iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

MINDY2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs148815862	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58797540	AGATTAATTTTACCT[A/G]TTTATTTTGACCTTT	54629
rs148852334	snp	G/T	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58829819	ATAATTATAGTGTGG[G/T]AAGTTTTTACAACCA	54629
rs148901278	snp	A/G	0.0102456	0.0708367	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771453	GTGGCGGCCGGGCCA[A/G]CGTCAGGGACAGGTT	54629
rs148911577	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58852972	TTTTTTTTTTTTTTA[A/T]GACAGAGTCTCACTC	54629
rs148921386	snp	A/T	0.00676609	0.0577691	intron-variant	FAM63B	GRCh38.p7	15:58817837	GCCATCTACTTTTGA[A/T]ACCAGTTTGGTTTAT	54629
rs148937869	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58784032	CTTGTGCTTATATTA[A/G]TAATTTTCCAGGGCC	54629
rs148974305	snp	C/T	0.00755907	0.0610114	intron-variant	FAM63B	GRCh38.p7	15:58821970	GTAACCATCCATAGG[C/T]TGGGCACAGTGGCTC	54629
rs148987164	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58798760	CACGCCCAGCAATCC[A/T]GTAAATATTCACTGA	54629
rs149009858	snp	A/C	0.0197687	0.0974348	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856590	GTATCTTGATTATAA[A/C]CTAGAATATGTATAC	54629
rs149057459	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58800058	ACGCTATAAAGCGAG[A/G]TCAATGTTGAAGCAT	54629
rs149114298	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58804463	AATTCATTTTACTTT[C/T]GTTGCCTAATCCTGA	54629
rs149125338	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58788428	CTAGGATGTAAAATA[C/T]TTACATTAGTAAGCA	54629
rs149150607	snp	A/G	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58837779	GAGACCAGCATGGAC[A/G]ATGAAGTAAGACCTT	54629
rs149179281	snp	C/T	0.0185938	0.0946107	intron-variant	FAM63B	GRCh38.p7	15:58792554	GACGTTGCAGTGAGC[C/T]GAGATCATGCGATTG	54629
rs149204761	snp	C/G	0.00795532	0.062565	intron-variant	FAM63B	GRCh38.p7	15:58842056	GATTACATAGCCCCT[C/G]TCTAGATCACATAGC	54629
rs149236816	snp	A/G	0.00993419	0.0697739	intron-variant	FAM63B	GRCh38.p7	15:58819239	GAATTGCTTGAGCCC[A/G]GGAGTTTGAGACCAG	54629
rs149252936	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786812	CTTGATTTTTTATAG[C/T]GTCCGTTTCTTTACT	54629
rs149293201	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58823876	AAAATTCCACTCACT[A/G]GAAGTTTGCATTCCT	54629
rs149329268	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859445	AATGTGAAGTTAAAT[C/T]CCTTTTAGAAAGTGA	54629
rs149374496	snp	A/G	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58775793	AAATGTCCAGTGGGG[A/G]GCATAAAAATATAAA	54629
rs149377776	snp	C/T	0.00517822	0.0506191	intron-variant	FAM63B	GRCh38.p7	15:58801175	AACAGGATTTCACCA[C/T]GTTGGCCAGGCTGGT	54629
rs149411975	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58811183	CAAAGGTCAAACCTC[C/T]CTTTGGGCAAGACCG	54629
rs149469623	snp	C/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58815566	GTTGCCCAGGCTGGT[C/G]TGAAACTCCTAGCCT	54629
rs149553731	snp	A/C	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58798664	TTTCATCATCTTGGC[A/C]AGGCTGGATTCAAAC	54629
rs149589736	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58831512	ATGAAATCCTTTGTA[A/G]TAGTAGGTGAAGTAT	54629
rs149645460	snp	A/G	0.00557542	0.0525036	intron-variant	FAM63B	GRCh38.p7	15:58836302	TGGAGTGCAGTGGCT[A/G]CTATCATTCTCAGTA	54629
rs149665785	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58829679	TACAGATATTACAGA[C/T]GGCAGTGGTACTTTT	54629
rs149694311	snp	C/T	0.0170251	0.090679	intron-variant	FAM63B	GRCh38.p7	15:58778851	GGAATCTCATTTAGT[C/T]GCCCAGGCTGGAGTG	54629
rs149703845	snp	C/T	0.0170251	0.090679	intron-variant	FAM63B	GRCh38.p7	15:58778816	TCTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTG	54629
rs149766678	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58850570	GGGAACTTTTTAAAA[A/G]ATTCTTTAAACCAAT	54629
rs149783080	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817462	TGGGCGCAGTGGCTC[A/G]CACCTGTAATCCCAG	54629
rs149824002	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856280	TTTTTTGTGTGTGGT[C/G]TGGGGTGACAAAAGA	54629
rs149893910	snp	C/T	0.0162398	0.0886349	intron-variant	FAM63B	GRCh38.p7	15:58843519	GTGCTTTCCTCCATA[C/T]TGGATCACAAAAGAA	54629
rs149908345	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58834004	TCCCTGCAGCCTTCC[A/G]CAGTGTTTTGTGTCT	54629
rs149993648	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58788338	TTAGAGCAGTGCTAC[C/T]GAAAGTGTGATTCAT	54629
rs150030755	snp	A/G	0.0189856	0.0955633	intron-variant	FAM63B	GRCh38.p7	15:58825990	TTCGTTAATTCAAAT[A/G]TTTATTGAGCCTTTA	54629
rs150046817	snp	A/G	0.0256215	0.110247	intron-variant	FAM63B	GRCh38.p7	15:58792463	ACATAAAAATTAGCC[A/G]GGCGTGGTGGCACAT	54629
rs150064127	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58773222	TCTGGAGGCTGACAC[A/G]AGACAATCGCTTGAG	54629
rs150084954	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853279	TTTTGATTCAGATAC[A/G]TAAGAAATTCTGATT	54629
rs150135213	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770651	CCCTTTCCTGTAGGG[C/G]GAATGTCTCACCAGT	54629
rs150138435	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858550	ATTAATGTTCACATG[G/T]GAACTACATATCTAA	54629
rs150140311	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797790	GAGACAAAATGAGCT[C/T]TTTTGCCATGAGTTC	54629
rs150170545	snp	C/T	0.0700422	0.173537	intron-variant	FAM63B	GRCh38.p7	15:58807651	TACAGGCGTGAGCCA[C/T]TGCGCCCGGCCTAAA	54629
rs150207762	snp	C/T	0.0103295	0.0711199	intron-variant	FAM63B	GRCh38.p7	15:58844847	TTGAACCCAAGAGGC[C/T]GAGGCTGCAGTGAGC	54629
rs150223890	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810760	CAGTTCATTACAGGG[C/T]AAAGATACAGGTTAA	54629
rs150226179	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835951	GGGTCTTGCTGTCAC[C/T]CAGGCTGGAGTGCAA	54629
rs150260870	snp	C/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58789739	CGCAACCTCCACCTC[C/G]TGGGTTCAAGTGATT	54629
rs150310692	snp	C/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58794032	TTAACCAGAGCTGGA[C/G]TTTTGCCTGATGAGC	54629
rs150335083	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58776880	AAAATTATAATAAGG[-/A]AAAAAGAGAGGTAGA	54629
rs150346838	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826959	TCCTTTTTTGTCGTT[C/T]ATGACATTGACTTTT	54629
rs150470952	snp	G/T	0.0185938	0.0946107	intron-variant	FAM63B	GRCh38.p7	15:58819004	TTGTTTTAGAGACAG[G/T]GTCTTGCTGCATTGC	54629
rs150500966	in-del	-/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857878	CAGAGTCTAAGTATA[-/T]TCCTTAAGGTTAGTA	54629
rs150526364	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58846322	ATGTAGGCCAGGCGC[A/G]GTGGCTCACGCCTGT	54629
rs150580878	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58792106	CATTGATAACCTTGA[C/T]GAGTGTATGGAATGA	54629
rs150612380	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800940	CTGGAAGGGTAGAGA[A/C]AGATTAACCAGTTGA	54629
rs150700550	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58839034	CACCTCCAGTTTCTT[C/T]ACTGGTTGTACCAAT	54629
rs150731431	in-del	-/TGTGTGTGTGTGTA			intron-variant	FAM63B	GRCh38.p7	15:58791649	GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTA]TGTGTGTGTGTGTAA	54629
rs150753685	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58782083	AAATTTTTATTTGCT[A/G]GAGCCAGAATTAAAG	54629
rs150805309	snp	C/G	0.0146672	0.084371	intron-variant	FAM63B	GRCh38.p7	15:58788039	ATTACCCAGTCTCAC[C/G]TTTCTGAAGTGCTAT	54629
rs150876792	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773031	CCTGTCAAATGAAGT[A/G]TCTCATTTAAGCTTG	54629
rs150879173	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58861995	GATTCACATTTACCT[A/G]TAACTCTTAGAATAT	54629
rs150914375	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58809073	AAACATTAGCTGGGC[A/G]TGTTAGCATATACCT	54629
rs150934206	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58803114	AAGCATAACTCATTT[G/T]TCTTGCAAAATTTCT	54629
rs150984593	snp	C/T	0.0341408	0.126114	intron-variant	FAM63B	GRCh38.p7	15:58807448	GCAAGCTCCGCCTCC[C/T]GGGTTTACGCCATTC	54629
rs151020531	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58840281	TTTATTGCACAGGAC[A/G]TTTTCCCTGACCACA	54629
rs151046532	in-del	-/AAAT	0.0107246	0.0724382	intron-variant	FAM63B	GRCh38.p7	15:58817731	TGTCTCAAAAAACAA[-/AAAT]AAAAAAATAAAAGTT	54629
rs151075332	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58785065	TAAAAAGACAAAGGA[A/G]TACAAGCCTTATTAG	54629
rs151113007	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822628	TTTTTCTAATCCTTA[A/G]CTAACTGGAATTCCT	54629
rs151198751	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774784	AGAAAAGGGTTTCTT[C/G]TACTTGGAACCTTCA	54629
rs151265753	snp	A/G	0.00517822	0.0506191	intron-variant	FAM63B	GRCh38.p7	15:58825082	AAATACCTCAAAGCC[A/G]ACTTGTTTCTAATCT	54629
rs151270452	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58848619	GGCATGGTGGCGGGC[A/G]CCTGTAGTCGCAGCT	54629
rs151286572	snp	C/T	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58814092	ACAGGCGCCCACCAC[C/T]ATGCCCAGTGAATTT	54629
rs151320209	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58852078	GATTGCTTGAGCCCA[G/T]GAGTTCGAGACCAGC	54629
rs180678659	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58783182	CACCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA	54629
rs180723687	snp	C/G	0.0111196	0.0737302	intron-variant	FAM63B	GRCh38.p7	15:58850932	AGCTTTCTTGGCTGC[C/G]TATATATGGCTTCCA	54629
rs180752025	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815547	AGAGACAGGATTTCA[A/C]CATGTTGCCCAGGCT	54629
rs180761720	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58830339	TGTTGATTCACTAGC[A/G]TTAAACTCACAGCCA	54629
rs180769839	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58799988	TTAAGAAAAATAATA[C/G]AGATGGTGGCATTGT	54629
rs180887897	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833731	AAGGCGGTTTTCCCC[C/T]GTCTCAGTAGATGGA	54629
rs180889119	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58845204	TGAGGTCAGGAATTC[A/G]AGACCAGCCTGGCCA	54629
rs180913433	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828220	GGCATTTGTCATTAA[A/G]ATAAATTGTTTTGCC	54629
rs180914902	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797513	ACCCTATCTCAAACA[A/C]ACAAACAAAAAAGAT	54629
rs180956441	snp	A/C	0.00478085	0.0486577	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855237	TAGATAGCAAAAATA[A/C]AGATTTGTATTTCTT	54629
rs181028516	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804936	AGTTCAAGACCAATC[C/T]GGGTGTGATATAGTA	54629
rs181052299	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58818612	TGACATCTTTTTTTA[C/T]TGGTACTCTAGAGAA	54629
rs181055264	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787449	AATACAGTAAAGACT[A/G]GTTATAGGCTGGGTG	54629
rs181066814	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770510	GCTTCCCACTCCATG[A/C]AAAGTGAAGCCAAGT	54629
rs181117845	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823178	GTTTCACTCTTGTTG[C/T]CCAGGCTGGAGTGCA	54629
rs181137563	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58808483	GCCTTTTCATATTAG[C/T]TTGTTTTCTTTACTA	54629
rs181142876	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773839	ATAGAATGGATATTG[C/T]GTGTTTATATGTTTA	54629
rs181197292	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816100	TAAATATTGACTGAT[A/G]GAATGCAGCATACAT	54629
rs181204720	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784317	GAGGACAGTGAGAAC[A/G]TGATGTCTTAAAAAT	54629
rs181209468	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838877	TGAGCCACTGAGCCC[A/G]GCCTAATTTTTATTA	54629
rs181217640	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860170	TGTAATATCCTGCTT[C/T]GAGAAGAAAGAATGC	54629
rs181225050	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58801560	AAAAGTTGCCACATA[C/T]ACCAAAAGGTTATAC	54629
rs181278684	snp	A/G	0.00755907	0.0610114	intron-variant	FAM63B	GRCh38.p7	15:58851672	GTGTATTTTTTAATA[A/G]CCATTCTTACAGCTT	54629
rs181334644	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830618	GAACGAAACCTATCT[A/T]GCACATGTATTTTCT	54629
rs181432504	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58827311	ATTTGGCATCCATTG[A/G]TTCTTGCCTGAATCA	54629
rs181437489	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805738	AGAGTTTAAAACCCT[G/T]TTAAAATAAGTTTGT	54629
rs181443513	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770714	AACCGACAGAGACTG[C/G]AATTTGTGCAGTGCA	54629
rs181445346	snp	A/G	0.00835141	0.0640778	intron-variant	FAM63B	GRCh38.p7	15:58811574	AACACAGCAAGATTG[A/G]TTAGTAAAGCACAGA	54629
rs181445585	snp	G/T	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58843747	GCTGAGGCAGGAGAA[G/T]GGCGTGAACCTGGGA	54629
rs181446918	snp	A/G	0.0158469	0.0875917	intron-variant	FAM63B	GRCh38.p7	15:58787671	GAACCGGAGAGGCGC[A/G]GCTTGCAGTGAGCCG	54629
rs181476535	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795911	TAAGATAGGAGAAAG[C/G]CCAGTACAGAGTGGT	54629
rs181524714	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855412	TGTGATTGAGTGTAT[A/G]GAGGAAAGCACAGTG	54629
rs181562095	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860678	GAAATACCTTACAAA[A/G]CAGTTCTAACTAATG	54629
rs181576323	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809036	GGTAACATAGTGAGA[A/C]CCCGTCTCTACAAAA	54629
rs181580621	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58823350	GCTGGGAGGTTTATG[C/T]TATTCTTCTACTTGC	54629
rs181619371	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778180	AACATACATACAAAA[A/T]ACTTACATGTAACCT	54629
rs181644581	snp	C/T	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58834418	AGCTACTTCTACTCT[C/T]CTCAAACCAGTGGTT	54629
rs181743414	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781967	TAGATTCACTGAAAA[C/G]TCTGAATTTGAGTAT	54629
rs181880528	snp	G/T	0.00953873	0.0683987	intron-variant	FAM63B	GRCh38.p7	15:58799438	CAGGCGTGGTGGCGG[G/T]TGCCTGTAGTCCCAG	54629
rs181882856	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58786849	TTTATTTTTTATTGA[A/G]ATGGAGTTTCACTCT	54629
rs181885443	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58829801	AGTCCTTGCAATAGT[A/G]TGATAATTATAGTGT	54629
rs181885849	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58804594	AGGCGGATTGCTTGA[A/G]CCCAGTAGTGAGACC	54629
rs181890023	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58773998	CCCTAATCTTTTTTG[G/T]AGGAAGGAATAACTA	54629
rs181961334	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769774	CAGTGAGCCGAGATC[A/G]CGCCACTGCACGCCA	54629
rs182004201	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58849713	ATGAGATAGTCATGC[C/T]ATATATATGACAAGA	54629
rs182018323	snp	C/G	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58811761	GGAATTCCAGTTGCT[C/G]CAGTCCATAGAGGTT	54629
rs182021898	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58778835	TTTTTTTTTTTGAGA[C/T]GGAATCTCATTTAGT	54629
rs182084521	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785014	TCTGTATTCTTAGCC[A/G]ACTATCTCATAACCT	54629
rs182088030	snp	C/T	0.00163735	0.0285656	intron-variant	FAM63B	GRCh38.p7	15:58802305	CAATTCTTTTTTTTT[C/T]TTTACAGGAGATTAC	54629
rs182090229	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58844468	GAGGCGGGAGAATGG[A/G]GTGAACCCAGGAGGC	54629
rs182135956	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792439	GGTAAAACCCCGTCT[C/T]TACTAAGAACATAAA	54629
rs182163466	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815084	TAGTTTTAGCACTTA[C/T]ATTTATGAATATGGT	54629
rs182245800	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861595	TTGTTTTAAATACTA[A/G]TTATTTTAAAACTAC	54629
rs182305283	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827823	AATGTGATATGGCCA[A/G]TGGGATGCCCTCAAG	54629
rs182319467	snp	A/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58796782	CCTGCCTTGGCCTCC[A/G]GAAGTGCTGGGATTA	54629
rs182436667	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769329	CTTGGGAGGCTGAGG[C/T]AGGAGAATCACTTGA	54629
rs182451519	snp	C/T	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58778886	GGCACGATCTTGGCT[C/T]ACTGCAACCTCTGCC	54629
rs182458087	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792574	TCATGCGATTGCACT[C/T]CAGCCTGGGCGACAG	54629
rs182584750	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775258	TAGATATAGATAGAT[A/G]TCCACATAGATGAAA	54629
rs182590318	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806717	CAAAAATAGAGGAAA[A/G]TCTGGTGGTTGTAAA	54629
rs182620597	snp	A/G	0.00159689	0.0282116	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771706	AGGCGCCTCTGAGAG[A/G]GCAGTACAAGGTGAC	54629
rs182643623	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840666	TATTATTATTATTAT[C/T]ATTATTTTGAGATGG	54629
rs182669947	snp	A/G	0.00795532	0.062565	intron-variant	FAM63B	GRCh38.p7	15:58793437	GCCTGGGCGACAGTG[A/G]GAAACTGTCTCAAAA	54629
rs182676700	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809791	GTCTTGTTTTGTTTC[A/G]TTTTTTGAGACAGAG	54629
rs182677940	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58840113	TGCTAGGATTACAGG[C/T]GTGAGCCACGCGTTT	54629
rs182679495	snp	C/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58809249	ACTTCCCCCAGTCCC[C/T]TGGAAACAACCATTC	54629
rs182691466	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774593	CATATAAACAATAAT[G/T]ACAGTGCAATGTGAG	54629
rs182778648	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837901	TTGAGTCCAGGAGAT[C/T]GAAGCTACAGTTAAC	54629
rs182790173	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58846809	ACAAAAGAAGTACAC[G/T]GATAATACAAACTAG	54629
rs182793033	snp	C/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58821226	CATATCTCCACTATA[C/T]TTTTCTAGGAAATAA	54629
rs182803916	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58807188	AGTCTACTGTTCTTA[C/T]TTTGTGTCTTTAGTA	54629
rs182806553	snp	G/T	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58853593	TGGGAGGCCAAGACA[G/T]GTGGATCTCGAGGCC	54629
rs182877793	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58820405	GCCGAGGTCACACCA[C/T]TGCACTCCAGCCTGG	54629
rs182886025	snp	A/C	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58788680	ATCACCAAATAGGAA[A/C]TCTTAATCCATATTC	54629
rs182909907	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789637	TAATTTTTGGGTTTT[G/T]GGTTTGTTTTTGTTT	54629
rs182910995	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801819	TAATTTTTGTATTTT[A/T]AGTAGAGTTGGCCAG	54629
rs182925950	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784528	GTGCCTTTGTATATG[A/T]TAAAGTACTTATTTA	54629
rs182932676	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857082	ATTCAGCCTTTTTCT[A/G]TGTAATATTTCCAAG	54629
rs183049102	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58825288	GATAACATTTGCTTT[C/T]CTTGATTCTAATGCC	54629
rs183101778	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58841928	TATACATATGATCAT[C/G]ACTGTTGGATTCCTA	54629
rs183106498	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859062	TGCACACTTTTTTCT[C/T]AATAACAAAATATAT	54629
rs183136154	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828510	CATTCATCACTTTCA[C/T]GTTCTCTAATAACTG	54629
rs183158876	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788553	CAAAACAGACCAGTA[A/G]TACAGTTTGTAGACT	54629
rs183161336	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806388	TTTGAGACAGGGTCT[C/T]ACTCTGTCACTTTGT	54629
rs183227060	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780561	GACAGTAGGTCTGGG[A/G]CAAAACAGGGTGGGA	54629
rs183228245	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856573	TAGAAAATATTTAAT[A/G]AGTATCTTGATTATA	54629
rs183232469	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820031	AGCACTTTGGGAGAC[C/T]GAGGCAGGCAGAGTA	54629
rs183232659	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835831	AGTGTCCCTGAAACA[G/T]AGCAAGTAAAAGGAA	54629
rs183242404	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832288	CTGGAGTGCAATGGC[A/G]TGATCTCGGCTCACT	54629
rs183305600	snp	A/G	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58798519	ATAGTGCAATGGCAC[A/G]ATCTTGGCTCACTGC	54629
rs183406554	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58853153	AGATGAGGTTTTACC[A/G]TATTGGCCAGGCTGG	54629
rs183415077	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58831201	AAATGGCATAAAAAA[A/C]CATTAAAAATGGCAT	54629
rs183432588	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58810601	TAGGGCCCAACTACA[A/G]GGTTAGAGGGAAGAG	54629
rs183463109	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58776508	GGAAAGAGAATGTAA[C/T]AAAAATGTAGTACAT	54629
rs183511662	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58813233	GGCACGGTGGCTCAC[A/G]CCTGTAATCTCAGCA	54629
rs183541414	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780159	ACTGTAATCCCAGCA[C/G]TTTGTGAGGCCGAGG	54629
rs183636584	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781407	ATTCTTTATTGCTCT[A/T]AAACACTTTGAAGTG	54629
rs183685063	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58829053	TTGAATCAATAACAC[C/T]TCTTTGAGCGTTATA	54629
rs183693111	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58816529	TCCCACCTCAGCCTC[C/T]CAAGTAGCTGGGGCT	54629
rs183695905	snp	A/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58814713	TGTGTCTTTTTGTAA[A/T]TGAGTTGCAAATGTT	54629
rs183700231	snp	A/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58793837	GGAGGAGTTGTTGAA[A/G]GTAAGAGGGAAGGTA	54629
rs183700317	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58848700	GCAGCGAGCCGAGAT[C/T]GTGCCACTGCACTCC	54629
rs183701393	snp	G/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58852269	CTCCAGTCAGGATGA[G/T]AGAGCAAGACTCCTT	54629
rs183826351	snp	C/G	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58826998	TCCAGGCCAGTTGTT[C/G]CACAGAATATTCCTC	54629
rs183835563	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811491	GTGTAGCATCTTAGA[A/C]CTAGCAACAGCAGAA	54629
rs183839766	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847106	GTGTGCCAATTATAA[A/C]CTATATTCAAAGCCG	54629
rs183843521	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843529	CCATATTGGATCACA[A/G]AAGAACACGGAATGA	54629
rs183850194	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58814285	CTGAACATCTTTTGA[G/T]GTGCTTGTTTGCCAT	54629
rs183945899	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58795316	CTTTCTTTTCGTTAT[A/T]GCCATTCTGAGGGGC	54629
rs183966605	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58778064	GGTATATAACATATA[C/T]ATTTTAGTGCTTACA	54629
rs184011596	snp	G/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58828648	CTCACTGAAAGCTCC[G/T]CCTCCCAGTTCACGC	54629
rs184027654	snp	A/T	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58798643	GTATTTTTAGTAGAG[A/T]TGGGGTTTCATCATC	54629
rs184392384	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58843772	CTGGGAGGCGGAGTT[C/T]GCAGTGAGCCAAGTC	54629
rs184400891	snp	C/T	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58838351	TGTAGTGAGCCAAGA[C/T]CATGCCACTGCACTC	54629
rs184425908	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808044	CCTCTCTCCCTCACT[A/C]CCTTCCTTCCATCCT	54629
rs184440265	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58773433	AAACCTTGCCATTGT[C/T]TGGTGCATAATGGCA	54629
rs184538642	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822398	ACTTTGGTATGGTCA[C/G]GTACCCAGAGGTTAC	54629
rs184540035	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859890	GGGTAAAATTCTTCA[A/G]CTATTGCCTCAAGTT	54629
rs184540580	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769646	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	54629
rs184540791	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58786346	CTTCTATCACTGATA[C/T]AGTAATTACTTTGAG	54629
rs184573598	snp	G/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58790472	GTAACAGCAATTTTG[G/T]TTTTTGCCATGAGTA	54629
rs184608293	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817707	AGCCTGGGCGACAGA[G/T]CGAGACTCTGTCTCA	54629
rs184622062	snp	G/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58803197	GTTGGCTGGGCGTGG[G/T]GGCTCAAGCCTGTAA	54629
rs184726146	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817141	AAACTGAGAATTTGT[A/G]TTCATCTAAAGGCAT	54629
rs184732886	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785803	TGCCTCAGTCTCCCA[A/G]GTAGCTGGGACTACA	54629
rs184750419	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58838240	CCATCTCTACTAAAA[A/G]TACAAAAACTAGCTG	54629
rs184760645	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58799846	AATAAAGTAAGGTGT[A/G]GAAGAGATGTAGGGA	54629
rs184763782	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815197	TACCATTTGCTGAAA[A/T]GGTTATTCTTACCCT	54629
rs184763810	snp	C/G/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859703	GGTAAATTTAACTTA[C/G/T]TTTGAATATCTATCT	54629
rs184825399	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58776768	GGCTCATGCCTGTCG[A/T]CCCAGCATTGTGGGA	54629
rs184852276	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58802842	CACATTTCTTGGCAT[A/G/T]TTCTTTAGAGATCCT	54629
rs184874856	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58822215	GCCGAGATTGCGCCG[C/T]TGTACTCCACCCTGG	54629
rs184877198	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782325	AGTGAAATTTTGACT[A/T]TTATTTAGTGCGTCC	54629
rs184881706	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769596	GGGCCGAGGTGGGCA[A/G]ATCACGAGGTCAGGA	54629
rs184896909	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829585	TGTCTTTTTGAAAGG[A/G]ATCTGTGGAGAGGAT	54629
rs184911379	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798959	CTGAGGAAGCAGAAC[A/G]TAGGACAGATAATTT	54629
rs184998941	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849168	TGAGCCAAGATCATG[C/T]CATTGCACTCCAACA	54629
rs185003709	snp	C/G	0.0115144	0.0749975	intron-variant	FAM63B	GRCh38.p7	15:58814952	CTGGACTTAATTTCA[C/G]TGAAGTTCACTTTAT	54629
rs185015322	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781856	GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	54629
rs185017874	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58818199	TTGTGTCTGTAGATT[C/T]TCTAGTGGCACCTTG	54629
rs185090945	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854855	ATTCATGAAAAATAC[C/T]GCACTTGTAGCCAGA	54629
rs185097202	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58833695	GCAGTATTGCTGCCA[C/G]CATGTCCCATCTTCA	54629
rs185238502	snp	C/G	0.0170251	0.090679	intron-variant	FAM63B	GRCh38.p7	15:58811634	AGAGGAATACTACCC[C/G]CAAGCTATGGCCCAG	54629
rs185241689	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58850956	GCTTCCAGAAAAAAT[G/T]TCAAATACATTCCCC	54629
rs185251300	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830514	CAGTATAATGCAGAC[A/G]TTCCAAAATCCAAAA	54629
rs185258587	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58832536	CCCAGACTTTTTTTT[C/T]TTTCTTTCTTGAGAC	54629
rs185336836	snp	G/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58854108	AGTTAGCCAGGCGTG[G/T]TGGCAGGTGCCTGTA	54629
rs185357749	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827567	CTTCCGGGTTCATGC[C/T]GTTCTCTTGCCTCAG	54629
rs185367361	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58815772	GCAACCTCCATCTCC[C/T]GGGTTCAAGTGATTT	54629
rs185367605	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58774707	CTGTGAACTAGATCC[A/G]AAGGATGAGTGAGAG	54629
rs185373674	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58793296	TCTCTACTAAAAATA[C/T]AAAAAATTAGTCGGG	54629
rs185374778	snp	C/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58849840	TCCACCTCCCAGGCT[C/T]AAGCAAACACCTCAG	54629
rs185381780	snp	G/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58800236	CCCATTAGTAGCAAG[G/T]TTTTCTTAATTCTTT	54629
rs185395525	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784180	AAAATACAAAAATTA[C/G]CCAGGTGTGGTGGTG	54629
rs185509894	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58812270	GTGAAACCCTGTGTC[C/T]ACTAAAAAATACAAA	54629
rs185520787	snp	C/T	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58828257	TTTGAGGAAAAAATA[C/T]ATTAATGTATTTGAT	54629
rs185522857	snp	A/G/T	0.0111196	0.0737302	intron-variant	FAM63B	GRCh38.p7	15:58798327	AGATGGGATTTGTCT[A/G/T]TGTTGGCCAGGCTGA	54629
rs185524144	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789937	CAGGCGTGAGCCACC[A/G]TGCCTGGTTAAGTTT	54629
rs185529602	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829831	TGGTAAGTTTTTACA[A/G]CCACTTTGTAGCTTG	54629
rs185539156	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58779642	TCCTGTAAAAAGAGA[C/T]TAAAACTTCACACAA	54629
rs185581416	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58808849	GACCTCGTGATCCAC[A/C]CGCCTCAGCCTCCCA	54629
rs185584700	snp	C/G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58845968	CACACTTCGCATGTT[C/G/T]TTTCTTATTTTTGCG	54629
rs185586244	snp	A/T	0.00676609	0.0577691	intron-variant	FAM63B	GRCh38.p7	15:58773855	GTGTTTATATGTTTA[A/T]TACATGACAGAAGTG	54629
rs185639027	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58807557	TTTAGTAGAGACGGG[A/G]TTTCACCGTGTTAGC	54629
rs185658797	snp	C/T	0.00398564	0.0444627	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860488	TTGAGGCGCAAGAAT[C/T]GCTTGAACCCGGAAG	54629
rs185661631	snp	A/G	0.0111196	0.0737302	intron-variant	FAM63B	GRCh38.p7	15:58826476	TCAGGTGATCCGCCC[A/G]CCTTGGCCTTCCAAA	54629
rs185663035	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823209	ATGGCGCGATCTCAG[C/T]TCACTGCAACCTCCG	54629
rs185668684	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839036	CCTCCAGTTTCTTTA[C/G]TGGTTGTACCAATTT	54629
rs185674299	snp	A/G	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58773160	CAAAACAAACTGGGT[A/G]TGGTGGTGTGCGCCT	54629
rs185678283	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769851	CAAATTAGCCAGGCA[C/T]GGTGGCGGGCGCCTA	54629
rs185701594	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58794434	TGGAGAAGAGGTCAA[A/G]GAACAGACAGGCAGG	54629
rs185803041	snp	A/G	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58787182	TCTGTTGCCCAGGCC[A/G]GAGGTGTCACCATGT	54629
rs185809592	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842667	AGATAGACACAGAAA[C/T]TGAGATCGATTTAGA	54629
rs185810794	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58819583	GAACTCCCGGCCTCA[A/G]GATACCCTCCTGCCT	54629
rs185816511	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834736	GTGGCTTATTAAAGT[C/T]GTGAATTACATCTTC	54629
rs185819856	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58811064	AGGGATCCATCATTA[A/G]TATAAACTGCAGGTG	54629
rs185892873	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840526	GCCCTAATTTCTGCT[A/G]TCATTTATATCACTT	54629
rs185898740	snp	A/C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58809538	CGTGGGTGTACAACT[A/C/G]TCTCTTCAAGATCCT	54629
rs185921596	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806200	TGCCTCAGCCTCCCA[A/G]TTAGCTGGGATTACA	54629
rs185931828	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770729	GAATTTGTGCAGTGC[A/T]GTAATCCAAAGCCGT	54629
rs185935738	snp	A/G/T	0.000106201	0.00728632	intron-variant	FAM63B	GRCh38.p7	15:58787881	AAAACATTTAATTTT[A/G/T]TAGAAATAATATTTT	54629
rs185988984	snp	C/G	0.00119737	0.0244387	downstream-variant-500B	FAM63B	GRCh38.p7	15:58861964	GATGAGCGGGGAGAT[C/G]GGGAACTGACATATT	54629
rs186012469	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824545	TACAAATTTGTAGTT[C/T]ATTTGAAATAATTAC	54629
rs186079412	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839427	ACCTCCACCTCCCCG[A/G]TTCAAGTGATTCTCC	54629
rs186140490	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860706	ATGCAATGTGTTTTT[A/T]AAAAATTTTTAATGA	54629
rs186172724	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855258	TGTATTTCTTTTCCA[A/G]TAGCAAAAAGTTACA	54629
rs186190316	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58818697	TTGTTCTTGCTACCC[A/T]GGTGTGATCTCGGCT	54629
rs186200525	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58787454	AGTAAAGACTGGTTA[C/T]AGGCTGGGTGCAGTG	54629
rs186294774	snp	A/T	0.00795532	0.062565	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856950	TGCTGCCATACTGCA[A/T]TCCCTCTGGAAGGAA	54629
rs186298397	snp	A/C	0.00557542	0.0525036	intron-variant	FAM63B	GRCh38.p7	15:58833999	AGAGGTCCCTGCAGC[A/C]TTCCGCAGTGTTTTG	54629
rs186328019	snp	A/C	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58804991	AAGAAAGAAAAATAA[A/C]AATGCTTGCAAATGT	54629
rs186430015	snp	C/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58835914	TTTTTGTTTTGTTTT[C/G]TTTTGTTTTGTTTTT	54629
rs186432802	snp	C/G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58820180	CTGAGGCAGGAGAGT[C/G/T]GCTTGAACCCAGGAG	54629
rs186486998	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770519	TCCATGCAAAGTGAA[G/T]CCAAGTTAGCAAAAC	54629
rs186519049	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778839	TTTTTTTGAGACGGA[A/G]TCTCATTTAGTCGCC	54629
rs186519804	snp	A/G	0.00755907	0.0610114	intron-variant	FAM63B	GRCh38.p7	15:58801576	ACCAAAAGGTTATAC[A/G]TATATTTAAAAGGTG	54629
rs186582708	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58853512	AATTCTCAGGGGTTC[C/T]TTTCTCCTTTTAAAA	54629
rs186586204	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816835	TGGCATCCCTGTAGT[C/T]GCAGTTACTCAGGAG	54629
rs186589534	snp	A/G	3.84349e-05	0.0043836	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831944	AATAGCTATTTAATC[A/G]TGATTCTAAATCAAA	54629
rs186590585	snp	C/G	0.0154538	0.0865337	intron-variant	FAM63B	GRCh38.p7	15:58796903	CAGCTCTTCCATATC[C/G]ATCCACTCTCCACCC	54629
rs186623118	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811082	TAAACTGCAGGTGTG[A/G]CCCAAGGGGCCCACA	54629
rs186737312	snp	A/G	1.67172e-05	0.00289108	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851839	TTGGGAACAAATCCC[A/G]GAAGGAATCAGTGAT	54629
rs186749184	snp	A/C/G	0.00478244	0.0486902	intron-variant	FAM63B	GRCh38.p7	15:58816276	ATTTCACTGAAAAGT[A/C/G]TCAACATGTCCAGCA	54629
rs186754108	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784343	AAAATAATAATAATA[A/G]TTTCCTCAGGAAATC	54629
rs186845813	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58778633	GGCTAATTTCCTTTT[C/T]TTCTTTTTTTTGAGA	54629
rs186885475	snp	A/T	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58814776	GATATATGACTTGGA[A/T]ATATTCTTTAATTTT	54629
rs186885869	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848823	AAACAGTTCTGAAAG[C/T]CGTGCTCATTTTCCT	54629
rs186892295	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829063	AACACCTCTTTGAGC[A/G]TTATAATGATTCTCT	54629
rs186898203	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798775	AGTAAATATTCACTG[A/G]GCATGTATTGTGAGC	54629
rs186908296	snp	A/T	0.00358779	0.0422022	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855631	AGACATTAATAAAAA[A/T]CTGAAAGGGCCGGGC	54629
rs187001612	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58823364	GCTATTCTTCTACTT[G/T]CAGTAAACATATAAA	54629
rs187009744	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792450	GTCTCTACTAAGAAC[A/T]TAAAAATTAGCCGGG	54629
rs187047659	snp	A/C	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58796275	GGTTGTTTGAGGGTT[A/C]GTTGGAAACTATCTT	54629
rs187083919	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58852515	AAAATAAGCCAATTT[A/G]GACGAAGTCCTTTCA	54629
rs187199817	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58841126	AGCTGGGATTATAGG[C/T]GCGCACCACCATGTC	54629
rs187202633	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809170	TGAGCCATGATCATA[A/C]CACTGCACTCTAGCC	54629
rs187225355	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58774249	GCATTTCGGGAGGCC[A/G]AGGCGGGTGGATCAC	54629
rs187323119	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824961	AGGCATAAGCCACCT[C/T]GCCCAGCCCATCATA	54629
rs187324510	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58793442	GGCGACAGTGAGAAA[C/T]TGTCTCAAAAAATAA	54629
rs187326324	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769626	AGATCAAGACCATCC[C/T]GGCTAACACGGTGAA	54629
rs187328932	snp	A/G	8.28631e-05	0.0064362	missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810318	TTCGAGTGTTTGAAT[A/G]TACACCAGAATGCAT	54629
rs187336717	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58775759	AAGTTGATGCCAAAG[C/T]TTGGTTGTGTTGAGT	54629
rs187384609	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806637	AAGGTATAAGCATGA[G/T]CCCAGAGCCATTAGA	54629
rs187416530	snp	A/T	0.0119091	0.0762411	intron-variant	FAM63B	GRCh38.p7	15:58828034	GGTCAGGAGTTCGAG[A/T]CCAGCCTGGCCAACA	54629
rs187447416	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58789881	TGAACTCCTGACCTC[A/G]GGTGATCCGCCCACC	54629
rs187454884	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58807258	AGTGTGTTAAATTTT[A/T]TGTATTGGTTTTTCT	54629
rs187457881	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772509	AGAAGGACTTAGAGC[A/G]TCTTAAATCTTATGA	54629
rs187500295	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859066	CACTTTTTTCTCAAT[A/G]ACAAAATATATCTTA	54629
rs187505412	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58838065	CTCTTTGGAACATCT[A/G]TCGCATAAATACATT	54629
rs187542648	snp	A/G	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58802205	TCAATTTTATATGTC[A/G]ACTATAGCTACAGTG	54629
rs187543066	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58785684	AAAAAATAATCTATC[C/G]AATTTTTTTTTAAAC	54629
rs187556754	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58784882	TCAAGTGATCCTTTC[A/C]CTTCAGCCTCCCAAA	54629
rs187592830	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842801	CTGTGAGGAGTGGAT[A/G]TTATTATTCTCACTT	54629
rs187625857	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58831057	TATATATATATATAT[A/G]TATGTTTTAAATTAT	54629
rs187639772	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816641	AGAGGCCTAAAAAGA[C/T]CACTATACAGATAGA	54629
rs187643089	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58844523	TGCCACTGCACTCCA[C/G]TACTCCAGCCTGGGC	54629
rs187655834	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58788604	GTTTAGAGAGCAAGC[A/G]GTTGTACATCACATT	54629
rs187675140	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812204	GTACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAT	54629
rs187796655	snp	C/G	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58789073	CCGGGCACGGTGGCT[C/G]ACGCCTGTAATCCCA	54629
rs187804519	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802653	TCTCATTCCATGAGA[G/T]ATCAAACCTAGTGTT	54629
rs187804657	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769489	TTCTCAGGTAAACAA[C/G]AATATAAGTATCCAA	54629
rs187837060	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857250	TTTCCTGCCCTTGAA[G/T]GGTATAAAGAATTTA	54629
rs187849218	snp	A/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58826496	GGCCTTCCAAAGTGC[A/T]GGTATTACAGACATG	54629
rs187860058	snp	A/T	0.0166325	0.0896639	intron-variant	FAM63B	GRCh38.p7	15:58820786	TGTGCAGATATATGT[A/T]GAGACCTGTGGTATT	54629
rs187909904	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58798702	TTCAGGTGATCCGCC[C/T]GCCTTGGCCTCCCAA	54629
rs187915913	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814307	GTTTGCCATTTGCAT[A/G]TTCTTTTTAGTAAAA	54629
rs187925739	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780966	TTATCAATTTTTGAG[C/G]GGGGAGATATTTCAG	54629
rs188019725	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58802993	GCTTCTTAGAGTGGA[A/T]GGAAGTATTAGCCAG	54629
rs188023775	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58832368	AGTAGCTGGGATTAC[A/C]GGCATGCACCACCAT	54629
rs188057226	snp	A/G	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58794583	AGGTGGGTAGATAAT[A/G]GGTAGAATTATCTGA	54629
rs188065278	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811197	CTCTTTGGGCAAGAC[C/G/T]GTATTCTTTATTGCA	54629
rs188067428	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58777187	TAGTTCGCTTATGTC[C/T]GGAAATAGGAGCAGG	54629
rs188155084	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806845	GTAAGCTGGTTGTTT[G/T]TAAGCGTTTAATTTT	54629
rs188161557	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781630	CTGATGGTGGCGAAG[C/T]GCAGTGGCTCATGCC	54629
rs188243968	snp	A/G	0.0154538	0.0865337	intron-variant	FAM63B	GRCh38.p7	15:58833710	GCATGTCCCATCTTC[A/G]GCCCTAAGGCGGTTT	54629
rs188260487	snp	G/T	0.0111196	0.0737302	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58855040	TTTTACAATGTTAAA[G/T]TATGATCTAATTCAT	54629
rs188270305	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58854029	GTGGGCGGATCACAA[A/G]GTCAGGAGTGTGAGA	54629
rs188279834	snp	A/C	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58846819	TACACTGATAATACA[A/C]ACTAGGTACAAAGTA	54629
rs188307979	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813734	TGCACCATTATGCCC[C/T]GTTAACTTGTGTATT	54629
rs188311431	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817199	AGAGTAGAAGATGAA[C/T]TGCAACTTTAAAAAA	54629
rs188319873	snp	C/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58780258	AAAAATACAAAATTA[C/G]CCGGGTGTGGTGGCA	54629
rs188416319	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58773568	AAGTTATATGAGACA[A/G]GTGGTAGGTAAACTG	54629
rs188422800	snp	A/C	0.00795532	0.062565	intron-variant	FAM63B	GRCh38.p7	15:58791452	AGACCCCCATCTCCA[A/C]TTAAAAATTCAAAAA	54629
rs188423597	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785825	GGGACTACAGGTGTG[C/T]GCCACCACACCTGGC	54629
rs188547524	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827126	TCAAATCGGGGGCAC[A/G]TGAGCCTGATTATCT	54629
rs188561129	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811515	AGCAGAAAATAATTG[C/G]CACTCCTAACTCTGA	54629
rs188561416	snp	A/G	0.0267878	0.112589	intron-variant	FAM63B	GRCh38.p7	15:58843742	AGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC	54629
rs188570951	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58828532	TAATAACTGTCCAGT[A/G]ACAGAGGAAAACAGT	54629
rs188573462	snp	C/G	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58795440	AGACGGAGTCTTGCT[C/G]TGTTGCCCAGGCTGG	54629
rs188609410	snp	A/C	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58798612	AAGCGCCTGCCACCA[A/C]ACCCAGCTAATTTTT	54629
rs188638781	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58825981	GGATATGTATTCGTT[A/T]ATTCAAATATTTATT	54629
rs188671470	snp	C/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58794038	AGAGCTGGACTTTTG[C/G]CTGATGAGCGTGTTG	54629
rs188778330	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860569	ACTGAGCGAGACTCT[C/T]ATATCTCAAAAAAAA	54629
rs188804820	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58828803	CCTGACCTCATGATC[C/T]GCCCGCCTTCCAAAG	54629
rs188807587	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58851050	GTGATCTCAGCTCAC[A/T]GCAACCTCTGCCTCC	54629
rs188866074	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58776517	ATGTAATAAAAATGT[A/C]GTACATTACTATTGT	54629
rs188907947	snp	A/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58841959	TCCTTACCTAATTCT[A/G]TATCCTAGATCTAGT	54629
rs188909316	snp	A/G	0.00517822	0.0506191	intron-variant	FAM63B	GRCh38.p7	15:58823316	TTTAGTAGAGATGGG[A/G]TTTTGTCATGTTGGT	54629
rs188911171	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58839394	TGGAGTGCAGTGGCA[C/T]AATCTTGGCTCACTG	54629
rs188918550	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792422	ACCAGCCTGGCCAAC[A/G]TGGTAAAACCCCGTC	54629
rs188923921	snp	A/C	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58808897	GTGGGAGCCACCGTG[A/C]CCAGCCACTTTTTCA	54629
rs188933458	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810801	GGAAAGAGACACATA[C/T]GGCAGAATCTAGGAG	54629
rs188935515	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58773947	TAAGGGCCCTCAACT[A/G]GGGAGTTAGTTAGAC	54629
rs188970477	snp	A/G	0.0136801	0.0815652	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771386	TAGAGCTGGGGGCGG[A/G]CGGCCCGGTATGGAG	54629
rs189098403	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847121	ACTATATTCAAAGCC[A/G]AGTGGATTTGAGGAA	54629
rs189155586	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58818365	CTGGGCTTAAGCAAT[C/T]CTGTCTCAGCTTCCT	54629
rs189160709	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787293	GCCACTGTGCCCAGC[C/T]CATTTCTTTACTTCT	54629
rs189199827	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58854138	AATCCTAGCTACTTG[A/G]GAGGCTGAGGCAGCA	54629
rs189206140	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58832605	CGTGATTTCAGTTCA[C/T]CGCAACCTCCGCCTC	54629
rs189314417	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822415	TACCCAGAGGTTACT[A/G]ATAATTACTTTCTTA	54629
rs189316255	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860168	ACTGTAATATCCTGC[C/T]TTGAGAAGAAAGAAT	54629
rs189321304	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58817788	GATGTGCAGCATAGA[G/T]AATTCTCATTCCTTG	54629
rs189338532	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58803768	TTGCAGTGAGCCGAG[A/G]TTGCGTCACTACACT	54629
rs189347162	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769665	TCTACTAAAAATACA[A/G]AAAGTTAGCTGGGCG	54629
rs189351088	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58786702	ATTGCAGGTCAAGAA[C/G]GTCGAAGAACAGAGC	54629
rs189368943	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770137	AGTGACAGACAGCAT[A/C]CAGCAACTTACTTGG	54629
rs189453565	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58804813	CCTGTTACAAAAAAA[A/G]AAAAGAAAAGAAAAG	54629
rs189472798	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58838282	GTGTGCCCGTAATGC[C/G]AGCTACTCAGAAGGC	54629
rs189482368	snp	A/C	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58830199	TTAGTGAATGCTGAA[A/C]CACTGTCCCTAGGAT	54629
rs189482513	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58799960	TGATGATGAGACTGG[C/T]GGGGGCGCATAGTTA	54629
rs189486427	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859769	GTGTTTTTGCTCTTA[C/G]ATGTTAGAGTTTAAT	54629
rs189503146	snp	A/G	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58782964	TTGCTCTGTCACCCA[A/G]GCTGGAGTGCAGTGG	54629
rs189533425	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856981	ACAAAACAAAACAAA[A/G]CTCACTCAAAACCAG	54629
rs189575411	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805143	TTGCATTTCTCATAA[A/G]CATATCAGGCAAAAA	54629
rs189582613	snp	A/C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58838701	AAGCGATTGTCCTGC[A/C/T]TCAGCCTCCCAAGTA	54629
rs189631133	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58778151	TTAGAAAGAATGTTA[C/T]AGGTTCTGAGGCCAA	54629
rs189659017	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834005	CCCTGCAGCCTTCCG[C/T]AGTGTTTTGTGTCTC	54629
rs189704809	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808045	CTCTCTCCCTCACTC[C/G]CTTCCTTCCATCCTT	54629
rs189811397	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797070	GTTATTGAGTCCTTG[A/C]AATGTGGCCAGTGTG	54629
rs189816001	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58828123	AGATAGCGCCACTGC[A/C]CTCCAGTCTGGAAAC	54629
rs189832674	snp	C/T	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58778875	TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG	54629
rs189932935	snp	A/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58818947	TGCCCAGCCTATTGA[A/T]CTTGTGTTTATTATT	54629
rs189941478	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855319	AGATATTAATGACTT[G/T]GTAGTGTTGTAAAAT	54629
rs189946449	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849322	CCTGGCTAACATGGT[A/G]AAACCCCGTCTTTAA	54629
rs189950570	snp	C/T	0.00597247	0.0543191	intron-variant	FAM63B	GRCh38.p7	15:58851047	GGCGTGATCTCAGCT[C/T]ACTGCAACCTCTGCC	54629
rs189956911	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830524	CAGACATTCCAAAAT[C/T]CAAAAGAATCCACAC	54629
rs189963029	snp	A/G	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58793309	TACAAAAAATTAGTC[A/G]GGTGTGGTGGCACAT	54629
rs189968381	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809604	CCTTCTTCCTCTTTG[A/T]CTTGAAAAACATTTG	54629
rs189972576	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58774823	TGAAGTGTGCAGCAT[A/G]GGAGGTAAACGAAAT	54629
rs189977969	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816020	AACTGTCATCTCCCA[C/G]TAGAATATAGGTTTT	54629
rs189982974	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814986	TTCTTTTGTCCCTTA[C/T]GCTTTTGGTGTCCTA	54629
rs190128854	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58787585	ACTAAAAATACAAAA[C/T]AATTAGCCAGGTGTG	54629
rs190135343	snp	G/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58827678	ACCGTGGTCTCGATC[G/T]CCTGACCTCGTGATT	54629
rs190136530	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770520	CCATGCAAAGTGAAG[C/T]CAAGTTAGCAAAACC	54629
rs190230492	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58799290	AAAGCAAACACGGCT[A/G]GGCGCGGTGGCTCAC	54629
rs190234947	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58829737	AGTATTCAATGAATT[C/T]CTTTTGGCTGTAGAC	54629
rs190248281	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58796561	ACTGGGTCTCTCTCT[C/G]TTGCCCAAGCTGGAG	54629
rs190298717	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58846768	AAACACGTACAAAAC[A/G]ATTGTGTTGTATCTA	54629
rs190307083	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828478	ATAGTACCTCTGTAA[C/T]TTCACCATCTTTAAG	54629
rs190324113	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58812855	AGAGCGAGACCCTGT[C/G]TCAAAATAAATAGAG	54629
rs190376952	snp	G/T	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58844290	CGGTGGCTCACGCCT[G/T]TAATCCCAGCACTTT	54629
rs190382719	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811728	CTTTGGCCAAATTCA[A/G]CTGATTATTAGAGAG	54629
rs190412068	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807595	GTCTCGATCTCCTGA[A/C]CTTGTGATCCGCCCG	54629
rs190446978	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58841606	GACACAGTTTCACCA[A/T]GTTCGTCAGGCTGGT	54629
rs190544134	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773208	GTAAGCTCAGCTACT[C/G]TGGAGGCTGACACAA	54629
rs190610354	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856418	GGAATTATTCTAAGG[A/G]AAAAATCCAGGGTCA	54629
rs190615634	snp	A/T	0.00993419	0.0697739	intron-variant	FAM63B	GRCh38.p7	15:58844619	CAGTTATAGTTTTTT[A/T]AAAAAAATAAACGTC	54629
rs190615742	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819754	TATAAAGTAAAGGTG[G/T]TGAGGAAAATAACAT	54629
rs190618098	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58835255	TAAGGATACATATCA[C/T]AAGCTGTGAGTGTTT	54629
rs190626002	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58788337	TTTAGAGCAGTGCTA[A/C]CGAAAGTGTGATTCA	54629
rs190632395	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806334	CTGTCTGGCATTACA[A/G]GCGTGAGTCAACGTG	54629
rs190633070	snp	A/G	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58820218	TTGCAGTGAGCCAAG[A/G]CTGTGTCAGTGCACT	54629
rs190634281	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770924	CCACACGCGACCCAG[C/G]GCTAAAGGGTCACAG	54629
rs190672475	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58822224	GCGCCGCTGTACTCC[A/G]CCCTGGGCAACAGAG	54629
rs190676665	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58790366	GATTTTGAGGAATAG[C/T]CAATATGACTGTCAA	54629
rs190714751	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58850329	ATAATCTTGGGAAAT[A/T]CTTATTTTCTTAAAC	54629
rs190735505	snp	A/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58788665	TTATATATTTATACT[A/G]TCACCAAATAGGAAA	54629
rs190874395	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806666	GAAATCATATTGCCC[C/T]TAAAGGAAGTTGGGT	54629
rs190878657	snp	C/G	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58836218	CCCGGCCTATTGCAT[C/G]TCAAAATTAACTATA	54629
rs190883390	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58824804	CCTCCTGAGTAGCTG[C/G]GACTACAGGCATGTG	54629
rs190937813	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58831089	CCCCGGATCACTTCT[G/T]TATATTTTATTGTAT	54629
rs190950665	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861008	CAGTATAACAGGAGA[G/T]TGGTGTGTGAATGCT	54629
rs190953515	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58862224	GCCTGAGCAACAGAG[C/T]GAGACCCTGTGTCAA	54629
rs190961723	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58852758	TTTTTAACATGTACT[A/G]GGCATTCAACAAAGG	54629
rs190973169	snp	C/G	0.0244538	0.107838	intron-variant	FAM63B	GRCh38.p7	15:58802295	GGCAATTTTACAATT[C/G]TTTTTTTTTTTTTAC	54629
rs190984105	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769211	GCGGATCACAAGGTC[A/G]GAAGTTAGAGACCAG	54629
rs190985560	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784978	ATTTAGAAAATCAGA[C/G]AGACTGCCACAACTG	54629
rs191088649	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828968	CATTAAGTTTTTTAC[C/G]TTTAGTATCATCAAT	54629
rs191098783	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814671	CCACCATGTCCAGCC[C/T]TTTTCCCCATTTTTT	54629
rs191107004	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847223	AGATACAGATTGTAA[A/C]ACTTTCCTTAAATAT	54629
rs191115370	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58798703	TCAGGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	54629
rs191135493	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781200	GATTACAGACACCTG[C/T]CCCCATGCCCAGCTA	54629
rs191168031	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58784290	ATGATCCTGCCACTG[C/T]GATCCAGCCTGGAGG	54629
rs191190734	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780135	TGAGGCCAGGTGTGG[C/T]TGGCTCACACTGTAA	54629
rs191211348	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840585	ACAATTAAACTGGGC[A/G]GATCCTCTTTGTGAA	54629
rs191425816	snp	A/G			missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851939	CAAGCAGCAGCTGCT[A/G]CTGCTGCTGCTTCTA	54629
rs191434241	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58826799	ATGGATCATTTAGTT[G/T]TCACATCTCTTTAGT	54629
rs191440224	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58853568	GCTCACACGTATAAT[C/T]CCAGCACTTTGGGAG	54629
rs191454609	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794934	GGCTCACGGCTGTAA[G/T]CTCAGTACTTTGGGA	54629
rs191466193	snp	A/G	0.00517822	0.0506191	intron-variant	FAM63B	GRCh38.p7	15:58811401	GACACACTGAAGGAT[A/G]ACTGTCAAAAGTTTA	54629
rs191468307	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58777572	TGAGCCCAGGAGTTT[A/G]AGACCAGCCTGGTCA	54629
rs191474457	snp	A/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832184	ATTATTTTCTTTCTG[A/T]GAGAAAAAAAAGATA	54629
rs191517021	snp	G/T	0.00517822	0.0506191	intron-variant	FAM63B	GRCh38.p7	15:58798329	ATGGGATTTGTCTAT[G/T]TTGGCCAGGCTGATC	54629
rs191545333	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784388	ATATTTATAGGGTAG[A/G]ACATTTTCCTAGATA	54629
rs191618449	snp	C/G	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58849103	TAACCCCAACTACTC[C/G]GGAGGCTGAGGTGAG	54629
rs191628124	snp	A/C	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58829327	GGGAGAGATATAATT[A/C]AAGTGGCATTTATAA	54629
rs191659979	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830698	GGCATTATGCTTGGA[C/T]GCTGTTTGAAACAGC	54629
rs191712381	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798639	TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAT	54629
rs191769116	snp	C/T	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58828603	TTTTTTTTTTGTCAC[C/T]CAGGCTGGAGTGCAG	54629
rs191788815	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801608	TACCAAATAAAAACT[C/T]GTATATAAAAATACC	54629
rs191841840	snp	A/G	0.00993419	0.0697739	intron-variant	FAM63B	GRCh38.p7	15:58807028	CAGTCTGTTAGAATG[A/G]AATTTTATGAATTAT	54629
rs191849262	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789324	GCCTGGGCAACAGAG[C/T]GAGACTCCGTCTCAA	54629
rs191981239	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774548	TGCAAATCTGCCCTC[A/G]TGTAGCTGACTATCT	54629
rs191992603	snp	C/T	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58786338	TTACTATTCTTCTAT[C/T]ACTGATATAGTAATT	54629
rs191995583	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58824980	CAGCCCATCATATAT[C/G]ATATTATCTTGAGTG	54629
rs191998062	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58793573	GTGAGTAGCTTGTAT[C/T]GTATGTGGATTATAC	54629
rs192000304	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769635	CCATCCTGGCTAACA[A/C]GGTGAAACCCCGTCT	54629
rs192037410	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809185	CCACTGCACTCTAGC[C/T]TGGGCAACAGAGTGA	54629
rs192084941	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58847090	TTCTTGTTATAGTGT[A/C]GTGTGCCAATTATAA	54629
rs192155753	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58790413	AGTTGTAGGAGATGA[A/G]ATCAGAGAGTTGATG	54629
rs192213692	snp	A/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58822363	TGGATTCTATTAAAA[A/T]TTTTTGGAATCACTT	54629
rs192219153	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859797	AATAAATTGTGATAC[A/G]CATATATTTTTTTAC	54629
rs192301832	snp	G/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58792521	TGAGGCAGAAGAATC[G/T]CTTGAACCCGGGAGG	54629
rs192313169	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58838175	GGCCAAGGCAGGTGG[A/G]TCACTTAAGGTCAGG	54629
rs192324740	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859579	AAACATGAAGAATTG[A/T]GGTTACTCTTCTCAG	54629
rs192333313	snp	A/G	0.02016	0.0983543	intron-variant	FAM63B	GRCh38.p7	15:58822148	AATCCCAGCTACTCA[A/G]GAGGCTGAGGCAGGA	54629
rs192336678	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58789922	AAAGTGCTGGGATTG[A/C]AGGCGTGAGCCACCG	54629
rs192344697	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807496	GAGTAGCTGAGAGAG[A/G]CTACAGGCGCCCGCC	54629
rs192372788	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823750	TTTTGTTACAGCATG[A/G]GGCAGCAGTGTTCAA	54629
rs192431261	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802773	GAAAGTTGAACAAAT[G/T]ATGTATATGGTATGT	54629
rs192440486	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854790	GTCACACAATACACT[C/G]TTTATGAGCTGGAGT	54629
rs192447511	snp	G/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58833047	GTCAAAAACATTTAC[G/T]GTTTTACTCTTTTTA	54629
rs192465692	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58818056	GGAATACTGTACTAC[A/G]GTGAAAACAAACATC	54629
rs192520860	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58807880	CGTTTTTGCACTGGC[A/G]TCTACTTTGGAATGC	54629
rs192555452	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773367	TGTTTATCAAACATG[C/G]CTTTATCTTCCTGTC	54629
rs192607468	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838318	CAGGAGAATCGCTTG[A/G]ATCCAGGAGGCGGAG	54629
rs192661066	snp	C/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58814902	CCCACCTCAGCCTCT[C/G]AGAGTGCCGAGGTTA	54629
rs192733234	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58781728	GCCAAGATGGTGAAA[C/T]GCTGTCTCTACTAAA	54629
rs192736335	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837821	AAACTTTAAAAAAAT[C/T]AGCCAGGCATGGTGG	54629
rs192800193	snp	C/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58843475	TAAGTAATTTGAATC[C/T]GAGCTAGTTAACCAA	54629
rs192804449	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817402	TTAGAGACCACTGTA[C/T]ATACATCAGACTGGC	54629
rs192812487	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58816858	CTCAGGAGGCTGAGG[C/T]AGGAGAATCACTTAA	54629
rs192838495	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58852140	AAAAATACAAAATTA[A/G]CCGGGCGTGGTGGTG	54629
rs192845847	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58854107	AAGTTAGCCAGGCGT[A/G]GTGGCAGGTGCCTGT	54629
rs192878464	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857954	CATTGCATCCACAAT[A/G]CTGTGATTTATAGTA	54629
rs192939313	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58820789	GCAGATATATGTTGA[C/G]ACCTGTGGTATTCAA	54629
rs192943590	snp	C/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58798874	AGCATGGGATTTTTC[C/T]TGGAAAGAGTAATAA	54629
rs192958246	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772863	TGGCTCTCCTTAAAT[A/G]GTTTGGCATTATTAC	54629
rs193006881	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58831497	TTTACTGCAACCTGC[A/C]TGAAATCCTTTGTAA	54629
rs193020099	snp	A/C	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58832371	AGCTGGGATTACAGG[A/C]ATGCACCACCATGCC	54629
rs193020451	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58802998	TTAGAGTGGAAGGAA[G/T]TATTAGCCAGGGAAG	54629
rs193064833	snp	C/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58842103	CATATAATGATATCT[C/G]CATAGCTCTTTTCCT	54629
rs193089808	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58776209	AGACTAAATGAATTC[G/T]CCAGAGAGTAGTGAG	54629
rs193113299	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810810	CACATACGGCAGAAT[C/G]TAGGAGGGTTCCAAC	54629
rs193115509	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776762	TGTGGTGGCTCATGC[C/T]TGTCGTCCCAGCATT	54629
rs193182661	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780447	CATAAAGTTTAAATA[A/G]CTAGTCCAAGGTAAG	54629
rs193237472	snp	A/T	0.0197687	0.0974348	intron-variant	FAM63B	GRCh38.p7	15:58826036	ACTGAACATTATAGT[A/T]TGGCTTATTATTATT	54629
rs193271889	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794166	TGTATAGAGAGTGAT[G/T]ATAATTATGGGCCAT	54629
rs199530409	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58813952	TTTTTTTTTTTTTTA[A/T]TTTGAGATGGAGTAT	54629
rs199568863	snp	C/G	1.70909e-05	0.00292321	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772073	GGAGGGGGAGGAGAC[C/G]GCTCAGGTGCTGGCG	54629
rs199583124	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58795777	TAAGTTTTTTTTTTC[C/T]TTTTTTTGGCCACCC	54629
rs199586636	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58844009	TGCATTAAAACCTAT[C/T]CTATATTATTATTTA	54629
rs199652795	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58832528	CCACCATGCCCAGAC[-/T]TTTTTTTTTTTCTTT	54629
rs199692730	snp	C/T	3.34605e-05	0.00409012	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772211	CTTGCTGGCCATCCT[C/T]AATGTTTTGCTCCTG	54629
rs199705219	snp	A/C/T	0.000285762	0.01195	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851819	CAGCAGAGCCAAGAG[A/C/T]TCAATTGGGAACAAA	54629
rs199820810	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58823669	AATCTGTCTCAAAAA[A/C]AAAACAAAACAAAAC	54629
rs199855361	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58804078	AGCTTGGAGTGAGCC[A/G]AGATCGCGCCACTGC	54629
rs199856038	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58784637	TTTTTTTTTTTTTTT[-/T]GAGATCGGATCTCTC	54629
rs199883149	snp	A/G	0.00136181	0.0260586	intron-variant	FAM63B	GRCh38.p7	15:58810427	GTAAACACAAATACA[A/G]GAAAAATGTATTAAT	54629
rs199885473	snp	A/C	0.000368664	0.0135719	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771757	TGGCCGGAGTGGGTC[A/C]TGAGTTGGGTACCGC	54629
rs199907753	snp	A/G	4.29212e-05	0.00463236	intron-variant	FAM63B	GRCh38.p7	15:58802425	TTAAAGTTTAAATAT[A/G]TACATTGGTTTCTAT	54629
rs199918524	in-del	-/TTATTATTATTA			intron-variant	FAM63B	GRCh38.p7	15:58840629	TCACTATTTATTTAC[-/TTATTATTATTA]TTATTATTATTATTA	54629
rs199933742	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58814616	ACTCCTGGGCTCAAA[C/T]CCTCCTCAGCCTCCC	54629
rs199979863	snp	A/G	0.000393751	0.0140257	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772071	GAGGAGGGGGAGGAG[A/G]CCGCTCAGGTGCTGG	54629
rs200049542	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58785547	GTGTTCCAAAAAAAC[A/G]TTTATTTAGAAAAAC	54629
rs200057987	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58792592	GCCTGGGCGACAGAG[C/T]AAGACTCTGTCTCAG	54629
rs200084198	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58776070	TCACCATGTTAGCCT[G/T]GCTGGTCTCGAACTC	54629
rs200119592	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58821693	ATCTTACCATGATTA[A/G]TGAGACAGTCATTTG	54629
rs200151819	in-del	-/TATG			intron-variant	FAM63B	GRCh38.p7	15:58791621	GACCCTGTCTCAAAA[-/TATG]TGTGTGTGTGTGTGT	54629
rs200160118	in-del	-/ACTC			intron-variant	FAM63B	GRCh38.p7	15:58810092	TGACACATAGTAGAT[-/ACTC]AATAATAAAAATATG	54629
rs200176779	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58853032	GTCTCGCTCATTGCC[-/A]ACCTCTGCTTCCTGG	54629
rs200197024	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58840986	TTTTTTTTTTTTTTA[A/T]TTTTTTTTGGTGTGT	54629
rs200199753	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58790588	GACAATAGACCTTAG[-/T]GGGGGGTAAGACAAG	54629
rs200212778	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58778814	TTCTTTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT	54629
rs200281746	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58803757	GGAGGCGGAGGTTGC[A/T]GTGAGCCGAGATTGC	54629
rs200321736	snp	A/G	0.196771	0.244268	intron-variant	FAM63B	GRCh38.p7	15:58831037	TGTGTGTGTGTGTGT[A/G]TGTGTATATATATAT	54629
rs200343509	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58794360	AAGTTTTTTTTGGGG[-/T]GTGTGTGTGTGTGTG	54629
rs200346069	snp	C/G/T	0.00204883	0.0319417	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772089	GCTCAGGTGCTGGCG[C/G/T]CCTCCAAGGAACGCT	54629
rs200349898	snp	A/G	8.30848e-05	0.0064448	synonymous-codon, intron-variant	FAM63B	GRCh38.p7	15:58821767	CTACAACCAACTAGT[A/G]GAGAAGATCATCTCT	54629
rs200412192	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817700	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	54629
rs200416592	snp	C/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58808511	CTACTACGCATTTAA[C/G]TTTCCTCTGTGTCTT	54629
rs200515353	in-del	-/GCACACCCT			intron-variant	FAM63B	GRCh38.p7	15:58834092	CATTTGTTTAACAAA[-/GCACACCCT]GCACAGCCCTTAATC	54629
rs200520643	in-del	-/ATT			intron-variant	FAM63B	GRCh38.p7	15:58835206	ATAATTACACAAATA[-/ATT]ATTAATTTATTTCTA	54629
rs200544208	snp	C/T	0.00134011	0.025851	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772223	CCTCAATGTTTTGCT[C/T]CTGGCCTGGAAGGTA	54629
rs200573929	in-del	-/AAG	0.0364938	0.130058	intron-variant	FAM63B	GRCh38.p7	15:58803482	ATAAAAAAAAAAAAA[-/AAG]AAGAAGAATCAACAA	54629
rs200668184	snp	A/C	0.000481604	0.0155103	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851949	CTGCTGCTGCTGCTG[A/C]TTCTACACAGGCTCA	54629
rs200678470	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58804083	GGAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC	54629
rs200746441	in-del	-/GG			intron-variant	FAM63B	GRCh38.p7	15:58790590	AATAGACCTTAGTGG[-/GG]GGGGTAAGACAAGTG	54629
rs200859113	in-del	-/A	0.0130921	0.0798413	intron-variant	FAM63B	GRCh38.p7	15:58785361	TGTGTATTTGCTTCT[-/A]AAAAAAAAATCATCT	54629
rs200865085	snp	C/T	0.00016617	0.00911357	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802326	AGGAGATTACATGCT[C/T]GATGCAAAGCCAAAA	54629
rs200880397	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860602	AAAAAAAAAAGTCAA[C/T]AAACTGAAATTCCCA	54629
rs200916603	in-del	-/TTATTATTA	0.256619	0.249912	intron-variant	FAM63B	GRCh38.p7	15:58840629	TCACTATTTATTTAC[-/TTATTATTA]TTATTATTATTATTA	54629
rs200923335	in-del	-/AAA	0.489665	0.0711382	intron-variant	FAM63B	GRCh38.p7	15:58853820	AGACTCCATCTCAAT[-/AAA]AAAAAAAAAAAAAAA	54629
rs200935094	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58837539	GAGCCATGATGGCAC[A/C]AAAAAAAAAAAAAAA	54629
rs200940138	in-del	-/C	0.00835141	0.0640778	intron-variant	FAM63B	GRCh38.p7	15:58783250	TCTAAAGAGCAGAGA[-/C]TGGCAAATACTCAAT	54629
rs200957358	snp	A/G	0.396	0.202938	intron-variant	FAM63B	GRCh38.p7	15:58831043	TGTGTGTGTGTGTGT[A/G]TATATATATATATAT	54629
rs200958606	in-del	-/AAA			intron-variant	FAM63B	GRCh38.p7	15:58812437	GCAACGGTCCGTCTC[-/AAA]AAAAAAAAAAAAGAA	54629
rs200979869	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58853546	GTTTATTATGGCTGG[G/T]GCGGTGGCTCACACG	54629
rs201039791	snp	A/G	1.84524e-05	0.00303741	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771588	AGGAGGAGCCTCCCG[A/G]ACTCGGCTTCTCCCG	54629
rs201055912	snp	A/T	0.000880445	0.020963	intron-variant	FAM63B	GRCh38.p7	15:58810431	ACACAAATACAGGAA[A/T]AATGTATTAATTTGG	54629
rs201095543	snp	C/G	1.91639e-05	0.00309541	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771845	CGCCGGCTCCGAAGA[C/G]CCCAGCAGCGCCGGC	54629
rs201125611	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58814617	CTCCTGGGCTCAAAC[C/G]CTCCTCAGCCTCCCA	54629
rs201194368	snp	A/C	1.70985e-05	0.00292386	intron-variant	FAM63B	GRCh38.p7	15:58821703	GATTAGTGAGACAGT[A/C]ATTTGTTTTCTAGAT	54629
rs201302916	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58781055	TCTTTTACTAGTTAA[-/T]TTTTTTTTTTCCAGA	54629
rs201307103	in-del	-/AT			intron-variant	FAM63B	GRCh38.p7	15:58791620	AGACCCTGTCTCAAA[-/AT]ATGTGTGTGTGTGTG	54629
rs201324950	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58794347	AAAGTAGAATAAAAG[-/T]TTTTTTTTGGGGTGT	54629
rs201346518	snp	A/C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58778709	ATGGCTCCGAATAGC[A/C/T]TCGACCTCCCGAGCT	54629
rs201372801	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58785154	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGCAAGC	54629
rs201394289	in-del	-/AA	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58817365	AATTGGTCATCAGAG[-/AA]AAATACAAATTAAAA	54629
rs201398191	snp	A/T	0.00199806	0.0315443	intron-variant	FAM63B	GRCh38.p7	15:58831761	TATCTAATGTTATGC[A/T]TTGGTTCTATAGGCT	54629
rs201445495	snp	C/G	9.94876e-05	0.00705223	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854527	AGTGGAAGACAATCT[C/G]GGAATAGTGAACGTA	54629
rs201478129	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58831045	TGTGTGTGTGTGTAT[A/G]TATATATATATATAT	54629
rs201519379	in-del	-/TTGGCTTTGGTGTC	0.0444908	0.142359	intron-variant	FAM63B	GRCh38.p7	15:58782718	TTGGTAATTTGGTAA[-/TTGGCTTTGGTGTC]TTGGCTTTGGTGTCT	54629
rs201605979	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58834627	CCATCATCTAGCTGT[C/T]ATTGGCTACATCATC	54629
rs201611014	snp	A/G	0.00123814	0.0248503	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771575	GGCGGCGGCCGCCAG[A/G]AGGAGCCTCCCGGAC	54629
rs201627819	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58795776	CTAAGTTTTTTTTTT[C/T]TTTTTTTTGGCCACC	54629
rs201692637	snp	C/T	1.67343e-05	0.00289255	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851890	CCAAGAGGAAGAGGA[C/T]AGACGGGCTTCTCAA	54629
rs201709279	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58846365	TTGGGAGGCTGAGGC[A/G]GGTGGATCACGAGGT	54629
rs201721647	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58842119	CATAGCTCTTTTCCT[A/T]TTATGACTTCTTGAT	54629
rs201743953	in-del	-/AA	0.342806	0.232136	intron-variant	FAM63B	GRCh38.p7	15:58800835	GTAAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA	54629
rs201747352	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58844008	ATGCATTAAAACCTA[A/T]TCTATATTATTATTT	54629
rs201749025	snp	A/C	2.64162e-05	0.0036342	intron-variant	FAM63B	GRCh38.p7	15:58802264	CTTTTGTAATCAGAA[A/C]AACAAGTTTTTAAAA	54629
rs201794845	snp	C/T	8.50087e-05	0.00651898	intron-variant	FAM63B	GRCh38.p7	15:58847486	GTAAATTTGTATTGT[C/T]GTCTTTATAGTGGTT	54629
rs201813804	snp	A/C	0.00199806	0.0315442	intron-variant	FAM63B	GRCh38.p7	15:58787976	TAGGTTAGTGTTGAA[A/C]AGTGGATTTTATATC	54629
rs201818932	in-del	-/T/TT	0.451181	0.164656	intron-variant	FAM63B	GRCh38.p7	15:58802295	TCTTTTTTTTTTTTT[-/T/TT]ACAGGAGATTACATG	54629
rs201832293	snp	A/G	4.9788e-05	0.00498914	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810251	AGTGATGCCATGGCA[A/G]TTTTGCACAAACTAC	54629
rs201918466	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58814618	TCCTGGGCTCAAACC[A/C]TCCTCAGCCTCCCAA	54629
rs202044789	in-del	-/T/TT			intron-variant	FAM63B	GRCh38.p7	15:58809418	TTCTTTCTTTTTTTT[-/T/TT]AAGGCTGAATAATAT	54629
rs202083877	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58818652	ATTTTTGTATATTGA[-/T]TTTTTTTTTTTTTTT	54629
rs202084928	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58852940	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	54629
rs202092838	snp	A/G	1.90718e-05	0.00308796	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771842	CGCCGCCGGCTCCGA[A/G]GAGCCCAGCAGCGCC	54629
rs202127103	in-del	-/GG			intron-variant	FAM63B	GRCh38.p7	15:58794355	ATAAAAGTTTTTTTT[-/GG]GGGGTGTGTGTGTGT	54629
rs202149402	snp	A/G	1.66211e-05	0.00288275	synonymous-codon, intron-variant	FAM63B	GRCh38.p7	15:58821761	CTGCAGCTACAACCA[A/G]CTAGTGGAGAAGATC	54629
rs202153129	snp	A/G	0.000116265	0.00762357	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772128	CAATCTGTGTATCAC[A/G]TCAAGTGGATCCAGT	54629
rs202230704	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58854244	TCAAAAAAAAAAAAA[-/A]GGAAAAGAAATTTTA	54629
rs202237736	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58785159	AAAAAAAAAAAAAAA[A/G]AAAAGCAAGCTTTTG	54629
rs367548869	snp	C/G/T	0.000334277	0.0129241	intron-variant	FAM63B	GRCh38.p7	15:58787857	CTGCAAGAAATACTT[C/G/T]AGTCACCTAAAACAT	54629
rs367557279	in-del	-/TTG	0.00517822	0.0506191	intron-variant	FAM63B	GRCh38.p7	15:58850494	ATGGTGATTTAAACT[-/TTG]TTGTTTATGGTTTTC	54629
rs367635563	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58841584	CTAATTTTGTACTTT[C/T]AGTAGAGACACAGTT	54629
rs367675511	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58821927	TTCTAAAAAACACAT[G/T]TTATATTACTTGTAT	54629
rs367678205	in-del	-/TAAA			intron-variant	FAM63B	GRCh38.p7	15:58817734	CTCAAAAAACAAAAA[-/TAAA]AAAATAAAAGTTTGA	54629
rs367746878	in-del	-/CCC			cds-indel, intron-variant, utr-variant-3-prime, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831803	AGTTTCTAAATAACA[-/CCC]CAGCCACTCAACTGA	54629
rs367795500	snp	A/G	5.51729e-05	0.00525199	intron-variant	FAM63B	GRCh38.p7	15:58852003	TTAAATGTGATGATC[A/G]TGGCTGGGTGTAGTG	54629
rs367893768	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58787609	AGGTGTGGTGGTGGG[C/T]GCCTGTAGTCCCAGC	54629
rs367902488	snp	G/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856108	TTGGAAAACTATCCT[G/T]AATAGTCTGTTTTAT	54629
rs367903515	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58842974	AAGAAAGTGCTTTTT[A/T]GGATAAGACTACATT	54629
rs367905371	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828655	AAAGCTCCGCCTCCC[A/G]GTTCACGCCATTCTC	54629
rs367911049	in-del	-/TAT			intron-variant	FAM63B	GRCh38.p7	15:58831545	GTAAATGCATTTGTT[-/TAT]AAAAAAGAATTTCAC	54629
rs367971694	snp	A/C			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770825	GCTGAGAAACCAAGT[A/C]CCCTGAGCCCTTCAG	54629
rs367974275	snp	A/G	1.67654e-05	0.00289524	intron-variant	FAM63B	GRCh38.p7	15:58847473	TCAGATAGATCAGGT[A/G]AATTTGTATTGTCGT	54629
rs368088728	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58847890	TGAAGAGATGAGCAC[A/G]TATCTGAGCTATATT	54629
rs368141938	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58781553	ACTGATGAAAGTGTT[C/T]CAGAATTTCAAAGCC	54629
rs368183475	snp	A/G	6.82932e-05	0.00584311	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854614	GTTATTTTGTAACAA[A/G]TGTTGGCTTCTGTTG	54629
rs368190295	in-del	-/AAG	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58835342	AGGAAAGATTTATTT[-/AAG]AAGGTCACATTTAAA	54629
rs368242993	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58792101	GAGGTCATTGATAAC[C/G]TTGATGAGTGTATGG	54629
rs368250977	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811428	TTTAATGAAGAGACT[A/G]TTTACAAAGGTGTGG	54629
rs368279818	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58833668	TACATAAACATCGCA[A/G]TGCCTTAAGGAGCAG	54629
rs368313830	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58825060	TAGCTTTCCCTTTAA[A/G]TCAATAAAATACCTC	54629
rs368390369	snp	A/G	0.000260359	0.0114066	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771561	GGGAATGGGCTGGGG[A/G]CGGCGGCCGCCAGGA	54629
rs368392429	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58840732	TGTGATCTCGGCTCA[C/G]TGCAAGCTCCGCCTC	54629
rs368398599	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860193	AAGAATGCCTCATAA[A/G]TTAGAGAAGGACAAA	54629
rs368546505	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58776085	GGCTGGTCTCGAACT[C/T]CTGACCTCAGGTGAT	54629
rs368658001	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58850142	ATTTTAGTCAACACC[A/G]ACTCTTAATAAAGTG	54629
rs368688031	in-del	-/CA/CACA			intron-variant	FAM63B	GRCh38.p7	15:58791622	acacacacacacaca[-/CA/CACA]TAttttgagacaggg	54629
rs368718141	in-del	-/T	0.00676609	0.0577691	intron-variant	FAM63B	GRCh38.p7	15:58818172	TGAAAGCATAAACCA[-/T]TTTGCTCACTGTTGT	54629
rs368749431	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58788857	TGTCTACTAAAAATA[C/T]AAAAATTAGCCAGGC	54629
rs368749490	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58808299	AAATGTATAATGTCA[C/T]GTATCTACCATTACA	54629
rs368815940	snp	A/C/G	1.68026e-05	0.00289845	intron-variant	FAM63B	GRCh38.p7	15:58810222	ACTTTCCCCTTTTCT[A/C/G]TTTTCAGAATATGAG	54629
rs368821954	snp	C/G	3.66603e-05	0.00428121	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771544	CGGCGGAGACCAGCG[C/G]CGGGAATGGGCTGGG	54629
rs368955858	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58848615	TCCGGGCATGGTGGC[A/G]GGCGCCTGTAGTCGC	54629
rs368981717	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58854327	GTAGCGGTAATGGCT[C/T]AGATACCATGTAATA	54629
rs368984789	snp	A/G	0.000146625	0.00856101	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771970	GTAGCTGCGAGTTCA[A/G]TAGTGAGGAGGGAGC	54629
rs368999952	snp	C/G			missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772049	GGCTGTTCCTCTGTG[C/G]AAGGAGGAGGAGGGG	54629
rs369050195	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58839845	TTTTTTTTTTTTTTT[C/T]TTTTTGGGACAGAGT	54629
rs369058006	snp	A/C/G/T	0.000238553	0.0109193	intron-variant	FAM63B	GRCh38.p7	15:58847284	CCTTTTTCTTTTGTT[A/C/G/T]CTTCTTATTAAGGGT	54629
rs369163190	snp	C/T	0.000325814	0.0127593	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851934	AGGAACAAGCAGCAG[C/T]TGCTGCTGCTGCTGC	54629
rs369293141	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793358	TTGGGAAACTGAGGA[A/G]GAGAATCGCTTGAAC	54629
rs369295246	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58814152	ACCATGTTAATCAGA[C/G]TGGTCATGAACTCCT	54629
rs369315665	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58830401	AAAATCCAAAATCCA[A/G]AATGCTCCAAAATCT	54629
rs369336748	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58826545	CACACACTCTTTTTC[C/T]CTAAATCTTGTGAGA	54629
rs369361866	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58785880	GTCCGTGTTTCACCA[A/G]GTTGGCCAGGCTCGT	54629
rs369442565	snp	A/T	0.000171985	0.00927163	stop-gained, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787961	AGCTGATGGAATATT[A/T]AGGTTAGTGTTGAAA	54629
rs369473023	snp	A/C/G	0.000172399	0.00928277	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772062	TGCAAGGAGGAGGAG[A/C/G]GGGAGGAGACCGCTC	54629
rs369491162	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58826189	TACCAATTGTTGATA[C/T]GTTGAATGTTTTCTT	54629
rs369503590	snp	C/T	0.0217236	0.101931	intron-variant	FAM63B	GRCh38.p7	15:58849184	CATTGCACTCCAACA[C/T]GGGTGACAGAGCAAG	54629
rs369638718	snp	A/T	4.98475e-05	0.00499212	intron-variant	FAM63B	GRCh38.p7	15:58787999	TTTATATCTCTTTCA[A/T]AACAAAAGTTTTCAA	54629
rs369643125	snp	C/T	6.7086e-05	0.00579124	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851824	GAGCCAAGAGATCAA[C/T]TGGGAACAAATCCCG	54629
rs369645565	in-del	-/TGTG			intron-variant	FAM63B	GRCh38.p7	15:58831016	TATATGAAGATCAGT[-/TGTG]TGTGTGTGTGTGTGT	54629
rs369656214	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58820735	TTACATCTTTTTAAC[A/G]AGCTCCCCGAGTTTG	54629
rs369660239	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58790165	AGGGTAGATTACTCT[A/G]AATACCTAGATGTCT	54629
rs369661661	snp	A/C	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58773787	CAGGGAAATGGAATT[A/C]CCAGGGGAGAGAAGA	54629
rs369710416	snp	A/C			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857533	AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA	54629
rs369777060	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793957	AGCCAGCATGGTGTT[A/G]TGTTTTCTCAGTCAC	54629
rs369778436	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58803431	TGGAATCGCGCCACT[A/G]TGATCCAGGCTGGTG	54629
rs369778461	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58778194	AAACTTACATGTAAC[C/G]TATACTATACATTGT	54629
rs369781724	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58835966	CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCGGC	54629
rs369822716	snp	C/T	3.83002e-05	0.00437592	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771896	CGACCCGAGCCCTCC[C/T]GGGGAATCTCCGAGC	54629
rs369827807	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855801	GTGGTGCGTGCCTGT[A/G]GTCCCAGCTACTCAG	54629
rs369836612	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58841340	AGATACAGTGGCTTA[C/T]GGCTATAATCCCAAC	54629
rs369897199	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58852150	AATTAGCCGGGCGTG[C/G]TGGTGGTGAACACTT	54629
rs369943466	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793603	CCTCAAAGCCATTTT[A/G]TAAAAGAGAAAACTA	54629
rs369959705	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58781521	ACTCTGAGGATAGGG[A/T]CTAAATTATGATAAA	54629
rs369970136	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58821241	CTTTTCTAGGAAATA[A/C]GTAATAAAATGGAAT	54629
rs369978762	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58825501	AGTTTAAAAAAAAGC[A/G]CAGTACCAGCAGCCA	54629
rs370019161	snp	C/T	1.65858e-05	0.00287969	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831840	ATGGATTATGTGAAC[C/T]AACTTCAACGGTTCA	54629
rs370053500	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58849726	GCTATATATATGACA[A/G]GATCTTTCCAGGCAA	54629
rs370228691	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58786822	TATAGCGTCCGTTTC[C/T]TTACTTAGTAATTTA	54629
rs370234869	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58828005	TGGGAGGCCGAGGTG[A/G]GTGGATCACCTGAGG	54629
rs370258121	snp	A/G			intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832155	TCACAGATCTTTGCA[A/G]TAAGAAGTATTTTAT	54629
rs370318666	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769768	AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	54629
rs370395693	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58812994	TCTTAACCCCTGACA[A/T]CCACTAATCTTTCTC	54629
rs370475639	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58853548	TTATTATGGCTGGTG[C/T]GGTGGCTCACACGTA	54629
rs370497106	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857288	CCTGTAATCCCAGTA[A/C]TTTGGGAGGCCGAGG	54629
rs370517669	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58778727	GACCTCCCGAGCTCA[A/G]GCAATCCTCCCACCT	54629
rs370550908	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58795672	GCCTCCCAAAGTGCC[A/G]GGATTACAGGCGTGA	54629
rs370571725	snp	A/C/G	1.6569e-05	0.00287824	synonymous-codon, missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847344	GTTTCTTACTGAAGA[A/C/G]AAAGTTGTTTGGGAA	54629
rs370632331	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58822690	TTTTCAACTGTGTTC[A/C]AGTCAATGATGAGAA	54629
rs370680041	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58839497	CCACCACATCCAGCT[A/G]ATTTTTGTATTTTTC	54629
rs370690583	snp	A/G	6.8171e-05	0.00583788	intron-variant	FAM63B	GRCh38.p7	15:58802412	AAAGTATATAATTTT[A/G]AAGTTTAAATATATA	54629
rs370705281	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58795026	TAAAAATACAAAAAA[A/G]TTAGCCGGGCGTGGT	54629
rs370725466	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58791981	ATTTCCTAGAATCGT[A/T]ATGAAGAAATGTTTC	54629
rs370865206	snp	A/G	6.64883e-05	0.00576539	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772119	TTCCCGGGACAATCT[A/G]TGTATCACATCAAGT	54629
rs370879219	snp	G/T	8.82013e-05	0.00664025	intron-variant	FAM63B	GRCh38.p7	15:58851976	CTCAGGTAAAAACTA[G/T]TGTTTTGAGTCTTAA	54629
rs370944697	in-del	-/TATT			intron-variant	FAM63B	GRCh38.p7	15:58840618	ACACATTGACCTCAC[-/TATT]TATTTACTTATTATT	54629
rs371008771	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58805251	AGCTTATATGGCTGG[A/G]CTGAGTCTAAGCTAA	54629
rs371021666	in-del	-/T	0.426354	0.177198	intron-variant	FAM63B	GRCh38.p7	15:58840970	ACTGCGCCTGGCCAA[-/T]TTTTTTTTTTTTTTA	54629
rs371048973	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58853128	CAACTAATTTTTGTA[A/T]TTTTAGTAGAGATGA	54629
rs371051421	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845203	TTGAGGTCAGGAATT[C/T]GAGACCAGCCTGGCC	54629
rs371056170	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58854100	ATACAAAAAGTTAGC[C/G]AGGCGTGGTGGCAGG	54629
rs371066566	snp	A/G	0.0115144	0.0749975	intron-variant	FAM63B	GRCh38.p7	15:58810480	TATTTTTTGTTACTT[A/G]CTTTTTTTGTACTTT	54629
rs371122704	snp	A/C	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58823323	GAGATGGGATTTTGT[A/C]ATGTTGGTCAAGCTG	54629
rs371202388	snp	A/G	1.68621e-05	0.00290358	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772085	GACCGCTCAGGTGCT[A/G]GCGGCCTCCAAGGAA	54629
rs371209026	snp	C/T	0.000207432	0.010182	intron-variant	FAM63B	GRCh38.p7	15:58802304	ACAATTCTTTTTTTT[C/T]TTTTACAGGAGATTA	54629
rs371230487	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58840892	CCAGGATGGTCTCGA[C/T]CTCCTGACCTCGTGA	54629
rs371311093	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58796654	TCAGCCTCCTGAGTA[G/T]CTGGGATTATAGGCA	54629
rs371316968	snp	A/C			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770004	AAAAAAAAAAAAAAA[A/C]AAAAGCAAAAACAAA	54629
rs371317518	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58782529	ATTGTATGGATCTTA[A/G]TTTTCAGAGTTTCCT	54629
rs371318892	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842051	ACTAAGATTACATAG[C/T]CCCTGTCTAGATCAC	54629
rs371335431	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58803410	GAGGCGGAAGTTGCA[A/G]TGAGCTGGAATCGCG	54629
rs371341008	in-del	-/A			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770263	ATGTATCAGGTATTT[-/A]TATGTCTGCGAAGGA	54629
rs371404635	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858817	TTACAAATAGTCTAC[A/G]GTTTGTATTTTAAGG	54629
rs371496214	snp	A/G/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58827699	CCTCGTGATTCTCCC[A/G/T]CCTCGTCCTCCCAAA	54629
rs371504408	in-del	-/TGTT			intron-variant	FAM63B	GRCh38.p7	15:58825595	TGTTTGTTTGTGTGG[-/TGTT]TGTTTGTTTGTTTGT	54629
rs371504717	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829813	AGTGTGATAATTATA[A/G]TGTGGTAAGTTTTTA	54629
rs371510189	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58851174	AGACGGGGTTGTACC[A/G]TGTTGGCCAGGGTGG	54629
rs371537788	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58846080	CAGGCAGGATGGATG[A/G]TTAATGGATGTTAAA	54629
rs371646360	in-del	-/ACAC	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58778530	AGCTTAAAAAAACAG[-/ACAC]ACACCAAAAAAAAAA	54629
rs371663320	snp	A/G	0.000232311	0.010775	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847440	AGATCCTGAAACTGT[A/G]TACAAAGGACAACAA	54629
rs371736184	snp	C/T	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58828661	CCGCCTCCCAGTTCA[C/T]GCCATTCTCCTGCCT	54629
rs371830694	snp	A/C/G	0.000147423	0.00858438	intron-variant	FAM63B	GRCh38.p7	15:58787871	TTAGTCACCTAAAAC[A/C/G]TTTAATTTTATAGAA	54629
rs371924375	snp	C/T	0.000167986	0.00916322	intron-variant	FAM63B	GRCh38.p7	15:58854466	AGTAATTTCTTGCTG[C/T]ATATTTTTCTTAAAG	54629
rs371980599	in-del	-/TACTT			intron-variant	FAM63B	GRCh38.p7	15:58833251	TATTTGCCAACACTT[-/TACTT]CAGCCAAAATGGTGT	54629
rs371997194	snp	A/G	1.67097e-05	0.00289043	missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810366	ATATTCCTTTGTACC[A/G]TGGGTGGTTAGTAGA	54629
rs372019523	snp	A/G	0.00167639	0.028903	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854658	GTCTTGAGAAACAAA[A/G]CCACAGGAGGAAAGG	54629
rs372061949	in-del	-/A	0.00993419	0.0697739	intron-variant	FAM63B	GRCh38.p7	15:58777483	CATTCATAATCTATT[-/A]AAGTAGTTGGCTAGG	54629
rs372080026	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793201	TCACGCCGTAATCCC[A/G]GCACTTTGGGTGCTT	54629
rs372111580	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58850036	GCCACTGCACCTGAC[C/T]ACAGGCAAAAACCAT	54629
rs372138465	snp	C/T	1.74272e-05	0.00295183	intron-variant	FAM63B	GRCh38.p7	15:58847508	ATAGTGGTTAAAATG[C/T]TGATTTTTTTCAAAT	54629
rs372145813	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58824625	AAAGACCGTAATAGA[C/T]ATTTTTACTTACTTT	54629
rs372152536	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58792557	GTTGCAGTGAGCCGA[G/T]ATCATGCGATTGCAC	54629
rs372248304	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58850709	CCACCTCAGCCTCCC[C/G]TAGTAGCTGGGACCA	54629
rs372256898	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58810729	GACTCCCTGAAACCT[A/G]TTATACTCACCATTA	54629
rs372260906	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58844893	GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTG	54629
rs372328740	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792555	ACGTTGCAGTGAGCC[A/G]AGATCATGCGATTGC	54629
rs372348584	snp	A/C	1.8493e-05	0.00304075	intron-variant	FAM63B	GRCh38.p7	15:58821863	TTGAAATTCTTGGCA[A/C]GATAATTTTTCTTAT	54629
rs372357840	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58825164	CATTTTATTTCCTAT[C/T]AAGGTATGAGGAATA	54629
rs372464935	snp	C/G	7.61107e-05	0.00616843	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771831	GCAGAACTGACCGCC[C/G]CCGGCTCCGAAGAGC	54629
rs372488999	snp	A/C/G	1.83869e-05	0.00303202	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771602	GGACTCGGCTTCTCC[A/C/G]GCGGGCTCTCCTGAG	54629
rs372492734	snp	A/C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58792297	AGAAGTGAAAACGTA[A/C/T]GTCCATACAGCTTGT	54629
rs372499674	snp	A/C/G/T	0.000100462	0.00708679	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851895	AGGAAGAGGACAGAC[A/C/G/T]GGCTTCTCAATACTA	54629
rs372500519	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58846596	AAAGTGAGACTCCTC[-/AA]AAAAAAAAAAAAAAA	54629
rs372515564	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858669	TGATTACATTTGATT[A/G]ACTTTTCCTATTCCA	54629
rs372556569	snp	A/C			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770960	CTGTCCGCCTCCTGC[A/C]TTCCCTTTAAAGAAG	54629
rs372682616	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58829402	CTCCTAGGTTACTGT[C/T]TTCCCTTTGCCATAA	54629
rs372692376	snp	A/G	6.69927e-05	0.00578722	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851829	AAGAGATCAATTGGG[A/G]ACAAATCCCGGAAGG	54629
rs372725568	snp	A/C	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58808072	CCTTCCTTCCTTTTC[A/C]GTGCATTCACTGCAA	54629
rs372758095	in-del	-/AGA			intron-variant	FAM63B	GRCh38.p7	15:58839198	CTGTGGGCTTTGACA[-/AGA]GGGGAAGGGAGGTAT	54629
rs372761998	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803772	AGTGAGCCGAGATTG[C/T]GTCACTACACTCCGT	54629
rs372782386	snp	A/T	0.000165986	0.00910855	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772001	GGAGAACAGGGTCCC[A/T]GAGGAGGAGGAGGGC	54629
rs372877912	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789601	TAACTGGGACTGCAC[A/G]CACATGCTACCACAC	54629
rs372926100	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58848587	TCTCTACTAAAAATA[C/T]AAAAATCAATTATCC	54629
rs372934800	in-del	-/GTCA			intron-variant	FAM63B	GRCh38.p7	15:58779182	TACAGGCGTGAGTCA[-/GTCA]CCATGGCCAACCCTA	54629
rs372938869	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58803970	AAAAAAAAAAAAAAA[-/T]ACAAAAAATTAGCCA	54629
rs372947751	snp	G/T	0.000166121	0.00911225	intron-variant	FAM63B	GRCh38.p7	15:58787996	GATTTTATATCTCTT[G/T]CAAAACAAAAGTTTT	54629
rs372998567	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58830484	TCATTTTCAGATTAG[A/G]GATGCTCAGCTGATC	54629
rs373004466	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855724	CCAGGAGTTCGAGAC[C/G]AGCCTGGCCAGCATG	54629
rs373021909	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58793515	TGATAGTTTCATAAT[C/T]CTGTGAATATACAAC	54629
rs373037565	snp	A/G	0.0189856	0.0955633	intron-variant	FAM63B	GRCh38.p7	15:58836426	CATTGCATTTGATAG[A/G]GTAACTCCATTTTGA	54629
rs373054908	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58777746	TAATTTTGTTTACCT[C/G]TCATTTTCAAGAGAT	54629
rs373136823	in-del	-/GTTT			intron-variant	FAM63B	GRCh38.p7	15:58825615	TTTGTTTGTTTGTTT[-/GTTT]TGAGACAGAGTCTTG	54629
rs373157618	snp	A/G	0.00835141	0.0640778	intron-variant	FAM63B	GRCh38.p7	15:58801235	CTCCTCGGCCTCCCA[A/G]TGTGCTGGGATTATA	54629
rs373213302	in-del	-/ATTTTTTGT	0.0283406	0.115616	intron-variant	FAM63B	GRCh38.p7	15:58818806	CACCACGCCTGGCTA[-/ATTTTTTGT]ATTTTTTGTAGAGAT	54629
rs373252934	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58848369	TAAAGATGCAGCCTA[G/T]TAGGGAAGGCAGATA	54629
rs373346972	in-del	-/GAA			intron-variant	FAM63B	GRCh38.p7	15:58803490	AAAAAAAAAGAAGAA[-/GAA]TCAACAACTTACATT	54629
rs373353968	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58773661	AGTCCTAGAAAACTT[A/C]ATGGGATTTATGGGT	54629
rs373379122	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58780532	TAAAGTTCAAGATAG[C/T]AATAAGTCTGGTGGA	54629
rs373385274	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58820746	TAACAAGCTCCCCGA[C/G]TTTGAAAACCACTGC	54629
rs373444154	snp	A/G	1.81681e-05	0.00301392	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771712	CTCTGAGAGGGCAGT[A/G]CAAGGTGACCGCCTC	54629
rs373474712	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58809172	AGCCATGATCATACC[A/G]CTGCACTCTAGCCTG	54629
rs373508712	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58846256	GAGAGGCTGGATACC[A/G]CATTTACCCTCATGT	54629
rs373513458	snp	A/G	9.95718e-05	0.00705521	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831848	TGTGAACTAACTTCA[A/G]CGGTTCAGGAAGGAG	54629
rs373550682	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786004	CACAGAGAATAAAAA[C/T]AATTTAGAATGAAAT	54629
rs373557115	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855864	GGCAGAGGTTGCAGT[A/G]AGCCGAGATCGCCCT	54629
rs373584089	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58837617	ATCTTCCATATCTTC[C/G]TACTGCCTTCTAGCA	54629
rs373587176	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58801602	AGGTGATACCAAATA[A/C]AAACTCGTATATAAA	54629
rs373597250	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58774813	CAACCTTGGTTGAAG[A/T]GTGCAGCATAGGAGG	54629
rs373599820	snp	C/T	0.0115144	0.0749975	intron-variant	FAM63B	GRCh38.p7	15:58823579	CTGAGGCTGAAAGAT[C/T]ACTTGAGCCCAGGAG	54629
rs373608138	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58826034	ACACTGAACATTATA[G/T]TTTGGCTTATTATTA	54629
rs373621883	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774833	AGCATAGGAGGTAAA[C/T]GAAATGGTGGTAATA	54629
rs373679248	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58785769	GAAGCCTCCGCCTCC[C/T]GGGTTCAAGCAATTC	54629
rs373685173	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58803847	GGCGTGGTGGCTCAC[A/G]CCTGTAATTCCAGCA	54629
rs373747083	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787073	AACCTCACGTGATCC[A/G]CCTGCGTTGGCCTTC	54629
rs373789647	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58805959	ACGTACTGTGGTCCC[A/G]GCTACTCGAGAGGCT	54629
rs373853478	snp	C/T	1.6664e-05	0.00288647	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772108	CCAAGGAACGCTTCC[C/T]GGGACAATCTGTGTA	54629
rs373879104	snp	A/G	0.00795532	0.062565	intron-variant	FAM63B	GRCh38.p7	15:58791112	TTGAACCCAGGCGGC[A/G]GAGGTTGCAGTGAGC	54629
rs373960560	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782021	GTAAATGAATAGTAC[A/C]TACAAGAAATTAAAA	54629
rs373988407	in-del	-/G			utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854742	TTTTTTCAGGGGAAC[-/G]GTTGTTACTTAGTTA	54629
rs374052441	snp	C/T	0.000102379	0.00715394	intron-variant	FAM63B	GRCh38.p7	15:58810183	ATATCTTTTTTGTTC[C/T]CGTTTTGATGTTTCT	54629
rs374071527	snp	C/G	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58847114	ATTATAAACTATATT[C/G]AAAGCCGAGTGGATT	54629
rs374080449	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833595	GTAAACACGTGAACA[A/C]ATGTCTCTGCATCAT	54629
rs374096042	snp	A/G	0.0146672	0.084371	intron-variant	FAM63B	GRCh38.p7	15:58824570	AATTACTTAACTCCA[A/G]TGGTTACTTGTATAA	54629
rs374263183	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58850064	CATTTACCCATCCTC[C/T]GTATTATTTAAAATT	54629
rs374273869	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58812660	GGCCCAGGAATTCAA[A/G]ACTAGCCTGGGCAAC	54629
rs374278754	snp	C/T	0.0126979	0.078662	intron-variant	FAM63B	GRCh38.p7	15:58790595	GACCTTAGTGGGGGG[C/T]AAGACAAGTGGGAAA	54629
rs374337673	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58823122	TTAGTTAAGGTTTAT[C/T]CTAATCTTTTTTTTT	54629
rs374433778	snp	A/G	1.81793e-05	0.00301485	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771714	CTGAGAGGGCAGTAC[A/G]AGGTGACCGCCTCCC	54629
rs374456156	snp	A/T	3.40124e-05	0.00412372	intron-variant	FAM63B	GRCh38.p7	15:58810200	GTTTTGATGTTTCTG[A/T]ATTAGAACTTTCCCC	54629
rs374479159	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58836262	TTTTTTGAGACAGGG[G/T]GGGGTCTCACTCCAT	54629
rs374626783	snp	A/C			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770884	CACCTCCAACCACCC[A/C]ACAATGCCTCAGGCC	54629
rs374637701	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58786366	ATTACTTTGAGTTTC[C/T]ATCCTACAGTATTTA	54629
rs374662199	in-del	-/TTGT			intron-variant	FAM63B	GRCh38.p7	15:58825587	TGTCTGTTTGTTTGT[-/TTGT]GTGGTGTTTGTTTGT	54629
rs374709665	snp	A/C/T	5.66421e-05	0.0053215	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771918	TCTCCGAGCCTGGAC[A/C/T]CTCTGGAGTCGTTCT	54629
rs374710177	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58841128	CTGGGATTATAGGCG[C/T]GCACCACCATGTCCA	54629
rs374742316	snp	A/G/T	0.000390778	0.0139727	intron-variant	FAM63B	GRCh38.p7	15:58796027	CAGTGTGGTTATTGT[A/G/T]ACCTTCATCAAACCG	54629
rs374770976	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58797121	GTAAAATATACACTG[G/T]ATTTCAAAGATTTGG	54629
rs374830274	snp	C/G	1.90221e-05	0.00308394	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771812	TCTCGCCGGCACCTG[C/G]CAAGCAGAACTGACC	54629
rs374853839	snp	C/G/T	3.68611e-05	0.00429295	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771751	CAGCCGTGGCCGGAG[C/G/T]GGGTCATGAGTTGGG	54629
rs374890330	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58845882	AAACAGAATGACATC[C/T]TGTCAAATGCAACAA	54629
rs374918992	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58813468	GCCACTTCTCTCCAG[A/C]CTGGGTGATGGAGCA	54629
rs374953277	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58823139	TAATCTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT	54629
rs374961079	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861642	ATGTCATCAGTTTCA[A/G]AACTTTCACTTTGGG	54629
rs374988159	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58819914	AAGAAAAGGATTTGG[C/T]ACTGCATCAAAAGAT	54629
rs374990794	snp	A/G	1.6607e-05	0.00288153	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847442	ATCCTGAAACTGTAT[A/G]CAAAGGACAACAAGA	54629
rs375021360	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58802193	AGGATTGGGGAGTCA[A/G]TTTTATATGTCAACT	54629
rs375059015	in-del	-/CTCT			intron-variant	FAM63B	GRCh38.p7	15:58834283	CAATCTGATCTCTCT[-/CTCT]TTTCCCCACAATATC	54629
rs375079140	snp	A/G	0.000116216	0.00762198	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787917	TCAGGTGAAACTTCC[A/G]CCGATGATGGAAATC	54629
rs375082729	snp	C/T	1.67097e-05	0.00289043	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772204	CCTGCCCCTTGCTGG[C/T]CATCCTCAATGTTTT	54629
rs375160149	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797493	AGCCTGGGTGACAAA[A/G]TGAGACCCTATCTCA	54629
rs375163362	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58820425	CTCCAGCCTGGGCAA[C/T]AGAGTGAGACTCCAT	54629
rs375169582	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855747	CCAGCATGGTGAAAC[C/G]CTGTCTCTACTAAAA	54629
rs375182500	snp	A/G	0.0119091	0.0762411	intron-variant	FAM63B	GRCh38.p7	15:58793533	GTGAATATACAACAA[A/G]AAATAATTGAATTGT	54629
rs375289325	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58819701	AATTCAGATTATTTG[A/G]AAAGACTTACTGAAG	54629
rs375392715	snp	A/G	1.7659e-05	0.00297139	intron-variant	FAM63B	GRCh38.p7	15:58851978	CAGGTAAAAACTAGT[A/G]TTTTGAGTCTTAAAT	54629
rs375406230	in-del	-/GAAA/TG			intron-variant	FAM63B	GRCh38.p7	15:58844944	AAAAAAAAAAAAAAT[-/GAAA/TG]GAAAGGACAACCCAC	54629
rs375464228	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58840697	AGTCTTTCTCTGTCA[C/T]CCAGGCTGGAGTGCA	54629
rs375476553	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859916	AAGTTCAGTTTTGTC[C/T]TATTGTCCTGAGAAA	54629
rs375486168	snp	A/C	6.75767e-05	0.00581238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772260	GCAGCTTTCTACTTC[A/C]TACAGCTTTTGGGGT	54629
rs375527908	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58852073	AGGCAGATTGCTTGA[A/G]CCCAGGAGTTCGAGA	54629
rs375583665	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58852470	TTCTGATTTTCAAAT[A/T]TATTTTTAAAATTCG	54629
rs375595054	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58825296	TTGCTTTCCTTGATT[C/T]TAATGCCTTATAAGT	54629
rs375647845	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860226	AAAATGTTTTGGAAG[A/G]TGATCCTGGCTCCTT	54629
rs375666296	snp	A/C	1.92439e-05	0.00310187	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771854	CGAAGAGCCCAGCAG[A/C]GCCGGCGGCCTCAGC	54629
rs375674270	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58786480	CATGTCATTCATTTG[A/T]CAACGCATTTGAACA	54629
rs375675087	snp	C/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769604	GTGGGCAGATCACGA[C/G]GTCAGGAGATCAAGA	54629
rs375703306	in-del	-/GT			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857598	AATTTTGCCCAAGGT[-/GT]AACGTTATATATCCC	54629
rs375711457	snp	A/G	0.00676609	0.0577691	intron-variant	FAM63B	GRCh38.p7	15:58833922	TCTTTCCCTTCCCAC[A/G]AGGCCATATTTCAGA	54629
rs375740068	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58775981	GATTCTCCTGTCTCA[A/G]CCTCTCGAGTAGCTG	54629
rs375781422	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58786871	TTTCACTCTTGTCAC[C/T]CAGGCTGGAGTGCAA	54629
rs375793771	snp	C/G	1.6574e-05	0.00287867	missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810323	GTGTTTGAATATACA[C/G]CAGAATGCATAGTAT	54629
rs375818972	snp	A/T	0.000167986	0.00916322	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851932	ACAGGAACAAGCAGC[A/T]GCTGCTGCTGCTGCT	54629
rs375842450	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58835514	AAAAATTAGCTGGGC[A/C]TGGTGGTGGGTGCCT	54629
rs375844578	in-del	-/AT	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58782045	ATTAAAATGTAAAAC[-/AT]GTGTAATAGCTTATA	54629
rs375892191	snp	A/T			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770265	GTATCAGGTATTTAT[A/T]TGTCTGCGAAGGAAG	54629
rs375899024	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842347	TTTAGGGATTAGAAG[C/T]GAAAAGTAGTTTAGA	54629
rs375991220	snp	A/C	0.000169986	0.00921758	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847337	ACCAGGGGTTTCTTA[A/C]TGAAGAGAAAGTTGT	54629
rs376052006	snp	A/T	0.00835141	0.0640778	intron-variant	FAM63B	GRCh38.p7	15:58790596	ACCTTAGTGGGGGGT[A/T]AGACAAGTGGGAAAA	54629
rs376143233	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58815756	GCGTGATCTCCTCAC[C/T]GCAACCTCCATCTCC	54629
rs376146570	snp	C/G	1.745e-05	0.00295376	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772053	GTTCCTCTGTGCAAG[C/G]AGGAGGAGGGGGAGG	54629
rs376189428	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58832616	TTCACCGCAACCTCC[A/G]CCTCAGGTTCAAGCA	54629
rs376256509	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58794773	AGATAATAAGGTGAA[G/T]GGAACATTCAGAGGA	54629
rs376359259	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58853006	TGCCCAGGCTGGAGT[A/G]CAGTGGCGCAGTCTC	54629
rs376382065	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58831161	CATCTACATGAGTGG[C/T]ATATGTTGGAGGAGA	54629
rs376405828	snp	C/T	0.000339942	0.0130329	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851781	ATTAGGATTATCTTA[C/T]GGCATTATCTCTACA	54629
rs376417807	in-del	-/GTGTGT			intron-variant	FAM63B	GRCh38.p7	15:58794359	AAAGTTTTTTTTGGG[-/GTGTGT]GTGTGTGTGTGTGTG	54629
rs376428367	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58837968	GTAAGACCTTCTTTC[-/A]AAAAAAAAAAAAAAA	54629
rs376505962	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848340	TACAAAGATAAATCA[C/T]TGAGTCCTGTCCTTA	54629
rs376512131	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58785160	AAAAAAAAAAAAAAG[-/AA]AAGCAAGCTTTTGGG	54629
rs376557423	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58784643	TTTTTTTTTTGAGAT[C/T]GGATCTCTCTCTGTT	54629
rs376589521	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58804108	CACTCCAGCCGGGGC[A/G]ACAAAAAAAAAAGGA	54629
rs376603942	snp	A/G	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58851290	CCAAAAATATTTAGA[A/G]CAATGACAGAATCAC	54629
rs376666617	snp	C/T	7.27603e-05	0.00603116	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771713	TCTGAGAGGGCAGTA[C/T]AAGGTGACCGCCTCC	54629
rs376719312	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809176	ATGATCATACCACTG[C/T]ACTCTAGCCTGGGCA	54629
rs376730103	snp	A/T	1.80647e-05	0.00300533	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771495	GGGCTACAGGAGACC[A/T]GGCTCGCCGCTGGTG	54629
rs376747016	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58827653	GTACTTTTAGTAGAG[A/C]CAGGGTTTCACCGTG	54629
rs376754806	in-del	-/AAG	0.0107246	0.0724382	intron-variant	FAM63B	GRCh38.p7	15:58839197	GCTGTGGGCTTTGAC[-/AAG]AGGGGAAGGGAGGTA	54629
rs376787067	in-del	-/GC			intron-variant	FAM63B	GRCh38.p7	15:58785134	TGGTGGTGAAGGAAA[-/GC]AAAAAAAAAAAAAAA	54629
rs376789264	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855643	AAATCTGAAAGGGCC[A/G]GGCGCAGTGGCTCAC	54629
rs376802759	snp	C/T	1.65729e-05	0.00287857	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847411	GACTCAGAATTTCAT[C/T]TTCGACCTCCTTCAG	54629
rs376896450	snp	C/T	1.81612e-05	0.00301335	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831925	ATACAAGGTATGATA[C/T]AGAAATAGCTATTTA	54629
rs376901688	snp	A/G	0.000117615	0.0076677	intron-variant	FAM63B	GRCh38.p7	15:58810430	AACACAAATACAGGA[A/G]AAATGTATTAATTTG	54629
rs376940442	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837780	AGACCAGCATGGACA[A/G]TGAAGTAAGACCTTG	54629
rs376960294	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861470	TCAATTGAGGAATAA[C/T]AACAACCCTAGAGAT	54629
rs377007175	snp	A/G	0.0119091	0.0762411	intron-variant	FAM63B	GRCh38.p7	15:58774856	TGGTAATAGCAGGAC[A/G]TAAAATTGATGGGTT	54629
rs377031195	snp	G/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58814389	TGAGTTTTGTTTTTG[G/T]TTTTGTTTTTTTTTT	54629
rs377073004	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58837968	AGTAAGACCTTCTTT[A/C]AAAAAAAAAAAAAAA	54629
rs377113579	in-del	-/CT			intron-variant	FAM63B	GRCh38.p7	15:58824793	CCTGCCTCAGCCTCC[-/CT]TGAGTAGCTGGGACT	54629
rs377152879	snp	A/T	3.38776e-05	0.00411554	intron-variant	FAM63B	GRCh38.p7	15:58831739	TTTGATTTTGAAATT[A/T]TTCTTCTATCTAATG	54629
rs377224689	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58785790	CAAGCAATTCTCCTG[C/T]CTCAGTCTCCCAAGT	54629
rs377286510	snp	C/G	0.000165986	0.00910854	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851960	GCTGCTTCTACACAG[C/G]CTCAGGTAAAAACTA	54629
rs377344843	snp	C/T	0.0119091	0.0762411	intron-variant	FAM63B	GRCh38.p7	15:58849278	GAGGCCAAGGCGGGC[C/T]GATCACGAGGTCGGG	54629
rs377347458	snp	C/T	1.67888e-05	0.00289726	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772091	TCAGGTGCTGGCGGC[C/T]TCCAAGGAACGCTTC	54629
rs377400860	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58844506	GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	54629
rs377408054	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58781833	CTTGAACCCAGGAGA[C/T]GGAGTTTGCAGTGAG	54629
rs377414162	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58799317	TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	54629
rs377415094	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58814404	TTTTGTTTTTTTTTT[-/T]GACACAGGGTCTTAC	54629
rs377418240	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836109	TAGAGACAGGGTTTC[A/G]CTGTGTTAGCCAGGA	54629
rs377511136	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58779141	GGCCTCAAGTAATCC[A/T]GCCTCAGCCTCCCAG	54629
rs377513194	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849134	AGAATCACTTGAACC[C/G]AGGGGGCGGAAGTTG	54629
rs377579907	in-del	-/AA			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859081	AACAAAATATATCTT[-/AA]GTCAGTTTTTTTAAT	54629
rs377635143	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58845157	ACACCTGTAATCCCA[G/T]CACTTTGGGAGGCCC	54629
rs377655802	in-del	-/A	0.0115144	0.0749975	intron-variant	FAM63B	GRCh38.p7	15:58797820	TGCAAATGAAGAGAT[-/A]ACAGTTGTGGTGGCA	54629
rs377735527	snp	C/T	5.51466e-05	0.00525074	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771746	GGAGACAGCCGTGGC[C/T]GGAGTGGGTCATGAG	54629
rs386383150	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58846106	TAAAAAAAAAAAAAA[-/AA]AGAAAAAACAGAATG	54629
rs386784458	in-del	AGT/GG/TG			intron-variant	FAM63B	GRCh38.p7	15:58790586	TTGACAATAGACCTT[AGT/GG/TG]GGGGGGTAAGACAAG	54629
rs386784459	multinucleotide-polymorphism	CC/TT			intron-variant	FAM63B	GRCh38.p7	15:58807651	TACAGGCGTGAGCCA[CC/TT]GCGCCCGGCCTAAAA	54629
rs397689418	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58837554	AAAAAAAAAAAAAAA[-/A]GGAAACCTTTTTTAA	54629
rs397699068	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58795775	CTAAGTTTTTTTTTT[-/T]CTTTTTTTTGGCCAC	54629
rs397706358	in-del	-/CT	0	0	intron-variant	FAM63B	GRCh38.p7	15:58824794	CTGCCTCAGCCTCCT[-/CT]GAGTAGCTGGGACTA	54629
rs397719705	in-del	-/A	0.5	0	intron-variant	FAM63B	GRCh38.p7	15:58785136	GTGGTGAAGGAAAGC[-/A]AAAAAAAAAAAAAAA	54629
rs397770822	in-del	-/T	0.5	0	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832243	TTTTTTTTTTTTTTT[-/T]GAAATGGAATTTCGC	54629
rs397818937	in-del	-/A	0	0	intron-variant	FAM63B	GRCh38.p7	15:58773144	CCTAGGAAAAAAAAA[-/A]CAAAACAAACTGGGT	54629
rs397853675	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58791180	GTGAGACTCCTTCTC[-/A]AAAAAAAAAAAAGGG	54629
rs397854334	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58803947	CCCCAGCTCTACTGA[-/A]AAAAAAAAAAAAAAA	54629
rs397935377	in-del	-/GTGT			intron-variant	FAM63B	GRCh38.p7	15:58794396	TGTGTGTGTGTGTGT[-/GTGT]TTTAAGAATAAAATA	54629
rs397942251	in-del	-/AAAT			intron-variant	FAM63B	GRCh38.p7	15:58795202	AATAAATAAATAAAT[-/AAAT]CTGTGGAAGTTGATA	54629
rs397958450	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58840194	TCACAATGGATGTGT[-/T]AATCAAACTGATCCA	54629
rs397978224	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58774510	AAAAAAAAAAAAAAA[-/A]GGAAATGCAAAGATG	54629
rs398027487	in-del	-/T	0	0	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770003	TTGTTTTTGCTTTTG[-/T]TTTTTTTTTTTTTTT	54629
rs398027488	in-del	-/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58785158	AAAAGCTTGCTTTTC[-/T]TTTTTTTTTTTTTTT	54629
rs398027489	in-del	-/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58802108	TATATACTATAGTGC[-/T]TTTGAACTTTTTACT	54629
rs398027492	in-del	-/A	0	0	intron-variant	FAM63B	GRCh38.p7	15:58826246	GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	54629
rs398027493	in-del	-/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58843855	ATGATATTGTCAGGA[-/T]TTTTTTTTTTTTTTT	54629
rs398027494	in-del	-/A	0	0	intron-variant	FAM63B	GRCh38.p7	15:58848093	AAAATCTCATCTGTC[-/A]AAAAAAAAAAAAAAA	54629
rs398043362	in-del	-/T	0.5	0	intron-variant	FAM63B	GRCh38.p7	15:58805777	CAGTTGTTGTTTTTT[-/T]ATTAAGACAGAGTCT	54629
rs527237699	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822457	TTATTTAGGAGTCCT[A/G]AATGGACTTTATCAT	54629
rs527271384	snp	A/G			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770672	TCTCACCAGTAGCTG[A/G]TGAGAAGCACAGCTC	54629
rs527296500	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58793834	AGGGGAGGAGTTGTT[C/G]AAAGTAAGAGGGAAG	54629
rs527303463	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815946	GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA	54629
rs527322704	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58779388	GCTCTATTTCTCCCT[A/C]CCTCCTTGATGACTT	54629
rs527345655	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772416	TACATATATCGAAAA[G/T]AATTGCCCCTAACCT	54629
rs527357758	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835395	CGGTGTCTCACGCCT[A/G]TAATCCCAGCACTTT	54629
rs527421477	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834661	TTTTAGCCCTTATTG[A/G]TTAATACCTAATTAC	54629
rs527421836	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810727	AGGACTCCCTGAAAC[C/G]TATTATACTCACCAT	54629
rs527455527	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58782278	TGCTACATATATACA[C/T]ACATGTGTATATACA	54629
rs527491900	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58841809	TATAGATAGTGAGAT[A/G]ACTATTTATCCATGC	54629
rs527552311	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805760	TAAGTTTGTTTGGTT[C/T]ATCAGTTGTTGTTTT	54629
rs527553558	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58848462	AAAGAATATTTAATT[C/T]TCCGGGTGCGGTGGC	54629
rs527619544	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58816187	GCTTTTTTTTCATCT[A/C]TGTCCATTGGTAAAA	54629
rs527670283	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854818	AGTTTCATGTTACAA[C/G]TTGGAAATGCTGTGT	54629
rs527753352	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58844689	TTGGGAAGCTGAGGC[A/G]GTGGATCATCTGAGG	54629
rs527774184	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823917	TCATTACCATAGATA[A/T]TTACTAAAAAGAAGC	54629
rs527795430	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780220	GACCAGCCTGACCAA[C/T]GTGGAGAAACCCCTT	54629
rs527838457	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824470	TCCATATTAAAGAAT[A/G]ATTATATGTGTCATT	54629
rs527855908	snp	A/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58780583	AGGGTGGGACAGCCA[A/G]TGATAAAGTCAGAGA	54629
rs527866810	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773794	ATGGAATTCCCAGGG[C/G]AGAGAAGAGTATAAA	54629
rs527896267	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58833819	GAAGCCTTCCTCTTA[C/T]CTCAACTGCAAAGAG	54629
rs527934836	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58774240	GTATTCCCAGCATTT[C/T]GGGAGGCCGAGGCGG	54629
rs527998229	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769514	ATCCAACATTCATGT[A/G]TTATATGTAATACAT	54629
rs528011366	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840154	TTATCTTTACATACT[G/T]TTTTAAGCCTTCTGC	54629
rs528017680	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58806381	TTTTTTTTTTGAGAC[A/G]GGGTCTCACTCTGTC	54629
rs528049516	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769731	GGCTGAGGCAGGAGA[A/C]TGGCGTGAACCCGGG	54629
rs528077126	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861354	TAATATATAGATTAC[A/G]TATGAGTGCCTATTT	54629
rs528077537	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58807013	TGTTTACAGTCTGTA[C/T]AGTCTGTTAGAATGG	54629
rs528132620	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853674	AAATATAAAAAATTA[G/T]CTGGGTGTGGTGGCG	54629
rs528179164	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58851543	TCCTGGGCTGAAGCA[A/G]TCCTCCTGCCTCAGC	54629
rs528195861	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853205	TGATTCACCCACCTC[A/G]GCCTCCCAAAGTGCT	54629
rs528280070	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58788129	TGTTACTGTTCTTAG[A/G]TGGTATAGTCTTCTT	54629
rs528293928	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58825355	AATACTTAATTGTAG[A/C]ATACACTGCTTTCGG	54629
rs528316150	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860390	AGCCTGGCCAACATG[A/G]TGAAACCCTGTCTCT	54629
rs528349781	snp	C/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58781625	AAATACTGATGGTGG[C/T]GAAGCGCAGTGGCTC	54629
rs528353491	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58827118	CCAGTGCATCAAATC[A/G]GGGGCACATGAGCCT	54629
rs528411827	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782055	AAAACATGTGTAATA[C/G]CTTATAATACATAAA	54629
rs528436136	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819636	TACTGGTGTGAGCCA[C/T]CACACCCAACTTAGT	54629
rs528460022	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58826471	CAACCTCAGGTGATC[C/T]GCCCGCCTTGGCCTT	54629
rs528469436	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58797150	GGTTAAAAAAGAATA[C/T]CAGTAATTTAAAAAT	54629
rs528474350	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58831227	GGCATCATTTATCCC[A/G]CGGCTTTCTGTTCAG	54629
rs528497135	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813551	TCTCTGGGTTAAATG[C/T]CCAGGAGTGCAGTTG	54629
rs528532764	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770615	TTTTGCTACGCATGT[C/G]AATGTCCACAATCAT	54629
rs528536494	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58838384	GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA	54629
rs528541024	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58799663	CTAGCTGAAGTACCC[C/G]AAGGAAATGGGAATT	54629
rs528543398	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58776310	CCATCCTGCCTCAGT[C/T]TCCCCATTCCCTCTC	54629
rs528554577	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813923	CATTGTAGTTTTAAC[C/T]TGCATTTCTTTTTTT	54629
rs528569593	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807851	ATGCTATTCCATGGA[C/G]ACAGTAATAAACTCG	54629
rs528587264	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58770977	TCCCTTTAAAGAAGC[C/G]GCACACAAGGGAGCT	54629
rs528617938	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58808338	CAGAATAGTTTCACT[C/G]TCCTAAAAGTTCTCT	54629
rs528675987	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792655	TATTCATAGTAGTCA[A/G]AAAATGGAAACAACC	54629
rs528679227	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844866	GCTGCAGTGAGCCAA[A/G]ATCACACCACTGCAC	54629
rs528687070	snp	A/G			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770841	CCCTGAGCCCTTCAG[A/G]GACAAGTTCTTTTCC	54629
rs528700067	snp	A/G	1.84439e-05	0.00303671	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802345	GCAAAGCCAAAAGAA[A/G]TTTCAGAAATTCAAC	54629
rs528740273	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58851116	GTAGTTAGAATTACA[G/T]GTGTGCACCACCACA	54629
rs528750522	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795744	GGCCCTTTGAAGGCT[A/G]TAAACCATTATAGTG	54629
rs528761473	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58802917	CTGGAAAAAAGCAAG[C/T]GGAGCTTCATTTTCT	54629
rs528762255	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58851469	TTATAGACAGGGTCT[C/G]TCTCTGTCACCCATG	54629
rs528806787	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58850566	AATGGGGAACTTTTT[A/T]AAAAATTCTTTAAAC	54629
rs528818688	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859433	ATGTTATTTGATAAT[A/G]TGAAGTTAAATCCCT	54629
rs528822769	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58796335	GGCATATTGAAGGAA[C/T]AGTGTATGTGTCTAA	54629
rs528871464	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58786398	TTTTTCTCCTAGTCT[A/G]TAAATATATCCTGGA	54629
rs528876269	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858680	GATTAACTTTTCCTA[C/T]TCCATGCACAAGTTA	54629
rs528884162	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58811151	AAGATTTAGAAGTTA[C/T]TTCATAGGAGCTGGG	54629
rs528933411	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58788799	CAGATCACTTGAGGT[C/T]AATAATTTGAGACCT	54629
rs528937482	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58783869	AGCATCACCTGAGCC[C/G]GGGGAGGTTGAGGGT	54629
rs528982970	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820710	GAAGCAACATGAGCC[C/T]GAAATTCTTTTACAT	54629
rs528999618	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784358	ATTTCCTCAGGAAAT[C/T]TAGTTAATTCAGTAA	54629
rs529060828	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58852166	TGGTGGTGAACACTT[A/G]TAATCCCAGCTACTG	54629
rs529107401	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58836820	AGACAGGATATCCCT[C/G]TGTTGCCCAAATTGG	54629
rs529153588	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58838649	TGGAGTGCGGTGGCA[C/G]AATCTCAGCTCACCA	54629
rs529172140	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836162	TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT	54629
rs529185512	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58803758	GAGGCGGAGGTTGCA[C/G]TGAGCCGAGATTGCG	54629
rs529220802	in-del	-/TTTTTTTTTTTTTTAA			intron-variant	FAM63B	GRCh38.p7	15:58852957	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTAA]GACAGAGTCTCACTC	54629
rs529237794	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843571	GTCCAGAAATACCCT[C/T]GTAAATTAATTCTAC	54629
rs529239366	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835621	ATGTGCCATTGCACT[C/T]CAGCCTAAGCGACAA	54629
rs529248069	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804582	GGAGGCCAAAGCAGG[A/C]GGATTGCTTGAGCCC	54629
rs529268882	in-del	-/TG			intron-variant	FAM63B	GRCh38.p7	15:58831016	TATATGAAGATCAGT[-/TG]TGTGTGTGTGTGTGT	54629
rs529300209	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842898	CCAGTGTGACTTTCA[A/G]GTCCACTTTCAACTT	54629
rs529307380	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797998	ATCTGGGCACCTTCT[A/G]TGATTTAAAGTATGC	54629
rs529326651	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849159	AAGTTGCAGTGAGCC[A/G]AGATCATGCCATTGC	54629
rs529458582	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785078	GAGTACAAGCCTTAT[G/T]AGGTCATTAAGAAAA	54629
rs529467549	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58822525	TGGTGCTCAAGTACT[C/G]TAGATTTTAGTAGAC	54629
rs529470413	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817029	AAAAGTTTGAAACTA[C/T]GTTCCTGATATTATG	54629
rs529477431	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58805564	TTTGACCATGTTAAA[A/C]GTTCATTTGAAAAGA	54629
rs529481339	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792043	GCTGCTAATAGCTCA[G/T]GCAGGAGGAATACTA	54629
rs529528659	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58823200	TGGAGTGCAATGGCG[C/T]GATCTCAGCTCACTG	54629
rs529537511	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58833896	GGGTGTCGGGCTGCC[A/G]GACGGTCAGGTCTTT	54629
rs529547048	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785584	TCGACAGTAATTTGC[A/C]GGAGTTTCAGTTTAA	54629
rs529547243	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781089	TGTTTCATTCTTGTT[A/G]CCCAGGCTGGAGTGC	54629
rs529554452	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58802137	TACATTGAAAAAATA[C/T]TTGACGTGATAGGAA	54629
rs529631700	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58779549	TCCAAGTGTGTTTAT[C/T]ACTTATAAAAAAGGA	54629
rs529646765	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834529	TAAATGAGAATCTCC[A/G]GAGGTGGGATCTGAG	54629
rs529695045	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772944	AAAATAAGAAAAGGT[A/T]TGTCTAAGGTGAAGG	54629
rs529708830	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772755	CAAATTCCATTTAAG[A/G]AAAAGCATTGGTCTG	54629
rs529712139	snp	C/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58841624	TCGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	54629
rs529764046	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58798747	AGACGTCAGCCACCA[C/T]GCCCAGCAATCCAGT	54629
rs529770147	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58811318	GTACATTGACCTTTG[A/G]TATATTAGTCTAGCA	54629
rs529773349	snp	A/G	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58841033	GTCACCCAGGCTAGA[A/G]TGCAGTGGCATGATC	54629
rs529833305	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805829	GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCTGAG	54629
rs529897121	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847085	CTTATTTCTTGTTAT[A/G]GTGTAGTGTGCCAAT	54629
rs529900770	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770839	TCCCCTGAGCCCTTC[A/T]GGGACAAGTTCTTTT	54629
rs529904649	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58793985	CACGTTCAGCTGCAC[A/G]AGTCCAGGCCTGAAT	54629
rs529906962	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854680	GAGGAAAGGAAGAAA[A/G]ACCGATCAATACCGT	54629
rs529910599	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58799363	ACGAGGTCGGGAGAT[C/G]GAGACCATCCTGGCT	54629
rs529934500	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58792356	CTTACGCCTGTAATC[C/T]CAGCATTTTGGGAGG	54629
rs529941729	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58820157	TGTAGTCTCAGCTAC[A/T]AGGGAGGCTGAGGCA	54629
rs529963406	snp	A/C	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58786654	ATATCCAGTTTAATA[A/C]ATTATTATAAAGCAA	54629
rs529975865	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792773	CATGCTATAACATGG[A/G]TGAACCCTGAAACTT	54629
rs530025541	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58854027	AGGTGGGCGGATCAC[A/G]AAGTCAGGAGTGTGA	54629
rs530037908	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793561	TGTACATTTTAAGTG[A/T]GTAGCTTGTATCGTA	54629
rs530101669	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58862023	TATTAGGGCCAACTT[C/T]TGATAAAGAGAAAAT	54629
rs530138845	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824520	AACTAGATTTTTGTT[C/T]ATAAGTAACTACAAA	54629
rs530144007	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58781330	GTGCTGGGATTACAG[C/G]CATGAGCCACCGCAC	54629
rs530152708	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780861	CTAGTTCAGGCCTTT[A/G]TCTCTCACCTGGACT	54629
rs530178178	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58833251	TATTTGCCAACACTT[C/T]ACTTCAGCCAAAATG	54629
rs530212646	snp	C/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58787603	TTAGCCAGGTGTGGT[C/G]GTGGGTGCCTGTAGT	54629
rs530228970	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58847982	ATGGGTGGATATTCT[A/G]AACCTTAGAGGCCAA	54629
rs530323966	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58812750	GTAGTCCCAGCTATT[A/C]AGGAAGCTGAGGTGG	54629
rs530357358	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58801004	TTTGAGACAGAGTCT[C/T]GCTGCATCACCCAGG	54629
rs530384810	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839140	AGTGTGCGTTAAAAT[C/G]TTTTGTCATCCAGAG	54629
rs530416312	snp	G/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58853148	AGTAGAGATGAGGTT[G/T]TACCATATTGGCCAG	54629
rs530447928	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846134	ATGATTGAGACCTAG[A/C]ATTTGCTAACACAAG	54629
rs530479744	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58794877	AGAAGTCATCAGTAT[A/G]AAAATGGTATTTAAA	54629
rs530498018	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58837900	TTTGAGTCCAGGAGA[C/T]CGAAGCTACAGTTAA	54629
rs530513767	snp	A/C	0.00755907	0.0610114	intron-variant	FAM63B	GRCh38.p7	15:58823548	CAGGCACCTCTAGCT[A/C]CACGTACTTGGGAGG	54629
rs530530953	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58801034	GCTGGAGTACAGTGG[C/T]GTGATCTTGGCTCAC	54629
rs530603141	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58789170	GTGAAACTCCGTCTC[C/G]ACTAAAAAATACAAA	54629
rs530637888	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58826728	TATCAGAATTCTCCC[A/G]TTTTCCCAGTAATGC	54629
rs530638033	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819766	GTGTTGAGGAAAATA[A/C]CATCTGAACAGATTG	54629
rs530642602	in-del	-/T	0.0279526	0.114869	intron-variant	FAM63B	GRCh38.p7	15:58834643	ATTGGCTACATCATC[-/T]TTTTTTAGCCCTTAT	54629
rs530651123	snp	C/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58788747	AGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	54629
rs530652935	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860282	GAAAATAAAAAGTCA[A/G]GAAACTGGCCCGGTG	54629
rs530663139	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58782756	CTTCTCATCACAGTA[C/G]TTCTACTTACTTTGG	54629
rs530670567	in-del	-/T	0.424814	0.178718	intron-variant	FAM63B	GRCh38.p7	15:58795765	ATTATAGTGTCTAAG[-/T]TTTTTTTTTTCTTTT	54629
rs530683688	in-del	-/TCCT	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58808056	ACTCCCTTCCTTCCA[-/TCCT]TCCTTCCTTTTCAGT	54629
rs530699773	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820146	TGGCGTGCACCTGTA[A/G]TCTCAGCTACTAGGG	54629
rs530700572	snp	C/T			downstream-variant-500B	FAM63B	GRCh38.p7	15:58862345	AATCTGGCAGTTCTC[C/T]CATTGATTAAATACA	54629
rs530714504	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782147	TTATTTTGAAAAAAG[C/T]GGGTAAAGCTTCTCT	54629
rs530815806	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58829850	CTTTGTAGCTTGAAG[G/T]ACTATGGTTTGACAC	54629
rs530823015	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814614	GAACTCCTGGGCTCA[A/G]ACCCTCCTCAGCCTC	54629
rs530834935	in-del	-/AAA	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58774235	GCCTGTATTCCCAGC[-/AAA]ATTTCGGGAGGCCGA	54629
rs530849183	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58799996	AATAATAGAGATGGT[A/G]GCATTGTCTTACTTT	54629
rs530881499	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844808	TATAGTTGCAGCTAC[C/T]TGGGGCTGAGGCAGG	54629
rs530894451	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771009	CCCGGGAGTTCAACT[G/T]CCGGCCACATAGTGA	54629
rs530939928	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844456	ACTTGGGAGGCTGAG[G/T]CGGGAGAATGGGGTG	54629
rs530940512	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58802963	TACTTGGTAATAGAA[G/T]GCAAGAAGGAATTGG	54629
rs530958825	snp	A/G	0.00272764	0.0368291	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771393	GGGGGCGGGCGGCCC[A/G]GTATGGAGAGCAGCC	54629
rs530994704	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58779041	TATTAAGATTACAGG[C/T]GTGAGCCACTGTGCC	54629
rs531000641	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58850377	CTAAGTGGAAAAGAA[A/G]ACATTACAGTAGTTT	54629
rs531082267	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58826807	TTTAGTTGTCACATC[C/T]CTTTAGTCTTCTGTA	54629
rs531120339	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58824047	TCAGAAAGTGGTAAC[A/G]GACAGAATGCTAGCC	54629
rs531125396	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58796587	TGGAGTGCAGTGGCA[C/T]GATCTTGCTCACTGC	54629
rs531187459	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858535	AATAATTGTTCATAT[A/G]TTAATGTTCACATGT	54629
rs531251974	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790587	TGACAATAGACCTTA[A/G]TGGGGGGTAAGACAA	54629
rs531255032	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778132	GTTATACTTTTTTTT[A/T]ATTTTAGAAAGAATG	54629
rs531369556	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772355	TCAGTCCCCTTCTTA[A/C]ATGAAATTCATTCCA	54629
rs531409910	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58835498	TCTTTACTAAAAATA[C/G]AAAAATTAGCTGGGC	54629
rs531416974	snp	A/C	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58815454	CTCCTGTGCTCAAGC[A/C]ATCCTCCCTACTCGG	54629
rs531417667	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822399	CTTTGGTATGGTCAG[A/G]TACCCAGAGGTTACT	54629
rs531444870	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778781	ACAGGTGTGTGCTAC[C/T]ATGCCCACCTAATTT	54629
rs531476892	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804634	AACATGGCAAAACCC[C/T]GTCTCTACAAAAAAT	54629
rs531477862	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815921	TTGACCTCGTGATCC[A/G]TCTGCCTCGGCCTCC	54629
rs531479795	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809637	TTTGGACTTTGTGGT[C/T]TAAAATAGGTCCTTC	54629
rs531545084	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810174	TGTACTTGAATATCT[C/T]TTTTGTTCTCGTTTT	54629
rs531594487	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791706	CTGAATTTTTAATTT[C/T]ATATAATATAAATTA	54629
rs531603629	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842727	TATGAAGCAGTTAGA[C/G]GCTTTGTACTATATT	54629
rs531607646	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810634	CATAGAAGACCACCC[A/G]TACTTCTCACACCAA	54629
rs531656445	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792189	AAATGTAAAATAATA[C/T]AGCCACTTTGGAAAG	54629
rs531664884	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58804946	CAATCCGGGTGTGAT[A/G]TAGTAAGACTCCATC	54629
rs531667391	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849085	TGTGGTGGTGCGCAC[C/T]TGTAACCCCAACTAC	54629
rs531714279	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58785682	TAAAAAAATAATCTA[C/T]CGAATTTTTTTTTAA	54629
rs531729786	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848510	GCACTTTGGGAGGCC[A/G]AGGCGGGTAGATCAC	54629
rs531731024	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798630	CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG	54629
rs531774237	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786274	ATTGCTGATTTAAAG[A/G]ATTTCTTTGGATGAA	54629
rs531805786	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58816845	GTAGTCGCAGTTACT[A/C]AGGAGGCTGAGGTAG	54629
rs531951639	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833889	CCTTTATGGGTGTCG[G/T]GCTGCCGGACGGTCA	54629
rs531951762	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823865	GTATGGGGAAAAAAA[A/T]TCCACTCACTAGAAG	54629
rs531979016	in-del	-/TT	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58808309	GTCACGTATCTACCA[-/TT]TTACAGTATCATACA	54629
rs531989591	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811874	TAAATAGGTTAGAGT[C/G]TTCTCTTTTCCACTG	54629
rs532000730	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58785906	CTCGTCTCGTACTCC[A/T]GACCTCAAGTGATCT	54629
rs532012242	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58840959	AGGTGTAAGCCACTG[C/T]GCCTGGCCAATTTTT	54629
rs532016179	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805894	TGCTGGCTAACACAG[C/T]GAAACCCCATCTCTA	54629
rs532019572	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58827230	TTGGTAGTTAATAAG[C/T]CACCTGTGATATTAT	54629
rs532042763	snp	C/T	1.65759e-05	0.00287883	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847422	TCATCTTCGACCTCC[C/T]TCAGATCCTGAAACT	54629
rs532134600	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833466	GGCCCAGGGGACCAG[C/T]GTTCAGCATGCGGAG	54629
rs532173918	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769340	GAGGCAGGAGAATCA[C/T]TTGAACCCGGGAGGT	54629
rs532204151	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800815	ACTCCAGCCTGGGCA[A/G]CAGAGTAAGACTCTG	54629
rs532204538	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806337	TCTGGCATTACAGGC[A/G]TGAGTCAACGTGCCA	54629
rs532227831	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858339	TTTCAAGTTCTTTCT[C/T]ATACTTCTTGATCTT	54629
rs532230892	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853269	AAACTGTTCATTTTG[A/T]TTCAGATACATAAGA	54629
rs532261280	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861664	CACTTTGGGAGGATA[C/T]TCCTTAAAAGGCATA	54629
rs532344443	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793645	CTGCAAAAAATACTT[C/T]ATACAAATAGAAAAA	54629
rs532409824	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787374	TGCCTGTTTTTAAGC[G/T]TTGCATTACTTTTAA	54629
rs532409940	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58775563	GCAGATAGCGCTTTG[A/G]TTAGAGAGTTCTTTG	54629
rs532447329	in-del	-/AAT	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58850430	ATGGGAATGTAGAAA[-/AAT]AATAATAAACTACTG	54629
rs532450160	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861139	TTGTGCAGAATAATT[G/T]GATTGAGGCACATAT	54629
rs532471430	snp	C/G	0.0119091	0.0762411	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769792	CCACTGCACGCCAGC[C/G]TGGGCGACAGAGCAA	54629
rs532501416	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775536	GTAGTGAGTGTAGCA[C/T]GAAGAATTGATGCAG	54629
rs532506699	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58820483	ATATTTATGCCTGTA[A/G]ACATTTTCCACAATT	54629
rs532524467	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58786365	AATTACTTTGAGTTT[C/T]CATCCTACAGTATTT	54629
rs532598849	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58782006	ATAGTATTACTAGTA[G/T]TAAATGAATAGTACA	54629
rs532632701	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58812818	AGCTGTGATCACACT[A/G]CTGCGTTCCAGCCTG	54629
rs532779935	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795638	CTCGATCTCCTGACC[A/T]CGTGATCCACCCGTC	54629
rs532805177	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58801796	AGGCACCCGCCACCA[C/T]GCCCGGCTAATTTTT	54629
rs532814760	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58789278	AGGAGGCATAGCTTG[C/T]AGTGAGCCGAGATTG	54629
rs532867820	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794991	AGGAGATCGAGACCA[C/T]GGTGAAACCCCGTCT	54629
rs532877186	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58782955	GACAGAGTCTTGCTC[C/T]GTCACCCAGGCTGGA	54629
rs532887542	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58789889	TGACCTCAGGTGATC[C/G]GCCCACCTGAGCCTC	54629
rs532894102	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58840458	AACATCCTCCATGAA[A/C]CCTTCATTAAACTTT	54629
rs532946860	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58775669	AGTAACAGCATTTTT[C/G]AAACCTGGGTAATAG	54629
rs532947594	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783697	CCAGCACTTCAGGAG[G/T]CTGAGGCAGGCAGAT	54629
rs533013060	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859584	TGAAGAATTGAGGTT[A/G]CTCTTCTCAGGTGAC	54629
rs533017757	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58777188	AGTTCGCTTATGTCC[A/G]GAAATAGGAGCAGGA	54629
rs533022995	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778336	TTTTGGTAGGGAATT[C/G]TTTTCCCAATTTTTT	54629
rs533057581	snp	A/C	0.0023933	0.0345097	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859115	TGTCAAAATTTGTAG[A/C]ATTTTCTTTGAGTAT	54629
rs533078522	snp	C/G	0.00038187	0.0138126	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771538	TATGGGCGGCGGAGA[C/G]CAGCGGCGGGAATGG	54629
rs533083865	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58852845	TTAATGGTGGGATTC[C/T]ACATGTTAAATCTCA	54629
rs533099669	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808982	GTTGAGAGGCTGAGG[C/T]GGAGAATCACTTGAG	54629
rs533136714	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58776609	TAGGGACAAGGTCAC[C/T]GAAAAGTCAGGATAA	54629
rs533153486	snp	C/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58780958	AAGTTTTATTATCAA[C/T]TTTTGAGGGGGGAGA	54629
rs533161461	snp	A/C/G	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58809435	AGGCTGAATAATATT[A/C/G]CATTGTATGTATATA	54629
rs533213580	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58850276	TATATGATGGCTACT[A/G]TGTTGGCTTTAAAAG	54629
rs533263549	in-del	-/AAAC			intron-variant	FAM63B	GRCh38.p7	15:58820266	TGAGATTCCATCTCA[-/AAAC]AAACAAACAAACAAA	54629
rs533292297	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797388	TGATGCTTACCAGTA[A/G]TCCCTGCTGCTCAGG	54629
rs533293928	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836955	GGTCAAAAGCACGTC[G/T]TCTTCACTGACCCAG	54629
rs533321521	snp	A/G	1.87651e-05	0.00306303	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771775	AGTTGGGTACCGCCG[A/G]AGACGCGGGAGCCCG	54629
rs533350700	snp	G/T	0.0138799	0.0821421	intron-variant	FAM63B	GRCh38.p7	15:58790590	CAATAGACCTTAGTG[G/T]GGGGTAAGACAAGTG	54629
rs533401262	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856599	TTATAACCTAGAATA[C/T]GTATACGTTAGTAAA	54629
rs533406133	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58827486	TTTATTCAGACAGAA[C/T]GGAGTCTTGTTGTGT	54629
rs533510246	in-del	-/TC	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58852614	CATTTCCTGCTCCTG[-/TC]TCTCTCCTTCTAGTT	54629
rs533525028	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855138	TAATTGTATATTGGA[C/G]TAGTTCAGCCCTTAA	54629
rs533561889	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797966	CCAATGTTCAGAGGG[C/G]TTAATGTGCTGTCTC	54629
rs533615613	snp	C/T			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770367	CTTTTCTGTAACAAG[C/T]TAGAATAGGACCCAC	54629
rs533620164	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58784742	CTCCCACCTCAGCCT[C/T]CCAAATAGCTGGAAC	54629
rs533647441	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58802951	GTATTCTTCCTTTAC[G/T]TGGTAATAGAAGGCA	54629
rs533677908	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827383	TTATTAGTTGTTATT[C/T]TTCTGTAACAGAACA	54629
rs533686869	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58829666	GAACATTTAGTAATA[C/T]AGATATTACAGACGG	54629
rs533709684	in-del	-/A	0.0134861	0.0810011	intron-variant	FAM63B	GRCh38.p7	15:58846671	CAAAAATTAAAAATT[-/A]AAAAAAAAATTTGTA	54629
rs533731433	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58815498	GGGACTACAGGTGCA[C/T]ACCAGCACGCCTGGC	54629
rs533737579	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58827055	CATTAGTAGATTCAG[A/G]TTATATATTTTTGGC	54629
rs533752982	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791025	TCCACTAAAAAATAC[A/C]AAAAATTAGCTGGGA	54629
rs533766782	snp	A/C/G	0.000106143	0.00728432	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772032	GCGGCGGTGTTGCCC[A/C/G]GGGCTGTTCCTCTGT	54629
rs533776957	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58787356	AACAATATAGTTAAA[G/T]TTTGCCTGTTTTTAA	54629
rs533799030	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833664	CATATACATAAACAT[C/T]GCAATGCCTTAAGGA	54629
rs533819125	in-del	-/ATCA	0.0023933	0.0345097	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856684	AAGTTTACTCTTGAT[-/ATCA]ATCACTCTGTTGGCT	54629
rs533865065	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58785337	TGTAAGTAAGTGAGT[C/T]GAAATATTTGTGTAT	54629
rs533869909	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840510	GCAACAAATAGGAAT[A/C]GCCCTAATTTCTGCT	54629
rs533923967	snp	A/C	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58779157	GCCTCAGCCTCCCAG[A/C]GTGCTGGGATTACAG	54629
rs533949923	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812999	ACCCCTGACAACCAC[C/T]AATCTTTCTCCATTT	54629
rs533962981	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58816275	AATTTCACTGAAAAG[C/T]CTCAACATGTCCAGC	54629
rs533986155	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58809208	CAGAGTGAGACCCTA[C/T]ATTCATCAAACAACC	54629
rs533995684	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772644	GATATCATGGACTAA[A/G]TTTTCATGGTTATAT	54629
rs534062701	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791882	GGTCAGTAGACCGAG[G/T]CTGGGATATGCCAGT	54629
rs534139590	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805424	GTAAGCAAAGAGCCT[A/T]TTTTTTCCAGTTTTG	54629
rs534144508	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811501	TTAGACCTAGCAACA[A/G]CAGAAAATAATTGCC	54629
rs534146021	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822753	CATAGCATGTAGATA[C/T]ACCTTCTCAGTCCCC	54629
rs534186255	snp	A/C	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58839755	AACCTGCACCTGGAC[A/C]AAGTATTCTCTGTTT	54629
rs534200889	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798812	TTTGGAGGTGTCAAC[A/G]TGTAGTTAGTGGGGC	54629
rs534224417	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58839007	GGACAAAAATGATTA[C/T]CTAGGAAGGGTCACC	54629
rs534250897	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846552	GAGCTGAGGTGGCAC[C/T]ACTGCACTCCAGCCT	54629
rs534262737	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58799566	CCTGGGCGACAGAGC[A/G]AGACTCCATCTCAAA	54629
rs534289188	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816875	GGAGAATCACTTAAG[A/G]CCAGGAGTTTGAGGC	54629
rs534291926	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58842831	TAATGGCTGAGGGAA[C/G]ATGTAAAGACCCTAA	54629
rs534304672	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58853424	CTTAATAGTTAAATC[C/T]TACCATGTTATGTGT	54629
rs534304740	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58862159	GGAGGATCACCTGAG[C/T]CCAGGAAGGCTGAGG	54629
rs534355610	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58811066	GGATCCATCATTAGT[A/G]TAAACTGCAGGTGTG	54629
rs534368601	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861491	CCCTAGAGATTCATA[A/G]GAAAGAGCATTGAAA	54629
rs534386782	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793725	TTACAAATAGGTGCA[A/G]GTAGGTGGGTGGATG	54629
rs534410798	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58824151	TCTGGCTACAAATAC[A/G]GTAAGGGTAGGACTT	54629
rs534442442	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845839	GAAAATGTGGTACAC[A/G]TACACAACGGAGCAC	54629
rs534460957	snp	C/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58844682	CAGCACTTTGGGAAG[C/T]TGAGGCGGTGGATCA	54629
rs534472064	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824746	ACGATCTCGGCTCAC[C/T]GTAACCTCTGCCCCA	54629
rs534487704	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58773688	GGTCTTGAACCAATC[-/T]TTTTTTTTTTTCGTT	54629
rs534493854	snp	A/G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58804278	TGAAATCTCATCCCA[A/G/T]CTTCCAATATATAAA	54629
rs534532617	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58832768	CCGACCTCAGATGAT[A/C]GCCCGCCTCAGCCTC	54629
rs534568334	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58841197	CATGTTGACCAGGCT[A/G]GTGTTGAACTCCTGA	54629
rs534600026	snp	A/G	1.81622e-05	0.00301343	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831926	TACAAGGTATGATAT[A/G]GAAATAGCTATTTAA	54629
rs534600726	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819187	TGCATGGTGGCTAAC[A/G]CCTGTGATCCCAACA	54629
rs534616108	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793017	CTAAAAAATGAAAGT[G/T]TAAAAAAACCAGAAT	54629
rs534642032	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859060	TGTGCACACTTTTTT[C/G]TCAATAACAAAATAT	54629
rs534644114	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58825529	CCAGACTTCACCATA[G/T]CTATTCATTTAATTC	54629
rs534657920	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812909	AGATATGGCACATTT[C/T]TGTTAACACAAGAAT	54629
rs534667484	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838732	GTTGGGATTACAGGC[A/G]GGTACCACCACTCCT	54629
rs534678288	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58801146	GCCTGGCTAATTTTT[A/G]TATTTTTACTAGAAA	54629
rs534684126	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786889	GGCTGGAGTGCAATG[C/G]TGCATTCTTGGCTCA	54629
rs534692945	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769870	GGCGGGCGCCTATAG[C/T]CCCAGCTACTCGGGA	54629
rs534710839	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58827909	GCACAGTAAAATGTT[C/T]TGGGCTCCCTACTGC	54629
rs534740312	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780368	GATAGCGCCATTGCA[C/T]TCCAGCCTGGGCAAC	54629
rs534742648	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58802938	TTCATTTTCTTCAGT[A/G]TTCTTCCTTTACTTG	54629
rs534760129	in-del	-/A	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769266	CTTTACTAAAAATAC[-/A]AAAAAAAATTAGCTG	54629
rs534801523	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781079	TTCCAGACAGTGTTT[C/T]ATTCTTGTTGCCCAG	54629
rs534802656	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845305	CAGCTACTCAGGAGC[C/G]TGAGACAGGAGAATC	54629
rs534825574	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58830020	CTTATGAAACTTTTT[A/G]GGGCATTCCCTTCCC	54629
rs534833417	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58845409	AGACTCCATCTTAAA[C/G]AAAAAAGATAAACAA	54629
rs534833789	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58799683	AAATGGGAATTTTGA[C/T]TGGCAAAGGTTAGAG	54629
rs534857365	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58778269	TTTTAGTAGAAAAAT[A/G]AATGCACTAATTTAA	54629
rs534865749	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58851530	TGTAACCTCAAACTC[A/C]TGGGCTGAAGCAATC	54629
rs534873413	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774558	CCCTCGTGTAGCTGA[C/G]TATCTAGTGGGATGA	54629
rs534886371	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837159	TTGTGCCTTTGTTCT[A/G]TTAAGGCTGTTCATC	54629
rs534891599	snp	A/G/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855450	GGCTTTGTAAATATG[A/G/T]GGATGTAGAAAAGCA	54629
rs534910509	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795082	TCGGGAGGCGGAGGC[A/G]GGAGAATAGCGTGAA	54629
rs534973746	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788970	TGAGCCAAGATCATG[C/G]CACTGCACTCCAGCC	54629
rs535007239	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58818224	ACCTTGCATGTAGTA[C/G]TATGTAATAGGCATC	54629
rs535010680	snp	A/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771260	CGCGCGCGTTCTTAG[A/T]ACTCTCCCCGGTGAC	54629
rs535049167	in-del	-/A			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769655	AACCCCGTCTCTACT[-/A]AAAAATACAAAAAGT	54629
rs535069738	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58843305	CAGGCATGTACCACT[A/G]CACCTGGCTAACTTT	54629
rs535075598	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782980	GCTGGAGTGCAGTGG[C/G]GTGATCTTTACTCAC	54629
rs535092948	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801182	TTTCACCATGTTGGC[C/T]AGGCTGGTCTTAAAC	54629
rs535133973	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58784914	TGCTGGGACTGTAGA[A/C]GTGAGCCACCGTACC	54629
rs535134718	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58776666	GAAAGGAACAACAAC[C/T]GTATTTTCTGAAGTA	54629
rs535152503	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849314	AAGACCATCCTGGCT[A/G]ACATGGTGAAACCCC	54629
rs535216705	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771151	GAAAGGGCTGGGCCA[A/C]GTGGGCGGCTGCTGA	54629
rs535245637	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808532	TCTGTGTCTTTTCAT[G/T]GCTTGATAGCTCATC	54629
rs535276846	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802611	TCCTTTTTTTCTCAT[C/T]TTTTTCTCAGTATTT	54629
rs535276965	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58831484	TTGTGTCTGCTTTTT[C/T]ACTGCAACCTGCATG	54629
rs535288035	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820919	TATATAACTTACTTA[C/T]ACAGCAATACACATA	54629
rs535351834	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843904	AAAGTAGAAGAAAAC[C/T]TGTCAAATTTAATAA	54629
rs535376827	snp	A/G	0.00243853	0.0348327	intron-variant	FAM63B	GRCh38.p7	15:58803481	CATAAAAAAAAAAAA[A/G]AAGAAGAAGAATCAA	54629
rs535393095	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58796853	TATATAATTTAAGTA[A/G]TGAGTTACATGTATT	54629
rs535418170	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845983	CTTTCTTATTTTTGC[A/G]GGCTAGAAATTAAAA	54629
rs535477515	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790085	CACCCGGCAGGAAGA[A/C]CCTTTTTAGAAAATA	54629
rs535488988	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857398	AATTAGCCAGGCATG[C/G]TGGCGGGCACCTGTC	54629
rs535490817	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770806	TTAATTTTCCATATT[A/C]GGAGCTGAGAAACCA	54629
rs535527777	snp	C/T	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58806639	GGTATAAGCATGAGC[C/T]CAGAGCCATTAGAAA	54629
rs535536549	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58784085	AATACCAGCAATTTG[C/T]GAGGCTGAGGTAGGA	54629
rs535539436	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58832531	CCATGCCCAGACTTT[C/T]TTTTTTTTCTTTCTT	54629
rs535549099	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58821196	TTCAGGAAAATAACA[C/T]TAGTTATCTCTACTC	54629
rs535552080	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856925	TCTTCTTAATTTGTT[C/G]CAAAGAAAATGCTGC	54629
rs535611885	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58822004	CCTGTAATCCCAGCA[A/T]TTTGAGAGGCCAAGG	54629
rs535647369	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58808292	TTTTGAAAAATGTAT[A/G]ATGTCACGTATCTAC	54629
rs535665245	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58779740	CAAGAATTAGAATTG[A/G]TGTTGTAACTCTGGA	54629
rs535791750	in-del	-/CGGAT	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58854019	GGAGGCCAAGGTGGG[-/CGGAT]CACAAAGTCAGGAGT	54629
rs535826388	in-del	-/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58797934	ATTGTAATGCCTCTG[-/T]TTTACAGAAGAGGAA	54629
rs535844495	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834840	AATACCCTTAAAGCC[A/G]TTGCTCTCCCATTCC	54629
rs535850434	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58773491	CTGCCCTTAAAAGGC[C/T]GTCAAGCTGTTTGAG	54629
rs535864715	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58841664	CCTGCCTCGGCCTCC[C/T]AGAGTGCTGGGATTA	54629
rs535902359	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790597	CCTTAGTGGGGGGTA[A/G]GACAAGTGGGAAAAC	54629
rs535911864	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58834273	GACACAGTAACAATC[A/T]GATCTCTCTCTCTTT	54629
rs535959897	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837132	TAATAAGGGAATAAG[A/G]CAGAGAGAGGATTGT	54629
rs535963439	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58848603	AAAAATCAATTATCC[A/G]GGCATGGTGGCGGGC	54629
rs535965261	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784875	CCTGGGCTCAAGTGA[A/T]CCTTTCACTTCAGCC	54629
rs535976750	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58841366	CCAACACTTTGGAAG[A/G]TTTATGATTCTATGA	54629
rs535987712	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58848792	AATATGCATCTTTCT[A/C]GGACTTTTCTTTGAA	54629
rs535996006	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791926	GGAAGGAGAAAGAGC[C/T]GGCACGGTCAGCCAG	54629
rs536076730	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58777464	ACTGCTAGAGAGTAG[A/G]CGATCATTCATAATC	54629
rs536101643	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839644	GCCTAGGGTTAGGCT[C/T]TTTGGTGATCCTCTA	54629
rs536153123	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58854147	TACTTGGGAGGCTGA[C/G]GCAGCAGAATCTCTT	54629
rs536160567	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846485	GTAGTCCCAGCTACT[C/G]AGGAGGCTGAGGCAG	54629
rs536224987	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773346	AAAATCAAGTAAAGG[C/G]AATAGTGTTTATCAA	54629
rs536233829	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58853319	AAGAAAGCAAGATGC[C/G]CTTTTAAGTCTCATA	54629
rs536233902	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58780262	ATACAAAATTAGCCG[A/G]GTGTGGTGGCACATG	54629
rs536257098	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804722	TGAGGTCAGAGGATC[G/T]CTTGAGCCCAGGAGG	54629
rs536289460	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58773859	TTATATGTTTATTAC[A/G]TGACAGAAGTGGTAA	54629
rs536321173	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58789502	TACTCTATTGCCCAG[C/G]CTGGAGTGCAGTGGC	54629
rs536330692	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58852152	TTAGCCGGGCGTGGT[C/G]GTGGTGAACACTTGT	54629
rs536338675	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789867	GGTCAGGCTTGTCTT[A/G]AACTCCTGACCTCAG	54629
rs536443054	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58832978	GTGACCAAACATTAA[A/G]TTCTTTAATAATGTG	54629
rs536445572	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58792298	GAAGTGAAAACGTAT[A/G]TCCATACAGCTTGTA	54629
rs536452947	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58806444	CTCACTGCAGCCTCA[A/C]ACTCCTGGGCTCAAG	54629
rs536506081	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58785826	GGACTACAGGTGTGC[A/G]CCACCACACCTGGCT	54629
rs536513645	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58831686	TATTGGCCTTTTTCC[A/G]TACTTGGAACACACT	54629
rs536545349	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823358	GTTTATGCTATTCTT[C/T]TACTTGCAGTAAACA	54629
rs536605701	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816926	CCTGTGAATAGCCAC[C/T]GTACTCCAGCCTGGG	54629
rs536692493	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812478	GAATGATCCCTCATA[C/T]CTTTTACCCAGTTTT	54629
rs536705348	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788222	ATACATCTTAATCCC[A/G]ATAAATTGTAGAATG	54629
rs536735711	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58853452	TGTAGGTTTTCACTC[-/A]AAAAAGGTGTCTTAT	54629
rs536736339	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58799180	TTATTCAGGGCCAGT[C/T]GTGCCAGAACAAATG	54629
rs536741911	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58825479	TTCATGGCAGCAAAA[A/G]TCAGCAAGTTTAAAA	54629
rs536763866	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860603	AAAAAAAAAGTCAAG[A/T]AACTGAAATTCCCAT	54629
rs536768590	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781760	ATGCAAAAATTAGCC[A/G]TGTGTGGTGGCGGGC	54629
rs536775436	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58783531	CTTAGGATGTTTTAC[A/C]TTCCTGTTTAAGATT	54629
rs536797979	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805981	CGAGAGGCTGAGGCA[C/G]ATGGAACCCTTGAAC	54629
rs536807692	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819241	ATTGCTTGAGCCCAG[C/G]AGTTTGAGACCAGCC	54629
rs536867793	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58813111	AAGCATCATCCAGAT[C/T]GTTGCATCTATCAGT	54629
rs536930897	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813592	TCATAGTTGCTTGTT[C/G]GTTTGTGTGTTTGTT	54629
rs536957881	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857838	TGAATGAACAAATAT[G/T]GTCATTGCACTTTCC	54629
rs536984787	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830858	TGGGAATGTGCACAT[G/T]GGGCCACTCAGAATT	54629
rs536991835	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58807889	ACTGGCATCTACTTT[C/G]GAATGCTCTTTGCCC	54629
rs537038967	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838070	TGGAACATCTATCGC[A/G]TAAATACATTTCATC	54629
rs537060651	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801944	TTCTTTTTTTTACTT[C/G]TCAGTGTTGCAGACA	54629
rs537099845	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837418	TCTCAACAAATAATT[C/T]TGAAAGTTAGCCAGT	54629
rs537100562	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58789649	TTTGGTTTGTTTTTG[-/T]TTTTTTTTGTTTTTT	54629
rs537109188	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58781122	TGGTGTGGTCTTGGC[G/T]CACTGCAACCTCCAC	54629
rs537118965	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780028	TGTGCATTATTTTAC[A/G]TGCATTGTATGTGTT	54629
rs537128657	in-del	-/AGTC	0.0107246	0.0724382	intron-variant	FAM63B	GRCh38.p7	15:58779177	GGGATTACAGGCGTG[-/AGTC]AGTCACCATGGCCAA	54629
rs537165218	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58844620	AGTTATAGTTTTTTT[A/G]AAAAAATAAACGTCA	54629
rs537180316	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828679	CATTCTCCTGCCTCA[C/G]CCTCCCGGGTAGCTG	54629
rs537181313	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58840501	TATCTATTGGCAACA[A/G]ATAGGAATAGCCCTA	54629
rs537221899	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775155	TTTTCAGGCTACATG[A/G]TGTAATGACATCGCT	54629
rs537233415	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58850698	AAGTGATCCTCCCAC[C/T]TCAGCCTCCCCTAGT	54629
rs537267085	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837729	GCAGTACTTTGAGAG[A/G]CAGAGGTGGGAAGAT	54629
rs537284742	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769936	GGAGGTTGCAGTGAG[C/T]CAAGATCGTGCCACT	54629
rs537296751	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58821553	TGAGCTGTAAACAAA[C/T]TTGGAAACTGTTGGG	54629
rs537299590	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859029	TCACAAATATTACAC[A/T]TCCTATGTTCTTGAA	54629
rs537302559	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843253	CTCTTGGGTTCAAGC[A/G]ATTCTTCTGCCTCAG	54629
rs537306428	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783077	GACACCTGCCACCGC[A/G]CCTGGCTAATTGTTT	54629
rs537316475	snp	C/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772398	TGAAGGAATATTCCT[C/T]TATACATATATCGAA	54629
rs537317265	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58776344	CCCTACCTCATTCTC[C/T]AGGAGACAGAGAGAA	54629
rs537321629	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58797294	GGCAGATCACTTGAG[C/G]TCAGGAGTTCAAGAC	54629
rs537324346	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58828233	AAAATAAATTGTTTT[A/G]CCCATCCTTTTGAGG	54629
rs537336809	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58807546	TTTTTGTATTTTTTA[A/G]TAGAGACGGGGTTTC	54629
rs537346303	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58831579	TAACTATTTAGGATA[G/T]GAATGTCTGTATACA	54629
rs537371786	in-del	-/AT			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859364	GTGGAATTCATTTAG[-/AT]ATCTCTCAAGTAATA	54629
rs537426432	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771215	GCGGAGGCAAGCTCA[C/G]AGCGCACGGACAGAG	54629
rs537486121	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58773783	ATAACAGGGAAATGG[A/G]ATTCCCAGGGGAGAG	54629
rs537489927	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855805	TGCGTGCCTGTAGTC[C/G]CAGCTACTCAGGGCT	54629
rs537515630	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795223	GAAGTTGATAAGATA[A/G]TAGAGAAAAGAAGAG	54629
rs537578780	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795796	TTTTGGCCACCCTCC[C/G]TCCTGCACCAAGAAC	54629
rs537580425	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58789060	TTGTCAACTGGGGCC[A/G]GGCACGGTGGCTCAC	54629
rs537585020	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58803337	GCTGGGCATGGTGAT[A/G]CGCGCCTGTAGTCCC	54629
rs537639388	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58789541	GACTTGCTGCAATCT[C/T]GACCTCCCTAGGCTC	54629
rs537716254	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58786964	CCTCCCAAGTAGCTG[A/G]GATTATAAGCATGCG	54629
rs537720057	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58797594	TAAAATTACATTTGA[A/G]CTCAAATTCGTGGCT	54629
rs537732137	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820243	TGCACTCTAGCCTGG[C/T]GACAGAGTGAGATTC	54629
rs537755640	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58811635	GAGGAATACTACCCC[C/T]AAGCTATGGCCCAGC	54629
rs537759676	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58785117	ACTTGCTTTTGAAGT[A/G]ATGGTGGTGAAGGAA	54629
rs537779441	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834093	ATTTGTTTAACAAAG[C/G]ACACCCTGCACAGCC	54629
rs537791529	in-del	-/GT	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58844555	ACAGAGCGAGACTCC[-/GT]CTCAAAAAAAAAAAA	54629
rs537795224	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58814388	TTGAGTTTTGTTTTT[C/G]GTTTTGTTTTTTTTT	54629
rs537825026	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58777431	GAGTAAGGACTGAGT[G/T]GAAAGTATTGGTTCA	54629
rs537825104	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856745	TTTTCCCGGGACAGA[C/T]AGTAGTGATAGTGCA	54629
rs537844882	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58841246	CCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG	54629
rs537850774	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784895	TCACTTCAGCCTCCC[A/G]AAGTGCTGGGACTGT	54629
rs537911572	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785245	TTAGTGTGAAGTAGG[C/T]ACTTTTTAGTTTTAA	54629
rs537914426	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58778534	TAAAAAAACAGACAC[A/C]CACCAAAAAAAAAAA	54629
rs537932203	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58807394	CGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG	54629
rs538002834	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816165	ATAATAGCAAGGACT[G/T]GGCAGTGCTTTTTTT	54629
rs538005830	in-del	-/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58815673	GATATTATTTCCTTC[-/T]TTTTTCTTTTTTCTT	54629
rs538096657	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58862308	GATGGGAATATAAAT[C/T]GGTGCAGTCACTTTG	54629
rs538127825	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810920	TCCTGGAAGTTCACC[C/T]CACCTTCAGTGTTCA	54629
rs538137433	snp	G/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58804780	CACTGCATTCCAGCC[G/T]GGACAACAGAGTGAG	54629
rs538196661	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58798474	TTTTTTTTTTTTTTG[A/G]GACAGAGTTTCACTC	54629
rs538263114	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58833051	AAAACATTTACTGTT[A/T]TACTCTTTTTATCTC	54629
rs538290985	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840573	ACCTGGTCTTCTACA[A/G]TTAAACTGGGCGGAT	54629
rs538300212	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58828061	AACATGGTGAGACCC[C/T]GTCTGTACTAAAAAT	54629
rs538320929	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58832851	TGACATCTAATCATG[A/G]AAGTTTATATTTCAG	54629
rs538350341	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854937	AGTTAGTAAGCTATT[A/G]TATCTTCTGTTCTAA	54629
rs538358109	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58821973	ACCATCCATAGGCTG[C/G]GCACAGTGGCTCCCG	54629
rs538358965	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58847125	TATTCAAAGCCGAGT[A/G]GATTTGAGGAAGTAA	54629
rs538533497	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861552	ATCTACCCAGCTTAG[A/G]GTTGAACTGAATTTC	54629
rs538563973	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58852231	AGGCAGAGGTTGCAG[C/T]GAGCTGAGATTGTGC	54629
rs538577822	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58826930	TTCCTTCCTTGCTTC[C/T]TCCCTCCTTTCCTTC	54629
rs538632123	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860533	GAGCCAAGATTGCCC[C/T]ACTGCACTCCAGCCT	54629
rs538754883	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832106	GAAGCATTACCTCAA[A/T]TCACTTTTTGTTTTT	54629
rs538820153	in-del	-/A	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58785538	GAGGGACTGTGTTCC[-/A]AAAAAAACGTTTATT	54629
rs538848446	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830758	GAAAAACATGGCACT[A/G]AATAGACCATGAAAG	54629
rs538855511	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824091	TGGATAAACTGACTT[A/G]TGGAGTATGAAGCTA	54629
rs538859178	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58801100	TGCCTCAGCCTCCTG[A/T]GTAGTTGGGACTACA	54629
rs538910729	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58830222	CCTAGGATAAATATG[A/T]GTGAGTTTTTAAGGA	54629
rs538913868	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817573	TATTAAAATACAAAA[A/C]TTAGCCGGGCATGGT	54629
rs538926594	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58794404	GTGTGTGTTTTAAGA[A/G]TAAAATATTTTTGTT	54629
rs538928767	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58837943	CACTGCACTCCAACC[C/T]GGATGACAGAGTAAG	54629
rs538948587	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773972	TTAGACTTGCTCTAA[C/T]GGGCCAGAGTCCCTA	54629
rs538974669	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58788314	TGAATTAAAGACAAA[G/T]GAGGTGATTTAGAGC	54629
rs539035846	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781827	GAATTGCTTGAACCC[A/G]GGAGACGGAGTTTGC	54629
rs539052062	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812233	ATGAAGTCAGGAGTT[C/G]GAGATCAGTCTGGCC	54629
rs539053731	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806172	TCCGCCTTTCAGGTT[C/T]AAGAGATTCTCATGC	54629
rs539069365	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817726	GACTCTGTCTCAAAA[A/G]ACAAAAATAAAAAAA	54629
rs539089919	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826424	AGTAGAGATGGGGTT[A/T]CTCTGTGTTGGTCAA	54629
rs539096991	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782221	CTTTACAATTTCTAC[G/T]AAAAAATCATGAATA	54629
rs539112635	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844022	ATTCTATATTATTAT[C/T]TATGAAATTTTTCAG	54629
rs539134209	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813220	TGTTTTCCCGCCGGG[C/T]ACGGTGGCTCACGCC	54629
rs539150805	snp	G/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58819805	AATTGTTTCTTAAGG[G/T]TCTAACTTCTCATTT	54629
rs539158782	in-del	-/AAAATAT	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857908	AACCAGTCTTTATTA[-/AAAATAT]AAAATTTTTCTTCAT	54629
rs539161552	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800598	CCATTCATTCTTCCC[C/T]TCAAAAGATGCTTTT	54629
rs539178579	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807260	TGTGTTAAATTTTAT[G/T]TATTGGTTTTTCTTT	54629
rs539223039	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793829	GGATGAGGGGAGGAG[C/T]TGTTGAAAGTAAGAG	54629
rs539243636	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770745	GTAATCCAAAGCCGT[A/C]GAGTAGATATGCCTG	54629
rs539263291	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814219	TGCTGCGATTACAGG[C/T]GTGAGCCATCGCACC	54629
rs539292370	snp	A/G			downstream-variant-500B	FAM63B	GRCh38.p7	15:58862223	AGCCTGAGCAACAGA[A/G]TGAGACCCTGTGTCA	54629
rs539320189	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58834905	TTCAACATTTTAGCT[A/G]GATGTATGTCAGATG	54629
rs539323789	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808501	GTTTTCTTTACTACT[A/G]CGCATTTAAGTTTCC	54629
rs539335388	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812426	TGGCCAACAGAGCAA[C/T]GGTCCGTCTCAAAAA	54629
rs539347009	snp	G/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58837303	AGAGGCTGGGCATGG[G/T]GGCTCATGTGTGTAA	54629
rs539383718	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58825710	TCCCAGGTTCAAGCA[A/G]TTCTTCTGCCTTAGC	54629
rs539406625	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844546	GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA	54629
rs539432243	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837093	TTTAGGGAAGGGGTT[C/T]TTCCAGCATGGTGTC	54629
rs539446741	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58819356	AGGAGGCTGAGGTGG[A/C]AGGATTGCTTGAGCC	54629
rs539460577	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849811	CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC	54629
rs539489941	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58850640	CTAGGCTACAGTGCA[A/G]TGGTGTGATCACAGC	54629
rs539526228	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860063	CTTCTTCTTCTGCCA[C/T]TAAGTCTCTCTTTAT	54629
rs539557445	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858808	ATGGAGGCATTACAA[A/G]TAGTCTACAGTTTGT	54629
rs539624595	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857499	AGATAGCACCACTGC[A/T]TGCAAGCCTGGGCAA	54629
rs539635499	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774433	AGGTTGCGGTTAGCC[A/G]AGATCACGCCACTGC	54629
rs539635735	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58842189	CTGTTTCCCCTATCT[A/C]TTGGTTTTAAATTAC	54629
rs539671686	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820942	TACACATAAATAATT[C/T]ATAAATAAATATAAA	54629
rs539673313	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797842	GTGGTGGCAGAGAAC[C/T]GATGAGCAGAGCCAT	54629
rs539686214	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804533	TTTGCAAGCACCAGG[C/T]GTGGTGGCTCATGCC	54629
rs539700300	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802118	TTCAAAGCACTATAG[C/T]ATATACATTGAAAAA	54629
rs539733376	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814954	GGACTTAATTTCAGT[C/G]AAGTTCACTTTATTT	54629
rs539761284	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855719	TGAGGCCAGGAGTTC[A/G]AGACCAGCCTGGCCA	54629
rs539766602	snp	C/T	3.6103e-05	0.00424855	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771638	CGGACCCTGCAGCTC[C/T]TCCGCGGGTTTGGAC	54629
rs539865183	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58796297	AACTATCTTAAGCTC[A/G]AGCTAGAGGTGGAAA	54629
rs539886194	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835767	GAACATGTATGCAAA[C/G]GCCCTGAGGAAGGAA	54629
rs539905735	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58789600	GTAACTGGGACTGCA[C/T]GCACATGCTACCACA	54629
rs539932529	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58789912	TGAGCCTCCCAAAGT[A/G]CTGGGATTGCAGGCG	54629
rs539950130	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843056	CTCTCTTAGAAATGT[A/G]TAAATTTTCAAATTA	54629
rs539952727	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843727	TAGTCCCAGCTACTC[A/C]GGAGGCTGAGGCAGG	54629
rs539965323	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835006	ATGGTGAATACTGCT[A/G]AATCATTTTATTTCT	54629
rs539967286	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789991	ACTGTGTTTCCCAGG[C/T]TTGTCTTGAACTCCT	54629
rs539967371	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783170	AGGTGATCCGCCCAC[A/C]TCGGCCTCCCAAAGT	54629
rs540028557	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784046	AATAATTTTCCAGGG[C/T]CGAGTGCAGTGGCTC	54629
rs540089689	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58821444	ATACATGTTTATGAC[C/T]TTAAGAAATAAAGTT	54629
rs540114618	snp	A/G	1.66214e-05	0.00288278	missense, intron-variant	FAM63B	GRCh38.p7	15:58821787	AGATCATCTCTTGTA[A/G]ACAGTCAGACAATAG	54629
rs540153450	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815268	ATCCTTCCCTTTACC[C/T]TTCCCTCCTCATTGC	54629
rs540165734	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58778650	TCTTTTTTTTGAGAT[A/G]GACTATCATTCTGTC	54629
rs540190279	snp	C/G	9.50616e-05	0.0068936	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771789	GGAGACGCGGGAGCC[C/G]GCCCGGATCTCGCCG	54629
rs540233004	in-del	-/A	0.410568	0.191619	intron-variant	FAM63B	GRCh38.p7	15:58803946	ACCCCAGCTCTACTG[-/A]AAAAAAAAAAAAAAA	54629
rs540248076	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803398	ACTTGATCCCAGGAG[A/G]CGGAAGTTGCAGTGA	54629
rs540314671	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804545	AGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	54629
rs540319944	in-del	-/AAAAC	0.0350946	0.127733	intron-variant	FAM63B	GRCh38.p7	15:58823669	ATCTGTCTCAAAAAC[-/AAAAC]AAAACAAAACAAAAC	54629
rs540334975	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58783217	TGACCGACTCTGCCC[A/G]GCCCCTGACTTCTTT	54629
rs540374499	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804886	TAATTCCAGGTACTC[A/C]GGAGACTGAGGCAGG	54629
rs540385263	snp	C/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58846010	AAAACAATTGAGCTC[C/T]TGGAGATAGAGAGTA	54629
rs540415835	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797988	TGCTGTCTCCATCTG[A/G]GCACCTTCTATGATT	54629
rs540445186	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58801980	AAGACTGATAATACC[C/T]ATTGTTGGTGAGGTA	54629
rs540520380	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58822273	AAAAAAAAGAAGAAG[A/T]AGTAATCATTCATAA	54629
rs540547307	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836673	ACCCAGGCTTGAGTG[A/C/T]GCTGCTGCAATCTCA	54629
rs540585861	snp	C/T	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58815467	GCAATCCTCCCTACT[C/T]GGCCCCCCAGTAGTT	54629
rs540617465	snp	A/G	1.67326e-05	0.00289241	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772213	TGCTGGCCATCCTCA[A/G]TGTTTTGCTCCTGGC	54629
rs540659937	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823713	GTATAGAGTCGTTGA[A/T]CATTGATTCATCTGA	54629
rs540735660	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774908	AGCATGCTAATGAAT[C/G/T]TGGAGATTATTTTGT	54629
rs540796474	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58845638	TGGAGAACAGTTTAG[A/C]GGTTCCTCAAGACAC	54629
rs540851333	snp	A/G	0.00557542	0.0525036	intron-variant	FAM63B	GRCh38.p7	15:58797215	TAAAATATATTATTA[A/G]GATTAATTTTGCCAG	54629
rs540867413	snp	A/G	3.35289e-05	0.0040943	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851905	CAGACGGGCTTCTCA[A/G]TACTATCAGGAACAG	54629
rs540892262	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791991	ATCGTAATGAAGAAA[A/T]GTTTCAAGGAAGAGT	54629
rs540893096	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811784	TAGAGGTTAGTCTCC[C/T]GAATAGAGAAGAAAT	54629
rs540952218	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793841	GAGTTGTTGAAAGTA[A/G]GAGGGAAGGTATAAA	54629
rs540959538	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785566	ATTTAGAAAAACAGA[C/G]AGTCGACAGTAATTT	54629
rs541020911	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58779435	TTCACATACTCTCCT[A/G]GTTTCCATCTAGGTT	54629
rs541032856	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786078	TAAATCTACTGGATG[A/G]CTAAATATAACTATT	54629
rs541062045	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58796329	ATGTAAGGCATATTG[A/C]AGGAACAGTGTATGT	54629
rs541067362	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858171	GTGTGCTTAGGTAAA[C/G]TAACTTCTTCCATGT	54629
rs541105597	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58849530	AAAACTGGAGAAGGG[A/G]AATGAAGGCAGAGTG	54629
rs541123606	snp	G/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772645	ATATCATGGACTAAG[G/T]TTTCATGGTTATATT	54629
rs541151555	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58830447	GCTCACAGGAAATGC[C/T]CATTGGAGGATTTCA	54629
rs541188291	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58849659	AGTTTGAAGAATTCA[C/G]AAGAACTTGAAGGAC	54629
rs541198227	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787763	AAAAAAAGCCTGGCT[A/G]TAAAGATTCTAATAT	54629
rs541221447	snp	G/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58781290	CTCCTGACCTCAGGC[G/T]ATCAGCCCACCTTGG	54629
rs541222965	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58774007	TTTTTGTAGGAAGGA[A/G]TAACTATTATTTTCC	54629
rs541226150	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58812437	GCAACGGTCCGTCTC[-/A]AAAAAAAAAAAAAAG	54629
rs541278462	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836845	AATTGGTCTTGAGCT[C/G]CTGGGCTCAAGCAGT	54629
rs541281944	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774785	GAAAAGGGTTTCTTC[C/T]ACTTGGAACCTTCAA	54629
rs541284623	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58794726	TATCACTTAAGAGAA[C/T]TGCATTGTCGTCAAG	54629
rs541320032	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58806298	ATGCTGGTCTCGAAC[C/T]CCTGGCCTCAAGTGA	54629
rs541332798	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58844270	TCTCCATTGTTGGCC[A/G]GGCACGGTGGCTCAC	54629
rs541350882	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58853507	CTCCCAATTCTCAGG[A/G]GTTCTTTTCTCCTTT	54629
rs541358180	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58838330	TTGAATCCAGGAGGC[A/G]GAGGTTGTAGTGAGC	54629
rs541359221	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58819896	CCCAAGGATCCTCTC[A/G]CAAAGAAAAGGATTT	54629
rs541381491	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58791314	AATTTCTGTAATGAT[A/G]GAAATGTTCTGTATC	54629
rs541385022	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828410	GCAACATTTTAAAAT[A/G]AATCAAGTTTCCTTC	54629
rs541442068	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770442	TGAAAACTGCATGGC[C/T]TTAAGAGGAGTCCAT	54629
rs541444974	snp	C/G	0.00716266	0.059414	intron-variant	FAM63B	GRCh38.p7	15:58800683	TTTTTTTTTTGAAAC[C/G]ATTAGCCAGGTGTGG	54629
rs541486708	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787194	GCCAGAGGTGTCACC[A/G]TGTTGGCCAGGCTGG	54629
rs541535768	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58841685	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	54629
rs541570311	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58794772	CAGATAATAAGGTGA[A/G]GGGAACATTCAGAGG	54629
rs541631591	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848276	CTGTTCAGTTAGCCA[A/G]TATTCACTGAGGAGT	54629
rs541670823	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58828808	CCTCATGATCCGCCC[A/G]CCTTCCAAAGTGCTG	54629
rs541680221	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58818822	TTTTTTGTATTTTTT[A/G]TAGAGATGGGGTTTC	54629
rs541728913	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769741	GGAGAATGGCGTGAA[C/G]CCGGGAGGCGGAGCT	54629
rs541729911	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58789162	CTAACACGGTGAAAC[C/T]CCGTCTCGACTAAAA	54629
rs541741774	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58819413	TGATCACGCCACTAC[A/G]TTCCAGCAAGAGTGA	54629
rs541789885	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820136	TTGGGCATGGTGGCG[G/T]GCACCTGTAGTCTCA	54629
rs541842408	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782043	AAATTAAAATGTAAA[A/G]CATGTGTAATAGCTT	54629
rs541853198	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820313	GTCAGGTGTGGTGGC[A/G]GGCGCCTGTAATCCC	54629
rs541873090	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58795746	CCCTTTGAAGGCTAT[A/G]AACCATTATAGTGTC	54629
rs541896508	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808142	CTGTTCCTCCTAACC[C/G]CATACACACAGCTTC	54629
rs541909135	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58817621	CCAGCTACTCAGGAG[G/T]CTGAGGCAGAGAATT	54629
rs541952558	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58814588	CTCGCCATATTGCTC[A/G]GGCTGGTCTCGAACT	54629
rs542016199	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808859	TCCACCCGCCTCAGC[C/T]TCCCAAAGTGCTGGG	54629
rs542114810	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857331	CTGAGATCAGGAGTT[C/T]GAGACCAGCCTGGCC	54629
rs542134628	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58803468	AAGACTCTGTCTCAT[-/A]AAAAAAAAAAAAAAA	54629
rs542135625	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58800556	TAAGCTGTTCGTGTG[A/T]CATGATCTTTCTTAT	54629
rs542170113	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846759	GGTGCTACGAAACAC[A/G]TACAAAACAATTGTG	54629
rs542203049	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783356	TATTGGTATTCTAAT[G/T]GTTAAGCATTTAAAA	54629
rs542203291	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827620	AGGCGCCCGCCACCA[C/T]GGCCGGCTAATTTTT	54629
rs542229160	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853616	TCGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC	54629
rs542270012	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790501	TAAGCTGGGAAGCTG[G/T]TGGAGGATTTTGAAC	54629
rs542297404	snp	C/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58777123	ATAAATTGAGGTTTT[C/G]TTTAAAAACTATTAG	54629
rs542332664	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58815986	CCCAGCCAAAAGGCT[A/G]TTATTTCTTTACCTG	54629
rs542357383	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58835702	TGATACCTAAAAAGT[A/G]AATCTTCTAGTTTAA	54629
rs542358731	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771337	TGTCATGGCGTCCAA[A/G]GCGCTGGCTGCGGAG	54629
rs542367824	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815143	TCGAGGAAAGGGCCC[A/G]ACTTTATTCATATAC	54629
rs542410186	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58778757	TCAGCCTCCTGAGTA[G/T]CTGGGACCACAGGTG	54629
rs542427922	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833289	TTCACTGATAACTCT[A/C]CATCCCATACACACA	54629
rs542428217	snp	C/T	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58840606	TCTTTGTGAAATACA[C/T]ATTGACCTCACTATT	54629
rs542465006	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58802918	TGGAAAAAAGCAAGC[A/G]GAGCTTCATTTTCTT	54629
rs542467341	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772312	GCTGCTGCATGTCAG[A/G]TGATGGCTTCCTTTC	54629
rs542534590	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838885	TGAGCCCGGCCTAAT[G/T]TTTATTACGACTTTT	54629
rs542657720	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845544	CCAAAAGACAGACAA[A/T]AACAAATGTTGGTGA	54629
rs542680906	snp	C/T	0.00597247	0.0543191	intron-variant	FAM63B	GRCh38.p7	15:58791072	GTAGTCCCAACTACT[C/T]GGGAGGCTGAGGCAG	54629
rs542698592	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798563	TGGGTTCAAGCGATT[A/G]TCTCACCTCAGACTC	54629
rs542700020	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58785594	TTTGCCGGAGTTTCA[G/T]TTTAAAAATATGCCA	54629
rs542723469	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844830	TGAGGCAGGACAGTC[A/G]CTTGAACCCAAGAGG	54629
rs542738573	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58805674	ATTTATATTTTGTAA[C/T]ATTAAGTATAATTTG	54629
rs542822633	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860067	TTCTTCTGCCATTAA[A/G]TCTCTCTTTATCTGA	54629
rs542874249	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822861	AGAAATCATGAGAAG[C/T]AGGGCATGAGTTTTA	54629
rs542876078	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815857	GCTAATCTTTGTATT[C/T]TTAGTAGAGACGGGG	54629
rs542914136	in-del	-/AG	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58792606	GCAAGACTCTGTCTC[-/AG]GGGGAAAAAAAGAAA	54629
rs542919403	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823760	GCATGAGGCAGCAGT[A/G]TTCAAATTTTAGGAG	54629
rs542982933	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58817216	GCAACTTTAAAAAAT[C/G]AATAAAGGATTAATA	54629
rs542986037	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786912	TTGGCTCACTGCAAC[C/T]TCTGCCTCCCGGGTC	54629
rs543287636	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58783814	GCCAAGCATGGTGGC[A/G]CACACCTGTGGTCCC	54629
rs543336812	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58777823	AGACGGGGTCTCACT[A/G]TAGTGCCCCAGCTAG	54629
rs543337405	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800730	TCCCAGCTACTCAGG[A/C]AGCTGAGGTGGGAGG	54629
rs543365136	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58839587	TCCACCCACCTTGGC[C/T]TCCCAAAGTGCTGAG	54629
rs543373277	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58775201	ATGTGTGCCTCTGTA[C/G]TTTGTGTTTTAAATT	54629
rs543453710	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58775196	ATGCAATGTGTGCCT[C/G]TGTACTTTGTGTTTT	54629
rs543490151	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856435	AAAATCCAGGGTCAA[A/G]CTGTATCTTTTATGT	54629
rs543496038	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811809	AGAAATGGAGAGTCA[A/C]TTGGAAGGGTGAAAG	54629
rs543496787	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774090	ACTGTGGTGTGGAGT[A/G]TTTGGGGATAGATGC	54629
rs543526450	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836741	CTCATGGCTCAGCCT[C/T]CCAAGCAACTGGGAC	54629
rs543556468	snp	G/T	0	0	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769294	CTGGACCTGGTGGCG[G/T]GCGCCTGTAGTCCCA	54629
rs543623398	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844088	GAGTCTTAAGAAAGC[A/G]TTGACTGCATAATCT	54629
rs543657771	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58800082	GAAGCATTTTAATTT[C/T]GCCCAGAGTTGCCTG	54629
rs543658377	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58793327	TGTGGTGGCACATGC[C/G]TGTAGTCCCAGCTAC	54629
rs543715027	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58827703	GTGATTCTCCCGCCT[A/C]GTCCTCCCAAAGTGC	54629
rs543721025	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770869	TCCAAATACTACAAC[C/T]ACCTCCAACCACCCA	54629
rs543724172	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58799293	GCAAACACGGCTGGG[C/T]GCGGTGGCTCACGCC	54629
rs543726956	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842254	TTGAGGTTGGTTGTT[G/T]TGTTGTTGTTATTTC	54629
rs543758729	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58825931	TCTTTAACAGTTGTT[C/T]CTAGGACAAAAATAT	54629
rs543774487	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857054	AGGAAAAACTAAAAA[A/G]TGTAATGTGTTAATT	54629
rs543786193	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58781252	AGACAGGGTTTTACC[A/G/T]TGTTGGCCAGGCTGG	54629
rs543789723	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58841610	CAGTTTCACCATGTT[C/G/T]GTCAGGCTGGTCTCG	54629
rs543839064	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58825033	TTTCATTTTCTGTTT[A/G]GCCTGCAATTGTAGC	54629
rs543848930	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794472	AAGAGACATCTCCAT[A/G]CATATTGAAATTACC	54629
rs543850010	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58848220	GGTCATGTTAAACAG[C/T]TGACATATATTTCAC	54629
rs543878795	snp	A/G	0.00042919	0.0146428	intron-variant	FAM63B	GRCh38.p7	15:58802292	AAAGGCAATTTTACA[A/G]TTCTTTTTTTTTTTT	54629
rs543882115	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58795521	GCCGTTCTCCTGCCT[C/G]AGCCTCCTGAGTAGC	54629
rs543910203	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788546	CTTATTTCAAAACAG[A/G]CCAGTAGTACAGTTT	54629
rs543940199	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789212	GCATGGTGGCAGACG[C/G]CTGATGTCCCAGCTA	54629
rs543942095	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58796256	TGTTGTAAAGAATAG[A/G]AAAGGTTGTTTGAGG	54629
rs543990082	snp	A/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58828246	TTGCCCATCCTTTTG[A/T]GGAAAAAATACATTA	54629
rs543998606	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58819474	TCCAGCGTGGGTGAC[A/G]GAGCGTGGGAGACAG	54629
rs544002604	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58789873	GCTTGTCTTGAACTC[C/T]TGACCTCAGGTGATC	54629
rs544045780	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775915	TTGCCCAGGCTAGAG[C/T]GCAGTGGCAGGATCT	54629
rs544050775	snp	A/C	0.000729032	0.0190784	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854499	GGGCCAGCCAGCACA[A/C]GCCTCTCCATCAAGT	54629
rs544051859	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835152	GCTATGGTTTTTGCC[A/T]ATTAAGGACCTCGTA	54629
rs544058635	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820011	TGGCTCACACCTGTA[A/T]TCCCAGCACTTTGGG	54629
rs544086728	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807791	TCTTAGACTTTATCT[C/T]CTACAACTTTTCACT	54629
rs544129721	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827092	GCTACGTAGGTGACA[C/T]TGTGTCTTTCCCAGT	54629
rs544140538	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58783552	GTTTAAGATTTCACT[C/T]ACAGTTTAAACAGAA	54629
rs544164455	in-del	-/TT	0.420096	0.183214	intron-variant	FAM63B	GRCh38.p7	15:58775860	AGTAAAGAGGCTAAA[-/TT]TTTTTTTTTTTTTTT	54629
rs544164512	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58814646	CAAAGTGTGAGACTA[C/T]GGCTGTGAGCCACCA	54629
rs544181808	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820393	AGGTTGCAGTGAGCC[C/G]AGGTCACACCACTGC	54629
rs544207972	snp	A/G	0.00993419	0.0697739	intron-variant	FAM63B	GRCh38.p7	15:58778016	TGAGGGCTGTGACCC[A/G]TGTAATTAGGTGTTT	54629
rs544229165	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815177	TAGATAGCCAGTTGT[C/T]CTAGTACCATTTGCT	54629
rs544276900	in-del	-/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58787735	GAGCGAGAGTCCGTC[-/T]CAAAAAAAAAAAAAA	54629
rs544285042	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58780783	CCTTTCCCATTGTAG[C/T]TTATTAAATATATTC	54629
rs544336845	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833184	CATCAGTAATATACC[A/G]AAAATGTTCAGTAGC	54629
rs544397745	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839931	TCCACCTCCCAGGTT[C/G]AAGCAATTCTCGTGC	54629
rs544435290	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58803559	CGGTGACTCCTGCCT[A/G]TAATCCCAGCACTTT	54629
rs544531741	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784201	TGTGGTGGTGCGTGC[C/T]TGTAGTTCCAGCTAC	54629
rs544651715	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860977	CTTGTTACAGATTCA[A/C]ACATTACAAGTAGGA	54629
rs544669057	snp	A/G	0.00156493	0.0279288	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771753	GCCGTGGCCGGAGTG[A/G]GTCATGAGTTGGGTA	54629
rs544669584	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770316	ATCCCCAACAGCCTA[A/G]AAAATGTTGAAAGAA	54629
rs544671549	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795703	GCCACTGCGCCCAGC[C/T]TATCGTATGTGTTTT	54629
rs544798146	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846643	CACAAATACATACAC[A/G]TACTATGTATCCACA	54629
rs544864897	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849030	GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA	54629
rs544920573	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845407	TGAGACTCCATCTTA[A/G]AGAAAAAAGATAAAC	54629
rs544931194	snp	A/T	0.473909	0.111197	intron-variant	FAM63B	GRCh38.p7	15:58852971	TTTTTTTTTTTTTTT[A/T]AGACAGAGTCTCACT	54629
rs544991141	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58846920	TGTAGGCTTAATTGG[-/A]AAAAAAAAACAGGCA	54629
rs545024421	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791932	AGAAAGAGCCGGCAC[A/G]GTCAGCCAGGTAGAA	54629
rs545024427	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784984	AAAATCAGACAGACT[A/G]CCACAACTGTTAATT	54629
rs545078562	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58792538	TTGAACCCGGGAGGC[A/G]GACGTTGCAGTGAGC	54629
rs545087904	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58785451	GGCTTTGCATGCCAT[A/G]CTGTCTCTGCTGCAC	54629
rs545103358	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58850305	AGTCATCTTTTAGAA[A/G/T]AATATTTAATAATCT	54629
rs545147452	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58799892	GCAGGAATATGAAAC[G/T]CAACATAAACTGGAA	54629
rs545162888	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858417	GATTAAACATTTTGC[A/G]CTTGCACAAAACCTT	54629
rs545174067	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859126	GTAGAATTTTCTTTG[A/G]GTATGGCGTGATCTC	54629
rs545186997	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772788	ACCCAATTACCGTAA[C/T]TTCTTGGTTTTCAAA	54629
rs545249291	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58810644	CACCCGTACTTCTCA[C/T]ACCAATCACAAGTTC	54629
rs545322650	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829547	ACATGAAAGTAATGT[A/G]CTATATCTCCACTGA	54629
rs545357492	in-del	-/TA	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58839811	CTATTTATTTATTTT[-/TA]CCACAGCTGATTTTA	54629
rs545379334	snp	C/T	0.00517822	0.0506191	intron-variant	FAM63B	GRCh38.p7	15:58824903	TCAAACTCCTGACCT[C/T]AGGTGATCCGCCAGC	54629
rs545384256	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828846	AGGCATGAGCCACTG[C/T]GCCCAGTCTTAAATT	54629
rs545422118	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58812576	GTAAAGTCGAGATAC[A/G]TGGCTGGACACAGTG	54629
rs545471823	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836674	CCCAGGCTTGAGTGC[A/G]CTGCTGCAATCTCAG	54629
rs545480119	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774744	TTCTGGGCAAAGAGA[A/G]TAGTGTATTGAAAGA	54629
rs545545460	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58807623	CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC	54629
rs545593950	snp	G/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855681	ATCCCAACATTTTGG[G/T]AGGCCAAGGTGGGCG	54629
rs545605852	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58775144	GTCCGTGGAGTTTTT[C/G]AGGCTACATGATGTA	54629
rs545620364	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58824341	ACATCATGGTGAAAG[C/T]AAAGAAAGAAACCCT	54629
rs545648879	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780534	AAGTTCAAGATAGCA[A/G]TAAGTCTGGTGGACA	54629
rs545701220	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58788530	ATTCTTCTCTAAGCT[G/T]CTTATTTCAAAACAG	54629
rs545717982	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58786030	GAAATGATGATCAAA[A/C]TTCAAAGACATCTCT	54629
rs545718404	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58774204	ATGCAAAGATGAGGC[C/T]GGGCGCGGTGGCTCA	54629
rs545784222	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58801629	TAAAAATACCATCTT[A/T]TTAAATGAAAAGAAA	54629
rs545813670	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769426	GAGACTGCGTCTCAA[A/G]TGGGAAAAAAAAAAA	54629
rs545830239	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826633	CAAGGAATTCTCTTA[C/T]ATAAATTCTCCTATA	54629
rs545840694	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58809725	TTGTTTTATATATAT[A/G]CATGTTTATCTCTCC	54629
rs545874528	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769678	CAAAAAGTTAGCTGG[C/G]CGTGGTGGCGGGCGC	54629
rs545932475	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58842262	GGTTGTTTTGTTGTT[A/G]TTATTTCTTTTTTAC	54629
rs545937278	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800905	GTCTAGCTCTCACAA[A/G]AAATCAGTTAACTAG	54629
rs545965616	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58838809	TGGTCTCAAATCCCT[A/G]ACATCAAGTGATCTG	54629
rs545980444	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820078	CAAGACCATCCTGGC[C/G]AACATAGTGAAACCG	54629
rs545995735	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794056	GATGAGCGTGTTGAC[A/G]AAAGAATCTAGGGTA	54629
rs546001567	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58849330	ACATGGTGAAACCCC[A/G]TCTTTAATTAGAAAA	54629
rs546014896	snp	C/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772567	TTCTTACTGACCTTA[C/T]CACATATGCAAAAAA	54629
rs546039405	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58787654	AGGCAGGAGAATGGC[A/C]TGAACCGGAGAGGCG	54629
rs546062761	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848944	GCCAGGCAAGGTGGC[C/T]CACACCTATAATCCC	54629
rs546082899	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58778711	GGCTCCGAATAGCCT[C/T]GACCTCCCGAGCTCA	54629
rs546119507	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58775586	GTTCTTTGTCCCCCT[C/T]TTTGATGAGGATAAT	54629
rs546120620	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795373	CTCACTTCAGGACAT[C/T]TTAATACTGTAGATA	54629
rs546121273	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856333	TTTTTTCAACTATGT[C/T]ATTAACTTTATGATC	54629
rs546193546	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840735	GATCTCGGCTCAGTG[C/T]AAGCTCCGCCTCCCA	54629
rs546196925	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789287	AGCTTGCAGTGAGCC[A/G]AGATTGCACCACTGC	54629
rs546250570	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775581	AGAGAGTTCTTTGTC[C/T]CCCTCTTTGATGAGG	54629
rs546269742	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782963	CTTGCTCTGTCACCC[A/G]GGCTGGAGTGCAGTG	54629
rs546284329	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58828175	AAAAAAAAAAATCAT[A/G]TGAGCTTTTATCTTT	54629
rs546311641	in-del	-/CT	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58811796	CCCGAATAGAGAAGA[-/CT]AATGGAGAGTCAATT	54629
rs546319880	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58839386	GTCCAGGCTGGAGTG[C/T]AGTGGCACAATCTTG	54629
rs546326305	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58796885	CTGACCCTGTTTCCT[A/T]TCCAGCTCTTCCATA	54629
rs546332969	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783761	GGAGTTTGTTCAACA[C/T]GTCAAAACCCCATCT	54629
rs546340906	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820304	CAAAAATTAGTCAGG[C/T]GTGGTGGCGGGCGCC	54629
rs546357547	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58853249	TGAGGCACCACGCCT[C/G]GCCTAAACTGTTCAT	54629
rs546383345	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846269	CCACATTTACCCTCA[C/T]GTGATTATTATGCAT	54629
rs546389066	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58820158	GTAGTCTCAGCTACT[A/C]GGGAGGCTGAGGCAG	54629
rs546396482	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58777275	GGGGTATAGGGGCAG[A/C]GAATTAGAGAATTGA	54629
rs546404035	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814531	AGCTGGGCACATGCC[A/G]CCATACCCTGCTCAC	54629
rs546409284	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827180	GATAAGATAATATCT[A/G]CCAGGTTTTTATATT	54629
rs546416607	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861120	TGTGAATCTTTTCCT[A/T]GAATTGTGCAGAATA	54629
rs546418972	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58852173	GAACACTTGTAATCC[C/T]AGCTACTGGGAGGCT	54629
rs546426817	snp	C/G	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58841497	TGCAACCTCTGCCTC[C/G]CAGGTTCAAGCAATT	54629
rs546426935	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58808502	TTTTCTTTACTACTA[C/T]GCATTTAAGTTTCCT	54629
rs546488347	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58838527	GTAATAAACAGGCAA[C/T]CAGACATAAATATCT	54629
rs546490286	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808988	AGGCTGAGGCGGAGA[A/C]TCACTTGAGCTCAGA	54629
rs546509503	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808813	GTTTCACCCTGTTAG[C/G]CAAGATGGTCTTGAT	54629
rs546525179	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58835157	GGTTTTTGCCTATTA[A/C]GGACCTCGTAGTTTG	54629
rs546551657	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803024	GGAAGAAAGAGACAT[C/T]GTTGGAACCTTCATA	54629
rs546551693	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58809505	TAGATAAAGAATTAT[A/G]AATAATGTTGCAATG	54629
rs546555387	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840200	ATGGATGTGTAATCA[A/G]ACTGATCCATTTTTT	54629
rs546599726	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58827447	TTAAAAAAAATTGTA[A/T]CCATATAAACTCATG	54629
rs546603322	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58826448	TGGTCAAGCTGGTCT[C/T]GAACTCCCAACCTCA	54629
rs546613058	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803647	ATGGAAAAACCCCAC[C/T]TCTACTAAAAATACA	54629
rs546641767	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58831265	CCTACTTTTAGTTTT[A/G]AAGCAAGAATTGAGA	54629
rs546664841	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826858	CTTATTCCTTCCTCC[C/T]TCCCTTCCTCCCTTC	54629
rs546690032	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811119	AACACAGTCACTCCT[A/G]TTGGTACAGCAATGC	54629
rs546697899	snp	A/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58796792	CCTCCGGAAGTGCTG[A/G]GATTATAGGCATTAG	54629
rs546703185	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830654	AGGCACATCACAGCC[G/T]TTGTCTACTGAATGC	54629
rs546742743	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58845848	GTACACATACACAAC[G/T]GAGCACTATTCACAC	54629
rs546746230	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58820650	CTCAAACTTCGCTAT[A/G]CATCGGAATCACCTG	54629
rs546756777	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849318	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	54629
rs546764254	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58807720	AGAAAACTGATGTGG[A/G]CAAAATGACTCCTTA	54629
rs546832190	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58862026	TAGGGCCAACTTTTG[A/G]TAAAGAGAAAATTTC	54629
rs546832560	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58829695	GGCAGTGGTACTTTT[C/T]AGCACAGGCATACCC	54629
rs546835534	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58821924	GACTTCTAAAAAACA[C/T]ATGTTATATTACTTG	54629
rs546842447	snp	C/T	0.000183594	0.00957932	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771545	GGCGGAGACCAGCGG[C/T]GGGAATGGGCTGGGG	54629
rs546898654	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822472	GAATGGACTTTATCA[C/T]TGATCCTGAATACTT	54629
rs546916655	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845050	GCTCTCTAGAAAAAA[A/G]AAAATCTCATAATCA	54629
rs546931412	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58792596	GGGCGACAGAGCAAG[A/T]CTCTGTCTCAGGGGG	54629
rs546978156	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58851163	GTTTTTAATAGAGAC[A/G]GGGTTGTACCATGTT	54629
rs547008527	snp	A/C	0.000798403	0.0199641	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772050	GCTGTTCCTCTGTGC[A/C]AGGAGGAGGAGGGGG	54629
rs547054269	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58797437	CACTTGAGCCTGGAA[A/G]TTCAAGGCTGCAGTG	54629
rs547123280	snp	A/G			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770765	AGATATGCCTGCTTT[A/G]AAATCTGCATCTCGT	54629
rs547168026	snp	C/G	0.000134954	0.00821333	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771886	GCAGTTGCAGCGACC[C/G]GAGCCCTCCTGGGGA	54629
rs547222275	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784767	TGGAACTACAGGCAC[A/G]TGCCACCACACCTGG	54629
rs547273562	snp	C/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58844538	GTACTCCAGCCTGGG[C/G]GACAGAGCGAGACTC	54629
rs547283514	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58785044	TGTTTCTCCTTTGAA[A/C]AAATCTAAAAAGACA	54629
rs547294043	in-del	-/CTC	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58798224	AAAGCTCAAGCAATT[-/CTC]CTGCCTCAGCTACCC	54629
rs547315609	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58839122	TTATTTAATTTTTTT[G/T]TGAGTGTGCGTTAAA	54629
rs547349784	snp	A/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58778852	GAATCTCATTTAGTC[A/G]CCCAGGCTGGAGTGC	54629
rs547363227	snp	A/C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772435	TGCCCCTAACCTCAG[A/C/T]CTTCTCTTGTAGTGT	54629
rs547419315	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792613	TCTGTCTCAGGGGGA[A/G]AAAAAGAAAAATGTT	54629
rs547441447	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858692	CTATTCCATGCACAA[C/G]TTACCTTAAAACATG	54629
rs547517156	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58780636	CCTTAGATCGATTCC[C/T]GGGATCTTGGTACCA	54629
rs547577785	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774253	TTCGGGAGGCCGAGG[C/T]GGGTGGATCACCTGA	54629
rs547614371	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855667	GGCTCACGCCTGTAA[C/T]CCCAACATTTTGGGA	54629
rs547646937	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58818085	TCTGCATACCACTAT[A/G]TACAACAACCTTACA	54629
rs547662909	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829097	AAGTTTACAAATAAA[G/T]AAACTGCTGTGTAAC	54629
rs547706591	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812036	ATCATACCAGCCAAT[A/G]CCTTTCAAATTTATT	54629
rs547727376	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836202	GGCGTGAGCGACCGC[A/G]CCCGGCCTATTGCAT	54629
rs547727686	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58828647	GCTCACTGAAAGCTC[C/T]GCCTCCCAGTTCACG	54629
rs547744514	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800320	GCAAACTGTATCATT[C/G]TTTGTCCCTAAATTA	54629
rs547806882	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800924	TCAGTTAACTAGTTG[C/T]CTGGAAGGGTAGAGA	54629
rs547830701	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58834606	AGGCAGAGTACAATT[C/T]TCTAACCATCATCTA	54629
rs547847226	snp	G/T			downstream-variant-500B	FAM63B	GRCh38.p7	15:58861990	ATATTGATTCACATT[G/T]ACCTATAACTCTTAG	54629
rs547856367	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823928	GATAATTACTAAAAA[G/T]AAGCTCCTATTTTAA	54629
rs547868392	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58783109	TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT	54629
rs547876237	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817444	AGTCTGATGGTATTA[C/T]GTTGGGCGCAGTGGC	54629
rs547880707	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58830221	CCCTAGGATAAATAT[C/G]AGTGAGTTTTTAAGG	54629
rs547919789	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824474	TATTAAAGAATAATT[A/G]TATGTGTCATTTAGC	54629
rs547940393	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58840207	TGTAATCAAACTGAT[A/C]CATTTTTTGTGAATA	54629
rs547959491	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58841074	GCAACCTCTGCCTCC[C/T]GGGTTCAAGAGATTC	54629
rs547962830	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794195	ATAGAATTTAAGCTG[C/T]GTAAAGAGGAAATGA	54629
rs547963574	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58825369	GAATACACTGCTTTC[A/G]GGTGTCGATACCTTT	54629
rs548021722	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58840411	CATTATTAGCAAACT[A/G]AAATCCATCTCTGTT	54629
rs548025813	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826111	TTTTATTTTAAAAAA[C/T]CTCAAACCTATAAAA	54629
rs548156292	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58827820	CTAAATGTGATATGG[C/T]CAGTGGGATGCCCTC	54629
rs548177543	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859336	AATACAGTATATAAA[C/T]TTCGTTTGCATTGGT	54629
rs548192175	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793752	GATGTGGTTGCAGCG[C/T]GTCTCTTGAGTGCTT	54629
rs548206119	in-del	-/A	0.00874735	0.0655527	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855084	TTAACATAGGGATTC[-/A]AAAAAAACAAAAACA	54629
rs548241726	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775633	TGACTTCTCCCAATG[A/G]TGACTATAAGAAGTG	54629
rs548282843	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770634	GTCCACAATCATACC[C/G]ACCCTTTCCTGTAGG	54629
rs548299930	in-del	-/A	0.357664	0.225629	intron-variant	FAM63B	GRCh38.p7	15:58803310	TTCTACTAAAAATAC[-/A]AAAAAAAATTAGCTG	54629
rs548329997	snp	C/T	0.00835141	0.0640778	intron-variant	FAM63B	GRCh38.p7	15:58799233	ATGTTCTGTTGAGAT[C/T]ACTCCATTTCTCTGG	54629
rs548373305	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788667	ATATATTTATACTAT[C/T]ACCAAATAGGAAATC	54629
rs548375990	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58775892	TTGAGACAGAGTCTC[A/G]CTCTGTCTTGCCCAG	54629
rs548405928	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847523	CTGATTTTTTTCAAA[A/T]GTGAATTCATGTATC	54629
rs548433092	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58787661	AGAATGGCCTGAACC[A/G]GAGAGGCGCAGCTTG	54629
rs548469292	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854742	TTTTTTCAGGGGAAC[C/G]GTTGTTACTTAGTTA	54629
rs548506073	snp	A/C	1.66128e-05	0.00288204	missense, nc-transcript-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854543	GGAATAGTGAACGTA[A/C]ACGGAAGGAACCACG	54629
rs548525268	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58797247	TGTGATGGCTCATGC[C/G]TTTTATCCCAGCACT	54629
rs548529368	in-del	-/TT	0.00119737	0.0244387	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832050	TTATGAAGGTAATTA[-/TT]AAATACAGTACTTCT	54629
rs548587707	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789340	GAGACTCCGTCTCAA[A/C]AACAAAAGAATCTTA	54629
rs548615273	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792111	ATAACCTTGATGAGT[A/G]TATGGAATGAAAACC	54629
rs548632531	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58777422	GATCAAACAGAGTAA[A/G]GACTGAGTTGAAAGT	54629
rs548657784	snp	A/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58808420	CTTTTTTACTGTCTC[A/T]GTAGTCTTGCCCTTT	54629
rs548659978	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58786782	CCTTCTGTTACCACT[A/G]GGGATAACCATAATC	54629
rs548682338	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58773474	TTAAGTGAAGACAGT[A/T]CCTGCCCTTAAAAGG	54629
rs548696115	snp	A/G	1.84978e-05	0.00304114	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771574	GGGCGGCGGCCGCCA[A/G]GAGGAGCCTCCCGGA	54629
rs548699364	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801926	CCCAGCCAGATGCCA[A/C]ACTTCTTTTTTTTAC	54629
rs548759982	snp	A/G	5.47166e-05	0.00523023	intron-variant	FAM63B	GRCh38.p7	15:58802402	AGTTTTTGTTAAAGT[A/G]TATAATTTTAAAGTT	54629
rs548802188	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58852110	TGGCCAACATGGCAA[A/C]ACCCTATCTCTATTA	54629
rs548823442	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795764	CCATTATAGTGTCTA[A/G]GTTTTTTTTTTCTTT	54629
rs548871511	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809053	CCGTCTCTACAAAAT[A/G]TCAAAAACATTAGCT	54629
rs548875415	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58831708	GAACACACTTTAAAT[A/G]GAAAAAGAATAACTT	54629
rs548886965	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58796518	AATAACAAGTTAAAT[A/G]TAGTTTCATTTTGTT	54629
rs548899258	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809040	ACATAGTGAGACCCC[A/G]TCTCTACAAAATATC	54629
rs548899543	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58841462	CCTTCCTGGAGTGCA[A/G]TGGTGTGATCTTGGC	54629
rs548910269	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789926	TGCTGGGATTGCAGG[C/T]GTGAGCCACCGTGCC	54629
rs548936435	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846180	AAAAATAATTTAATT[G/T]TACATTTTAAAATAA	54629
rs548973482	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783888	GAGGTTGAGGGTACA[A/G]TGAGCCATGATTTTG	54629
rs548974194	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838727	AAGTAGTTGGGATTA[C/T]AGGCGGGTACCACCA	54629
rs549035485	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845790	AGCCAAGATGTGGAA[A/T]CAAGCTGTGTCCATT	54629
rs549105324	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58821492	TTAATCTTATTTTGC[A/G]TAATTAAAATAATAC	54629
rs549122799	snp	A/C	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58790655	AAGATGGTGGCTTTA[A/C]ACAAGGTAAAATAAG	54629
rs549127241	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58851490	GTCACCCATGCTGGG[A/G]TGCAGTGAGGAGATC	54629
rs549140608	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58844484	GTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	54629
rs549188645	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859744	TCATGCATGTTCTTA[C/T]TTAATCCTGGTGTTT	54629
rs549251677	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58803765	AGGTTGCAGTGAGCC[A/G]AGATTGCGTCACTAC	54629
rs549317915	in-del	-/TA			intron-variant	FAM63B	GRCh38.p7	15:58831037	GTGTGTGTGTGTGTG[-/TA]TGTGTATATATATAT	54629
rs549343971	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58816343	GCCAGATAATTTAGA[C/T]TGTGAAGAATGACAG	54629
rs549347505	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58850472	GTTATCTCTATGTAA[A/T]GATATTATGGTGATT	54629
rs549386176	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58779598	AAGGTTCCATCTTAG[C/T]CTCTGCCCACCTTGT	54629
rs549406993	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829894	GGGAGTGGAATAAAC[C/T]TATGTTATCTGCTTC	54629
rs549431117	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58781123	GGTGTGGTCTTGGCT[C/T]ACTGCAACCTCCACC	54629
rs549560249	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805769	TTGGTTTATCAGTTG[C/T]TGTTTTTTATTAAGA	54629
rs549725395	snp	C/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772961	GTCTAAGGTGAAGGA[C/G]CAAAAAAGGGAAAGA	54629
rs549777371	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805237	AATAGTGTATGTCAA[G/T]CTTATATGGCTGGGC	54629
rs549817494	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834737	TGGCTTATTAAAGTC[A/G]TGAATTACATCTTCA	54629
rs549840680	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855062	CTAATTCATGAGAAA[C/G]CACGGGTTTAACATA	54629
rs549846012	snp	A/G	0.0115144	0.0749975	intron-variant	FAM63B	GRCh38.p7	15:58787295	CACTGTGCCCAGCCC[A/G]TTTCTTTACTTCTTA	54629
rs549885066	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824539	AGTAACTACAAATTT[C/G]TAGTTCATTTGAAAT	54629
rs549907481	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58780865	TTCAGGCCTTTATCT[C/T]TCACCTGGACTACCT	54629
rs549994439	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835528	CATGGTGGTGGGTGC[C/T]TGTAATTCCAGCTAC	54629
rs550016229	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792782	ACATGGATGAACCCT[C/G]AAACTTTTAAGTGAA	54629
rs550025305	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786718	GTCGAAGAACAGAGC[A/G]TTGTCAGCACCTCAG	54629
rs550064330	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823957	AAAAATGTCTATCTA[C/T]GGAATCCTTCTTTTT	54629
rs550064724	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854985	TGATTTAGTCTGATT[C/G]CTTCCTGAAATCTAA	54629
rs550107644	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58842757	TAAGCATTTTATATG[A/G]ATTATCTCATTTAAT	54629
rs550112729	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794342	TGAGATAAAGTAGAA[C/T]AAAAGTTTTTTTTGG	54629
rs550138899	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807237	TAGCAGTAGGGATTC[A/G]GTAAAAGTGTGTTAA	54629
rs550200088	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58845179	GGGAGGCCCAGGTGG[G/T]CAGATCACTTGAGGT	54629
rs550208739	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840960	GGTGTAAGCCACTGC[A/G]CCTGGCCAATTTTTT	54629
rs550226199	in-del	-/AATT	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58843980	TTTGAACTAATACAC[-/AATT]AAGAATTTAATGCAT	54629
rs550226449	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58828575	TTTATTATTGAATTT[-/C]TTTTTTTTTTTTTTT	54629
rs550236486	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848525	GAGGCGGGTAGATCA[C/G]AAGGTCAGGAGATCG	54629
rs550238667	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58818290	GGAAGACAAGATCTT[A/C]CTCTGACACCCAGGC	54629
rs550239614	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788881	GCCAGGCGTGGTGTC[A/G]TGCACCTATAGTCCC	54629
rs550268209	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840295	CATTTTCCCTGACCA[C/G]AGATATTAATTGACT	54629
rs550295128	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792381	GGGAGGCCAAGGCAG[A/G]TGGATCACAATGTCA	54629
rs550301649	snp	C/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58819001	GTTTTGTTTTAGAGA[C/T]AGTGTCTTGCTGCAT	54629
rs550312661	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806459	AACTCCTGGGCTCAA[A/G]TGATCTGCTCACTTC	54629
rs550331573	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847020	AATGAGATTATAAAC[C/G]CCCCCAAAGGTGTTT	54629
rs550337565	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58819784	TCTGAACAGATTGTG[C/T]CCTCAAATTGTTTCT	54629
rs550351160	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833489	ATGCGGAGGATCCAC[A/G]CCGGCACCGGCCTCT	54629
rs550365017	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812779	GGGAGGATCACTTGT[A/G]CCCAGGAGGTTGAAG	54629
rs550393029	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58846409	CCATCCTGGCTAACA[C/T]GGTGAAACTCTGTCT	54629
rs550395975	in-del	-/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58796532	TGTAGTTTCATTTTG[-/T]TTTGTTTTTTGAAAC	54629
rs550418286	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826401	CACCTGGCTAATTTT[A/G]TATTTTTAGTAGAGA	54629
rs550423654	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58852261	CCACTACACTCCAGT[C/T]AGGATGATAGAGCAA	54629
rs550501335	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58801624	GTATATAAAAATACC[A/G]TCTTTTTAAATGAAA	54629
rs550578463	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58826955	TCCTTCCTTTTTTGT[C/T]GTTTATGACATTGAC	54629
rs550601906	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58776804	ACACAGGAGGATCGC[G/T]TGAGCCCAGGAGTTT	54629
rs550659143	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58833382	CCTGTGGGTGTTTCT[C/T]ATTAGGTGGAACAAG	54629
rs550661986	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861143	GCAGAATAATTGGAT[C/T]GAGGCACATATTTTG	54629
rs550672775	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58781618	TGTTTTGAAATACTG[A/T]TGGTGGCGAAGCGCA	54629
rs550682898	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58779230	GAGCCCTTATAAATT[A/G]GAAAAGGGTGAACAG	54629
rs550727139	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58811888	TCTTCTCTTTTCCAC[A/T]GATCTGTGTTATGTC	54629
rs550728413	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802464	GGCAGCATTTTTCTA[C/T]AAAGGATTAGATAGT	54629
rs550728974	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826742	CGTTTTCCCAGTAAT[A/G]CCCCTAATAGCTTTT	54629
rs550753498	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782873	ATAAAATTGAATGAC[A/C]ATTAGTAGATGTTCA	54629
rs550788421	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853738	AGGCAGGAGAATCGC[C/T]TGAACCTGGGAGGCA	54629
rs550792443	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820149	CGTGCACCTGTAGTC[C/T]CAGCTACTAGGGAGG	54629
rs550825868	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58776460	GATGTGGAATGAGAA[C/T]TAGAAATAGGGCAAT	54629
rs550850642	snp	G/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857573	AGAGCTATTGTGTCT[G/T]TATTTTCTTAAATTT	54629
rs550877217	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58831614	TTTCATTGCAAAATT[A/T]AAAACACAAATGTCC	54629
rs550938489	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838667	TCTCAGCTCACCACA[A/G]CCTCCACCTCTCAGG	54629
rs551036912	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58777456	GGTTCAGAACTGCTA[C/G]AGAGTAGGCGATCAT	54629
rs551042228	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802986	GGAATTGGCTTCTTA[C/G]AGTGGAAGGAAGTAT	54629
rs551106623	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58778427	TCCTGAAGCAGGATT[G/T]TTTTTATATAAAGTT	54629
rs551109762	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58796732	TTCCCCATGTTGGCC[A/G]GGCTGGTCTTGAATT	54629
rs551222839	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772384	CAAGACTTCCATGTT[A/G]AAGGAATATTCCTTT	54629
rs551242396	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58789066	ACTGGGGCCGGGCAC[A/G]GTGGCTCACGCCTGT	54629
rs551262366	snp	A/C	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58838034	TTTTCCATCTTTCTA[A/C]TCCTGTGAACTCTTT	54629
rs551274970	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58787072	CAACCTCACGTGATC[C/T]GCCTGCGTTGGCCTT	54629
rs551304032	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845673	AGTAGAGCTGTTATA[C/G]AATCCGGCAATCCCA	54629
rs551315724	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58791711	TTTTTAATTTTATAT[A/G]ATATAAATTAAATTT	54629
rs551367368	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845122	AGAAGTCATGCAAAT[C/G]AGGCCAGGTGTGGTG	54629
rs551367371	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58852026	GTGTAGTGGCTCACA[C/T]CTGTATTCCCAGCCC	54629
rs551379355	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58792232	TCTTTAAAAAGTTAA[A/G]CAGAATTACCGTATG	54629
rs551429518	snp	C/T	0.000148846	0.00862558	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771939	GAGTCGTTCTCTAAC[C/T]TGCATTCTTTTCCCA	54629
rs551440382	snp	G/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58785724	CTCTGTCACCCAGGC[G/T]GGAGCGTAGTGGCAC	54629
rs551527133	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844298	CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC	54629
rs551566862	snp	C/T	0.0001366	0.00826326	intron-variant	FAM63B	GRCh38.p7	15:58810184	TATCTTTTTTGTTCT[C/T]GTTTTGATGTTTCTG	54629
rs551573463	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842629	AGAGATTCATCTTTT[C/T]CTCTTAAATAGGAGA	54629
rs551580276	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804693	ACGCCTATAGTCCCA[G/T]CTACTTGGGAGGCTG	54629
rs551592964	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849273	TTTGGGAGGCCAAGG[C/T]GGGCCGATCACGAGG	54629
rs551655597	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856737	GGGTTTGTTTTTCCC[A/G]GGACAGATAGTAGTG	54629
rs551655744	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811490	GGTGTAGCATCTTAG[A/T]CCTAGCAACAGCAGA	54629
rs551715036	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58805904	CACAGTGAAACCCCA[C/T]CTCTACTAAAAATAC	54629
rs551724081	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817246	ATTCAGAAAGTAGGA[A/G]CTCCTACAGATAATT	54629
rs551758871	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773776	ATTTAGAATAACAGG[A/G]AAATGGAATTCCCAG	54629
rs551781641	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829265	TGACAGGAGAATTAC[A/G]AAACATTGTTTTTTC	54629
rs551784179	snp	C/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58806341	GCATTACAGGCGTGA[C/G]TCAACGTGCCAACTT	54629
rs551809114	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828474	AATTATAGTACCTCT[C/G]TAACTTCACCATCTT	54629
rs551864928	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823292	ACAGGCATGCAATAA[G/T]TTTGTATTTTTAGTA	54629
rs551871402	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58827868	CTTTTGTATCTCCTC[A/G]TCTTTACTTAAGCAC	54629
rs551891951	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58779666	CACACAATTGTGGGG[G/T]TTTGTTTACACAAAA	54629
rs551977129	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800235	TCCCATTAGTAGCAA[C/G]GTTTTCTTAATTCTT	54629
rs552001737	snp	C/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58835481	AACATGGTGAAACCC[C/T]GTCTTTACTAAAAAT	54629
rs552181084	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58807058	TTTCATAAAACAGAA[A/C]TTCATTTTTGTAACC	54629
rs552199644	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58825187	GAGGAATAAGAAATA[C/T]ATTCACTAACATTCC	54629
rs552227872	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58824733	GGAGTGTAGTGGCAC[A/G]ATCTCGGCTCACTGT	54629
rs552241732	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58792873	CCAGGCTGGTGGTGC[A/G]TGCCTATGGTCCCAG	54629
rs552288934	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861380	TATTTTTTCCTCCTC[C/G]TTTCATTTTTTATCT	54629
rs552361308	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769841	ACAACAACAACAAAT[C/T]AGCCAGGCATGGTGG	54629
rs552391628	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58841821	GATGACTATTTATCC[A/G]TGCAGGAAATTTGAA	54629
rs552395731	snp	A/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58824617	GGAAAATAAAAGACC[A/G]TAATAGACATTTTTA	54629
rs552444118	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58773327	CTTCTAAACACTTAG[A/G]TAGAAAATCAAGTAA	54629
rs552488257	snp	C/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58802660	CCATGAGAGATCAAA[C/T]CTAGTGTTTTTCTTG	54629
rs552489633	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774536	AGATGAGTATGATGC[A/G]AATCTGCCCTCGTGT	54629
rs552493888	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58820526	TTTTTGAATTAACTG[A/T]TTGTTTACTCAACCA	54629
rs552578364	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795032	TACAAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG	54629
rs552584721	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817951	TCCTAGAATTTTTCA[C/G]AGCAGTGTTATTTGC	54629
rs552673179	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770571	AATACAAGCTAATTT[A/T]TTATTATTGGCGCAA	54629
rs552684608	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771041	AGGATGTTTTCCTAC[C/T]GGAGCTGAGCCGCGG	54629
rs552694924	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58854054	GTGAGACCAGCCTGG[C/T]CAACATAGTGAAACC	54629
rs552697395	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801130	AGGTGCATGCCACTA[C/T]GCCTGGCTAATTTTT	54629
rs552698808	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775271	ATATCCACATAGATG[A/G]AAGTTATTGGGGGTC	54629
rs552701378	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813462	GATCGTGCCACTTCT[C/T]TCCAGCCTGGGTGAT	54629
rs552717661	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58794215	AGAGGAAATGATGTA[A/T]GTGTGTTGAAGGAAA	54629
rs552737457	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58813222	TTTTCCCGCCGGGCA[C/T]GGTGGCTCACGCCTG	54629
rs552761946	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770120	TCCACTATGGCATCT[C/G]CAGTGACAGACAGCA	54629
rs552764672	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807817	TCACTTTTATTTTGT[C/G]CCAGCCGCACTGGGC	54629
rs552842686	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802588	TTTTTAGCTCACAGC[C/G]AGATTTTTCCTTTTT	54629
rs552879475	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795639	TCGATCTCCTGACCT[C/T]GTGATCCACCCGTCT	54629
rs552891954	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58782327	TGAAATTTTGACTAT[C/T]ATTTAGTGCGTCCAT	54629
rs552900665	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859799	TAAATTGTGATACGC[A/G]TATATTTTTTTACAT	54629
rs552919534	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845326	CAGGAGAATCACTTG[C/G]ACCTGGTAGATGGAG	54629
rs552920072	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833439	GACAAAGTATAGAGA[A/C]AGAAAAAAGGGGGCC	54629
rs552965620	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859086	AATATATCTTAAGTC[A/G]GTTTTTTTAATGCTG	54629
rs552977791	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58819850	CTGGAACTCATAGAT[G/T]TTTTTTTGTGCAATG	54629
rs553000284	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775758	AAAGTTGATGCCAAA[C/G]TTTGGTTGTGTTGAG	54629
rs553036724	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58838747	GGGTACCACCACTCC[C/T]GGCTTATTTTTTTTA	54629
rs553090827	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58838478	CTTCAGTGGTGTTTA[C/T]AACTAGGGGCTTATA	54629
rs553129192	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830041	TTCCCTTCCCTCCTC[C/T]CCCATTGCTTCCGAG	54629
rs553163753	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58804682	CATGGTGGCACACGC[C/T]TATAGTCCCAGCTAC	54629
rs553181596	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58803082	ATACTTTCACCAGTA[C/T]CAAATTTGCAAAAAG	54629
rs553186864	snp	C/T	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58778535	AAAAAAACAGACACA[C/T]ACCAAAAAAAAAAAC	54629
rs553192556	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829445	CCTTGGGCAAGTCAC[G/T]TATTCTCTCTGAGCC	54629
rs553209793	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820305	AAAAATTAGTCAGGT[A/G]TGGTGGCGGGCGCCT	54629
rs553224817	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844704	GGTGGATCATCTGAG[C/G]TCAGGAGTTCGAGAC	54629
rs553273072	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814535	GGGCACATGCCACCA[C/T]ACCCTGCTCACTTTT	54629
rs553295435	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771333	CAGCTGTCATGGCGT[C/T]CAAGGCGCTGGCTGC	54629
rs553317474	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836058	GGGACTACAGGCGCC[C/T]GCCACCACACCCAGC	54629
rs553464446	in-del	-/ATTG	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58846837	TAGGTACAAAGTATT[-/ATTG]GTGTATAAAAGAAGA	54629
rs553497322	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58846507	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	54629
rs553522820	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797139	TTCAAAGATTTGGTT[A/G]AAAAAGAATATCAGT	54629
rs553550723	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784065	GTGCAGTGGCTCACA[C/G]CTGTAATACCAGCAA	54629
rs553572919	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58784925	TAGACGTGAGCCACC[A/G]TACCCAGCCTGTTAT	54629
rs553596891	snp	A/C/T	0.000487038	0.0155981	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771641	ACCCTGCAGCTCCTC[A/C/T]GCGGGTTTGGACTTG	54629
rs553608293	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58777688	GATGCTCTAACATCA[A/G]GAAAGACATCTATTT	54629
rs553707888	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791906	TGCCAGTGATTAGAA[A/G]GTGGGGAAGGAGAAA	54629
rs553760162	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843447	TGAGCCACCACACCC[A/G]ACCTAGAGATGTTAA	54629
rs553772600	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809778	GAGCATGGACTTTGT[A/C]TTGTTTTGTTTCGTT	54629
rs553802766	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58833237	TACAAGATATGTTCT[A/G]TTTGCCAACACTTTA	54629
rs553851645	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58804912	GCAGGAGGATTACTT[C/G]AGCCTAGGAGTTCAA	54629
rs553894208	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791048	AGCTGGGAGTGGTGG[C/T]GGGCACGTGTAGTCC	54629
rs553919179	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827621	GGCGCCCGCCACCAC[A/G]GCCGGCTAATTTTTT	54629
rs553920124	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805441	TTTTTCCAGTTTTGT[C/T]TAATAGTGTACTGAC	54629
rs553923285	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58816878	GAATCACTTAAGGCC[A/G]GGAGTTTGAGGCTGC	54629
rs553960807	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856928	TCTTAATTTGTTCCA[A/G]AGAAAATGCTGCCAT	54629
rs553980155	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798817	AGGTGTCAACATGTA[C/G]TTAGTGGGGCTGTGT	54629
rs554005374	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58785408	AACTTTTTCTGTAAA[G/T]GATCAGATAGTAAAT	54629
rs554023982	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856127	AGTCTGTTTTATATG[C/T]CTTATATTTAAAAGT	54629
rs554041167	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58799666	GCTGAAGTACCCCAA[A/G]GAAATGGGAATTTTG	54629
rs554163132	snp	A/G	0.000122535	0.0078264	intron-variant	FAM63B	GRCh38.p7	15:58847259	TACTAGTTTTGATCA[A/G]TTTAACAGTCCTTTT	54629
rs554177519	snp	C/T			downstream-variant-500B	FAM63B	GRCh38.p7	15:58862251	TCAAAAAAAAAGGTA[C/T]GTGTTGGTGAGAAAA	54629
rs554181049	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58842887	TATCAGCATTTCCAG[G/T]GTGACTTTCAAGTCC	54629
rs554239509	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58787390	TTGCATTACTTTTAA[C/T]AGCAAAACCGCAATT	54629
rs554248418	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834939	GCCCAGAGTCATCCA[C/T]ACTCCTCAGAAATCT	54629
rs554261803	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824792	CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAC	54629
rs554268746	in-del	-/AGA	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58834199	ACAGCATCTCAAGGC[-/AGA]AGAATTTTTCTTAAT	54629
rs554278605	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812202	CAGTACTTTGGGAGG[C/T]CGAGGCGGGTGGATC	54629
rs554292101	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786899	CAATGGTGCATTCTT[A/G]GCTCACTGCAACCTC	54629
rs554309803	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834292	CTCTCTCTCTTTTCC[C/T]CACAATATCTCACTC	54629
rs554324899	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58818495	TCCTGGACTGAAGCC[A/G]TCCTCCCCTGCTAGC	54629
rs554371041	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58841373	TTTGGAAGGTTTATG[A/G]TTCTATGAAGATAAT	54629
rs554389387	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58822214	AGCCGAGATTGCGCC[A/G]CTGTACTCCACCCTG	54629
rs554400237	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58801174	AAACAGGATTTCACC[A/G]TGTTGGCCAGGCTGG	54629
rs554440238	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855075	AACCACGGGTTTAAC[A/G]TAGGGATTCAAAAAA	54629
rs554443631	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839646	CTAGGGTTAGGCTTT[G/T]TGGTGATCCTCTATA	54629
rs554445975	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792462	AACATAAAAATTAGC[C/T]GGGCGTGGTGGCACA	54629
rs554455602	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58833627	AACAAGGTAAAGAAA[A/G]AAGTGCTGTGCTGTT	54629
rs554511710	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786101	TAACTATTGACTGTC[A/G]TATATGCTTACAGAT	54629
rs554514571	in-del	-/TTTTG	0.0166325	0.0896639	intron-variant	FAM63B	GRCh38.p7	15:58835899	GTAAAGTCTTGGGTT[-/TTTTG]TTTTGTTTTGTTTTG	54629
rs554533040	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769619	GGTCAGGAGATCAAG[A/G]CCATCCTGGCTAACA	54629
rs554573645	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58828089	AATACAAAAAATTAG[C/T]TGGGTGTGCAGTGAG	54629
rs554634258	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58787457	AAAGACTGGTTATAG[G/T]CTGGGTGCAGTGGCT	54629
rs554650585	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837180	GCTGTTCATCATTAA[A/G]ATTATTATTCTCTCC	54629
rs554685259	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58775036	AAGTAGAGCAGTATT[C/T]TCAAAGTGAGCCAGG	54629
rs554728185	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811785	AGAGGTTAGTCTCCC[A/G]AATAGAGAAGAAATG	54629
rs554743647	snp	A/C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774029	TTATTTTCCTTTAGT[A/C/G]TTTTTTCTTATGTAG	54629
rs554755110	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58852447	TAGTAAAATGTTTTC[C/T]CCTGAGGTTCTGATT	54629
rs554816616	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58788441	TATTTACATTAGTAA[C/G]CACACTGTTTATTTC	54629
rs554853017	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813017	TCTTTCTCCATTTCT[A/G]TAATTTTGTTATTTT	54629
rs554881013	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775822	AATGTTCGTTATGCT[C/G]TTAGAAGCATGGACT	54629
rs554888418	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781917	AAAAAAGAAAAAAAA[A/G]AGAAAGAAATACTGA	54629
rs554915046	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846524	CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG	54629
rs554915426	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807508	GAGACTACAGGCGCC[C/T]GCCATCATGCCTGGC	54629
rs554942593	snp	A/T	0.00755907	0.0610114	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770812	TTCCATATTAGGAGC[A/T]GAGAAACCAAGTCCC	54629
rs554944382	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58776732	GGTCACGTTAAGATA[G/T]AGAGGTAGGCCGTGT	54629
rs554947104	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855495	TACCTTTTTCTAGAA[C/T]TACCTTGAACCTTAA	54629
rs554967585	snp	C/T	0.00874735	0.0655527	intron-variant	FAM63B	GRCh38.p7	15:58800694	AAACGATTAGCCAGG[C/T]GTGGTGGTGCGTGTC	54629
rs554975647	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58822864	AATCATGAGAAGTAG[A/G]GCATGAGTTTTAGTC	54629
rs555044846	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813785	AAACTGTTTACTAGA[C/T]TACCTGTAGAAAAGT	54629
rs555089765	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794468	TTGGAAGAGACATCT[C/T]CATACATATTGAAAT	54629
rs555161223	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58795109	TGAACCTGGGAGGCG[A/G]AGCTTGCAGTGTACC	54629
rs555168754	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789006	GATGGAGTGAGACTC[C/T]GTCTCAAAAACAAAA	54629
rs555169852	snp	A/C	0.000966837	0.0219655	intron-variant	FAM63B	GRCh38.p7	15:58796046	TTCATCAAACCGTGT[A/C]ACTGCAGTGATGAGA	54629
rs555220263	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860110	TTCTTCAAACTACTT[A/C]ATAATTTGTCACCAT	54629
rs555300560	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58850874	ATATAGGTGTGTGCC[A/G]TTGTACCTGGCTCCC	54629
rs555361801	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789771	TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGATT	54629
rs555380040	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820181	TGAGGCAGGAGAGTC[A/G]CTTGAACCCAGGAGG	54629
rs555385279	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814332	GTAAAATGTCTCTTC[A/T]TGTCTTTTGCCCACT	54629
rs555432047	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58804933	AGGAGTTCAAGACCA[A/G]TCCGGGTGTGATATA	54629
rs555446508	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58808595	ATTATAAAATATATG[G/T]TTTTTTTGTTTTTGT	54629
rs555456745	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815144	CGAGGAAAGGGCCCA[A/G]CTTTATTCATATACA	54629
rs555502567	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837502	CACTTGAGCCCTGAG[C/T]CCAGGAGGGTGAGGC	54629
rs555518062	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815642	CATGAGCCACTGTGC[G/T]TGGCTCAAGAAGAAA	54629
rs555552179	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58813255	ATCTCAGCACTTTGG[A/C]AGGCTGAGGCAGGTG	54629
rs555565389	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844643	AAACGTCAGGCCAGG[C/T]GCGGTGGCTCATACC	54629
rs555624242	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58850056	GCAAAAACCATTTAC[C/T]CATCCTCTGTATTAT	54629
rs555685962	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790128	TTTAATCCCCATTCA[C/G]TGGCTAGGGACCTCA	54629
rs555687903	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857923	AAAATATAAAATTTT[G/T]CTTCATGTCTAATCC	54629
rs555701152	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842331	GCTTTTTTACTCTAT[C/G]TTTAGGGATTAGAAG	54629
rs555762577	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58848741	ACAGAGCGAGACTCC[A/G]TCTCAAAACAAAAAA	54629
rs555796826	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58845321	TGAGACAGGAGAATC[A/T]CTTGGACCTGGTAGA	54629
rs555833862	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793466	AAAATAAGTAAATAA[A/G]TAAATAAATTTAAAA	54629
rs555845517	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849284	AAGGCGGGCCGATCA[C/T]GAGGTCGGGAGATCA	54629
rs555902990	snp	A/C	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58828683	CTCCTGCCTCAGCCT[A/C]CCGGGTAGCTGGGAC	54629
rs555908482	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856850	ATAATTATATACTTA[C/T]CTGTTTATTGCCCAT	54629
rs555934787	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778444	TTTTATATAAAGTTG[A/G]TTTCTCCAAACATCA	54629
rs555945171	snp	C/T	3.66146e-05	0.00427855	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771740	CTCCCCGGAGACAGC[C/T]GTGGCCGGAGTGGGT	54629
rs556031761	snp	C/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58804107	GCACTCCAGCCGGGG[C/T]GACAAAAAAAAAAGG	54629
rs556091566	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849228	AAAAAAAAGGCTGGG[C/T]ACGGTGGCTCACACC	54629
rs556100707	snp	C/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58785836	TGTGCGCCACCACAC[C/T]TGGCTAATTTTTGTG	54629
rs556131446	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827887	TTACTTAAGCACTTA[C/T]TTTTTGGCACAGTAA	54629
rs556135775	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823428	CCTGTAATCCCAGCA[A/C]TTTGGGAGGCTGAGG	54629
rs556159429	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797805	CTTTTGCCATGAGTT[C/T]TGCAAATGAAGAGAT	54629
rs556208104	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855884	GAGATCGCCCTGCTG[A/C]ACTCCAGCCTGGGTG	54629
rs556220745	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798413	TACAGGCGTGAGCCA[C/G]CACACCCAGACCTTT	54629
rs556281795	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791927	GAAGGAGAAAGAGCC[A/G]GCACGGTCAGCCAGG	54629
rs556317617	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58833721	CTTCAGCCCTAAGGC[A/G]GTTTTCCCCTGTCTC	54629
rs556356072	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58777268	GACACCTGGGGTATA[C/G]GGGCAGAGAATTAGA	54629
rs556369119	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793308	ATACAAAAAATTAGT[C/T]GGGTGTGGTGGCACA	54629
rs556382875	snp	G/T	0.00636936	0.0560724	intron-variant	FAM63B	GRCh38.p7	15:58806036	CCGAGATCACGCCAC[G/T]GCACTCCAGCCCGGG	54629
rs556428866	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793786	TTTTCTCAATGAAAT[A/G]GGAAACAAAGTCATC	54629
rs556431456	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58827532	GTAGTGGCGCGATCT[C/T]GGCTCACTGTAAGCT	54629
rs556449374	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58839669	CCTCTATACACCAAA[C/G]TGGTGTTTAAAGGAC	54629
rs556496820	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811179	GGGACAAAGGTCAAA[A/C]CTCTCTTTGGGCAAG	54629
rs556512273	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816927	CTGTGAATAGCCACC[A/G]TACTCCAGCCTGGGC	54629
rs556560093	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805690	ATTAAGTATAATTTG[A/G]AATTAGGAACAAAGT	54629
rs556589498	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58818569	CCTTGAGTGAAATAC[G/T]AATGTACAGATTCTG	54629
rs556608074	in-del	-/AAACA	0.00159617	0.0282053	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856964	ATTCCCTCTGGAAGG[-/AAACA]AAACAAAACAAAACT	54629
rs556627606	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58774644	AGTGCAGAGAAAACG[C/G]TAATTGGGGAGGGGA	54629
rs556628874	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861559	CAGCTTAGGGTTGAA[C/G]TGAATTTCTGTGAAA	54629
rs556632130	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58841273	CAGGCATGAGCCACT[G/T]CACTGAGCCAACTTC	54629
rs556649864	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819307	TTAAAAATTAGCTGG[A/G]TGTGGTGGCGTCTGC	54629
rs556693646	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847846	GTCCAAGCAAGAGCT[C/G]ATGATGGCTTAGCCT	54629
rs556698111	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781148	TCCACCTCCTGGGTT[A/C/T]AAGCTATTCTCCTGC	54629
rs556709226	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58813460	AAGATCGTGCCACTT[A/C]TCTCCAGCCTGGGTG	54629
rs556755010	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58847172	ATTTATTGTGTTGTA[C/G]AGATCTAAACAGTAG	54629
rs556765599	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774666	GGGAGGGGATTATCA[A/G]GGGAAGACTTCATAG	54629
rs556799534	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58862369	AAATACAGAGTTTCC[A/G]TATGACCCAGCAATT	54629
rs556807740	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786961	CAGCCTCCCAAGTAG[A/C]TGGGATTATAAGCAT	54629
rs556837425	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58845939	TTAAGTGAGATAAGC[C/G]AGGCACAGAAAGACA	54629
rs556846441	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58843332	CTTTTTGTATTTTTA[G/T]TAGAGACGGGGTTTC	54629
rs556885947	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812666	GGAATTCAAGACTAG[C/T]CTGGGCAACATGGCA	54629
rs556898773	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58845447	ACAGGTATGTGAAAA[G/T]GTGCTGAACATCACT	54629
rs556902847	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58782088	TTTATTTGCTGGAGC[A/C]AGAATTAAAGGCATG	54629
rs556912265	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58850871	GGAATATAGGTGTGT[G/T]CCGTTGTACCTGGCT	54629
rs556912799	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838857	AAGAACTGAGATTAC[A/G]GGTGTGAGCCACTGA	54629
rs556947020	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58778474	AAACCTAGAAACTGT[A/G]AAATAAGGATTAATA	54629
rs556964251	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58841694	ACAGGCGTGAGCCAC[C/T]GCGCCCGGCTGATCT	54629
rs556967204	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58825566	CTCTCAGGAATGGTT[A/C]TTTTTTGTCTGTTTG	54629
rs556980036	snp	A/G	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58801313	AGAAAAGATAGGCCA[A/G]GAACGGTGGCTCATG	54629
rs557037889	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806934	AAGGTCAAAGACTGC[A/G]GTATAACAATGTTAT	54629
rs557066199	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775169	GATGTAATGACATCG[C/T]TCTGTCAGTTAATGC	54629
rs557090411	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839455	TCCTGCCTCAGCCCC[C/T]GGAGTAGCTGGGATT	54629
rs557121218	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855772	CTAAAAATACAAAAA[A/G]TCAGCCTGGCATGGT	54629
rs557157652	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859918	GTTCAGTTTTGTCCT[A/G]TTGTCCTGAGAAAGG	54629
rs557198384	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58826543	CCCACACACTCTTTT[C/T]CCCTAAATCTTGTGA	54629
rs557202197	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769975	GCCTGGGCGACAGAG[A/G]GAGACTCCGTTTCAA	54629
rs557219421	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838269	TGGGCATGGTGGTGT[G/T]TGCCCGTAATGCCAG	54629
rs557223270	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807892	GGCATCTACTTTGGA[A/G]TGCTCTTTGCCCAGA	54629
rs557227296	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782545	TTTTCAGAGTTTCCT[C/G]AGCCTTAGAGTCAAC	54629
rs557290905	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802112	AAAAAGTTCAAAGCA[C/G]TATAGTATATACATT	54629
rs557342297	snp	C/G	1.83041e-05	0.00302518	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771610	CTTCTCCCGCGGGCT[C/G]TCCTGAGGTTCCCGG	54629
rs557378782	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830272	TCAGCTGATCAGTAC[A/G]TAAACTTGTTTTATG	54629
rs557422160	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795304	GCAGTGTTTCAACTT[C/T]CTTTTCGTTATTGCC	54629
rs557441447	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837330	GTAATCCTAGCACTT[C/T]GGGAGGCCAAGGCTG	54629
rs557486043	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58785246	TAGTGTGAAGTAGGC[A/G]CTTTTTAGTTTTAAT	54629
rs557544198	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58789542	ACTTGCTGCAATCTC[A/G]ACCTCCCTAGGCTCA	54629
rs557622419	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790922	TGGTGGCTCACGCCT[G/T]TAATCTCAGCAGTTT	54629
rs557686094	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784897	ACTTCAGCCTCCCAA[A/T]GTGCTGGGACTGTAG	54629
rs557698493	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797606	TGAGCTCAAATTCGT[A/G]GCTTGCATTATATTT	54629
rs557705806	in-del	-/AAAAA	0.495963	0.0447464	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769431	TGCGTCTCAAGTGGG[-/AAAAA]AAAAAAAAAAAAAAA	54629
rs557712456	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58808644	GAGTCTCGCCCTGTC[A/G]CCCAGGCTGGAGTGC	54629
rs557758931	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808678	GGCACAATCTTGGCT[C/T]ACTGCAAGCTCTGCC	54629
rs557777880	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815682	TTCCTTCTTTTTCTT[C/T]TTTCTTTTTCTTTTT	54629
rs557822863	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58783129	TTTCACCATGTTAGC[C/T]AGGCTGGTCTTGAAC	54629
rs557826473	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809129	AGATGGGAGGATCAC[A/T]TGAGCCCAGGAGTTT	54629
rs557835517	in-del	-/A	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58778507	TTGATTCTGTAAAAT[-/A]AAAAAAAAGCTTAAA	54629
rs557904412	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58810499	TTTTTGTACTTTTGC[C/T]TGGAATTAGCCAAAC	54629
rs557921964	snp	C/G			synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771572	GGGGGCGGCGGCCGC[C/G]AGGAGGAGCCTCCCG	54629
rs557941108	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58850002	TTGGCCCCCTAAAGT[A/G]CTGGGATTACAGGCG	54629
rs557949867	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58779002	CCTGACCTCAAGTGA[C/G]CTGCCCGCCTCAGCC	54629
rs557982482	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816207	CATTGGTAAAAGCTG[C/T]TGGGATTCAGGAGAA	54629
rs558008343	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58849337	GAAACCCCGTCTTTA[A/T]TTAGAAAAATGCAAA	54629
rs558027621	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805379	GAGCTGCAATATTCC[C/T]ATTTAAAACTCTTTA	54629
rs558066049	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856960	CTGCATTCCCTCTGG[A/T]AGGAAACAAAACAAA	54629
rs558087172	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848216	ATATGGTCATGTTAA[A/G]CAGTTGACATATATT	54629
rs558091178	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855733	CGAGACCAGCCTGGC[C/T]AGCATGGTGAAACCC	54629
rs558098396	snp	C/G	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58838205	GAGTTCGAGACCAGC[C/G]TGGCCAACATGGTGA	54629
rs558118677	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58822217	CGAGATTGCGCCGCT[A/G]TACTCCACCCTGGGC	54629
rs558146881	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58809883	CTACTGGGTTCAAGT[C/G]ATCCTCCCACCTCAG	54629
rs558161225	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58841605	AGACACAGTTTCACC[A/G]TGTTCGTCAGGCTGG	54629
rs558219166	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58809272	AACCATTCTGCTTTC[C/T]GTTTTTATGATTTTG	54629
rs558289765	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792435	ACATGGTAAAACCCC[A/G]TCTCTACTAAGAACA	54629
rs558300565	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835044	CCTGACCTCTCAAGT[C/G]TAGGATTTATTCATT	54629
rs558364440	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842202	CTCTTGGTTTTAAAT[C/T]ACTGACATCTCTGAA	54629
rs558366481	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804789	CCAGCCTGGACAACA[C/G]AGTGAGACCCTGTTA	54629
rs558395775	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824874	GAGATTTCACCATGT[G/T]GGCCAGGCTGGTCTC	54629
rs558423677	snp	C/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58798505	TTGTCACCCAGCCTA[C/T]AGTGCAATGGCACAA	54629
rs558433633	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833665	ATATACATAAACATC[G/T]CAATGCCTTAAGGAG	54629
rs558456983	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58824092	GGATAAACTGACTTA[C/T]GGAGTATGAAGCTAT	54629
rs558499006	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58822047	CTGAGGACAGGAGTT[C/T]AGGATCAGCCTGGCC	54629
rs558499221	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58833147	ATTTCTTCAGTAGTA[C/T]AGTAGAATACTGTTC	54629
rs558546149	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791956	GGTAGAAGAAAAATA[A/G]GAGGCTGTGATTTCC	54629
rs558553819	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773984	TAACGGGCCAGAGTC[C/G]CTAATCTTTTTTGTA	54629
rs558641222	in-del	-/AAAAT	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58786293	TCTTTGGATGAACAC[-/AAAAT]AATTGGTGAAGAATT	54629
rs558700321	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817096	AAACCTATTAACTGT[A/G]AGGAAACATTAGTAA	54629
rs558778524	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58846592	TGACAAAGTGAGACT[C/T]CTCAAAAAAAAAAAA	54629
rs558806030	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780343	TGGGAGGGAGGTTGC[A/G]GTGAGCCGAGATAGC	54629
rs558808445	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58781261	TTTACCATGTTGGCC[A/G]GGCTGGTCTTGAACT	54629
rs558846248	in-del	-/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58818830	ATTTTTTGTAGAGAT[-/G]GGGTTTCCTCGTGTT	54629
rs558848991	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813292	TTGAGACCAGGAGTT[C/T]GAGACCAGCCTGGCC	54629
rs558896093	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58776468	ATGAGAACTAGAAAT[A/G]GGGCAATGTCATGAT	54629
rs558941630	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58799908	CAACATAAACTGGAA[A/T]GTATATTGTGACTTC	54629
rs558966713	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806184	GTTCAAGAGATTCTC[A/G]TGCCTCAGCCTCCCA	54629
rs558968859	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806965	CCTATTATAAATGCA[C/T]CATTCATTAATTTAA	54629
rs559168074	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58797631	ATATTTCAACTGGAC[A/G]GTGTTAAACTGTGCT	54629
rs559194051	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800908	TAGCTCTCACAAAAA[A/G]TCAGTTAACTAGTTG	54629
rs559218754	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861501	TCATAGGAAAGAGCA[A/T]TGAAATACATTTTTT	54629
rs559231499	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58815225	CCTGTTGAATTGTCT[A/T]GAACTTAGCATGAAC	54629
rs559251846	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58824918	CAGGTGATCCGCCAG[C/G]CTCAACCTCCCAAAG	54629
rs559284975	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58812585	AGATACATGGCTGGA[C/G]ACAGTGGCTCATGCC	54629
rs559305076	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769679	AAAAAGTTAGCTGGG[C/T]GTGGTGGCGGGCGCC	54629
rs559307823	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856959	ACTGCATTCCCTCTG[A/G]AAGGAAACAAAACAA	54629
rs559314265	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58825719	CAAGCAATTCTTCTG[C/T]CTTAGCCTCCCAGGT	54629
rs559315957	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826648	TATAAATTCTCCTAT[A/G]TAATCACAATGCAAT	54629
rs559335749	in-del	-/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58793064	CAGAAAGTAGATTAG[-/T]TGGTTGCTTAGGGCT	54629
rs559342164	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58854177	TGAACCCAGGAAGTG[C/G]AGGTTGCAGTGAGAC	54629
rs559406458	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858356	TACTTCTTGATCTTG[G/T]CTTAACTAAGCAAGT	54629
rs559445963	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58844285	GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC	54629
rs559450259	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861506	GGAAAGAGCATTGAA[A/G]TACATTTTTTGCATA	54629
rs559469584	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857206	ATGTTCAATTGTATT[A/C]AAACAAACAAGCTTT	54629
rs559528833	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837719	ACATGTAATTGCAGT[A/T]CTTTGAGAGGCAGAG	54629
rs559536736	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794707	GTATGAGAGAGAACA[G/T]AACTATCACTTAAGA	54629
rs559542517	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813526	TTTGTGTACAGGTAC[A/G]TTTTTCATTTCTCTG	54629
rs559558126	snp	A/G	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58830493	GATTAGGGATGCTCA[A/G]CTGATCAGTATAATG	54629
rs559569534	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770598	GCAAATTAGCCACTT[A/T]CTTTTGCTACGCATG	54629
rs559622041	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788053	CCTTTCTGAAGTGCT[A/G]TTATATAATCTATTT	54629
rs559624076	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828810	TCATGATCCGCCCGC[C/T]TTCCAAAGTGCTGGG	54629
rs559700217	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58843751	AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGGCG	54629
rs559718530	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843594	AATTCTACATGGAGT[A/C]GTTACTTGTATTAAC	54629
rs559754099	in-del	-/T	0.262985	0.249663	intron-variant	FAM63B	GRCh38.p7	15:58824672	CTTCATCATATTATC[-/T]TTTTTTTTTTTTTTT	54629
rs559755087	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820125	ACAAAAATTAGTTGG[G/T]CATGGTGGCGTGCAC	54629
rs559766288	in-del	-/TGTTTGTT/TGTTTGTTTGTT/TTTTTTT	0.0134861	0.0810011	intron-variant	FAM63B	GRCh38.p7	15:58839316	TCTGTTAAGTTAGAC[lengthTooLong]TGTTTTTTTGTTTGT	54629
rs559771061	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58791731	AAATTAAATTTAATA[A/G]CCACATATTGCTACT	54629
rs559808785	snp	G/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58834618	ATTCTCTAACCATCA[G/T]CTAGCTGTTATTGGC	54629
rs559814638	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58783775	ATGTCAAAACCCCAT[C/T]TGTACAAAAAATACA	54629
rs559817883	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813918	TATTTCATTGTAGTT[C/T]TAACTTGCATTTCTT	54629
rs559819275	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782182	TTCCCATTAATACTT[A/C]TAATATTTTCTAAAG	54629
rs559847205	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58797005	TTAGATCATTGCCAT[A/G]TATCACCTAAACCTG	54629
rs559866022	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58777293	ATTAGAGAATTGAAA[A/G]TGAAAACAGCTGATC	54629
rs559904910	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58778436	AGGATTTTTTTTATA[C/T]AAAGTTGGTTTCTCC	54629
rs559939341	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778050	AAGTTAAGCCAGAAG[G/T]TATATAACATATATA	54629
rs559951601	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58819443	ACACAGTGAGACCCA[A/G]ATCACACCACTGCAC	54629
rs559970910	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808300	AATGTATAATGTCAC[A/G]TATCTACCATTACAG	54629
rs559982417	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842508	AAGTTTAGCTATTTT[C/T]AAAGCTGGTTGATAT	54629
rs559990784	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58790457	TGGGGCCCTAAAGAT[A/G]TAACAGCAATTTTGG	54629
rs560043362	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848836	AGTCGTGCTCATTTT[C/T]CTTCAGAAGCTATAC	54629
rs560094652	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803667	CTAAAAATACAAAAA[G/T]TGGCCGAGTGTAATA	54629
rs560099358	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802908	TTATTGGTGCTGGAA[A/G]AAAGCAAGCGGAGCT	54629
rs560130667	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58789913	GAGCCTCCCAAAGTG[C/G]TGGGATTGCAGGCGT	54629
rs560156400	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58804561	GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCCAAA	54629
rs560204386	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815782	TCTCCCGGGTTCAAG[C/T]GATTTTCCTGCCTCA	54629
rs560240691	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58813500	GACTCTATCTCAAAC[G/T]GCTGTAAACATTTGT	54629
rs560266969	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809977	AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG	54629
rs560285557	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58798552	CCTCTGCCTCCTGGG[G/T]TCAAGCGATTATCTC	54629
rs560319019	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820655	ACTTCGCTATGCATC[A/G]GAATCACCTGGGCAG	54629
rs560350964	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815291	CTCATTGCCTTAAAA[C/G]CATCCAGTTTAATTA	54629
rs560441467	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58823198	GCTGGAGTGCAATGG[C/T]GCGATCTCAGCTCAC	54629
rs560460181	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855271	CAATAGCAAAAAGTT[A/C]CATAACACTAATACT	54629
rs560513711	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58783627	AATTTACTTTACTCT[G/T]TAGATGATTAAGAAT	54629
rs560524249	in-del	-/AAG	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58804119	GGGCGACAAAAAAAA[-/AAG]GAGGAGGAGGAGAAG	54629
rs560621252	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785571	GAAAAACAGACAGTC[A/G]ACAGTAATTTGCCGG	54629
rs560625990	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861591	AAATTTGTTTTAAAT[A/G]CTAATTATTTTAAAA	54629
rs560650467	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833827	CCTCTTATCTCAACT[A/G]CAAAGAGGCGTTCCT	54629
rs560686639	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58830330	AATATATACTGTTGA[C/T]TCACTAGCGTTAAAC	54629
rs560695206	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772668	GTTATATTTAGTTTG[A/C]TTTCCAACTAATGCC	54629
rs560696862	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58833310	CATACACACACTATA[A/C]CTTCTAATTTCTGCA	54629
rs560729979	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58796672	GGGATTATAGGCACC[A/G]CCACCATGCCCAGCT	54629
rs560735354	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58775152	AGTTTTTCAGGCTAC[A/G]TGATGTAATGACATC	54629
rs560738121	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58846247	TAAATGTTTGAGAGG[A/C]TGGATACCACATTTA	54629
rs560760172	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840114	GCTAGGATTACAGGC[A/G]TGAGCCACGCGTTTG	54629
rs560775908	snp	A/C/G	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58817176	AACAGAATGTAAAAG[A/C/G]AAGCCACAGAGTAGA	54629
rs560794446	in-del	-/T/TT	0.386308	0.245145	intron-variant	FAM63B	GRCh38.p7	15:58809410	GACAGGATTTCTTTC[-/T/TT]TTTTTTTTAAGGCTG	54629
rs560800125	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853191	CTCCTGACCTCAAGT[A/G]ATTCACCCACCTCGG	54629
rs560812521	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58836981	CCCAGTGACAGATTA[C/T]CTGATTTACAACAGA	54629
rs560830100	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58779436	TCACATACTCTCCTA[A/G]TTTCCATCTAGGTTA	54629
rs560837952	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811317	TGTACATTGACCTTT[A/G]GTATATTAGTCTAGC	54629
rs560881089	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772942	CTAAAATAAGAAAAG[A/G]TATGTCTAAGGTGAA	54629
rs560942306	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773510	AAGCTGTTTGAGGTG[C/G]CATCATTAACTTACT	54629
rs560953127	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853634	GACCAGCCTGGCCAA[C/T]ATGATGAAACCCTGT	54629
rs560960372	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58782412	TGTGTTCCAAATTCA[A/G]CTCCCTGTTTGAATG	54629
rs561035850	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58780688	GGTTTTTAGCTCTCT[C/G]TACTTTATCTTATGT	54629
rs561096318	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781304	CGATCAGCCCACCTT[A/G]GCCTCCCAAAGTGCT	54629
rs561105570	snp	A/G	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58799334	GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC	54629
rs561106729	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58774334	CTAAACATACAAAAA[A/C]TTAGACGGGCATGGT	54629
rs561107766	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806299	TGCTGGTCTCGAACT[C/G]CTGGCCTCAAGTGAT	54629
rs561109955	in-del	-/AG	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58776363	AGACAGAGAGAAAAC[-/AG]AGGAATAAAGATTAC	54629
rs561119532	in-del	-/A	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58823610	GTCAAGGCTGCAGTG[-/A]GCCAATATCATGCCA	54629
rs561164084	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58828988	GTATCATCAATTACA[A/G]TAACAATAAAATTGA	54629
rs561168830	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800039	TTATCTTTTGAATAT[A/G]AATACGCTATAAAGC	54629
rs561212011	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822636	ATCCTTAGCTAACTG[A/G]AATTCCTAAATTCAT	54629
rs561221622	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58775341	AAAGTTTGAGAAATG[C/T]TTTAGTAGAGAAAAA	54629
rs561282422	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58793851	AAGTAAGAGGGAAGG[C/T]ATAAAATAATTGGTT	54629
rs561284836	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770456	CCTTAAGAGGAGTCC[A/G]TTCTAATTAGGAAAA	54629
rs561293584	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793953	AACCAGCCAGCATGG[G/T]GTTATGTTTTCTCAG	54629
rs561294215	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58790577	GCATTTATGTTGACA[A/G]TAGACCTTAGTGGGG	54629
rs561384097	snp	A/C	0	0	intron-variant	FAM63B	GRCh38.p7	15:58801597	TTAAAAGGTGATACC[A/C]AATAAAAACTCGTAT	54629
rs561395301	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824988	CATATATCATATTAT[C/G]TTGAGTGGTGTTCAG	54629
rs561398770	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859347	TAAACTTCGTTTGCA[C/T]TGGTGGAATTCATTT	54629
rs561409566	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769744	GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC	54629
rs561410958	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58847965	CATATAGTGTATAAA[A/G]AATGGGTGGATATTC	54629
rs561422405	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787795	TGTGAATGTTAATGT[A/G]TAAGTATAGTAGATA	54629
rs561435852	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807140	TTTCCTTCATTTTCA[C/T]CCTTTTTATTATCAA	54629
rs561508258	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795475	CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC	54629
rs561539410	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58788775	AGCACTTTGGGAGGT[C/G]AAGGCAGGCAGATCA	54629
rs561546377	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826294	GAGTACAATGGCGCA[A/G]CCTTGGCTTACCACA	54629
rs561555813	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58814544	CCACCATACCCTGCT[C/G]ACTTTTTAATTTTTT	54629
rs561579483	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58777971	AAAAATCTTATTTTA[A/G]CTGTAATAAGTGCTA	54629
rs561630745	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829718	GCATACCCAAGAAGT[C/T]GCAAGTATTCAATGA	54629
rs561641280	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855674	GCCTGTAATCCCAAC[A/G]TTTTGGGAGGCCAAG	54629
rs561673567	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820139	GGCATGGTGGCGTGC[A/G]CCTGTAGTCTCAGCT	54629
rs561737002	snp	C/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58820386	GAGGTGGAGGTTGCA[C/G]TGAGCCGAGGTCACA	54629
rs561737196	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814147	GTTTCACCATGTTAA[G/T]CAGACTGGTCATGAA	54629
rs561808608	snp	A/C/T			intron-variant	FAM63B	GRCh38.p7	15:58834423	CTTCTACTCTCCTCA[A/C/T]ACCAGTGGTTCTCAA	54629
rs561827328	snp	C/T	0.00874735	0.0655527	intron-variant	FAM63B	GRCh38.p7	15:58836775	AGGTGTACACGATCA[C/T]ACCTGGCCAATTTAA	54629
rs561834961	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58811650	CAAGCTATGGCCCAG[C/G]AGGGAAAGAGCATAG	54629
rs561884416	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58849506	CAAGACTCCGTCTCA[A/G]AAAAGAAAAAAACTG	54629
rs561884448	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783481	TTTCCTTTGGATTAT[C/G]AAAATCATAGGTGTC	54629
rs561891932	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836140	TGGTCTCAATCTCCT[C/G]ATCTCGTGATCTGCC	54629
rs561947117	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58789165	ACACGGTGAAACTCC[A/G]TCTCGACTAAAAAAT	54629
rs561957216	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857064	AAAAAATGTAATGTG[C/T]TAATTCAGCCTTTTT	54629
rs561981393	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826727	ATATCAGAATTCTCC[C/T]GTTTTCCCAGTAATG	54629
rs562018572	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58804805	GTGAGACCCTGTTAC[-/A]AAAAAAAAAAAAGAA	54629
rs562032316	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58778989	CTGTTCTTGAACTCC[G/T]GACCTCAAGTGACCT	54629
rs562087194	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58770998	CAAGGGAGCTGCCCG[A/G]GAGTTCAACTTCCGG	54629
rs562106743	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58789005	TGATGGAGTGAGACT[A/C]CGTCTCAAAAACAAA	54629
rs562119467	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860524	GGTTGCAGTGAGCCA[A/G]GATTGCCCCACTGCA	54629
rs562124944	in-del	-/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58840136	CGCGTTTGGCCTCGA[-/T]TTTTATCTTTACATA	54629
rs562145826	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58813815	TTTACATTCCCACCA[C/G]TAACATATGAGTGAT	54629
rs562172345	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58841620	ATGTTCGTCAGGCTG[C/G]TCTCGAACTCCTGAC	54629
rs562181647	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58848383	AGTAGGGAAGGCAGA[C/T]ATTTGACCAACTCAT	54629
rs562181943	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803505	GAATCAACAACTTAC[A/C]TTGCATTATATCATA	54629
rs562192429	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856507	TTCTTCAAATTTCCT[A/G]TGGTAGCATGATAAA	54629
rs562235627	snp	A/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58840984	ATTTTTTTTTTTTTT[A/T]AATTTTTTTTGGTGT	54629
rs562243944	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835168	ATTAAGGACCTCGTA[A/G]TTTGACAAGGGGCAG	54629
rs562261447	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58819040	CTGATGTGTAGTAGC[A/G]TGATCATAGCTCATT	54629
rs562282978	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58815958	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	54629
rs562365441	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772318	GCATGTCAGGTGATG[G/T]CTTCCTTTCTTTCCT	54629
rs562373951	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58797221	ATATTATTAAGATTA[A/T]TTTTGCCAGGTGTGA	54629
rs562378852	in-del	-/TAT	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58850475	ATCTCTATGTAATGA[-/TAT]TATGGTGATTTAAAC	54629
rs562405664	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58827719	GTCCTCCCAAAGTGC[C/T]GGGATTACAGGCATG	54629
rs562432753	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58784973	TTAAAATTTAGAAAA[G/T]CAGACAGACTGCCAC	54629
rs562435268	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790547	TCTAACTTTGGATTT[A/C]ATAAGAATTCTCTAG	54629
rs562493955	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791111	CTTGAACCCAGGCGG[C/T]GGAGGTTGCAGTGAG	54629
rs562496521	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778768	AGTAGCTGGGACCAC[A/G]GGTGTGTGCTACCAT	54629
rs562498406	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855218	ATGGAGCTTAGTTTT[A/G]ATTTAGATAGCAAAA	54629
rs562533168	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784495	GAGAATATTTAAACT[A/C]CTTAAAGTGCCTTCC	54629
rs562594629	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778120	AATCCCTACTTGGTT[A/G]TACTTTTTTTTTATT	54629
rs562621441	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58854025	CAAGGTGGGCGGATC[A/T]CAAAGTCAGGAGTGT	54629
rs562656314	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810620	TAGAGGGAAGAGCTC[A/C]TAGAAGACCACCCGT	54629
rs562661099	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815899	TGGTCAGGATGGTCT[C/G]GATCTCTTGACCTCG	54629
rs562711202	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58792520	ATGAGGCAGAAGAAT[C/G]GCTTGAACCCGGGAG	54629
rs562713624	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827106	ATTGTGTCTTTCCCA[A/G]TGCATCAAATCGGGG	54629
rs562717510	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804937	GTTCAAGACCAATCC[A/G]GGTGTGATATAGTAA	54629
rs562840508	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58844269	ATCTCCATTGTTGGC[C/T]GGGCACGGTGGCTCA	54629
rs562866577	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817228	AATGAATAAAGGATT[A/G]ATATTCAGAAAGTAG	54629
rs562892537	in-del	-/ATTATTATTATT			intron-variant	FAM63B	GRCh38.p7	15:58840661	ATTATTATTATTATT[-/ATTATTATTATT]TTGAGATGGAGTCTT	54629
rs562968829	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58809606	TTCTTCCTCTTTGAC[C/T]TGAAAAACATTTGAC	54629
rs563032355	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780153	GCTCACACTGTAATC[C/G]CAGCACTTTGTGAGG	54629
rs563039985	snp	A/C	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58808218	TAAACTGGCAATGCC[A/C]CATCATTATCACCCA	54629
rs563064933	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58783982	TGGAATATTTGGAGT[C/T]GGAGTAGCTATTTTC	54629
rs563066448	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58785681	TTAAAAAAATAATCT[A/G]TCGAATTTTTTTTTA	54629
rs563098925	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846662	TATGTATCCACAAAA[A/G]TTAAAAATTAAAAAA	54629
rs563160884	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846124	AAAAAACAGAATGAT[A/T]GAGACCTAGCATTTG	54629
rs563185874	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58785869	TTTTTAGTAAAGTCC[A/G]TGTTTCACCAAGTTG	54629
rs563215934	snp	A/T	0.00398564	0.0444627	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860215	AAGGACAAAACAAAA[A/T]GTTTTGGAAGGTGAT	54629
rs563227587	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58845692	CCGGCAATCCCACTC[C/G]TAAGAATATACTCAA	54629
rs563233693	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58773705	TTTTTTTTTTCGTTT[G/T]TTTGTTTGTTTTAAA	54629
rs563242717	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853076	TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGGGATT	54629
rs563248626	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806336	GTCTGGCATTACAGG[C/T]GTGAGTCAACGTGCC	54629
rs563250057	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780448	ATAAAGTTTAAATAA[C/G]TAGTCCAAGGTAAGA	54629
rs563288441	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58852041	CCTGTATTCCCAGCC[C/T]TTTGGGAGGCTGAGG	54629
rs563294481	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774132	ACTCATTCAATTCAG[A/G]CAGATTCAAGTGAAT	54629
rs563304370	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860997	TACAAGTAGGACAGT[A/G]TAACAGGAGATTGGT	54629
rs563310174	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800149	TAACTTATGCCAAGC[C/G]CTCTCTTCCATTTTT	54629
rs563347966	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58849320	ATCCTGGCTAACATG[G/T]TGAAACCCCGTCTTT	54629
rs563366679	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844806	CCTATAGTTGCAGCT[A/C]CTTGGGGCTGAGGCA	54629
rs563416200	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58819632	GCATTACTGGTGTGA[C/G]CCACCACACCCAACT	54629
rs563426061	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844319	TTGGGAGGCCGAGGC[A/G]GGTGGATCACAAGGT	54629
rs563428531	snp	A/G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58851013	GAGTCTTCCTCTGTC[A/G/T]CCCAGGCTGGAGCGC	54629
rs563475958	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806702	ACAAACAAGAATTTA[C/G]AAAAATAGAGGAAAA	54629
rs563507894	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793627	AAAACTAGAGAAAGG[A/G]AACTGCAAAAAATAC	54629
rs563563925	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781396	ACTGCAACAACATTC[C/T]TTATTGCTCTAAAAC	54629
rs563599814	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58799294	CAAACACGGCTGGGC[A/G]CGGTGGCTCACGCCT	54629
rs563604055	snp	C/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772782	TCTGAGACCCAATTA[C/T]CGTAACTTCTTGGTT	54629
rs563624261	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770903	ATGCCTCAGGCCGAG[A/G]GTGGGCCACACGCGA	54629
rs563652738	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792215	GAAAGCAGTTTGGCA[A/G]TTCTTTAAAAAGTTA	54629
rs563656003	in-del	-/GCT			intron-variant	FAM63B	GRCh38.p7	15:58828691	CAGCCTCCCGGGTAG[-/GCT]CTGGGACTACAGGCG	54629
rs563671866	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58854068	GCCAACATAGTGAAA[C/T]CCCGTCTCTACTAAA	54629
rs563682183	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770009	AAAAAAAAAACAAAA[A/G]CAAAAACAAAAACAA	54629
rs563686006	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58835730	TAATCAGTTGGCCAA[A/G]AAAGAGTTAACTTAG	54629
rs563726500	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836999	GATTTACAACAGAAT[C/G]TATAACACTTTGGCT	54629
rs563739082	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858478	GTCAATTCACTAAGA[A/G]ACAGATCATGAGAGG	54629
rs563773084	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828888	GAAATATTTTCAAAT[A/T]TAGTAATCTTCTCAG	54629
rs563778223	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807795	AGACTTTATCTCCTA[C/T]AACTTTTCACTTTTA	54629
rs563784663	in-del	-/TT			intron-variant	FAM63B	GRCh38.p7	15:58775877	TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCAC	54629
rs563796080	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58781989	TTTGAGTATTTTTAA[A/G]TATAGTATTACTAGT	54629
rs563811961	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58820411	GTCACACCACTGCAC[G/T]CCAGCCTGGGCAACA	54629
rs563827186	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819522	AAAAATATTTTTATT[A/T]TATTTTTAGAGACAG	54629
rs563834466	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801709	CAGTGGCGCGATCTC[A/G]GCTCACTGCAGCCTC	54629
rs563859859	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813451	CAGTGAGCCAAGATC[A/G]TGCCACTTCTCTCCA	54629
rs563863412	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775520	GGCTAGAAGTAAGAT[G/T]GTAGTGAGTGTAGCA	54629
rs563911394	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58838329	CTTGAATCCAGGAGG[A/C]GGAGGTTGTAGTGAG	54629
rs563979575	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857293	AATCCCAGTACTTTG[A/G]GAGGCCGAGGCAGGT	54629
rs563982423	snp	C/G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58808187	TCCCGCATCAGAGTG[C/G/T]TTCATTTATTATTGA	54629
rs564021863	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58836088	CTAATTTTTTTGTAT[G/T]TTTAGTAGAGACAGG	54629
rs564060554	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58826787	GAGGCTCCAATTATG[G/T]ATCATTTAGTTGTCA	54629
rs564074969	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58808616	TTGTTTTTGTTTTTG[G/T]TTTTTTGAGACAGAG	54629
rs564081532	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858650	TTAAAAAGCAAAAGC[A/G]AATTGATTACATTTG	54629
rs564083042	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58782940	TTTTTTTTTTTTTGA[A/G]ACAGAGTCTTGCTCT	54629
rs564104474	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58805005	AAAATGCTTGCAAAT[A/G]TTATCAGCATTTGGT	54629
rs564126909	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808967	CTGTAATCCCAATAC[G/T]TTGAGAGGCTGAGGC	54629
rs564143285	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58802825	TTGATAGTTTCAGTA[A/T]CCACATTTCTTGGCA	54629
rs564230333	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58849216	GTCTGTCTCAAAAAA[A/T]AAAAGGCTGGGCACG	54629
rs564270499	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58780840	TCTGTTTCTACTGCT[A/G]CTACCCTAGTTCAGG	54629
rs564311462	snp	A/G/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769786	ATCGCGCCACTGCAC[A/G/T]CCAGCCTGGGCGACA	54629
rs564360141	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848984	AGAGGCTGAGGCAGG[C/T]GGATCACCTGAGGTC	54629
rs564417685	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856374	TATAGGATGAATCTG[C/T]ATGTAAAAATAGAGT	54629
rs564483130	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792118	TGATGAGTGTATGGA[A/G]TGAAAACCTGACTGG	54629
rs564550998	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791879	AAAGGTCAGTAGACC[A/G]AGTCTGGGATATGCC	54629
rs564558769	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834350	CATTCCTTTTTGCCT[A/G]TCCCAATTTTACCCA	54629
rs564559338	snp	A/G	0.000115997	0.00761478	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847409	GTGACTCAGAATTTC[A/G]TCTTCGACCTCCTTC	54629
rs564620531	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58846860	ATAAAAGAAGAGCAA[C/G]TAATGGTGTAGAGAA	54629
rs564640683	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827698	ACCTCGTGATTCTCC[C/T]GCCTCGTCCTCCCAA	54629
rs564643913	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58813931	TTTTAACTTGCATTT[-/C]TTTTTTTTTTTTTTT	54629
rs564646994	in-del	-/TGAGCC	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58852065	CTGAGGCAGGCAGAT[-/TGAGCC]TGCTTGAGCCCAGGA	54629
rs564672232	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770326	GCCTAGAAAATGTTG[A/G]AAGAAAAAAGATGGG	54629
rs564673143	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797324	CCAGGCTGGGCAACA[G/T]GGCAAAACCCTATCT	54629
rs564688588	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853715	GTCCCAGCTACTCGG[A/G]AGACTTGAGGCAGGA	54629
rs564699730	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793784	TATTTTCTCAATGAA[A/G]TAGGAAACAAAGTCA	54629
rs564703397	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827205	TATATTGTAAAGATG[G/T]CCTTTTCCCTTGGTA	54629
rs564726920	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857605	GCCCAAGGTAACGTT[A/G]TATATCCCACCACTT	54629
rs564763014	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58791250	ATATATATATATATA[C/T]ATATATCTTGAGTTC	54629
rs564798084	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833834	TCTCAACTGCAAAGA[G/T]GCGTTCCTTCCTCTT	54629
rs564827321	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784991	GACAGACTGCCACAA[C/G]TGTTAATTCTGTATT	54629
rs564850219	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816498	TCACTGCAGCCTCAG[A/G]TGGCTCAAGGAATCC	54629
rs564854480	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58840904	CGATCTCCTGACCTC[A/G]TGATCTGCCTGACTC	54629
rs564873423	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772800	TAACTTCTTGGTTTT[C/T]AAAGATTGTTTTCAT	54629
rs564893102	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58822436	TACTTTCTTAAAAAA[C/T]GTTTATTATTTAGGA	54629
rs564893471	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785454	TTTGCATGCCATACT[C/G]TCTCTGCTGCACAAA	54629
rs564953363	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815944	CGGCCTCCCAAAGTG[A/C]TGGGATTACAGGCGT	54629
rs564991064	in-del	-/A/AA	0.455977	0.141681	intron-variant	FAM63B	GRCh38.p7	15:58773135	GCAATGTTTCCTAGG[-/A/AA]AAAAAAAAACAAAAC	54629
rs565002783	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861121	GTGAATCTTTTCCTT[C/G]AATTGTGCAGAATAA	54629
rs565053928	in-del	-/G	0.0115144	0.0749975	intron-variant	FAM63B	GRCh38.p7	15:58795407	AGTATGTGTTATTTT[-/G]TTTTGTTTTGTTTTT	54629
rs565117316	in-del	-/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58806888	GAAAATATGTTGTTT[-/G]GGGGGAACAGTAGAA	54629
rs565119643	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58804990	AAAGAAAGAAAAATA[A/G]AAATGCTTGCAAATG	54629
rs565185256	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805747	AACCCTTTTAAAATA[A/T]GTTTGTTTGGTTTAT	54629
rs565197982	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58798642	TGTATTTTTAGTAGA[G/T]ATGGGGTTTCATCAT	54629
rs565292309	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838652	AGTGCGGTGGCACAA[C/T]CTCAGCTCACCACAA	54629
rs565298637	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58792624	GGGAAAAAAAGAAAA[A/C]TGTTCAAAGCAGTAT	54629
rs565331203	snp	A/G	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58824447	GATGAAATTCTACAT[A/G]CCATATTTCCATATT	54629
rs565359502	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845646	AGTTTAGAGGTTCCT[C/T]AAGACACTAAAAGTA	54629
rs565374803	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793339	TGCCTGTAGTCCCAG[C/G]TACTTGGGAAACTGA	54629
rs565509008	snp	A/C/G	0.00557542	0.0525036	intron-variant	FAM63B	GRCh38.p7	15:58840054	GCCCAGCCTAGTCTC[A/C/G]AACTCCTGACCTCAG	54629
rs565523720	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58799522	AGGCGGAGCTTGCAG[C/T]GAGCCGAGATGGCAC	54629
rs565543452	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824743	GGCACGATCTCGGCT[C/T]ACTGTAACCTCTGCC	54629
rs565587515	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792918	GAGGTGGGAGGATCA[C/T]TTGAACCCAGGAGTT	54629
rs565606782	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58825259	AGAGTTAGGTGTTCT[C/T]TCAACTTCTTTTAGA	54629
rs565614361	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774771	AAGATACTGAAGCAG[A/T]AAAGGGTTTCTTCTA	54629
rs565615732	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58833383	CTGTGGGTGTTTCTC[A/G]TTAGGTGGAACAAGA	54629
rs565673383	in-del	-/ACT			cds-indel	FAM63B	GRCh38.p7	15:58859052	TTCTTGAATGTGCAC[-/ACT]TTTTTCTCAATAACA	54629
rs565685685	snp	A/C	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58850582	AAAAATTCTTTAAAC[A/C]AATTTACTTATTTAT	54629
rs565754798	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858747	ATCACACAGTACTTA[C/T]GCATAAACTTATAAT	54629
rs565776236	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58793717	AGACTGTATTACAAA[C/T]AGGTGCAGGTAGGTG	54629
rs565786025	in-del	-/TA			intron-variant	FAM63B	GRCh38.p7	15:58831041	GTGTGTGTGTGTGTG[-/TA]TATATATATATATAT	54629
rs565812014	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857456	GGAGAATCGCTTGAA[C/T]CCAGGAGGCAGTGAT	54629
rs565815120	snp	G/T	3.52858e-05	0.0042002	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772035	GCGGTGTTGCCCGGG[G/T]CTGTTCCTCTGTGCA	54629
rs565866026	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812277	CCTGTGTCTACTAAA[A/G]AATACAAAAATTAGT	54629
rs565896220	in-del	-/G			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770840	CCCCTGAGCCCTTCA[-/G]GGACAAGTTCTTTTC	54629
rs565903995	in-del	-/T	0.00993419	0.0697739	intron-variant	FAM63B	GRCh38.p7	15:58778425	GGTCCTGAAGCAGGA[-/T]TTTTTTTATATAAAG	54629
rs565917268	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58794303	GGTAATAATGAAACT[A/G]TATTACCATGGGAAA	54629
rs565918729	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781055	TTCTTTTACTAGTTA[A/G]TTTTTTTTTTCCAGA	54629
rs565991705	snp	C/T	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58851216	TGGGCTCAAGCGATC[C/T]ACCTGCCTTGGCCTC	54629
rs566006282	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855683	CCCAACATTTTGGGA[A/G]GCCAAGGTGGGCGGA	54629
rs566017092	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775015	AAGAGATGGATAAGC[C/G]AAGCAAAGTAGAGCA	54629
rs566036408	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836206	TGAGCGACCGCACCC[A/G]GCCTATTGCATCTCA	54629
rs566056245	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812870	CTCAAAATAAATAGA[A/G]AAATAAGTAAATAAA	54629
rs566099350	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835662	CTGTCTCAGTAATTA[A/C]TTAATTCATTAAATA	54629
rs566108913	in-del	-/GA	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58811801	AATAGAGAAGAAATG[-/GA]GAGTCAATTGGAAGG	54629
rs566119133	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794449	GGAACAGACAGGCAG[C/G]GTATTGGAAGAGACA	54629
rs566193762	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58807824	TATTTTGTCCCAGCC[A/G]CACTGGGCCCCATGC	54629
rs566218418	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58776634	GGATAACATGGAATC[C/G]TCAGTTCTCTTTAGA	54629
rs566228171	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771069	CGGGGGCGCGCCCCC[C/T]GGCCGCGCCCTCCTA	54629
rs566318635	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789294	AGTGAGCCGAGATTG[C/T]ACCACTGCACTCCAG	54629
rs566355592	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776319	CTCAGTCTCCCCATT[C/T]CCTCTCCTCCCCTAC	54629
rs566363460	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788959	GGAGGTTACAGTGAG[C/T]CAAGATCATGCCACT	54629
rs566388092	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58838567	TTATTTTGTTAGTGG[A/G]GCTACTTTTTAGGGA	54629
rs566412803	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58840428	AATCCATCTCTGTTA[A/G]TTATTACTTGTAATA	54629
rs566447453	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803025	GAAGAAAGAGACATC[A/G]TTGGAACCTTCATAT	54629
rs566478714	snp	A/C	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58826909	CTCCCTTGCTTCCTC[A/C]CTCCTTTCCTTCCTT	54629
rs566485122	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58808771	CACCATGCCCGACTA[A/G]TTTTTTGTATTTTTA	54629
rs566491198	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58786316	TGGTGAAGAATTTTT[A/G]ACAATGTTACTATTC	54629
rs566528703	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58820159	TAGTCTCAGCTACTA[A/G]GGAGGCTGAGGCAGG	54629
rs566540037	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814731	AGTTGCAAATGTTCT[C/T]GATGTGTTCTAAGCA	54629
rs566561884	snp	A/G	3.66932e-05	0.00428314	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771547	CGGAGACCAGCGGCG[A/G]GAATGGGCTGGGGGC	54629
rs566613614	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771130	GCGAGCTCGGTCGGA[C/T]GCACGGAAAGGGCTG	54629
rs566633071	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847642	ACATTAATTATGTAC[A/T]TTGGTGCAGAAGGCC	54629
rs566708875	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58777290	AGAATTAGAGAATTG[A/G]AAGTGAAAACAGCTG	54629
rs566788830	snp	A/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58822489	GATCCTGAATACTTC[A/G]ACTGACTGAGATGAG	54629
rs566823101	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853375	AAATAAGTATAAAAT[A/T]TCTATTTCTAGCTCA	54629
rs566834709	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58796828	GCACCTGGCCATTTA[C/T]ATATAACTATATATA	54629
rs566898711	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58790017	CTCCTGGGCTCAAGC[A/G]ATCCTCCCACCTTGG	54629
rs566913786	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784778	GCACGTGCCACCACA[C/G]CTGGCTAAGTTTTGT	54629
rs566944287	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58862077	AGTTAACTCTAAACC[A/G]TGTTAAAAAATTAGC	54629
rs566974531	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848728	TCCAGCCTGGGCAAC[A/T]GAGCGAGACTCCATC	54629
rs567005628	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861418	CATTTTACTTCTGAA[A/G]TAATTCATCTGTTTT	54629
rs567018836	in-del	-/T	0.00795532	0.062565	intron-variant	FAM63B	GRCh38.p7	15:58798374	CGTGATCCACCCACC[-/T]TTACACTCTCAAAGT	54629
rs567037501	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58803037	ATCGTTGGAACCTTC[A/G]TATTTACTTTCAAAG	54629
rs567095236	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778413	GAGGAATGCCAGGGT[C/T]CTGAAGCAGGATTTT	54629
rs567126455	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860325	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG	54629
rs567151855	snp	A/G/T	3.49713e-05	0.00418147	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772051	CTGTTCCTCTGTGCA[A/G/T]GGAGGAGGAGGGGGA	54629
rs567159280	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58778862	TAGTCGCCCAGGCTG[A/G]AGTGCAGTGGCACGA	54629
rs567163325	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58832653	CTGCCTCAGCCTCCC[C/G]AGTAGCTGGGATTAT	54629
rs567180289	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809779	AGCATGGACTTTGTC[A/T]TGTTTTGTTTCGTTT	54629
rs567202612	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58779726	TTCCCAGTCTCCTCC[A/G]AGAATTAGAATTGGT	54629
rs567224687	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839246	ATTAATGGTATTGTT[C/T]ACATCTCTATTCTAA	54629
rs567226668	snp	G/T	1.68705e-05	0.0029043	intron-variant	FAM63B	GRCh38.p7	15:58831743	ATTTTGAAATTATTC[G/T]TCTATCTAATGTTAT	54629
rs567281520	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776766	GTGGCTCATGCCTGT[C/T]GTCCCAGCATTGTGG	54629
rs567297249	snp	A/G	1.88866e-05	0.00307294	intron-variant	FAM63B	GRCh38.p7	15:58810422	ATTATGTAAACACAA[A/G]TACAGGAAAAATGTA	54629
rs567320808	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58804721	CTGAGGTCAGAGGAT[A/C]GCTTGAGCCCAGGAG	54629
rs567332314	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845801	GGAATCAAGCTGTGT[C/G]CATTGACAGACAAGT	54629
rs567349430	snp	A/G	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58780261	AATACAAAATTAGCC[A/G]GGTGTGGTGGCACAT	54629
rs567352161	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58851520	CATAACTCACTGTAA[C/T]CTCAAACTCCTGGGC	54629
rs567387642	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805130	ATCTAACAACTGCTT[C/G]CATTTCTCATAAACA	54629
rs567387682	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798337	TGTCTATGTTGGCCA[C/G]GCTGATCTCGAACTC	54629
rs567458807	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58789421	TTTGTGAGATACAGA[A/C]TTAGTGATATAACTG	54629
rs567474073	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817512	AGGTGGATCACCTGA[A/G]GTCAGGAGTTTGAGA	54629
rs567575052	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58799684	AATGGGAATTTTGAT[A/T]GGCAAAGGTTAGAGG	54629
rs567600687	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843863	AAAAAAAATCCTGAC[A/G]ATATCATCACAATTT	54629
rs567616258	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786633	ATAGAAAAATACATA[A/G]AACAGATATCCAGTT	54629
rs567646111	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58829973	ATACCACAGATTTAT[C/G]TTTAGTCCCTGTATC	54629
rs567664467	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816889	GGCCAGGAGTTTGAG[G/T]CTGCAGTGCACTATG	54629
rs567682916	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811521	AAATAATTGCCACTC[C/T]TAACTCTGAAGAGAT	54629
rs567726017	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817451	TGGTATTACGTTGGG[C/T]GCAGTGGCTCACACC	54629
rs567760045	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794277	ATTCCTGATAGAGCT[A/G]AGGAATTTTTGGTAA	54629
rs567790878	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824793	TCCTGCCTCAGCCTC[A/C]TGAGTAGCTGGGACT	54629
rs567836380	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812163	AAAGAACAGTCTGGG[C/T]GCAGTGGCTCACGCC	54629
rs567899937	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806425	TGCCGTGGTGCTATC[A/G]TGGCTCACTGCAGCC	54629
rs567907359	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849810	ACAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT	54629
rs567928116	snp	A/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58850554	GTTTCTTTTGTAAAT[A/G]GGGAACTTTTTAAAA	54629
rs567965504	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857362	AACATGGCAAAACCC[G/T]GTCTCTACTAAAAAT	54629
rs568063597	snp	C/G			downstream-variant-500B	FAM63B	GRCh38.p7	15:58862337	TGGAAAACAATCTGG[C/G]AGTTCTCTCATTGAT	54629
rs568076449	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58828106	GGGTGTGCAGTGAGC[C/T]GAGATAGCGCCACTG	54629
rs568151411	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58788197	ATCTAGGTAACGTCT[A/G]GAAAACAAGATACAT	54629
rs568177441	snp	A/C	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58806213	CAATTAGCTGGGATT[A/C]CAGGCATGTGCCACC	54629
rs568189796	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782110	AAAGGCATGTTAAAA[G/T]AATCCTTAAGTTTTT	54629
rs568198892	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58803720	ATTCAGGAGGTTGAG[C/G]CATGAGAATTGCTTG	54629
rs568200119	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58827541	CGATCTCGGCTCACT[A/G]TAAGCTCCGCCTTCC	54629
rs568212229	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58781672	CACTTTGGGAGGCCA[A/G]GGCGGGTGGATCACA	54629
rs568217978	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859341	AGTATATAAACTTCG[C/T]TTGCATTGGTGGAAT	54629
rs568228511	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813070	AATCTTTTTGGATTG[C/T]ATTTCATACTCACCA	54629
rs568296388	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775145	TCCGTGGAGTTTTTC[A/T]GGCTACATGATGTAA	54629
rs568309097	in-del	-/T	0.00159617	0.0282053	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855951	GAGAGTAGCTAAGAA[-/T]TTATGTAAAAGCAAT	54629
rs568335022	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827921	GTTCTGGGCTCCCTA[C/T]TGCACTCCTGGAATC	54629
rs568351973	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58835529	ATGGTGGTGGGTGCC[C/T]GTAATTCCAGCTACT	54629
rs568361274	snp	G/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769899	GAGGCTGAGGCAGGA[G/T]AATCGCTTGAACCCG	54629
rs568414296	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808439	GTCTTGCCCTTTCCA[A/G]AATGTCATTTGGAAT	54629
rs568415656	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834745	TAAAGTCGTGAATTA[C/T]ATCTTCATATTTTCT	54629
rs568425563	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770637	CACAATCATACCGAC[C/G]CTTTCCTGTAGGGCG	54629
rs568457033	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58823937	TAAAAAGAAGCTCCT[A/G]TTTTAAAAATGTCTA	54629
rs568478327	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842022	CACCCTCTGATAACT[G/T]CTGCTTGCTCTTAAC	54629
rs568547005	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58777429	CAGAGTAAGGACTGA[A/G]TTGAAAGTATTGGTT	54629
rs568568129	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58776175	AGTAAATATGGTAGT[A/C]CTACATAGAGTAAAT	54629
rs568584144	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795189	CCAAAAAATAAATAA[A/G]TAAATAAATAAATCT	54629
rs568614119	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847887	AGATGAAGAGATGAG[A/C]ACATATCTGAGCTAT	54629
rs568616932	in-del	-/G			utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854795	CAATACACTCTTTAT[-/G]GAGCTGGAGTTTCAT	54629
rs568639158	in-del	-/T	0.407502	0.194147	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832228	AACTAGGATGACTTC[-/T]TTTTTTTTTTTTTTT	54629
rs568639386	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58855012	CTAAATATTAGCACA[A/G]TAGTTTCTGAAATTT	54629
rs568648551	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795792	TTTTTTTTGGCCACC[C/T]TCCCTCCTGCACCAA	54629
rs568678227	snp	C/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58789535	GATCATGACTTGCTG[C/G]AATCTCGACCTCCCT	54629
rs568684908	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FAM63B	GRCh38.p7	15:58862380	TTCCATATGACCCAG[C/T]AATTCATTCCCAGAT	54629
rs568688376	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58809168	GGTGAGCCATGATCA[C/T]ACCACTGCACTCTAG	54629
rs568723475	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827256	ATTATTCTTTGAACT[C/G]TGTGAATATGCTATT	54629
rs568726937	snp	C/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58839577	CCTCAGATGATCCAC[C/G]CACCTTGGCCTCCCA	54629
rs568727465	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783924	GCACTCCAGCCTGGA[C/G]GATAGAATAATTGGG	54629
rs568740354	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783070	GATTACAGACACCTG[C/T]CACCGCGCCTGGCTA	54629
rs568774485	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789929	TGGGATTGCAGGCGT[A/G]AGCCACCGTGCCTGG	54629
rs568786468	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846430	AACTCTGTCTCTACT[A/G]AAAATACAAAAAATT	54629
rs568867982	snp	C/T	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58814338	TGTCTCTTCATGTCT[C/T]TTGCCCACTTTCTAA	54629
rs568868324	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820808	TGTGGTATTCAAAGA[A/G]TAAGTCTTCAAGGTG	54629
rs568890402	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798194	CGATCTTGGCTCATT[A/G]CAACCTCCGCTTCCA	54629
rs568890728	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790706	TAGATACTGGATACA[C/G]AGTTGACAGAATTTG	54629
rs568921515	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833574	TAGTGCAGAGAAGGT[C/G]AGAAGGTAAACACGT	54629
rs568934184	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58814904	CACCTCAGCCTCTCA[A/G]AGTGCCGAGGTTACA	54629
rs568936548	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58841549	TAGCTGGGATTACAG[A/G]TGCATACCACCATGC	54629
rs568951648	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791705	ACTGAATTTTTAATT[C/T]TATATAATATAAATT	54629
rs568957834	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809060	TACAAAATATCAAAA[A/G]CATTAGCTGGGCATG	54629
rs568989198	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58812065	TTTTGTTTTATGGTA[A/T]GAGGTGAGAATTTAC	54629
rs569019253	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58803267	GTCAGGAGATGGAGA[C/T]CATCCTTGTCAACAT	54629
rs569039170	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58836189	TGCTGGGATTACAGG[C/G]GTGAGCGACCGCACC	54629
rs569114514	in-del	-/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58815456	CCTGTGCTCAAGCAA[-/T]CCTCCCTACTCGGCC	54629
rs569152452	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58808503	TTTCTTTACTACTAC[A/G]CATTTAAGTTTCCTC	54629
rs569167714	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816843	CTGTAGTCGCAGTTA[C/T]TCAGGAGGCTGAGGT	54629
rs569177915	in-del	-/CA	0.00360071	0.0422775	intron-variant	FAM63B	GRCh38.p7	15:58830646	CTCTATAAGGCACAT[-/CA]CACAGCCTTTGTCTA	54629
rs569221202	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860584	TATATCTCAAAAAAA[A/G]AAAAAAAAAAAAGTC	54629
rs569232310	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58810856	GGATCCTCAGGACAT[C/G]ATACCCTCCTGGAAC	54629
rs569240997	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861280	GGTCAATTTGCTGTG[A/G]CATATCAAAGATCTC	54629
rs569287814	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822596	ATTCTGGATCAGAGT[A/G]TGCCTCTGAAAATCA	54629
rs569320419	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778953	TTTTAGTAGAGATAG[G/T]GTTTCAGCATGTTGG	54629
rs569432658	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823248	GATGAAGCCATTCTC[C/T]TTCCTCAGCCTCCTG	54629
rs569437933	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58830856	GCTGGGAATGTGCAC[A/G]TTGGGCCACTCAGAA	54629
rs569459591	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58831627	TTAAAAACACAAATG[C/T]CCAGTTTGGAGCCAT	54629
rs569597130	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798754	AGCCACCACGCCCAG[C/T]AATCCAGTAAATATT	54629
rs569626359	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800439	AGTCAGCCAAACTTA[G/T]CAGCATATTATTTAG	54629
rs569633153	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58852810	CTTTCTGTAGTTAAA[C/T]GGTTTAAAGCACTGA	54629
rs569684621	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845171	AGCACTTTGGGAGGC[C/G/T]CAGGTGGGCAGATCA	54629
rs569686944	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58776168	TACATAGAGTAAATA[C/T]GGTAGTACTACATAG	54629
rs569717607	snp	A/G			upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58770975	CTTCCCTTTAAAGAA[A/G]CCGCACACAAGGGAG	54629
rs569745835	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58851289	TCCAAAAATATTTAG[A/G]ACAATGACAGAATCA	54629
rs569809989	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769577	TGTAATCCTAGCACT[C/T]TGGGGGCCGAGGTGG	54629
rs569823462	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58837672	TTGAGGGACATCTTA[G/T]GCATTCATATTTAAT	54629
rs569837699	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58792818	CAAAGTACAAAAGAC[A/C]ATATAGTGTATGATT	54629
rs569906673	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773971	GTTAGACTTGCTCTA[A/G]CGGGCCAGAGTCCCT	54629
rs569926214	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58849729	ATATATATGACAAGA[G/T]CTTTCCAGGCAACAA	54629
rs569930359	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843236	CTCACTGGATCCTCT[A/G]TCTCTTGGGTTCAAG	54629
rs569960357	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787308	CCATTTCTTTACTTC[C/T]TAATAGTTTTATCTC	54629
rs569963805	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848238	ACATATATTTCACTC[A/G]TAACAATTTAAGTGC	54629
rs569992299	snp	A/G	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58849274	TTGGGAGGCCAAGGC[A/G]GGCCGATCACGAGGT	54629
rs569998975	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817538	TGAGACGCCTGGCCA[A/G]CATGGTGAAACCTTG	54629
rs570020464	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794400	GTGTGTGTGTGTTTT[A/C]AGAATAAAATATTTT	54629
rs570037410	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58836247	TAATTCTTTTTTTTT[G/T]TTTTTGAGACAGGGT	54629
rs570042152	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58817699	TGCACTCCAGCCTGG[C/G]CGACAGAGCGAGACT	54629
rs570063803	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58818339	TCATAGCTCACTGCA[A/G]CCTGGTACTTCTGGG	54629
rs570064383	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774441	GTTAGCCGAGATCAC[A/G]CCACTGCACTCCAGC	54629
rs570075373	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806461	CTCCTGGGCTCAAGT[A/G]ATCTGCTCACTTCAG	54629
rs570085853	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788254	GAGATGGTACAGAAT[C/T]GCTGACATTGCATGT	54629
rs570131446	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58800569	TGACATGATCTTTCT[A/T]ATATGTGCTTTCTCC	54629
rs570188387	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58812802	GGTTGAAGCTGCAGT[A/G]AGCTGTGATCACACT	54629
rs570202932	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792397	TGGATCACAATGTCA[A/G]GAGTTTGAGACCAGC	54629
rs570234404	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58827047	TATTTCCTCATTAGT[A/T]GATTCAGGTTATATA	54629
rs570273673	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827873	GTATCTCCTCATCTT[C/T]ACTTAAGCACTTATT	54629
rs570275033	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801099	CTGCCTCAGCCTCCT[A/G]AGTAGTTGGGACTAC	54629
rs570281223	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58845601	ACACTGTTGATGGGA[A/G]TATAAATGAGTACAA	54629
rs570294254	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856739	GTTTGTTTTTCCCGG[A/G]ACAGATAGTAGTGAT	54629
rs570335792	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827460	TATCCATATAAACTC[A/G]TGGATTCCTTTTTAT	54629
rs570371375	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814191	GTGATCCACCCGCTT[C/T]GGCCTCCCAGAGTGC	54629
rs570371468	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808014	TCCCATTTACACTCC[C/T]CACTCCCCTCCCTCC	54629
rs570386615	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58781795	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	54629
rs570431730	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855778	ATACAAAAAATCAGC[C/G]TGGCATGGTGGTGCG	54629
rs570497364	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826409	TAATTTTGTATTTTT[A/G]GTAGAGATGGGGTTT	54629
rs570514631	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58777523	TAACGCCTGGAATCC[C/T]AGCACTTTGGGAGGC	54629
rs570550224	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820151	TGCACCTGTAGTCTC[A/T]GCTACTAGGGAGGCT	54629
rs570561874	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819786	TGAACAGATTGTGCC[C/T]TCAAATTGTTTCTTA	54629
rs570575657	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58802896	CTAGGCTTAAAATTA[C/T]TGGTGCTGGAAAAAA	54629
rs570581886	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775717	CCAAAGATAGGGAAG[A/G]TATGAAGGGAATTAT	54629
rs570605739	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58781785	GCGGGCGCCTGTAAT[C/T]CCAGCTACTCGGGAG	54629
rs570638048	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58826500	TTCCAAAGTGCTGGT[A/G]TTACAGACATGAGCC	54629
rs570697288	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58797798	ATGAGCTCTTTTGCC[A/G]TGAGTTCTGCAAATG	54629
rs570708318	snp	C/T	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58841130	GGGATTATAGGCGCG[C/T]ACCACCATGTCCAGC	54629
rs570711886	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58834008	TGCAGCCTTCCGCAG[C/T]GTTTTGTGTCTCTGG	54629
rs570739019	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771024	TCCGGCCACATAGTG[A/G]GAGGATGTTTTCCTA	54629
rs570769283	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58804086	GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC	54629
rs570812048	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802550	TTTTCTTTTTTTATG[C/T]CTCTTTAAAAATATG	54629
rs570825664	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58788792	AGGCAGGCAGATCAC[C/T]TGAGGTCAATAATTT	54629
rs570831724	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836146	CAATCTCCTGATCTC[A/G]TGATCTGCCTGCCTC	54629
rs570857422	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58774414	TCTTGAACCCAGGAG[G/T]TGGAGGTTGCGGTTA	54629
rs570862854	in-del	-/TCTC	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58834276	ACAGTAACAATCTGA[-/TCTC]TCTCTCTTTTCCCCA	54629
rs570869240	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847746	AAGTATTAAACACAG[A/G]AGTGATGGGATCTTC	54629
rs570969157	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789547	CTGCAATCTCGACCT[C/T]CCTAGGCTCAGGTGA	54629
rs570980438	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58824417	ATTACTTCCTTGATA[C/T]ATAAATTTCATAATG	54629
rs571010489	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58827070	GTTATATATTTTTGG[C/G]AGGGATGCTACGTAG	54629
rs571028490	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789990	CACTGTGTTTCCCAG[G/T]CTTGTCTTGAACTCC	54629
rs571090779	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784040	TATATTAATAATTTT[A/C]CAGGGCCGAGTGCAG	54629
rs571114626	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58833449	AGAGAAAGAAAAAAG[A/G]GGGCCCAGGGGACCA	54629
rs571121173	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853253	GCACCACGCCTGGCC[C/T]AAACTGTTCATTTTG	54629
rs571150634	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815489	CCAGTAGTTGGGACT[A/G]CAGGTGCACACCAGC	54629
rs571157968	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58784710	CTTCAGCTTCAAATT[C/G]CTGGGTTCAAGTGGT	54629
rs571172591	snp	C/G	1.8274e-05	0.00302269	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771977	CGAGTTCAATAGTGA[C/G]GAGGGAGCGGAGAAC	54629
rs571182035	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58852210	GGAGAATTGCTTGAA[A/C]CTGGGAGGCAGAGGT	54629
rs571240615	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860531	GTGAGCCAAGATTGC[C/T]CCACTGCACTCCAGC	54629
rs571256996	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58789103	AGCACTTTGGGAGGC[C/T]GAGGCGGGCCGATCA	54629
rs571280024	snp	C/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58785285	AAAGTACTTTACTGG[C/G]TATGATTCAGGAAAT	54629
rs571286493	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58832844	ACTAGGATGACATCT[A/G]ATCATGGAAGTTTAT	54629
rs571302102	snp	A/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58838754	ACCACTCCTGGCTTA[A/T]TTTTTTTAGTAGAGA	54629
rs571323642	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58809728	TTTTATATATATACA[A/T]GTTTATCTCTCCCAA	54629
rs571340679	snp	G/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58803833	AAAATAAGAGGCCGG[G/T]CGTGGTGGCTCACGC	54629
rs571342165	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58814089	ATTACAGGCGCCCAC[A/C]ACCATGCCCAGTGAA	54629
rs571350989	in-del	-/AG	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58841172	ATTTTTAGTAGAGAC[-/AG]AGTTTCACCATGTTG	54629
rs571365814	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58845879	ACAAAACAGAATGAC[A/G]TCCTGTCAAATGCAA	54629
rs571383536	snp	A/G	5.1181e-05	0.00505845	intron-variant	FAM63B	GRCh38.p7	15:58810185	ATCTTTTTTGTTCTC[A/G]TTTTGATGTTTCTGA	54629
rs571401530	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798265	GGGATTACAGGCGCC[C/T]GCCACCATGCCCAGC	54629
rs571405424	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58797709	TAACAAGTTGATACC[A/C]TTTACCTAACCTCTT	54629
rs571443580	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58811942	ATTTTCACTTACTTA[C/G]ATTTTTTAACATAAA	54629
rs571546233	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58838800	TGTCCAGACTGGTCT[C/T]AAATCCCTGACATCA	54629
rs571620020	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58822665	ATCGTCACAAAATCA[A/G]TTTAATATTTTTTCA	54629
rs571630378	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58805930	AATACAAAAAATTAG[C/T]TGGGCGTGGTGGCAC	54629
rs571650518	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58779119	TCCAGTCTGGCCTTG[A/T]ACTCCTGGCCTCAAG	54629
rs571675238	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58842733	GCAGTTAGAGGCTTT[G/T]TACTATATTAAGCAT	54629
rs571755924	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789427	AGATACAGACTTAGT[A/G]ATATAACTGAGACAG	54629
rs571792797	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784689	CAGTGGCATGATAGC[A/G]GCTCACTTCAGCTTC	54629
rs571832263	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58837268	ATTTAATAAGGACAC[A/C]AATAATAATTTTTAA	54629
rs571850707	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824108	GGAGTATGAAGCTAT[G/T]TGAAACACTGTTAAC	54629
rs571890786	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845105	AGTAGACATTTCTCC[A/G]AAGAAGTCATGCAAA	54629
rs572019358	snp	A/T	0.0640965	0.167152	intron-variant	FAM63B	GRCh38.p7	15:58844006	TAATGCATTAAAACC[A/T]ATTCTATATTATTAT	54629
rs572047225	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785460	TGCCATACTGTCTCT[C/G]CTGCACAAATTCATC	54629
rs572087172	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817099	CCTATTAACTGTAAG[G/T]AAACATTAGTAAACA	54629
rs572210858	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817646	AGAATTGCTTGAACC[C/T]GAGAGGCGGAGGTTG	54629
rs572243859	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780359	GTGAGCCGAGATAGC[A/G]CCATTGCACTCCAGC	54629
rs572274664	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58811283	CATATATCCATCACT[C/T]TAACTGTACATTTCT	54629
rs572343460	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58781289	ACTCCTGACCTCAGG[C/T]GATCAGCCCACCTTG	54629
rs572406282	snp	A/G	0.0119091	0.0762411	intron-variant	FAM63B	GRCh38.p7	15:58781857	CAGTGAGCCAAGATC[A/G]TGCCACTGCACTCCA	54629
rs572442877	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855098	TCAAAAAAACAAAAA[C/G]AAAAGAATAGGAATA	54629
rs572464066	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806589	TAGTTGTTTTAATAT[C/T]AAATAATGGGGAATA	54629
rs572480804	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58775274	TCCACATAGATGAAA[C/G]TTATTGGGGGTCCTC	54629
rs572494062	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58828139	CTCCAGTCTGGAAAC[A/G]GAGTGAGACTCCATC	54629
rs572518114	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793858	AGGGAAGGTATAAAA[C/T]AATTGGTTAGAGAAA	54629
rs572524629	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58800647	AGTTTTGCTCATTTT[A/T]CTGCATCCAGTTTAG	54629
rs572554556	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827674	TTTCACCGTGGTCTC[A/G]ATCTCCTGACCTCGT	54629
rs572554592	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834975	CAAAGGACATAAGGA[G/T]CAGATTTATTGATAC	54629
rs572559255	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58841389	TTCTATGAAGATAAT[A/G]CGCTTTTCCTTTCTT	54629
rs572604618	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58807353	GCATTTTAAAATAGT[-/C]TTTTTTTTTTTTTTT	54629
rs572608384	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58790223	CTTTTAGGCTAGCTT[A/G]GTGATTCTTTTTATT	54629
rs572620331	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58848012	AGGTAAGGAGGAGTA[A/G]TAGACATTTGTAGCA	54629
rs572628678	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58818708	ACCCAGGTGTGATCT[C/T]GGCTCACTGCAACCT	54629
rs572673390	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58788645	ATAATCTGACAAATA[A/T]GAATTTATATATTTA	54629
rs572688855	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802172	TAACATTGATTTTCT[C/T]TGGGTAGGATTGGGG	54629
rs572717483	snp	C/G			intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832351	CCTACCTCAGCTTCC[C/G]GAGTAGCTGGGATTA	54629
rs572737599	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819389	GGAGGTCGAGGCTGC[A/G]GTGGGCTGTGATCAC	54629
rs572754102	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58818039	ATTATGGTATATTCT[A/G]TGGAATACTGTACTA	54629
rs572783567	snp	A/C	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58833053	AACATTTACTGTTTT[A/C]CTCTTTTTATCTCTT	54629
rs572815141	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813767	TTTTTTTAAGAAAGC[A/G]ACAAACTGTTTACTA	54629
rs572841994	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58814209	CCTCCCAGAGTGCTG[C/T]GATTACAGGCGTGAG	54629
rs572846556	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58839730	TTGAAAAGTATATAG[C/G]TGTTTCTAAAACCTG	54629
rs572846638	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832366	CGAGTAGCTGGGATT[A/G]CAGGCATGCACCACC	54629
rs572910397	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838904	ATTACGACTTTTCAG[A/G]GGATCTTTATGCTTC	54629
rs572955103	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58829135	GTTGTTTTCCAAAAT[C/T]TGTTTAAATAGTTGT	54629
rs572977778	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58820312	AGTCAGGTGTGGTGG[C/T]GGGCGCCTGTAATCC	54629
rs572997970	snp	C/G			missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771840	ACCGCCGCCGGCTCC[C/G]AAGAGCCCAGCAGCG	54629
rs573040182	snp	C/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58821169	TCCCCCATTAACATA[C/T]ATTAACTTTTCTTCA	54629
rs573044520	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58795428	TTTTGTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT	54629
rs573107704	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789153	ACATCCTGGCTAACA[C/T]GGTGAAACTCCGTCT	54629
rs573123247	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58774659	GTAATTGGGGAGGGG[A/T]TTATCAAGGGAAGAC	54629
rs573133394	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58789709	CTGGAGTGCAATGGC[A/G]TGATCTCAGCTCACC	54629
rs573165956	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846534	GGAGGCGGAGGTTGC[A/G]GTGAGCTGAGGTGGC	54629
rs573180687	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58841695	CAGGCGTGAGCCACC[A/G]CGCCCGGCTGATCTG	54629
rs573291079	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58846712	GAGTTTATGTGATAA[A/G]GCAGGAAAATACAAT	54629
rs573319884	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58852484	TTTATTTTTAAAATT[C/T]GTAATAGCTGCAAAG	54629
rs573325426	in-del	-/TG			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859401	TAGGGCTATATAAAT[-/TG]TGTTTTTAGTGTAAA	54629
rs573351259	snp	A/G	0.000300978	0.0122637	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851884	GAAACTCCAAGAGGA[A/G]GAGGACAGACGGGCT	54629
rs573354419	in-del	-/CAAAA			intron-variant	FAM63B	GRCh38.p7	15:58823689	CAAAACAAAACAAAA[-/CAAAA]AACAGTATAGAGTCG	54629
rs573358621	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771336	CTGTCATGGCGTCCA[A/G]GGCGCTGGCTGCGGA	54629
rs573385040	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58777000	GTAAAGCATTTGACC[C/T]GGTGAATTTTGTGAG	54629
rs573387340	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58808851	CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA	54629
rs573394169	snp	G/T	1.80042e-05	0.0030003	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771645	TGCAGCTCCTCCGCG[G/T]GTTTGGACTTGAAGG	54629
rs573474714	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860681	ATACCTTACAAAGCA[C/G]TTCTAACTAATGCAA	54629
rs573513576	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58777994	AAGTGCTATTTATAG[A/G]TTTATTTGAGGGCTG	54629
rs573516173	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58815366	TTTGTTTTTTGTTTT[C/T]TTGAGACAGAGTCTC	54629
rs573540202	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860161	AATCTGCACTGTAAT[A/G]TCCTGCTTTGAGAAG	54629
rs573599860	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58818508	CCGTCCTCCCCTGCT[A/G]GCCTCCTAAAGTGCT	54629
rs573605303	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803454	GGCTGGTGACAGAGC[A/G]AGACTCTGTCTCATA	54629
rs573607541	snp	A/G	8.4553e-05	0.00650149	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772265	TTTCTACTTCCTACA[A/G]CTTTTGGGGTGGAGG	54629
rs573632353	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859064	CACACTTTTTTCTCA[A/G]TAACAAAATATATCT	54629
rs573668280	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58803899	GGATCACGAGGTCAG[C/G]AGATTGAGACCATCC	54629
rs573671285	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791053	GGAGTGGTGGCGGGC[A/C]CGTGTAGTCCCAACT	54629
rs573672460	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58797142	AAAGATTTGGTTAAA[A/G]AAGAATATCAGTAAT	54629
rs573734309	snp	C/T	0.00478085	0.0486577	intron-variant	FAM63B	GRCh38.p7	15:58784945	CAGCCTGTTATTTTT[C/T]TCATTGTAAAGCTTA	54629
rs573735731	snp	C/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58797788	CTGAGACAAAATGAG[C/G]TCTTTTGCCATGAGT	54629
rs573760751	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58838135	TGGTGTGGTGGTTCA[C/T]GCCTGTAATCCCAGC	54629
rs573788551	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844646	CGTCAGGCCAGGCGC[A/G]GTGGCTCATACCTGT	54629
rs573824182	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58805613	ACCATTGCCTTAAAG[A/G]ATCCACTAGTACTCC	54629
rs573824443	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58798559	CTCCTGGGTTCAAGC[A/G]ATTATCTCACCTCAG	54629
rs573852301	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58850893	TACCTGGCTCCCCGC[A/T]ACTTTTTGTTTGGTT	54629
rs573886004	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58850141	AATTTTAGTCAACAC[C/T]GACTCTTAATAAAGT	54629
rs573892942	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58822286	AGAAGTAATCATTCA[C/T]AAAGGTGCCAATGAA	54629
rs573954755	snp	C/T	0.00398564	0.0444627	intron-variant	FAM63B	GRCh38.p7	15:58844248	TAAAGGAACTGTGGA[C/T]TAATAATCTCCATTG	54629
rs574013684	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58793193	ACAGTGGCTCACGCC[A/G]TAATCCCAGCACTTT	54629
rs574036773	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58843301	ACTACAGGCATGTAC[C/G]ACTACACCTGGCTAA	54629
rs574037076	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58835246	ACAGTTTGTTAAGGA[C/T]ACATATCACAAGCTG	54629
rs574040165	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857102	ATATTTCCAAGTCAG[A/C]CTTTCTTACATTCCT	54629
rs574098393	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58842334	TTTTTACTCTATGTT[C/T]AGGGATTAGAAGTGA	54629
rs574106289	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824264	ATTATTTCTCTGACA[C/T]TGATTCCTCAGGATA	54629
rs574120050	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58809390	GTTCATCTGGTTGTA[A/G]CATCTGACAGGATTT	54629
rs574132822	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58829404	CCTAGGTTACTGTCT[C/T]CCCTTTGCCATAACT	54629
rs574157223	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58850543	CCTATAGGCATGTTT[C/G]TTTTGTAAATGGGGA	54629
rs574168490	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58817767	ACAATATTAAATGTT[G/T]GTGAAGATGTGCAGC	54629
rs574208104	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58808118	GTCCTGAGGCTTTCT[A/G]TATACCTCCTGTTCC	54629
rs574228588	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58818516	CCCTGCTAGCCTCCT[A/G]AAGTGCTGGGATTAT	54629
rs574255730	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828311	AATTCTTAAAAGTTA[C/G]ATTGTTTAAAGCTGT	54629
rs574276663	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58847612	TCCTGAATAGTTGGT[G/T]ATCATTCTACATGTA	54629
rs574330939	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58775052	TCAAAGTGAGCCAGG[G/T]GTACTAGAAGTCAAA	54629
rs574339897	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58839256	TTGTTTACATCTCTA[G/T]TCTAACTCCCATCTC	54629
rs574352807	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58786910	TCTTGGCTCACTGCA[A/G]CCTCTGCCTCCCGGG	54629
rs574464705	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780110	TTCTTATTTTATATA[C/T]ATAGAAAATTGAGGC	54629
rs574475766	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855968	TATGTAAAAGCAATC[A/C]GAGTTTTTAATTTAT	54629
rs574483826	snp	A/T	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58811798	CCGAATAGAGAAGAA[A/T]TGGAGAGTCAATTGG	54629
rs574499204	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58799178	CTTTATTCAGGGCCA[G/T]TCGTGCCAGAACAAA	54629
rs574527800	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58780429	AGAAAGAAAATTGAA[A/G]TGCATAAAGTTTAAA	54629
rs574545283	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58806327	GATCCACCTGTCTGG[C/T]ATTACAGGCGTGAGT	54629
rs574565290	in-del	-/A	0.424348	0.179172	intron-variant	FAM63B	GRCh38.p7	15:58837539	AGCCATGATGGCACC[-/A]AAAAAAAAAAAAAAA	54629
rs574571905	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58853735	TTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	54629
rs574573374	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58812432	ACAGAGCAACGGTCC[A/G]TCTCAAAAAAAAAAA	54629
rs574593774	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58774050	TCTTATGTAGTACTG[C/T]AGAAATTCAGAGGAA	54629
rs574656727	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774614	GCAATGTGAGAAGCT[C/G]TAATATGCTATGGAA	54629
rs574675249	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58822736	AGAATGCTATCAAAA[A/G]GCATAGCATGTAGAT	54629
rs574707988	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58841601	GTAGAGACACAGTTT[C/T]ACCATGTTCGTCAGG	54629
rs574735579	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58775384	TGTGAAGGTGGTTGT[C/T]AGATTTCAGAGGACC	54629
rs574737840	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58796740	GTTGGCCGGGCTGGT[C/T]TTGAATTCCTGACCT	54629
rs574757092	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834174	GGGTTGGGGGTAGGG[G/T]TACAGATTAACAGCA	54629
rs574780114	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58838547	CATAAATATCTATAC[C/T]TCTATTATTTTGTTA	54629
rs574792415	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58827108	TGTGTCTTTCCCAGT[A/G]CATCAAATCGGGGGC	54629
rs574799326	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58775883	TTTTTTTTTTTGAGA[C/G]AGAGTCTCACTCTGT	54629
rs574799406	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770470	CATTCTAATTAGGAA[A/G]AAAGTCACCTTTTCA	54629
rs574869402	snp	A/C/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58793983	GTCACGTTCAGCTGC[A/C/G]CGAGTCCAGGCCTGA	54629
rs574877360	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801258	GGATTATAGGCATGA[A/G]CCATCATGCCCAGCC	54629
rs574901636	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58778958	GTAGAGATAGGGTTT[C/T]AGCATGTTGGCCAGG	54629
rs574928086	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771174	GCTGCTGAGTGGTTC[C/G]CCTTCGCCTCTCAGC	54629
rs574940770	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58794470	GGAAGAGACATCTCC[A/G]TACATATTGAAATTA	54629
rs574976090	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782456	GTCACAGTTCCAAAG[A/C]AGACATCATTTTCTT	54629
rs575015386	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58795494	CACTGCAAGCTCCAC[C/T]TTCGGGTTCACGCCG	54629
rs575067768	snp	C/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769875	GCGCCTATAGTCCCA[C/G]CTACTCGGGAGGCTG	54629
rs575079480	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58796089	GGTGAGTTGAAGAGT[A/G]TCTGGGAGGCAAGGA	54629
rs575091226	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58847207	GTTTAATATATTCTG[A/T]AGATACAGATTGTAA	54629
rs575096712	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58819468	CTGCACTCCAGCGTG[G/T]GTGACAGAGCGTGGG	54629
rs575152100	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846758	TGGTGCTACGAAACA[A/C/T]GTACAAAACAATTGT	54629
rs575158101	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819994	ATATGGGCCAGGCAC[A/T]GTGGCTCACACCTGT	54629
rs575160147	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813363	AGCTGGCTGTCATGG[C/T]ATGTGCCTATAATCC	54629
rs575167282	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861568	GTTGAACTGAATTTC[C/T]GTGAAATAAATTTGT	54629
rs575175607	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58808152	TAACCCCATACACAC[A/G]GCTTCCCCCACTGTC	54629
rs575192263	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820388	GGTGGAGGTTGCAGT[A/G]AGCCGAGGTCACACC	54629
rs575195380	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58807737	AAAATGACTCCTTAA[C/T]CTGACAAACAAGTCT	54629
rs575209895	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58808635	TTTGAGACAGAGTCT[C/T]GCCCTGTCGCCCAGG	54629
rs575239275	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845463	GTGCTGAACATCACT[A/G]GTCATCTGAGAAATG	54629
rs575246034	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813805	TGTAGAAAAGTTTAC[A/G]TTCCCACCAGTAACA	54629
rs575256738	snp	C/T	2.40775e-05	0.00346961	intron-variant	FAM63B	GRCh38.p7	15:58802290	TAAAAGGCAATTTTA[C/T]AATTCTTTTTTTTTT	54629
rs575257543	snp	A/G	0.00914312	0.0669923	intron-variant	FAM63B	GRCh38.p7	15:58785152	AAAAAAAAAAAAAAA[A/G]AAAAAAGAAAAGCAA	54629
rs575364692	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58780509	CTCAGGATGTTTGAT[G/T]GGGAAGATAAAGTTC	54629
rs575366229	in-del	-/C	0.0126979	0.078662	intron-variant	FAM63B	GRCh38.p7	15:58786594	TATCTTTACTTTTAA[-/C]CTTCTTATTGTGAAA	54629
rs575411819	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832226	TAGAACTAGGATGAC[G/T]TCTTTTTTTTTTTTT	54629
rs575427876	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58831139	ATATCTATTTCCGAA[C/T]TTGATACATCTACAT	54629
rs575443531	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58849592	TGAGATTGTTATCTG[A/G]AAGCAGCAAGAAAGA	54629
rs575502839	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783534	AGGATGTTTTACATT[C/T]CTGTTTAAGATTTCA	54629
rs575532725	in-del	-/T	0.0142736	0.0832652	intron-variant	FAM63B	GRCh38.p7	15:58821385	ATGGATATTTTCTTA[-/T]TTTTTTCTTCTGGAA	54629
rs575562683	snp	C/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58777168	TTTGTTTTTGGTCTT[C/T]CCCTAGTTCGCTTAT	54629
rs575602457	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58835694	AAATAAAATGATACC[C/T]AAAAAGTGAATCTTC	54629
rs575643054	in-del	-/GTGA	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58835261	TACATATCACAAGCT[-/GTGA]GTGTTTTTATCAGGA	54629
rs575662718	snp	A/G	1.6853e-05	0.0029028	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851815	AGAACAGCAGAGCCA[A/G]GAGATCAATTGGGAA	54629
rs575680089	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58851026	TCGCCCAGGCTGGAG[C/T]GCAGTGGCGTGATCT	54629
rs575693464	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58793585	TATCGTATGTGGATT[A/T]TACCTCAAAGCCATT	54629
rs575699226	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58778512	TTCTGTAAAATAAAA[A/C]AAAGCTTAAAAAAAC	54629
rs575717818	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859939	CTGAGAAAGGAGATT[C/T]AGACTTGTCTGCCTA	54629
rs575725657	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809244	TTTCCACTTCCCCCA[G/T]TCCCCTGGAAACAAC	54629
rs575737716	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859293	TCTTTGCCTTTTTCT[C/T]CATGGAATACGGTGG	54629
rs575747801	snp	A/G	0.00279162	0.0372561	intron-variant	FAM63B	GRCh38.p7	15:58809841	CTGGAATGCAGTGGC[A/G]GAATCTCAGCTCACT	54629
rs575787697	snp	C/T	0.00438332	0.0466095	intron-variant	FAM63B	GRCh38.p7	15:58803544	AATCTAGGCCAGATG[C/T]GGTGACTCCTGCCTA	54629
rs575918342	snp	C/T	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58804762	CTGTGAGCCAAATCA[C/T]ACCACTGCATTCCAG	54629
rs575923180	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58773418	AAGAAATAAAATTAG[A/G]AACCTTGCCATTGTC	54629
rs575944339	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58830335	ATACTGTTGATTCAC[C/T]AGCGTTAAACTCACA	54629
rs575947400	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58819236	GGAGAATTGCTTGAG[C/T]CCAGGAGTTTGAGAC	54629
rs575954635	in-del	-/A	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58848750	ACTCCATCTCAAAAC[-/A]AAAAAAAAGAATATT	54629
rs576025964	snp	A/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58797823	CAAATGAAGAGATAC[A/T]GTTGTGGTGGCAGAG	54629
rs576065508	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58785433	GTAAATACTAATATT[A/T]TAGGCTTTGCATGCC	54629
rs576075627	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793080	TGGTTGCTTAGGGCT[A/G]GGGAAGAGATGGGGT	54629
rs576089302	snp	G/T	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58798433	CCCAGACCTTTTCTT[G/T]CCTTTTTTAATGCAG	54629
rs576126611	snp	C/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58779376	GGCTGAGTTTTTGCT[C/G]TATTTCTCCCTACCT	54629
rs576141864	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58789985	GGTTTCACTGTGTTT[C/T]CCAGGCTTGTCTTGA	54629
rs576150493	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791931	GAGAAAGAGCCGGCA[C/T]GGTCAGCCAGGTAGA	54629
rs576194195	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58823434	ATCCCAGCACTTTGG[G/T]AGGCTGAGGCGGGAG	54629
rs576243163	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58844067	ATGAAATTAGAAGGA[A/C]GATTTGAGTCTTAAG	54629
rs576253367	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857807	CAAATCATCATTAGA[C/T]TTGAAAATAGGCAGA	54629
rs576274556	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58793802	GGAAACAAAGTCATC[A/G]GCTGGGAGTGAGGAT	54629
rs576276751	snp	A/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787046	TGTTGGCTAGGCTGG[A/T]CTCGAACTCCCAACC	54629
rs576337308	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58787635	CCAGCTACTCGGAAG[C/G]CTGAGGCAGGAGAAT	54629
rs576354119	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58805719	GTGGCAAAATACTTA[C/T]CCAAGAGTTTAAAAC	54629
rs576365812	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58800663	TGCATCCAGTTTAGC[-/T]TTTTTTTTTTTTTTG	54629
rs576377065	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816944	ACTCCAGCCTGGGCA[A/G]TATACTAAGGTCCTG	54629
rs576432910	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58848219	TGGTCATGTTAAACA[A/G]TTGACATATATTTCA	54629
rs576468838	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58828675	ACGCCATTCTCCTGC[C/G]TCAGCCTCCCGGGTA	54629
rs576497718	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855208	TATCTTGATCATGGA[A/G]CTTAGTTTTAATTTA	54629
rs576500182	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58812552	ATCAAAACCAGGAAA[C/T]TGACATTAGTAAAGT	54629
rs576500279	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58811691	CTCTGACTCCCACTT[G/T]CTGATTTCCTCTAGT	54629
rs576505533	snp	A/G	0.00159617	0.0282053	intron-variant	FAM63B	GRCh38.p7	15:58799875	GAGAAGGCAGGAAAT[A/G]GGCAGGAATATGAAA	54629
rs576528343	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58788210	CTAGAAAACAAGATA[C/T]ATCTTAATCCCAATA	54629
rs576559403	in-del	-/A	0.000314361	0.0125332	intron-variant	FAM63B	GRCh38.p7	15:58847263	AGTTTTGATCAATTT[-/A]ACAGTCCTTTTTCTT	54629
rs576559432	snp	A/C/G	5.02503e-05	0.00501229	intron-variant	FAM63B	GRCh38.p7	15:58854435	TAACCATGAGTAAGT[A/C/G]CCTCAGAATAGTTAG	54629
rs576560177	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58843337	TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT	54629
rs576563443	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813213	ATCTGGGTGTTTTCC[C/T]GCCGGGCACGGTGGC	54629
rs576574723	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58835063	GATTTATTCATTTAT[G/T]TAACAAATATTTATT	54629
rs576614728	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58839943	GTTCAAGCAATTCTC[A/G]TGCCTCAGCCTCCCA	54629
rs576620560	in-del	-/GT	0.00755907	0.0610114	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857596	TAAATTTTGCCCAAG[-/GT]GTAACGTTATATATC	54629
rs576643394	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58824329	AATTTAGGAAGAACA[C/T]CATGGTGAAAGCAAA	54629
rs576650162	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58834352	TTCCTTTTTGCCTGT[A/C]CCAATTTTACCCATC	54629
rs576717665	snp	C/T	0.00517822	0.0506191	intron-variant	FAM63B	GRCh38.p7	15:58824902	CTCAAACTCCTGACC[C/T]CAGGTGATCCGCCAG	54629
rs576833554	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58819316	AGCTGGGTGTGGTGG[C/T]GTCTGCCTGTAGTCC	54629
rs576932910	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58778698	GTGGTGCAATCATGG[C/T]TCCGAATAGCCTCGA	54629
rs576966951	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58828823	GCCTTCCAAAGTGCT[A/G]GGATTACAGGCATGA	54629
rs577028180	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58801356	ACACTTTGGGAGGCT[A/G]CAACATGGCAAGACC	54629
rs577066987	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770018	ACAAAAGCAAAAACA[A/G]AAACAAAAAAACATA	54629
rs577086705	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802115	AAGTTCAAAGCACTA[C/T]AGTATATACATTGAA	54629
rs577178126	snp	A/C	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58840570	TCCACCTGGTCTTCT[A/C]CAATTAAACTGGGCG	54629
rs577180578	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58833154	CAGTAGTACAGTAGA[A/G]TACTGTTCTGATCCC	54629
rs577248597	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58826570	GTGAGAATTAATTGC[A/G]AATATAGCACTTTAC	54629
rs577294211	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58788575	TTGTAGACTGGCTAC[A/G]TTGAGTTGAACTTGT	54629
rs577303927	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58823590	AGATCACTTGAGCCC[A/C]GGAGGTCAAGGCTGC	54629
rs577371315	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58820300	CAAACAAAAATTAGT[C/T]AGGTGTGGTGGCGGG	54629
rs577394339	snp	C/T	0.00358779	0.0422022	intron-variant	FAM63B	GRCh38.p7	15:58776848	GCAATATAGTGAGAC[C/T]CCCATCTCTGTAAAA	54629
rs577400793	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58790371	TGAGGAATAGCCAAT[A/G]TGACTGTCAAGGAGT	54629
rs577426744	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58782581	TTATTCTTTCCTCAT[C/T]GTGCTTCACTTTTCA	54629
rs577450188	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58846624	AAAAAAATCTCATGT[A/G]ACCCACAAATACATA	54629
rs577457201	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771293	GCCTGACCGAGGCCG[C/T]GCCAGGGCGCTGTTG	54629
rs577461845	snp	A/C	0.00318978	0.0398085	intron-variant	FAM63B	GRCh38.p7	15:58791013	TGAAACCCCATCTCC[A/C]CTAAAAAATACAAAA	54629
rs577485303	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58783169	CAGGTGATCCGCCCA[A/C]CTCGGCCTCCCAAAG	54629
rs577516145	snp	C/T	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58846039	TAGAATGATGGTTAC[C/T]AGAGGCTGGGATGCA	54629
rs577518174	snp	G/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58813899	AGCCATTCTTAGGTA[G/T]CAATATTTCATTGTA	54629
rs577552374	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58851578	CAAGTAGCTAGGACT[A/G]TAGGTGCACACCACC	54629
rs577563766	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58802800	ATGTCATTAGGACAA[A/G]TTTTGCTATTTGATA	54629
rs577579877	snp	A/C	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58814467	TCATAGCTCACTGCA[A/C]CCTCAAACTCCTGAG	54629
rs577612116	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58850994	TTGTTTTTTTTTCAC[A/G]ACTGAGTCTTCCTCT	54629
rs577622513	in-del	-/CGTCTCAAA			intron-variant	FAM63B	GRCh38.p7	15:58789332	AACAGAGCGAGACTC[-/CGTCTCAAA]AACAAAAGAATCTTA	54629
rs577627314	snp	A/G	0.00119737	0.0244387	intron-variant	FAM63B	GRCh38.p7	15:58796291	GTTGGAAACTATCTT[A/G]AGCTCAAGCTAGAGG	54629
rs577707547	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58809134	GGAGGATCACTTGAG[C/G]CCAGGAGTTTGAGGC	54629
rs577735272	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858397	GACTAGTTGACTGAA[C/G]CCAAGATTAAACATT	54629
rs577743243	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58810543	ACAGAGTCCTCCAGA[C/G]TACTAAGTCTGCCCA	54629
rs577798436	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831991	TTGTCTTTTGATCTG[C/G]TTATAAATAAAAGAT	54629
rs577840964	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58845400	AACAGAATGAGACTC[C/T]ATCTTAAAGAAAAAA	54629
rs577869580	snp	A/G	0.000798403	0.0199641	intron-variant	FAM63B	GRCh38.p7	15:58778036	ATTAGGTGTTTATGA[A/G]GTTAAGCCAGAAGGT	54629
rs577894777	snp	A/G	0.00199481	0.0315187	intron-variant	FAM63B	GRCh38.p7	15:58844778	AAAAATTAGCCAGGC[A/G]TGGTGGTGTGCTCCT	54629
rs577964966	snp	C/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58815711	TTTTTTGGACAGAGT[C/G]TCACTCTGTCGCCAG	54629
rs578021876	snp	C/T	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58816238	TGGAAGGATGGCTTA[C/T]TATAAGCAAGGCAAC	54629
rs578041309	snp	A/C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772626	AAGTTACCATCAATC[A/C/T]GTGATATCATGGACT	54629
rs578059905	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58777416	AAAAATGATCAAACA[C/G]AGTAAGGACTGAGTT	54629
rs578076255	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58774651	AGAAAACGGTAATTG[A/G]GGAGGGGATTATCAA	54629
rs578166672	snp	C/T	0.0023933	0.0345097	intron-variant	FAM63B	GRCh38.p7	15:58833587	GTCAGAAGGTAAACA[C/T]GTGAACAAATGTCTC	54629
rs578198564	snp	A/G	0.000399281	0.0141238	intron-variant	FAM63B	GRCh38.p7	15:58791974	GGCTGTGATTTCCTA[A/G]AATCGTAATGAAGAA	54629
rs745318425	snp	C/G	8.35596e-05	0.00646319	intron-variant	FAM63B	GRCh38.p7	15:58854450	CCCTCAGAATAGTTA[C/G]AGTAATTTCTTGCTG	54629
rs745335327	snp	A/G	0.000128607	0.00801791	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771550	AGACCAGCGGCGGGA[A/G]TGGGCTGGGGGCGGC	54629
rs745341739	snp	C/T			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770490	TCACCTTTTCAGAAG[C/T]AGGCGCTTCCCACTC	54629
rs745379734	snp	G/T			upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771001	GGGAGCTGCCCGGGA[G/T]TTCAACTTCCGGCCA	54629
rs745427934	snp	A/G	1.65715e-05	0.00287845	synonymous-codon, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810316	TGTTCGAGTGTTTGA[A/G]TATACACCAGAATGC	54629
rs745446759	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842760	GCATTTTATATGGAT[C/T]ATCTCATTTAATCTT	54629
rs745484008	snp	C/T	9.51068e-05	0.00689524	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771830	AGCAGAACTGACCGC[C/T]GCCGGCTCCGAAGAG	54629
rs745493092	snp	A/G	2.01713e-05	0.00317572	intron-variant	FAM63B	GRCh38.p7	15:58810435	AAATACAGGAAAAAT[A/G]TATTAATTTGGCAAA	54629
rs745500166	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58778700	GGTGCAATCATGGCT[A/C]CGAATAGCCTCGACC	54629
rs745593136	snp	C/G/T	6.87301e-05	0.00586183	intron-variant	FAM63B	GRCh38.p7	15:58847277	TAACAGTCCTTTTTC[C/G/T]TTTGTTACTTCTTAT	54629
rs745599827	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58789497	AGTCTTACTCTATTG[C/T]CCAGGCTGGAGTGCA	54629
rs745708557	snp	C/T	1.66327e-05	0.00288376	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772159	GGAAGGAAGAGAACA[C/T]ACCCATCATCACCCA	54629
rs745727188	in-del	-/GATCAAAACTAGTAATA	1.65583e-05	0.00287731	intron-variant	FAM63B	GRCh38.p7	15:58847477	TAGATCAGGTAAATT[-/GATCAAAACTAGTAATA]TGTATTGTCGTCTTT	54629
rs745765854	snp	C/G	1.83128e-05	0.0030259	stop-gained, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771457	CGGCCGGGCCAGCGT[C/G]AGGGACAGGTTCTTC	54629
rs745772245	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58847631	ATTCTACATGTACAT[G/T]AATTATGTACTTTGG	54629
rs745790809	snp	C/T	1.68915e-05	0.00290611	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772259	TGCAGCTTTCTACTT[C/T]CTACAGCTTTTGGGG	54629
rs745803920	in-del	-/AGG	0.000104972	0.00724397	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772051	CTGTTCCTCTGTGCA[-/AGG]AGGAGGAGGGGGAGG	54629
rs745858555	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58773726	TTGTTTTAAAGACAA[A/G]TTAGAGCAATTTAAC	54629
rs745868892	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58847026	ATTATAAACCCCCCC[A/G]AAGGTGTTTATAAGT	54629
rs745881727	snp	C/T	1.68018e-05	0.00289838	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851820	AGCAGAGCCAAGAGA[C/T]CAATTGGGAACAAAT	54629
rs745894330	snp	C/G	1.65974e-05	0.0028807	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787954	GCTGAGCAGCTGATG[C/G]AATATTTAGGTTAGT	54629
rs745897636	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58793848	TGAAAGTAAGAGGGA[A/C]GGTATAAAATAATTG	54629
rs745903891	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58843690	AATACAAAAATTAGC[C/T]GGGCGTGGTGGTGGG	54629
rs745947406	snp	A/C	1.80641e-05	0.00300528	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771637	CCGGACCCTGCAGCT[A/C]CTCCGCGGGTTTGGA	54629
rs746069940	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817445	GTCTGATGGTATTAC[A/G]TTGGGCGCAGTGGCT	54629
rs746074293	snp	G/T	1.81701e-05	0.00301409	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771707	GGCGCCTCTGAGAGG[G/T]CAGTACAAGGTGACC	54629
rs746077983	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58837315	TGGTGGCTCATGTGT[G/T]TAATCCTAGCACTTT	54629
rs746096621	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58806052	GCACTCCAGCCCGGG[C/T]GACAGAGCGAGACTC	54629
rs746098469	in-del	-/TC			intron-variant	FAM63B	GRCh38.p7	15:58782395	ATAAAAATCTTATCT[-/TC]TGTGTTCCAAATTCA	54629
rs746117802	in-del	-/TTTTG			intron-variant	FAM63B	GRCh38.p7	15:58835900	GTAAAGTCTTGGGTT[-/TTTTG]TTTTGTTTTGTTTTG	54629
rs746121283	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58807482	TGCCTCAGCCTCCCG[A/T]GTAGCTGAGAGAGAC	54629
rs746135385	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58792792	ACCCTGAAACTTTTA[A/C]GTGAAAGAGGCAAAG	54629
rs746154698	in-del	-/TTTTTTT			intron-variant	FAM63B	GRCh38.p7	15:58852923	AGACTGCTGTTCCTG[-/TTTTTTT]TTTTTTTTTTTTTTT	54629
rs746172667	in-del	-/C			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855146	ATTGGACTAGTTCAG[-/C]CCCTTAAACAGCTTT	54629
rs746175236	in-del	-/TGTA/TGTGTA			intron-variant	FAM63B	GRCh38.p7	15:58791648	GTGTGTGTGTGTGTG[-/TGTA/TGTGTA]TGTGTGTGTGTGTAT	54629
rs746181361	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58816339	CAATGCCAGATAATT[C/T]AGATTGTGAAGAATG	54629
rs746191215	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58786813	TTGATTTTTTATAGC[A/G]TCCGTTTCTTTACTT	54629
rs746193870	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58774848	CGAAATGGTGGTAAT[A/G]GCAGGACATAAAATT	54629
rs746198882	snp	C/T	1.92851e-05	0.00310519	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771885	AGCAGTTGCAGCGAC[C/T]CGAGCCCTCCTGGGG	54629
rs746232920	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58775784	TTGAGTTGGAAATGT[C/T]CAGTGGGGGGCATAA	54629
rs746240767	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58831455	TTTACTTGCTTTCAT[A/G]GCTTTTAGTTTTATT	54629
rs746319749	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58793984	TCACGTTCAGCTGCA[C/T]GAGTCCAGGCCTGAA	54629
rs746347370	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58828685	CCTGCCTCAGCCTCC[C/T]GGGTAGCTGGGACTA	54629
rs746375374	in-del	-/TTTT			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856263	TCCACTTGGAGAGTG[-/TTTT]TTTTGTGTGTGGTCT	54629
rs746404468	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58829642	CTTTTAAAAACATCT[C/T]TCTGAAGGGAACATT	54629
rs746428455	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58852634	TCCTTCTAGTTGCAA[A/C]CTCTTGGATGACGTC	54629
rs746463424	snp	A/G	6.7891e-05	0.00582588	intron-variant	FAM63B	GRCh38.p7	15:58821708	GTGAGACAGTCATTT[A/G]TTTTCTAGATTGATG	54629
rs746491841	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58778470	CATCAAACCTAGAAA[C/G]TGTAAAATAAGGATT	54629
rs746550352	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58791515	CCAGCTACTTGGGAC[A/G]CTCAGGTGGGAGGAT	54629
rs746559761	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855206	ATTATCTTGATCATG[C/G]AGCTTAGTTTTAATT	54629
rs746560479	snp	A/C	1.75878e-05	0.0029654	intron-variant	FAM63B	GRCh38.p7	15:58821851	ATTTCCTGACTTTTG[A/C]AATTCTTGGCAAGAT	54629
rs746613701	snp	A/G	1.82643e-05	0.00302189	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771978	GAGTTCAATAGTGAG[A/G]AGGGAGCGGAGAACA	54629
rs746649540	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58802944	TTCTTCAGTATTCTT[C/T]CTTTACTTGGTAATA	54629
rs746664937	in-del	-/AT			intron-variant	FAM63B	GRCh38.p7	15:58848077	AATGAGACAGATGAG[-/AT]TTTTTTTTTTTTTTT	54629
rs746711321	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58838789	TTGCACCATGTTGTC[C/T]AGACTGGTCTCAAAT	54629
rs746795225	snp	C/G	1.86007e-05	0.00304959	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771557	CGGCGGGAATGGGCT[C/G]GGGGCGGCGGCCGCC	54629
rs746848059	snp	C/G	1.65979e-05	0.00288074	missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854482	ATATTTTTCTTAAAG[C/G]AGGGCCAGCCAGCAC	54629
rs746851593	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58776912	GAAAATTGAAGCCTC[A/G]TATTTTTCAGTTTGG	54629
rs746862134	snp	C/T	1.80716e-05	0.0030059	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772000	CGGAGAACAGGGTCC[C/T]TGAGGAGGAGGAGGG	54629
rs746877065	in-del	-/GT			intron-variant	FAM63B	GRCh38.p7	15:58794360	AGTTTTTTTTGGGGT[-/GT]GTGTGTGTGTGTGTG	54629
rs746926052	in-del	-/GCT	0.000545312	0.0165033	cds-indel, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851932	CAGGAACAAGCAGCA[-/GCT]GCTGCTGCTGCTGCT	54629
rs746960227	snp	C/T	1.82028e-05	0.0030168	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771621	GGCTCTCCTGAGGTT[C/T]CCGGACCCTGCAGCT	54629
rs746968284	snp	A/G	1.67304e-05	0.00289222	missense, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854566	GAACCACGAGAAAAA[A/G]ATAAAGAAAAAGAAA	54629
rs746979174	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58799038	AGAGGTTTGGGAATC[-/A]ACTGGTGAGAGGACT	54629
rs747006656	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58824831	TGTGCCACCATGCCC[A/G]ACTAATTTTTGTATT	54629
rs747027694	snp	C/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772424	TCGAAAAGAATTGCC[C/T]CTAACCTCAGTCTTC	54629
rs747092414	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58822738	AATGCTATCAAAAGG[C/T]ATAGCATGTAGATAT	54629
rs747165402	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58829609	AGAGGATATTGGGTG[A/C]GTAAGGTATGGAAGG	54629
rs747177069	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58851562	TCCTGCCTCAGCCTC[C/T]CAAGTAGCTAGGACT	54629
rs747206408	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849956	TACCCACACTGGTCT[C/T]GAACTCCTGGGCTCA	54629
rs747227801	in-del	-/G			intron-variant	FAM63B	GRCh38.p7	15:58793137	ACAGGGTTTCTTTTA[-/G]GGAAGACCAAAATGT	54629
rs747278490	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58845403	AGAATGAGACTCCAT[A/C]TTAAAGAAAAAAGAT	54629
rs747279792	snp	C/G/T	0.00015634	0.00884014	intron-variant	FAM63B	GRCh38.p7	15:58851751	TCATAGCTAATGATG[C/G/T]TTATAATTTAATTTA	54629
rs747293166	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58774815	ACCTTGGTTGAAGTG[G/T]GCAGCATAGGAGGTA	54629
rs747327648	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784781	CGTGCCACCACACCT[A/G]GCTAAGTTTTGTTGT	54629
rs747337172	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58809814	AGACAGAGTCTCGCT[C/G]TGTTGACCAGGCTGG	54629
rs747356913	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58798202	GCTCATTGCAACCTC[C/T]GCTTCCAAAGCTCAA	54629
rs747378765	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58782841	TGCTTCATAGGATTG[C/T]TGAGGATTCAGGTAA	54629
rs747381099	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58785671	TAAAACTGCTTTAAA[A/C]AAATAATCTATCGAA	54629
rs747429061	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58841263	GCTGGGATTACAGGC[A/G]TGAGCCACTGCACTG	54629
rs747467058	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58828107	GGTGTGCAGTGAGCC[A/G]AGATAGCGCCACTGC	54629
rs747475259	snp	A/G	3.35065e-05	0.00409293	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851828	CAAGAGATCAATTGG[A/G]AACAAATCCCGGAAG	54629
rs747517100	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58797066	TGTGGTTATTGAGTC[C/T]TTGAAATGTGGCCAG	54629
rs747560631	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842719	CTTCTGTTTATGAAG[C/T]AGTTAGAGGCTTTGT	54629
rs747575998	in-del	-/G			intron-variant	FAM63B	GRCh38.p7	15:58853029	GCAGTCTCGCTCATT[-/G]CCAACCTCTGCTTCC	54629
rs747589374	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58831596	AATGTCTGTATACAC[A/G]TATTTCATTGCAAAA	54629
rs747597557	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58810446	AAATGTATTAATTTG[G/T]CAAATTAATCTCAAT	54629
rs747614507	snp	C/G	1.66012e-05	0.00288103	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831851	GAACTAACTTCAACG[C/G]TTCAGGAAGGAGAAC	54629
rs747667525	snp	A/G	0.000104028	0.00721131	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772056	CCTCTGTGCAAGGAG[A/G]AGGAGGGGGAGGAGA	54629
rs747668524	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58789190	AAAAATACAAAAAAT[A/T]AGCTGGGCATGGTGG	54629
rs747672209	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58832446	GTTGGTCAGGCTGGT[A/G]TCAAACTCCTGACCT	54629
rs747719683	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58776723	CAGAGACAAGGTCAC[A/G]TTAAGATAGAGAGGT	54629
rs747740122	in-del	-/G	1.91558e-05	0.00309476	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771852	CCGAAGAGCCCAGCA[-/G]GCGCCGGCGGCCTCA	54629
rs747752426	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817654	TTGAACCCGAGAGGC[A/G]GAGGTTGCAGTGAGC	54629
rs747756159	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58846204	AAAATAACTAAAAGT[A/G]TAATTGGATTGTTTG	54629
rs747844523	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58830942	TTTGGGGGATCTAAA[C/T]AAATTTTAGCCAGTT	54629
rs747857972	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58781767	AATTAGCCGTGTGTG[A/G]TGGCGGGCGCCTGTA	54629
rs747862484	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58816676	GGGCACTCTAGAGCA[A/G]TGGGGAAAGGCAATC	54629
rs747883436	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58801702	TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG	54629
rs747895968	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58839456	CCTGCCTCAGCCCCC[A/G]GAGTAGCTGGGATTA	54629
rs747902112	snp	G/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771276	ACTCTCCCCGGTGAC[G/T]TGCCTGACCGAGGCC	54629
rs747903042	snp	C/T	1.81342e-05	0.00301111	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771628	CTGAGGTTCCCGGAC[C/T]CTGCAGCTCCTCCGC	54629
rs747913062	snp	A/G			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772404	AATATTCCTTTATAC[A/G]TATATCGAAAAGAAT	54629
rs747945882	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842109	ATGATATCTGCATAG[C/T]TCTTTTCCTATTATG	54629
rs748051845	snp	A/G	0.000205994	0.0101467	intron-variant	FAM63B	GRCh38.p7	15:58821865	GAAATTCTTGGCAAG[A/G]TAATTTTTCTTATAA	54629
rs748059919	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58822075	GCCAACATGATGAAA[C/T]CACGTGTCTACTAAA	54629
rs748112852	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792542	ACCCGGGAGGCGGAC[A/G]TTGCAGTGAGCCGAG	54629
rs748117587	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58823352	TGGGAGGTTTATGCT[A/G]TTCTTCTACTTGCAG	54629
rs748134172	in-del	-/AAA			intron-variant	FAM63B	GRCh38.p7	15:58846596	AAAGTGAGACTCCTC[-/AAA]AAAAAAAAAAAAAAA	54629
rs748166019	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58780657	CTTGGTACCAGTTGG[C/T]CTTTATACAGACTCC	54629
rs748176378	snp	C/G	1.89935e-05	0.00308162	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771813	CTCGCCGGCACCTGC[C/G]AAGCAGAACTGACCG	54629
rs748181683	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58815018	CTAAGAGGGCTTTGC[C/T]TAACCAAAAATCAAG	54629
rs748274253	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58774670	GGGGATTATCAAGGG[A/C]AGACTTCATAGAAGA	54629
rs748297932	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842160	CCATAGCAACCTTTA[C/T]ATTCATGTCATAACT	54629
rs748303597	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58847956	GGAAGGTAGCATATA[A/G]TGTATAAAGAATGGG	54629
rs748355069	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58823093	AGGAAAATAAGAAGA[A/G]AATGCATAGTATTTT	54629
rs748361834	snp	A/C/T	8.34517e-05	0.00645911	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772196	GAACGGACCCTGCCC[A/C/T]TTGCTGGCCATCCTC	54629
rs748363533	snp	A/G	1.65663e-05	0.002878	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847372	GAAAGCCTACACAAC[A/G]TAGATGGTGATGGAA	54629
rs748396625	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58783630	TTACTTTACTCTTTA[G/T]ATGATTAAGAATTAC	54629
rs748416708	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58813685	TCAAGTGATCCTCTT[A/G]CCGCAGCCTCCCAAG	54629
rs748620361	snp	G/T	1.85005e-05	0.00304137	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771763	GAGTGGGTCATGAGT[G/T]GGGTACCGCCGGAGA	54629
rs748699574	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855120	ATAGGAATAAATAAC[C/G]CTTAATTGTATATTG	54629
rs748720731	snp	A/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772340	TTCTTTCCTCATTCA[A/T]CAGTCCCCTTCTTAC	54629
rs748723480	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58778137	ACTTTTTTTTTATTT[C/T]AGAAAGAATGTTATA	54629
rs748729620	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836305	AGTGCAGTGGCTACT[A/G]TCATTCTCAGTATCT	54629
rs748741979	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58799858	TGTGGAAGAGATGTA[A/G]GGAGAAGGCAGGAAA	54629
rs748744801	in-del	-/CA			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855570	AAACCAATGAAAAAG[-/CA]CATTTCTGAAATGAA	54629
rs748744878	snp	A/G	0.00142628	0.0266666	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771349	CAAGGCGCTGGCTGC[A/G]GAGAAGTGGCCGCGG	54629
rs748766222	snp	A/C			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857703	TAATACTTGAAAATT[A/C]TTAGATGTATACTGC	54629
rs748798122	snp	A/C	1.87485e-05	0.00306169	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771445	AACACGGGGTGGCGG[A/C]CGGGCCAGCGTCAGG	54629
rs748816856	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58845856	ACACAACGGAGCACT[A/G]TTCACACACAAAACA	54629
rs748922297	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859236	AGCATTTAAAAATCT[A/G]TTTTTTTCTAGTATC	54629
rs748930746	in-del	-/TCT	1.79874e-05	0.0029989	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831924	ATACAAGGTATGATA[-/TCT]TAGAAATAGCTATTT	54629
rs748940395	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58823107	AAAATGCATAGTATT[G/T]TAGTTAAGGTTTATC	54629
rs748940829	in-del	-/GAG	0.000126683	0.00795773	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772002	GAGAACAGGGTCCCT[-/GAG]GAGGAGGAGGGCGCG	54629
rs748962305	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860698	TCTAACTAATGCAAT[A/G]TGTTTTTTAAAAATT	54629
rs748974515	in-del	-/TT			intron-variant	FAM63B	GRCh38.p7	15:58814794	TTCTTTAATTTTAAC[-/TT]TTTTTTTTTTTTTTT	54629
rs748995834	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58811358	TTGCCTCTTGTTAAG[C/T]GTATCAGGGTCCTGG	54629
rs748996077	snp	C/G			upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771052	CTACTGGAGCTGAGC[C/G]GCGGGGGCGCGCCCC	54629
rs749081327	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58794326	ATGGGAAATGAGTTT[C/T]TGAGATAAAGTAGAA	54629
rs749083295	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58819654	CACCCAACTTAGTGT[A/G]GCTATATTTTTGTGG	54629
rs749085113	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58780536	GTTCAAGATAGCAAT[A/G]AGTCTGGTGGACAGT	54629
rs749093639	snp	A/T	1.69484e-05	0.002911	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831899	AATAATCATTTTAGC[A/T]CCATGACCAAATACA	54629
rs749230287	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836190	GCTGGGATTACAGGC[A/G]TGAGCGACCGCACCC	54629
rs749241675	in-del	-/CT			intron-variant	FAM63B	GRCh38.p7	15:58794562	GTCAGGAGATAACTG[-/CT]CAACAAGGTGGGTAG	54629
rs749259801	in-del	-/TTG			intron-variant	FAM63B	GRCh38.p7	15:58842254	TTGAGGTTGGTTGTT[-/TTG]TTGTTGTTATTTCTT	54629
rs749266654	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58812849	AGAGAAAGAGCGAGA[A/C]CCTGTCTCAAAATAA	54629
rs749382054	snp	C/G	1.69824e-05	0.00291392	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772287	GGGTGGAGGAAAACG[C/G]GGTGAGGGAGCTGCT	54629
rs749382736	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58773026	AGTTACCTGTCAAAT[A/G]AAGTGTCTCATTTAA	54629
rs749419676	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58812066	TTTGTTTTATGGTAT[A/G]AGGTGAGAATTTACC	54629
rs749440772	snp	A/G	5.1507e-05	0.00507453	intron-variant	FAM63B	GRCh38.p7	15:58847496	ATTGTCGTCTTTATA[A/G]TGGTTAAAATGCTGA	54629
rs749491844	snp	A/G	3.31884e-05	0.00407346	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787933	CCGATGATGGAAATC[A/G]TAACTGCTGAGCAGC	54629
rs749502556	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58825084	ATACCTCAAAGCCGA[A/C]TTGTTTCTAATCTTT	54629
rs749509963	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58808583	TAAAAACCACATATT[A/T]TAAAATATATGGTTT	54629
rs749599962	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58818163	TAAGCTTTATGAAAG[C/T]ATAAACCATTTTGCT	54629
rs749612015	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58807659	TGAGCCATTGCGCCC[A/G]GCCTAAAATAGTCTT	54629
rs749613016	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58849727	CTATATATATGACAA[G/T]ATCTTTCCAGGCAAC	54629
rs749623291	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776738	GTTAAGATAGAGAGG[C/T]AGGCCGTGTGTGGTG	54629
rs749629010	snp	C/T	1.65699e-05	0.00287831	synonymous-codon, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810301	TGTAAGATTCACTGG[C/T]GTTCGAGTGTTTGAA	54629
rs749643001	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58790873	TTGTTTTTAGATGTT[G/T]ATTTACATCAAAATG	54629
rs749672851	snp	C/T	1.90431e-05	0.00308564	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771826	GCCAAGCAGAACTGA[C/T]CGCCGCCGGCTCCGA	54629
rs749751848	snp	A/C	1.92933e-05	0.00310584	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771873	GGCGGCCTCAGCAGC[A/C]GTTGCAGCGACCCGA	54629
rs749804735	in-del	-/TCT			intron-variant	FAM63B	GRCh38.p7	15:58780905	CAAAATGGTCTCTTG[-/TCT]TCTTACCCTATTCTC	54629
rs749806751	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58786956	TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTATA	54629
rs749809062	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776016	ACAGATGTGTGCCAC[C/T]ACACCAGCTAATTTT	54629
rs749855963	snp	C/T	9.97672e-05	0.00706213	intron-variant	FAM63B	GRCh38.p7	15:58787903	TAATATTTTGTTTTT[C/T]AGGTGAAACTTCCAC	54629
rs749857752	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58787991	AAGTGGATTTTATAT[C/G]TCTTTCAAAACAAAA	54629
rs749892867	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837879	GAGGCTGAGATGGGA[A/G]GATAATTTGAGTCCA	54629
rs749948754	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58781315	CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	54629
rs749986165	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58801225	GTGATCCACCCTCCT[C/T]GGCCTCCCAATGTGC	54629
rs750020946	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58851031	CAGGCTGGAGCGCAG[G/T]GGCGTGATCTCAGCT	54629
rs750075515	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58836962	AGCACGTCTTCTTCA[C/G]TGACCCAGTGACAGA	54629
rs750079041	snp	C/T	1.79745e-05	0.00299782	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771662	TTTGGACTTGAAGGA[C/T]AGTGGTTTGGAGAGT	54629
rs750122888	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58792355	GCTTACGCCTGTAAT[C/G]CCAGCATTTTGGGAG	54629
rs750170877	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58815929	GTGATCCGTCTGCCT[C/T]GGCCTCCCAAAGTGC	54629
rs750220479	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58824490	TATGTGTCATTTAGC[A/G]TAATTAAAAAGCTAA	54629
rs750268448	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58775160	AGGCTACATGATGTA[A/G]TGACATCGCTCTGTC	54629
rs750278841	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58851548	GGCTGAAGCAATCCT[A/C]CTGCCTCAGCCTCCC	54629
rs750303322	snp	A/G	4.96956e-05	0.00498451	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847358	AGAAAGTTGTTTGGG[A/G]AAGCCTACACAACGT	54629
rs750356584	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58827665	GAGACAGGGTTTCAC[C/T]GTGGTCTCGATCTCC	54629
rs750356643	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58843289	TGAGTAGCTGAGACT[A/G]CAGGCATGTACCACT	54629
rs750358484	snp	C/G	1.66358e-05	0.00288402	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847453	GTATACAAAGGACAA[C/G]AAGATCAGATAGATC	54629
rs750385991	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58785297	TGGCTATGATTCAGG[A/G]AATGAATATACTACT	54629
rs750409662	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58829295	CTAGTTCTTAATAAG[C/T]TATGCTTTATGGTTT	54629
rs750581884	snp	C/G	2.12452e-05	0.00325916	intron-variant	FAM63B	GRCh38.p7	15:58802386	TGAACAGGTAATAAA[C/G]AGTTTTTGTTAAAGT	54629
rs750589720	snp	G/T			utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854697	CCGATCAATACCGTC[G/T]GTGCCTGATTTCCTA	54629
rs750615032	snp	C/G	3.55177e-05	0.00421397	intron-variant	FAM63B	GRCh38.p7	15:58851983	AAAAACTAGTGTTTT[C/G]AGTCTTAAATGTGAT	54629
rs750665909	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58833666	TATACATAAACATCG[C/T]AATGCCTTAAGGAGC	54629
rs750672952	in-del	-/C			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860559	GCCTGGGCGACTGAG[-/C]CGAGACTCTTATATC	54629
rs750698453	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776706	ATGGAACAAGAAAAA[C/T]ACAGAGACAAGGTCA	54629
rs750715877	in-del	-/AAGTT			intron-variant	FAM63B	GRCh38.p7	15:58828336	AGCTGTCACAGTGAC[-/AAGTT]AAGTTCTCACTAAGC	54629
rs750717594	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58801116	GTAGTTGGGACTACA[A/G]GTGCATGCCACTACG	54629
rs750726890	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58830753	AATGTGAAAAACATG[A/G]CACTAAATAGACCAT	54629
rs750754829	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58787631	AGTCCCAGCTACTCG[C/G]AAGGCTGAGGCAGGA	54629
rs750762084	snp	C/G	1.70432e-05	0.00291913	intron-variant	FAM63B	GRCh38.p7	15:58821834	GGTGGGTGAGTGCTG[C/G]TATTTCCTGACTTTT	54629
rs750832826	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58802492	AGTAAACACTTTAGA[C/G]TTTGCAAGCCACATG	54629
rs750881289	in-del	-/TGTGT			intron-variant	FAM63B	GRCh38.p7	15:58794380	GTGTGTGTGTGTGTG[-/TGTGT]GTGTGTGTGTGTTTT	54629
rs750906673	in-del	-/AAAA			intron-variant	FAM63B	GRCh38.p7	15:58844560	GCGAGACTCCGTCTC[-/AAAA]AAAAAAAAAAAAAAA	54629
rs750949107	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58818934	GCATGAGCCACTATG[A/C]CCAGCCTATTGATCT	54629
rs750994184	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58782390	GCAAAATAAAAATCT[C/T]ATCTTCTGTGTTCCA	54629
rs751033931	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58805305	TGTAATAGTGTTCTT[C/T]TTTGTGTAATTTTAC	54629
rs751081705	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58800664	TGCATCCAGTTTAGC[-/T]TTTTTTTTTTTTTGA	54629
rs751198967	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806023	AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC	54629
rs751233361	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58774420	ACCCAGGAGGTGGAG[A/G]TTGCGGTTAGCCGAG	54629
rs751265019	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58815852	GCCCAGCTAATCTTT[C/G]TATTTTTAGTAGAGA	54629
rs751300147	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58827487	TTATTCAGACAGAAC[A/G]GAGTCTTGTTGTGTC	54629
rs751352727	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58797599	TTACATTTGAGCTCA[A/C]ATTCGTGGCTTGCAT	54629
rs751374749	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58827244	GTCACCTGTGATATT[A/T]TTCTTTGAACTGTGT	54629
rs751379906	snp	A/C	1.69009e-05	0.00290692	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851812	ACAAGAACAGCAGAG[A/C]CAAGAGATCAATTGG	54629
rs751409936	snp	C/T	0.000182617	0.00955379	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787919	AGGTGAAACTTCCAC[C/T]GATGATGGAAATCAT	54629
rs751441741	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58809313	ATATCTCATATAAGT[A/G]GAATCATACAGTATT	54629
rs751474529	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58826314	GGCTTACCACAACCT[C/T]TGCCTCCCAGGCTCA	54629
rs751499297	snp	A/G	1.80935e-05	0.00300773	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771684	TTGGAGAGTCCTGCT[A/G]CCGCCGAGGCGCCTC	54629
rs751507416	in-del	-/TC			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859276	TCTAAATATTTAGAT[-/TC]TCTTTGCCTTTTTCT	54629
rs751525843	snp	A/T	1.65916e-05	0.00288019	synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831844	ATTATGTGAACTAAC[A/T]TCAACGGTTCAGGAA	54629
rs751591897	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58796478	TAATAGGATGCTTAA[C/T]CTATTTTAGTTTCCT	54629
rs751611114	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58787618	GGTGGGTGCCTGTAG[A/T]CCCAGCTACTCGGAA	54629
rs751621839	snp	A/G	3.60211e-05	0.00424373	intron-variant	FAM63B	GRCh38.p7	15:58851994	TTTTGAGTCTTAAAT[A/G]TGATGATCATGGCTG	54629
rs751664044	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58776528	ATGTAGTACATTACT[A/G]TTGTCAAATGCAGCA	54629
rs751698669	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849375	CCGGGCATGGTGGCA[C/T]GCACCTGTAGTCTCA	54629
rs751746090	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58845350	GATGGAGGTTGCAGT[A/G]AGCCAAGGTCACACC	54629
rs751778422	snp	A/G	1.91342e-05	0.00309301	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771804	CGCCCGGATCTCGCC[A/G]GCACCTGCCAAGCAG	54629
rs751785835	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58838105	AGAATTCAAGATATA[C/G]TTTCAGGCCAGGTGT	54629
rs751818302	snp	A/G	2.04338e-05	0.00319632	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831958	CGTGATTCTAAATCA[A/G]AGGAGCTTGATTTAG	54629
rs751825887	snp	C/T	3.83318e-05	0.00437772	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771846	GCCGGCTCCGAAGAG[C/T]CCAGCAGCGCCGGCG	54629
rs751841920	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58786485	CATTCATTTGACAAC[G/T]CATTTGAACAATTAA	54629
rs751866822	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811462	AAGTTAAGGGGAACA[A/G]CAAGTAAGAGATGGT	54629
rs751872040	snp	A/C	1.67553e-05	0.00289437	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772094	GGTGCTGGCGGCCTC[A/C]AAGGAACGCTTCCCG	54629
rs751880390	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58799291	AAGCAAACACGGCTG[G/T]GCGCGGTGGCTCACG	54629
rs751949601	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58798015	GATTTAAAGTATGCT[G/T]AAAAGCTCATATGCT	54629
rs751963278	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811773	GCTGCAGTCCATAGA[A/G]GTTAGTCTCCCGAAT	54629
rs751981135	snp	C/G/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860293	GTCAGGAAACTGGCC[C/G/T]GGTGCGGTGGCTCAT	54629
rs751990695	snp	A/G	1.67775e-05	0.00289629	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851910	GGGCTTCTCAATACT[A/G]TCAGGAACAGGAACA	54629
rs751994149	snp	A/G	1.78299e-05	0.00298574	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772019	GGAGGAGGAGGGCGC[A/G]GCGGTGTTGCCCGGG	54629
rs752010287	in-del	-/T	0.0452658	0.143471	intron-variant	FAM63B	GRCh38.p7	15:58802296	GCAATTTTACAATTC[-/T]TTTTTTTTTTTTACA	54629
rs752069504	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858973	TGTTTTGCACTCCTG[A/G]ATAAAGGGCATAGTA	54629
rs752096657	snp	G/T	2.35059e-05	0.00342818	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771415	AGAGCAGCCCCGAGA[G/T]CCTGCAGCCGCTAGA	54629
rs752098631	in-del	-/GCCTCCCGGACTCG	5.54729e-05	0.00526625	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771580	CGGCCGCCAGGAGGA[-/GCCTCCCGGACTCG]GCTTCTCCCGCGGGC	54629
rs752127718	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58773623	GATATTCAAAAAGGG[G/T]ACATTTTCCTTTGGT	54629
rs752159998	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58822594	CCATTCTGGATCAGA[A/G]TATGCCTCTGAAAAT	54629
rs752263217	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58804045	GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC	54629
rs752272527	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58788465	TTATTTCAACTGAAA[-/T]TTTTTTATAGGGAAA	54629
rs752286425	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58775335	GAACAAAAAGTTTGA[C/G]AAATGCTTTAGTAGA	54629
rs752339266	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58825983	ATATGTATTCGTTAA[G/T]TCAAATATTTATTGA	54629
rs752341008	snp	C/T	1.66502e-05	0.00288527	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847312	GGTCAACTGTATTTG[C/T]TGGTAACGGACCAGG	54629
rs752341396	snp	G/T	1.66932e-05	0.002889	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772102	CGGCCTCCAAGGAAC[G/T]CTTCCCGGGACAATC	54629
rs752362495	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784026	AATATTCTTGTGCTT[A/G]TATTAATAATTTTCC	54629
rs752385343	snp	A/T	0.000195829	0.00989323	intron-variant	FAM63B	GRCh38.p7	15:58796208	AGAACATGTGACTTG[A/T]ATCCGGCTTTGAAGC	54629
rs752392473	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58827446	ATTAAAAAAAATTGT[A/G]TCCATATAAACTCAT	54629
rs752433859	in-del	-/GGTGT			intron-variant	FAM63B	GRCh38.p7	15:58794358	AAAAGTTTTTTTTGG[-/GGTGT]GTGTGTGTGTGTGTG	54629
rs752439012	snp	A/G	1.94192e-05	0.00311596	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771433	TGCAGCCGCTAGAAC[A/G]CGGGGTGGCGGCCGG	54629
rs752475568	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58840235	ATAATATCTACCACA[C/T]TTCCGAACGAATATA	54629
rs752487811	snp	C/T	3.34806e-05	0.00409136	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851894	GAGGAAGAGGACAGA[C/T]GGGCTTCTCAATACT	54629
rs752539072	snp	C/G	5.62562e-05	0.00530329	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802360	ATTTCAGAAATTCAA[C/G]GTTTAAATTATGAAC	54629
rs752541947	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58796277	TTGTTTGAGGGTTAG[C/T]TGGAAACTATCTTAA	54629
rs752541990	snp	C/T	9.06002e-05	0.00672993	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771697	CTGCCGCCGAGGCGC[C/T]TCTGAGAGGGCAGTA	54629
rs752553541	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58782874	TAAAATTGAATGACA[A/G]TTAGTAGATGTTCAA	54629
rs752558946	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58852707	AGAACTCTTAAGTTT[C/G]TTGTGAAGAACAAAT	54629
rs752669206	snp	C/T			missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851906	AGACGGGCTTCTCAA[C/T]ACTATCAGGAACAGG	54629
rs752694924	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58777591	CCAGCCTGGTCAACA[A/T]AATGAGACCCCATCT	54629
rs752722534	snp	C/T	1.66252e-05	0.00288311	stop-gained, intron-variant	FAM63B	GRCh38.p7	15:58821789	ATCATCTCTTGTAAA[C/T]AGTCAGACAATAGTG	54629
rs752723472	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58799198	GCCAGAACAAATGTT[C/T]AATTTTCTAAGCTAT	54629
rs752724261	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58827535	GTGGCGCGATCTCGG[C/T]TCACTGTAAGCTCCG	54629
rs752737177	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58829982	ATTTATCTTTAGTCC[C/G]TGTATCTATATCTCT	54629
rs752769901	snp	A/T	1.81529e-05	0.00301266	intron-variant	FAM63B	GRCh38.p7	15:58810407	AGTCGAAGAATTTAA[A/T]TTATGTAAACACAAA	54629
rs752782282	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58785360	TTGTGTATTTGCTTC[C/T]AAAAAAAAAATCATC	54629
rs752827017	snp	C/T	1.92236e-05	0.00310023	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771857	AGAGCCCAGCAGCGC[C/T]GGCGGCCTCAGCAGC	54629
rs752849204	snp	C/T	1.85779e-05	0.00304772	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771942	TCGTTCTCTAACCTG[C/T]ATTCTTTTCCCAGTA	54629
rs752901270	snp	A/G			missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810335	ACACCAGAATGCATA[A/G]TATTTGATCTTCTTG	54629
rs752901656	snp	C/T			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770910	AGGCCGAGGGTGGGC[C/T]ACACGCGACCCAGCG	54629
rs752935175	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58820667	ATCGGAATCACCTGG[A/G]CAGTGGAATGAAAAC	54629
rs752935729	in-del	-/ATTTATTTATATATG			intron-variant	FAM63B	GRCh38.p7	15:58850591	TAAACCAATTTACTT[-/ATTTATTTATATATG]ATTTATTTATATATG	54629
rs752998824	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58843339	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATAT	54629
rs753031354	snp	A/G	1.80455e-05	0.00300373	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771513	CTCGCCGCTGGTGAT[A/G]GTCCTGGGGTATGGG	54629
rs753067745	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856066	ATTATGAGGCCACAC[A/G]TATTTTCCTGTGTTT	54629
rs753082139	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58776303	ATCCTCTCCATCCTG[C/G]CTCAGTCTCCCCATT	54629
rs753110926	snp	C/G	1.65759e-05	0.00287883	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810268	TTTGCACAAACTACA[C/G]ACAGGCCTGGATGTA	54629
rs753138906	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58780309	CTCGGGAGGCTGAGG[C/T]AGGAGAATCACTTTA	54629
rs753163741	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58835258	GGATACATATCACAA[A/G]CTGTGAGTGTTTTTA	54629
rs753167326	snp	G/T	1.85555e-05	0.00304588	intron-variant	FAM63B	GRCh38.p7	15:58852011	GATGATCATGGCTGG[G/T]TGTAGTGGCTCACAC	54629
rs753172039	in-del	-/A	1.65844e-05	0.00287957	frameshift-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810260	ATGGCAATTTTGCAC[-/A]AACTACAGACAGGCC	54629
rs753186876	in-del	-/AACCACCTATATGTCTTGAGAAAC	3.44566e-05	0.00415056	cds-indel, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854631	GTTGGCTTCTGTTGG[-/AACCACCTATATGTCTTGAGAAAC]AAAACCACAGGAGGA	54629
rs753194404	in-del	-/TTTTTTTTTT			intron-variant	FAM63B	GRCh38.p7	15:58852943	TTTTTTTTTTTTTTT[-/TTTTTTTTTT]TTTTTTTTTTTTTTT	54629
rs753222491	snp	A/C	1.65806e-05	0.00287924	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854525	CAAGTGGAAGACAAT[A/C]TGGGAATAGTGAACG	54629
rs753228798	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58849484	CACTCCAGCCTGGAC[A/G]ACAGAGCAAGACTCC	54629
rs753247953	snp	A/G	4.98293e-05	0.00499121	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847320	GTATTTGTTGGTAAC[A/G]GACCAGGGGTTTCTT	54629
rs753272709	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58819404	AGTGGGCTGTGATCA[C/T]GCCACTACATTCCAG	54629
rs753307650	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58790002	CAGGCTTGTCTTGAA[A/C]TCCTGGGCTCAAGCG	54629
rs753361790	snp	A/G	1.68117e-05	0.00289923	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772238	CCTGGCCTGGAAGGT[A/G]CATTCTGCAGCTTTC	54629
rs753458448	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58824162	ATACAGTAAGGGTAG[C/G]ACTTAGTACTATAAT	54629
rs753493083	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58794178	GATTATAATTATGGG[C/T]CATAGAATTTAAGCT	54629
rs753541761	snp	C/T	1.83761e-05	0.00303112	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771604	ACTCGGCTTCTCCCG[C/T]GGGCTCTCCTGAGGT	54629
rs753547954	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58781555	TGATGAAAGTGTTTC[A/C]GAATTTCAAAGCCTT	54629
rs753581174	snp	A/G	1.67259e-05	0.00289183	splice-acceptor-variant	FAM63B	GRCh38.p7	15:58810229	CCTTTTCTATTTTCA[A/G]AATATGAGTGATGCC	54629
rs753626481	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58786903	GGTGCATTCTTGGCT[C/T]ACTGCAACCTCTGCC	54629
rs753675620	snp	C/T	7.66401e-05	0.00618984	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771793	ACGCGGGAGCCCGCC[C/T]GGATCTCGCCGGCAC	54629
rs753688339	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58852446	TTAGTAAAATGTTTT[C/G]TCCTGAGGTTCTGAT	54629
rs753692377	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837026	GGCTGTTGGTGTAGA[A/G]TAGAACCCCTAAAGG	54629
rs753755139	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58809207	ACAGAGTGAGACCCT[A/G]TATTCATCAAACAAC	54629
rs753778051	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58851264	TAGGCGTGAGCCACC[A/G]CACCTGGCCTCCAAA	54629
rs753785421	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58775412	ACCCATGGCTATAGG[G/T]GTTTAGACTTTATAT	54629
rs753874610	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58791494	TGATGGTGTGCACCT[A/G]TAGTCCCAGCTACTT	54629
rs753894601	in-del	-/GACACTT			intron-variant	FAM63B	GRCh38.p7	15:58830775	ATAGACCATGAAAGG[-/GACACTT]GTTTACAGTATGCGA	54629
rs753929105	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58850990	TTTTTGTTTTTTTTT[-/C]CACGACTGAGTCTTC	54629
rs753935871	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769301	TGGTGGCGTGCGCCT[A/G]TAGTCCCAGCTACTT	54629
rs753950388	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58832845	CTAGGATGACATCTA[A/G]TCATGGAAGTTTATA	54629
rs753975695	snp	A/G	1.68329e-05	0.00290106	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851817	AACAGCAGAGCCAAG[A/G]GATCAATTGGGAACA	54629
rs754030178	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842123	GCTCTTTTCCTATTA[C/T]GACTTCTTGATTGTC	54629
rs754094679	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855791	GCCTGGCATGGTGGT[A/G]CGTGCCTGTAGTCCC	54629
rs754110092	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58809574	CAGTTATTTTAGATT[C/G]ACCAGTAGGAGAGGC	54629
rs754112304	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58820537	ACTGATTGTTTACTC[A/T]ACCAATCATCAGTTC	54629
rs754213911	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58798292	CAGCTAATTTTTGTA[-/T]TTTTTTTTTTTTTTA	54629
rs754224353	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58816030	TCCCACTAGAATATA[C/G]GTTTTATAAGGGCTG	54629
rs754269053	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789890	GACCTCAGGTGATCC[A/G]CCCACCTGAGCCTCC	54629
rs754279247	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793751	GGATGTGGTTGCAGC[A/G]CGTCTCTTGAGTGCT	54629
rs754281791	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58773345	GAAAATCAAGTAAAG[G/T]GAATAGTGTTTATCA	54629
rs754358050	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58813250	CTGTAATCTCAGCAC[A/T]TTGGAAGGCTGAGGC	54629
rs754385615	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58801455	GAAAAAAGTATGTAC[A/G]TACAGTTAATACATA	54629
rs754387073	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58816559	TGCAGTTGTGCATCA[C/G]CATGCCCAGCTCACA	54629
rs754391768	snp	C/T	1.66382e-05	0.00288424	synonymous-codon, intron-variant	FAM63B	GRCh38.p7	15:58821797	TTGTAAACAGTCAGA[C/T]AATAGTGAGCTGGTT	54629
rs754400975	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58832414	GTGTATTTTTAGGAG[A/G]GATGGGGTTTCTCCA	54629
rs754415482	snp	G/T	1.84201e-05	0.00303475	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771958	ATTCTTTTCCCAGTA[G/T]CTGCGAGTTCAATAG	54629
rs754423089	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58844072	ATTAGAAGGAAGATT[C/T]GAGTCTTAAGAAAGC	54629
rs754453622	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58846597	AAGTGAGACTCCTCA[-/AA]AAAAAAAAAAAAAAA	54629
rs754466978	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58847093	TTGTTATAGTGTAGT[G/T]TGCCAATTATAAACT	54629
rs754484365	snp	C/T	5.36658e-05	0.00517977	intron-variant	FAM63B	GRCh38.p7	15:58821856	CTGACTTTTGAAATT[C/T]TTGGCAAGATAATTT	54629
rs754616116	snp	A/C/G	3.47049e-05	0.00416551	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772055	TCCTCTGTGCAAGGA[A/C/G]GAGGAGGGGGAGGAG	54629
rs754637869	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58794301	TTGGTAATAATGAAA[C/G]TGTATTACCATGGGA	54629
rs754654398	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58841457	GTTGCCCTTCCTGGA[C/G]TGCAATGGTGTGATC	54629
rs754660494	snp	A/C			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772262	AGCTTTCTACTTCCT[A/C]CAGCTTTTGGGGTGG	54629
rs754714189	snp	A/G	3.37268e-05	0.00410637	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851814	AAGAACAGCAGAGCC[A/G]AGAGATCAATTGGGA	54629
rs754722498	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58852455	TGTTTTCTCCTGAGG[C/T]TCTGATTTTCAAATT	54629
rs754735334	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860825	TCAGAATTTTTATTA[C/T]TGTTTTTCACATATG	54629
rs754766972	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837039	GAATAGAACCCCTAA[A/G]GGAATACTTTTAAAA	54629
rs754794164	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58854080	AACCCCGTCTCTACT[-/A]AAAAATACAAAAAGT	54629
rs754804718	snp	A/G	6.64055e-05	0.0057618	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787920	GGTGAAACTTCCACC[A/G]ATGATGGAAATCATA	54629
rs754837030	snp	A/G			missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851867	GATTTGGAACTAGCA[A/G]AGAAACTCCAAGAGG	54629
rs754857679	snp	A/T	0.000375164	0.0136909	intron-variant	FAM63B	GRCh38.p7	15:58796086	AGTGGTGAGTTGAAG[A/T]GTATCTGGGAGGCAA	54629
rs754859746	snp	C/T	1.82005e-05	0.00301661	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771623	CTCTCCTGAGGTTCC[C/T]GGACCCTGCAGCTCC	54629
rs754915126	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58805884	ATCGAGACCATGCTG[C/G]CTAACACAGTGAAAC	54629
rs754955755	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792531	GAATCGCTTGAACCC[A/G]GGAGGCGGACGTTGC	54629
rs754969558	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58807052	GAATTATTTCATAAA[A/G]CAGAACTTCATTTTT	54629
rs754987830	snp	A/G	1.81164e-05	0.00300963	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771693	CCTGCTGCCGCCGAG[A/G]CGCCTCTGAGAGGGC	54629
rs755003332	snp	A/G	1.65806e-05	0.00287924	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810262	GGCAATTTTGCACAA[A/G]CTACAGACAGGCCTG	54629
rs755007027	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58790187	TAGATGTCTGCAAAT[C/T]GCCTTAAAAAGAAAA	54629
rs755077307	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784471	GAGATACTTTGTTCA[A/G]ATTTTACGGAGAATA	54629
rs755092897	snp	A/T	3.81526e-05	0.00436748	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771807	CCGGATCTCGCCGGC[A/T]CCTGCCAAGCAGAAC	54629
rs755093667	in-del	-/TA			intron-variant	FAM63B	GRCh38.p7	15:58846197	ACATTTTAAAATAAC[-/TA]AAAGTATAATTGGAT	54629
rs755095723	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855866	CAGAGGTTGCAGTGA[A/G]CCGAGATCGCCCTGC	54629
rs755106100	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842130	TCCTATTATGACTTC[C/T]TGATTGTCCTTTTAC	54629
rs755146699	in-del	-/GAG			intron-variant	FAM63B	GRCh38.p7	15:58811599	CACAGAGCTCCTGAC[-/GAG]GAGATGTGACCTTCA	54629
rs755194048	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58840633	TATTTATTTACTTAT[C/T]ATTATTATTATTATT	54629
rs755213669	snp	C/T	1.9128e-05	0.00309251	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771848	CGGCTCCGAAGAGCC[C/T]AGCAGCGCCGGCGGC	54629
rs755238932	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58779249	AAGGGTGAACAGCAC[A/G]ATGGCAAAATGAACA	54629
rs755253019	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58775814	AAAATATAAATGTTC[A/G]TTATGCTGTTAGAAG	54629
rs755305136	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58778041	GTGTTTATGAAGTTA[A/G]GCCAGAAGGTATATA	54629
rs755308950	snp	A/G	1.67368e-05	0.00289277	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772095	GTGCTGGCGGCCTCC[A/G]AGGAACGCTTCCCGG	54629
rs755327834	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58818220	TGGCACCTTGCATGT[A/C]GTAGTATGTAATAGG	54629
rs755360096	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58833852	GTTCCTTCCTCTTTT[A/C]CTAATCTTCCTCAGC	54629
rs755375372	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58832437	TTTCTCCATGTTGGT[C/T]AGGCTGGTGTCAAAC	54629
rs755381158	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58809372	CAGCATGATGTCCTC[-/A]AGGTTCATCTGGTTG	54629
rs755416711	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58802808	AGGACAAGTTTTGCT[A/G]TTTGATAGTTTCAGT	54629
rs755437672	snp	A/G	4.44336e-05	0.00471326	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771419	CAGCCCCGAGAGCCT[A/G]CAGCCGCTAGAACAC	54629
rs755443929	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58848406	CAACTCATGTTATAT[A/G]TTCTATAATGGCAAT	54629
rs755466687	snp	G/T	1.67837e-05	0.00289682	stop-gained, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851911	GGCTTCTCAATACTA[G/T]CAGGAACAGGAACAA	54629
rs755493233	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58798189	TGGTGCGATCTTGGC[G/T]CATTGCAACCTCCGC	54629
rs755510792	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58796465	TTTGAATTTACTGTA[A/G]TAGGATGCTTAATCT	54629
rs755552301	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58821223	ACTCATATCTCCACT[A/G]TACTTTTCTAGGAAA	54629
rs755553313	in-del	-/GTTT			intron-variant	FAM63B	GRCh38.p7	15:58773701	ATCTTTTTTTTTTTC[-/GTTT]GTTTGTTTGTTTTAA	54629
rs755573819	in-del	-/CTCCTC	1.80822e-05	0.00300679	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771635	TCCCGGACCCTGCAG[-/CTCCTC]CGCGGGTTTGGACTT	54629
rs755580203	snp	C/T			upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58771014	GAGTTCAACTTCCGG[C/T]CACATAGTGAGAGGA	54629
rs755581774	in-del	-/TCTA	1.68705e-05	0.0029043	intron-variant	FAM63B	GRCh38.p7	15:58831743	TTTTGAAATTATTCT[-/TCTA]TCTATCTAATGTTAT	54629
rs755598950	in-del	-/G	1.93373e-05	0.00310939	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771880	TCAGCAGCAGTTGCA[-/G]CGACCCGAGCCCTCC	54629
rs755605677	snp	C/T	5.27904e-05	0.00513736	intron-variant	FAM63B	GRCh38.p7	15:58847252	ATTATATTACTAGTT[C/T]TGATCAATTTAACAG	54629
rs755620613	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58824027	ACTTGAAGGAACAAT[A/G]GGATTCAGAAAGTGG	54629
rs755660637	snp	C/T	3.33812e-05	0.00408528	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772103	GGCCTCCAAGGAACG[C/T]TTCCCGGGACAATCT	54629
rs755726428	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58836988	ACAGATTACCTGATT[C/T]ACAACAGAATCTATA	54629
rs755727723	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811299	TAACTGTACATTTCT[A/G]AATGTACATTGACCT	54629
rs755741260	snp	A/G	1.90874e-05	0.00308923	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771438	CCGCTAGAACACGGG[A/G]TGGCGGCCGGGCCAG	54629
rs755781535	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58819359	AGGCTGAGGTGGAAG[A/G]ATTGCTTGAGCCTGG	54629
rs755785268	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58793369	AGGAGGAGAATCGCT[G/T]GAACCCAGCAGTCGG	54629
rs755785293	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58780499	AGAGCTCTCACTCAG[A/G]ATGTTTGATTGGGAA	54629
rs755806656	snp	A/G	1.89593e-05	0.00307885	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802367	AAATTCAACGTTTAA[A/G]TTATGAACAGGTAAT	54629
rs755884612	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58836098	TGTATTTTTAGTAGA[C/G]ACAGGGTTTCGCTGT	54629
rs755898513	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849715	GAGATAGTCATGCTA[C/T]ATATATGACAAGATC	54629
rs755912172	snp	C/G	3.62739e-05	0.0042586	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771699	GCCGCCGAGGCGCCT[C/G]TGAGAGGGCAGTACA	54629
rs755930073	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58805722	GCAAAATACTTACCC[A/G]AGAGTTTAAAACCCT	54629
rs755936811	in-del	-/AT			intron-variant	FAM63B	GRCh38.p7	15:58782281	TACATATATACACAC[-/AT]GTGTATATACACTGC	54629
rs755999458	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58830317	ACACACCTTATTTAA[C/T]ATATACTGTTGATTC	54629
rs756016282	snp	C/G	1.84103e-05	0.00303394	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771747	GAGACAGCCGTGGCC[C/G]GAGTGGGTCATGAGT	54629
rs756041973	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58814911	GCCTCTCAGAGTGCC[A/G]AGGTTACAAATGTGA	54629
rs756047364	snp	C/T	1.67049e-05	0.00289002	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831881	CTTTGTGTGTTCTTT[C/T]GGAATAATCATTTTA	54629
rs756086188	snp	A/G	5.77417e-05	0.00537285	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771859	AGCCCAGCAGCGCCG[A/G]CGGCCTCAGCAGCAG	54629
rs756093635	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58804595	GGCGGATTGCTTGAG[C/T]CCAGTAGTGAGACCA	54629
rs756202324	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58795306	AGTGTTTCAACTTTC[C/T]TTTCGTTATTGCCAT	54629
rs756292579	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58818081	AACATCTGCATACCA[C/G]TATATACAACAACCT	54629
rs756305846	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58791480	AAATTAGCCAGGCGT[A/G]ATGGTGTGCACCTGT	54629
rs756336896	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776722	ACAGAGACAAGGTCA[C/T]GTTAAGATAGAGAGG	54629
rs756359477	snp	C/G	1.70638e-05	0.00292089	intron-variant	FAM63B	GRCh38.p7	15:58847489	AATTTGTATTGTCGT[C/G]TTTATAGTGGTTAAA	54629
rs756392145	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58818515	CCCTGCTAGCCTCCT[-/A]AAAGTGCTGGGATTA	54629
rs756395413	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58815826	CTGGGACTATAGGCG[C/T]GCACCAGCATGCCCA	54629
rs756401978	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58793485	ATAAATTTAAAAAAT[A/C]AAATTAGATTATGAT	54629
rs756456185	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58830777	AGACCATGAAAGGGA[C/T]ACTTGTTTACAGTAT	54629
rs756496390	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58846929	TAATTGGAAAAAAAA[A/T]CAGGCAACATGGTAT	54629
rs756510991	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58845674	GTAGAGCTGTTATAC[A/G]ATCCGGCAATCCCAC	54629
rs756538849	snp	A/T	1.67262e-05	0.00289185	intron-variant	FAM63B	GRCh38.p7	15:58854431	TAGATAACCATGAGT[A/T]AGTCCCTCAGAATAG	54629
rs756547153	snp	C/T	1.65721e-05	0.0028785	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810275	AAACTACAGACAGGC[C/T]TGGATGTAAATGTAA	54629
rs756609224	snp	A/G	1.85561e-05	0.00304594	intron-variant	FAM63B	GRCh38.p7	15:58810416	ATTTAAATTATGTAA[A/G]CACAAATACAGGAAA	54629
rs756628298	in-del	-/TGTGTA			intron-variant	FAM63B	GRCh38.p7	15:58831038	GTGTGTGTGTGTGTG[-/TGTGTA]TATATATATATATAT	54629
rs756642962	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58799682	GAAATGGGAATTTTG[A/C]TTGGCAAAGGTTAGA	54629
rs756643082	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58812114	TTTTTATTTTGAGGT[A/C]ATTATAGATTCACAT	54629
rs756657053	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58836341	TCTAGTCCATATTCA[A/C]ATTTGCCACTTGTCC	54629
rs756676322	in-del	-/TT			intron-variant	FAM63B	GRCh38.p7	15:58807353	CATTTTAAAATAGTC[-/TT]TTTTTTTTTTTTTTT	54629
rs756713696	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58774220	GGGCGCGGTGGCTCA[C/T]GCCTGTATTCCCAGC	54629
rs756774934	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58776413	GAATATTAAGGGTGA[C/G]AGAGTGAAAAACCAG	54629
rs756779460	snp	C/T	1.68352e-05	0.00290126	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772243	CCTGGAAGGTACATT[C/T]TGCAGCTTTCTACTT	54629
rs756805124	snp	A/G	9.16515e-05	0.00676885	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771546	GCGGAGACCAGCGGC[A/G]GGAATGGGCTGGGGG	54629
rs756823679	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792306	AACGTATGTCCATAC[A/G]GCTTGTATAAAAATG	54629
rs756855108	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58779592	GAGCCAAAGGTTCCA[A/T]CTTAGCCTCTGCCCA	54629
rs756867485	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58821195	CTTCAGGAAAATAAC[A/T]TTAGTTATCTCTACT	54629
rs756877016	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58804564	TGTAATCCCAGCACT[C/T]TGGGAGGCCAAAGCA	54629
rs756900375	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58834057	TGGTGATGACTCTTA[A/T]CTAGCATGCTGCCTT	54629
rs756929862	snp	A/C	1.83256e-05	0.00302696	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771608	GGCTTCTCCCGCGGG[A/C]TCTCCTGAGGTTCCC	54629
rs756944603	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58790258	TTATTATTTTAAGTT[G/T]TTTTTTCCCCATGGG	54629
rs756945687	snp	A/C/G	0.000307101	0.0123881	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771801	GCCCGCCCGGATCTC[A/C/G]CCGGCACCTGCCAAG	54629
rs756954662	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58798727	TCCCAAAGTGCTGGG[A/G]TTACAGACGTCAGCC	54629
rs756973050	in-del	-/TT	3.88576e-05	0.00440764	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831948	GCTATTTAATCGTGA[-/TT]CTAAATCAAAGGAGC	54629
rs757027625	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58848674	TGGCATGAACCAAGG[A/T]GGCAGAGCTTGCAGC	54629
rs757045521	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58773686	ATGGGTCTTGAACCA[A/G]TCTTTTTTTTTTTCG	54629
rs757064499	in-del	-/GGGA			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769914	GAATCGCTTGAACCC[-/GGGA]GGCGGAGGTTGCAGT	54629
rs757094928	snp	A/C	3.48056e-05	0.00417152	intron-variant	FAM63B	GRCh38.p7	15:58847266	TTTGATCAATTTAAC[A/C]GTCCTTTTTCTTTTG	54629
rs757174687	in-del	-/AAAG			intron-variant	FAM63B	GRCh38.p7	15:58844946	AAAAAAAAAAAAATG[-/AAAG]GACAACCCACAAAAT	54629
rs757197606	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58813479	CCAGCCTGGGTGATG[A/G]AGCAAGACTCTATCT	54629
rs757220789	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58841925	TATTATACATATGAT[C/G]ATGACTGTTGGATTC	54629
rs757223495	snp	C/G	1.65825e-05	0.00287941	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847333	ACGGACCAGGGGTTT[C/G]TTACTGAAGAGAAAG	54629
rs757227051	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58783201	GCTGGGATTACAGGA[A/G]TGACCGACTCTGCCC	54629
rs757248590	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58851589	GACTATAGGTGCACA[A/C]CACCACACCTGGCTG	54629
rs757258952	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58776555	AGCAGCATCAGAGAG[C/G]TAATAGAGTAGGGAA	54629
rs757277240	snp	A/C	1.72883e-05	0.00294004	intron-variant	FAM63B	GRCh38.p7	15:58847504	CTTTATAGTGGTTAA[A/C]ATGCTGATTTTTTTC	54629
rs757378124	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58830623	AAACCTATCTAGCAC[A/T]TGTATTTTCTCTATA	54629
rs757384574	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58853091	CCAAGTAGCTGGGAT[C/T]ACAGGTGTGTGCCAC	54629
rs757421554	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58818048	TATTCTATGGAATAC[C/T]GTACTACAGTGAAAA	54629
rs757429402	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817283	AGATAGCCCAGCCAA[A/G]AAAAGGAGCAAATGA	54629
rs757452700	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58786746	CAGAATCCCCTTAAA[A/C]GCCCCTTTCCAACTA	54629
rs757475783	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58807442	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTTACG	54629
rs757489597	snp	A/C/G			intron-variant	FAM63B	GRCh38.p7	15:58787630	TAGTCCCAGCTACTC[A/C/G]GAAGGCTGAGGCAGG	54629
rs757504122	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58775631	GATGACTTCTCCCAA[C/T]GATGACTATAAGAAG	54629
rs757681012	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58780426	AAAAGAAAGAAAATT[A/G]AAGTGCATAAAGTTT	54629
rs757685585	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58829631	TATGGAAGGGGCTTT[C/T]AAAAACATCTTTCTG	54629
rs757705930	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58798558	CCTCCTGGGTTCAAG[C/T]GATTATCTCACCTCA	54629
rs757706594	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858996	GCATAGTATAAGCAC[A/G]AAGTATGACTTAATT	54629
rs757733869	snp	G/T	1.92847e-05	0.00310516	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771875	CGGCCTCAGCAGCAG[G/T]TGCAGCGACCCGAGC	54629
rs757734537	snp	A/G			upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58770993	GCACACAAGGGAGCT[A/G]CCCGGGAGTTCAACT	54629
rs757746031	snp	G/T	1.67998e-05	0.00289821	intron-variant	FAM63B	GRCh38.p7	15:58821822	CTGGTTAGTGAAGGT[G/T]GGTGAGTGCTGCTAT	54629
rs757784143	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58811225	GCATAGCTTTGAAAA[G/T]AGATTTTGTATTACC	54629
rs757787184	in-del	-/AGTG			intron-variant	FAM63B	GRCh38.p7	15:58790586	TTGACAATAGACCTT[-/AGTG]GGGGGTAAGACAAGT	54629
rs757872676	snp	C/T	5.52501e-05	0.00525567	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771959	TTCTTTTCCCAGTAG[C/T]TGCGAGTTCAATAGT	54629
rs757892501	snp	A/G	8.30875e-05	0.00644491	missense, nc-transcript-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854546	ATAGTGAACGTAAAC[A/G]GAAGGAACCACGAGA	54629
rs757910331	snp	A/G	1.80127e-05	0.003001	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771672	AAGGACAGTGGTTTG[A/G]AGAGTCCTGCTGCCG	54629
rs757994545	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58789196	ACAAAAAATTAGCTG[C/G]GCATGGTGGCAGACG	54629
rs758021886	in-del	-/AG			intron-variant	FAM63B	GRCh38.p7	15:58782943	TTTTTTTTTTGAGAC[-/AG]AGTCTTGCTCTGTCA	54629
rs758057812	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58801268	CATGAGCCATCATGC[C/G]CAGCCCAGTTTAGCT	54629
rs758062893	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58847149	GAAGTAAAATATCTA[C/T]TTGGTCTATTTATTG	54629
rs758072147	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58802872	TGTTCTGCAATGTAG[A/G]AGGTATCACTAGGCT	54629
rs758112793	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58773635	GGGGACATTTTCCTT[C/T]GGTATGGCGTAGTCC	54629
rs758147973	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58824529	TTTGTTCATAAGTAA[C/G]TACAAATTTGTAGTT	54629
rs758267212	snp	A/C/T	4.96975e-05	0.00498465	missense, synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847371	GGAAAGCCTACACAA[A/C/T]GTAGATGGTGATGGA	54629
rs758280065	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58849210	GCAAGAGTCTGTCTC[-/A]AAAAAAAAAAGGCTG	54629
rs758298665	snp	A/T	5.52888e-05	0.00525751	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771551	GACCAGCGGCGGGAA[A/T]GGGCTGGGGGCGGCG	54629
rs758318042	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58787757	AAAAAAAAAAAAAGC[C/T]TGGCTATAAAGATTC	54629
rs758320665	snp	A/G	1.67458e-05	0.00289355	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847470	AGATCAGATAGATCA[A/G]GTAAATTTGTATTGT	54629
rs758343561	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58774685	AAGACTTCATAGAAG[A/G]GATAACCTGTGAACT	54629
rs758395335	snp	A/T	6.64938e-05	0.00576563	splice-acceptor-variant	FAM63B	GRCh38.p7	15:58787904	AATATTTTGTTTTTC[A/T]GGTGAAACTTCCACC	54629
rs758397304	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58829435	AGTTTGATGTCCTTG[A/G]GCAAGTCACTTATTC	54629
rs758404425	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58811286	ATATCCATCACTCTA[A/C]CTGTACATTTCTAAA	54629
rs758410156	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58786421	ATCCTGGAATGTGCT[C/T]GTCACTGTCAGCTAA	54629
rs758433626	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58810718	GTGACTAACAGGACT[-/C]CCTGAAACCTATTAT	54629
rs758437312	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849080	CCAGGTGTGGTGGTG[C/T]GCACCTGTAACCCCA	54629
rs758468140	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58846092	TGGTTAATGGATGTT[-/AA]AAAAAAAAAAAAAAA	54629
rs758469829	snp	C/G	1.67604e-05	0.00289481	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851903	GACAGACGGGCTTCT[C/G]AATACTATCAGGAAC	54629
rs758471510	snp	G/T	4.85343e-05	0.00492593	intron-variant	FAM63B	GRCh38.p7	15:58802288	TTTAAAAGGCAATTT[G/T]ACAATTCTTTTTTTT	54629
rs758542697	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58830547	ATCCACACCCAAAAC[C/G]CTTCTGATCTCAAGC	54629
rs758595500	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58797911	TGCAAAAATAAAGCC[A/G]TCACAAAATTGTAAT	54629
rs758648556	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58799231	AGATGTTCTGTTGAG[A/G]TTACTCCATTTCTCT	54629
rs758654520	snp	A/C	1.66131e-05	0.00288206	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810245	AATATGAGTGATGCC[A/C]TGGCAATTTTGCACA	54629
rs758690068	snp	C/G			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770914	CGAGGGTGGGCCACA[C/G]GCGACCCAGCGCTAA	54629
rs758728476	snp	G/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856269	TGGAGAGTGTTTTTT[G/T]TGTGTGTGGTCTGGG	54629
rs758780006	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58780323	GCAGGAGAATCACTT[G/T]AACCTGGGAGGGAGG	54629
rs758780205	snp	A/G	1.65822e-05	0.00287938	synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831832	GACATACCATGGATT[A/G]TGTGAACTAACTTCA	54629
rs758789078	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58819450	GAGACCCAGATCACA[C/G]CACTGCACTCCAGCG	54629
rs758817564	in-del	-/AAA			intron-variant	FAM63B	GRCh38.p7	15:58800835	GTAAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA	54629
rs758826908	snp	A/G	1.83162e-05	0.00302618	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771973	GCTGCGAGTTCAATA[A/G]TGAGGAGGGAGCGGA	54629
rs758840375	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58809755	CCAATAGAATGTTAG[C/T]TGCATAAGAGCATGG	54629
rs758864141	snp	A/G/T	0.000123991	0.00787289	intron-variant	FAM63B	GRCh38.p7	15:58810396	ACCCTCAGGTAAGTC[A/G/T]AAGAATTTAAATTAT	54629
rs758864254	in-del	-/TGT/TGTT			intron-variant	FAM63B	GRCh38.p7	15:58794395	GTGTGTGTGTGTGTG[-/TGT/TGTT]TTTTAAGAATAAAAT	54629
rs758916717	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58783931	AGCCTGGACGATAGA[A/C]TAATTGGGCTAAATT	54629
rs758952437	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58778177	GCCAACATACATACA[A/G]AAAACTTACATGTAA	54629
rs758990549	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58795949	AGTCAAGAGAGGGTG[A/G]AGATTGTTAGAAGAA	54629
rs759009713	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58779345	TGAGGCACCATGAAG[A/G]TGAGCCTCTTGCCAG	54629
rs759046395	snp	A/G/T	7.34033e-05	0.00605783	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771741	TCCCCGGAGACAGCC[A/G/T]TGGCCGGAGTGGGTC	54629
rs759110636	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58827373	TTCCTTCTGTTTATT[A/C]GTTGTTATTCTTCTG	54629
rs759145993	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58796273	AAGGTTGTTTGAGGG[C/T]TAGTTGGAAACTATC	54629
rs759153259	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58840135	CACGCGTTTGGCCTC[A/G]ATTTTATCTTTACAT	54629
rs759171383	snp	G/T	7.55373e-05	0.00614515	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771780	GGTACCGCCGGAGAC[G/T]CGGGAGCCCGCCCGG	54629
rs759196489	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58841595	CTTTTAGTAGAGACA[C/T]AGTTTCACCATGTTC	54629
rs759214857	snp	G/T	3.52367e-05	0.00419727	intron-variant	FAM63B	GRCh38.p7	15:58847249	AATATTATATTACTA[G/T]TTTTGATCAATTTAA	54629
rs759248866	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58832589	GGCTGGAGTACAATG[C/G]CGTGATTTCAGTTCA	54629
rs759299232	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58808758	TACAGGTGCCCACCA[C/T]CATGCCCGACTAATT	54629
rs759309948	snp	A/C	6.79625e-05	0.00582895	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772077	GGGGAGGAGACCGCT[A/C]AGGTGCTGGCGGCCT	54629
rs759328410	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58777274	TGGGGTATAGGGGCA[C/G]AGAATTAGAGAATTG	54629
rs759357119	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58796500	AGTTTCCTAAATGGG[-/A]ATAATAACAAGTTAA	54629
rs759386546	snp	C/T	5.68618e-05	0.00533176	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771362	GCGGAGAAGTGGCCG[C/T]GGTCTCCATAGAGCT	54629
rs759412691	snp	A/G	1.74595e-05	0.00295456	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851965	TTCTACACAGGCTCA[A/G]GTAAAAACTAGTGTT	54629
rs759413882	snp	C/G	1.67307e-05	0.00289224	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851887	ACTCCAAGAGGAAGA[C/G]GACAGACGGGCTTCT	54629
rs759420356	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58854167	CAGAATCTCTTGAAC[A/C]CAGGAAGTGGAGGTT	54629
rs759435128	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58776417	ATTAAGGGTGAGAGA[C/G]TGAAAAACCAGCATG	54629
rs759459794	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58787319	CTTCTTAATAGTTTT[A/G]TCTCCTATGTGTGCA	54629
rs759460498	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58808128	TTTCTATATACCTCC[C/T]GTTCCTCCTAACCCC	54629
rs759462020	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58802162	TAGGAAAAGTTAACA[C/T]TGATTTTCTCTGGGT	54629
rs759462453	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58818577	GAAATACTAATGTAC[A/G]GATTCTGTCTATGAA	54629
rs759513186	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58788626	CATCACATTGTGGCC[G/T]TTTATAATCTGACAA	54629
rs759518456	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58833311	ATACACACACTATAC[C/T]TTCTAATTTCTGCAC	54629
rs759541005	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771339	TCATGGCGTCCAAGG[C/T]GCTGGCTGCGGAGAA	54629
rs759566999	snp	A/G	1.85644e-05	0.00304661	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802354	AAAGAAATTTCAGAA[A/G]TTCAACGTTTAAATT	54629
rs759571775	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58799760	AGAGCAGAGCCAGAC[A/T]TGGACATGGCTTTTT	54629
rs759578063	snp	A/G			utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854630	TGTTGGCTTCTGTTG[A/G]AACCACCTATATGTC	54629
rs759581881	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859691	ATGCAGGACTCTGGT[A/G]AATTTAACTTACTTT	54629
rs759588488	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58776559	CATCAGAGAGCTAAT[-/A]AGAGTAGGGAAGATT	54629
rs759616267	snp	A/C			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770828	GAGAAACCAAGTCCC[A/C]TGAGCCCTTCAGGGA	54629
rs759644795	snp	A/C	1.65791e-05	0.00287911	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854521	CCATCAAGTGGAAGA[A/C]AATCTGGGAATAGTG	54629
rs759655388	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858362	TTGATCTTGGCTTAA[C/T]TAAGCAAGTTAGTAT	54629
rs759696760	snp	A/C	1.6617e-05	0.00288239	synonymous-codon, intron-variant	FAM63B	GRCh38.p7	15:58821776	ACTAGTGGAGAAGAT[A/C]ATCTCTTGTAAACAG	54629
rs759709197	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58820564	GTTCCAGTTGTATGA[A/G]TTAAGAGGCTTTTAG	54629
rs759712563	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58824551	TTTGTAGTTCATTTG[-/A]AATAATTACTTAACT	54629
rs759724704	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58840331	TGTTGGAAAGTCCTC[-/T]TTATCATTCCTAGTT	54629
rs759737011	in-del	-/TAAGGTGAA			intron-variant	FAM63B	GRCh38.p7	15:58780750	GTCTCTTTGGGGCAC[-/TAAGGTGAA]TAAGGTGAATCAGCT	54629
rs759802427	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849395	CTGTAGTCTCAGCTA[C/T]TCGGGAGACTGAGGC	54629
rs759821206	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58791997	ATGAAGAAATGTTTC[A/G]AGGAAGAGTGAGAGA	54629
rs759833970	snp	G/T	5.03664e-05	0.00501803	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847297	TTACTTCTTATTAAG[G/T]GTCAACTGTATTTGT	54629
rs759862181	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58834913	TTTAGCTAGATGTAT[A/G]TCAGATGTGGGCCCA	54629
rs759880630	snp	G/T	1.67407e-05	0.00289311	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772215	CTGGCCATCCTCAAT[G/T]TTTTGCTCCTGGCCT	54629
rs759902143	in-del	-/A	1.65791e-05	0.00287911	frameshift-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854521	CATCAAGTGGAAGAC[-/A]AATCTGGGAATAGTG	54629
rs759914591	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58789969	ATTTTTGTAGAGATT[C/G]GGTTTCACTGTGTTT	54629
rs759937759	snp	A/G	1.80945e-05	0.00300781	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771504	GAGACCAGGCTCGCC[A/G]CTGGTGATGGTCCTG	54629
rs759958688	snp	A/G	3.31461e-05	0.00407086	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847415	CAGAATTTCATCTTC[A/G]ACCTCCTTCAGATCC	54629
rs760041782	snp	C/G	1.90047e-05	0.00308253	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771838	TGACCGCCGCCGGCT[C/G]CGAAGAGCCCAGCAG	54629
rs760065481	snp	C/G	1.85579e-05	0.00304608	intron-variant	FAM63B	GRCh38.p7	15:58787864	AAATACTTTAGTCAC[C/G]TAAAACATTTAATTT	54629
rs760087666	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58774312	ACATGGTGAAACCCC[A/G]TCTCTACTAAACATA	54629
rs760111861	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58794127	CGGTGGGGGAGGAGG[A/G]GAGGAATCTAAGGTA	54629
rs760218290	snp	A/G	1.66214e-05	0.00288278	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847318	CTGTATTTGTTGGTA[A/G]CGGACCAGGGGTTTC	54629
rs760297702	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58777115	TAGCATGAATAAATT[A/G]AGGTTTTCTTTAAAA	54629
rs760346781	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58834452	AACCCAAATTGTATG[C/G]TAAAACTGTATGGGA	54629
rs760353615	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806659	GCCATTAGAAATCAT[A/G]TTGCCCCTAAAGGAA	54629
rs760372162	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776228	GAGAGTAGTGAGCAA[C/T]AGTTCTCAACTTTTC	54629
rs760378669	in-del	-/GT/TA			intron-variant	FAM63B	GRCh38.p7	15:58794359	AAGTTTTTTTTGGGG[-/GT/TA]TGTGTGTGTGTGTGT	54629
rs760394970	in-del	-/CCTAT			intron-variant	FAM63B	GRCh38.p7	15:58844004	TTTAATGCATTAAAA[-/CCTAT]TCTATATTATTATTT	54629
rs760432142	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58798421	TGAGCCACCACACCC[-/A]GACCTTTTCTTGCCT	54629
rs760462325	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58787053	TAGGCTGGTCTCGAA[C/T]TCCCAACCTCACGTG	54629
rs760472985	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58786466	TTGACTGTAATATCC[A/G]TGTCATTCATTTGAC	54629
rs760478601	snp	A/G	7.21774e-05	0.00600695	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771476	GACAGGTTCTTCGCA[A/G]GAAGGGCTACAGGAG	54629
rs760560185	snp	G/T	1.68312e-05	0.00290092	intron-variant	FAM63B	GRCh38.p7	15:58810219	AGAACTTTCCCCTTT[G/T]CTATTTTCAGAATAT	54629
rs760586675	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58817085	AAACAAGATACAAAC[C/G]TATTAACTGTAAGGA	54629
rs760614335	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58791777	CAGTACAAGTCTAGC[C/G]TGTAAATATATATTT	54629
rs760617703	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58831190	GATTAGCATAAAAAT[A/G]GCATAAAAAACCATT	54629
rs760627000	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58800241	TAGTAGCAAGGTTTT[A/C]TTAATTCTTTCCTTG	54629
rs760644816	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58816223	TGGGATTCAGGAGAA[C/T]GGAAGGATGGCTTAC	54629
rs760655848	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859756	TTACTTAATCCTGGT[A/G]TTTTTGCTCTTAGAT	54629
rs760687084	snp	G/T	0.000399555	0.0141286	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771790	GAGACGCGGGAGCCC[G/T]CCCGGATCTCGCCGG	54629
rs760706342	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58830406	CCAAAATCCAAAATG[C/G]TCCAAAATCTAAACA	54629
rs760722573	snp	C/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772659	GTTTTCATGGTTATA[C/T]TTAGTTTGATTTCCA	54629
rs760749070	snp	A/T	1.66252e-05	0.00288311	missense, intron-variant	FAM63B	GRCh38.p7	15:58821790	TCATCTCTTGTAAAC[A/T]GTCAGACAATAGTGA	54629
rs760789538	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58820307	AAATTAGTCAGGTGT[A/G]GTGGCGGGCGCCTGT	54629
rs760849673	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58833693	GAGCAGTATTGCTGC[C/T]AGCATGTCCCATCTT	54629
rs760901153	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58819117	GAATAGCTGGGACTA[G/T]GGACGTGCACCACCA	54629
rs760967304	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58843790	AGTGAGCCAAGTCAC[A/G]CCACTGCACTCCAGC	54629
rs760974401	snp	C/T	1.81381e-05	0.00301143	intron-variant	FAM63B	GRCh38.p7	15:58787877	ACCTAAAACATTTAA[C/T]TTTATAGAAATAATA	54629
rs760993871	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58848010	CAAGGTAAGGAGGAG[G/T]AGTAGACATTTGTAG	54629
rs761005515	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58781169	ATTCTCCTGCCTCAG[C/T]ATCCCAAGTACCTGA	54629
rs761010643	in-del	-/AA			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858060	AAGAATTCAGAACTT[-/AA]CAATTTAAGAATCAC	54629
rs761014613	snp	C/T	1.83785e-05	0.00303132	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771601	CGGACTCGGCTTCTC[C/T]CGCGGGCTCTCCTGA	54629
rs761053943	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58840687	TTTGAGATGGAGTCT[G/T]TCTCTGTCACCCAGG	54629
rs761094058	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58827082	TGGCAGGGATGCTAC[A/G]TAGGTGACATTGTGT	54629
rs761097048	snp	C/T	1.66062e-05	0.00288146	intron-variant	FAM63B	GRCh38.p7	15:58787979	GTTAGTGTTGAAAAG[C/T]GGATTTTATATCTCT	54629
rs761147403	in-del	-/A	1.74576e-05	0.00295441	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854654	TATGTCTTGAGAAAC[-/A]AAAACCACAGGAGGA	54629
rs761158466	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58795940	GTAGAATGAAGTCAA[A/G]AGAGGGTGAAGATTG	54629
rs761158580	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58782479	ATTTTCTTCTACAAA[C/G]TTAATCTTCACTTGC	54629
rs761199933	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58825818	ACCATGTTGCCCAGG[C/G]TGGTCTCAAACTCCT	54629
rs761213511	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58783780	AAAACCCCATCTGTA[C/T]AAAAAATACAAAAAA	54629
rs761245615	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58828544	AGTAACAGAGGAAAA[C/T]AGTTTAATGAACTAA	54629
rs761270122	snp	A/G	1.74227e-05	0.00295145	intron-variant	FAM63B	GRCh38.p7	15:58787883	AACATTTAATTTTAT[A/G]GAAATAATATTTTGT	54629
rs761323255	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58830246	TTAAGGAGCATTTGG[C/T]AACATTTTCATCAGC	54629
rs761326236	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58803615	TGAGGCCAGGAGTTC[A/G]AGACCAGCTGTTCAA	54629
rs761373359	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58806628	AAATATATGAAGGTA[C/T]AAGCATGAGCCCAGA	54629
rs761380349	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58816816	CTGTAAAAGCCAGGT[A/G]AGGTGGCATCCCTGT	54629
rs761426876	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58852125	AACCCTATCTCTATT[A/T]AAAATACAAAATTAG	54629
rs761428842	snp	A/G	1.9693e-05	0.00313785	intron-variant	FAM63B	GRCh38.p7	15:58851766	GTTATAATTTAATTT[A/G]TTAGGATTATCTTAT	54629
rs761448754	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836920	CCACTACACCCAGAC[A/G]TGAGTGCATTCTTTA	54629
rs761481794	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58815917	TCTCTTGACCTCGTG[A/T]TCCGTCTGCCTCGGC	54629
rs761592649	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58791702	GGAACTGAATTTTTA[A/G]TTTTATATAATATAA	54629
rs761597359	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58775133	CTCTTACAAGTGTCC[A/G]TGGAGTTTTTCAGGC	54629
rs761597400	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58787004	CCAGCTAATTTTTGT[A/G]GTTTTAGTAGAGGCA	54629
rs761612772	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58798920	TGGTATGTTAAATTT[A/G]TCTAACTCTTAGCTA	54629
rs761652425	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58780067	TAAGTTTCTCAACCA[C/T]ATCATGAAATCCTTA	54629
rs761667345	snp	G/T	1.66291e-05	0.00288345	missense, intron-variant	FAM63B	GRCh38.p7	15:58821753	GTTGGTAACTGCAGC[G/T]ACAACCAACTAGTGG	54629
rs761686826	snp	A/G	6.69456e-05	0.00578518	intron-variant	FAM63B	GRCh38.p7	15:58831751	ATTATTCTTCTATCT[A/G]ATGTTATGCATTGGT	54629
rs761687462	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58843237	TCACTGGATCCTCTA[G/T]CTCTTGGGTTCAAGC	54629
rs761689194	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58797725	TTTACCTAACCTCTT[A/C]CCTGCTCGTTATCAC	54629
rs761710811	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58829103	ACAAATAAATAAACT[G/T]CTGTGTAACACTTAC	54629
rs761735588	snp	A/G	1.90583e-05	0.00308688	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771843	GCCGCCGGCTCCGAA[A/G]AGCCCAGCAGCGCCG	54629
rs761744971	in-del	-/CT			intron-variant	FAM63B	GRCh38.p7	15:58833054	ACATTTACTGTTTTA[-/CT]CTTTTTATCTCTTAT	54629
rs761750460	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58773045	TGTCTCATTTAAGCT[C/T]GCAGTGTTAGGGTGC	54629
rs761772241	in-del	-/AAAAAAAAAA			intron-variant	FAM63B	GRCh38.p7	15:58853820	AGACTCCATCTCAAT[-/AAAAAAAAAA]AAAAAAAAAAAAAGT	54629
rs761775293	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857750	TTAAACATTTTTGTT[C/T]TTATCATTTATAGCC	54629
rs761782013	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58837585	ACAAACTATGGCTAT[C/T]TTTAAATCTACATTA	54629
rs761790179	snp	C/T			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770761	GAGTAGATATGCCTG[C/T]TTTAAAATCTGCATC	54629
rs761816910	in-del	-/A			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860393	CTGGCCAACATGGTG[-/A]AACCCTGTCTCTACT	54629
rs761904921	in-del	-/TTG	2.38535e-05	0.00345343	intron-variant	FAM63B	GRCh38.p7	15:58802292	AAGGCAATTTTACAA[-/TTG]TTCTTTTTTTTTTTT	54629
rs761926720	snp	C/G	3.52088e-05	0.00419561	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772038	GTGTTGCCCGGGGCT[C/G]TTCCTCTGTGCAAGG	54629
rs761928488	snp	A/G/T	5.62554e-05	0.00530331	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831936	GATATAGAAATAGCT[A/G/T]TTTAATCGTGATTCT	54629
rs761934930	in-del	-/GATC			intron-variant	FAM63B	GRCh38.p7	15:58799360	ATCACGAGGTCGGGA[-/GATC]GAGACCATCCTGGCT	54629
rs761982196	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58846783	AATTGTGTTGTATCT[A/T]TTATTGGTATACAAA	54629
rs762018576	in-del	-/ATT			intron-variant	FAM63B	GRCh38.p7	15:58851396	TTTTATTTTATTTTA[-/ATT]ATTTTGTTATTTTAT	54629
rs762080724	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58820887	GTAATTCTAAAATTT[G/T]TATTTGTTTTATTAG	54629
rs762106717	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812927	TTAACACAAGAATCC[C/T]GCCTGATGCCCTTTT	54629
rs762161171	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58844562	GAGACTCCGTCTCAA[-/AA]AAAAAAAAAAAAAAA	54629
rs762168180	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58845950	AAGCCAGGCACAGAA[A/C]GACACACTTCGCATG	54629
rs762224127	snp	C/G	1.8265e-05	0.00302195	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771729	AAGGTGACCGCCTCC[C/G]CGGAGACAGCCGTGG	54629
rs762240794	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58839656	GCTTTTTGGTGATCC[G/T]CTATACACCAAAGTG	54629
rs762279014	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58807804	CTCCTACAACTTTTC[A/C]CTTTTATTTTGTCCC	54629
rs762283264	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58793304	AAAAATACAAAAAAT[C/T]AGTCGGGTGTGGTGG	54629
rs762308474	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58774395	AGGTTGAGGCAGGAG[A/T]ATCTCTTGAACCCAG	54629
rs762337201	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58825305	TTGATTCTAATGCCT[C/T]ATAAGTAAAGGTGCA	54629
rs762337505	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811847	TAATTCTACTGTAAC[A/G]TACTAAATTTTTAAA	54629
rs762409600	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58781137	TCACTGCAACCTCCA[C/T]CTCCTGGGTTCAAGC	54629
rs762425363	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58823902	TTCCTATACAAGCTC[C/T]CATTACCATAGATAA	54629
rs762443632	snp	G/T	6.63779e-05	0.0057606	missense, intron-variant, synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831776	ATTGGTTCTATAGGC[G/T]TTGTAGCTGAGCAGT	54629
rs762490890	snp	C/G	1.67167e-05	0.00289103	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851875	ACTAGCAAAGAAACT[C/G]CAAGAGGAAGAGGAC	54629
rs762492631	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58785838	TGCGCCACCACACCT[A/G]GCTAATTTTTGTGTT	54629
rs762508905	snp	A/G			missense, intron-variant, downstream-variant-500B, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831885	GTGTGTTCTTTCGGA[A/G]TAATCATTTTAGCAC	54629
rs762543406	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58828079	CTGTACTAAAAATAC[-/A]AAAAATTAGCTGGGT	54629
rs762604674	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849499	GACAGAGCAAGACTC[C/T]GTCTCAAAAAAGAAA	54629
rs762642665	snp	C/G	1.82687e-05	0.00302225	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771736	CCGCCTCCCCGGAGA[C/G]AGCCGTGGCCGGAGT	54629
rs762666328	snp	C/T	0.000433092	0.0147091	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771922	CGAGCCTGGACTCTC[C/T]GGAGTCGTTCTCTAA	54629
rs762686327	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58790585	TTGACAATAGACCTT[-/A]AGTGGGGGGTAAGAC	54629
rs762688334	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58826538	CTGGCCCCACACACT[C/G]TTTTTCCCTAAATCT	54629
rs762728294	snp	C/T			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769797	GCACGCCAGCCTGGG[C/T]GACAGAGCAAGACTC	54629
rs762737969	snp	A/C			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770582	ATTTATTATTATTGG[A/C]GCAAATTAGCCACTT	54629
rs762775903	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58819005	TGTTTTAGAGACAGT[A/G]TCTTGCTGCATTGCC	54629
rs762784012	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58789708	GCTGGAGTGCAATGG[C/T]GTGATCTCAGCTCAC	54629
rs762863290	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58813135	TATCAGTAGTTTGCT[A/C]CTGTTCATTACTGAG	54629
rs762867633	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58810013	AACTCCTGACCTCAA[C/G]TGATCCGCCCACCTC	54629
rs762902176	in-del	-/AATG			intron-variant	FAM63B	GRCh38.p7	15:58794294	GGAATTTTTGGTAAT[-/AATG]AAACTGTATTACCAT	54629
rs762916353	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789265	ATGGTGTGAACCCAG[A/G]AGGCATAGCTTGCAG	54629
rs762933434	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58840184	CCATCATGAGGTCAC[A/G]ATGGATGTGTAATCA	54629
rs762979446	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58846697	TTGTATGCACGTACA[C/G]AGTTTATGTGATAAG	54629
rs763010220	snp	A/G			downstream-variant-500B	FAM63B	GRCh38.p7	15:58862309	ATGGGAATATAAATT[A/G]GTGCAGTCACTTTGG	54629
rs763019671	snp	A/C	1.76633e-05	0.00297176	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851785	GGATTATCTTATGGC[A/C]TTATCTCTACAACAA	54629
rs763060685	snp	C/T	0.000133229	0.00816067	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771408	GGTATGGAGAGCAGC[C/T]CCGAGAGCCTGCAGC	54629
rs763071811	snp	C/T	1.78589e-05	0.00298817	intron-variant	FAM63B	GRCh38.p7	15:58851987	ACTAGTGTTTTGAGT[C/T]TTAAATGTGATGATC	54629
rs763072020	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58845225	AGCCTGGCCAACATG[A/G]TAAAACCCCATCTCT	54629
rs763076924	snp	A/C/G			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772483	AATTGTGGTTGATAC[A/C/G]CTTAGAAACAAGAAG	54629
rs763099257	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58778057	GCCAGAAGGTATATA[A/G]CATATATATTTTAGT	54629
rs763156915	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793075	ATTAGTGGTTGCTTA[A/G]GGCTGGGGAAGAGAT	54629
rs763187587	snp	C/G/T	0.000130967	0.00809132	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771773	TGAGTTGGGTACCGC[C/G/T]GGAGACGCGGGAGCC	54629
rs763210960	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58823709	AACAGTATAGAGTCG[G/T]TGATCATTGATTCAT	54629
rs763235034	in-del	-/A	5.01098e-05	0.00500524	intron-variant	FAM63B	GRCh38.p7	15:58854448	TCCCTCAGAATAGTT[-/A]AGAGTAATTTCTTGC	54629
rs763251641	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58781038	TCTGAATGGAAGATG[C/G]CTTCTTTTACTAGTT	54629
rs763262517	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58811646	CCCCCAAGCTATGGC[C/G]CAGCAGGGAAAGAGC	54629
rs763271181	snp	C/T	1.91797e-05	0.00309669	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831943	AAATAGCTATTTAAT[C/T]GTGATTCTAAATCAA	54629
rs763286799	in-del	-/TTTTG			intron-variant	FAM63B	GRCh38.p7	15:58835904	GTCTTGGGTTTTTTG[-/TTTTG]TTTTGTTTTGTTTTG	54629
rs763294541	in-del	-/AGTT			intron-variant	FAM63B	GRCh38.p7	15:58773951	GGCCCTCAACTAGGG[-/AGTT]AGTTAGACTTGCTCT	54629
rs763322463	in-del	-/A			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860576	AGACTCTTATATCTC[-/A]AAAAAAAAAAAAAAA	54629
rs763323920	in-del	-/C	0.00134483	0.025896	intron-variant	FAM63B	GRCh38.p7	15:58802295	GGCAATTTTACAATT[-/C]TTTTTTTTTTTTTAC	54629
rs763388609	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806543	TTAACCGTTTTATTA[A/G]TCTTTATGAAGATAT	54629
rs763419193	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58820937	AGCAATACACATAAA[C/T]AATTTATAAATAAAT	54629
rs763436183	in-del	-/TG			intron-variant	FAM63B	GRCh38.p7	15:58850412	GGGTTGGTTTGAATT[-/TG]TATGGGAATGTAGAA	54629
rs763442331	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58846296	GCATTGCATGCCTGT[A/G]TCAAAATACCATGTA	54629
rs763477345	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58837457	ACGCACCTATAGTCC[C/T]AGTTACTAGGGTGGC	54629
rs763482004	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58805085	CTTGAAGGGAATTTG[A/G]AATATTGGCTCAAAG	54629
rs763516373	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58850895	CCTGGCTCCCCGCTA[A/C]TTTTTGTTTGGTTTT	54629
rs763549735	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58792086	TGATTTAGCCATAAG[A/G]AGGTCATTGATAACC	54629
rs763565199	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58836700	CTCAGATCACTGCAA[A/C]CTCTGCCTCCTGGGT	54629
rs763570415	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58774994	AGTCATAAGTAATCA[A/T]TGATGAAGAGATGGA	54629
rs763586984	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58804464	ATTCATTTTACTTTC[A/G]TTGCCTAATCCTGAG	54629
rs763587065	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58815819	TGAGCAGCTGGGACT[A/G]TAGGCGCGCACCAGC	54629
rs763637356	snp	C/T	3.32358e-05	0.00407637	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847319	TGTATTTGTTGGTAA[C/T]GGACCAGGGGTTTCT	54629
rs763639890	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58805102	ATATTGGCTCAAAGT[C/T]GAAACAAAGGATATC	54629
rs763662407	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58823807	AACTATTACAAAAGT[A/G]TATTCTCTCAATTAA	54629
rs763695056	snp	A/G	1.67939e-05	0.0028977	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772233	TTGCTCCTGGCCTGG[A/G]AGGTACATTCTGCAG	54629
rs763773813	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58841696	AGGCGTGAGCCACCG[C/T]GCCCGGCTGATCTGT	54629
rs763787850	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58785212	AAATAATTAAGATCT[C/G]TGGATGGCTCCACAG	54629
rs763803050	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58774400	GAGGCAGGAGAATCT[A/C]TTGAACCCAGGAGGT	54629
rs763890633	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58832822	TGAGCCACCGTGTGC[G/T]GCCAGAACTAGGATG	54629
rs763901310	snp	C/T	1.90073e-05	0.00308274	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771791	AGACGCGGGAGCCCG[C/T]CCGGATCTCGCCGGC	54629
rs763932867	in-del	AAGGGAAACTCTTTCTAAAAA/GTCACGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCTGTCTC			intron-variant	FAM63B	GRCh38.p7	15:58843785	TTTGCAGTGAGCCAA[lengthTooLong]AAAAAAAAAAAAAAA	54629
rs763980435	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58796422	TAAGTAGATTGTGGC[A/G]AGACAGTCTTGTGAG	54629
rs764041681	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58784320	GACAGTGAGAACATG[A/T]TGTCTTAAAAATAAT	54629
rs764048178	snp	A/G	1.65737e-05	0.00287864	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771957	CATTCTTTTCCCAGT[A/G]GCTGCGAGTTCAATA	54629
rs764056368	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58830606	TAACTCATGCCTGAA[C/T]GAAACCTATCTAGCA	54629
rs764106464	snp	C/G	1.89921e-05	0.00308151	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771839	GACCGCCGCCGGCTC[C/G]GAAGAGCCCAGCAGC	54629
rs764141019	in-del	-/AGAG			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769971	TCCAGCCTGGGCGAC[-/AGAG]AGAGACTCCGTTTCA	54629
rs764174987	snp	C/G			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770881	AACCACCTCCAACCA[C/G]CCAACAATGCCTCAG	54629
rs764203911	in-del	-/AG			intron-variant	FAM63B	GRCh38.p7	15:58793608	AAGCCATTTTATAAA[-/AG]AGAAAACTAGAGAAA	54629
rs764248098	snp	C/T	1.66779e-05	0.00288768	intron-variant	FAM63B	GRCh38.p7	15:58831756	TCTTCTATCTAATGT[C/T]ATGCATTGGTTCTAT	54629
rs764262655	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58831626	ATTAAAAACACAAAT[C/G]TCCAGTTTGGAGCCA	54629
rs764286016	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58845237	ATGGTAAAACCCCAT[C/G]TCTACTAAAAATACA	54629
rs764318725	in-del	-/TTA			intron-variant	FAM63B	GRCh38.p7	15:58840635	TTTATTTACTTATTA[-/TTA]TTATTATTATTATTA	54629
rs764338661	snp	A/G	5.29956e-05	0.00514733	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772033	CGGCGGTGTTGCCCG[A/G]GGCTGTTCCTCTGTG	54629
rs764362747	in-del	-/CTT			cds-indel	FAM63B	GRCh38.p7	15:58858175	GCTTAGGTAAAGTAA[-/CTT]CTTCCATGTTTCAAG	54629
rs764370579	snp	G/T	1.88963e-05	0.00307372	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771782	TACCGCCGGAGACGC[G/T]GGAGCCCGCCCGGAT	54629
rs764390895	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58818320	CTAGAGTGCAGTGGC[A/G]TGATCATAGCTCACT	54629
rs764398800	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858876	TTGTGTCTATAAACC[C/T]GACTTTCTATCTTGC	54629
rs764410055	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58795352	TAGACACTTTTGTCC[A/T]AATGGCTCACTTCAG	54629
rs764512075	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793270	AGCCTGGGCAACATG[A/G]CAAAACCCCGTCTCT	54629
rs764540000	snp	A/G/T	3.60648e-05	0.00424633	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771642	CCCTGCAGCTCCTCC[A/G/T]CGGGTTTGGACTTGA	54629
rs764554299	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58778895	TTGGCTCACTGCAAC[C/T]TCTGCCTCCTGGGTT	54629
rs764573238	snp	C/G/T	4.98031e-05	0.00498994	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854539	TCTGGGAATAGTGAA[C/G/T]GTAAACGGAAGGAAC	54629
rs764675554	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58814198	ACCCGCTTCGGCCTC[C/T]CAGAGTGCTGCGATT	54629
rs764712063	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58840861	TTTTAGTAGAGATGG[C/G]TTTTCACCGTGTTAG	54629
rs764714447	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58803764	GAGGTTGCAGTGAGC[C/T]GAGATTGCGTCACTA	54629
rs764716438	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784932	GAGCCACCGTACCCA[A/G]CCTGTTATTTTTTTC	54629
rs764754775	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836762	CAACTGGGACTACAG[A/G]TGTACACGATCACAC	54629
rs764755121	snp	A/C	1.66341e-05	0.00288388	missense, intron-variant	FAM63B	GRCh38.p7	15:58821796	CTTGTAAACAGTCAG[A/C]CAATAGTGAGCTGGT	54629
rs764770913	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58813311	ACCAGCCTGGCCAAC[A/G]TGGCGAAACCCCATC	54629
rs764785298	snp	A/G	1.7306e-05	0.00294155	intron-variant	FAM63B	GRCh38.p7	15:58787884	ACATTTAATTTTATA[A/G]AAATAATATTTTGTT	54629
rs764812639	snp	C/G	5.39428e-05	0.00519312	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771651	TCCTCCGCGGGTTTG[C/G]ACTTGAAGGACAGTG	54629
rs764820518	snp	C/G	1.81926e-05	0.00301595	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851777	ATTTATTAGGATTAT[C/G]TTATGGCATTATCTC	54629
rs764834859	in-del	-/TATATATATATATATA			intron-variant	FAM63B	GRCh38.p7	15:58791226	AATTTTATATATATA[-/TATATATATATATATA]TATATATATATATAT	54629
rs764860036	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58807664	CATTGCGCCCGGCCT[-/A]AAATAGTCTTTATTC	54629
rs765017040	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58840177	CCTTCTGCCATCATG[A/G]GGTCACAATGGATGT	54629
rs765029536	in-del	-/CTC			intron-variant	FAM63B	GRCh38.p7	15:58826608	TGCTTCATCATTTGT[-/CTC]CTAAGAACAAGGAAT	54629
rs765107261	snp	A/C/G	0.000131953	0.00812163	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771921	CCGAGCCTGGACTCT[A/C/G]TGGAGTCGTTCTCTA	54629
rs765118758	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58808135	ATACCTCCTGTTCCT[C/T]CTAACCCCATACACA	54629
rs765124209	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58848775	AATATTTAATTCAAA[C/G]AAATATGCATCTTTC	54629
rs765136759	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789123	CGGGCCGATCACAAG[A/G]TCAGGAGATCAAGAA	54629
rs765162051	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58777547	GGGAGGCCGAGGCCA[A/G]AGGATCAGTTGAGCC	54629
rs765162211	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812844	GCCTGAGAGAAAGAG[C/T]GAGACCCTGTCTCAA	54629
rs765183959	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58776500	GTATTCAGGGAAAGA[A/G]AATGTAATAAAAATG	54629
rs765208636	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58817974	TTATTTGCCATAGTC[C/T]GAAACTGAAAACAAC	54629
rs765255338	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58852457	TTTTCTCCTGAGGTT[C/G]TGATTTTCAAATTTA	54629
rs765264920	in-del	-/TG	7.1617e-05	0.00598359	intron-variant	FAM63B	GRCh38.p7	15:58802293	AGGCAATTTTACAAT[-/TG]TCTTTTTTTTTTTTT	54629
rs765288060	snp	A/G	1.66092e-05	0.00288172	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847445	CTGAAACTGTATACA[A/G]AGGACAACAAGATCA	54629
rs765294966	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811098	CCCAAGGGGCCCACA[A/G]TAAATAACACAGTCA	54629
rs765297037	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58797841	TGTGGTGGCAGAGAA[C/T]CGATGAGCAGAGCCA	54629
rs765315932	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58822303	AAGGTGCCAATGAAA[C/G]GTTTTTCCTAGAACT	54629
rs765384856	snp	A/G			missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810242	CAGAATATGAGTGAT[A/G]CCATGGCAATTTTGC	54629
rs765415034	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858482	ATTCACTAAGAGACA[C/G]ATCATGAGAGGAAAG	54629
rs765426418	snp	C/T	0.000179185	0.00946363	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771345	CGTCCAAGGCGCTGG[C/T]TGCGGAGAAGTGGCC	54629
rs765450984	snp	C/T	3.65611e-05	0.00427542	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771392	TGGGGGCGGGCGGCC[C/T]GGTATGGAGAGCAGC	54629
rs765547899	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836537	ATTTCCTATATTCCT[A/G]TTGTACCAGCTTTCC	54629
rs765563831	snp	C/T	1.9029e-05	0.0030845	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802368	AATTCAACGTTTAAA[C/T]TATGAACAGGTAATA	54629
rs765594881	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58803835	AATAAGAGGCCGGGC[A/G]TGGTGGCTCACGCCT	54629
rs765599174	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58806354	AGTCAACGTGCCAAC[-/T]TTTTTTTTTTTTTTT	54629
rs765619395	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58805013	TGCAAATGTTATCAG[C/G]ATTTGGTTTAAGTCC	54629
rs765660502	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58828571	TAATTTATTATTGAA[-/T]TTTCTTTTTTTTTTT	54629
rs765668427	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58820620	GAAAATAAATTATAG[C/T]ATAGAATGGTGGTTC	54629
rs765719244	snp	G/T	1.68278e-05	0.00290062	intron-variant	FAM63B	GRCh38.p7	15:58821824	GGTTAGTGAAGGTGG[G/T]TGAGTGCTGCTATTT	54629
rs765734805	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58833869	TAATCTTCCTCAGCA[C/G]AGACCCTTTATGGGT	54629
rs765747635	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58779309	GAATGGACGTATGCT[A/G]TTGTCTCATCACCTG	54629
rs765747983	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58792032	CTGAATCAAATGCTG[C/T]TAATAGCTCAGGCAG	54629
rs765762311	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58795655	GTGATCCACCCGTCT[C/T]GGCCTCCCAAAGTGC	54629
rs765774402	snp	A/G	1.65781e-05	0.00287902	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831797	GCTGAGCAGTTTCTA[A/G]ATAACACAGCCACTC	54629
rs765785228	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58818722	TCGGCTCACTGCAAC[C/T]TCCACCTCCCAGTTT	54629
rs765836105	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58823128	AGGTTTATCCTAATC[-/T]TTTTTTTTTTCTTTT	54629
rs765842661	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58825881	AAAGTGCTGGGATTA[C/G]AGGCGTGAGATGCCA	54629
rs765855733	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58839961	CCTCAGCCTCCCAGG[C/T]AGCTGGGATTATGGG	54629
rs765881093	snp	C/G	1.80657e-05	0.00300542	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771681	GGTTTGGAGAGTCCT[C/G]CTGCCGCCGAGGCGC	54629
rs765889777	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793430	CACTCCAGCCTGGGC[A/G]ACAGTGAGAAACTGT	54629
rs765898070	snp	A/T	1.82587e-05	0.00302142	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771737	CGCCTCCCCGGAGAC[A/T]GCCGTGGCCGGAGTG	54629
rs765902781	snp	A/G	3.50116e-05	0.00418384	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772046	CGGGGCTGTTCCTCT[A/G]TGCAAGGAGGAGGAG	54629
rs765906911	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849461	AGTGAGCCAAGATGA[C/T]GCCACTGCACTCCAG	54629
rs765951798	snp	A/G	1.84245e-05	0.00303511	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802330	GATTACATGCTTGAT[A/G]CAAAGCCAAAAGAAA	54629
rs765989819	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58808054	TCACTCCCTTCCTTC[C/G]ATCCTTCCTTCCTTT	54629
rs766087273	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58844392	TCTACTAAAAAATAC[-/A]AAAAAAAAAATTAGC	54629
rs766089393	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58838275	TGGTGGTGTGTGCCC[A/G]TAATGCCAGCTACTC	54629
rs766110614	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806683	AAAGGAAGTTGGGTG[A/G]TTGACAAACAAGAAT	54629
rs766173340	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58852370	AGGTGTTAACTCTTC[A/C]ATTTTGTTAGGATTT	54629
rs766233358	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58787061	TCTCGAACTCCCAAC[A/C]TCACGTGATCCGCCT	54629
rs766247931	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58817140	AAAACTGAGAATTTG[C/T]GTTCATCTAAAGGCA	54629
rs766279574	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789725	TGATCTCAGCTCACC[A/G]CAACCTCCACCTCCT	54629
rs766293485	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58786217	TTGATAACGTAAACA[C/G]CTAGAGGACCTTTTT	54629
rs766297284	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817855	CAGTTTGGTTTATCC[A/G]TTAAAGTTGATGCTA	54629
rs766348258	snp	A/G	3.38301e-05	0.00411265	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851811	AACAAGAACAGCAGA[A/G]CCAAGAGATCAATTG	54629
rs766394757	snp	C/T	1.78873e-05	0.00299054	intron-variant	FAM63B	GRCh38.p7	15:58851989	TAGTGTTTTGAGTCT[C/T]AAATGTGATGATCAT	54629
rs766419006	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58820489	ATGCCTGTAAACATT[G/T]TCCACAATTTCCTGC	54629
rs766480099	snp	C/T	0.000589449	0.0171574	intron-variant	FAM63B	GRCh38.p7	15:58796030	TGTGGTTATTGTGAC[C/T]TTCATCAAACCGTGT	54629
rs766503918	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58810168	TGTGCTTGTACTTGA[A/G]TATCTTTTTTGTTCT	54629
rs766515973	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58779008	CTCAAGTGACCTGCC[C/T]GCCTCAGCCTTCCAA	54629
rs766525674	snp	C/T	1.66045e-05	0.00288132	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810249	TGAGTGATGCCATGG[C/T]AATTTTGCACAAACT	54629
rs766526919	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855672	ACGCCTGTAATCCCA[A/G]CATTTTGGGAGGCCA	54629
rs766559531	snp	C/T	1.65748e-05	0.00287874	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854504	AGCCAGCACAAGCCT[C/T]TCCATCAAGTGGAAG	54629
rs766561644	snp	A/C/T	3.61045e-05	0.00424867	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771498	CTACAGGAGACCAGG[A/C/T]TCGCCGCTGGTGATG	54629
rs766580169	snp	A/C			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857842	TGAACAAATATGGTC[A/C]TTGCACTTTCCTTTT	54629
rs766633067	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58838041	TCTTTCTACTCCTGT[C/G]AACTCTTTCTCTTTG	54629
rs766648385	snp	C/T	3.53307e-05	0.00420287	intron-variant	FAM63B	GRCh38.p7	15:58810395	GACCCTCAGGTAAGT[C/T]GAAGAATTTAAATTA	54629
rs766672470	in-del	-/TG			intron-variant	FAM63B	GRCh38.p7	15:58776259	TTCCATCCCAATATA[-/TG]TGAGAGTGACAAATT	54629
rs766740571	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58813217	GGGTGTTTTCCCGCC[A/G]GGCACGGTGGCTCAC	54629
rs766832121	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58783817	AAGCATGGTGGCGCA[C/T]ACCTGTGGTCCCAGC	54629
rs766834298	snp	C/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772591	CAAAAAAGTGAAGAA[C/T]TGGAGAAAGTAATCT	54629
rs766844742	in-del	-/TT	0.0228885	0.1045	intron-variant	FAM63B	GRCh38.p7	15:58802296	GCAATTTTACAATTC[-/TT]TTTTTTTTTTTACAG	54629
rs766846926	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58802308	TCTTTTTTTTTTTTT[-/A]ACAGGAGATTACATG	54629
rs766855930	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58820981	TATATATGGAAAGGC[A/G]ACTATATAAGTTGTT	54629
rs766863248	in-del	-/C	2.8054e-05	0.00374516	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771406	CGGTATGGAGAGCAG[-/C]CCCCGAGAGCCTGCA	54629
rs766871587	in-del	-/TTTTA			intron-variant	FAM63B	GRCh38.p7	15:58775296	GGGGTCCTCAATCAT[-/TTTTA]AGACTGTAAAGGGCT	54629
rs766888846	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58852147	CAAAATTAGCCGGGC[A/G]TGGTGGTGGTGAACA	54629
rs766889317	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58773309	AGAAAAATAACCTGG[A/G]TTCTTCTAAACACTT	54629
rs766890038	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58789069	GGGGCCGGGCACGGT[C/G]GCTCACGCCTGTAAT	54629
rs766900131	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58803704	ACCTGTAGTCCCAGC[C/T]ATTCAGGAGGTTGAG	54629
rs767004614	snp	A/G	2.43858e-05	0.00349175	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771412	TGGAGAGCAGCCCCG[A/G]GAGCCTGCAGCCGCT	54629
rs767031279	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58836942	CATTCTTTATAAGGG[C/T]CAAAAGCACGTCTTC	54629
rs767053041	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58846323	TGTAGGCCAGGCGCG[G/T]TGGCTCACGCCTGTA	54629
rs767082000	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58786202	GTGACATTATTACAT[G/T]TGATAACGTAAACAC	54629
rs767087507	snp	A/G/T	7.04517e-05	0.0059348	intron-variant	FAM63B	GRCh38.p7	15:58847250	ATATTATATTACTAG[A/G/T]TTTGATCAATTTAAC	54629
rs767101840	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58805387	ATATTCCCATTTAAA[A/C]CTCTTTACCAGAAGT	54629
rs767128288	snp	A/G	5.01928e-05	0.00500938	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772096	TGCTGGCGGCCTCCA[A/G]GGAACGCTTCCCGGG	54629
rs767135563	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58787737	GCGAGAGTCCGTCTC[-/AA]AAAAAAAAAAAAAAA	54629
rs767165749	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58822757	GCATGTAGATATACC[G/T]TCTCAGTCCCCACTT	54629
rs767203776	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58798925	TGTTAAATTTATCTA[A/T]CTCTTAGCTAGCAAA	54629
rs767214285	snp	C/T	1.66624e-05	0.00288633	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847310	AGGGTCAACTGTATT[C/T]GTTGGTAACGGACCA	54629
rs767237268	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58775149	TGGAGTTTTTCAGGC[A/T]ACATGATGTAATGAC	54629
rs767250771	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58815920	CTTGACCTCGTGATC[C/T]GTCTGCCTCGGCCTC	54629
rs767317932	snp	A/G	1.87103e-05	0.00305856	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802359	AATTTCAGAAATTCA[A/G]CGTTTAAATTATGAA	54629
rs767328469	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58794787	AGGGAACATTCAGAG[A/G]AGTTGAATACCTAGG	54629
rs767377130	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58830257	TTGGTAACATTTTCA[A/T]CAGCTGATCAGTACA	54629
rs767423928	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58797736	TCTTCCCTGCTCGTT[A/G]TCACTAGCACTCTAC	54629
rs767469172	snp	G/T	1.78204e-05	0.00298494	intron-variant	FAM63B	GRCh38.p7	15:58810399	CTCAGGTAAGTCGAA[G/T]AATTTAAATTATGTA	54629
rs767487734	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58788904	ATAGTCCCAACTATT[C/T]GGGAGGCTGAGGTGG	54629
rs767501715	snp	G/T	1.69749e-05	0.00291327	intron-variant	FAM63B	GRCh38.p7	15:58810205	GATGTTTCTGAATTA[G/T]AACTTTCCCCTTTTC	54629
rs767503407	snp	A/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856568	TCTGATAGAAAATAT[A/T]TAATGAGTATCTTGA	54629
rs767575745	in-del	-/A			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769988	GAGAGACTCCGTTTC[-/A]AAAAAAAAAAAAAAA	54629
rs767615888	snp	A/G	1.73012e-05	0.00294114	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854635	GCTTCTGTTGGAACC[A/G]CCTATATGTCTTGAG	54629
rs767629252	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58777697	ACATCAAGAAAGACA[C/T]CTATTTATTACATTT	54629
rs767630007	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58843252	TCTCTTGGGTTCAAG[C/T]GATTCTTCTGCCTCA	54629
rs767683510	snp	C/G			missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851879	GCAAAGAAACTCCAA[C/G]AGGAAGAGGACAGAC	54629
rs767721786	snp	A/C			utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854696	ACCGATCAATACCGT[A/C]TGTGCCTGATTTCCT	54629
rs767773826	in-del	-/AAAGAA	3.34846e-05	0.0040916	cds-indel, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854569	CCACGAGAAAAAGAT[-/AAAGAA]AAAGAAAAGGAAAAA	54629
rs767782795	snp	C/T			synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831886	TGTGTTCTTTCGGAA[C/T]AATCATTTTAGCACC	54629
rs767885466	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58818430	TGGCTAGATTTTTTA[-/T]TTTTTTGTGAAGACA	54629
rs767911572	snp	G/T	1.84449e-05	0.00303679	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771594	AGCCTCCCGGACTCG[G/T]CTTCTCCCGCGGGCT	54629
rs767965458	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58811919	TACTCCTATACTGTT[G/T]TAATATTATTTTCAC	54629
rs767972711	snp	A/G	9.94728e-05	0.0070517	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854523	ATCAAGTGGAAGACA[A/G]TCTGGGAATAGTGAA	54629
rs767980295	snp	A/C			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772557	TTCCTACATTTTCTT[A/C]CTGACCTTATCACAT	54629
rs767991445	in-del	-/TTA			intron-variant	FAM63B	GRCh38.p7	15:58826041	ACATTATAGTTTGGC[-/TTA]TTATTATTTTTATTA	54629
rs767997894	in-del	-/AAA			intron-variant	FAM63B	GRCh38.p7	15:58844561	CGAGACTCCGTCTCA[-/AAA]AAAAAAAAAAAAAAA	54629
rs768015371	snp	C/T	1.80439e-05	0.0030036	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771512	GCTCGCCGCTGGTGA[C/T]GGTCCTGGGGTATGG	54629
rs768020759	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812937	AATCCCGCCTGATGC[C/T]CTTTTATATCCACAC	54629
rs768050449	snp	C/T	1.90416e-05	0.00308552	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771907	CTCCTGGGGAATCTC[C/T]GAGCCTGGACTCTCT	54629
rs768103293	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58776124	AAGAGGCTATAAAAT[G/T]ATAGAGAAAAATCAA	54629
rs768154542	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811359	TGCCTCTTGTTAAGC[A/G]TATCAGGGTCCTGGC	54629
rs768162980	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58812306	GTCGGGTGCAGTGGC[A/G]GGCGCCTGTAATCCT	54629
rs768179681	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58816649	AAAAAGATCACTATA[C/T]AGATAGAACTAGGGC	54629
rs768200325	snp	A/C			missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772131	TCTGTGTATCACATC[A/C]AGTGGATCCAGTGGA	54629
rs768250862	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58843951	AAATTGTGACAATAT[G/T]GACATTTATATAATT	54629
rs768264473	snp	A/G	5.44183e-05	0.00521596	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771993	GAGGGAGCGGAGAAC[A/G]GGGTCCCTGAGGAGG	54629
rs768269501	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58838876	GTGAGCCACTGAGCC[C/T]GGCCTAATTTTTATT	54629
rs768337558	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58786958	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTATAAG	54629
rs768386438	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58798870	TGTCAGCATGGGATT[A/T]TTCTTGGAAAGAGTA	54629
rs768389508	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860866	AGTTTTTTCAGGGTA[C/T]ATAGGGTATCTTTGT	54629
rs768397954	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837353	CAAGGCTGGACAGTC[A/G]CTTGAGGCCCAGAGT	54629
rs768419097	snp	C/T	1.65894e-05	0.00288	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854487	TTTCTTAAAGCAGGG[C/T]CAGCCAGCACAAGCC	54629
rs768425348	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58785885	TGTTTCACCAAGTTG[G/T]CCAGGCTCGTCTCGT	54629
rs768436945	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58790781	CATTTTTGGTTTGAA[C/G]AAGTAGAAGGATGGA	54629
rs768447793	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58789075	GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC	54629
rs768493624	snp	A/C/T	7.00395e-05	0.00591739	intron-variant	FAM63B	GRCh38.p7	15:58821848	GCTATTTCCTGACTT[A/C/T]TGAAATTCTTGGCAA	54629
rs768493940	snp	A/G	1.6641e-05	0.00288448	missense, intron-variant	FAM63B	GRCh38.p7	15:58821745	TAAAAGCTGTTGGTA[A/G]CTGCAGCTACAACCA	54629
rs768523812	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836211	GACCGCACCCGGCCT[A/G]TTGCATCTCAAAATT	54629
rs768526234	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58843084	TTATAAAGTACCTTA[C/G]AAACTTCAAAATTTC	54629
rs768537909	snp	A/C	1.67649e-05	0.0028952	missense, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854573	GAGAAAAAGATAAAG[A/C]AAAAGAAAAGGAAAA	54629
rs768548732	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58810746	TATACTCACCATTAC[A/T]GTTCATTACAGGGCA	54629
rs768549586	snp	A/C			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857440	TTGGGAGGCTGAGGC[A/C]GGAGAATCGCTTGAA	54629
rs768574450	snp	A/C			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859277	CTAAATATTTAGATT[A/C]TCTTTGCCTTTTTCT	54629
rs768592897	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58779893	AAAAACCTTCTCACT[C/G]CCCATTCAACCTTGT	54629
rs768599630	snp	A/T	1.65814e-05	0.00287931	synonymous-codon, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810334	TACACCAGAATGCAT[A/T]GTATTTGATCTTCTT	54629
rs768639573	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58812614	CTGTAATCCTAGAAC[-/T]TTTGGGAGGCCAAGG	54629
rs768669924	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58813545	TTCATTTCTCTGGGT[A/T]AAATGCCCAGGAGTG	54629
rs768701180	in-del	-/TATT			intron-variant	FAM63B	GRCh38.p7	15:58839096	AAAAGTTTTTTTAAA[-/TATT]TATTTATTTATTTAA	54629
rs768709836	snp	C/T	1.8434e-05	0.0030359	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771755	CGTGGCCGGAGTGGG[C/T]CATGAGTTGGGTACC	54629
rs768716728	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58782264	GCTGAATATATAAAT[C/G]CTACATATATACACA	54629
rs768756578	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58847748	GTATTAAACACAGAA[A/G]TGATGGGATCTTCTT	54629
rs768794685	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58847285	CTTTTTCTTTTGTTA[C/T]TTCTTATTAAGGGTC	54629
rs768819831	in-del	-/G			intron-variant	FAM63B	GRCh38.p7	15:58794547	GGGGATTGGCCTGAA[-/G]GTCAGGAGATAACTG	54629
rs768832986	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58802164	GGAAAAGTTAACATT[G/T]ATTTTCTCTGGGTAG	54629
rs768871965	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58853654	TGAAACCCTGTCACT[A/G]CTAAAAATATAAAAA	54629
rs768878032	in-del	-/GTTT			intron-variant	FAM63B	GRCh38.p7	15:58785546	GTGTTCCAAAAAAAC[-/GTTT]GTTTATTTAGAAAAA	54629
rs768881618	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58795505	CCACCTTCGGGTTCA[C/T]GCCGTTCTCCTGCCT	54629
rs768904109	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58845422	AAGAAAAAAGATAAA[C/G]AAATGGCAGACAGGT	54629
rs768931673	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58825131	TGGTCACAGGTGATA[A/G]CTTTTTAAAAATTCA	54629
rs768950737	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58783000	TCTTTACTCACTGCA[G/T]CCTTTGTCTTCTGGG	54629
rs768997850	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58807669	CGCCCGGCCTAAAAT[A/G]GTCTTTATTCCAGAT	54629
rs769019098	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58831657	TCATAAAGTAGTAGG[A/G]AAAGTATTATAATTA	54629
rs769087941	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806554	ATTAATCTTTATGAA[A/G]ATATCAAATGGTGTT	54629
rs769106230	snp	G/T	0.00947237	0.0681649	intron-variant	FAM63B	GRCh38.p7	15:58802296	GCAATTTTACAATTC[G/T]TTTTTTTTTTTTACA	54629
rs769147293	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58844837	GGACAGTCGCTTGAA[A/C]CCAAGAGGCTGAGGC	54629
rs769174261	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58776022	GTGTGCCACCACACC[A/G]GCTAATTTTGTATTT	54629
rs769259652	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58842823	TTCTCACTTAATGGC[C/T]GAGGGAACATGTAAA	54629
rs769262523	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58814553	CTGCTCACTTTTTAA[-/T]TTTTTTGTAGAAATG	54629
rs769266468	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58821590	TTTTAGTGCTGATTT[G/T]GTTTTTCGTAAATAA	54629
rs769312581	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58828751	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCAGGT	54629
rs769354340	snp	A/C			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770494	CTTTTCAGAAGCAGG[A/C]GCTTCCCACTCCATG	54629
rs769503123	snp	A/T	1.88963e-05	0.00307372	intron-variant	FAM63B	GRCh38.p7	15:58802308	TTCTTTTTTTTTTTT[A/T]ACAGGAGATTACATG	54629
rs769535093	snp	C/G	1.67128e-05	0.00289069	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851844	AACAAATCCCGGAAG[C/G]AATCAGTGATTTGGA	54629
rs769559285	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58833332	ATTTCTGCACTTTAC[C/T]GCCATATCTTGAAGG	54629
rs769561046	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58789457	GGAAATTTTAGAAGA[-/T]TTTTTTTTTTTTCTT	54629
rs769580175	snp	C/T	3.42079e-05	0.00413555	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851937	AACAAGCAGCAGCTG[C/T]TGCTGCTGCTGCTTC	54629
rs769580220	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58797239	TTGCCAGGTGTGATG[C/G]CTCATGCCTTTTATC	54629
rs769582095	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58803032	GAGACATCGTTGGAA[C/G]CTTCATATTTACTTT	54629
rs769626083	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58834143	AGTTGACACAGCACA[A/C]GTTTCAGGGAGCACA	54629
rs769632397	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58778702	TGCAATCATGGCTCC[A/G]AATAGCCTCGACCTC	54629
rs769638148	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855380	TAACCTGGACCACAG[C/T]TACTATTTATTGACA	54629
rs769667230	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58837601	TTTAAATCTACATTA[C/T]ATCTTCCATATCTTC	54629
rs769667425	snp	C/T	1.92165e-05	0.00309966	intron-variant	FAM63B	GRCh38.p7	15:58821866	AAATTCTTGGCAAGA[C/T]AATTTTTCTTATAAC	54629
rs769678763	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58820092	CCAACATAGTGAAAC[C/T]GCAACTCTACTAAAA	54629
rs769707125	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58818929	TACAGGCATGAGCCA[C/T]TATGCCCAGCCTATT	54629
rs769723809	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58839504	ATCCAGCTAATTTTT[A/G]TATTTTTCGTAGGAA	54629
rs769723895	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58789518	CTGGAGTGCAGTGGC[A/G]TGATCATGACTTGCT	54629
rs769723929	snp	A/G	9.02861e-05	0.00671825	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772005	AACAGGGTCCCTGAG[A/G]AGGAGGAGGGCGCGG	54629
rs769830843	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58773977	CTTGCTCTAACGGGC[C/T]AGAGTCCCTAATCTT	54629
rs769863791	snp	A/G	1.65669e-05	0.00287805	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847388	TAGATGGTGATGGAA[A/G]TTTCTGTGACTCAGA	54629
rs769883061	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58849703	CTTTATATCCATGAG[A/G]TAGTCATGCTATATA	54629
rs769902878	in-del	-/GCTGCTTCTACACAGCA	1.71322e-05	0.00292674	frameshift-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851944	GCAGCTGCTGCTGCT[-/GCTGCTTCTACACAGCA]GCTGCTTCTACACAG	54629
rs769909906	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58811571	CAGAACACAGCAAGA[C/T]TGATTAGTAAAGCAC	54629
rs769915400	snp	C/G	3.60653e-05	0.00424633	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771491	GGAAGGGCTACAGGA[C/G]ACCAGGCTCGCCGCT	54629
rs769940541	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58825315	TGCCTTATAAGTAAA[C/G]GTGCAGAACTTTTAC	54629
rs769998704	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837367	CGCTTGAGGCCCAGA[A/G]TTCAAAGCCAGCCTG	54629
rs770015247	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58854244	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAGGA	54629
rs770068812	in-del	-/TGTT			intron-variant	FAM63B	GRCh38.p7	15:58825598	TGTTTGTGTGGTGTT[-/TGTT]TGTTTGTTTGTTTGT	54629
rs770092541	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806221	TGGGATTACAGGCAT[A/G]TGCCACCACTCCTGG	54629
rs770102832	snp	G/T	1.85672e-05	0.00304684	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771766	TGGGTCATGAGTTGG[G/T]TACCGCCGGAGACGC	54629
rs770120774	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58775796	TGTCCAGTGGGGGGC[A/C]TAAAAATATAAATGT	54629
rs770156743	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58780998	CTAGTAAGCTTGCTG[A/G]GCTTCTTAAATATAA	54629
rs770158695	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793902	GGATTAGAGAGCTGT[A/G]GTATGATTTTTGGGT	54629
rs770192873	snp	C/G	1.82424e-05	0.00302007	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771732	GTGACCGCCTCCCCG[C/G]AGACAGCCGTGGCCG	54629
rs770218802	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58829669	CATTTAGTAATACAG[A/G]TATTACAGACGGCAG	54629
rs770402589	in-del	-/ATT			cds-indel	FAM63B	GRCh38.p7	15:58855620	GTCTTATAAAAAGAC[-/ATT]AATAAAAATCTGAAA	54629
rs770418677	snp	C/G	1.86221e-05	0.00305135	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771447	CACGGGGTGGCGGCC[C/G]GGCCAGCGTCAGGGA	54629
rs770462079	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856579	ATATTTAATGAGTAT[C/T]TTGATTATAACCTAG	54629
rs770463855	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58841275	GGCATGAGCCACTGC[A/C]CTGAGCCAACTTCAT	54629
rs770532660	snp	A/G	3.475e-05	0.00416819	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851959	TGCTGCTTCTACACA[A/G]GCTCAGGTAAAAACT	54629
rs770637235	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58818494	TTCCTGGACTGAAGC[C/T]GTCCTCCCCTGCTAG	54629
rs770657499	snp	A/C	3.34549e-05	0.00408978	intron-variant	FAM63B	GRCh38.p7	15:58854440	ATGAGTAAGTCCCTC[A/C]GAATAGTTAGAGTAA	54629
rs770657678	in-del	-/AT			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861047	TCAGCAAAAGGAATC[-/AT]ATGTTTGCTTGTGAA	54629
rs770658151	in-del	-/GGC	1.79412e-05	0.00299505	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772009	GGTCCCTGAGGAGGA[-/GGC]GGAGGGCGCGGCGGT	54629
rs770707266	snp	C/G	1.78026e-05	0.00298345	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772022	GGAGGAGGGCGCGGC[C/G]GTGTTGCCCGGGGCT	54629
rs770712491	snp	C/G	1.65699e-05	0.00287831	missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810305	AGATTCACTGGTGTT[C/G]GAGTGTTTGAATATA	54629
rs770732516	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58847487	TAAATTTGTATTGTC[A/G]TCTTTATAGTGGTTA	54629
rs770755113	snp	C/T	1.69755e-05	0.00291332	synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831901	TAATCATTTTAGCAC[C/T]ATGACCAAATACAAG	54629
rs770806476	snp	A/G	1.70586e-05	0.00292045	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772074	GAGGGGGAGGAGACC[A/G]CTCAGGTGCTGGCGG	54629
rs770828001	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58846677	ATTAAAAATTAAAAA[A/G]AAATTTGTATGCACG	54629
rs770852844	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58780307	TACTCGGGAGGCTGA[A/G]GCAGGAGAATCACTT	54629
rs770866408	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58802119	TCAAAGCACTATAGT[A/G]TATACATTGAAAAAA	54629
rs770883004	snp	A/G/T	0.000118781	0.00770577	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771351	AGGCGCTGGCTGCGG[A/G/T]GAAGTGGCCGCGGTC	54629
rs770902321	in-del	-/AT			intron-variant	FAM63B	GRCh38.p7	15:58794380	TGTGTGTGTGTGTGT[-/AT]GTGTGTGTGTGTGTG	54629
rs770942550	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58837100	AAGGGGTTCTTCCAG[C/G]ATGGTGTCCATTTGC	54629
rs770964944	snp	A/G	1.65949e-05	0.00288048	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787939	ATGGAAATCATAACT[A/G]CTGAGCAGCTGATGG	54629
rs771047799	snp	C/G	1.67223e-05	0.00289151	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851881	AAAGAAACTCCAAGA[C/G]GAAGAGGACAGACGG	54629
rs771083598	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58805154	ATAAACATATCAGGC[A/C]AAAAGTACCCTGCTT	54629
rs771117598	in-del	-/TTTTTTTT			intron-variant	FAM63B	GRCh38.p7	15:58852923	AGACTGCTGTTCCTG[-/TTTTTTTT]TTTTTTTTTTTTTTT	54629
rs771120623	snp	A/G	3.42906e-05	0.00414055	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854616	TATTTTGTAACAAGT[A/G]TTGGCTTCTGTTGGA	54629
rs771123951	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58774818	TTGGTTGAAGTGTGC[A/C]GCATAGGAGGTAAAC	54629
rs771142580	snp	A/C	1.94972e-05	0.00312221	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771432	CTGCAGCCGCTAGAA[A/C]ACGGGGTGGCGGCCG	54629
rs771143612	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58816218	GCTGCTGGGATTCAG[A/G]AGAATGGAAGGATGG	54629
rs771147807	in-del	-/AGT			intron-variant	FAM63B	GRCh38.p7	15:58824005	CAGAGTATGCTATTC[-/AGT]AGTAGTACTTGAAGG	54629
rs771183759	snp	C/T	1.90376e-05	0.0030852	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771827	CCAAGCAGAACTGAC[C/T]GCCGCCGGCTCCGAA	54629
rs771283237	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58791825	ACAGTAGTTAGATTG[G/T]GTGAGATCATTAAGG	54629
rs771305481	snp	A/G	1.80856e-05	0.00300707	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771633	GTTCCCGGACCCTGC[A/G]GCTCCTCCGCGGGTT	54629
rs771326020	in-del	-/GT	0.000284017	0.0119134	intron-variant	FAM63B	GRCh38.p7	15:58854449	CCCTCAGAATAGTTA[-/GT]GAGTAATTTCTTGCT	54629
rs771478463	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817677	CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA	54629
rs771478849	snp	C/T	1.65721e-05	0.0028785	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847410	TGACTCAGAATTTCA[C/T]CTTCGACCTCCTTCA	54629
rs771481023	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769455	AAAAAAAAAAAAAAA[A/G]GGGGCACAGTCTTCT	54629
rs771540542	snp	A/C			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770387	ATAGGACCCACATAC[A/C]TTTTGTTACTAACAA	54629
rs771570297	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58831136	ATAATATCTATTTCC[A/G]AACTTGATACATCTA	54629
rs771574422	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58801712	TGGCGCGATCTCGGC[C/T]CACTGCAGCCTCCAC	54629
rs771616292	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58790917	GGGTGTGGTGGCTCA[C/T]GCCTGTAATCTCAGC	54629
rs771621020	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58807823	TTATTTTGTCCCAGC[C/T]GCACTGGGCCCCATG	54629
rs771637833	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58788228	CTTAATCCCAATAAA[C/T]TGTAGAATGGGAGAT	54629
rs771662826	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58818378	ATCCTGTCTCAGCTT[C/T]CTGAGTAGCTGGGAC	54629
rs771676218	in-del	-/TG			intron-variant	FAM63B	GRCh38.p7	15:58785211	AAAATAATTAAGATC[-/TG]TGGATGGCTCCACAG	54629
rs771699087	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58798782	ATTCACTGAGCATGT[A/G]TTGTGAGCTAGTTAT	54629
rs771707903	snp	A/T	6.48179e-05	0.00569252	intron-variant	FAM63B	GRCh38.p7	15:58810440	CAGGAAAAATGTATT[A/T]ATTTGGCAAATTAAT	54629
rs771715909	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58787036	GGTTTCACCATGTTG[A/G]CTAGGCTGGTCTCGA	54629
rs771764241	snp	A/G	5.28388e-05	0.00513971	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771370	GTGGCCGCGGTCTCC[A/G]TAGAGCTGGGGGCGG	54629
rs771775683	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58776849	CAATATAGTGAGACC[C/G]CCATCTCTGTAAAAA	54629
rs771787087	in-del	-/A	7.25049e-05	0.00602057	intron-variant	FAM63B	GRCh38.p7	15:58851730	CATTCATTCTTGGGT[-/A]AAATCTCATAGCTAA	54629
rs771829717	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859365	GTGGAATTCATTTAG[A/G]TCTCTCAAGTAATAT	54629
rs771834223	snp	A/G			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772408	TTCCTTTATACATAT[A/G]TCGAAAAGAATTGCC	54629
rs771867371	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58776185	GTAGTACTACATAGA[A/G]TAAATATGAGACTAA	54629
rs771874617	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58780695	AGCTCTCTGTACTTT[A/G]TCTTATGTCTCCTGA	54629
rs771875342	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861255	CTCCACTTTATTGTT[C/G]GACTAATTGGGTCAA	54629
rs771884073	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58810863	CAGGACATCATACCC[-/T]CCTGGAACTGATGTA	54629
rs771897526	snp	C/T	1.66333e-05	0.00288381	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772166	AGAGAACACACCCAT[C/T]ATCACCCAGAATGAG	54629
rs771931576	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58811077	TAGTATAAACTGCAG[A/G]TGTGGCCCAAGGGGC	54629
rs771933344	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58823533	AAATAAAAAATTAGC[C/T]AGGCACCTCTAGCTC	54629
rs771940907	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58800162	GCCCTCTCTTCCATT[C/T]TTTTGGCCTAAAGTA	54629
rs771962386	snp	A/C	1.66888e-05	0.00288862	intron-variant	FAM63B	GRCh38.p7	15:58854455	AGAATAGTTAGAGTA[A/C]TTTCTTGCTGTATAT	54629
rs771965796	in-del	-/GA			intron-variant	FAM63B	GRCh38.p7	15:58843283	GCCTCCTGAGTAGCT[-/GA]GACTACAGGCATGTA	54629
rs772005974	snp	A/G	1.75496e-05	0.00296217	intron-variant	FAM63B	GRCh38.p7	15:58851972	CAGGCTCAGGTAAAA[A/G]CTAGTGTTTTGAGTC	54629
rs772026956	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58846223	TTGGATTGTTTGTAA[C/G]ACAAACAGTAAATGT	54629
rs772053794	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58848077	AATGAGACAGATGAG[-/A]TTTTTTTTTTTTTTT	54629
rs772085113	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58804657	CAAAAAATACAAAAC[A/G]TTTGCCAGGCATGGT	54629
rs772089892	in-del	-/GGG	1.72958e-05	0.00294068	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772060	GTGCAAGGAGGAGGA[-/GGG]GGGGGAGGAGACCGC	54629
rs772095570	snp	A/G	3.63531e-05	0.00426324	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771710	GCCTCTGAGAGGGCA[A/G]TACAAGGTGACCGCC	54629
rs772103923	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58817877	TTGATGCTAAGCATT[C/T]CTTAAGACTCAGCAA	54629
rs772117221	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849157	GGAAGTTGCAGTGAG[C/T]CAAGATCATGCCATT	54629
rs772138564	in-del	-/AAAAAAA/AAAAAAAAAA			intron-variant	FAM63B	GRCh38.p7	15:58852287	GCAAGACTCCTTCTC[-/AAAAAAA/AAAAAAAAAA]AAAAAAAAAAAAAAA	54629
rs772150878	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58773241	CAATCGCTTGAGCCC[A/C]GAAGTTTGAGACCAG	54629
rs772168712	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58849858	GCAAACACCTCAGCC[G/T]CCTGAGTAGCTGGGA	54629
rs772179950	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58803276	TGGAGACCATCCTTG[C/T]CAACATGGTGAAACC	54629
rs772195560	snp	A/C	1.69017e-05	0.00290699	intron-variant	FAM63B	GRCh38.p7	15:58831742	GATTTTGAAATTATT[A/C]TTCTATCTAATGTTA	54629
rs772200901	snp	A/C			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859507	TAGCGTTCTTAAGTT[A/C]TCTGATAATTTAGTA	54629
rs772241046	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58789721	GGCGTGATCTCAGCT[A/C]ACCGCAACCTCCACC	54629
rs772252190	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58784730	GTTCAAGTGGTGCTC[A/C]CACCTCAGCCTCCCA	54629
rs772266193	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58815129	TTTTTGTATGTGGTT[C/T]GAGGAAAGGGCCCAA	54629
rs772279033	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58807807	CTACAACTTTTCACT[A/T]TTATTTTGTCCCAGC	54629
rs772295845	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58841132	GATTATAGGCGCGCA[C/T]CACCATGTCCAGCTA	54629
rs772340803	in-del	-/ATGTAAAA			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856375	ATAGGATGAATCTGT[-/ATGTAAAA]ATAGAGTCTTATTTA	54629
rs772354083	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58813735	GCACCATTATGCCCC[C/G]TTAACTTGTGTATTT	54629
rs772363600	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58774209	AAGATGAGGCCGGGC[A/G]CGGTGGCTCACGCCT	54629
rs772365008	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58805488	ATGTGTGTATTCATA[A/T]CAAATTTTTAATGAG	54629
rs772438552	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58852682	TCATTTTCCCTATCT[A/G]TAAAATAGAAGAACT	54629
rs772519053	snp	C/T	0.000143403	0.00846647	intron-variant	FAM63B	GRCh38.p7	15:58851735	ATTCTTGGGTAAAAT[C/T]TCATAGCTAATGATG	54629
rs772550336	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58818437	GATTTTTTATTTTTT[A/G]TGAAGACAGGGCCTT	54629
rs772570406	snp	A/G	1.65968e-05	0.00288065	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787955	CTGAGCAGCTGATGG[A/G]ATATTTAGGTTAGTG	54629
rs772572285	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58795790	TCTTTTTTTTGGCCA[C/T]CCTCCCTCCTGCACC	54629
rs772575916	in-del	-/C			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770029	ACAAAAACAAAAAAA[-/C]CATATAAGTATGTAT	54629
rs772592180	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58808669	GAGTGCAGTGGCACA[A/G]TCTTGGCTCACTGCA	54629
rs772596047	in-del	-/C			downstream-variant-500B	FAM63B	GRCh38.p7	15:58862041	ATAAAGAGAAAATTT[-/C]CCCACTCCCAGGAAG	54629
rs772601276	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58808714	GGTTCATGCCATTCT[A/C]CTGCCTCAGCCTCCC	54629
rs772721513	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58794065	GTTGACGAAAGAATC[C/T]AGGGTATGTTGCTCT	54629
rs772723798	snp	A/G	1.85417e-05	0.00304475	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58802321	TTTACAGGAGATTAC[A/G]TGCTTGATGCAAAGC	54629
rs772726246	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58816908	CAGTGCACTATGATA[A/G]CACCTGTGAATAGCC	54629
rs772729267	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58807833	CCAGCCGCACTGGGC[A/C]CCATGCTATTCCATG	54629
rs772777415	snp	A/G	1.82523e-05	0.0030209	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771734	GACCGCCTCCCCGGA[A/G]ACAGCCGTGGCCGGA	54629
rs772804002	snp	A/G	1.77947e-05	0.00298279	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851783	TAGGATTATCTTATG[A/G]CATTATCTCTACAAC	54629
rs772809322	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58794322	ACCATGGGAAATGAG[-/T]TTTCTGAGATAAAGT	54629
rs772814275	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855507	GAACTACCTTGAACC[C/T]TAAATTTTAAGTCAT	54629
rs772849267	snp	A/G	3.3418e-05	0.00408753	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851849	ATCCCGGAAGGAATC[A/G]GTGATTTGGAACTAG	54629
rs772855859	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58788279	GCATGTAGAAAGTGT[A/T]CAAAAATATTGGGTA	54629
rs772879354	snp	A/G			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772418	CATATATCGAAAAGA[A/G]TTGCCCCTAACCTCA	54629
rs772904945	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58787050	GGCTAGGCTGGTCTC[A/G]AACTCCCAACCTCAC	54629
rs772935337	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776221	TTCTCCAGAGAGTAG[C/T]GAGCAATAGTTCTCA	54629
rs772962410	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58839855	TTTTTCTTTTTGGGA[C/T]AGAGTCTCACTCTGT	54629
rs772986384	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58814850	GACACGCTTGAACTC[A/C]CAGGCTGGTCTTGAA	54629
rs773018968	snp	G/T	1.70119e-05	0.00291644	intron-variant	FAM63B	GRCh38.p7	15:58831730	GAATAACTTTTTGAT[G/T]TTGAAATTATTCTTC	54629
rs773044211	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861539	GATACCTAAAACCAT[C/T]TACCCAGCTTAGGGT	54629
rs773053969	in-del	-/AC			intron-variant	FAM63B	GRCh38.p7	15:58787138	CCAGCCCATTTCTTT[-/AC]ACTTTTTTTTTTTTT	54629
rs773072005	snp	C/G	1.78902e-05	0.00299078	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772015	CTGAGGAGGAGGAGG[C/G]CGCGGCGGTGTTGCC	54629
rs773074110	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58813134	CTATCAGTAGTTTGC[A/T]CCTGTTCATTACTGA	54629
rs773078737	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58830281	CAGTACATAAACTTG[A/T]TTTATGTGTGTTTCT	54629
rs773144943	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771338	GTCATGGCGTCCAAG[A/G]CGCTGGCTGCGGAGA	54629
rs773167434	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859653	AAATTGCAAAATAGC[A/G]ATAATGGCATGGGAG	54629
rs773198765	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58811489	TGGTGTAGCATCTTA[C/G]ACCTAGCAACAGCAG	54629
rs773200909	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58785546	TGTGTTCCAAAAAAA[-/C]GTTTATTTAGAAAAA	54629
rs773266959	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58799033	AGCTAAAGAGGTTTG[A/G]GAATCACTGGTGAGA	54629
rs773391457	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58848000	CCTTAGAGGCCAAGG[A/T]AAGGAGGAGTAGTAG	54629
rs773459447	snp	A/G	1.66971e-05	0.00288934	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772199	CGGACCCTGCCCCTT[A/G]CTGGCCATCCTCAAT	54629
rs773463204	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58777921	ACATTTTTGTTTTGC[G/T]TCTTTTTGACTATAT	54629
rs773492031	in-del	-/TAGT	1.67144e-05	0.00289084	intron-variant	FAM63B	GRCh38.p7	15:58854444	GTAAGTCCCTCAGAA[-/TAGT]TAGAGTAATTTCTTG	54629
rs773510290	in-del	-/G			intron-variant	FAM63B	GRCh38.p7	15:58802294	GGCAATTTTACAATT[-/G]CTTTTTTTTTTTTTA	54629
rs773512320	snp	C/T	1.80713e-05	0.00300588	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771493	AAGGGCTACAGGAGA[C/T]CAGGCTCGCCGCTGG	54629
rs773544806	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58783655	AATTACAGAATGGTC[C/T]GGGCATGGTGGCTTA	54629
rs773588839	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58839775	ATTCTCTGTTTATTA[A/G]CTTCATGATTTCATC	54629
rs773600015	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784756	TCCCAAATAGCTGGA[A/G]CTACAGGCACGTGCC	54629
rs773633276	snp	C/T	5.5686e-05	0.00527635	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771568	GGCTGGGGGCGGCGG[C/T]CGCCAGGAGGAGCCT	54629
rs773637311	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58803427	GAGCTGGAATCGCGC[C/T]ACTATGATCCAGGCT	54629
rs773648199	snp	C/T	3.71416e-05	0.00430922	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771767	GGGTCATGAGTTGGG[C/T]ACCGCCGGAGACGCG	54629
rs773658874	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58773272	CCTGGGCAATACAGT[A/G]AGACCCTATATTAAA	54629
rs773726916	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58813803	CCTGTAGAAAAGTTT[A/G]CATTCCCACCAGTAA	54629
rs773767131	snp	C/T	1.89238e-05	0.00307596	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831939	ATAGAAATAGCTATT[C/T]AATCGTGATTCTAAA	54629
rs773780555	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58783478	TCTTTTCCTTTGGAT[C/T]ATCAAAATCATAGGT	54629
rs773821981	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58841238	TCCACCCACCTCAGC[C/G]TCCCAAAGTGCTGGG	54629
rs773867876	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817647	GAATTGCTTGAACCC[A/G]AGAGGCGGAGGTTGC	54629
rs773992902	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58834297	TCTCTTTTCCCCACA[A/G]TATCTCACTCCTTAA	54629
rs774028909	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58776069	TTCACCATGTTAGCC[C/T]GGCTGGTCTCGAACT	54629
rs774029128	snp	A/C	5.11051e-05	0.0050547	intron-variant	FAM63B	GRCh38.p7	15:58810197	CTCGTTTTGATGTTT[A/C]TGAATTAGAACTTTC	54629
rs774035906	snp	C/T	1.70304e-05	0.00291803	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772075	AGGGGGAGGAGACCG[C/T]TCAGGTGCTGGCGGC	54629
rs774049892	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58844260	GGACTAATAATCTCC[A/G]TTGTTGGCCGGGCAC	54629
rs774051563	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58810714	CAGAGTGACTAACAG[G/T]ACTCCCTGAAACCTA	54629
rs774087308	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58817653	CTTGAACCCGAGAGG[C/T]GGAGGTTGCAGTGAG	54629
rs774105028	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58830081	CTTACTCCAAAAGGA[A/T]GGAGGGAAAGAAGAA	54629
rs774110459	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58806679	CCCTAAAGGAAGTTG[A/G]GTGGTTGACAAACAA	54629
rs774111482	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58800062	TATAAAGCGAGGTCA[A/G]TGTTGAAGCATTTTA	54629
rs774116551	snp	C/T			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770719	ACAGAGACTGGAATT[C/T]GTGCAGTGCAGTAAT	54629
rs774167568	in-del	-/TA			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770262	TATGTATCAGGTATT[-/TA]TATGTCTGCGAAGGA	54629
rs774194069	in-del	-/AGC	1.78924e-05	0.00299097	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772014	CTGAGGAGGAGGAGG[-/AGC]GCGCGGCGGTGTTGC	54629
rs774211067	snp	C/T	1.90405e-05	0.00308544	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771829	AAGCAGAACTGACCG[C/T]CGCCGGCTCCGAAGA	54629
rs774212936	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58785887	TTTCACCAAGTTGGC[C/T]AGGCTCGTCTCGTAC	54629
rs774229451	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58842549	GTCACTTTTTAAATT[-/A]AAAGGGGAGGGGGCA	54629
rs774229927	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859284	TTTAGATTCTCTTTG[C/T]CTTTTTCTCCATGGA	54629
rs774231370	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856050	ATATTTATTTAACTT[C/T]ATTATGAGGCCACAC	54629
rs774250683	snp	A/G	2.52567e-05	0.00355355	intron-variant	FAM63B	GRCh38.p7	15:58802281	ACAAGTTTTTAAAAG[A/G]CAATTTTACAATTCT	54629
rs774259562	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58820192	AGTCGCTTGAACCCA[G/T]GAGGCAGAGGTTGCA	54629
rs774312337	snp	A/G	1.65765e-05	0.00287888	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854513	AAGCCTCTCCATCAA[A/G]TGGAAGACAATCTGG	54629
rs774316892	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58821956	ATGAATTTTAAGAAG[C/T]AACCATCCATAGGCT	54629
rs774369522	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58783564	ACTTACAGTTTAAAC[A/G]GAAGGTTTTGTTGTT	54629
rs774390885	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58810020	GACCTCAAGTGATCC[A/G]CCCACCTCAGTGTCT	54629
rs774394847	snp	A/G	1.74579e-05	0.00295443	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851964	CTTCTACACAGGCTC[A/G]GGTAAAAACTAGTGT	54629
rs774452832	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857676	TTAAAGTCTTTCCTT[C/G]CAAGTATTTTGTAAT	54629
rs774456404	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58840243	TACCACACTTCCGAA[C/T]GAATATAGTACAAAC	54629
rs774480268	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58812868	GTCTCAAAATAAATA[A/G]AGAAATAAGTAAATA	54629
rs774496528	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58803116	GCATAACTCATTTGT[C/T]TTGCAAAATTTCTTG	54629
rs774556777	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58773163	AACAAACTGGGTGTG[A/G]TGGTGTGCGCCTGTA	54629
rs774562152	snp	A/T	1.80651e-05	0.00300536	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771636	CCCGGACCCTGCAGC[A/T]CCTCCGCGGGTTTGG	54629
rs774631747	snp	C/T	1.71882e-05	0.00293152	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854625	ACAAGTGTTGGCTTC[C/T]GTTGGAACCACCTAT	54629
rs774649945	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58780618	GAAATGGACTTCATG[A/C]TTCCTTAGATCGATT	54629
rs774704093	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58825220	TTTAAGGGAAAAGAA[A/G]TGTTATTTAGCAAAT	54629
rs774717829	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58852063	AGGCTGAGGCAGGCA[A/G]ATTGCTTGAGCCCAG	54629
rs774732941	in-del	-/TTC	3.32519e-05	0.00407736	intron-variant	FAM63B	GRCh38.p7	15:58854473	TCTTGCTGTATATTT[-/TTC]TTAAAGCAGGGCCAG	54629
rs774775231	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793300	TACTAAAAATACAAA[A/G]AATTAGTCGGGTGTG	54629
rs774780306	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58823794	AAGAAGCAATAAAAA[C/G]TATTACAAAAGTATA	54629
rs774780691	snp	A/C	1.68937e-05	0.0029063	intron-variant	FAM63B	GRCh38.p7	15:58847291	CTTTTGTTACTTCTT[A/C]TTAAGGGTCAACTGT	54629
rs774797262	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58782269	ATATATAAATGCTAC[A/G]TATATACACACATGT	54629
rs774811219	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58844005	TAATGCATTAAAACC[-/C]TATTCTATATTATTA	54629
rs774940535	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58836864	GGCTCAAGCAGTCTG[C/T]CCAACTCAACCTCCC	54629
rs774944345	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58853672	AAAAATATAAAAAAT[A/T]AGCTGGGTGTGGTGG	54629
rs774990845	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58815783	CTCCCGGGTTCAAGT[C/G]ATTTTCCTGCCTCAG	54629
rs774992890	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58829758	GGCTGTAGACCTCTT[C/T]ATAGTTTTTGTACTT	54629
rs775085372	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58774344	AAAAAATTAGACGGG[A/C]ATGGTGGTGGGCACC	54629
rs775146620	snp	C/G			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770528	AGTGAAGCCAAGTTA[C/G]CAAAACCGCAAAGAC	54629
rs775161605	snp	C/T	1.75844e-05	0.00296511	intron-variant	FAM63B	GRCh38.p7	15:58851974	GGCTCAGGTAAAAAC[C/T]AGTGTTTTGAGTCTT	54629
rs775171731	snp	C/T	5.4536e-05	0.00522159	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771467	AGCGTCAGGGACAGG[C/T]TCTTCGCAGGAAGGG	54629
rs775174435	snp	C/G	3.79564e-05	0.00435623	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771832	CAGAACTGACCGCCG[C/G]CGGCTCCGAAGAGCC	54629
rs775229500	snp	C/T	1.92443e-05	0.0031019	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771890	TTGCAGCGACCCGAG[C/T]CCTCCTGGGGAATCT	54629
rs775253275	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58796970	GATTGAGTCAAATTG[G/T]ACTCATTTACTATTC	54629
rs775255094	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58842856	CCCTAAGTAACTTGC[C/G]CAAGACCATTTAGCT	54629
rs775256599	snp	C/T	9.24582e-05	0.00679857	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771951	AACCTGCATTCTTTT[C/T]CCAGTAGCTGCGAGT	54629
rs775286624	snp	C/T	1.69135e-05	0.002908	intron-variant	FAM63B	GRCh38.p7	15:58810212	CTGAATTAGAACTTT[C/T]CCCTTTTCTATTTTC	54629
rs775329424	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58834245	GGAGTCTCCTATGTC[C/T]ACTTTCTGCACAGAC	54629
rs775348101	snp	C/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856638	ATATACTACAGAACT[C/G]TCTATTGGCTCAAAC	54629
rs775378401	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58834430	TCTCCTCAAACCAGT[A/G]GTTCTCAACCCAAAT	54629
rs775458968	in-del	-/ATG			intron-variant	FAM63B	GRCh38.p7	15:58805470	ACAGCACAAGAAAAC[-/ATG]ATGTGTGTATTCATA	54629
rs775469664	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58789608	GACTGCACGCACATG[C/G]TACCACACCCAGCTA	54629
rs775482485	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58833381	ACCTGTGGGTGTTTC[G/T]CATTAGGTGGAACAA	54629
rs775494585	snp	A/G	1.66454e-05	0.00288486	intron-variant	FAM63B	GRCh38.p7	15:58854467	GTAATTTCTTGCTGT[A/G]TATTTTTCTTAAAGC	54629
rs775537374	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58818952	AGCCTATTGATCTTG[C/T]GTTTATTATTGTAGT	54629
rs775549330	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58800443	AGCCAAACTTATCAG[C/T]ATATTATTTAGGATT	54629
rs775549688	snp	C/T	1.65743e-05	0.00287869	missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810321	GAGTGTTTGAATATA[C/T]ACCAGAATGCATAGT	54629
rs775586461	snp	G/T			downstream-variant-500B	FAM63B	GRCh38.p7	15:58861956	TTAAGAAAGATGAGC[G/T]GGGAGATGGGGAACT	54629
rs775588661	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769688	GCTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC	54629
rs775613801	snp	G/T	1.73267e-05	0.0029433	missense, intron-variant, downstream-variant-500B, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831911	AGCACCATGACCAAA[G/T]ACAAGGTATGATATA	54629
rs775613942	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58823604	CAGGAGGTCAAGGCT[C/G]CAGTGAGCCAATATC	54629
rs775638069	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58793928	TGGGTGTTACCTTTG[A/G]GGTTAGTGAAACCAG	54629
rs775639880	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58812811	TGCAGTGAGCTGTGA[A/T]CACACTACTGCGTTC	54629
rs775665148	snp	A/G	1.73661e-05	0.00294665	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854643	TGGAACCACCTATAT[A/G]TCTTGAGAAACAAAA	54629
rs775710524	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58845329	GAGAATCACTTGGAC[C/T]TGGTAGATGGAGGTT	54629
rs775764524	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58822317	AGGTTTTTCCTAGAA[C/T]TCTTTTTCATTTAAC	54629
rs775791907	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58781032	GTGAATTCTGAATGG[A/G]AGATGCCTTCTTTTA	54629
rs775819151	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58805764	TTTGTTTGGTTTATC[A/G]GTTGTTGTTTTTTAT	54629
rs775826868	in-del	-/AT			intron-variant	FAM63B	GRCh38.p7	15:58831038	TGTGTGTGTGTGTGT[-/AT]GTGTATATATATATA	54629
rs775837482	snp	C/T	2.26267e-05	0.00336346	intron-variant	FAM63B	GRCh38.p7	15:58851749	TCTCATAGCTAATGA[C/T]GGTTATAATTTAATT	54629
rs775839019	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58837393	GCCTGGACAACATAG[A/G]AAGACCCCATCTCAA	54629
rs775842560	in-del	-/TGTG			intron-variant	FAM63B	GRCh38.p7	15:58831015	TATATGAAGATCAGT[-/TGTG]TGTGTGTGTGTGTGT	54629
rs775909312	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58803522	TGCATTATATCATAA[A/G]ATAGGAAATCTAGGC	54629
rs775927116	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58836644	TTTTCCCTGAAACAG[A/G]GTCTTGCTCTGTCAC	54629
rs775950318	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58792955	TGCAATGAGCTATGA[C/T]CATACCACTGCATTC	54629
rs775964289	snp	C/T	1.65987e-05	0.00288082	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787959	GCAGCTGATGGAATA[C/T]TTAGGTTAGTGTTGA	54629
rs775975297	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58851012	TGAGTCTTCCTCTGT[C/T]GCCCAGGCTGGAGCG	54629
rs775987064	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58854243	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGG	54629
rs776005436	snp	C/T	0.000129734	0.00805296	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771598	TCCCGGACTCGGCTT[C/T]TCCCGCGGGCTCTCC	54629
rs776026867	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58826213	TTTTCTTTTTTTCTG[C/T]ATTCACACAATCTTT	54629
rs776032962	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58797147	TTTGGTTAAAAAAGA[A/G]TATCAGTAATTTAAA	54629
rs776048269	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58841325	TCAATTTTGGGGGCC[A/G]GATACAGTGGCTTAC	54629
rs776142115	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58783919	CCACTGCACTCCAGC[C/G]TGGACGATAGAATAA	54629
rs776145192	snp	A/T	6.64901e-05	0.00576547	intron-variant	FAM63B	GRCh38.p7	15:58851752	CATAGCTAATGATGG[A/T]TATAATTTAATTTAT	54629
rs776166130	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58850813	GCTGGTCTCAAACTC[C/T]TGGGCTCAAGCAGCC	54629
rs776177503	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58796167	GGGTATGGGAAGTGG[A/G]TAAGGAGTAGGAAAA	54629
rs776196679	snp	A/G	3.32176e-05	0.00407526	intron-variant	FAM63B	GRCh38.p7	15:58787987	TGAAAAGTGGATTTT[A/G]TATCTCTTTCAAAAC	54629
rs776220227	snp	C/T	3.31934e-05	0.00407377	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847441	GATCCTGAAACTGTA[C/T]ACAAAGGACAACAAG	54629
rs776254659	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58809923	TAGCTGGGACTACAG[A/G]CGCATGCCACCATGC	54629
rs776364356	snp	C/T	1.65902e-05	0.00288008	stop-gained, nc-transcript-variant	FAM63B	GRCh38.p7	15:58854497	CAGGGCCAGCCAGCA[C/T]AAGCCTCTCCATCAA	54629
rs776393870	in-del	-/CTAT			intron-variant	FAM63B	GRCh38.p7	15:58774558	CCCTCGTGTAGCTGA[-/CTAT]CTAGTGGGATGACAG	54629
rs776397217	snp	C/T	1.6722e-05	0.00289149	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851838	ATTGGGAACAAATCC[C/T]GGAAGGAATCAGTGA	54629
rs776411856	snp	A/G	1.68023e-05	0.00289843	missense, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854579	AAGATAAAGAAAAAG[A/G]AAAGGAAAAAAATAG	54629
rs776419878	snp	C/T	1.66515e-05	0.00288539	missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810360	TTCTTGATATTCCTT[C/T]GTACCATGGGTGGTT	54629
rs776444836	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58789380	TAATTTGTCTCTACC[C/G]TTCCAGGCAACTAGT	54629
rs776463923	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58806097	AACAAAAGAAAAGAC[-/AA]AGTCTCCCTCTGTTG	54629
rs776481683	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58822115	AAAAATTAGTTGGCC[A/G]TGGTGTTGCATGCCT	54629
rs776484790	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58847557	AATTTTTCAACTAAA[G/T]ATTAATTCATCAATA	54629
rs776525512	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58817884	TAAGCATTCCTTAAG[A/T]CTCAGCAATTTGGCA	54629
rs776539303	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812630	TTTGGGAGGCCAAGG[C/T]AAGAGGACCACTTGG	54629
rs776540326	snp	A/C	1.66319e-05	0.00288369	missense, intron-variant	FAM63B	GRCh38.p7	15:58821750	GCTGTTGGTAACTGC[A/C]GCTACAACCAACTAG	54629
rs776552840	in-del	-/CTCA	1.67181e-05	0.00289115	frameshift-variant, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772208	CCCTTGCTGGCCATC[-/CTCA]CTCAATGTTTTGCTC	54629
rs776622905	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58846694	AATTTGTATGCACGT[A/T]CAGAGTTTATGTGAT	54629
rs776630669	snp	G/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858301	CTACTTATCCCATAT[G/T]CTGTTTCAAATTCTT	54629
rs776654683	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58822213	GAGCCGAGATTGCGC[C/T]GCTGTACTCCACCCT	54629
rs776755868	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58831486	GTGTCTGCTTTTTTA[C/G]TGCAACCTGCATGAA	54629
rs776771403	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58836373	CAGAATAGTTCTATG[G/T]ATGGTTTGTTCAAAC	54629
rs776798597	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58800836	TAAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA	54629
rs776804667	snp	C/G	1.66291e-05	0.00288345	intron-variant	FAM63B	GRCh38.p7	15:58831764	CTAATGTTATGCATT[C/G]GTTCTATAGGCTTTG	54629
rs776807370	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58780850	CTGCTACTACCCTAG[C/T]TCAGGCCTTTATCTC	54629
rs776821621	snp	C/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772775	GCATTGGTCTGAGAC[C/T]CAATTACCGTAACTT	54629
rs776833295	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58792678	AAACAACCGAAATGT[C/G]TTATCAACTGATGAG	54629
rs776838185	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58797266	TATCCCAGCACTTCG[C/T]GAGACTGAGGCAGGC	54629
rs776856734	snp	G/T	1.87362e-05	0.00306068	intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58831935	TGATATAGAAATAGC[G/T]ATTTAATCGTGATTC	54629
rs776897534	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58799346	GCCGAGGCAGGCGGA[C/T]CACGAGGTCGGGAGA	54629
rs776910100	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58834850	AAGCCGTTGCTCTCC[A/C]ATTCCTATCTTAGTT	54629
rs776920141	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58826225	TGTATTCACACAATC[-/T]TTTTTTTTTTTTTTT	54629
rs776928267	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58820542	TTGTTTACTCAACCA[A/G]TCATCAGTTCCAGTT	54629
rs776955313	snp	A/G	4.46399e-05	0.00472419	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771384	CATAGAGCTGGGGGC[A/G]GGCGGCCCGGTATGG	54629
rs776970147	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58774311	AACATGGTGAAACCC[C/T]GTCTCTACTAAACAT	54629
rs776987019	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58827342	GTTATTACTGTGGTG[G/T]TTATAATTTCTGTTA	54629
rs777023175	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58774842	GGTAAACGAAATGGT[A/G]GTAATAGCAGGACAT	54629
rs777026801	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58843906	AGTAGAAGAAAACTT[A/G]TCAAATTTAATAATA	54629
rs777038305	snp	A/C	1.66427e-05	0.00288462	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772174	CACCCATCATCACCC[A/C]GAATGAGAACGGACC	54629
rs777042098	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58814082	AGCTGGGATTACAGG[C/T]GCCCACCACCATGCC	54629
rs777050477	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58805970	TCCCAGCTACTCGAG[A/G]GGCTGAGGCAGATGG	54629
rs777065911	snp	C/T	1.8238e-05	0.00301972	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771727	ACAAGGTGACCGCCT[C/T]CCCGGAGACAGCCGT	54629
rs777105070	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58842752	TATATTAAGCATTTT[A/G]TATGGATTATCTCAT	54629
rs777128810	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58808230	GCCACATCATTATCA[C/T]CCAGAGTCTATAATT	54629
rs777137950	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58789200	AAAATTAGCTGGGCA[C/T]GGTGGCAGACGCCTG	54629
rs777239480	snp	C/G	5.99431e-05	0.0054743	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771348	CCAAGGCGCTGGCTG[C/G]GGAGAAGTGGCCGCG	54629
rs777240344	snp	A/G/T			intron-variant	FAM63B	GRCh38.p7	15:58773644	TTCCTTTGGTATGGC[A/G/T]TAGTCCTAGAAAACT	54629
rs777282592	in-del	-/TAG	0.000117609	0.00766749	intron-variant	FAM63B	GRCh38.p7	15:58831747	GAAATTATTCTTCTA[-/TAG]TCTAATGTTATGCAT	54629
rs777283654	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58807905	GAATGCTCTTTGCCC[A/C]GAGCTTCCTAACATT	54629
rs777319598	in-del	-/TTAC			intron-variant	FAM63B	GRCh38.p7	15:58833051	AAAACATTTACTGTT[-/TTAC]TCTTTTTATCTCTTA	54629
rs777362398	snp	A/G	1.87908e-05	0.00306514	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771444	GAACACGGGGTGGCG[A/G]CCGGGCCAGCGTCAG	54629
rs777370355	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58811940	TATTTTCACTTACTT[-/A]ACATTTTTTAACATA	54629
rs777384114	in-del	-/AAG			intron-variant	FAM63B	GRCh38.p7	15:58789285	TAGCTTGCAGTGAGC[-/AAG]CGAGATTGCACCACT	54629
rs777386086	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58790087	CCCGGCAGGAAGACC[A/C]TTTTTAGAAAATATA	54629
rs777412032	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58796679	TAGGCACCGCCACCA[G/T]GCCCAGCTAATTTTT	54629
rs777438357	in-del	-/GAG	0.000126683	0.00795773	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772001	GAGAACAGGGTCCCT[-/GAG]GAGGAGGAGGAGGGC	54629
rs777449590	in-del	-/AAAAT			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860211	AGAGAAGGACAAAAC[-/AAAAT]GTTTTGGAAGGTGAT	54629
rs777455607	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58784621	TCTTTCTTTCTTTCC[-/T]TTTTTTTTTTTTTTT	54629
rs777476634	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58844756	ACTCCATCTCTACTA[A/C]AAATACAAAAATTAG	54629
rs777521400	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58812593	GGCTGGACACAGTGG[C/T]TCATGCCTGTAATCC	54629
rs777551191	snp	G/T	1.69329e-05	0.00290967	intron-variant	FAM63B	GRCh38.p7	15:58847289	TTCTTTTGTTACTTC[G/T]TATTAAGGGTCAACT	54629
rs777551361	snp	A/T	0.000119678	0.00773463	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851938	ACAAGCAGCAGCTGC[A/T]GCTGCTGCTGCTTCT	54629
rs777572292	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58813431	AACCCAAGAGGTGGC[A/G]GCTGCAGTGAGCCAA	54629
rs777612618	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58832650	CTACTGCCTCAGCCT[A/C]CCGAGTAGCTGGGAT	54629
rs777612709	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58848472	TAATTCTCCGGGTGC[C/G]GTGGCTCACACCTGT	54629
rs777638278	snp	G/T	1.75894e-05	0.00296553	intron-variant	FAM63B	GRCh38.p7	15:58847254	TATATTACTAGTTTT[G/T]ATCAATTTAACAGTC	54629
rs777643086	in-del	-/GTG			intron-variant	FAM63B	GRCh38.p7	15:58794359	AAAGTTTTTTTTGGG[-/GTG]TGTGTGTGTGTGTGT	54629
rs777653273	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58801879	CACCTCAGCCTCCCA[A/T]AGTGCTGGGATCACA	54629
rs777705700	in-del	-/TG			intron-variant	FAM63B	GRCh38.p7	15:58804153	AAAAGAAAGGAAATC[-/TG]TAGCTAAAGCCAGAT	54629
rs777706371	snp	C/T	1.69289e-05	0.00290933	synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831898	GAATAATCATTTTAG[C/T]ACCATGACCAAATAC	54629
rs777708957	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58783107	TGTATTTTTAGTAGA[A/G]ACGGGATTTCACCAT	54629
rs777750453	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58824616	TGGAAAATAAAAGAC[A/C]GTAATAGACATTTTT	54629
rs777797619	snp	C/T	5.13053e-05	0.00506458	intron-variant	FAM63B	GRCh38.p7	15:58847490	ATTTGTATTGTCGTC[C/T]TTATAGTGGTTAAAA	54629
rs777800610	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58780217	TGAGACCAGCCTGAC[C/G]AACGTGGAGAAACCC	54629
rs777828067	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58786422	TCCTGGAATGTGCTC[A/G]TCACTGTCAGCTAAA	54629
rs777860337	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58782308	ACTGCATATTTCAAA[-/T]TAGTGAAATTTTGAC	54629
rs777903757	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58774772	AGATACTGAAGCAGA[A/G]AAGGGTTTCTTCTAC	54629
rs777915927	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58809614	CTTTGACTTGAAAAA[-/C]ATTTGACTTTGGACT	54629
rs777936320	snp	C/T	1.65674e-05	0.00287809	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58847391	ATGGTGATGGAAATT[C/T]CTGTGACTCAGAATT	54629
rs777963654	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58842675	ACAGAAATTGAGATC[A/G]ATTTAGATGATACTC	54629
rs777976397	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58816115	GGAATGCAGCATACA[C/T]GTGTGCATCCATTAA	54629
rs778017521	snp	A/G	1.65699e-05	0.00287831	synonymous-codon, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810289	CCTGGATGTAAATGT[A/G]AGATTCACTGGTGTT	54629
rs778028962	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58805912	AACCCCATCTCTACT[A/G]AAAATACAAAAAATT	54629
rs778074754	snp	A/G	0.000151808	0.00871098	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771818	CGGCACCTGCCAAGC[A/G]GAACTGACCGCCGCC	54629
rs778079953	snp	G/T	1.69502e-05	0.00291115	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772280	GCTTTTGGGGTGGAG[G/T]AAAACGGGGTGAGGG	54629
rs778160363	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58788662	AATTTATATATTTAT[A/G]CTATCACCAAATAGG	54629
rs778204259	snp	G/T	1.65987e-05	0.00288082	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787923	GAAACTTCCACCGAT[G/T]ATGGAAATCATAACT	54629
rs778232003	in-del	-/TGAA			intron-variant	FAM63B	GRCh38.p7	15:58782806	CCTTAGTTTATTCTT[-/TGAA]TGGAGGTAATAATGC	54629
rs778237916	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58787981	TAGTGTTGAAAAGTG[A/G]ATTTTATATCTCTTT	54629
rs778245707	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855195	ACATTTTAGGTATTA[C/T]CTTGATCATGGAGCT	54629
rs778246542	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58830913	AACAAGCATGAAAAT[A/G]CTGCAAGTATTGATT	54629
rs778317699	snp	G/T	1.67103e-05	0.00289048	intron-variant	FAM63B	GRCh38.p7	15:58854444	GTAAGTCCCTCAGAA[G/T]AGTTAGAGTAATTTC	54629
rs778371289	in-del	-/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859053	CTTGAATGTGCACAC[-/T]TTTTTTCTCAATAAC	54629
rs778398259	snp	C/T	1.9347e-05	0.00311017	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771869	CGCCGGCGGCCTCAG[C/T]AGCAGTTGCAGCGAC	54629
rs778400210	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58809811	TTGAGACAGAGTCTC[A/G]CTCTGTTGACCAGGC	54629
rs778431166	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770111	GCTCCGTGATCCACT[A/G]TGGCATCTCCAGTGA	54629
rs778491215	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58798736	GCTGGGATTACAGAC[A/G]TCAGCCACCACGCCC	54629
rs778502490	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58832440	CTCCATGTTGGTCAG[G/T]CTGGTGTCAAACTCC	54629
rs778530187	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58787738	CGAGAGTCCGTCTCA[-/A]AAAAAAAAAAAAAAA	54629
rs778538364	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58774231	CTCACGCCTGTATTC[C/G]CAGCATTTCGGGAGG	54629
rs778542103	snp	A/T			intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772654	ACTAAGTTTTCATGG[A/T]TATATTTAGTTTGAT	54629
rs778561193	in-del	-/TGTA			intron-variant	FAM63B	GRCh38.p7	15:58846980	TATTTTTCAGGAATT[-/TGTA]TGGTATTTTTCTATT	54629
rs778561233	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58780597	AATGATAAAGTCAGA[A/G]AAGCAGAAATGGACT	54629
rs778614769	snp	A/C/G	3.32338e-05	0.00407627	synonymous-codon, missense, nc-transcript-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854545	AATAGTGAACGTAAA[A/C/G]GGAAGGAACCACGAG	54629
rs778649851	snp	A/G	4.9708e-05	0.00498513	missense, intron-variant, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810306	GATTCACTGGTGTTC[A/G]AGTGTTTGAATATAC	54629
rs778687261	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58824410	CATATTTATTACTTC[C/T]TTGATATATAAATTT	54629
rs778701494	in-del	-/GAGTAGTC			intron-variant	FAM63B	GRCh38.p7	15:58779861	TTCTCCCCTTGGTAT[-/GAGTAGTC]GAGTAGTCTTTTAGT	54629
rs778783996	snp	A/T	3.37058e-05	0.00410509	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772250	GGTACATTCTGCAGC[A/T]TTCTACTTCCTACAG	54629
rs778800639	snp	C/T	5.19827e-05	0.00509791	intron-variant	FAM63B	GRCh38.p7	15:58847270	ATCAATTTAACAGTC[C/T]TTTTTCTTTTGTTAC	54629
rs778809055	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58781675	TTTGGGAGGCCAAGG[C/T]GGGTGGATCACAGTG	54629
rs778845755	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58844988	ACATTTGCAAACTAC[C/T]TATGTGACAAGGGAT	54629
rs778853942	snp	C/G	0.00021597	0.0103893	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58772139	TCACATCAAGTGGAT[C/G]CAGTGGAAGGAAGAG	54629
rs778934209	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58807080	TTTGTAACCTAAATT[C/T]GTCTTTTTCAAATTT	54629
rs778935083	snp	A/G	7.90378e-05	0.00628591	intron-variant	FAM63B	GRCh38.p7	15:58802268	TGTAATCAGAAAAAC[A/G]AGTTTTTAAAAGGCA	54629
rs778968248	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58836237	AATTAACTATAATTC[-/T]TTTTTTTTTTTTTTT	54629
rs779036113	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58784477	CTTTGTTCAAATTTT[A/G]CGGAGAATATTTAAA	54629
rs779036480	in-del	-/AA			intron-variant	FAM63B	GRCh38.p7	15:58846921	TGTAGGCTTAATTGG[-/AA]AAAAAAACAGGCAAC	54629
rs779072508	snp	C/T	1.65946e-05	0.00288046	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58787941	GGAAATCATAACTGC[C/T]GAGCAGCTGATGGAA	54629
rs779080216	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855094	GGATTCAAAAAAACA[A/G]AAACAAAAGAATAGG	54629
rs779087545	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58827804	TGATGCTTTAATTGT[G/T]CTAAATGTGATATGG	54629
rs779088845	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58774064	GCAGAAATTCAGAGG[A/C]AAGGGCAAGTACTGT	54629
rs779127539	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58819398	GGCTGCAGTGGGCTG[C/T]GATCACGCCACTACA	54629
rs779131249	in-del	-/TGATTTTGTTTTT			intron-variant	FAM63B	GRCh38.p7	15:58821584	TGTTGATTTTAGTGC[-/TGATTTTGTTTTT]CGTAAATAATAGTTT	54629
rs779181948	snp	A/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855961	AAGAATTTATGTAAA[A/T]GCAATCAGAGTTTTT	54629
rs779237308	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58842132	CTATTATGACTTCTT[C/G]ATTGTCCTTTTACCA	54629
rs779239155	in-del	-/TGT			intron-variant	FAM63B	GRCh38.p7	15:58831384	CTATTGGGAGGTAGC[-/TGT]TGACTGACATTTTTC	54629
rs779265537	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58841107	ATGCCTCAGACTCCT[A/G]AGTAGCTGGGATTAT	54629
rs779270459	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58795689	GATTACAGGCGTGAG[A/C]CACTGCGCCCAGCCT	54629
rs779282834	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58809717	ACTTGACATTGTTTT[A/G]TATATATACATGTTT	54629
rs779435402	snp	A/T	1.73033e-05	0.00294132	intron-variant	FAM63B	GRCh38.p7	15:58847505	TTTATAGTGGTTAAA[A/T]TGCTGATTTTTTTCA	54629
rs779444438	snp	A/G	1.9316e-05	0.00310767	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771877	GCCTCAGCAGCAGTT[A/G]CAGCGACCCGAGCCC	54629
rs779471998	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58841336	GGCCAGATACAGTGG[C/G]TTACGGCTATAATCC	54629
rs779477129	in-del	-/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769455	AAAAAAAAAAAAAAA[-/G]GGGGCACAGTCTTCT	54629
rs779497209	snp	C/G	1.83994e-05	0.00303305	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771962	TTTTCCCAGTAGCTG[C/G]GAGTTCAATAGTGAG	54629
rs779515745	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58790933	GCCTGTAATCTCAGC[A/T]GTTTGGGAGGCCGAG	54629
rs779533761	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58781438	CATATAAAATAAGAC[A/G]TTCTTGCAAATTTAA	54629
rs779540905	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58818268	TGAATGGAATTCTGG[C/G]GGTGGGGGAAGACAA	54629
rs779551340	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58776850	AATATAGTGAGACCC[A/C]CATCTCTGTAAAAAA	54629
rs779570592	in-del	-/A			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770653	CTTTCCTGTAGGGCG[-/A]ATGTCTCACCAGTAG	54629
rs779577572	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860691	AAGCAGTTCTAACTA[A/G]TGCAATGTGTTTTTT	54629
rs779622865	snp	A/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859173	ACAGTTTTTTGTGTG[A/T]TCTATAGACTATAGA	54629
rs779627832	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58828156	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAT	54629
rs779628885	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58845837	AAGAAAATGTGGTAC[A/C]CATACACAACGGAGC	54629
rs779641245	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58823095	GAAAATAAGAAGAAA[A/G]TGCATAGTATTTTAG	54629
rs779693868	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58811336	TATTAGTCTAGCAAT[C/G]CAGATTTTGCCTCTT	54629
rs779800022	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58790670	AACAAGGTAAAATAA[A/G]TGAAGTTTGTAAGAA	54629
rs779859903	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58836144	CTCAATCTCCTGATC[C/T]CGTGATCTGCCTGCC	54629
rs779903527	snp	A/C	1.67253e-05	0.00289178	missense, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854565	GGAACCACGAGAAAA[A/C]GATAAAGAAAAAGAA	54629
rs779915824	snp	A/G	1.82533e-05	0.00302098	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771616	CCGCGGGCTCTCCTG[A/G]GGTTCCCGGACCCTG	54629
rs779976761	snp	G/T	1.8582e-05	0.00304806	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771554	CAGCGGCGGGAATGG[G/T]CTGGGGGCGGCGGCC	54629
rs780001346	in-del	-/GCT	0.000545312	0.0165033	cds-indel, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851933	CAGGAACAAGCAGCA[-/GCT]GCTGCTGCTGCTGCT	54629
rs780014715	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58849737	GACAAGATCTTTCCA[A/G]GCAACAACCTTTTTT	54629
rs780020877	snp	A/G/T	8.45321e-05	0.00650075	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772264	CTTTCTACTTCCTAC[A/G/T]GCTTTTGGGGTGGAG	54629
rs780022153	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58796663	TGAGTAGCTGGGATT[A/G]TAGGCACCGCCACCA	54629
rs780073430	snp	A/G	1.84188e-05	0.00303464	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771752	AGCCGTGGCCGGAGT[A/G]GGTCATGAGTTGGGT	54629
rs780130595	snp	A/G	1.68977e-05	0.00290665	intron-variant	FAM63B	GRCh38.p7	15:58802404	TTTTTGTTAAAGTAT[A/G]TAATTTTAAAGTTTA	54629
rs780140528	in-del	-/TTT			intron-variant	FAM63B	GRCh38.p7	15:58838582	GCTACTTTTTAGGGA[-/TTT]TTTTTTTTTTTTTTT	54629
rs780157372	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58795369	ATGGCTCACTTCAGG[A/G]CATTTTAATACTGTA	54629
rs780173235	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58787778	ATAAAGATTCTAATA[C/T]ATGTGAATGTTAATG	54629
rs780199032	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58816015	TGGTTAACTGTCATC[G/T]CCCACTAGAATATAG	54629
rs780267433	snp	C/T	8.30517e-05	0.00644352	intron-variant	FAM63B	GRCh38.p7	15:58787985	GTTGAAAAGTGGATT[C/T]TATATCTCTTTCAAA	54629
rs780268244	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58811327	CCTTTGGTATATTAG[G/T]CTAGCAATCCAGATT	54629
rs780271404	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58831594	GGAATGTCTGTATAC[A/G]CATATTTCATTGCAA	54629
rs780272243	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58777842	TGCCCCAGCTAGTCT[C/G]AAACTCCTGGGCTCA	54629
rs780307827	snp	A/C/G			intron-variant	FAM63B	GRCh38.p7	15:58783238	TGACTTCTTTTTTCT[A/C/G]AAGAGCAGAGACTGG	54629
rs780350091	snp	A/G			intron-variant, downstream-variant-500B	FAM63B	GRCh38.p7	15:58832301	GCGTGATCTCGGCTC[A/G]CTGCAACCTCTGCCT	54629
rs780350145	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58817513	GGTGGATCACCTGAG[A/G]TCAGGAGTTTGAGAC	54629
rs780411927	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58853528	TTTCTCCTTTTAAAA[C/T]CTGTTTATTATGGCT	54629
rs780438110	in-del	-/CTCCCTCT			intron-variant	FAM63B	GRCh38.p7	15:58808025	TCCCCACTCCCCTCC[-/CTCCCTCT]CTCCCTCTCTCCCTC	54629
rs780458157	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857448	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	54629
rs780513424	in-del	-/AAAG			intron-variant	FAM63B	GRCh38.p7	15:58833620	CATCATAAACAAGGT[-/AAAG]AAAAAAGTGCTGTGC	54629
rs780535245	in-del	-/CAGCAGCGCCGGCGGCCT	1.91408e-05	0.00309354	cds-indel, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771847	CGGCTCCGAAGAGCC[-/CAGCAGCGCCGGCGGCCT]CAGCAGCGCCGGCGG	54629
rs780551648	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58779600	GGTTCCATCTTAGCC[C/T]CTGCCCACCTTGTTT	54629
rs780606569	snp	A/G			upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58770428	TTGTCTTTCTTCTTT[A/G]AAAACTGCATGGCCT	54629
rs780617990	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58856684	CAAGTTTACTCTTGA[C/T]ATCACTCTGTTGGCT	54629
rs780644145	in-del	-/G			intron-variant	FAM63B	GRCh38.p7	15:58806887	GAAAATATGTTGTTT[-/G]GGGGGGAACAGTAGA	54629
rs780659564	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769559	GGCATGGTGGCTCAC[A/G]CCTGTAATCCTAGCA	54629
rs780697864	snp	C/T	1.65968e-05	0.00288065	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	FAM63B	GRCh38.p7	15:58831849	GTGAACTAACTTCAA[C/T]GGTTCAGGAAGGAGA	54629
rs780789395	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58780430	GAAAGAAAATTGAAG[C/T]GCATAAAGTTTAAAT	54629
rs780841442	in-del	-/AAAT			intron-variant	FAM63B	GRCh38.p7	15:58829090	CTCTGATAAGTTTAC[-/AAAT]AAATAAACTGCTGTG	54629
rs780864154	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58849670	TTCAGAAGAACTTGA[A/T]GGACAAATTCTTTAT	54629
rs780930651	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58802975	GAAGGCAAGAAGGAA[C/T]TGGCTTCTTAGAGTG	54629
rs780952893	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58800795	AGTCGTGATCACGCC[-/A]CTGCACTCCAGCCTG	54629
rs780966009	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58782167	AAAGCTTCTCTTTGA[C/T]TCCCATTAATACTTC	54629
rs781000300	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58804583	GAGGCCAAAGCAGGC[A/G]GATTGCTTGAGCCCA	54629
rs781046356	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58813499	AGACTCTATCTCAAA[A/C]TGCTGTAAACATTTG	54629
rs781052905	snp	A/C/T			intron-variant	FAM63B	GRCh38.p7	15:58834123	CCTTAATCCATTTAA[A/C/T]CCTTAGTTGACACAG	54629
rs781084653	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58833471	AGGGGACCAGCGTTC[A/C]GCATGCGGAGGATCC	54629
rs781111103	snp	C/T	3.6297e-05	0.00425995	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771627	CCTGAGGTTCCCGGA[C/T]CCTGCAGCTCCTCCG	54629
rs781111164	snp	A/G	0.000188875	0.00971607	intron-variant	FAM63B	GRCh38.p7	15:58796174	GGAAGTGGGTAAGGA[A/G]TAGGAAAAGGCTTAA	54629
rs781125726	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58849519	CAAAAAAGAAAAAAA[C/T]TGGAGAAGGGGAATG	54629
rs781142353	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58838891	CGGCCTAATTTTTAT[A/T]ACGACTTTTCAGAGG	54629
rs781150334	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58808213	ATTGATAAACTGGCA[A/G]TGCCACATCATTATC	54629
rs781214009	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58784397	GGGTAGGACATTTTC[C/G]TAGATAATAAAAATT	54629
rs781217733	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58772997	AAAAATAGGTATGTT[A/G]AGGACTCAGAGCGAG	54629
rs781232058	snp	C/T	3.62404e-05	0.00425663	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771696	GCTGCCGCCGAGGCG[C/T]CTCTGAGAGGGCAGT	54629
rs781234468	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58801730	CTGCAGCCTCCACCT[C/T]CCAGGTTCAAGCGAT	54629
rs781241864	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58776592	GCTGAAAATGACAGG[G/T]GTAGGGACAAGGTCA	54629
rs781285275	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58804669	AACGTTTGCCAGGCA[C/T]GGTGGCACACGCCTA	54629
rs781319613	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58838283	TGTGCCCGTAATGCC[A/G]GCTACTCAGAAGGCT	54629
rs781339067	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58803004	GGAAGGAAGTATTAG[-/C]CCAGGGAAGAAAGAG	54629
rs781424246	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58788444	TTACATTAGTAAGCA[C/T]ACTGTTTATTTCAAC	54629
rs781437702	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58786800	GATAACCATAATCTT[C/G]ATTTTTTATAGCGTC	54629
rs781445651	snp	C/T	1.69714e-05	0.00291298	missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851931	AACAGGAACAAGCAG[C/T]AGCTGCTGCTGCTGC	54629
rs781496908	snp	A/T	4.4153e-05	0.00469836	intron-variant	FAM63B	GRCh38.p7	15:58802427	AAAGTTTAAATATAT[A/T]CATTGGTTTCTATTA	54629
rs781530560	snp	A/G			missense, nc-transcript-variant	FAM63B	GRCh38.p7	15:58851808	TACAACAAGAACAGC[A/G]GAGCCAAGAGATCAA	54629
rs781530762	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58817357	GAACATATGAATTGG[A/T]CATCAGAGAAATACA	54629
rs781554577	snp	C/T	1.71284e-05	0.00292642	intron-variant	FAM63B	GRCh38.p7	15:58847280	CAGTCCTTTTTCTTT[C/T]GTTACTTCTTATTAA	54629
rs781679672	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58798699	GACTTCAGGTGATCC[A/G]CCCGCCTTGGCCTCC	54629
rs781692328	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58843578	AATACCCTCGTAAAT[C/T]AATTCTACATGGAGT	54629
rs781717460	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859022	TAATTTATCACAAAT[A/G]TTACACATCCTATGT	54629
rs781754932	snp	A/G	1.65767e-05	0.00287891	synonymous-codon, nc-transcript-variant	FAM63B	GRCh38.p7	15:58810265	AATTTTGCACAAACT[A/G]CAGACAGGCCTGGAT	54629
rs781755468	in-del	-/T			intron-variant	FAM63B	GRCh38.p7	15:58775859	AGTAAAGAGGCTAAA[-/T]TTTTTTTTTTTTTTT	54629
rs796068340	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58797228	TAAGATTAATTTTGC[C/T]AGGTGTGATGGCTCA	54629
rs796084946	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58782513	ATTTCCATTGTTATC[A/T]ATTGTATGGATCTTA	54629
rs796091777	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58852943	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	54629
rs796154538	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58848930	ATAAAAAATACTGGG[A/C]CAGGCAAGGTGGCTC	54629
rs796202449	in-del	-/GA			intron-variant	FAM63B	GRCh38.p7	15:58829313	GCTTTATGGTTTTGG[-/GA]GAGAGATATAATTCA	54629
rs796244986	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58788170	TTAAAATTCTGTAAT[-/A]ACCCATAAGGAATCT	54629
rs796262241	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58846108	AAAAAAAAAAAAAAA[A/G]AAAAAACAGAATGAT	54629
rs796266115	multinucleotide-polymorphism	AC/GT			intron-variant	FAM63B	GRCh38.p7	15:58781857	AGTGAGCCAAGATCG[AC/GT]CCACTGCACTCCAGC	54629
rs796312207	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58801731	TGCAGCCTCCACCTC[C/G]CAGGTTCAAGCGATT	54629
rs796322953	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58785728	GTCACCCAGGCTGGA[C/G]CGTAGTGGCACGATC	54629
rs796445339	in-del	-/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58858662	AGCGAATTGATTACA[-/T]TTGATTAACTTTTCC	54629
rs796446034	snp	C/T			intron-variant	FAM63B	GRCh38.p7	15:58845153	GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG	54629
rs796500879	in-del	-/GT			intron-variant	FAM63B	GRCh38.p7	15:58794359	AAAGTTTTTTTTGGG[-/GT]GTGTGTGTGTGTGTG	54629
rs796570869	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58799655	CCTAATACCTAGCTG[A/C]AGTACCCCAAGGAAA	54629
rs796577724	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58828738	GCTAATTTTTTTGTA[A/T]TTTTAGTAGAGACGG	54629
rs796600813	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58793099	AAGAGATGGGGTGAA[A/T]TGGGGGTTGACTGCT	54629
rs796705620	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58803067	GCAACCTTTTTTAAC[A/T]TACTTTCACCAGTAT	54629
rs796709849	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58784054	TCCAGGGCCGAGTGC[A/C]GTGGCTCACACCTGT	54629
rs796719330	snp	A/G			upstream-variant-2KB, intron-variant	FAM63B, LOC101928725	GRCh38.p7	15:58769995	CTCCGTTTCAAAAAA[A/G]AAAAAAAACAAAAGC	54629
rs796723831	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58798247	TCAGCTACCCGAGCA[C/G]CTGGGATTACAGGCG	54629
rs796733579	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58849209	GCAAGAGTCTGTCTC[-/A]AAAAAAAAAAAGGCT	54629
rs796745379	in-del	-/C			intron-variant	FAM63B	GRCh38.p7	15:58853031	AGTCTCGCTCATTGC[-/C]AACCTCTGCTTCCTG	54629
rs796763352	in-del	-/TG			intron-variant	FAM63B	GRCh38.p7	15:58844944	AAAAAAAAAAAAAAA[-/TG]AAAGGACAACCCACA	54629
rs796817376	snp	A/G			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857585	TCTTTATTTTCTTAA[A/G]TTTTGCCCAAGGTAA	54629
rs796838847	in-del	-/A			intron-variant	FAM63B	GRCh38.p7	15:58799594	AAAAAAAAAAAAAAA[-/A]GCAAACACTAGTAGA	54629
rs796869478	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58844462	GAGGCTGAGGCGGGA[C/G]AATGGGGTGAACCCA	54629
rs796915893	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58852935	CTGTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	54629
rs796923981	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58796710	GTATTTTTCGTAGAG[A/G]TGGGGTTTCCCCATG	54629
rs796924176	in-del	-/CT			intron-variant	FAM63B	GRCh38.p7	15:58854235	GGCGACGGTGCAAGA[-/CT]CTGTCTCAAAAAAAA	54629
rs796935192	snp	G/T			intron-variant	FAM63B	GRCh38.p7	15:58807328	TTAATGTGTTAACGT[G/T]CTTAGAAAAGCATTT	54629

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