| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs189067 | snp | G/T | 0 | 0 | intron-variant | PELI1 | GRCh38.p7 | 2:64104285 | TATTAGAAGCACATT[G/T]GGATGAGGTAATTTT | 57162 |
| rs191298 | snp | C/T | 0 | 0 | intron-variant | PELI1 | GRCh38.p7 | 2:64104348 | CTGTTACTAGAGGGG[C/T]CTCCCTGGCCTGGAT | 57162 |
| rs329481 | snp | C/T | 0.441021 | 0.161279 | intron-variant | PELI1 | GRCh38.p7 | 2:64107745 | TGCAGTGGCGCGATC[C/T]CAGCTCACTGCAACC | 57162 |
| rs329482 | snp | A/G | 0.440746 | 0.161604 | intron-variant | PELI1 | GRCh38.p7 | 2:64110016 | ttgggaagcggaggc[A/G]ggaagatcacttgat | 57162 |
| rs329497 | snp | A/G | 0.445722 | 0.155558 | synonymous-codon, utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64100458 | CATATCATATACTTT[A/G]TCTCGGGCCCAGACT | 57162 |
| rs329498 | snp | A/C | 0.446543 | 0.154538 | synonymous-codon, utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64100410 | TCATGACAGCAACAC[A/C]GATATGTTTCAGGTA | 57162 |
| rs329499 | snp | A/C | 0.221141 | 0.248329 | intron-variant | PELI1 | GRCh38.p7 | 2:64096942 | TCTAAAGAGAAAAAA[A/C]CTACATGATACACAT | 57162 |
| rs714672 | snp | C/T | 0.485255 | 0.0845871 | intron-variant | PELI1 | GRCh38.p7 | 2:64119188 | GAGATTTATTTAACT[C/T]CTTCCCTAAGATGGA | 57162 |
| rs717382 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | PELI1 | GRCh38.p7 | 2:64120001 | TTTATGCCTGGGATA[A/G]TATAGTATTTTATAA | 57162 |
| rs1370389 | snp | G/T | 0 | 0 | utr-variant-3-prime | PELI1 | GRCh38.p7 | 2:64093101 | CACTCAGGAAATGCA[G/T]GTCAGGAAACTTGTA | 57162 |
| rs1814406 | snp | C/G | 0.441158 | 0.161117 | intron-variant | PELI1 | GRCh38.p7 | 2:64117937 | CTGTAGTCCCAGCTA[C/G]TTAGGAGGCTGAGGC | 57162 |
| rs1837484 | snp | A/G | 0.440609 | 0.161766 | intron-variant | PELI1 | GRCh38.p7 | 2:64110607 | tctcttgaatcttct[A/G]aattttgtctgatgg | 57162 |
| rs2017833 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PELI1 | GRCh38.p7 | 2:64114585 | TGTAGGTGATATACT[A/G]TCAGCATGCTATTTG | 57162 |
| rs2017834 | snp | G/T | 0.48491 | 0.0855403 | intron-variant | PELI1 | GRCh38.p7 | 2:64114589 | TCCCTGTAGGTGATA[G/T]ACTATCAGCATGCTA | 57162 |
| rs2422114 | snp | C/T | 0 | 0 | intron-variant | PELI1 | GRCh38.p7 | 2:64104316 | CCTGAATACACATAT[C/T]ATACATCACATTCTT | 57162 |
| rs2576836 | snp | A/T | 0.499587 | 0.0143711 | | | GRCh38.p7 | 2:64102856 | TTTTTTTTTTTTTTT[A/T]AACTGAGACAGGGTC | 57162 |
| rs2576837 | snp | C/T | 0.437401 | 0.165472 | | | GRCh38.p7 | 2:64112143 | TTAAATTGTATTAAA[C/T]AGAATTAGTAAGTGC | 57162 |
| rs2901645 | snp | A/G | 0.455977 | 0.141681 | intron-variant | PELI1 | GRCh38.p7 | 2:64112773 | ATATAATCAATCAAT[A/G]TACAACTGGCCTTAT | 57162 |
| rs3731962 | snp | C/T | 0.0999349 | 0.199951 | utr-variant-3-prime | PELI1 | GRCh38.p7 | 2:64094689 | TAACAGACCATTGTC[C/T]TGCAGGACTACATTA | 57162 |
| rs3755112 | snp | C/G | 0.151668 | 0.229849 | utr-variant-3-prime | PELI1 | GRCh38.p7 | 2:64093799 | TAGAAAAAAATCATT[C/G]CCATAAGAAAAAGTA | 57162 |
| rs4671081 | snp | C/T | 0.48435 | 0.0870631 | intron-variant | PELI1 | GRCh38.p7 | 2:64115821 | ACTAGAATGTATTCA[C/T]ATGTAAAATAAACTG | 57162 |
| rs4671082 | snp | C/T | 0.483345 | 0.0897213 | intron-variant | PELI1 | GRCh38.p7 | 2:64116098 | AGGAAGAAAAACATA[C/T]ACATTAGAAGTGAGT | 57162 |
| rs4671548 | snp | A/G | 0.423726 | 0.179776 | intron-variant | PELI1 | GRCh38.p7 | 2:64128057 | GTAGATTAAAAAAAA[A/G]TATCAACCAGTTTTC | 57162 |
| rs5831679 | in-del | -/G | 0.22263 | 0.248497 | intron-variant | PELI1 | GRCh38.p7 | 2:64119013 | TAAGTACTGTAGCTT[-/G]GATTGCAAAAATATT | 57162 |
| rs6717575 | snp | A/G | 0.488363 | 0.0753851 | utr-variant-5-prime, upstream-variant-2KB | PELI1 | GRCh38.p7 | 2:64144435 | TGACATACACTCGCA[A/G]GGAGGGGAGGGGTCT | 57162 |
| rs6717990 | snp | A/G | 0.486595 | 0.0807641 | upstream-variant-2KB | PELI1 | GRCh38.p7 | 2:64144830 | TGACTTTCTCTCCAT[A/G]TTTCAGTCTTCCCTG | 57162 |
| rs6718082 | snp | A/G | 0.44858 | 0.151875 | intron-variant | PELI1 | GRCh38.p7 | 2:64107322 | ATGGCAAGTTTAAGT[A/G]GAATAAATTGAAATA | 57162 |
| rs6726519 | snp | C/T | 0.213937 | 0.247385 | intron-variant | PELI1 | GRCh38.p7 | 2:64139897 | atttggtaccccaaa[C/T]gaaatttatttgctg | 57162 |
| rs6730262 | snp | C/T | 0.366885 | 0.220993 | intron-variant | PELI1 | GRCh38.p7 | 2:64140560 | AGGTAGGTAAGCTAA[C/T]TGAAAGACTCCAATC | 57162 |
| rs6730543 | snp | A/C | 0.208779 | 0.246578 | intron-variant | PELI1 | GRCh38.p7 | 2:64140800 | TGCAAAAAAAAAAAA[A/C]AAACAAACAAAAAAA | 57162 |
| rs6733160 | snp | C/T | 0.366679 | 0.221102 | intron-variant | PELI1 | GRCh38.p7 | 2:64137498 | ATGTGTGTGTGTGTG[C/T]GCGCATTTTGTGaga | 57162 |
| rs6741845 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PELI1 | GRCh38.p7 | 2:64113020 | tggtggctcatgccc[A/G]taatcccagcacttt | 57162 |
| rs6742704 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PELI1 | GRCh38.p7 | 2:64113888 | ATCTTTGTCTCTCAA[C/T]CTAACAAATGTTTTC | 57162 |
| rs6746080 | snp | C/G | 0.233527 | 0.249457 | upstream-variant-2KB | PELI1 | GRCh38.p7 | 2:64144481 | CCTGAGGGAGGGGAC[C/G]GGGCAGGGCCACAGC | 57162 |
| rs6761204 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64123364 | AAGAAAGCTAGGTAT[C/G]AAAAGTACTGCCATa | 57162 |
| rs6761307 | snp | C/G | 0.0138799 | 0.0821421 | utr-variant-3-prime | PELI1 | GRCh38.p7 | 2:64093230 | CCAAAAGAAAATTCA[C/G]AACAGTTTTGTAATA | 57162 |
| rs6761890 | snp | C/T | 0.448836 | 0.15154 | upstream-variant-2KB | PELI1 | GRCh38.p7 | 2:64144908 | CCTCACTTCCCTCAA[C/T]TGAATCTTCTCCGGC | 57162 |
| rs7349403 | snp | A/G | 0.186421 | 0.24178 | intron-variant | PELI1 | GRCh38.p7 | 2:64115335 | TTAAAAGCAGGTTTT[A/G]GCAAGCATGGGAGAA | 57162 |
| rs7558544 | snp | C/T | 0.439641 | 0.162899 | intron-variant | PELI1 | GRCh38.p7 | 2:64129440 | CCATAAACCCAGATA[C/T]TGTATTTGTTTAAAC | 57162 |
| rs7558568 | snp | A/C | 0.435837 | 0.167226 | intron-variant | PELI1 | GRCh38.p7 | 2:64129511 | ACAACCATATTCAAA[A/C]AAGTTTTGTCTAATT | 57162 |
| rs7559410 | snp | C/T | 0.446318 | 0.165006 | intron-variant, upstream-variant-2KB | PELI1 | GRCh38.p7 | 2:64124321 | tatacctcaataaag[C/T]GAAGCAAGCAAGCAA | 57162 |
| rs7562080 | snp | A/G | 0.21725 | 0.247846 | intron-variant | PELI1 | GRCh38.p7 | 2:64130072 | GACTTTTGATTTTGA[A/G]ATTTTGAATCATGTG | 57162 |
| rs7563423 | snp | A/G | 0.484279 | 0.0872533 | intron-variant | PELI1 | GRCh38.p7 | 2:64118268 | GTTAGCACATTAAAA[A/G]TACCCCAATTAGGTA | 57162 |
| rs7572397 | snp | C/T | 0.439641 | 0.162899 | intron-variant | PELI1 | GRCh38.p7 | 2:64129300 | GTCAAGGGAAATTTT[C/T]AGACAGCAATAAGTT | 57162 |
| rs7573532 | snp | A/G | 0.365439 | 0.221752 | intron-variant | PELI1 | GRCh38.p7 | 2:64133299 | TTAAGCTCATACAGT[A/G]AGTTTCAACCCTGAG | 57162 |
| rs7574193 | snp | C/T | 0.43598 | 0.167067 | intron-variant, upstream-variant-2KB | PELI1 | GRCh38.p7 | 2:64124852 | aagttaaagggctca[C/T]gccacaagactcccc | 57162 |
| rs7575383 | snp | A/G | 0.441295 | 0.160954 | intron-variant | PELI1 | GRCh38.p7 | 2:64121885 | ACTCCAGCCTGGACA[A/G]CAAGAGCAAAACTCC | 57162 |
| rs7577356 | snp | C/T | 0.439641 | 0.162899 | intron-variant, upstream-variant-2KB | PELI1 | GRCh38.p7 | 2:64125326 | agttacctattatga[C/T]cagaaagggggttgt | 57162 |
| rs7579814 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PELI1 | GRCh38.p7 | 2:64110169 | gtaatcgcttgaacc[C/T]gggaggcagagcttg | 57162 |
| rs7579828 | snp | C/T | 0.14665 | 0.227637 | intron-variant | PELI1 | GRCh38.p7 | 2:64110214 | tgcgccactgcactc[C/T]agcctgggcgacaga | 57162 |
| rs7581647 | snp | A/C | 0.21303 | 0.247251 | intron-variant | PELI1 | GRCh38.p7 | 2:64128828 | TTTTATGTAAGTTAA[A/C]ATGATTATTTTTTCA | 57162 |
| rs7585957 | snp | A/C | 0.492775 | 0.059668 | intron-variant, upstream-variant-2KB | PELI1 | GRCh38.p7 | 2:64124274 | accactgaagtgtac[A/C]ctttaagtgtttaca | 57162 |
| rs7587919 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | PELI1 | GRCh38.p7 | 2:64112765 | AAAATGGCATATAAT[A/C]AATCAATATACAACT | 57162 |
| rs7604199 | snp | C/T | 0.484209 | 0.0874434 | intron-variant | PELI1 | GRCh38.p7 | 2:64118511 | GTTCAATTATACTTT[C/T]TCTTCTGGTGAAAAT | 57162 |
| rs7604693 | snp | A/C | 0.213333 | 0.247296 | intron-variant | PELI1 | GRCh38.p7 | 2:64122068 | TCTCATATATGCTTT[A/C]TTTACAATGATGTTT | 57162 |
| rs9309358 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | PELI1 | GRCh38.p7 | 2:64118980 | CTAAAATATGTTTTT[G/T]TTTTTTTTTTTAAAG | 57162 |
| rs10169847 | snp | A/G | 0.151334 | 0.229706 | intron-variant | PELI1 | GRCh38.p7 | 2:64097605 | AGTGACAAGTGTCAC[A/G]GGGCTTTAAAGCAAA | 57162 |
| rs10175483 | snp | A/G | 0.14665 | 0.227637 | intron-variant, utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64106006 | ATATATAGAAACTAC[A/G]TTGACCCTTTATAAA | 57162 |
| rs10176596 | snp | C/G | 0.148661 | 0.22854 | intron-variant | PELI1 | GRCh38.p7 | 2:64099800 | TTGGAACTGACTGTC[C/G]TAAAATCTATCAGTT | 57162 |
| rs10185776 | snp | A/T | 0.486067 | 0.0822953 | intron-variant, utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64122999 | CTAAGTAGTGCAGCT[A/T]GCTAACTGATCTTGG | 57162 |
| rs10186108 | snp | C/T | 0.486067 | 0.0822953 | intron-variant, utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64123280 | GATAGAGCACTGCCT[C/T]CCTAAATTGGCTGTT | 57162 |
| rs10189454 | snp | C/T | 0.0275645 | 0.114116 | utr-variant-3-prime | PELI1 | GRCh38.p7 | 2:64094131 | AATTCCATATTTAGA[C/T]TGGGGTGGGGAGAGA | 57162 |
| rs10191854 | snp | C/T | 0.148661 | 0.22854 | intron-variant | PELI1 | GRCh38.p7 | 2:64100184 | ggaaactgaggcata[C/T]aatggttatgtaaTA | 57162 |
| rs10192642 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | PELI1 | GRCh38.p7 | 2:64127107 | AGACTACCAAGACCA[A/G]AGAAAAGATTCCCTT | 57162 |
| rs10496105 | snp | A/G | 0.197703 | 0.244469 | utr-variant-3-prime | PELI1 | GRCh38.p7 | 2:64093612 | GTGGCAATCTCCTTA[A/G]GATTCAAACCCAGAG | 57162 |
| rs10496106 | snp | A/G | 0.485255 | 0.0845871 | intron-variant | PELI1 | GRCh38.p7 | 2:64119530 | TCACTTAAGCACCTC[A/G]TAACGTGTGTAGGTG | 57162 |
| rs10496107 | snp | A/C | 0.407502 | 0.194147 | intron-variant | PELI1 | GRCh38.p7 | 2:64142202 | TACATGCAACTTTCC[A/C]TACATATAACTGTTC | 57162 |
| rs10713817 | in-del | -/G | 0.438386 | 0.164349 | intron-variant | PELI1 | GRCh38.p7 | 2:64133833 | CTCAGATGGTTTTAT[-/G]GGCATTATAGGATTT | 57162 |
| rs11454015 | in-del | -/A | 0.483199 | 0.0901004 | intron-variant | PELI1 | GRCh38.p7 | 2:64117498 | ATCAAATATCTAAAT[-/A]AGAGCATATATTCTC | 57162 |
| rs11673747 | snp | C/T | 0.437542 | 0.165312 | intron-variant | PELI1 | GRCh38.p7 | 2:64115305 | TCTGGACTAAGGGGC[C/T]CATATTTAGAAAAAT | 57162 |
| rs11679748 | snp | C/T | 0.455024 | 0.143057 | intron-variant | PELI1 | GRCh38.p7 | 2:64115492 | GCCCTGTGAATTGGG[C/T]AGGAAAGTCTGAACT | 57162 |
| rs11695959 | snp | C/G | 0 | 0 | intron-variant | PELI1 | GRCh38.p7 | 2:64120874 | CACAGGACAATAGTT[C/G]TGGTTCACAGTAAGG | 57162 |
| rs11898031 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PELI1 | GRCh38.p7 | 2:64135386 | CCAAGGCACACACCA[A/C/G]AAATAGGCAAGGAAA | 57162 |
| rs12472736 | snp | C/T | 0.185472 | 0.241529 | intron-variant | PELI1 | GRCh38.p7 | 2:64109455 | ggaggtcgaggcagg[C/T]ggatcacttgaggtt | 57162 |
| rs12472816 | snp | C/T | 0.190833 | 0.242898 | intron-variant | PELI1 | GRCh38.p7 | 2:64130686 | TTAGATCTTACGAAA[C/T]CTTCATTTTAATTTG | 57162 |
| rs12477310 | snp | A/G | 0.151001 | 0.229563 | intron-variant, utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64143452 | GCGGTAGAAGATCAA[A/G]CGTATCCATCAATTT | 57162 |
| rs12479211 | snp | C/T | 0.191147 | 0.242974 | intron-variant | PELI1 | GRCh38.p7 | 2:64141464 | TACATTGATGTATTA[C/T]GGTAAAATGTGTATG | 57162 |
| rs12614186 | snp | A/C | 0.368733 | 0.220005 | intron-variant | PELI1 | GRCh38.p7 | 2:64141310 | ATGTTTCCCGCCCCC[A/C]CCCCAAAGGAGCTCC | 57162 |
| rs12624273 | snp | C/T | 0.482831 | 0.0910472 | intron-variant | PELI1 | GRCh38.p7 | 2:64115043 | CCGTGTAGTTGAAGG[C/T]GGGTGTAGTTTCAGT | 57162 |
| rs12713504 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | PELI1 | GRCh38.p7 | 2:64140808 | AAAAAAACAAACAAA[A/C]AAAAAAAAACCTAGG | 57162 |
| rs12988261 | snp | A/G | 0.190833 | 0.242898 | intron-variant | PELI1 | GRCh38.p7 | 2:64138775 | ACTGCATCCTCCTCC[A/G]AACCTCATACACATA | 57162 |
| rs13005731 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PELI1 | GRCh38.p7 | 2:64114191 | CTCAGATAAAACAGA[G/T]TTCCATCTATACTAG | 57162 |
| rs13009123 | snp | C/T | 0 | 0 | intron-variant | PELI1 | GRCh38.p7 | 2:64102553 | TAAACAGCTCACTTT[C/T]CAATGAAACAATTAC | 57162 |
| rs13031772 | snp | C/T | 0 | 0 | intron-variant | PELI1 | GRCh38.p7 | 2:64102274 | ATATTTCTTTCTACA[C/T]ATTTAGGTATTCATA | 57162 |
| rs13031800 | snp | A/T | | | intron-variant | PELI1 | GRCh38.p7 | 2:64102372 | catatacatataTAt[A/T]tgtttaagagaccag | 57162 |
| rs13031999 | snp | A/G | 0 | 0 | intron-variant | PELI1 | GRCh38.p7 | 2:64102450 | ggaaaatggcacact[A/G]cagctttaaactcct | 57162 |
| rs13032018 | snp | C/G | 0 | 0 | intron-variant | PELI1 | GRCh38.p7 | 2:64102429 | tgcagtggctattta[C/G]aggcaggaaaatggc | 57162 |
| rs13032032 | snp | A/T | | | intron-variant | PELI1 | GRCh38.p7 | 2:64102498 | ctgcctctgcctccc[A/T]aggagctgggactaa | 57162 |
| rs13386653 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PELI1 | GRCh38.p7 | 2:64133983 | ATTCTTACTTCATGT[A/G]GAGTTTTTCCATATG | 57162 |
| rs13392453 | snp | C/T | | | intron-variant | PELI1 | GRCh38.p7 | 2:64114605 | TATCACCTACAGGGA[C/T]AACTTATTTCATCCT | 57162 |
| rs13408188 | snp | A/C | 0.147321 | 0.227941 | intron-variant | PELI1 | GRCh38.p7 | 2:64108516 | TTATGGGACATTTTG[A/C]CCAATAATGATTATA | 57162 |
| rs13412068 | snp | A/G | 0.14933 | 0.228835 | intron-variant | PELI1 | GRCh38.p7 | 2:64109537 | aatacaaaattagcc[A/G]ggcgtggtggcacat | 57162 |
| rs13419918 | snp | C/T | 0.151001 | 0.229563 | intron-variant | PELI1 | GRCh38.p7 | 2:64106393 | ATTAACTGAGGAACC[C/T]ATAGGCTAAGACTGG | 57162 |
| rs13421554 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64108374 | GGACACCTTTTGCAT[C/T]ATTTCCTAGAGGGGA | 57162 |
| rs13422540 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PELI1 | GRCh38.p7 | 2:64112450 | ATTTTTTTGCTTAGA[C/G]AAGAAACTAAAAAAC | 57162 |
| rs13428357 | snp | G/T | 0.150667 | 0.229419 | intron-variant | PELI1 | GRCh38.p7 | 2:64110031 | gggaagatcacttga[G/T]gtcaggagttcgaga | 57162 |
| rs17028389 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | PELI1 | GRCh38.p7 | 2:64105749 | ACTGCTTCATTGAGG[C/G]ATGAGCAGTAGCTTA | 57162 |
| rs17028445 | snp | C/T | 0.046775 | 0.145601 | intron-variant | PELI1 | GRCh38.p7 | 2:64120639 | AGCCACCTAAGTAAA[C/T]GGCTATCCAGACAAT | 57162 |
| rs17028475 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | PELI1 | GRCh38.p7 | 2:64127426 | ATGAAATTTGTTGGG[A/G]TACCATGCTTTAGTA | 57162 |
| rs17028480 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | PELI1 | GRCh38.p7 | 2:64128699 | CATTTACTGCGGAGT[A/G]TATGATAAATTTAAA | 57162 |