| SNP - dbSNP | 						
			| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene | 			
		| rs6281522 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Bcl6, Gm31527 | Mm_Celera | 16:23988744 | GCGCCCTCCCGGCCG[A/G]CAGAATGCCTCGGGG | 12053 | 		
		| rs6281669 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Bcl6, Gm31527 | Mm_Celera | 16:23988833 | ACACCGGGGGTCCCG[A/C]GGCGGGCGCGCGCGG | 12053 | 		
		| rs13460079 | snp | C/G |  |  | utr-variant-3-prime | Bcl6 | Mm_Celera | 16:23965778 | AGGAATGTAAATGAT[C/G]TGTGGGAACAGAGGT | 12053 | 		
		| rs45718920 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23974564 | GATGTCAGCAAAAGG[C/G]CCATGGAAAAGGCTT | 12053 | 		
		| rs45755003 | snp | C/G/T | 0.345679 | 0.230967 | intron-variant | Bcl6 | GRCm38.p3 | 16:23973440 | AGCCACTCATATAAC[C/G/T]TGTGTTTCATTGGAT | 12053 | 		
		| rs45828037 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Bcl6 | Mm_Celera | 16:23977409 | TGAGATCTGGAGACT[A/G]AGGAAATGTCATCTC | 12053 | 		
		| rs45883749 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23971049 | AGCCAACTGAGGCCC[A/G]GTGCGAGATGCATGA | 12053 | 		
		| rs45916774 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B | Bcl6 | Mm_Celera | 16:23964741 | ACTCGTTAGAGGTTG[G/T]AGAGACTATGACGTT | 12053 | 		
		| rs46050893 | snp | C/G | 0.375 | 0.216506 | intron-variant | Bcl6 | Mm_Celera | 16:23977490 | ATCCCCATTTCTGCA[C/G]TCCCTTCATGCCGAG | 12053 | 		
		| rs46223839 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Bcl6 | Mm_Celera | 16:23965007 | AAGCAAAGACCACTC[C/T]GATCTCTCTCCATGC | 12053 | 		
		| rs46438581 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23970931 | TTTTCACCAGGTTAA[A/G]AACTGAGGGAGCCAA | 12053 | 		
		| rs46451262 | snp | G/T | 0.32 | 0.24 | intron-variant | Bcl6 | Mm_Celera | 16:23971616 | TGTGGGCAGGAAAAA[G/T]GAGCCTCAGGACTCA | 12053 | 		
		| rs46610787 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Bcl6 | Mm_Celera | 16:23974211 | GATAAGCCTCAAGTA[C/G]CTGCTCCATTTACCA | 12053 | 		
		| rs46773519 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Bcl6 | Mm_Celera | 16:23967064 | AGCACCGAATGAATT[A/C]GTTCCCTAAACATGG | 12053 | 		
		| rs46851330 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Bcl6 | Mm_Celera | 16:23977456 | CTATACATTTGTCTC[A/G]CTGGCTGTCAATCCA | 12053 | 		
		| rs46903089 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23969201 | CTGAGCAGAGGCCGG[A/G]CAGAGGAAACCAATC | 12053 | 		
		| rs47086276 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Bcl6 | Mm_Celera | 16:23975352 | CTCATCTGCTCCTAC[C/T]TCGTGTGTGTGGTAC | 12053 | 		
		| rs47276674 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime | Bcl6 | GRCm38.p3 | 16:23965712 | GCCTTCTCTTTGACA[A/G]CATACTGAAGTCTTG | 12053 | 		
		| rs47326807 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bcl6 | Mm_Celera | 16:23967178 | TGTCAAGAAACAAAG[A/G]GCAAGTACAAAGCCC | 12053 | 		
		| rs47352936 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23969415 | CAGTCCATGTTGCCT[C/T]TATCAGCATTAGTCT | 12053 | 		
		| rs47395590 | snp | C/T | 0.165289 | 0.235211 | synonymous-codon | Bcl6 | Mm_Celera | 16:23972352 | CGCGGGCTCCATAGG[C/T]GGCTGGCAAGCGGGC | 12053 | 		
		| rs48034790 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Bcl6 | Mm_Celera | 16:23975671 | GCAGGAAGTAGCTCT[A/T]CAGCTGTGGCTAATA | 12053 | 		
		| rs48121547 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Bcl6 | Mm_Celera | 16:23977481 | AATCCAAGCATCCCC[A/G]TTTCTGCAGTCCCTT | 12053 | 		
		| rs48188272 | snp | C/T | 0.32 | 0.24 | intron-variant | Bcl6 | Mm_Celera | 16:23974530 | CAAAAGGCTGCCCGC[C/T]AAACACAGATGAGCT | 12053 | 		
		| rs48383064 | snp | G/T | 0.32 | 0.24 | intron-variant | Bcl6 | Mm_Celera | 16:23971297 | TATTGCTGGAGACGG[G/T]AAGTGCCAGAGGCCT | 12053 | 		
		| rs48431946 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Bcl6 | Mm_Celera | 16:23964610 | TGTGTGGCTTCAGCC[A/G]GATGCCTTTGACCTG | 12053 | 		
		| rs48581432 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23970239 | TTTTTCTTAGTTTTT[C/T]AGAGTCTCAGTCAGA | 12053 | 		
		| rs48645351 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23970956 | AGCCAATACTGACCA[C/T]GTGGAGATGCTAATT | 12053 | 		
		| rs48774433 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Bcl6 | Mm_Celera | 16:23969313 | AAAGAGACTGTGAGA[C/T]GAGTCCCCAGGAAAA | 12053 | 		
		| rs48931252 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23970098 | CATGGAGGGATGCCT[C/G]GTTAGCATGAGGAGA | 12053 | 		
		| rs48947901 | snp | A/G | 0.32 | 0.24 | intron-variant | Bcl6 | Mm_Celera | 16:23966837 | GGGAGTCTTGAGTCT[A/G]GGAGATGGTTTTCTT | 12053 | 		
		| rs48948288 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Bcl6 | Mm_Celera | 16:23964906 | CTACCTGGACAAGCC[C/T]CAGTCTGGCTCTCAG | 12053 | 		
		| rs49330404 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Bcl6 | GRCm38.p3 | 16:23965261 | AAAAAGGGATGGCGC[A/G]CACCCGTCCATCATT | 12053 | 		
		| rs49377043 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bcl6 | Mm_Celera | 16:23967092 | TGGCCACCTTATGAC[A/G]TAGGCACTGTTTTCT | 12053 | 		
		| rs49430128 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Bcl6 | Mm_Celera | 16:23971308 | ACGGTAAGTGCCAGA[A/G]GCCTTCTAATCTGGG | 12053 | 		
		| rs49489804 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23969877 | CCTGTAACCGATCAC[A/G]GAGCCCTCGGCTTGG | 12053 | 		
		| rs49518701 | snp | C/T | 0.32 | 0.24 | intron-variant | Bcl6 | Mm_Celera | 16:23967947 | CTCCTGACCACTGGC[C/T]CATGTGTACACTAGA | 12053 | 		
		| rs49718993 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23971084 | CTAAGGCCAGCTATT[C/T]CTTCACAGAGGACTG | 12053 | 		
		| rs49884556 | snp | A/G | 0.345679 | 0.230967 | synonymous-codon | Bcl6 | GRCm38.p3 | 16:23968093 | TGTGTGGATGCGCAG[A/G]TGGCTCTTCAGAGTC | 12053 | 		
		| rs50001661 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bcl6 | Mm_Celera | 16:23966983 | AAACAGCACTTTCAA[C/T]TCTTACTGCCACTAA | 12053 | 		
		| rs50135833 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Bcl6 | Mm_Celera | 16:23975486 | GGCCTTGCTCCAAGT[A/C]CAACAATACCAGAAA | 12053 | 		
		| rs50259726 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23978264 | CTTATAATCCTGGCA[C/G]TGTAGGCAACCAGGT | 12053 | 		
		| rs50434480 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23973876 | GTACTCCCAAATGAC[A/G]GCAATGATGCACTTG | 12053 | 		
		| rs50639321 | snp | A/G | 0.18 | 0.24 | intron-variant | Bcl6 | Mm_Celera | 16:23973330 | GAGTCAGTGAGACTC[A/G]GGAGATGTGACTCTG | 12053 | 		
		| rs50727819 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Bcl6 | GRCm38.p3 | 16:23969916 | CGTACCCGTGTGGAC[A/G]GTCTTGTGGCTGGCG | 12053 | 		
		| rs50840590 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Bcl6 | Mm_Celera | 16:23973769 | GCACAAAAGCCCTGG[C/T]GATGGAGCAGCCTGG | 12053 | 		
		| rs51063837 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Bcl6 | Mm_Celera | 16:23964566 | GTCGGTCACCCAGGA[A/G]GCTCTGAATGCGTGG | 12053 | 		
		| rs51674070 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Bcl6 | Mm_Celera | 16:23977381 | TGAGAGTCCACAATG[C/G]CAGGCCATTTGCTGA | 12053 | 		
		| rs51807807 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Bcl6 | Mm_Celera | 16:23971660 | GTCCACGTGGTGGCC[A/G]TGCTAACCTCTCTCT | 12053 | 		
		| rs51978935 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Bcl6 | Mm_Celera | 16:23970164 | TCTGCCAATGTCTCA[C/G]CAGAGCCTGGGCTCC | 12053 | 		
		| rs211755463 | snp | G/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23985562 | GTTTTTGGGTTTTTG[G/T]TTTTTGGTTTTTGGT | 12053 | 		
		| rs211865339 | snp | A/C |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23984496 | AAACTGAAGTCGGAA[A/C]ACATTTAGTTGAGTA | 12053 | 		
		| rs212258195 | snp | A/C |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23982041 | ACGTGCTCCGGAATT[A/C]AGTGTCTTATTTTCC | 12053 | 		
		| rs212296361 | snp | A/G |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23970547 | CCTCAAGAGCCATGA[A/G]ACACAGTTCTAACCC | 12053 | 		
		| rs212376661 | snp | A/G |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23980945 | GAGAGACAGAAAGAG[A/G]GAGGGAGAGAGAATC | 12053 | 		
		| rs212390837 | in-del | -/CCAAGACAC |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23970367 | TCTTCTCTGGGAGCT[-/CCAAGACAC]CTTACAAACAGGTTC | 12053 | 		
		| rs212407270 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23970137 | AGCCCGGACGCCTCC[C/T]GCCTCTGGAACTCTG | 12053 | 		
		| rs212614614 | snp | A/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23976572 | CCTGAAATTCAGAAA[A/T]ATTTGAAGAATAAGC | 12053 | 		
		| rs212616676 | snp | A/G |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23967096 | CACCTTATGACATAG[A/G]CACTGTTTTCTAAAT | 12053 | 		
		| rs212706051 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23967496 | ACGCATGCAGGTACC[C/T]GGGGAGGCCACAAGA | 12053 | 		
		| rs212780438 | snp | A/G |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23975211 | TTTACATTAACCGGC[A/G]TTCTCCCTAATCCTG | 12053 | 		
		| rs212796875 | snp | C/T |  |  | upstream-variant-2KB, intron-variant | Bcl6, Gm31527 | Mm_Celera | 16:23989527 | CAGAAGCTTACATTT[C/T]TGGCCACATATGACA | 12053 | 		
		| rs212933472 | in-del | -/AGC |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23978082 | ATTTTCCAAAATAGG[-/AGC]AGCAATACCTATGTG | 12053 | 		
		| rs213209640 | snp | C/T |  |  | synonymous-codon | Bcl6 | GRCm38.p3 | 16:23973192 | CTCTTCACGGGGAGG[C/T]TTAAGTGCAGGGGCC | 12053 | 		
		| rs213269964 | snp | C/T |  |  | downstream-variant-500B | Bcl6 | Mm_Celera | 16:23964685 | CAGGATGGGACTTCT[C/T]ACTTTAGAAAAGAAT | 12053 | 		
		| rs213345354 | in-del | -/GGGA |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23979970 | GGTAGGAAATGGAGG[-/GGGA]GAGAGGACAGAAAAA | 12053 | 		
		| rs213443498 | snp | A/G |  |  | upstream-variant-2KB, intron-variant | Bcl6, Gm31527 | Mm_Celera | 16:23990554 | GAAGACTGCTGGCTT[A/G]TGGGGTACAGAGGAC | 12053 | 		
		| rs213467344 | in-del | -/A |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23978492 | GGTAAAATTCATGAG[-/A]AAAAAAAATCACCTA | 12053 | 		
		| rs213486180 | snp | G/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23974490 | ATATATAGACCAATG[G/T]TAGAAGTCAGGTTGG | 12053 | 		
		| rs213523040 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23966446 | AGGTTAGGTATACAC[C/T]GTGCAAATGCCCCAG | 12053 | 		
		| rs213541332 | snp | A/G |  |  | upstream-variant-2KB, intron-variant | Bcl6, Gm31527 | Mm_Celera | 16:23989484 | TCTCTCTCTCTAAAG[A/G]TGCAATATTTCAACC | 12053 | 		
		| rs213566678 | snp | C/T |  |  | utr-variant-3-prime | Bcl6 | Mm_Celera | 16:23965861 | GAAAATGAATTTGCT[C/T]TTTGCTGACAGGGTT | 12053 | 		
		| rs213843264 | snp | A/G |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23967041 | AGCTATGTGCTTGAG[A/G]AACTCAAAGCACCGA | 12053 | 		
		| rs213974787 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23975149 | CGAATGACTTCTACA[C/T]GTGGAAAGCCTAGCA | 12053 | 		
		| rs213995186 | snp | C/G |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23984332 | GGATCCAGACAACAC[C/G]GCTTCGGGCGCAAAC | 12053 | 		
		| rs214298995 | snp | A/C |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23971229 | CAGTTCAACACCTAA[A/C]CCCTGTTGGCTTGCT | 12053 | 		
		| rs214349855 | in-del | -/A |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23968941 | ATTGTCATTAGGGTC[-/A]CTGCCTCTGGGGCTT | 12053 | 		
		| rs214356688 | snp | C/G |  |  | downstream-variant-500B | Bcl6 | Mm_Celera | 16:23964631 | CTTTGACCTGCCAGG[C/G]GTAGCCAAGTAAAGA | 12053 | 		
		| rs214480698 | snp | A/C |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23976881 | AAGGATGGTTGTGAG[A/C]CACCATGTGGTTGCT | 12053 | 		
		| rs214540057 | in-del | -/CTC |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23984290 | TTGGACAATGCCCTT[-/CTC]CTCCTCAGTCCTAGC | 12053 | 		
		| rs214548355 | snp | A/G |  |  | missense | Bcl6 | Mm_Celera | 16:23972746 | TTCCGAGCAGAAGGG[A/G]CAGCAGGCTTGGGGC | 12053 | 		
		| rs214572673 | in-del | -/AAA |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23981925 | GAGGACTAAACCTGG[-/AAA]AAAAAAAAGTAAACT | 12053 | 		
		| rs214648827 | snp | C/G |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23968948 | TTAGGGTCACTGCCT[C/G]TGGGGCTTGGGCAAG | 12053 | 		
		| rs214936673 | snp | A/C |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23968296 | TCCCTTCGCCATGCT[A/C]CCCTGCTCACCTGAA | 12053 | 		
		| rs215087240 | snp | A/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23967580 | AGTGCTGGCAACTGG[A/T]CACTCCTCTACAACC | 12053 | 		
		| rs215161230 | snp | A/C |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23968492 | TAACCGGGGGCTCCA[A/C]TGACTCTTAATTTCA | 12053 | 		
		| rs215187306 | in-del | -/TTTTTTTTTTT |  |  | intron-variant, upstream-variant-2KB | Bcl6, Gm31527 | Mm_Celera | 16:23987370 | TATACCCAGGGCCAC[-/TTTTTTTTTTT]TTTTTTTTTTTAAAC | 12053 | 		
		| rs215498021 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23966354 | GAAGAGAGGCAACTC[C/T]GTGAGGGTTGGGTGC | 12053 | 		
		| rs215564915 | snp | A/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23967017 | TAAAATTCTAGCAGT[A/T]CAGGATACAGCTATG | 12053 | 		
		| rs215576112 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23977424 | AAGGAAATGTCATCT[C/T]GGACATAGAGAATGG | 12053 | 		
		| rs215697537 | snp | A/C |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23975340 | TCTAACTTAGCACTC[A/C]TCTGCTCCTACTTCG | 12053 | 		
		| rs216009400 | in-del | -/AAAA |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23976971 | TCTAGCCCCCCCCCC[-/AAAA]AAAAAAAAAACTTTT | 12053 | 		
		| rs216179821 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23976805 | AAGATTTATTTATTG[C/T]TACATGTAAGTACAC | 12053 | 		
		| rs216623509 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23969133 | CAGAACATAGTTTTC[C/T]GCTTGTGGCAACTAC | 12053 | 		
		| rs216767760 | snp | A/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23968638 | ATCATTTTTGTCGCT[A/T]CTTCATAACTGTAAT | 12053 | 		
		| rs216768067 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23979420 | GAAATATATACTCTC[C/T]CCAAATTGGTTTCTC | 12053 | 		
		| rs216793154 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23982812 | TAGGGAAGGACAATA[C/T]TGTTGCTCTTGCCTC | 12053 | 		
		| rs216865622 | snp | C/T |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23977696 | GTTTGCCTGAACAGA[C/T]GTTAAAACTCCTATT | 12053 | 		
		| rs216982827 | snp | A/G |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23980892 | TAGTGTGCTTTGAAT[A/G]AGGCAGCTTCAAGTA | 12053 | 		
		| rs217375041 | snp | A/C |  |  | intron-variant | Bcl6 | Mm_Celera | 16:23979743 | TCTCAGTTTTAAACT[A/C]CTTTGCCCACACAAA | 12053 |