SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9288 | snp | A/G | 1.72982e-05 | 0.00294088 | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113815 | GTAAAGGCGCATGGC[A/G]TCCTCGGCCCGCGCA | 1155 |
rs1046975 | snp | A/C | 0 | 0 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121555 | TTTCCTGAAGCGCAG[A/C]AAGCTCGGCCGGTAC | 1155 |
rs1048259 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114755 | GAAGGCGGGCGAGGA[A/G]TGGCTCCAGGACTAA | 1155 |
rs1801989 | snp | C/T | 0.000375607 | 0.013699 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125751 | CGGTGGGGGACTTCC[C/T]GGAGGAGGACTACGG | 1155 |
rs1801990 | snp | A/C | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125502 | TCCGCTATGATGAGC[A/C]ACTGGGGAAAAATGA | 1155 |
rs1803271 | snp | A/T | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121707 | CTCGCCGGGGCACCG[A/T]CATGTATGTAGGTCT | 1155 |
rs1803272 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125795 | TGACACCTAAGGAAT[G/T]CCCCTGCTTCAGCTC | 1155 |
rs2072606 | snp | C/T | 0.4628 | 0.13121 | intron-variant | TBCB | GRCh38.p7 | 19:36121324 | GTGCAGGCGGCACCC[C/T]TTCCATTTACGATTG | 1155 |
rs2075474 | snp | A/G | 0.477098 | 0.104529 | intron-variant | TBCB | GRCh38.p7 | 19:36121494 | TTAGGCCCGGCCGAC[A/G]CCCCAACTGACCCCA | 1155 |
rs2227260 | snp | C/T | 0.452595 | 0.146476 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114745 | GTGCCAGGGGTTAGT[C/T]CTGGAGCCATTCCTC | 1155 |
rs2230684 | snp | C/T | 0.000611101 | 0.0174693 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114227 | CCAGATTATCGCCGA[C/T]GTGTCCCAGGACCCC | 1155 |
rs2231566 | snp | A/G | 0.143717 | 0.226283 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114650 | GCCGGGGAAGACCCC[A/G]GCGCTCACCGCGTAG | 1155 |
rs2231567 | snp | C/T | 0.0114531 | 0.0748023 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114680 | GAGCAGAATGCGGTT[C/T]TCCTTGTCTTCCTTG | 1155 |
rs2231568 | snp | C/T | 0.455003 | 0.143087 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114892 | GCCCTCCCAGCCTTC[C/T]GCGCTTGCTCCGCCG | 1155 |
rs2231569 | snp | G/T | 0.0490535 | 0.14873 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114973 | CGGAGCTGCGCACAC[G/T]TGCTGGCTCCCCGCC | 1155 |
rs2231570 | snp | C/T | 0.0543475 | 0.155628 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115182 | GGACAGAAGCCAAGG[C/T]GCTTGGCTTGGTTGA | 1155 |
rs2231571 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115242 | TCGCGGACTGGGCGA[A/G]CTCTTGCCACTCCTA | 1155 |
rs2231572 | snp | C/G | 0.0150606 | 0.0854603 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115386 | AGAGCCCTCTTCCTG[C/G]CGGTGGGGAAGGGAC | 1155 |
rs2231573 | snp | C/T | 0.00191612 | 0.0308932 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120727 | CATTGACCACAGTGG[C/T]GCCCGCCTTGGTGAG | 1155 |
rs2231574 | snp | G/T | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36120833 | TGGGCGTCGAGGGGT[G/T]CGTGGGGGCCAGAGG | 1155 |
rs2231575 | snp | A/G | 0.00759075 | 0.0611372 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121579 | CCGGTACAACGAGGA[A/G]GAGCGGGCTCAGCAG | 1155 |
rs2231576 | snp | A/G | 0.0152535 | 0.0859889 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121744 | CGCGGGCCCGGTCCC[A/G]GGCTCCAGGGCTCCA | 1155 |
rs2231577 | snp | A/G | 0.0038934 | 0.0439493 | intron-variant | TBCB | GRCh38.p7 | 19:36125654 | ACCACACCCACCCCT[A/G]TCCTTTCCTGCAGTG | 1155 |
rs2239509 | snp | C/T | 0.114387 | 0.210022 | intron-variant | TBCB | GRCh38.p7 | 19:36120359 | CAGCTTAGGAGAGTC[C/T]CAGAGGCCCATCGAG | 1155 |
rs2239510 | snp | A/G | 0.383824 | 0.211166 | intron-variant | TBCB | GRCh38.p7 | 19:36120382 | CCATCGAGGAGATGC[A/G]CTGTGCACAGGGCTG | 1155 |
rs4555271 | snp | A/G | 0.337841 | 0.23406 | intron-variant | TBCB | GRCh38.p7 | 19:36119288 | ACGCTTCATCCGGAG[A/G]TAAAGGCCATTCCTA | 1155 |
rs4806277 | snp | C/T | 0.279726 | 0.248226 | intron-variant | TBCB | GRCh38.p7 | 19:36124646 | cctcccgggttcaaa[C/T]ggttctcctgcctca | 1155 |
rs6510521 | snp | G/T | 0.497855 | 0.0326773 | intron-variant | TBCB | GRCh38.p7 | 19:36124781 | atctcctgacctcgt[G/T]atccaccctcctcag | 1155 |
rs7258441 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115456 | TTGGTCAGGCACGGA[G/T]CAGGAGGCGGGGCTG | 1155 |
rs8100250 | snp | A/G | 0.466824 | 0.124448 | intron-variant | TBCB | GRCh38.p7 | 19:36124851 | cccggccAgtatgtc[A/G]tcttttgagaagtgt | 1155 |
rs8103791 | snp | C/T | 0.201727 | 0.245295 | intron-variant | TBCB | GRCh38.p7 | 19:36119890 | gacagagcgagactc[C/T]gtcaaaaaaaaaaaa | 1155 |
rs8104047 | snp | A/G | 0.482757 | 0.0912364 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122012 | GGCAGTGTCAGTCGC[A/G]GTGGGGAAACGGGCG | 1155 |
rs8104053 | snp | A/G | 0.477175 | 0.104362 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122023 | TCGCGGTGGGGAAAC[A/G]GGCGGCGTGACCAAG | 1155 |
rs8106074 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126088 | TGTAGCTACCAGGAA[A/G]AAAGGGAAGGGAAGG | 1155 |
rs8106396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117234 | atttactctctgtct[C/T]cctggattcgagtgc | 1155 |
rs8110206 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36125987 | GACCCACTGGGTAAA[C/T]AGTGGCCCTTCGGTA | 1155 |
rs8113579 | snp | A/G | 0.202651 | 0.245475 | intron-variant | TBCB | GRCh38.p7 | 19:36119361 | GTGTTCCTTGGGCCC[A/G]CTCTCTCCCTCACCC | 1155 |
rs10407011 | snp | A/G | 0.383824 | 0.211166 | intron-variant | TBCB | GRCh38.p7 | 19:36119883 | CCTGGGTGACAGAGC[A/G]AGACTCCGTCAAAAA | 1155 |
rs10410489 | snp | C/T | 0.029116 | 0.117091 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121963 | GGAGGAAGCAGAAGC[C/T]AGAGGCACGCGGCCT | 1155 |
rs10410926 | snp | A/G | 0.279726 | 0.248226 | intron-variant | TBCB | GRCh38.p7 | 19:36122874 | caaattgtgaacatc[A/G]tacccaacagataat | 1155 |
rs10417569 | snp | A/G | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36123535 | ctcccaaagtgctgg[A/G]attacaggtgtgagc | 1155 |
rs10417577 | snp | A/G | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36123545 | gctgggattacaggt[A/G]tgagccaccatgcta | 1155 |
rs10418079 | snp | C/G | 0.398714 | 0.200958 | intron-variant | TBCB | GRCh38.p7 | 19:36123073 | cttttgtaactggcg[C/G]cttccactgagcaga | 1155 |
rs10419924 | snp | A/C | 0.339203 | 0.233544 | intron-variant | TBCB | GRCh38.p7 | 19:36123560 | gtgagccaccatgct[A/C]ggcctgaacattctt | 1155 |
rs10420582 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TBCB | GRCh38.p7 | 19:36118254 | TGTTGGCTAAATGGC[C/T]AGAGGACTGAATGTG | 1155 |
rs10425477 | snp | C/T | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36123544 | tgctgggattacagg[C/T]gtgagccaccatgct | 1155 |
rs10425700 | snp | A/G | 0.338069 | 0.233974 | intron-variant | TBCB | GRCh38.p7 | 19:36118888 | GTGTGTGGGGAACAG[A/G]TGGTGGAGGACAGGA | 1155 |
rs11267762 | in-del | -/TCATGGCCAACATG | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116829 | TTTGCCATGTTGGCC[-/TCATGGCCAACATG]AGGCTGGTCTGGAAC | 1155 |
rs11310846 | in-del | -/T | 0.125874 | 0.217008 | intron-variant | TBCB | GRCh38.p7 | 19:36121200 | GGACGGATCGAGTGT[-/T]GGGGGAGACCGGGGG | 1155 |
rs11540331 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115145 | CGATGCGCATCGTAA[A/C]CCGCAAAACACTGAG | 1155 |
rs11545600 | snp | A/C/T | 6.22452e-05 | 0.00557842 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115545 | CGCGCTGCAGGCATC[A/C/T]GCAGGGCGCGGCAAG | 1155 |
rs11545601 | snp | A/G | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121623 | CCCAGCGCCTGGCCG[A/G]GGAGAAGGCCCAGGC | 1155 |
rs12971639 | snp | C/T | 0.472241 | 0.114494 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126204 | AGGGCGGGTGGATCA[C/T]GAGGTCAGGAGATCG | 1155 |
rs12971936 | snp | C/T | 0.472241 | 0.114494 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126338 | GAGGCAGGAGAATGG[C/T]GAGAACCTGGGAGGC | 1155 |
rs12972828 | snp | A/G | 0.449979 | 0.150028 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126371 | AGCTTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 1155 |
rs12981995 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36122666 | aggctgaggtgggag[A/G]atggcttgagcccgg | 1155 |
rs34390728 | in-del | -/A | 0.0954561 | 0.19651 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113834 | TGGCAGAAATGATGC[-/A]TGGTTAGGAAGGATT | 1155 |
rs34683365 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116835 | ATGTTGGCCAGGCTG[-/AG]GTCTGGAACTCCTGA | 1155 |
rs34701186 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117236 | TACTCTCTGTCTCCC[-/C]TGGATTCGAGTGCCC | 1155 |
rs35581971 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121651 | GCCAGCTCCATCCCC[-/C]GTGGGCAGCCGCTGT | 1155 |
rs35625281 | in-del | -/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36119949 | TGTCTTCCACTCTCC[-/C]TCTGGCTCGCTCCAC | 1155 |
rs35947741 | in-del | -/A | | | intron-variant | TBCB | GRCh38.p7 | 19:36122590 | AAAAAAAAAAAAAAA[-/A]TCCCACAAAACTTTT | 1155 |
rs36073528 | in-del | -/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36119387 | ACCCCCACATCCACT[-/G]CTCATCAAATCCTCT | 1155 |
rs45471297 | snp | C/G | 0.0119091 | 0.0762411 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115262 | TGCCACTCCTACCTC[C/G]GGGCTTCAGTCTTCG | 1155 |
rs55911548 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36120568 | CTCCCTTCCGCTGGG[A/C]TCAGGAGAGAAGAGA | 1155 |
rs57123860 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123274 | TTTTTTTTTTTTTTT[-/T]CTAATTTGAGACAGC | 1155 |
rs57766416 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124993 | TTCTGCTCAGTTTTT[-/T]CATTGGGATGCTGTC | 1155 |
rs58457494 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116052 | ACAGTGTAAACTGGA[A/G]TTGCTGGTGGGCAGC | 1155 |
rs60393405 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | TBCB | GRCh38.p7 | 19:36118165 | TCTCGTTGATTAACT[C/G]TTCATTCCCCATCTG | 1155 |
rs60910092 | in-del | -/G | 0.0678174 | 0.1712 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126174 | ACGCCTGTAATCCCA[-/G]CACTTTGGGAGGCCA | 1155 |
rs61736267 | snp | A/C | 0.020313 | 0.0987111 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113458 | ATCTGTGCAGGGATC[A/C]GGCCCTTCCGCTGCA | 1155 |
rs62111380 | snp | C/T | 0.118933 | 0.212888 | intron-variant | TBCB | GRCh38.p7 | 19:36117504 | TGTGCACCACCACGC[C/T]TGGCTAATTTTGTAA | 1155 |
rs62111381 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | TBCB | GRCh38.p7 | 19:36118350 | CTGATGCATCAGTGA[C/T]GTCTGGGAGGACATC | 1155 |
rs62111382 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36119912 | AAAAAAAAAAAAACC[A/C]AAAGTCTCCAGCAGT | 1155 |
rs73036138 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113076 | TGTATGTGGGGTATG[A/G]AGAATCAAGACATGA | 1155 |
rs73601689 | snp | A/G | 0.0626037 | 0.165477 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122173 | GGAGTAGCGGGTGCA[A/G]GTGAGCAGAGCGCAG | 1155 |
rs73601695 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | TBCB | GRCh38.p7 | 19:36124370 | GGATTATAGGTGAGC[A/G]CTACAACACCTGGCT | 1155 |
rs74172781 | in-del | -/G | 0.5 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36118714 | AGGTTAACTGAAGAT[-/G]GGGGAAGGGGTGCCC | 1155 |
rs74572952 | snp | A/C | 0.5 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36122757 | AGACCCTGTCTCCAA[A/C]AAAAAAAAAAAAAAA | 1155 |
rs74892215 | in-del | -/AAAAA | | | intron-variant | TBCB | GRCh38.p7 | 19:36118696 | AAAAAAAAAAAAAAA[-/AAAAA]GGTTAACTGAAGATG | 1155 |
rs74928101 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116495 | AAGGGTGACTTAAGA[A/G]AAAGAGGTGGAAAGG | 1155 |
rs75130259 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TBCB | GRCh38.p7 | 19:36119991 | CACCCACTCTAGAGC[A/G]TGAAGGACATTTCTA | 1155 |
rs75674576 | snp | A/G | 0.000175731 | 0.00937203 | intron-variant | TBCB | GRCh38.p7 | 19:36121491 | CTGTTAGGCCCGGCC[A/G]ACACCCCAACTGACC | 1155 |
rs75735458 | snp | A/G | 0.0325976 | 0.123435 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117192 | TAATTCTCCTCTGAC[A/G]CACTCTGGATTTCTC | 1155 |
rs75814442 | snp | A/G | 0.0383715 | 0.133092 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116392 | AATCCCAGGGGACTG[A/G]AGCCACCAAGAAGAG | 1155 |
rs76039766 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | TBCB | GRCh38.p7 | 19:36123108 | TTTCAAGTTTCATCC[A/G]TGGCATGCCTGTGTC | 1155 |
rs76334680 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TBCB | GRCh38.p7 | 19:36118776 | AAGGTGGGAGGGAGC[A/G]CGGTGGGGATTAAGA | 1155 |
rs76448723 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116255 | ACAGACACTTGCTGG[A/G]CTTTGCCCTCAGTCA | 1155 |
rs76559835 | snp | C/G | 0.109108 | 0.206518 | intron-variant | TBCB | GRCh38.p7 | 19:36122979 | CCATCCCCCAGTCGT[C/G]TTCAGCCACTAATTT | 1155 |
rs76615582 | in-del | -/CC | | | intron-variant | TBCB | GRCh38.p7 | 19:36122753 | AGGGAGACCCTGTCT[-/CC]AAAAAAAAAAAAAAA | 1155 |
rs76953459 | snp | C/G | 0.0130508 | 0.0797186 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114007 | TAGAAAGCCCTCGCG[C/G]CACTTACCTCGGCCC | 1155 |
rs77095979 | snp | A/C | 0.5 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36122759 | ACCCTGTCTCCAAAA[A/C]AAAAAAAAAAAAAAG | 1155 |
rs77581492 | in-del | -/AGC | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115490 | CCCAGCAGCAGCAGC[-/AGC]GGCGGCGGCGGCTGC | 1155 |
rs78029023 | snp | A/G | 0.111224 | 0.207945 | intron-variant | TBCB | GRCh38.p7 | 19:36123448 | TGTGGTTTTTTTTGT[A/G]GGATGGGATTTCGCC | 1155 |
rs78464082 | in-del | -/CAACA | 0.200801 | 0.245111 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116833 | CCATGTTGGCCAGGC[-/CAACA]TGGTCTGGAACTCCT | 1155 |
rs78689013 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TBCB | GRCh38.p7 | 19:36120085 | TTTTGGGAAGCCTAC[C/T]CTCCCATGCTCCTTA | 1155 |
rs78849072 | snp | A/G | 0.108048 | 0.20579 | intron-variant | TBCB | GRCh38.p7 | 19:36122209 | CCACCTGGGGAAGGG[A/G]AGCGGGAGGAGAGGG | 1155 |
rs78885567 | snp | A/G | 0.105569 | 0.204058 | intron-variant | TBCB | GRCh38.p7 | 19:36124976 | TTCTTTGAGTTCCTT[A/G]TATATTCTTCTGCTC | 1155 |
rs79608574 | snp | C/T | 0.0952156 | 0.196321 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121992 | CTGTGCGCTTCGAAG[C/T]GTGGGGCAGTGTCAG | 1155 |
rs79645164 | snp | A/G | 0.109108 | 0.206518 | intron-variant | TBCB | GRCh38.p7 | 19:36125228 | TTCACCCAGTGAATG[A/G]GGGACAGGGGTGGAA | 1155 |
rs79831274 | snp | A/G | 0.0383715 | 0.133092 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122092 | AGGAAGCACCTGGAG[A/G]CTGGGAGCATCTGAA | 1155 |
rs111515084 | snp | C/G/T | 0 | 0 | upstream-variant-2KB, splice-acceptor-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114252 | ATCTGGGTCAGTTCG[C/G/T]TGCAGGGACGCGGGG | 1155 |
rs111540586 | snp | G/T | 0.000937023 | 0.0216248 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114897 | CCCAGCCTTCCGCGC[G/T]TGCTCCGCCGCGCTA | 1155 |
rs111579854 | snp | C/T | 0.00403031 | 0.0447092 | intron-variant | TBCB | GRCh38.p7 | 19:36125660 | CCCACCCCTATCCTT[C/T]CCTGCAGTGTGAATG | 1155 |
rs111804819 | snp | A/G | 0.5 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36119209 | TTATAAATATCACCC[A/G]TATTCATTGTTTAAA | 1155 |
rs111846720 | snp | A/G | 0.5 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36120970 | GGAGTGGGGACAGAC[A/G]GAGGCCTGGGGTGGG | 1155 |
rs112154946 | snp | A/G | 0.00153551 | 0.0276658 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121846 | GGGGGACTCGAAACG[A/G]TCTCAGTCCCTGGAG | 1155 |
rs112357049 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36123875 | GCAAGACTCCATCTC[A/G]AAAAATAAAAAATAC | 1155 |
rs112419799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36118277 | TGAATGTGAAGGGTC[A/G]GGGGAGACAAGGGTT | 1155 |
rs112545487 | snp | A/G | 0.00159688 | 0.0282115 | intron-variant | TBCB | GRCh38.p7 | 19:36125565 | TGTGTGTGCATTTGT[A/G]TGTAAGTCCATGCGT | 1155 |
rs112665309 | snp | A/C/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125942 | TTCACTAGAAACCCA[A/C/G]AAAGTATTTAGAGGA | 1155 |
rs112987109 | snp | C/G | 0 | 0 | upstream-variant-2KB, splice-donor-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114338 | AGGGCCCGCCACTCA[C/G]TCCACTTCGTGCGTG | 1155 |
rs113183340 | snp | C/G/T | 0.5 | 0 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121583 | TACAACGAGGAGGAG[C/G/T]GGGCTCAGCAGGAGG | 1155 |
rs113199583 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36121201 | GGACGGATCGAGTGT[G/T]GGGGGAGACCGGGGG | 1155 |
rs113237625 | snp | A/C/G/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, splice-donor-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114658 | AGACCCCGGCGCTCA[A/C/G/T]CGCGTAGAGCAGAAT | 1155 |
rs113238123 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | TBCB | GRCh38.p7 | 19:36118432 | GGGCATGGTGGTTCA[C/T]GCCTGTAATCCCAGT | 1155 |
rs113244426 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116439 | GGGAGAATCAGAGAG[G/T]GCTTCCTGGAGGAAG | 1155 |
rs113262039 | snp | C/T | 0.00167955 | 0.0289302 | intron-variant | TBCB | GRCh38.p7 | 19:36125646 | GTCCTCTGACCACAC[C/T]CACCCCTATCCTTTC | 1155 |
rs113538709 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36117888 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGGTGGGAT | 1155 |
rs113563085 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113653 | CGCGCCCTGCACCGC[A/G]CAGCCTGATACGGTG | 1155 |
rs113599287 | snp | A/C/G | 0 | 0 | upstream-variant-2KB, splice-donor-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114797 | GCTCCCTCCGCCTCA[A/C/G]CATTCCTGGCAGAAG | 1155 |
rs113893724 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | TBCB | GRCh38.p7 | 19:36123790 | TGAGGCAGGAGAATC[A/G]CTTGAGCCTGGGAGG | 1155 |
rs114053980 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | TBCB | GRCh38.p7 | 19:36123757 | GCGGGTGCCTGTGAT[C/T]GCAGCTACCCGGAAG | 1155 |
rs114198513 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | TBCB | GRCh38.p7 | 19:36119495 | CTCCCTGGCCTCCCC[A/G]CTCCCCATCTCAGCC | 1155 |
rs114740448 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | TBCB | GRCh38.p7 | 19:36119969 | GCTCGCTCCACCCCA[A/C]CCGCACCACCCACTC | 1155 |
rs115149643 | snp | C/T | 0.0387552 | 0.1337 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113947 | GCAGGGTCACCCACA[C/T]TGATATCCCCGCCCC | 1155 |
rs115382811 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115491 | CCCAGCAGCAGCAGC[A/G]GCGGCGGCGGCTGCG | 1155 |
rs115665245 | snp | A/C | 0.0137092 | 0.0816496 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113985 | GACCAAACAAGCCCC[A/C]GATACTTAGAAAGCC | 1155 |
rs116462592 | snp | A/G | 0.00633087 | 0.0559049 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114073 | TGGCCGCACCTGAGA[A/G]GGTAGGGGCTCGGTC | 1155 |
rs116557391 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117099 | GTATTCTAGTGAAGT[C/T]TTCACCGGCCTCAGT | 1155 |
rs117273296 | snp | A/C | 0.15665 | 0.231917 | intron-variant | TBCB | GRCh38.p7 | 19:36125268 | CCAGTGAAGTGGCTA[A/C]CATATTAGTCCCGGC | 1155 |
rs117692728 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TBCB | GRCh38.p7 | 19:36120139 | CTCCATAGCCATCCT[C/T]CAGTGTTTCATAGGT | 1155 |
rs117966240 | snp | A/G | 0.00159033 | 0.0281538 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113544 | GGTGCATGGACAGCC[A/G]GCCAGCTACGCTTAC | 1155 |
rs118094953 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116478 | GAGCTGAGGGATGAG[A/G]AAAGGGTGACTTAAG | 1155 |
rs118095168 | snp | C/G | 0.114738 | 0.210248 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116937 | CTTTCTGTCCTTATT[C/G]CCTCCCGACCTCACT | 1155 |
rs137946199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117321 | ATAGTGCCTGGGACA[C/G]GGAGGATAGTCCGTG | 1155 |
rs138199063 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125509 | TGATGAGCCACTGGG[A/G]AAAAATGATGGCAGG | 1155 |
rs138428261 | snp | C/T | 1.65261e-05 | 0.0028745 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120758 | TATGAGGACGTGTCC[C/T]GGGTGGAGAAGTACA | 1155 |
rs138638369 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113358 | TTGGAATAGGTACCA[A/G]AAATGCTCAACACTG | 1155 |
rs138844822 | snp | C/T | 1.65252e-05 | 0.00287443 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120751 | TGGTGAGTATGAGGA[C/T]GTGTCCCGGGTGGAG | 1155 |
rs138947982 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TBCB | GRCh38.p7 | 19:36125121 | CAAGATCAAGCTGTC[A/G]GCAGGTTGGATTTAT | 1155 |
rs138984946 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TBCB | GRCh38.p7 | 19:36121162 | AATGCGAGTGGACAG[A/G]GTGGCGGTCAGTGAG | 1155 |
rs139279016 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TBCB | GRCh38.p7 | 19:36119230 | ATTGTTTAAAATAAC[A/G]GAACTTCAAATTTGT | 1155 |
rs139507463 | snp | C/T | 0.0219847 | 0.102514 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114329 | CCCCAGCTCAGGGCC[C/T]GCCACTCACTCCACT | 1155 |
rs139731164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36123767 | GTGATCGCAGCTACC[C/T]GGAAGGCTGAGGCAG | 1155 |
rs140157747 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36118352 | GATGCATCAGTGACG[A/T]CTGGGAGGACATCCT | 1155 |
rs140607574 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125482 | GCCTGGCTACTGGAT[C/T]GGTGTCCGCTATGAT | 1155 |
rs140740967 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TBCB | GRCh38.p7 | 19:36120191 | TGGCCTTCTCCCTGC[A/T]CAATGAGCACAGCCT | 1155 |
rs140846484 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116693 | GGAGTGCAGTGGCAC[C/T]ATCGGGCTCACTGCA | 1155 |
rs140883777 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116828 | TTTTGCCATGTTGGC[-/CT]CAGGCTGGTCTGGAA | 1155 |
rs141361922 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TBCB | GRCh38.p7 | 19:36123860 | AGCCTGGGCAACCAT[G/T]CAAGACTCCATCTCA | 1155 |
rs141544940 | snp | A/G | 5.36639e-05 | 0.00517968 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125752 | GGTGGGGGACTTCCC[A/G]GAGGAGGACTACGGG | 1155 |
rs141686471 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114471 | TCCAGACAAGATTGG[C/G]AGGAGAGGGCAGGGT | 1155 |
rs141926543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36118065 | GCCACCGCACCCGGC[C/T]CAGAATCTACTTTCT | 1155 |
rs142309046 | snp | C/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115627 | TCCCTCAACACCTTC[C/T]GCTCCGAGAAGCGAT | 1155 |
rs142727772 | snp | C/T | 0.000408145 | 0.0142796 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125710 | CCAGGCCAAGTATGG[C/T]GCCTTTGTCAAGCCA | 1155 |
rs142763699 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36122820 | TGGGTGTGTTGCCTG[C/T]TAGTGGGTGGGGACC | 1155 |
rs142894953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117148 | CCTTTCCCCTTCTTT[C/G]CTTTATTTTAGATTT | 1155 |
rs143109145 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126319 | CCCAGCTGCTGGGGA[A/G]GCTGAGGCAGGAGAA | 1155 |
rs143211071 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113008 | TGCTGGGCCCCAGGT[A/G]GGGATGGAAGGAAAT | 1155 |
rs143733124 | snp | C/T | 5.01878e-05 | 0.00500913 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116222 | ACTCCCCCACCCCAC[C/T]TTTCATTTGGTTATT | 1155 |
rs143912330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118987 | TCAGGCCTCTGCTGG[A/G]TGCACAGGACTGAGC | 1155 |
rs143966459 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | TBCB | GRCh38.p7 | 19:36117615 | CCTCAGCCTCGCAAA[C/G]TGCTGGGATTACAGG | 1155 |
rs144358732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119754 | AAAAATTAGCCGGGT[A/G]TGGTGGTGTGTGCCT | 1155 |
rs144534068 | snp | C/T | 0.000113106 | 0.00751933 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115656 | ATACAGCCGCAGCCT[C/T]ACCATCGCTGAGTTC | 1155 |
rs145056144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36124187 | TCTTTGCATGGCCAT[C/T]TGTGTATCTTCTTTG | 1155 |
rs145076637 | snp | C/G/T | 0.000148747 | 0.00862288 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115571 | GCAAGATGGAGGTGA[C/G/T]GGGGGTGTCGGCACC | 1155 |
rs145279646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119704 | CTAGACCAGCCTGAC[C/T]AGCATGGCAAAATGT | 1155 |
rs145653505 | snp | A/T | 0.000378803 | 0.0137571 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125492 | TGGATTGGTGTCCGC[A/T]ATGATGAGCCACTGG | 1155 |
rs146109844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36120983 | ACGGAGGCCTGGGGT[A/G]GGAATGAGGGCCGGG | 1155 |
rs146129583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118155 | TTCTTTTTTCTCTCG[C/T]TGATTAACTGTTCAT | 1155 |
rs146133484 | snp | A/G | 6.62295e-05 | 0.00575416 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114347 | CACTCACTCCACTTC[A/G]TGCGTGATCTTGTTG | 1155 |
rs146159771 | snp | C/G/T | 0.0001246 | 0.00789224 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125731 | TGTCAAGCCAGCAGT[C/G/T]GTGACGGTGGGGGAC | 1155 |
rs146299612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119039 | TGAAGCTAAGGGGTG[C/T]GGGTGTTCATAGGCA | 1155 |
rs146402521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122136 | CAGCCAGGTGAAAAG[A/G]GAGGAAGAGTTCCCG | 1155 |
rs146645834 | snp | A/G | 0.00944938 | 0.0680838 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114765 | AGCCATTCCTCGCCC[A/G]CCTTCTAACATCACC | 1155 |
rs146919750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117232 | TTATTTACTCTCTGT[C/T]TCCCTGGATTCGAGT | 1155 |
rs147021992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36119972 | CGCTCCACCCCACCC[A/G]CACCACCCACTCTAG | 1155 |
rs147357335 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113901 | AGAGAACTTCACCAA[C/T]AGGTAAGGGCCCGGC | 1155 |
rs147557343 | snp | A/G | 0.000245598 | 0.0110787 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115610 | CCGTTTTCATCAGCA[A/G]CTCCCTCAACACCTT | 1155 |
rs147822873 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36123806 | CTTGAGCCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 1155 |
rs147974947 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36120099 | CCCTCCCATGCTCCT[C/T]AAGCCTCTTCCCTGT | 1155 |
rs148135859 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TBCB | GRCh38.p7 | 19:36118009 | GACCTCAGGTAATCC[A/G]CCCACCTCGGCCTCC | 1155 |
rs148196307 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TBCB | GRCh38.p7 | 19:36124393 | ACCTGGCTAATTTCT[A/G]TATTTTTAGTAGAGA | 1155 |
rs148366566 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125744 | GTCGTGACGGTGGGG[C/G]ACTTCCCGGAGGAGG | 1155 |
rs148426844 | snp | A/G | 3.19474e-05 | 0.00399658 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115566 | GCGCGGCAAGATGGA[A/G]GTGACGGGGGTGTCG | 1155 |
rs148504570 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | TBCB | GRCh38.p7 | 19:36122679 | AGGATGGCTTGAGCC[C/T]GGGAGTTGAGGCTGC | 1155 |
rs148725233 | snp | C/T | 0.0178098 | 0.0926698 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126264 | TTTCTCTACTAAAAA[C/T]ACAAAAAAATTAGCC | 1155 |
rs148944876 | snp | A/C | | | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116184 | CGGCTGCCGCATCCA[A/C]GTGAGGACTCTCTAT | 1155 |
rs149117559 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TBCB | GRCh38.p7 | 19:36124205 | TGTATCTTCTTTGGA[G/T]AAATGTCTATTCAGA | 1155 |
rs149169812 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TBCB | GRCh38.p7 | 19:36119721 | GCATGGCAAAATGTC[A/G]TCTCTACTTAAAAAT | 1155 |
rs149272294 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TBCB | GRCh38.p7 | 19:36120965 | GGCTGGGAGTGGGGA[C/T]AGACGGAGGCCTGGG | 1155 |
rs149642132 | snp | A/G | 0.00716266 | 0.059414 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126074 | CCCACCTCATCTGCT[A/G]TAGCTACCAGGAAGA | 1155 |
rs149812865 | snp | A/G | 0.000199117 | 0.00997592 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114686 | AATGCGGTTCTCCTT[A/G]TCTTCCTTGGGGTAC | 1155 |
rs150004516 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36119643 | CTGTAATCCCACCCA[C/G]TACATTGGGAGGCTG | 1155 |
rs150055773 | snp | A/G | 3.50422e-05 | 0.00418568 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114609 | GCAGGGGGCAGGGCG[A/G]GGCCACGCTGGGAAC | 1155 |
rs150091844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36120527 | GGGGGTGAGGAAGGG[A/G]AGGTGGCCAGTGTAC | 1155 |
rs150163654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116892 | TACTAAAGTGCTGGG[A/T]TTACAGGCGTGAGCC | 1155 |
rs150338841 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120729 | TTGACCACAGTGGCG[C/T]CCGCCTTGGTGAGTA | 1155 |
rs150615061 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | TBCB | GRCh38.p7 | 19:36123593 | ATAAATTTCTGTGTG[G/T]CTGGGCATGGTGGCT | 1155 |
rs150874978 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114568 | TGAGGTGCAGCGGAG[A/G]GCGAACAGGGAGTCC | 1155 |
rs150983591 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116583 | CTGGACAGCTTGGGA[C/G]AAACCAGAACACAGG | 1155 |
rs151215211 | snp | A/C/G/T | 4.9465e-05 | 0.00497299 | missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116115 | AGTTGACGACAAGTT[A/C/G/T]TACAGCAAGCTGGAT | 1155 |
rs180762158 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TBCB | GRCh38.p7 | 19:36119523 | GCCAGAGGGAGCCTG[G/T]GACCACCTGAGTCAG | 1155 |
rs180995760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36124975 | GTTCTTTGAGTTCCT[C/T]GTATATTCTTCTGCT | 1155 |
rs181039739 | snp | A/C/G | 0.000316568 | 0.0125779 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113554 | CAGCCGGCCAGCTAC[A/C/G]CTTACCGTGAGCGCC | 1155 |
rs181537145 | snp | C/G | 0.00279162 | 0.0372561 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126323 | GCTGCTGGGGAGGCT[C/G]AGGCAGGAGAATGGC | 1155 |
rs182212578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119079 | CAGTGGCATCTTTGA[G/T]CAGGTTTCATAACAG | 1155 |
rs182243336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123983 | GACTTTTTTGAGGAC[C/T]TGCCACACTGCTTCC | 1155 |
rs182394863 | snp | A/G | 0.00102226 | 0.022585 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114075 | GCCGCACCTGAGAGG[A/G]TAGGGGCTCGGTCAC | 1155 |
rs182485837 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113049 | GCTGGGCTGTGGAGT[A/G]TCCATGGTTTGTGTA | 1155 |
rs182578152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118046 | GCTGGGATTACAGGC[A/T]TGAGCCACCGCACCC | 1155 |
rs183594454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116505 | TAAGAGAAAGAGGTG[C/G]AAAGGAGGGAGCAGG | 1155 |
rs183609890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36125013 | TCATTGGGATGCTGT[C/T]TTTTGTCGCTGAGTT | 1155 |
rs183907368 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TBCB | GRCh38.p7 | 19:36122677 | GGAGGATGGCTTGAG[C/T]CCGGGAGTTGAGGCT | 1155 |
rs184064924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36118777 | AGGTGGGAGGGAGCG[C/T]GGTGGGGATTAAGAC | 1155 |
rs184798875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36124630 | CTCGTTCCAACCTCC[A/G]CCTCCCGGGTTCAAA | 1155 |
rs185116917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119111 | CGGTTCAGGTACACA[C/T]AGACCTCCCAGGCCA | 1155 |
rs185188027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36124222 | AATGTCTATTCAGAT[C/G]CTTTGCCTTTTGTTT | 1155 |
rs185255944 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36119008 | AGGACTGAGCCTTTG[G/T]GCCACCCTGGGCAGC | 1155 |
rs185607477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36119720 | AGCATGGCAAAATGT[C/T]GTCTCTACTTAAAAA | 1155 |
rs185949069 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114490 | AGAGGGCAGGGTGAT[A/C]CCGGAGGATATGACG | 1155 |
rs186078536 | snp | A/G | 0.000692281 | 0.018592 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113620 | ACCAGCTCCCGGCCC[A/G]ACACCTACGCACAGC | 1155 |
rs186553587 | snp | A/T | 0.00279162 | 0.0372561 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126324 | CTGCTGGGGAGGCTG[A/T]GGCAGGAGAATGGCG | 1155 |
rs186625543 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36118416 | ATAAAAAGAATTGGT[C/T]GGGCATGGTGGTTCA | 1155 |
rs186773102 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122030 | GGGGAAACGGGCGGC[G/T]TGACCAAGGCAGGAG | 1155 |
rs186805158 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126051 | TGTTCCCCCATCTTC[C/T]CATCATTCCCACCTC | 1155 |
rs186887842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122943 | ACTGTCTGGTATTTC[C/T]GTCTTTATGCCTGTG | 1155 |
rs187326286 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36124006 | CTGCTTCCCACAGCC[A/G]CTGCAGCAGTTTTCA | 1155 |
rs188017612 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36119275 | GAAATTCTCAGTGAC[A/G]CTTCATCCGGAGGTA | 1155 |
rs188499583 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | TBCB | GRCh38.p7 | 19:36124312 | TGCATCCTCTGCCTC[C/G]CGGGTTCAAGCAATT | 1155 |
rs188602623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118862 | CAGGTGTTCACAGGC[A/C]CCCTCTGGCTGTGTG | 1155 |
rs188936111 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117252 | TGGATTCGAGTGCCC[G/T]GAGGGTGGAAATTTT | 1155 |
rs189261942 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124636 | CCAACCTCCGCCTCC[C/T]GGGTTCAAACGGTTC | 1155 |
rs189575453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36125021 | ATGCTGTCTTTTGTC[C/G]CTGAGTTGTGTATTA | 1155 |
rs189970762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123166 | GCATTGAGCGCCTAG[A/G]CCACAGTGTATCCAG | 1155 |
rs190063242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121226 | CGGGGGCCTCAGGGC[C/T]GGAGGAGGGCGGAGG | 1155 |
rs190119611 | snp | C/T | 8.24627e-05 | 0.00642063 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114062 | CAGCCTCCTTGTGGC[C/T]GCACCTGAGAGGGTA | 1155 |
rs190577677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119011 | ACTGAGCCTTTGGGC[C/T]ACCCTGGGCAGCTGA | 1155 |
rs190582219 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113271 | GGAGAGTGGAGACAC[A/G]GGTGTCTGGCCCATG | 1155 |
rs190610117 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116454 | GGCTTCCTGGAGGAA[A/G]GGATGTCTGAGCTGA | 1155 |
rs191712186 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126115 | AAGGGAGGGGATATC[A/C]TTTGCCTTTAAAAAT | 1155 |
rs191826859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36118501 | GGAGTTCGAGACGGT[A/G]AAACCCCGTCTCTCC | 1155 |
rs191984966 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TBCB | GRCh38.p7 | 19:36122284 | GAGCAGTGTGGATTT[G/T]TTTAAAAAGAACAGG | 1155 |
rs192908734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124026 | AGCAGTTTTCATTCC[C/T]GCCAGCAGTGCAGAA | 1155 |
rs192974805 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36119007 | CAGGACTGAGCCTTT[A/G]GGCCACCCTGGGCAG | 1155 |
rs193114952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124517 | AACATGAGCCACTGC[A/G]CCCATCGGTATGTCG | 1155 |
rs193248118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117268 | GAGGGTGGAAATTTT[A/G]ATCACTATAATTCAC | 1155 |
rs199554432 | snp | C/T | 0.000549382 | 0.0165647 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116023 | CCTCCTTCTTCTCAC[C/T]CTGCCTCCTCCTCAC | 1155 |
rs199564247 | snp | A/G | 0.00118714 | 0.0243343 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114080 | ACCTGAGAGGGTAGG[A/G]GCTCGGTCACCGGAG | 1155 |
rs199646187 | in-del | -/CAG | 0.206642 | 0.246211 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115477 | GCGGGGCTGATAGCC[-/CAG]CAGCAGCAGCAGCGG | 1155 |
rs199647655 | snp | C/T | 4.96085e-05 | 0.00498014 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114366 | GTGATCTTGTTGACA[C/T]AGATGCAGCTGTTGT | 1155 |
rs199754543 | snp | C/T | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126133 | TGCCTTTAAAAATGA[C/T]GTACAGCCAGCTGGG | 1155 |
rs199881119 | snp | C/T | 1.64846e-05 | 0.0028709 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114789 | CATCACCCGCTCCCT[C/T]CGCCTCACCATTCCT | 1155 |
rs200039146 | snp | A/C/G/T | 6.65059e-05 | 0.00576616 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116203 | AGGACTCTCTATCTG[A/C/G/T]GACACTCCCCCACCC | 1155 |
rs200123490 | snp | A/G | 0.00211789 | 0.0324725 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121678 | CTGTGAGGTGCGGGC[A/G]GCGGGACAATCCCCT | 1155 |
rs200166261 | snp | C/G/T | 0.000103551 | 0.00719491 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113722 | ACTCACGCATGGAAT[C/G/T]TGGTGTTTATTACAC | 1155 |
rs200251576 | snp | C/G | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125732 | GTCAAGCCAGCAGTC[C/G]TGACGGTGGGGGACT | 1155 |
rs200345741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115724 | GCGAAGAAATTGGGG[A/G]GTTCCCGGAAGGGGG | 1155 |
rs200481198 | snp | C/T | 0.00236363 | 0.0342962 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116210 | TCTATCTGGGACACT[C/T]CCCCACCCCACCTTT | 1155 |
rs200549990 | snp | C/G/T | 0.00102696 | 0.0226368 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114888 | CGCAGCCCTCCCAGC[C/G/T]TTCCGCGCTTGCTCC | 1155 |
rs200864904 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120375 | CAGAGGCCCATCGAG[C/G]AGATGCGCTGTGCAC | 1155 |
rs200919588 | snp | A/G | 4.95921e-05 | 0.00497932 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114719 | CATGTTGTTACTGTG[A/G]GGAGGGGGAGGTGCC | 1155 |
rs200939642 | in-del | -/AAAAAAAA | | | intron-variant | TBCB | GRCh38.p7 | 19:36122755 | GGAGACCCTGTCTCC[-/AAAAAAAA]AAAAAAAAAAAGATA | 1155 |
rs200990838 | snp | C/G/T | 3.29974e-05 | 0.00406175 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114132 | CCTTCGCCCAGTGAG[C/G/T]AGACGAGCCTCACTT | 1155 |
rs201075532 | snp | C/G | 8.35806e-05 | 0.006464 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114875 | GACGCGCAGCCCGCG[C/G]AGCCCTCCCAGCCTT | 1155 |
rs201232718 | in-del | -/GA | 0.200801 | 0.245111 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116834 | CATGTTGGCCAGGCT[-/GA]GGTCTGGAACTCCTG | 1155 |
rs201239089 | snp | G/T | 0.000269614 | 0.0116075 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115720 | CGGGGCGAAGAAATT[G/T]GGGGGTTCCCGGAAG | 1155 |
rs201373916 | snp | A/G | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126245 | GGCTAACACGGTGAA[A/G]CCCTTTCTCTACTAA | 1155 |
rs201433073 | snp | C/G/T | 1.64928e-05 | 0.00287161 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114172 | AGTACCAGCTGAACG[C/G/T]TCACTTTTGGCACGG | 1155 |
rs201582028 | snp | C/G | 1.67184e-05 | 0.00289118 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114877 | CGCGCAGCCCGCGCA[C/G]CCCTCCCAGCCTTCC | 1155 |
rs201692898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36125622 | CTTCTAGAGTGGAGC[C/T]ATGTGAGGGTCCTCT | 1155 |
rs201763604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115680 | TGAGTTCAAGGTGTG[C/G]CCATGGGGGCGGGGT | 1155 |
rs201890657 | in-del | -/TTTTTTT | | | intron-variant | TBCB | GRCh38.p7 | 19:36123255 | CTATGAACCTTCTTC[-/TTTTTTT]TTTTTTTTTTTTTCT | 1155 |
rs202004947 | snp | A/T | 0.000115455 | 0.007597 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116139 | GCTGGATCAAGAGGA[A/T]GCGCTCCTGGGCTCC | 1155 |
rs202044151 | snp | A/C/G | 0.000245045 | 0.0110667 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114610 | CAGGGGGCAGGGCGG[A/C/G]GCCACGCTGGGAACA | 1155 |
rs202058207 | snp | A/G | 3.45167e-05 | 0.00415417 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113824 | CATGGCGTCCTGGCA[A/G]AAATGATGCATGGTT | 1155 |
rs202093479 | snp | C/T | 0.000362671 | 0.0134612 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114800 | CCCTCCGCCTCACCA[C/T]TCCTGGCAGAAGCGA | 1155 |
rs202182379 | in-del | -/TG | 0.0252325 | 0.109451 | intron-variant | TBCB | GRCh38.p7 | 19:36121201 | GGACGGATCGAGTGT[-/TG]GGGGAGACCGGGGGC | 1155 |
rs367614069 | snp | A/C | 0.000873946 | 0.0208856 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114133 | CTTCGCCCAGTGAGG[A/C]GACGAGCCTCACTTT | 1155 |
rs367634558 | snp | A/G | 0.000379278 | 0.0137657 | intron-variant | TBCB | GRCh38.p7 | 19:36125417 | ATTTCTTCTATGTCC[A/G]GAAGCTTCACAGGGA | 1155 |
rs367733273 | snp | G/T | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126215 | ATCACGAGGTCAGGA[G/T]ATCGAGACCATCCTG | 1155 |
rs367832263 | snp | A/G | 0.000214527 | 0.0103546 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114006 | TTAGAAAGCCCTCGC[A/G]CCACTTACCTCGGCC | 1155 |
rs367941648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122399 | ACAGTGAGCTATGAT[G/T]GTGTCATTGCACCCT | 1155 |
rs368104936 | snp | C/T | 1.69092e-05 | 0.00290763 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113859 | AGGATTTGGACCCAG[C/T]AGCGCCTTACCCCAA | 1155 |
rs368197432 | snp | A/G | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126194 | TTGGGAGGCCAGGGC[A/G]GGTGGATCACGAGGT | 1155 |
rs368386652 | snp | A/G | 3.3534e-05 | 0.00409461 | intron-variant | TBCB | GRCh38.p7 | 19:36120812 | CAGAGGCAAGGTACG[A/G]GCAGGTGGGCGTCGA | 1155 |
rs368480740 | snp | C/T | 1.64928e-05 | 0.00287161 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114151 | CGAGCCTCACTTTAC[C/T]TCCCCAGTACCAGCT | 1155 |
rs368763862 | snp | C/T | 1.6593e-05 | 0.00288031 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114416 | ACAGTTCCGGCACTA[C/T]GAGAGGGCGAGTGTG | 1155 |
rs368952201 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113963 | TGATATCCCCGCCCC[C/G]AGAAAGGACCAAACA | 1155 |
rs369134537 | snp | G/T | 0.000117021 | 0.00764831 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116010 | GGGGCCTCCGTGGCC[G/T]CCTTCTTCTCACCCT | 1155 |
rs369219038 | snp | A/C | 8.35317e-05 | 0.00646211 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114307 | CCTCCAGAGCCAACA[A/C]CCCCGCCCCCAGCTC | 1155 |
rs369336555 | snp | A/G | 5.36476e-05 | 0.00517889 | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113785 | GTGGCCGCAGTGTGG[A/G]GCTGTGCACACGTAG | 1155 |
rs369422481 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124198 | CCATTTGTGTATCTT[C/T]TTTGGAGAAATGTCT | 1155 |
rs369595160 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36123464 | GGATGGGATTTCGCC[A/G]TGTGGCCCAGGCTGG | 1155 |
rs369615453 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36117869 | CTCCCCGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 1155 |
rs369674679 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | TBCB | GRCh38.p7 | 19:36125561 | TGTCTGTGTGTGCAT[A/T]TGTGTGTAAGTCCAT | 1155 |
rs369679191 | snp | A/C | 3.7701e-05 | 0.00434155 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113719 | AAAACTCACGCATGG[A/C]ATCTGGTGTTTATTA | 1155 |
rs369762368 | snp | A/G | 1.66338e-05 | 0.00288386 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114434 | GAGGGCGAGTGTGGG[A/G]GAAAGGGGGTCACGG | 1155 |
rs369798257 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36118728 | ATGGGGAAGGGGTGC[A/C]CTAGGAGTGGGGCAC | 1155 |
rs370055101 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36120871 | TGCAGGTATGAGGGC[G/T]GGCAGGTTAGACAGG | 1155 |
rs370131754 | snp | A/G/T | 4.98098e-05 | 0.00499027 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114860 | GTCGGGCTCCATGGC[A/G/T]ACGCGCAGCCCGCGC | 1155 |
rs370138891 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116107 | CTGTATGGAGTTGAC[A/G]ACAAGTTCTACAGCA | 1155 |
rs370183718 | snp | A/G | 1.76098e-05 | 0.00296725 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125677 | CTGCAGTGTGAATGG[A/G]AAACGCTACTTCGAA | 1155 |
rs370358153 | snp | C/G | 5.01081e-05 | 0.00500515 | intron-variant | TBCB | GRCh38.p7 | 19:36120660 | TGCACCCAGCACCCA[C/G]GCCTCCCTGGCCAGA | 1155 |
rs370420591 | snp | C/T | 0.00156912 | 0.027966 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121705 | CCCTCGCCGGGGCAC[C/T]GTCATGTATGTAGGT | 1155 |
rs370522612 | snp | A/G | 0.000102496 | 0.00715803 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115528 | GTGTGAGGCGGCTGG[A/G]CCGCGCTGCAGGCAT | 1155 |
rs370560092 | snp | A/G | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126150 | TACAGCCAGCTGGGC[A/G]CGGTGGCTCACGCCT | 1155 |
rs370733896 | snp | A/G | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126195 | TGGGAGGCCAGGGCG[A/G]GTGGATCACGAGGTC | 1155 |
rs370865201 | snp | A/C | | | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121924 | GGAAGTGGGAGGCGC[A/C]GGCGGAGTGATCTGT | 1155 |
rs371046526 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118509 | AGACGGTGAAACCCC[A/G]TCTCTCCTAAAAATA | 1155 |
rs371349439 | snp | G/T | 3.36933e-05 | 0.00410433 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114889 | GCAGCCCTCCCAGCC[G/T]TCCGCGCTTGCTCCG | 1155 |
rs371393156 | snp | C/T | 3.30235e-05 | 0.00406333 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113983 | AGGACCAAACAAGCC[C/T]CAGATACTTAGAAAG | 1155 |
rs371592763 | snp | A/G | 0.000115669 | 0.00760402 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120752 | GGTGAGTATGAGGAC[A/G]TGTCCCGGGTGGAGA | 1155 |
rs371607562 | snp | A/C/G | 0.000137883 | 0.00830219 | intron-variant | TBCB | GRCh38.p7 | 19:36120835 | GGCGTCGAGGGGTGC[A/C/G]TGGGGGCCAGAGGGA | 1155 |
rs371720256 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123268 | TCTTTTTTTTTTTTT[C/T]TTTTTTCTAATTTGA | 1155 |
rs371808930 | snp | C/T | 0.000233715 | 0.0108075 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116014 | CCTCCGTGGCCTCCT[C/T]CTTCTCACCCTGCCT | 1155 |
rs371957619 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116192 | GCATCCACGTGAGGA[C/T]TCTCTATCTGGGACA | 1155 |
rs372008072 | snp | C/G | 2.97517e-05 | 0.00385681 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113727 | CGCATGGAATCTGGT[C/G]TTTATTACACTCGGG | 1155 |
rs372170589 | snp | A/C | 1.6483e-05 | 0.00287076 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114766 | GCCATTCCTCGCCCG[A/C]CTTCTAACATCACCC | 1155 |
rs372238547 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36123388 | ACCTCGGCCTCCTGA[C/G]TAGCTGGGAATACAG | 1155 |
rs372267761 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36122256 | GGCATGGGCAGGGCG[C/G]CGTCACAGTGGAGAG | 1155 |
rs372327571 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125498 | GGTGTCCGCTATGAT[A/G]AGCCACTGGGGAAAA | 1155 |
rs372384224 | snp | G/T | 1.64982e-05 | 0.00287208 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114134 | TTCGCCCAGTGAGGA[G/T]ACGAGCCTCACTTTA | 1155 |
rs372405358 | in-del | -/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118724 | GAAGATGGGGAAGGG[-/G]TGCCCTAGGAGTGGG | 1155 |
rs372428065 | snp | G/T | 1.65378e-05 | 0.00287552 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114240 | ACGTCGGCGATAATC[G/T]GGGTCAGTTCGCTGC | 1155 |
rs372511743 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114470 | TTCCAGACAAGATTG[C/G]GAGGAGAGGGCAGGG | 1155 |
rs372632284 | in-del | -/AG | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122057 | GGAGTGAGGGAACAC[-/AG]GGGGCTGTGTGAGCC | 1155 |
rs372875479 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36121455 | CCGTGAACGTGGGCC[C/T]CTCGTGGGTGGAGCG | 1155 |
rs373082247 | snp | A/C/G/T | 0.000133205 | 0.00816019 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114868 | CCATGGCGACGCGCA[A/C/G/T]CCCGCGCAGCCCTCC | 1155 |
rs373092686 | snp | C/T | 6.65979e-05 | 0.00577014 | intron-variant | TBCB | GRCh38.p7 | 19:36120688 | AGACCCTGATCCCCA[C/T]GGAGCCCCTCCCCTC | 1155 |
rs373142265 | snp | A/G | 6.00811e-05 | 0.0054806 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113749 | ACACTCGGGGGAGAG[A/G]GGAGGTCACTCGGTC | 1155 |
rs373252386 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36120996 | GTGGGAATGAGGGCC[A/G]GGAGGTGTCAGGGGT | 1155 |
rs373271375 | snp | A/G | 5.09135e-05 | 0.00504521 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113842 | ATGATGCATGGTTAG[A/G]AAGGATTTGGACCCA | 1155 |
rs373516015 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36121398 | GGTGGGAGACCTGGG[A/G]CTTGGGTGACAGCCC | 1155 |
rs373584395 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36117456 | TTCAAGCTATTCTCC[G/T]GCCTCAGCCTCCCAA | 1155 |
rs373659436 | snp | G/T | 0.000122137 | 0.00781369 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114621 | GCGGGGCCACGCTGG[G/T]AACAGGTGGACCTGC | 1155 |
rs373777567 | snp | G/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114085 | AGAGGGTAGGGGCTC[G/T]GTCACCGGAGGCTTC | 1155 |
rs373869094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118182 | TCATTCCCCATCTGT[A/G]TTGTGCCAGGGGTTT | 1155 |
rs373949149 | snp | A/G | 4.95528e-05 | 0.00497734 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114730 | TGTGGGGAGGGGGAG[A/G]TGCCAGGGGTTAGTT | 1155 |
rs374618000 | snp | A/G | 0.000181622 | 0.00952774 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113986 | ACCAAACAAGCCCCA[A/G]ATACTTAGAAAGCCC | 1155 |
rs374667464 | snp | A/G/T | 1.76505e-05 | 0.00297068 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125682 | GTGTGAATGGGAAAC[A/G/T]CTACTTCGAATGCCA | 1155 |
rs374745788 | snp | C/G | 0.000412035 | 0.0143474 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114764 | GAGCCATTCCTCGCC[C/G]GCCTTCTAACATCAC | 1155 |
rs375170781 | snp | A/G | 0.000155988 | 0.00883005 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115536 | CGGCTGGACCGCGCT[A/G]CAGGCATCCGCAGGG | 1155 |
rs375335190 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36122337 | GTAAACTCAGCACTT[G/T]GGGAGAACAAGGTGG | 1155 |
rs375391541 | snp | C/G/T | 3.29464e-05 | 0.00405861 | intron-variant | TBCB | GRCh38.p7 | 19:36125536 | CAGGTAACAAGAATT[C/G/T]CCACTCAGGTGTCTG | 1155 |
rs375409074 | snp | A/T | 0.000159987 | 0.00894248 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121703 | TCCCCTCGCCGGGGC[A/T]CCGTCATGTATGTAG | 1155 |
rs375409909 | snp | A/T | 1.66685e-05 | 0.00288686 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114278 | CGGGGGTGCAAAATT[A/T]CGCTCAGACCCAGCC | 1155 |
rs375469729 | snp | A/G | 0.000923224 | 0.0214653 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114139 | CCAGTGAGGAGACGA[A/G]CCTCACTTTACCTCC | 1155 |
rs375476178 | snp | C/T | 0.000374436 | 0.0136776 | intron-variant | TBCB | GRCh38.p7 | 19:36120825 | CGGGCAGGTGGGCGT[C/T]GAGGGGTGCGTGGGG | 1155 |
rs375610951 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126152 | CAGCCAGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 1155 |
rs375706556 | snp | C/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114774 | TCGCCCGCCTTCTAA[C/G]ATCACCCGCTCCCTC | 1155 |
rs375713982 | snp | A/G | 0.000108017 | 0.00734824 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125765 | CCGGAGGAGGACTAC[A/G]GGTTGGACGAGATAT | 1155 |
rs375765443 | snp | A/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123270 | TTTTTTTTTTTTTTT[A/T]TTTTCTAATTTGAGA | 1155 |
rs375775148 | snp | A/G | 1.6513e-05 | 0.00287336 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114737 | AGGGGGAGGTGCCAG[A/G]GGTTAGTTCTGGAGC | 1155 |
rs375909698 | snp | A/G | 3.59706e-05 | 0.00424075 | intron-variant | TBCB | GRCh38.p7 | 19:36120853 | GGGGCCAGAGGGAGT[A/G]TGTGCAGGTATGAGG | 1155 |
rs375946363 | snp | A/G | 0.000169811 | 0.00921285 | intron-variant | TBCB | GRCh38.p7 | 19:36120823 | TACGGGCAGGTGGGC[A/G]TCGAGGGGTGCGTGG | 1155 |
rs376057216 | snp | A/C/G | 3.30531e-05 | 0.00406518 | synonymous-codon, missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120742 | CGCCCGCCTTGGTGA[A/C/G]TATGAGGACGTGTCC | 1155 |
rs376064713 | snp | A/C/G/T | 6.6103e-05 | 0.00574872 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120759 | ATGAGGACGTGTCCC[A/C/G/T]GGTGGAGAAGTACAC | 1155 |
rs376077742 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36117488 | TAGCTGGGATTACAG[A/G]TGTGCACCACCACGC | 1155 |
rs376216521 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TBCB | GRCh38.p7 | 19:36121236 | AGGGCCGGAGGAGGG[C/T]GGAGGAGGAAGGCGG | 1155 |
rs376333650 | snp | C/T | 3.65925e-05 | 0.00427726 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113775 | CGGTCCAGCGGTGGC[C/T]GCAGTGTGGGGCTGT | 1155 |
rs376659596 | snp | A/G | 4.96052e-05 | 0.00497998 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114368 | GATCTTGTTGACATA[A/G]ATGCAGCTGTTGTCG | 1155 |
rs376782710 | snp | A/G | 0.000437904 | 0.0147905 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113958 | CACATTGATATCCCC[A/G]CCCCCAGAAAGGACC | 1155 |
rs376822383 | snp | C/T | 0.000197892 | 0.0099452 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114056 | AGAACACAGCCTCCT[C/T]GTGGCCGCACCTGAG | 1155 |
rs376901763 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36120443 | TCTGTGACTTTGGGG[C/T]CCTTGGCGATGTTGA | 1155 |
rs377048349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123563 | AGCCACCATGCTAGG[C/G]CTGAACATTCTTTTA | 1155 |
rs377070718 | snp | A/T | 0.000211201 | 0.010274 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125674 | TTCCTGCAGTGTGAA[A/T]GGGAAACGCTACTTC | 1155 |
rs377393551 | snp | C/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115726 | GAAGAAATTGGGGGG[C/T]TCCCGGAAGGGGGAG | 1155 |
rs377495271 | snp | A/G | 9.96115e-05 | 0.00705662 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114422 | CCGGCACTACGAGAG[A/G]GCGAGTGTGGGGGAA | 1155 |
rs377670806 | snp | A/G | 0.000134562 | 0.00820141 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121584 | ACAACGAGGAGGAGC[A/G]GGCTCAGCAGGAGGC | 1155 |
rs377738858 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36118497 | GTCAGGAGTTCGAGA[C/T]GGTGAAACCCCGTCT | 1155 |
rs386808976 | in-del | AGGCT/TCATGGCCAACATGA | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116830 | TTTGCCATGTTGGCC[AGGCT/TCATGGCCAACATGA]GGTCTGGAACTCCTG | 1155 |
rs397746956 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124998 | TTCTGCTCAGTTTTT[-/T]CATTGGGATGCTGTC | 1155 |
rs398079851 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124997 | CTTCTGCTCAGTTTT[-/T]TCATTGGGATGCTGT | 1155 |
rs527410432 | in-del | -/GT | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36123318 | CCAGGCTGGAATGCA[-/GT]GGCACAATCTCGGCC | 1155 |
rs527462711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122968 | CCTGTGTGTACCCAT[C/T]CCCCAGTCGTCTTCA | 1155 |
rs527882913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, splice-donor-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115929 | CTGGATTGCGGCCCC[C/G]TGCGTCCTGACTGGG | 1155 |
rs527992928 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36119471 | CAACCTCGCCATCCC[A/G]GCAGCTTCCTCCCTG | 1155 |
rs528053425 | snp | C/T | 0.000632606 | 0.0177737 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114869 | CATGGCGACGCGCAG[C/T]CCGCGCAGCCCTCCC | 1155 |
rs528089905 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120728 | ATTGACCACAGTGGC[A/G]CCCGCCTTGGTGAGT | 1155 |
rs528128853 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126409 | CCTGGGCGACAGAGC[A/G]AGACTGTCTCAAAAA | 1155 |
rs528465448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123159 | TAGTCCTGCATTGAG[C/T]GCCTAGACCACAGTG | 1155 |
rs528495306 | snp | C/G | 1.6646e-05 | 0.00288491 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114440 | GAGTGTGGGGGAAAG[C/G]GGGTCACGGAAGGAT | 1155 |
rs528837914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115995 | ATTGATGCAAGGGGC[A/G]GGGCCTCCGTGGCCT | 1155 |
rs528874843 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115383 | AGGAGAGCCCTCTTC[C/T]TGGCGGTGGGGAAGG | 1155 |
rs528896565 | snp | A/G | 0.00100886 | 0.0224369 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121687 | GCGGGCGGCGGGACA[A/G]TCCCCTCGCCGGGGC | 1155 |
rs529542468 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125862 | CATGGCCCTTTTCTC[C/T]TGACCCCATTTTAAT | 1155 |
rs529899718 | snp | C/G/T | 0.000945245 | 0.0217204 | upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113699 | CACGAGGCAAATAAA[C/G/T]ACAGAAAACTCACGC | 1155 |
rs529983063 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113101 | ACATGATGTCTCTCG[A/G]ACCCCAGTGGGTGGG | 1155 |
rs530012297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118661 | CTCCAGTTTGGATGA[C/T]AGAGTGAGATCCTAT | 1155 |
rs530054979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36118062 | TGAGCCACCGCACCC[A/G]GCCCAGAATCTACTT | 1155 |
rs530055094 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36124331 | GTTCAAGCAATTCTC[A/C]TGCCTCAGCCTCCCG | 1155 |
rs530087123 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TBCB | GRCh38.p7 | 19:36123768 | TGATCGCAGCTACCC[A/G]GAAGGCTGAGGCAGG | 1155 |
rs530309557 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36125443 | AGGGATTTCTCTTCT[A/G]TTGGCAGGTCTCACA | 1155 |
rs530407200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119987 | GCACCACCCACTCTA[C/G]AGCGTGAAGGACATT | 1155 |
rs530442640 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126030 | CTCTGTCTCCTCATA[C/T]CTTGCTGTTCCCCCA | 1155 |
rs530514300 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126400 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTG | 1155 |
rs530772350 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36117765 | GGTGGAGTTTATTTA[C/T]TTATTTTTTATTTTT | 1155 |
rs530998004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124383 | GCGCTACAACACCTG[G/T]CTAATTTCTGTATTT | 1155 |
rs531082662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124812 | CCTACTAAAGTGCTG[C/G]GATTACAGGCGTGAG | 1155 |
rs531419400 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36117334 | CAGGGAGGATAGTCC[A/G]TGAATCGTTTTTTGT | 1155 |
rs531513013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117846 | TCTCGGCTCACTGCA[A/T]CCTCCGCCTCCCCGG | 1155 |
rs531559939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36119001 | GGTGCACAGGACTGA[A/G]CCTTTGGGCCACCCT | 1155 |
rs531716929 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TBCB | GRCh38.p7 | 19:36122254 | GGGGCATGGGCAGGG[C/T]GGCGTCACAGTGGAG | 1155 |
rs531906877 | snp | A/G | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125676 | CCTGCAGTGTGAATG[A/G]GAAACGCTACTTCGA | 1155 |
rs532355652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123735 | CAAAAATTAACTGGG[C/T]GTGGTGGCGGGTGCC | 1155 |
rs532391105 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36123160 | AGTCCTGCATTGAGC[A/G]CCTAGACCACAGTGT | 1155 |
rs532523248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36117501 | AGGTGTGCACCACCA[C/T]GCCTGGCTAATTTTG | 1155 |
rs532928521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122130 | AGGCAGCAGCCAGGT[A/G]AAAAGGGAGGAAGAG | 1155 |
rs533098626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116022 | GCCTCCTTCTTCTCA[C/T]CCTGCCTCCTCCTCA | 1155 |
rs533132349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121822 | CTCTGCCTAGGGGCG[C/T]GGGGTTGGGGGGGAC | 1155 |
rs533290416 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114577 | GCGGAGGGCGAACAG[C/G]GAGTCCGATCACAGA | 1155 |
rs533334515 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115158 | AAACCGCAAAACACT[C/G]AGCATCCAGGACAGA | 1155 |
rs533725351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120562 | CTACTTCTCCCTTCC[A/G]CTGGGCTCAGGAGAG | 1155 |
rs534129652 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120315 | GGGGGCAGAACAGGA[A/G]GAGATGCTCTGGGGC | 1155 |
rs534178324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121253 | GAGGAGGAAGGCGGA[A/T]GATGAAGGCAGATGT | 1155 |
rs534539036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36125376 | GGGTAGGCATGGATC[C/T]AGGGTGATCCTGAAA | 1155 |
rs535197021 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113364 | TAGGTACCAGAAATG[C/T]TCAACACTGGAAAGC | 1155 |
rs535254823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120874 | AGGTATGAGGGCGGG[C/T]AGGTTAGACAGGGCC | 1155 |
rs535287446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120187 | TGGTTGGCCTTCTCC[C/T]TGCACAATGAGCACA | 1155 |
rs536109140 | snp | A/G | 0.000161642 | 0.0089886 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113460 | CTGTGCAGGGATCCG[A/G]CCCTTCCGCTGCAGT | 1155 |
rs536110935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119369 | TGGGCCCGCTCTCTC[C/T]CTCACCCCCACATCC | 1155 |
rs536244607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118949 | GAGAGTCCTGATGAG[C/G]GGACGAGGTCTGGAG | 1155 |
rs536273323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124524 | GCCACTGCGCCCATC[A/G]GTATGTCGGGGTTTG | 1155 |
rs536301670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117550 | AGAGTTGGGGTTTCA[C/T]CATGTTGGCCAGGCT | 1155 |
rs536317660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124124 | TGTGAAGTGGAACAT[C/T]ATCATGGTTTTGATT | 1155 |
rs536436667 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36123296 | TGAGACAGCATCTGG[C/G]TATTGCCCAGGCTGG | 1155 |
rs536848739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124600 | GCTGGAATACAGTGG[C/T]ATGATCTCAGCTCGC | 1155 |
rs536894584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124733 | TATTTTTAGTAGAGA[C/T]GGGGCTTCACCGTGT | 1155 |
rs536999466 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36119494 | CCTCCCTGGCCTCCC[C/T]GCTCCCCATCTCAGC | 1155 |
rs537074306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119411 | ATCCTCTCGGCTCCA[C/T]CTACAAAAACTTCCC | 1155 |
rs537106821 | snp | C/T | 0 | 0 | intron-variant | TBCB | GRCh38.p7 | 19:36125177 | CAGTAGTGCCATCCC[C/T]CTTAGGTTTTTACAA | 1155 |
rs537267259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117576 | AGGCTGGTCTTGAAC[G/T]CCTGACCTCAAGTGA | 1155 |
rs537308364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123391 | TCGGCCTCCTGAGTA[A/G]CTGGGAATACAGGTA | 1155 |
rs537805628 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36120133 | ATTTTTCTCCATAGC[C/T]ATCCTCCAGTGTTTC | 1155 |
rs537875609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121907 | CCAGAGTGTTTGTGG[A/G]GGGAAGTGGGAGGCG | 1155 |
rs538667715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123454 | TTTTTTTGTAGGATG[C/G]GATTTCGCCATGTGG | 1155 |
rs538686782 | snp | C/G | | | upstream-variant-2KB, stop-gained, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113553 | ACAGCCGGCCAGCTA[C/G]GCTTACCGTGAGCGC | 1155 |
rs538717890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122370 | GGCTTGCTTGAGCCC[C/G]GGAGTTGGAGGTTAC | 1155 |
rs539075422 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116320 | AGTGCAGCCTGACGA[C/G]AGACAGACCCATCAT | 1155 |
rs539279158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121237 | GGGCCGGAGGAGGGC[A/G]GAGGAGGAAGGCGGA | 1155 |
rs539284419 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36118917 | GAAGAGTAGGGAGAC[C/T]AGGAAGGGGCTGCTG | 1155 |
rs539642411 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114926 | TACAGGTCGCGGGAG[A/G]GGCCAGGCCTAGGTG | 1155 |
rs539680282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120916 | GCCAGTGGTGTAGAC[A/G]GGGGGCCGAGAGCTT | 1155 |
rs540024634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118259 | GCTAAATGGCCAGAG[A/G]ACTGAATGTGAAGGG | 1155 |
rs540111520 | snp | A/T | | | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114581 | AGGGCGAACAGGGAG[A/T]CCGATCACAGAGGCA | 1155 |
rs540259579 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114983 | CACACGTGCTGGCTC[C/T]CCGCCGCCTCGGGCT | 1155 |
rs540632039 | snp | A/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123387 | CACCTCGGCCTCCTG[A/T]GTAGCTGGGAATACA | 1155 |
rs540652509 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114753 | GGTTAGTTCTGGAGC[C/G]ATTCCTCGCCCGCCT | 1155 |
rs540698307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120439 | GGACTCTGTGACTTT[C/G]GGGCCCTTGGCGATG | 1155 |
rs540889563 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36124652 | GGGTTCAAACGGTTC[C/T]CCTGCCTCAGCCTCC | 1155 |
rs541195061 | snp | C/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117295 | TCACTACTGTGTCCC[C/T]AGTACTTGGAATAGT | 1155 |
rs541679670 | snp | C/T | 0.000291265 | 0.0120643 | upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113708 | AATAAACACAGAAAA[C/T]TCACGCATGGAATCT | 1155 |
rs541932467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124341 | TTCTCATGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 1155 |
rs542244918 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124757 | ACCGTGTTAGCCAGG[A/T]TGGTCTCGATCTCCT | 1155 |
rs542408165 | snp | C/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116716 | TCACTGCAGCCTTCA[C/T]CTCCTGGGTTCAAGT | 1155 |
rs542704293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117749 | GAAAATTTAGCTTCA[C/G]GGTGGAGTTTATTTA | 1155 |
rs542842067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116428 | TGACTCCACCTGGGA[A/G]AATCAGAGAGGGCTT | 1155 |
rs542880578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115942 | CCGTGCGTCCTGACT[A/G]GGGGGTCTTTTGGAG | 1155 |
rs542917348 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121651 | GGCCAGCTCCATCCC[C/T]GTGGGCAGCCGCTGT | 1155 |
rs543286615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117851 | GCTCACTGCAACCTC[C/T]GCCTCCCCGGTTCAA | 1155 |
rs543670639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117233 | TATTTACTCTCTGTC[G/T]CCCTGGATTCGAGTG | 1155 |
rs543718013 | snp | A/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113402 | GGGCGCTTTAGTCCA[A/G]AGCCCATTGCCCTCT | 1155 |
rs543899115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122062 | GAGGGAACACAGGGG[A/G]CTGTGTGAGCCCAGA | 1155 |
rs544473914 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36121033 | AGTCAGACGTGGTCG[G/T]GGGAGGGCTGGGAAA | 1155 |
rs544675321 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115080 | CAATTTTTGGGCATC[A/G]CCGCCTCAGTTTACA | 1155 |
rs544810902 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36120351 | GTTGGGGCCAGCTTA[G/T]GAGAGTCCCAGAGGC | 1155 |
rs544856891 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TBCB | GRCh38.p7 | 19:36120518 | AGCTTGGATGGGGGT[G/T]AGGAAGGGGAGGTGG | 1155 |
rs545262140 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115827 | TCGCGGCGGGGCGGG[C/T]CCGGAGAGAACTCGA | 1155 |
rs545300614 | snp | A/G | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121575 | TCGGCCGGTACAACG[A/G]GGAGGAGCGGGCTCA | 1155 |
rs545646952 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | TBCB | GRCh38.p7 | 19:36121073 | GTTGAGGGGTAGGTG[G/T]GGGGGCTGGGTGTTG | 1155 |
rs545875990 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36120322 | GAACAGGAAGAGATG[A/C]TCTGGGGCCTGAGGT | 1155 |
rs545984688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124823 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 1155 |
rs546206464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36119749 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGTGTG | 1155 |
rs546222868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121182 | CGGTCAGTGAGGGCG[C/T]CTGGGACGGATCGAG | 1155 |
rs546274765 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115267 | CTCCTACCTCCGGGC[G/T]TCAGTCTTCGCCGCC | 1155 |
rs546409595 | snp | C/G | 0.0023933 | 0.0345097 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126218 | ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 1155 |
rs546973797 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36120995 | GGTGGGAATGAGGGC[C/T]GGGAGGTGTCAGGGG | 1155 |
rs547256831 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36119360 | GGTGTTCCTTGGGCC[C/G]GCTCTCTCCCTCACC | 1155 |
rs547285685 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36118882 | CTGGCTGTGTGTGGG[A/G]AACAGGTGGTGGAGG | 1155 |
rs547327415 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36124520 | ATGAGCCACTGCGCC[C/T]ATCGGTATGTCGGGG | 1155 |
rs548172260 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113153 | GGGCCTGTCACGGAA[G/T]GCAGAGTGCAGACGG | 1155 |
rs548208966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36118701 | AAAAAAAAAAAAAAA[A/G]GTTAACTGAAGATGG | 1155 |
rs548212644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36125092 | ATTTCTCACAGTAAT[A/G]GAGGCTAGAAGTTCA | 1155 |
rs548543657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123330 | GCAGTGGCACAATCT[C/T]GGCCATTTCAGCCTT | 1155 |
rs548764451 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125859 | GCCCATGGCCCTTTT[C/T]TCCTGACCCCATTTT | 1155 |
rs548804190 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36124096 | TGTCTTTTGCTTACA[C/G]TCATCCACTGGGTGT | 1155 |
rs548928150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120503 | GAGGCAGCCTCTGGG[A/T]GCTTGGATGGGGGTG | 1155 |
rs549231820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116890 | CCTACTAAAGTGCTG[A/G]GATTACAGGCGTGAG | 1155 |
rs549272767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122236 | AGGGGAGAAGTGTAG[C/T]CAGGGGCATGGGCAG | 1155 |
rs549321058 | in-del | -/TCC | 0.00478085 | 0.0486577 | intron-variant | TBCB | GRCh38.p7 | 19:36121436 | CCTGGAAGAGAGAGT[-/TCC]TCCGTGAACGTGGGC | 1155 |
rs550021603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117392 | CCTTGTTCCCCAGGC[C/T]GGAATGCAGTGGTGT | 1155 |
rs550101841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116946 | CTTATTCCCTCCCGA[C/T]CTCACTCAGTCTGTA | 1155 |
rs550411605 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36122432 | CCTGGGCAGCAGAGA[A/G]AGACCCAGTCTCAAA | 1155 |
rs550414394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121227 | GGGGGCCTCAGGGCC[A/G]GAGGAGGGCGGAGGA | 1155 |
rs550798736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120891 | GGTTAGACAGGGCCC[C/T]TGCAGGGAGGCCAGT | 1155 |
rs550998216 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36125976 | CATGATTTGGGGACC[C/T]ACTGGGTAAATAGTG | 1155 |
rs551104316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36117835 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC | 1155 |
rs551162265 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123572 | GCTAGGCCTGAACAT[C/T]CTTTTATAAATTTCT | 1155 |
rs551195625 | snp | A/T | 1.64844e-05 | 0.00287087 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114784 | TCTAACATCACCCGC[A/T]CCCTCCGCCTCACCA | 1155 |
rs551232461 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114519 | CGACAGGACTCTCTT[C/T]GGGGATGGGCAGGAC | 1155 |
rs551307928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119378 | TCTCTCCCTCACCCC[A/C]ACATCCACTCTCATC | 1155 |
rs551330146 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114601 | TCACAGAGGCAGGGG[A/G]CAGGGCGGGGCCACG | 1155 |
rs551378932 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36119126 | CAGACCTCCCAGGCC[A/T]CTCAAGGAAGGTGTT | 1155 |
rs551389690 | in-del | -/GGA | 0.00318978 | 0.0398085 | intron-variant | TBCB | GRCh38.p7 | 19:36121227 | GGGGGCCTCAGGGCC[-/GGA]GGAGGGCGGAGGAGG | 1155 |
rs551440729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117634 | TGGGATTACAGGCAT[A/G]AGCCACCACGCCCAG | 1155 |
rs551634038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121247 | AGGGCGGAGGAGGAA[A/G]GCGGATGATGAAGGC | 1155 |
rs551640599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121830 | AGGGGCGCGGGGTTG[A/G]GGGGGACTCGAAACG | 1155 |
rs551750579 | snp | C/G | 0.000297349 | 0.0121896 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114827 | GCGAATACCCACGAA[C/G]CCCGGCTCGTAAGTC | 1155 |
rs551787672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120657 | CCCTGCACCCAGCAC[C/T]CAGGCCTCCCTGGCC | 1155 |
rs552218790 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113321 | GCAGATGGTGGGTCA[C/T]GGGCGGAAGAGTCTG | 1155 |
rs552355079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119163 | TGGAGCCACTGGGGA[A/G]TTTTTACATTTTCTA | 1155 |
rs552642437 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36118797 | GGGATTAAGACAGGC[C/G]ACTTCTGTGGCCAAA | 1155 |
rs552793566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36119582 | CCCTGGTGGCACTTC[A/G]CTCCAGATAAAAACC | 1155 |
rs552834549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36125395 | GTGATCCTGAAATTT[C/T]ATGGGGATTTCTTCT | 1155 |
rs552873811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36124669 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGAACTAC | 1155 |
rs552953067 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124688 | AGCTGGAACTACAGG[C/T]GCCCGCCACCACACC | 1155 |
rs553332370 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113384 | CACTGGAAAGCAGGG[C/T]GGGGGCGCTTTAGTC | 1155 |
rs553863698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122373 | TTGCTTGAGCCCCGG[A/G]GTTGGAGGTTACAGT | 1155 |
rs553890719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123461 | GTAGGATGGGATTTC[A/G]CCATGTGGCCCAGGC | 1155 |
rs553901841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121993 | TGTGCGCTTCGAAGC[A/G]TGGGGCAGTGTCAGT | 1155 |
rs553990836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116363 | GCCTAGAGTGGTCTG[G/T]GCTGGGATCAGGAAA | 1155 |
rs554217333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117105 | TAGTGAAGTCTTCAC[C/T]GGCCTCAGTGTTAAC | 1155 |
rs554351170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124539 | GGTATGTCGGGGTTT[C/G]GTTTTGTTTTTTTTC | 1155 |
rs554368387 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115305 | GTCCTTTCCCGGGCC[G/T]CTATTGGAAGAACCG | 1155 |
rs554653527 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36118951 | GAGTCCTGATGAGGG[A/G]ACGAGGTCTGGAGCT | 1155 |
rs554656166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117554 | TTGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC | 1155 |
rs554726725 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124939 | CACTTTGTAATGGGA[-/T]TTTTTTTTTGCAAAG | 1155 |
rs554825687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122610 | ACAAAACTTTTGTCA[C/G]TTGTGGTGGTGAGCA | 1155 |
rs555842522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121256 | GAGGAAGGCGGATGA[G/T]GAAGGCAGATGTGCG | 1155 |
rs555846824 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114996 | TCCCCGCCGCCTCGG[A/G]CTCGGCTCTCTCCGC | 1155 |
rs556423640 | snp | A/G | | | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113045 | AGGTGCTGGGCTGTG[A/G]AGTGTCCATGGTTTG | 1155 |
rs556466555 | in-del | -/GCGG | 0.000199621 | 0.00998852 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121730 | GTAGGTGCGTGGCTC[-/GCGG]GCCCGGTCCCGGGCT | 1155 |
rs556634287 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116279 | TCAGTCATACCCGAG[A/T]TAGGTCCTGCCTTCG | 1155 |
rs556778162 | snp | A/C/G | 5.02175e-05 | 0.00501065 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114665 | GGCGCTCACCGCGTA[A/C/G]AGCAGAATGCGGTTC | 1155 |
rs556827384 | snp | G/T | 0.00398564 | 0.0444627 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126401 | CACTCCAGCCTGGGC[G/T]ACAGAGCGAGACTGT | 1155 |
rs557725741 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36117577 | GGCTGGTCTTGAACT[C/T]CTGACCTCAAGTGAT | 1155 |
rs557748390 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114957 | CTTCGCCAAAAGAGG[A/G]CGGAGCTGCGCACAC | 1155 |
rs557784888 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36120917 | CCAGTGGTGTAGACG[G/T]GGGGCCGAGAGCTTG | 1155 |
rs557848921 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114212 | GGTCCGCGGCAACGT[A/G]GGGTCCTGGGACACG | 1155 |
rs557975377 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115482 | GGCTGATAGCCCAGC[A/G]GCAGCAGCGGCGGCG | 1155 |
rs558272582 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126273 | TAAAAATACAAAAAA[A/C]TTAGCCGGGCATGGT | 1155 |
rs558312255 | snp | C/T | 1.65086e-05 | 0.00287298 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114116 | ACACCCTTCCCTCCT[C/T]CCTTCGCCCAGTGAG | 1155 |
rs558351115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119470 | CCAACCTCGCCATCC[C/T]GGCAGCTTCCTCCCT | 1155 |
rs558665200 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113561 | CCAGCTACGCTTACC[A/G]TGAGCGCCGCGAGAA | 1155 |
rs558898294 | snp | A/T | 0.0010714 | 0.0231204 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113582 | GCCGCGAGAAGCTGC[A/T]CGTGTGCGAGGACTG | 1155 |
rs559178787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36117609 | TGCCCACCTCAGCCT[C/T]GCAAAGTGCTGGGAT | 1155 |
rs559221345 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TBCB | GRCh38.p7 | 19:36123403 | GTAGCTGGGAATACA[C/G]GTACTCATCACCACC | 1155 |
rs559279608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36124313 | GCATCCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 1155 |
rs559923022 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115007 | TCGGGCTCGGCTCTC[G/T]CCGCGCAGAGGTTTC | 1155 |
rs560009153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116633 | CAGTACATCCTTTCT[A/G]TCTTTTTTTGAGACA | 1155 |
rs560175907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117275 | GAAATTTTGATCACT[A/G]TAATTCACTACTGTG | 1155 |
rs560324494 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118260 | CTAAATGGCCAGAGG[A/G]CTGAATGTGAAGGGT | 1155 |
rs560434867 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TBCB | GRCh38.p7 | 19:36121074 | TTGAGGGGTAGGTGT[A/G]GGGGCTGGGTGTTGT | 1155 |
rs560783684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115897 | CGGTCCAGAGGGCGG[A/G]GGCAAGAGGCGAGGG | 1155 |
rs561018315 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TBCB | GRCh38.p7 | 19:36117333 | ACAGGGAGGATAGTC[C/T]GTGAATCGTTTTTTG | 1155 |
rs561227240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122997 | CAGCCACTAATTTAC[A/G]TCTGTCTCTAATTTG | 1155 |
rs561270405 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115959 | GGGGTCTTTTGGAGG[A/C]AAAGGGACGTGGCGA | 1155 |
rs561444430 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TBCB | GRCh38.p7 | 19:36121212 | GTGTTGGGGGAGACC[A/G]GGGGCCTCAGGGCCG | 1155 |
rs561746561 | in-del | -/GTG | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36122613 | AAACTTTTGTCAGTT[-/GTG]GTGGTGAGCACCTAT | 1155 |
rs561924622 | snp | A/G | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116520 | GAAAGGAGGGAGCAG[A/G]GTGTACAGAGGCCTA | 1155 |
rs562187386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120455 | GGGCCCTTGGCGATG[C/T]TGATGCCAGCAAGCG | 1155 |
rs562469990 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36117328 | CTGGGACAGGGAGGA[C/T]AGTCCGTGAATCGTT | 1155 |
rs562470083 | snp | C/T | 0.00022414 | 0.0105839 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121808 | CCTCGGAGACCACGC[C/T]CTGCCTAGGGGCGCG | 1155 |
rs562813476 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36122752 | GAGGGAGACCCTGTC[-/T]CCAAAAAAAAAAAAA | 1155 |
rs562983821 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115088 | GGGCATCGCCGCCTC[A/G]GTTTACAGAATAGTA | 1155 |
rs563049872 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | TBCB | GRCh38.p7 | 19:36121043 | GGTCGGGGGAGGGCT[C/G]GGAAAGTGGAGGGAG | 1155 |
rs563155940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122680 | GGATGGCTTGAGCCC[A/G]GGAGTTGAGGCTGCA | 1155 |
rs563220853 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114293 | ACGCTCAGACCCAGC[C/T]TCCAGAGCCAACACC | 1155 |
rs563223760 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36125427 | TGTCCAGAAGCTTCA[C/T]AGGGATTTCTCTTCT | 1155 |
rs563479394 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36117643 | AGGCATGAGCCACCA[C/T]GCCCAGCCCTGTGAA | 1155 |
rs564277934 | snp | A/C | 1.65318e-05 | 0.002875 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114373 | TGTTGACATAGATGC[A/C]GCTGTTGTCGGCCTC | 1155 |
rs564422218 | snp | G/T | 1.65121e-05 | 0.00287329 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114738 | GGGGGAGGTGCCAGG[G/T]GTTAGTTCTGGAGCC | 1155 |
rs564598712 | snp | A/G | 1.77294e-05 | 0.00297731 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125703 | TCGAATGCCAGGCCA[A/G]GTATGGCGCCTTTGT | 1155 |
rs564868800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36118056 | CAGGCATGAGCCACC[A/G]CACCCGGCCCAGAAT | 1155 |
rs565023152 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36124251 | TTTTTGACACACAGT[C/G]TCACTCCGTCACCCA | 1155 |
rs565212338 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36123694 | AGCCTGGCCAACATG[A/G]TGAAACCCCATCTCT | 1155 |
rs565295736 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36125112 | CTAGAAGTTCAAGAT[C/G]AAGCTGTCAGCAGGT | 1155 |
rs565650867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124523 | AGCCACTGCGCCCAT[C/T]GGTATGTCGGGGTTT | 1155 |
rs565835693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117518 | CCTGGCTAATTTTGT[A/G]ATTTTGTATTTTAAG | 1155 |
rs565869005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123250 | TGCTGCTATGAACCT[C/T]CTTCTTTTTTTTTTT | 1155 |
rs566547940 | in-del | -/CAC | 0.00517822 | 0.0506191 | intron-variant | TBCB | GRCh38.p7 | 19:36119851 | CGTGAGCTGAGATCA[-/CAC]CACCACCACACTCCA | 1155 |
rs566766837 | snp | A/G | 0.000928649 | 0.0215282 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121834 | GCGCGGGGTTGGGGG[A/G]GACTCGAAACGATCT | 1155 |
rs566809755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121249 | GGCGGAGGAGGAAGG[C/T]GGATGATGAAGGCAG | 1155 |
rs567173941 | snp | C/T | 1.66479e-05 | 0.00288508 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114866 | CTCCATGGCGACGCG[C/T]AGCCCGCGCAGCCCT | 1155 |
rs567479047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36122242 | GAAGTGTAGTCAGGG[A/G]CATGGGCAGGGCGGC | 1155 |
rs567591791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116246 | GGTTATTCAACAGAC[A/G]CTTGCTGGGCTTTGC | 1155 |
rs567631275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121857 | AACGATCTCAGTCCC[A/T]GGAGGTGACGGAACC | 1155 |
rs567678589 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115268 | TCCTACCTCCGGGCT[G/T]CAGTCTTCGCCGCCT | 1155 |
rs567950881 | snp | C/T | | | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121888 | ATCTGCCGACACTGA[C/T]GGCCCAGAGTGTTTG | 1155 |
rs568166506 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126151 | ACAGCCAGCTGGGCA[C/T]GGTGGCTCACGCCTG | 1155 |
rs568640646 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115392 | CTCTTCCTGGCGGTG[A/G]GGAAGGGACGGCGGC | 1155 |
rs568677325 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114919 | GCCGCGCTACAGGTC[A/G]CGGGAGGGGCCAGGC | 1155 |
rs568819164 | snp | A/C | 0.00318978 | 0.0398085 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126404 | TCCAGCCTGGGCGAC[A/C]GAGCGAGACTGTCTC | 1155 |
rs568827996 | in-del | -/TGAG | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36118579 | AGCTACTCAGGAGGC[-/TGAG]TGAGGCAGGAGGATC | 1155 |
rs568960844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120915 | GGCCAGTGGTGTAGA[C/G]GGGGGGCCGAGAGCT | 1155 |
rs568981397 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36119648 | ATCCCACCCAGTACA[C/T]TGGGAGGCTGAGGTG | 1155 |
rs569461772 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123726 | CTAAAAATTCAAAAA[G/T]TAACTGGGCGTGGTG | 1155 |
rs569517836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119403 | CTCATCAAATCCTCT[C/T]GGCTCCACCTACAAA | 1155 |
rs569565933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119983 | ACCCGCACCACCCAC[A/T]CTAGAGCGTGAAGGA | 1155 |
rs569666594 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113198 | ATTCAGGCTCCAGAT[A/C]GAAAGGCAAGGGAAG | 1155 |
rs569740030 | snp | C/T | 0.000384837 | 0.0138662 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121844 | GGGGGGGACTCGAAA[C/T]GATCTCAGTCCCTGG | 1155 |
rs569771690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124564 | TTTTTCTTTTGAGAC[A/G]TAATCTCGCTTTGTG | 1155 |
rs569840535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118154 | CTTCTTTTTTCTCTC[A/G]TTGATTAACTGTTCA | 1155 |
rs569883482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117563 | CACCATGTTGGCCAG[A/G]CTGGTCTTGAACTCC | 1155 |
rs570231851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123378 | CCATCCTCCCACCTC[A/G]GCCTCCTGAGTAGCT | 1155 |
rs570449082 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TBCB | GRCh38.p7 | 19:36120072 | GAAACATCCCCTCTT[G/T]TGGGAAGCCTACCCT | 1155 |
rs570915178 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36118861 | TCAGGTGTTCACAGG[A/C]CCCCTCTGGCTGTGT | 1155 |
rs571159810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124478 | CACCTGAGCTGGTGG[A/G]TCTCCCAAAGTGCTA | 1155 |
rs571171724 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124704 | GCCCGCCACCACACC[C/T]GGCTAATTTTTTGTA | 1155 |
rs571479055 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36117404 | GGCCGGAATGCAGTG[C/G]TGTGATCTCAGCTCA | 1155 |
rs571575962 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116962 | CTCACTCAGTCTGTA[C/G]CAGCCACATTGCTCC | 1155 |
rs571684813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121981 | AGGCACGCGGCCTGT[C/G]CGCTTCGAAGCGTGG | 1155 |
rs571711743 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TBCB | GRCh38.p7 | 19:36122317 | AGGCATGATGGCTCA[C/T]GCCTGTAAACTCAGC | 1155 |
rs571919198 | snp | A/G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115131 | CAGAGCCGGGAAAAC[A/G/T]ATGCGCATCGTAAAC | 1155 |
rs572071761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117720 | TAATGTAATTATCCC[C/T]ATTTTGCAGAAGAGA | 1155 |
rs572073621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36124082 | CCAGCACTTTAGTCT[A/G]TCTTTTGCTTACAGT | 1155 |
rs572212663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123481 | GTGGCCCAGGCTGGT[C/T]TCAAACTCTTCCCGC | 1155 |
rs572445789 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121595 | GAGCGGGCTCAGCAG[C/G]AGGCCGAGGCCGCCC | 1155 |
rs572482980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117115 | TTCACCGGCCTCAGT[A/G]TTAACGTTTACCTCA | 1155 |
rs573419882 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126276 | AAATACAAAAAAATT[A/C]GCCGGGCATGGTGGT | 1155 |
rs573537333 | snp | G/T | 0.000648649 | 0.0179973 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115679 | CTGAGTTCAAGGTGT[G/T]GCCATGGGGGCGGGG | 1155 |
rs573557650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36122059 | AGTGAGGGAACACAG[A/G]GGGCTGTGTGAGCCC | 1155 |
rs573848407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36119750 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGTGT | 1155 |
rs574046756 | snp | C/T | 7.3918e-05 | 0.00607894 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115682 | AGTTCAAGGTGTGGC[C/T]ATGGGGGCGGGGTCC | 1155 |
rs574083436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121264 | CGGATGATGAAGGCA[A/G]ATGTGCGCTGAAGGG | 1155 |
rs574083522 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115079 | CCAATTTTTGGGCAT[C/T]GCCGCCTCAGTTTAC | 1155 |
rs574220491 | snp | A/G | 3.44394e-05 | 0.00414952 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114640 | AGGTGGACCTGCCGG[A/G]GAAGACCCCGGCGCT | 1155 |
rs574223732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36121032 | CAGTCAGACGTGGTC[A/G]GGGGAGGGCTGGGAA | 1155 |
rs574254238 | in-del | -/A | 0.235854 | 0.249599 | intron-variant | TBCB | GRCh38.p7 | 19:36119894 | GAGCGAGACTCCGTC[-/A]AAAAAAAAAAAAAAA | 1155 |
rs574255340 | snp | C/T | 0.000231237 | 0.0107501 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114224 | CGTGGGGTCCTGGGA[C/T]ACGTCGGCGATAATC | 1155 |
rs575091751 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36124836 | GCGTGAGCCACCGCA[A/C]CCGGCCAGTATGTCA | 1155 |
rs575536095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36120321 | AGAACAGGAAGAGAT[A/G]CTCTGGGGCCTGAGG | 1155 |
rs575992607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36118970 | AGGTCTGGAGCTGTG[A/G]GTCAGGCCTCTGCTG | 1155 |
rs576105478 | snp | C/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116441 | GAGAATCAGAGAGGG[C/T]TTCCTGGAGGAAGGG | 1155 |
rs576200699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36123579 | CTGAACATTCTTTTA[C/T]AAATTTCTGTGTGGC | 1155 |
rs576247297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36118369 | TGGGAGGACATCCTG[A/G]AGGTGGTGCTGCTGG | 1155 |
rs576371967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116472 | ATGTCTGAGCTGAGG[A/G]ATGAGGAAAGGGTGA | 1155 |
rs576479190 | snp | C/T | 0.000962464 | 0.0219159 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113508 | TACGCAGCGCTGCTC[C/T]CTGGAAGCTCACCTT | 1155 |
rs576771790 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TBCB | GRCh38.p7 | 19:36124257 | ACACACAGTCTCACT[C/G]CGTCACCCAGGCTGG | 1155 |
rs576902033 | snp | A/G/T | 0.000156752 | 0.00885164 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113570 | CTTACCGTGAGCGCC[A/G/T]CGAGAAGCTGCACGT | 1155 |
rs576979156 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TBCB | GRCh38.p7 | 19:36118453 | TAATCCCAGTGCCTT[C/G]GGAGGCTGAGGTGGA | 1155 |
rs577499599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TBCB | GRCh38.p7 | 19:36117614 | ACCTCAGCCTCGCAA[A/G]GTGCTGGGATTACAG | 1155 |
rs577517228 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TBCB | GRCh38.p7 | 19:36122386 | GGAGTTGGAGGTTAC[A/G]GTGAGCTATGATTGT | 1155 |
rs577534375 | snp | A/C | 0.00011623 | 0.00762243 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114261 | AGTTCGCTGCAGGGA[A/C]GCGGGGGTGCAAAAT | 1155 |
rs577588738 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36120512 | TCTGGGAGCTTGGAT[-/G]GGGGTGAGGAAGGGG | 1155 |
rs577837830 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36120154 | CCAGTGTTTCATAGG[C/T]ACCTGTTCCTTTGTT | 1155 |
rs577883760 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118151 | CTGCTTCTTTTTTCT[C/G]TCGTTGATTAACTGT | 1155 |
rs578031132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116299 | TCCTGCCTTCGTGGA[A/G]CCTCCAGTGCAGCCT | 1155 |
rs578073589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115775 | GTGACTGGGCGGGCC[C/G]GGAGGTGATCCCAGG | 1155 |
rs578101320 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121566 | GCAGCAAGCTCGGCC[A/G]GTACAACGAGGAGGA | 1155 |
rs578115893 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TBCB | GRCh38.p7 | 19:36121052 | AGGGCTGGGAAAGTG[A/G]AGGGAGTTGAGGGGT | 1155 |
rs745327942 | snp | C/G | 5.00672e-05 | 0.00500311 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114288 | AAATTACGCTCAGAC[C/G]CAGCCTCCAGAGCCA | 1155 |
rs745392814 | snp | C/T | 1.65693e-05 | 0.00287826 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116036 | ACCCTGCCTCCTCCT[C/T]ACAGTGTAAACTGGA | 1155 |
rs745439910 | in-del | -/CTCACCCTGCCTCCTCCTC | 1.66852e-05 | 0.0028883 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116017 | CGTGGCCTCCTTCTT[-/CTCACCCTGCCTCCTCCTC]CTCACCCTGCCTCCT | 1155 |
rs745573676 | snp | G/T | 1.83159e-05 | 0.00302615 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115709 | GTCCGGAGGGGCGGG[G/T]CGAAGAAATTGGGGG | 1155 |
rs745600584 | snp | C/T | 1.77128e-05 | 0.00297591 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125695 | ACGCTACTTCGAATG[C/T]CAGGCCAAGTATGGC | 1155 |
rs745609799 | snp | C/T | 0.000156458 | 0.00884333 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121704 | CCCCTCGCCGGGGCA[C/T]CGTCATGTATGTAGG | 1155 |
rs745611800 | snp | A/G/T | 3.33496e-05 | 0.00408337 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114874 | CGACGCGCAGCCCGC[A/G/T]CAGCCCTCCCAGCCT | 1155 |
rs745664823 | snp | A/G | 0.000128775 | 0.00802314 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121578 | GCCGGTACAACGAGG[A/G]GGAGCGGGCTCAGCA | 1155 |
rs745723037 | in-del | -/AAAC | 7.77031e-05 | 0.00623262 | upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113696 | CCCCACGAGGCAAAT[-/AAAC]ACAGAAAACTCACGC | 1155 |
rs745740675 | snp | C/G | 4.9476e-05 | 0.00497348 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114164 | ACCTCCCCAGTACCA[C/G]CTGAACGCTCACTTT | 1155 |
rs745830410 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115118 | ATGGATCTGGTGCCA[A/G]AGCCGGGAAAACGAT | 1155 |
rs745915124 | snp | C/G | 1.66056e-05 | 0.00288141 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116196 | CCACGTGAGGACTCT[C/G]TATCTGGGACACTCC | 1155 |
rs745979083 | snp | A/G | 5.42677e-05 | 0.00520873 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125818 | TTCAGCTCCTAGCTC[A/G]GCCACTGACTGCCCC | 1155 |
rs746006777 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36119634 | GGATCGTGCCTGTAA[C/T]CCCACCCAGTACATT | 1155 |
rs746063380 | snp | G/T | 1.67992e-05 | 0.00289816 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113867 | GACCCAGCAGCGCCT[G/T]ACCCCAAAAGAACAG | 1155 |
rs746128501 | snp | A/T | 1.75065e-05 | 0.00295854 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115518 | TGCGGAGCGGGTGTG[A/T]GGCGGCTGGACCGCG | 1155 |
rs746171850 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115280 | GCTTCAGTCTTCGCC[G/T]CCTGTTCTGGTCCTT | 1155 |
rs746256753 | snp | A/G | 1.74549e-05 | 0.00295417 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114620 | GGCGGGGCCACGCTG[A/G]GAACAGGTGGACCTG | 1155 |
rs746278701 | snp | G/T | | | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113063 | TGTCCATGGTTTGTG[G/T]ATGTGGGGTATGGAG | 1155 |
rs746280802 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36118060 | CATGAGCCACCGCAC[A/C]CGGCCCAGAATCTAC | 1155 |
rs746394866 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118493 | TAAGGTCAGGAGTTC[A/G]AGACGGTGAAACCCC | 1155 |
rs746409274 | in-del | -/TT | | | intron-variant | TBCB | GRCh38.p7 | 19:36121200 | GGGACGGATCGAGTG[-/TT]GGGGGAGACCGGGGG | 1155 |
rs746452751 | snp | C/T | 3.33034e-05 | 0.00408051 | intron-variant | TBCB | GRCh38.p7 | 19:36120685 | GCCAGACCCTGATCC[C/T]CACGGAGCCCCTCCC | 1155 |
rs746470826 | snp | A/T | 5.50252e-05 | 0.00524496 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115695 | GCCATGGGGGCGGGG[A/T]CCGGAGGGGCGGGGC | 1155 |
rs746524119 | snp | C/G/T | 7.67672e-05 | 0.00619506 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115629 | CCTCAACACCTTCCG[C/G/T]TCCGAGAAGCGATAC | 1155 |
rs746535006 | snp | C/G | 4.9423e-05 | 0.00497082 | intron-variant | TBCB | GRCh38.p7 | 19:36125544 | AAGAATTCCCACTCA[C/G]GTGTCTGTGTGTGCA | 1155 |
rs746572229 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36121218 | GGGGAGACCGGGGGC[C/G]TCAGGGCCGGAGGAG | 1155 |
rs746701422 | snp | A/T | 1.64751e-05 | 0.00287007 | splice-acceptor-variant | TBCB | GRCh38.p7 | 19:36125449 | TTCTCTTCTGTTGGC[A/T]GGTCTCACAGATTTC | 1155 |
rs746798283 | snp | G/T | 3.79564e-05 | 0.00435623 | intron-variant | TBCB | GRCh38.p7 | 19:36121478 | GTGGAGCGTCATCCT[G/T]TTAGGCCCGGCCGAC | 1155 |
rs746884656 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36125579 | TGTGTAAGTCCATGC[A/G]TGCTGCTTGCTGAGC | 1155 |
rs746969929 | snp | A/G | | | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113199 | TTCAGGCTCCAGATC[A/G]AAAGGCAAGGGAAGG | 1155 |
rs746983863 | snp | A/G | 3.29843e-05 | 0.00406092 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114158 | CACTTTACCTCCCCA[A/G]TACCAGCTGAACGCT | 1155 |
rs747018552 | snp | C/T | 2.32951e-05 | 0.00341277 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113738 | TGGTGTTTATTACAC[C/T]CGGGGGAGAGAGGAG | 1155 |
rs747030232 | snp | C/T | 1.77779e-05 | 0.00298138 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125724 | GCGCCTTTGTCAAGC[C/T]AGCAGTCGTGACGGT | 1155 |
rs747215485 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36125359 | ACAGGCTTCTACTCA[A/G]TGGGTAGGCATGGAT | 1155 |
rs747265303 | snp | C/T | 0.000123054 | 0.00784296 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121561 | GAAGCGCAGCAAGCT[C/T]GGCCGGTACAACGAG | 1155 |
rs747325887 | snp | C/T | 0.000133416 | 0.0081664 | intron-variant | TBCB | GRCh38.p7 | 19:36120676 | GCCTCCCTGGCCAGA[C/T]CCTGATCCCCACGGA | 1155 |
rs747327622 | snp | A/C | 1.65466e-05 | 0.00287628 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114401 | CTCCTGCTGGTAATC[A/C]CAGTTCCGGCACTAC | 1155 |
rs747379011 | snp | C/T | 1.65466e-05 | 0.00287628 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116176 | GTAGATGACGGCTGC[C/T]GCATCCACGTGAGGA | 1155 |
rs747425593 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36124010 | TTCCCACAGCCGCTG[A/C]AGCAGTTTTCATTCC | 1155 |
rs747609968 | snp | A/G | 1.80876e-05 | 0.00300724 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125806 | GAATTCCCCTGCTTC[A/G]GCTCCTAGCTCAGCC | 1155 |
rs747640061 | snp | C/T | 1.64912e-05 | 0.00287147 | intron-variant | TBCB | GRCh38.p7 | 19:36125422 | TTCTATGTCCAGAAG[C/T]TTCACAGGGATTTCT | 1155 |
rs747694485 | snp | C/T | 0.000205952 | 0.0101456 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121747 | GGGCCCGGTCCCGGG[C/T]TCCAGGGCTCCAAGG | 1155 |
rs747749333 | snp | C/G | | | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113082 | TGGGGTATGGAGAAT[C/G]AAGACATGATGTCTC | 1155 |
rs747911063 | snp | A/C | 1.6501e-05 | 0.00287232 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114082 | CTGAGAGGGTAGGGG[A/C]TCGGTCACCGGAGGC | 1155 |
rs747990069 | snp | A/G | 3.73993e-05 | 0.00432414 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115683 | GTTCAAGGTGTGGCC[A/G]TGGGGGCGGGGTCCG | 1155 |
rs747995551 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36118032 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 1155 |
rs748105331 | snp | C/G | 5.10478e-05 | 0.00505186 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115587 | GGGGGTGTCGGCACC[C/G]ACGGTGACCGTTTTC | 1155 |
rs748107757 | snp | A/C | | | upstream-variant-2KB, intron-variant, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113438 | CAGCCCTCCCCTCTG[A/C]GCCCATCTGTGCAGG | 1155 |
rs748192004 | snp | C/G | 1.65261e-05 | 0.0028745 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114830 | AATACCCACGAAGCC[C/G]GGCTCGTAAGTCCCG | 1155 |
rs748342415 | in-del | -/TGAAT | | | intron-variant | TBCB | GRCh38.p7 | 19:36117673 | ATCATTGTTGAATGA[-/TGAAT]TGAATCCATAAAGTA | 1155 |
rs748400617 | snp | C/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117120 | CGGCCTCAGTGTTAA[C/T]GTTTACCTCATTCCT | 1155 |
rs748460579 | snp | C/G | 1.65105e-05 | 0.00287315 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116055 | GTGTAAACTGGAGTT[C/G]CTGGTGGGCAGCCCT | 1155 |
rs748462445 | snp | C/G | 1.66396e-05 | 0.00288436 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120801 | AAGCCTACGACCAGA[C/G]GCAAGGTACGGGCAG | 1155 |
rs748491400 | snp | A/G | 1.80729e-05 | 0.00300601 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125791 | GATATGACACCTAAG[A/G]AATTCCCCTGCTTCA | 1155 |
rs748514103 | snp | C/T | 3.54717e-05 | 0.00421125 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125705 | GAATGCCAGGCCAAG[C/T]ATGGCGCCTTTGTCA | 1155 |
rs748600183 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36122315 | CTAGGCATGATGGCT[C/T]ACGCCTGTAAACTCA | 1155 |
rs748822839 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124133 | GAACATCATCATGGT[G/T]TTGATTTGCACTTCT | 1155 |
rs748848558 | snp | C/G | 1.65356e-05 | 0.00287533 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114383 | GATGCAGCTGTTGTC[C/G]GCCTCCTGCTGGTAA | 1155 |
rs748987713 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36125203 | TACAAAGCCCTCACT[A/G]GCTGGTGTCTTCACC | 1155 |
rs749008755 | snp | C/T | 3.31186e-05 | 0.00406918 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116169 | CTACCCTGTAGATGA[C/T]GGCTGCCGCATCCAC | 1155 |
rs749039089 | snp | A/G | 3.30333e-05 | 0.00406393 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113970 | CCCGCCCCCAGAAAG[A/G]ACCAAACAAGCCCCA | 1155 |
rs749067440 | snp | A/T | 2.75433e-05 | 0.00371091 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115577 | TGGAGGTGACGGGGG[A/T]GTCGGCACCCACGGT | 1155 |
rs749093161 | snp | A/C/T | 1.74089e-05 | 0.00295029 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115521 | GGAGCGGGTGTGAGG[A/C/T]GGCTGGACCGCGCTG | 1155 |
rs749145680 | in-del | -/CTCA | 1.64939e-05 | 0.0028717 | upstream-variant-2KB, downstream-variant-500B, splice-donor-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114172 | AGTACCAGCTGAACG[-/CTCA]CTTTTGGCACGGGTG | 1155 |
rs749239611 | snp | A/G | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116831 | TTGCCATGTTGGCCA[A/G]GCTGGTCTGGAACTC | 1155 |
rs749250106 | snp | A/G | 0.0001999 | 0.0099955 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121732 | AGGTGCGTGGCTCGC[A/G]GGCCCGGTCCCGGGC | 1155 |
rs749271575 | in-del | -/CT | 1.65868e-05 | 0.00287978 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116192 | GCATCCACGTGAGGA[-/CT]CTCTATCTGGGACAC | 1155 |
rs749328790 | snp | C/T | 1.65364e-05 | 0.0028754 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120774 | GGGTGGAGAAGTACA[C/T]GATCTCACAAGAAGC | 1155 |
rs749382657 | snp | A/G | 1.6641e-05 | 0.00288448 | intron-variant | TBCB | GRCh38.p7 | 19:36120689 | GACCCTGATCCCCAC[A/G]GAGCCCCTCCCCTCA | 1155 |
rs749580258 | snp | G/T | 0.000160038 | 0.00894391 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113523 | CCTGGAAGCTCACCT[G/T]GCTAAGGTGCATGGA | 1155 |
rs749590541 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | TBCB | GRCh38.p7 | 19:36125571 | TGCATTTGTGTGTAA[A/G]TCCATGCGTGCTGCT | 1155 |
rs749821371 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120615 | GAGGGAGGGAGATGC[A/G]TTTTTCCCAGATGGA | 1155 |
rs749857259 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116146 | CAAGAGGATGCGCTC[C/T]TGGGCTCCTACCCTG | 1155 |
rs749869720 | in-del | -/TTGTGTGTAA | 0.000148252 | 0.00860837 | intron-variant | TBCB | GRCh38.p7 | 19:36125561 | TGTCTGTGTGTGCAT[-/TTGTGTGTAA]GTCCATGCGTGCTGC | 1155 |
rs749914527 | snp | A/C/G | 3.6096e-05 | 0.00424817 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125774 | GACTACGGGTTGGAC[A/C/G]AGATATGACACCTAA | 1155 |
rs749979189 | snp | C/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116576 | GACCAGGCTGGACAG[C/T]TTGGGAGAAACCAGA | 1155 |
rs750070195 | snp | A/C | | | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114327 | GCCCCCAGCTCAGGG[A/C]CCGCCACTCACTCCA | 1155 |
rs750122644 | snp | A/C/T | 3.34148e-05 | 0.00408736 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114668 | GCTCACCGCGTAGAG[A/C/T]AGAATGCGGTTCTCC | 1155 |
rs750144346 | snp | A/G | 1.64792e-05 | 0.00287042 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113715 | ACAGAAAACTCACGC[A/G]TGGAATCTGGTGTTT | 1155 |
rs750378782 | snp | A/T | 1.66593e-05 | 0.00288607 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114446 | GGGGGAAAGGGGGTC[A/T]CGGAAGGATTCCAGA | 1155 |
rs750422254 | snp | A/G | 6.72518e-05 | 0.00579839 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116232 | CCCACCTTTCATTTG[A/G]TTATTCAACAGACAC | 1155 |
rs750433581 | snp | A/G/T | 6.13032e-05 | 0.00553611 | synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115668 | CCTCACCATCGCTGA[A/G/T]TTCAAGGTGTGGCCA | 1155 |
rs750447186 | snp | A/G | 1.64939e-05 | 0.0028717 | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114060 | CACAGCCTCCTTGTG[A/G]CCGCACCTGAGAGGG | 1155 |
rs750627271 | snp | C/G | 2.90964e-05 | 0.0038141 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115572 | CAAGATGGAGGTGAC[C/G]GGGGTGTCGGCACCC | 1155 |
rs750629354 | snp | A/G | 8.23608e-05 | 0.00641667 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125490 | ACTGGATTGGTGTCC[A/G]CTATGATGAGCCACT | 1155 |
rs750912229 | snp | C/T | 3.30235e-05 | 0.00406333 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114136 | CGCCCAGTGAGGAGA[C/T]GAGCCTCACTTTACC | 1155 |
rs750948687 | snp | C/T | 1.77134e-05 | 0.00297597 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113790 | CGCAGTGTGGGGCTG[C/T]GCACACGTAGTAAAG | 1155 |
rs751154557 | in-del | -/ACCGCGCTGCAGGCATCCGC | 1.70124e-05 | 0.00291649 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115527 | GTGTGAGGCGGCTGG[-/ACCGCGCTGCAGGCATCCGC]ACCGCGCTGCAGGCA | 1155 |
rs751185128 | snp | C/T | 0.000160759 | 0.00896401 | upstream-variant-2KB, stop-gained, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113497 | GGGAAAGCGTTTACG[C/T]AGCGCTGCTCCCTGG | 1155 |
rs751215242 | snp | A/C | 5.60041e-05 | 0.0052914 | intron-variant | TBCB | GRCh38.p7 | 19:36121492 | TGTTAGGCCCGGCCG[A/C]CACCCCAACTGACCC | 1155 |
rs751228111 | snp | A/G | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116491 | AGGAAAGGGTGACTT[A/G]AGAGAAAGAGGTGGA | 1155 |
rs751273646 | snp | C/T | 1.64846e-05 | 0.0028709 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114783 | TTCTAACATCACCCG[C/T]TCCCTCCGCCTCACC | 1155 |
rs751330176 | snp | A/T | 1.6537e-05 | 0.00287545 | upstream-variant-2KB, stop-gained | TBCB, POLR2I | GRCh38.p7 | 19:36114365 | CGTGATCTTGTTGAC[A/T]TAGATGCAGCTGTTG | 1155 |
rs751408863 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120420 | GGCCTGAGCTCTGCC[A/G]GTTGGACTCTGTGAC | 1155 |
rs751435819 | snp | A/G | | | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121594 | GGAGCGGGCTCAGCA[A/G]GAGGCCGAGGCCGCC | 1155 |
rs751528263 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116120 | ACGACAAGTTCTACA[A/G]CAAGCTGGATCAAGA | 1155 |
rs751556288 | snp | A/C | | | upstream-variant-2KB, stop-gained, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113481 | CCGCTGCAGTGCTTG[A/C]GGGAAAGCGTTTACG | 1155 |
rs751594919 | snp | A/C | 0.000144987 | 0.00851308 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121820 | CGCTCTGCCTAGGGG[A/C]GCGGGGTTGGGGGGG | 1155 |
rs751617520 | snp | C/G | 0.000129879 | 0.00805744 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115512 | GGCGGCTGCGGAGCG[C/G]GTGTGAGGCGGCTGG | 1155 |
rs751849925 | snp | C/G | 4.99496e-05 | 0.00499723 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114439 | CGAGTGTGGGGGAAA[C/G]GGGGTCACGGAAGGA | 1155 |
rs752004943 | snp | A/G | 1.64914e-05 | 0.00287149 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114046 | TGTGACTGGAAGAAC[A/G]CAGCCTCCTTGTGGC | 1155 |
rs752123070 | snp | A/G | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126093 | CTACCAGGAAGAAAG[A/G]GAAGGGAAGGGAGGG | 1155 |
rs752276884 | snp | G/T | 1.71261e-05 | 0.00292622 | intron-variant | TBCB | GRCh38.p7 | 19:36120828 | GCAGGTGGGCGTCGA[G/T]GGGTGCGTGGGGGCC | 1155 |
rs752334905 | snp | A/G/T | 9.93105e-05 | 0.00704602 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114702 | TCTTCCTTGGGGTAC[A/G/T]GCATGTTGTTACTGT | 1155 |
rs752752701 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125518 | ACTGGGGAAAAATGA[C/T]GGCAGGTAACAAGAA | 1155 |
rs752759135 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124885 | TTCATGTCCTTTGGC[C/T]ATGATCGTGGCTCAC | 1155 |
rs752761965 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123254 | CTATGAACCTTCTTC[-/T]TTTTTTTTTTTTTTT | 1155 |
rs752777983 | snp | G/T | 1.72457e-05 | 0.00293642 | splice-acceptor-variant | TBCB | GRCh38.p7 | 19:36121526 | CCCCCTCTGCCCACA[G/T]ACACGGTCCGCTCTT | 1155 |
rs753126354 | in-del | -/G | 0.00029244 | 0.0120886 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121828 | TAGGGGCGCGGGGTT[-/G]GGGGGGGACTCGAAA | 1155 |
rs753188537 | snp | C/T | 0.000289771 | 0.0120334 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121680 | GTGAGGTGCGGGCGG[C/T]GGGACAATCCCCTCG | 1155 |
rs753249807 | snp | A/G | 1.66966e-05 | 0.00288929 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114453 | AGGGGGTCACGGAAG[A/G]ATTCCAGACAAGATT | 1155 |
rs753262434 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36123919 | CATTTGTTTTCATTT[A/C]TCTGTGCCTAGGAGT | 1155 |
rs753346359 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118954 | TCCTGATGAGGGGAC[A/G]AGGTCTGGAGCTGTG | 1155 |
rs753497265 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36118775 | CAAGGTGGGAGGGAG[C/T]GCGGTGGGGATTAAG | 1155 |
rs753525918 | snp | A/G | 0.000151895 | 0.00871346 | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113005 | AGTTGCTGGGCCCCA[A/G]GTGGGGATGGAAGGA | 1155 |
rs753567779 | snp | C/T | 1.64999e-05 | 0.00287222 | upstream-variant-2KB, downstream-variant-500B, splice-donor-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114014 | CCCTCGCGCCACTTA[C/T]CTCGGCCCGCGCACT | 1155 |
rs753677773 | snp | A/G | 1.64953e-05 | 0.00287182 | intron-variant | TBCB | GRCh38.p7 | 19:36125411 | ATGGGGATTTCTTCT[A/G]TGTCCAGAAGCTTCA | 1155 |
rs753729533 | snp | A/G | 0.000775194 | 0.0196722 | intron-variant | TBCB | GRCh38.p7 | 19:36117817 | GTCTCCCAGGCTGGC[A/G]TGCAGTGGCATGATC | 1155 |
rs753849983 | snp | A/C | 1.6519e-05 | 0.00287388 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114226 | TGGGGTCCTGGGACA[A/C]GTCGGCGATAATCTG | 1155 |
rs754049267 | snp | C/G | 1.64928e-05 | 0.00287161 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114141 | AGTGAGGAGACGAGC[C/G]TCACTTTACCTCCCC | 1155 |
rs754050010 | snp | C/T | 3.37445e-05 | 0.00410744 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115678 | GCTGAGTTCAAGGTG[C/T]GGCCATGGGGGCGGG | 1155 |
rs754080444 | snp | C/T | 3.3548e-05 | 0.00409547 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116000 | TGCAAGGGGCGGGGC[C/T]TCCGTGGCCTCCTTC | 1155 |
rs754167789 | in-del | -/CGCGCAGCC | 0.000116232 | 0.00762249 | upstream-variant-2KB, cds-indel | TBCB, POLR2I | GRCh38.p7 | 19:36114862 | CGGGCTCCATGGCGA[-/CGCGCAGCC]CGCGCAGCCCTCCCA | 1155 |
rs754271132 | snp | C/G | 1.84374e-05 | 0.00303618 | intron-variant | TBCB | GRCh38.p7 | 19:36121496 | AGGCCCGGCCGACAC[C/G]CCAACTGACCCCAGC | 1155 |
rs754347856 | snp | A/C | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116397 | CAGGGGACTGGAGCC[A/C]CCAAGAAGAGGTGCC | 1155 |
rs754433036 | snp | A/G | 7.01557e-05 | 0.00592224 | intron-variant | TBCB | GRCh38.p7 | 19:36120846 | GTGCGTGGGGGCCAG[A/G]GGGAGTATGTGCAGG | 1155 |
rs754541678 | snp | A/G | 1.67321e-05 | 0.00289236 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114461 | ACGGAAGGATTCCAG[A/G]CAAGATTGGGAGGAG | 1155 |
rs754781762 | snp | C/G | 2.6872e-05 | 0.00366541 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115580 | AGGTGACGGGGGTGT[C/G]GGCACCCACGGTGAC | 1155 |
rs754827802 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116511 | AAGAGGTGGAAAGGA[-/GG]GGGAGCAGGGTGTAC | 1155 |
rs754832985 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | TBCB | GRCh38.p7 | 19:36125413 | GGGGATTTCTTCTAT[A/G]TCCAGAAGCTTCACA | 1155 |
rs754852252 | snp | C/T | 6.58903e-05 | 0.00573941 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125501 | GTCCGCTATGATGAG[C/T]CACTGGGGAAAAATG | 1155 |
rs754911161 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36118008 | TGACCTCAGGTAATC[C/T]GCCCACCTCGGCCTC | 1155 |
rs755102214 | snp | A/T | 8.84119e-05 | 0.00664817 | intron-variant | TBCB | GRCh38.p7 | 19:36120850 | GTGGGGGCCAGAGGG[A/T]GTATGTGCAGGTATG | 1155 |
rs755138122 | snp | C/T | 6.59652e-05 | 0.00574267 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114145 | AGGAGACGAGCCTCA[C/T]TTTACCTCCCCAGTA | 1155 |
rs755143881 | in-del | -/CCATGT | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113282 | ACACAGGTGTCTGGC[-/CCATGT]CTGCACTGGGTGACG | 1155 |
rs755291376 | in-del | -/CGCGCAGCC | 0.000116232 | 0.00762249 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114861 | CGGGCTCCATGGCGA[-/CGCGCAGCC]CGCGCAGCCCGCGCA | 1155 |
rs755321802 | snp | C/G | 1.77568e-05 | 0.00297961 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125700 | ACTTCGAATGCCAGG[C/G]CAAGTATGGCGCCTT | 1155 |
rs755478432 | snp | C/T | 0.000137466 | 0.00828941 | intron-variant | TBCB | GRCh38.p7 | 19:36121515 | ACTGACCCCAGCCCC[C/T]TCTGCCCACAGACAC | 1155 |
rs755612213 | in-del | -/AC | 1.78188e-05 | 0.00298481 | frameshift-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125735 | AAGCCAGCAGTCGTG[-/AC]GGTGGGGGACTTCCC | 1155 |
rs755616103 | snp | C/G | 1.65329e-05 | 0.0028751 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114375 | TTGACATAGATGCAG[C/G]TGTTGTCGGCCTCCT | 1155 |
rs755669359 | snp | A/G | 1.64996e-05 | 0.0028722 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116148 | AGAGGATGCGCTCCT[A/G]GGCTCCTACCCTGTA | 1155 |
rs755856375 | snp | A/G | 5.10382e-05 | 0.00505139 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113836 | GCAGAAATGATGCAT[A/G]GTTAGGAAGGATTTG | 1155 |
rs755931712 | snp | A/C | 0.000395491 | 0.0140566 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121848 | GGGACTCGAAACGAT[A/C]TCAGTCCCTGGAGGT | 1155 |
rs755950581 | snp | A/G | 1.66843e-05 | 0.00288823 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114448 | GGGAAAGGGGGTCAC[A/G]GAAGGATTCCAGACA | 1155 |
rs755983311 | in-del | -/A | 1.64886e-05 | 0.00287124 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116118 | GACGACAAGTTCTAC[-/A]AGCAAGCTGGATCAA | 1155 |
rs756160109 | snp | A/G | 8.24681e-05 | 0.00642085 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114137 | GCCCAGTGAGGAGAC[A/G]AGCCTCACTTTACCT | 1155 |
rs756266441 | snp | C/G | 1.65285e-05 | 0.00287471 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115574 | AGATGGAGGTGACGG[C/G]GGTGTCGGCACCCAC | 1155 |
rs756513984 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118149 | AACTGCTTCTTTTTT[C/G]TCTCGTTGATTAACT | 1155 |
rs756522622 | snp | A/G | 1.65241e-05 | 0.00287433 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114724 | TGTTACTGTGGGGAG[A/G]GGGAGGTGCCAGGGG | 1155 |
rs756764691 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114977 | GCTGCGCACACGTGC[G/T]GGCTCCCCGCCGCCT | 1155 |
rs756822724 | snp | C/T | 1.66045e-05 | 0.00288132 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116030 | CTTCTCACCCTGCCT[C/T]CTCCTCACAGTGTAA | 1155 |
rs756856387 | snp | A/G | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116493 | GAAAGGGTGACTTAA[A/G]AGAAAGAGGTGGAAA | 1155 |
rs756938765 | in-del | -/T | 0.00141784 | 0.0265877 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115726 | GAAGAAATTGGGGGG[-/T]TCCCGGAAGGGGGAG | 1155 |
rs757252462 | snp | A/G | 1.6865e-05 | 0.00290383 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113863 | TTTGGACCCAGCAGC[A/G]CCTTACCCCAAAAGA | 1155 |
rs757305397 | snp | G/T | 0.000137127 | 0.00827918 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115514 | CGGCTGCGGAGCGGG[G/T]GTGAGGCGGCTGGAC | 1155 |
rs757384043 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113490 | TGCTTGCGGGAAAGC[A/G]TTTACGCAGCGCTGC | 1155 |
rs757401505 | snp | C/T | 0.000154907 | 0.00879939 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121696 | GGGACAATCCCCTCG[C/T]CGGGGCACCGTCATG | 1155 |
rs757680879 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124092 | AGTCTGTCTTTTGCT[C/T]ACAGTCATCCACTGG | 1155 |
rs757690138 | snp | C/G | 1.66646e-05 | 0.00288652 | intron-variant | TBCB | GRCh38.p7 | 19:36120680 | CCCTGGCCAGACCCT[C/G]ATCCCCACGGAGCCC | 1155 |
rs757697193 | snp | A/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36125131 | CTGTCAGCAGGTTGG[A/T]TTTATTCTGAAGCCT | 1155 |
rs757795005 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115232 | AGTTTACCCTTCGCG[C/G]ACTGGGCGAGCTCTT | 1155 |
rs757839104 | snp | C/G | 1.64914e-05 | 0.00287149 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114050 | ACTGGAAGAACACAG[C/G]CTCCTTGTGGCCGCA | 1155 |
rs757892608 | snp | C/T | 0.000484457 | 0.0155561 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113463 | TGCAGGGATCCGGCC[C/T]TTCCGCTGCAGTGCT | 1155 |
rs758151373 | snp | C/T | 1.64931e-05 | 0.00287163 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114153 | AGCCTCACTTTACCT[C/T]CCCAGTACCAGCTGA | 1155 |
rs758344941 | snp | C/T | 4.52294e-05 | 0.00475528 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115690 | GTGTGGCCATGGGGG[C/T]GGGGTCCGGAGGGGC | 1155 |
rs758386805 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115031 | AGGTTTCATGGCTTG[C/T]TTCAATCTTTTGATA | 1155 |
rs758456577 | snp | C/T | 1.70851e-05 | 0.00292271 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121537 | CACAGACACGGTCCG[C/T]TCTTTCCTGAAGCGC | 1155 |
rs758481337 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36124930 | CCTGTTGCCCACTTT[A/G]TAATGGGATTTTTTT | 1155 |
rs758504002 | snp | A/G | 0.000142217 | 0.00843139 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121683 | AGGTGCGGGCGGCGG[A/G]ACAATCCCCTCGCCG | 1155 |
rs758557800 | in-del | -/A | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126205 | GGCGGGTGGATCACG[-/A]AGGTCAGGAGATCGA | 1155 |
rs758606833 | snp | A/G | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36117272 | GTGGAAATTTTGATC[A/G]CTATAATTCACTACT | 1155 |
rs758606909 | snp | A/C | 1.65529e-05 | 0.00287683 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114350 | TCACTCCACTTCGTG[A/C]GTGATCTTGTTGACA | 1155 |
rs758791153 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123963 | CACATGGTAACACTG[C/T]GCTTGACTTTTTTGA | 1155 |
rs758803988 | snp | C/T | 1.68074e-05 | 0.00289887 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125799 | ACCTAAGGAATTCCC[C/T]TGCTTCAGCTCCTAG | 1155 |
rs758865837 | snp | G/T | 6.77644e-05 | 0.00582045 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113846 | TGCATGGTTAGGAAG[G/T]ATTTGGACCCAGCAG | 1155 |
rs758884640 | snp | C/T | 1.70889e-05 | 0.00292304 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114901 | GCCTTCCGCGCTTGC[C/T]CCGCCGCGCTACAGG | 1155 |
rs759175524 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120246 | CACTGAGTCCCCAGC[A/G]TGAGGCCCAGCTGGG | 1155 |
rs759194413 | snp | C/G/T | 0.000279096 | 0.0118097 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113619 | CACCAGCTCCCGGCC[C/G/T]GACACCTACGCACAG | 1155 |
rs759198666 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36121157 | GGTGGAATGCGAGTG[C/G]ACAGGGTGGCGGTCA | 1155 |
rs759329403 | snp | G/T | 1.65776e-05 | 0.00287898 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114850 | CGTAAGTCCCGTCGG[G/T]CTCCATGGCGACGCG | 1155 |
rs759344300 | snp | A/G | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125709 | GCCAGGCCAAGTATG[A/G]CGCCTTTGTCAAGCC | 1155 |
rs759525452 | snp | A/C | 7.56902e-05 | 0.00615137 | intron-variant | TBCB | GRCh38.p7 | 19:36121486 | TCATCCTGTTAGGCC[A/C]GGCCGACACCCCAAC | 1155 |
rs759527658 | snp | C/T | 1.6486e-05 | 0.00287102 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114760 | TCTGGAGCCATTCCT[C/T]GCCCGCCTTCTAACA | 1155 |
rs759620718 | snp | C/T | 1.67683e-05 | 0.00289549 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116003 | AAGGGGCGGGGCCTC[C/T]GTGGCCTCCTTCTTC | 1155 |
rs759620803 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124838 | GTGAGCCACCGCACC[C/T]GGCCAGTATGTCATC | 1155 |
rs759693852 | snp | A/G | 1.64879e-05 | 0.00287118 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116111 | ATGGAGTTGACGACA[A/G]GTTCTACAGCAAGCT | 1155 |
rs759711385 | in-del | -/AA | | | intron-variant | TBCB | GRCh38.p7 | 19:36122571 | AGACCCTGTCTCTAC[-/AA]AAAAAAAAAAAAAAA | 1155 |
rs759923303 | snp | C/G | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126370 | GAGCTTGCAGTGAGC[C/G]AAGATCATGCCACTG | 1155 |
rs759953460 | snp | C/T | 4.57268e-05 | 0.00478135 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121764 | CCAGGGCTCCAAGGC[C/T]GGGAGGAAATGTTGG | 1155 |
rs760002581 | snp | A/G | 0.000141213 | 0.00840158 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121676 | CGCTGTGAGGTGCGG[A/G]CGGCGGGACAATCCC | 1155 |
rs760031036 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36117610 | GCCCACCTCAGCCTC[A/G]CAAAGTGCTGGGATT | 1155 |
rs760048653 | in-del | -/GGGCTCCA | 3.99114e-05 | 0.004467 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121744 | CGCGGGCCCGGTCCC[-/GGGCTCCA]GGGCTCCAAGGCCGG | 1155 |
rs760184169 | snp | C/T | 1.65075e-05 | 0.00287289 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114105 | CCGGAGGCTTCACAC[C/T]CTTCCCTCCTCCCTT | 1155 |
rs760259893 | in-del | -/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36122953 | ATTTCCGTCTTTATG[-/C]CTGTGTGTACCCATC | 1155 |
rs760313102 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36118834 | GGAAGCTGGGGAGGA[C/T]CCTGACCTGGCTCAG | 1155 |
rs760368927 | snp | A/C | 1.6489e-05 | 0.00287128 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114752 | GGGTTAGTTCTGGAG[A/C]CATTCCTCGCCCGCC | 1155 |
rs760434848 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123506 | TCCCGCTCAAGTGAT[C/T]GTCCTGCTTCAGCCT | 1155 |
rs760462636 | snp | C/T | 8.02407e-05 | 0.00633356 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115537 | GGCTGGACCGCGCTG[C/T]AGGCATCCGCAGGGC | 1155 |
rs760524762 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124744 | GAGACGGGGCTTCAC[C/T]GTGTTAGCCAGGATG | 1155 |
rs760561784 | snp | C/T | | | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114602 | CACAGAGGCAGGGGG[C/T]AGGGCGGGGCCACGC | 1155 |
rs760605384 | snp | C/T | 3.30579e-05 | 0.00406544 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120733 | CCACAGTGGCGCCCG[C/T]CTTGGTGAGTATGAG | 1155 |
rs760716753 | snp | A/G | 1.67959e-05 | 0.00289787 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115996 | TTGATGCAAGGGGCG[A/G]GGCCTCCGTGGCCTC | 1155 |
rs760716904 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36117414 | CAGTGGTGTGATCTC[A/G]GCTCACTGCAACCTC | 1155 |
rs760833130 | snp | C/T | 0.000121073 | 0.00777957 | intron-variant | TBCB | GRCh38.p7 | 19:36125645 | GGTCCTCTGACCACA[C/T]CCACCCCTATCCTTT | 1155 |
rs760845257 | in-del | -/T | 1.71258e-05 | 0.00292619 | intron-variant | TBCB | GRCh38.p7 | 19:36120832 | GTGGGCGTCGAGGGG[-/T]GCGTGGGGGCCAGAG | 1155 |
rs761085834 | in-del | -/AC | 1.64833e-05 | 0.00287078 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114773 | CTCGCCCGCCTTCTA[-/AC]ATCACCCGCTCCCTC | 1155 |
rs761086607 | snp | C/T | 3.73281e-05 | 0.00432003 | intron-variant | TBCB | GRCh38.p7 | 19:36121493 | GTTAGGCCCGGCCGA[C/T]ACCCCAACTGACCCC | 1155 |
rs761212910 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114537 | GGATGGGCAGGACAT[-/GA]GAGTCAGGATCACTT | 1155 |
rs761231003 | snp | C/T | 1.68224e-05 | 0.00290016 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114887 | GCGCAGCCCTCCCAG[C/T]CTTCCGCGCTTGCTC | 1155 |
rs761232326 | snp | A/G | 1.64893e-05 | 0.0028713 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116084 | CTGCTTCCTGCATGG[A/G]ACTGGAGCTGTATGG | 1155 |
rs761357864 | in-del | -/CA | 1.64743e-05 | 0.00287 | frameshift-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125455 | TCTGTTGGCAGGTCT[-/CA]CAGATTTCAAGCCTG | 1155 |
rs761488464 | snp | C/T | 1.6571e-05 | 0.0028784 | intron-variant | TBCB | GRCh38.p7 | 19:36120707 | GCCCCTCCCCTCACA[C/T]AGGTCATTGACCACA | 1155 |
rs761580234 | snp | A/C | 3.32945e-05 | 0.00407997 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114864 | GGCTCCATGGCGACG[A/C]GCAGCCCGCGCAGCC | 1155 |
rs761613863 | snp | A/G | 3.4859e-05 | 0.00417472 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121626 | AGCGCCTGGCCGAGG[A/G]GAAGGCCCAGGCCAG | 1155 |
rs761959312 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120220 | CTGAGGGCAGAGTGC[A/G]TCTGTGTTTACACTG | 1155 |
rs762151648 | in-del | -/GGAAGGATTCCAGACAAGATTGGGA | 1.66763e-05 | 0.00288753 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114447 | GGGAAAGGGGGTCAC[-/GGAAGGATTCCAGACAAGATTGGGA]GGAAGGATTCCAGAC | 1155 |
rs762184762 | snp | C/T | 3.29935e-05 | 0.00406149 | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114185 | CGCTCACTTTTGGCA[C/T]GGGTGGTCCTCGGTC | 1155 |
rs762281580 | snp | C/T | 2.88405e-05 | 0.00379729 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115659 | CAGCCGCAGCCTCAC[C/T]ATCGCTGAGTTCAAG | 1155 |
rs762364907 | snp | C/T | 1.71428e-05 | 0.00292765 | intron-variant | TBCB | GRCh38.p7 | 19:36125633 | GAGCCATGTGAGGGT[C/T]CTCTGACCACACCCA | 1155 |
rs762400432 | snp | C/T | 0.000112564 | 0.00750129 | intron-variant | TBCB | GRCh38.p7 | 19:36121490 | CCTGTTAGGCCCGGC[C/T]GACACCCCAACTGAC | 1155 |
rs762426435 | snp | C/T | 6.64022e-05 | 0.00576166 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114859 | CGTCGGGCTCCATGG[C/T]GACGCGCAGCCCGCG | 1155 |
rs762607735 | snp | A/G | 1.71316e-05 | 0.00292669 | intron-variant | TBCB | GRCh38.p7 | 19:36120830 | AGGTGGGCGTCGAGG[A/G]GTGCGTGGGGGCCAG | 1155 |
rs762801071 | snp | C/G | 1.80955e-05 | 0.00300789 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125825 | CCTAGCTCAGCCACT[C/G]ACTGCCCCTCCTGTG | 1155 |
rs762920438 | snp | C/T | 0.000296575 | 0.0121737 | upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113679 | CGGTGTGCCAGCGTC[C/T]TCCCCACGAGGCAAA | 1155 |
rs763030152 | snp | C/T | | | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113477 | CCTTCCGCTGCAGTG[C/T]TTGCGGGAAAGCGTT | 1155 |
rs763096351 | snp | A/G | 1.66349e-05 | 0.00288395 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114432 | GAGAGGGCGAGTGTG[A/G]GGGAAAGGGGGTCAC | 1155 |
rs763101901 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120016 | TTTCTACCTCTGGCC[C/G]TCTGCACCTGCCGTT | 1155 |
rs763191211 | snp | C/T | 9.00179e-05 | 0.00670827 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125764 | CCCGGAGGAGGACTA[C/T]GGGTTGGACGAGATA | 1155 |
rs763258952 | snp | G/T | 4.23576e-05 | 0.00460185 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115555 | GCATCCGCAGGGCGC[G/T]GCAAGATGGAGGTGA | 1155 |
rs763313015 | snp | A/G | 0.000209754 | 0.0102388 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121797 | GCACAGTGGAGCCTC[A/G]GAGACCACGCTCTGC | 1155 |
rs763353057 | snp | A/T | 2.73901e-05 | 0.00370058 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115651 | AAGCGATACAGCCGC[A/T]GCCTCACCATCGCTG | 1155 |
rs763387255 | snp | C/G | 4.94931e-05 | 0.00497434 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114015 | CCTCGCGCCACTTAC[C/G]TCGGCCCGCGCACTG | 1155 |
rs763404243 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125467 | TCTCACAGATTTCAA[A/G]CCTGGCTACTGGATT | 1155 |
rs763575144 | snp | A/C | 9.4585e-05 | 0.0068763 | upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113685 | GCCAGCGTCCTCCCC[A/C]CGAGGCAAATAAACA | 1155 |
rs763602355 | snp | C/T | 4.94474e-05 | 0.00497205 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114767 | CCATTCCTCGCCCGC[C/T]TTCTAACATCACCCG | 1155 |
rs763657480 | snp | C/T | 1.72207e-05 | 0.00293429 | intron-variant | TBCB | GRCh38.p7 | 19:36120834 | GGGCGTCGAGGGGTG[C/T]GTGGGGGCCAGAGGG | 1155 |
rs763825459 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36120415 | GGCAAGGCCTGAGCT[C/T]TGCCGGTTGGACTCT | 1155 |
rs763948769 | snp | C/G | 1.8105e-05 | 0.00300868 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113779 | CCAGCGGTGGCCGCA[C/G]TGTGGGGCTGTGCAC | 1155 |
rs764045771 | snp | C/T | 1.64886e-05 | 0.00287124 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116118 | TGACGACAAGTTCTA[C/T]AGCAAGCTGGATCAA | 1155 |
rs764140794 | snp | A/G | 0.000142725 | 0.00844642 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121684 | GGTGCGGGCGGCGGG[A/G]CAATCCCCTCGCCGG | 1155 |
rs764160411 | snp | C/T | 1.76443e-05 | 0.00297016 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125681 | AGTGTGAATGGGAAA[C/T]GCTACTTCGAATGCC | 1155 |
rs764199200 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125842 | CTGCCCCTCCTGTGT[G/T]TGCCCATGGCCCTTT | 1155 |
rs764258836 | snp | A/G | | | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113480 | TCCGCTGCAGTGCTT[A/G]CGGGAAAGCGTTTAC | 1155 |
rs764267370 | snp | A/C/G | 1.66324e-05 | 0.00288374 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114431 | CGAGAGGGCGAGTGT[A/C/G]GGGGAAAGGGGGTCA | 1155 |
rs764313748 | in-del | -/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36120136 | TTTCTCCATAGCCAT[-/C]CTCCAGTGTTTCATA | 1155 |
rs764389666 | snp | A/G | 1.65496e-05 | 0.00287655 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114351 | CACTCCACTTCGTGC[A/G]TGATCTTGTTGACAT | 1155 |
rs764406339 | snp | C/T | 2.82298e-05 | 0.00375688 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115654 | CGATACAGCCGCAGC[C/T]TCACCATCGCTGAGT | 1155 |
rs764424073 | snp | C/T | 3.33417e-05 | 0.00408286 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116213 | ATCTGGGACACTCCC[C/T]CACCCCACCTTTCAT | 1155 |
rs764441829 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118557 | TGGTGGCAGATGCCT[A/G]TAATCCTAGCTACTC | 1155 |
rs764593397 | snp | C/T | 1.64928e-05 | 0.00287161 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114031 | TCGGCCCGCGCACTG[C/T]GTGACTGGAAGAACA | 1155 |
rs764610620 | snp | C/T | 3.92549e-05 | 0.00443012 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115557 | ATCCGCAGGGCGCGG[C/T]AAGATGGAGGTGACG | 1155 |
rs764795310 | snp | C/T | 4.9666e-05 | 0.00498302 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114701 | GTCTTCCTTGGGGTA[C/T]AGCATGTTGTTACTG | 1155 |
rs765017565 | snp | C/G | 0.000161616 | 0.00898788 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113459 | TCTGTGCAGGGATCC[C/G]GCCCTTCCGCTGCAG | 1155 |
rs765119301 | snp | A/C | 1.65778e-05 | 0.002879 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114851 | GTAAGTCCCGTCGGG[A/C]TCCATGGCGACGCGC | 1155 |
rs765186291 | snp | A/G | 5.27079e-05 | 0.00513334 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125671 | CCTTTCCTGCAGTGT[A/G]AATGGGAAACGCTAC | 1155 |
rs765273375 | snp | C/T | 1.65921e-05 | 0.00288024 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114334 | GCTCAGGGCCCGCCA[C/T]TCACTCCACTTCGTG | 1155 |
rs765452764 | snp | A/G | 1.6528e-05 | 0.00287467 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114233 | CTGGGACACGTCGGC[A/G]ATAATCTGGGTCAGT | 1155 |
rs765500716 | snp | C/T | 3.34952e-05 | 0.00409225 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116008 | GCGGGGCCTCCGTGG[C/T]CTCCTTCTTCTCACC | 1155 |
rs765520282 | snp | A/C | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116487 | GATGAGGAAAGGGTG[A/C]CTTAAGAGAAAGAGG | 1155 |
rs765563080 | snp | C/T | 5.3465e-05 | 0.00517007 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125736 | AGCCAGCAGTCGTGA[C/T]GGTGGGGGACTTCCC | 1155 |
rs765591077 | snp | A/G | 4.64954e-05 | 0.00482136 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121765 | CAGGGCTCCAAGGCC[A/G]GGAGGAAATGTTGGG | 1155 |
rs765604385 | in-del | -/T | 0.000110455 | 0.00743068 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115525 | CGGGTGTGAGGCGGC[-/T]GGACCGCGCTGCAGG | 1155 |
rs765697863 | snp | C/T | 8.66574e-05 | 0.00658188 | intron-variant | TBCB | GRCh38.p7 | 19:36121521 | CCCAGCCCCCTCTGC[C/T]CACAGACACGGTCCG | 1155 |
rs765764373 | snp | C/G | 1.69619e-05 | 0.00291216 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114893 | CCCTCCCAGCCTTCC[C/G]CGCTTGCTCCGCCGC | 1155 |
rs766144945 | snp | C/T | 1.70003e-05 | 0.00291545 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113838 | AGAAATGATGCATGG[C/T]TAGGAAGGATTTGGA | 1155 |
rs766182004 | snp | C/T | 1.66588e-05 | 0.00288602 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114673 | CCGCGTAGAGCAGAA[C/T]GCGGTTCTCCTTGTC | 1155 |
rs766238358 | snp | A/C | 3.29745e-05 | 0.00406031 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114757 | AGTTCTGGAGCCATT[A/C]CTCGCCCGCCTTCTA | 1155 |
rs766312403 | snp | C/T | 1.65291e-05 | 0.00287476 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120734 | CACAGTGGCGCCCGC[C/T]TTGGTGAGTATGAGG | 1155 |
rs766398720 | in-del | -/C | 1.74187e-05 | 0.00295111 | intron-variant | TBCB | GRCh38.p7 | 19:36120842 | AGGGGTGCGTGGGGG[-/C]CAGAGGGAGTATGTG | 1155 |
rs766515350 | snp | C/T | 5.03808e-05 | 0.00501875 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115999 | ATGCAAGGGGCGGGG[C/T]CTCCGTGGCCTCCTT | 1155 |
rs766568555 | snp | C/G | 1.65839e-05 | 0.00287953 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115671 | CACCATCGCTGAGTT[C/G]AAGGTGTGGCCATGG | 1155 |
rs766657294 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125493 | GGATTGGTGTCCGCT[A/C]TGATGAGCCACTGGG | 1155 |
rs766834250 | snp | A/G | 1.66145e-05 | 0.00288218 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114330 | CCCAGCTCAGGGCCC[A/G]CCACTCACTCCACTT | 1155 |
rs766834719 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36123012 | GTCTGTCTCTAATTT[A/G]CCGATTCTGGATGTT | 1155 |
rs766955849 | in-del | -/CGGCT | 1.65222e-05 | 0.00287417 | upstream-variant-2KB, frameshift-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114830 | AATACCCACGAAGCC[-/CGGCT]CGTAAGTCCCGTCGG | 1155 |
rs767086932 | snp | C/G | 1.6649e-05 | 0.00288518 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114865 | GCTCCATGGCGACGC[C/G]CAGCCCGCGCAGCCC | 1155 |
rs767111430 | snp | C/T | 3.60959e-05 | 0.00424813 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125773 | GGACTACGGGTTGGA[C/T]GAGATATGACACCTA | 1155 |
rs767146628 | snp | A/G | | | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121738 | GTGGCTCGCGGGCCC[A/G]GTCCCGGGCTCCAGG | 1155 |
rs767210100 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36117725 | TAATTATCCCCATTT[G/T]GCAGAAGAGAAAATT | 1155 |
rs767250100 | in-del | -/G | 1.64732e-05 | 0.0028699 | frameshift-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125523 | GGAAAAATGATGGCA[-/G]GTAACAAGAATTCCC | 1155 |
rs767284541 | snp | C/T | 0.000143916 | 0.00848158 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121661 | ATCCCCGTGGGCAGC[C/T]GCTGTGAGGTGCGGG | 1155 |
rs767305846 | snp | G/T | 1.67787e-05 | 0.00289639 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116229 | CACCCCACCTTTCAT[G/T]TGGTTATTCAACAGA | 1155 |
rs767370945 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36123125 | GGCATGCCTGTGTCA[C/G]TGCCACACTGTTGCC | 1155 |
rs767442722 | in-del | -/GGACCTGCCGGG | 1.74142e-05 | 0.00295073 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114629 | ACGCTGGGAACAGGT[-/GGACCTGCCGGG]GAAGACCCCGGCGCT | 1155 |
rs767456172 | snp | G/T | 4.99679e-05 | 0.00499815 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114443 | TGTGGGGGAAAGGGG[G/T]TCACGGAAGGATTCC | 1155 |
rs767649804 | snp | C/T | 0.000115303 | 0.00759199 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125489 | TACTGGATTGGTGTC[C/T]GCTATGATGAGCCAC | 1155 |
rs767723785 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36122436 | GGCAGCAGAGAAAGA[A/C]CCAGTCTCAAAAAAA | 1155 |
rs767816881 | snp | A/G | 1.65002e-05 | 0.00287225 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114190 | ACTTTTGGCACGGGT[A/G]GTCCTCGGTCCGCGG | 1155 |
rs768020512 | snp | C/T | 2.98976e-05 | 0.00386625 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115665 | CAGCCTCACCATCGC[C/T]GAGTTCAAGGTGTGG | 1155 |
rs768020937 | snp | C/T | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126210 | GGTGGATCACGAGGT[C/T]AGGAGATCGAGACCA | 1155 |
rs768034001 | snp | C/T | 1.67671e-05 | 0.00289539 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114882 | AGCCCGCGCAGCCCT[C/T]CCAGCCTTCCGCGCT | 1155 |
rs768130016 | snp | A/C | 1.65356e-05 | 0.00287533 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114385 | TGCAGCTGTTGTCGG[A/C]CTCCTGCTGGTAATC | 1155 |
rs768176232 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120251 | AGTCCCCAGCATGAG[A/G]CCCAGCTGGGCCCCT | 1155 |
rs768197238 | snp | G/T | 1.97814e-05 | 0.00314489 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121740 | GGCTCGCGGGCCCGG[G/T]CCCGGGCTCCAGGGC | 1155 |
rs768478513 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115499 | CAGCAGCGGCGGCGG[C/T]GGCTGCGGAGCGGGT | 1155 |
rs768489222 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115277 | CGGGCTTCAGTCTTC[C/G]CCGCCTGTTCTGGTC | 1155 |
rs768523192 | in-del | -/CG | 0.000266276 | 0.0115355 | intron-variant | TBCB | GRCh38.p7 | 19:36120688 | AGACCCTGATCCCCA[-/CG]GAGCCCCTCCCCTCA | 1155 |
rs768558990 | snp | G/T | 1.81023e-05 | 0.00300846 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125828 | AGCTCAGCCACTGAC[G/T]GCCCCTCCTGTGTGT | 1155 |
rs768848063 | snp | C/T | 3.30316e-05 | 0.00406383 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114731 | GTGGGGAGGGGGAGG[C/T]GCCAGGGGTTAGTTC | 1155 |
rs768903201 | snp | A/G | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120788 | ACGATCTCACAAGAA[A/G]CCTACGACCAGAGGC | 1155 |
rs768903225 | snp | A/C | 1.71513e-05 | 0.00292837 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114646 | ACCTGCCGGGGAAGA[A/C]CCCGGCGCTCACCGC | 1155 |
rs768956234 | snp | C/T | 0.000132895 | 0.00815044 | intron-variant | TBCB | GRCh38.p7 | 19:36120694 | TGATCCCCACGGAGC[C/T]CCTCCCCTCACACAG | 1155 |
rs768968774 | in-del | -/C | 1.8178e-05 | 0.00301474 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114307 | CCTCCAGAGCCAACA[-/C]CCCCGCCCCCAGCTC | 1155 |
rs768992524 | snp | A/C | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125468 | CTCACAGATTTCAAG[A/C]CTGGCTACTGGATTG | 1155 |
rs769026359 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36119766 | GGTGTGGTGGTGTGT[A/G]CCTATAGTTTCAGCT | 1155 |
rs769044915 | snp | A/G | 1.70406e-05 | 0.0029189 | intron-variant | TBCB | GRCh38.p7 | 19:36125627 | AGAGTGGAGCCATGT[A/G]AGGGTCCTCTGACCA | 1155 |
rs769051373 | snp | C/T | 1.84096e-05 | 0.00303389 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115710 | TCCGGAGGGGCGGGG[C/T]GAAGAAATTGGGGGG | 1155 |
rs769074048 | snp | C/T | 0.00111474 | 0.0235823 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113543 | AGGTGCATGGACAGC[C/T]GGCCAGCTACGCTTA | 1155 |
rs769207178 | snp | G/T | 1.67136e-05 | 0.00289076 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114294 | CGCTCAGACCCAGCC[G/T]CCAGAGCCAACACCC | 1155 |
rs769260239 | snp | A/T | 1.65449e-05 | 0.00287614 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116041 | GCCTCCTCCTCACAG[A/T]GTAAACTGGAGTTGC | 1155 |
rs769446521 | snp | G/T | 1.86991e-05 | 0.00305765 | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113767 | AGGTCACTCGGTCCA[G/T]CGGTGGCCGCAGTGT | 1155 |
rs769502265 | snp | C/T | 1.64936e-05 | 0.00287168 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114174 | TACCAGCTGAACGCT[C/T]ACTTTTGGCACGGGT | 1155 |
rs769569144 | snp | A/G | 0.000122242 | 0.00781703 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115519 | GCGGAGCGGGTGTGA[A/G]GCGGCTGGACCGCGC | 1155 |
rs769646346 | snp | A/G | 6.60338e-05 | 0.00574566 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114214 | TCCGCGGCAACGTGG[A/G]GTCCTGGGACACGTC | 1155 |
rs769734404 | snp | A/G | 3.76719e-05 | 0.00433988 | intron-variant | TBCB | GRCh38.p7 | 19:36121488 | ATCCTGTTAGGCCCG[A/G]CCGACACCCCAACTG | 1155 |
rs769747933 | snp | C/G | 9.99151e-05 | 0.00706736 | intron-variant | TBCB | GRCh38.p7 | 19:36120686 | CCAGACCCTGATCCC[C/G]ACGGAGCCCCTCCCC | 1155 |
rs769902946 | snp | A/G | 1.66125e-05 | 0.00288201 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114425 | GCACTACGAGAGGGC[A/G]AGTGTGGGGGAAAGG | 1155 |
rs769955794 | snp | A/C | 6.64297e-05 | 0.00576285 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116198 | ACGTGAGGACTCTCT[A/C]TCTGGGACACTCCCC | 1155 |
rs769998670 | snp | A/G | 0.000132127 | 0.00812686 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113965 | ATATCCCCGCCCCCA[A/G]AAAGGACCAAACAAG | 1155 |
rs770095381 | snp | C/G | 1.80915e-05 | 0.00300756 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125819 | TCAGCTCCTAGCTCA[C/G]CCACTGACTGCCCCT | 1155 |
rs770257075 | snp | C/G | | | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113070 | GGTTTGTGTATGTGG[C/G]GTATGGAGAATCAAG | 1155 |
rs770328765 | snp | A/C | | | intron-variant | TBCB | GRCh38.p7 | 19:36118496 | GGTCAGGAGTTCGAG[A/C]CGGTGAAACCCCGTC | 1155 |
rs770448084 | snp | A/G | 1.64751e-05 | 0.00287007 | intron-variant | TBCB | GRCh38.p7 | 19:36125563 | TCTGTGTGTGCATTT[A/G]TGTGTAAGTCCATGC | 1155 |
rs770612740 | snp | C/T | 7.05542e-05 | 0.00593903 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115697 | CATGGGGGCGGGGTC[C/T]GGAGGGGCGGGGCGA | 1155 |
rs770614655 | snp | C/T | 0.000115551 | 0.00760013 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114106 | CGGAGGCTTCACACC[C/T]TTCCCTCCTCCCTTC | 1155 |
rs770619530 | snp | C/T | 1.65504e-05 | 0.00287662 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114841 | AGCCCGGCTCGTAAG[C/T]CCCGTCGGGCTCCAT | 1155 |
rs770634310 | snp | C/T | 8.23635e-05 | 0.00641677 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125461 | GGCAGGTCTCACAGA[C/T]TTCAAGCCTGGCTAC | 1155 |
rs770725751 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36125602 | TGCTGAGCTGCCCAT[C/G]CCAGCTTCTAGAGTG | 1155 |
rs770754202 | snp | A/C | 5.69687e-05 | 0.00533677 | intron-variant | TBCB | GRCh38.p7 | 19:36121484 | CGTCATCCTGTTAGG[A/C]CCGGCCGACACCCCA | 1155 |
rs770807018 | snp | C/G | 5.08023e-05 | 0.0050397 | intron-variant | TBCB | GRCh38.p7 | 19:36120821 | GGTACGGGCAGGTGG[C/G]CGTCGAGGGGTGCGT | 1155 |
rs770815405 | snp | C/G | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113268 | GAGGGAGAGTGGAGA[C/G]ACAGGTGTCTGGCCC | 1155 |
rs770915376 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36119072 | TCATAGGCAGTGGCA[C/T]CTTTGAGCAGGTTTC | 1155 |
rs771018246 | snp | A/G | 0.000147918 | 0.00859867 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113597 | ACGTGTGCGAGGACT[A/G]CGGCTTCACCAGCTC | 1155 |
rs771055770 | snp | C/T | 1.64738e-05 | 0.00286995 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113739 | GGTGTTTATTACACT[C/T]GGGGGAGAGAGGAGG | 1155 |
rs771108967 | snp | C/G | 3.55745e-05 | 0.00421734 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125727 | CCTTTGTCAAGCCAG[C/G]AGTCGTGACGGTGGG | 1155 |
rs771118928 | snp | A/C | 1.66549e-05 | 0.00288568 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114871 | TGGCGACGCGCAGCC[A/C]GCGCAGCCCTCCCAG | 1155 |
rs771277915 | in-del | -/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120916 | GCCAGTGGTGTAGAC[-/G]GGGGGCCGAGAGCTT | 1155 |
rs771304333 | snp | G/T | 1.65778e-05 | 0.002879 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116189 | GCCGCATCCACGTGA[G/T]GACTCTCTATCTGGG | 1155 |
rs771336554 | snp | C/T | 1.65641e-05 | 0.00287781 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114408 | TGGTAATCACAGTTC[C/T]GGCACTACGAGAGGG | 1155 |
rs771359463 | snp | C/G | 1.80876e-05 | 0.00300724 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125807 | AATTCCCCTGCTTCA[C/G]CTCCTAGCTCAGCCA | 1155 |
rs771391427 | snp | A/C | | | upstream-variant-2KB, stop-gained, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113628 | CCGGCCCGACACCTA[A/C]GCACAGCACCGCGCC | 1155 |
rs771472271 | snp | G/T | 1.65059e-05 | 0.00287275 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114002 | ATACTTAGAAAGCCC[G/T]CGCGCCACTTACCTC | 1155 |
rs771486730 | snp | C/G | 1.64885e-05 | 0.00287123 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116106 | GCTGTATGGAGTTGA[C/G]GACAAGTTCTACAGC | 1155 |
rs771527034 | snp | C/T | 9.75467e-05 | 0.00698311 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115530 | GTGAGGCGGCTGGAC[C/T]GCGCTGCAGGCATCC | 1155 |
rs771559535 | snp | A/T | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125480 | AAGCCTGGCTACTGG[A/T]TTGGTGTCCGCTATG | 1155 |
rs771613420 | snp | C/T | | | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113117 | ACCCCAGTGGGTGGG[C/T]GTAAGGTGGCACCAA | 1155 |