| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs771748897 | snp | G/T | 1.64901e-05 | 0.00287137 | intron-variant | TBCB | GRCh38.p7 | 19:36125424 | CTATGTCCAGAAGCT[G/T]CACAGGGATTTCTCT | 1155 |
| rs771802288 | snp | C/T | 2.18936e-05 | 0.00330852 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121758 | CGGGCTCCAGGGCTC[C/T]AAGGCCGGGAGGAAA | 1155 |
| rs771981393 | snp | C/T | 1.65064e-05 | 0.00287279 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114091 | TAGGGGCTCGGTCAC[C/T]GGAGGCTTCACACCC | 1155 |
| rs772041810 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124563 | TTTTTTCTTTTGAGA[C/T]GTAATCTCGCTTTGT | 1155 |
| rs772199820 | snp | C/T | 1.6713e-05 | 0.00289072 | intron-variant | TBCB | GRCh38.p7 | 19:36120810 | ACCAGAGGCAAGGTA[C/T]GGGCAGGTGGGCGTC | 1155 |
| rs772302217 | snp | A/G | 1.7979e-05 | 0.00299819 | intron-variant | TBCB | GRCh38.p7 | 19:36120855 | GGCCAGAGGGAGTAT[A/G]TGCAGGTATGAGGGC | 1155 |
| rs772329724 | snp | C/G | 3.30885e-05 | 0.00406733 | upstream-variant-2KB, stop-gained | TBCB, POLR2I | GRCh38.p7 | 19:36114836 | CACGAAGCCCGGCTC[C/G]TAAGTCCCGTCGGGC | 1155 |
| rs772377609 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36117361 | TTGTTTTGTTTTGTT[C/T]GAGACAGAGTTTTGC | 1155 |
| rs772408823 | in-del | -/ACACAGGT | 0.000132777 | 0.00814683 | intron-variant | TBCB | GRCh38.p7 | 19:36120698 | CCCACGGAGCCCCTC[-/ACACAGGT]CCCTCACACAGGTCA | 1155 |
| rs772415437 | snp | C/G | 5.00571e-05 | 0.00500261 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116171 | ACCCTGTAGATGACG[C/G]CTGCCGCATCCACGT | 1155 |
| rs772468648 | snp | C/T | 1.65105e-05 | 0.00287315 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116056 | TGTAAACTGGAGTTG[C/T]TGGTGGGCAGCCCTG | 1155 |
| rs772475664 | snp | A/G | 5.03056e-05 | 0.005015 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114312 | AGAGCCAACACCCCC[A/G]CCCCCAGCTCAGGGC | 1155 |
| rs772525357 | snp | A/G | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115725 | CGAAGAAATTGGGGG[A/G]TTCCCGGAAGGGGGA | 1155 |
| rs772537980 | snp | C/T | | | upstream-variant-2KB, intron-variant | TBCB, OVOL3 | GRCh38.p7 | 19:36113155 | GCCTGTCACGGAATG[C/T]AGAGTGCAGACGGAT | 1155 |
| rs772580345 | snp | G/T | 0.000137377 | 0.00828671 | intron-variant | TBCB | GRCh38.p7 | 19:36125637 | CATGTGAGGGTCCTC[G/T]GACCACACCCACCCC | 1155 |
| rs772723019 | snp | C/G | 1.65053e-05 | 0.0028727 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114004 | ACTTAGAAAGCCCTC[C/G]CGCCACTTACCTCGG | 1155 |
| rs772790170 | snp | G/T | 5.12177e-05 | 0.00506026 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115628 | CCCTCAACACCTTCC[G/T]CTCCGAGAAGCGATA | 1155 |
| rs772996074 | snp | A/G | 0.000134161 | 0.00818916 | intron-variant | TBCB | GRCh38.p7 | 19:36120811 | CCAGAGGCAAGGTAC[A/G]GGCAGGTGGGCGTCG | 1155 |
| rs772998768 | snp | C/T | 9.33402e-05 | 0.00683091 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115532 | GAGGCGGCTGGACCG[C/T]GCTGCAGGCATCCGC | 1155 |
| rs773011907 | snp | A/G | 3.30589e-05 | 0.00406551 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120732 | ACCACAGTGGCGCCC[A/G]CCTTGGTGAGTATGA | 1155 |
| rs773048188 | snp | A/G | 9.01652e-05 | 0.00671375 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121762 | CTCCAGGGCTCCAAG[A/G]CCGGGAGGAAATGTT | 1155 |
| rs773056557 | snp | C/T | 8.25335e-05 | 0.00642339 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114098 | TCGGTCACCGGAGGC[C/T]TCACACCCTTCCCTC | 1155 |
| rs773140399 | in-del | -/CCTACGA | 1.65626e-05 | 0.00287768 | frameshift-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120789 | CGATCTCACAAGAAG[-/CCTACGA]CCAGAGGCAAGGTAC | 1155 |
| rs773207072 | snp | C/T | 0.000189863 | 0.00974143 | intron-variant | TBCB | GRCh38.p7 | 19:36125643 | AGGGTCCTCTGACCA[C/T]ACCCACCCCTATCCT | 1155 |
| rs773276065 | snp | A/C/T | 3.30903e-05 | 0.00406746 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114837 | ACGAAGCCCGGCTCG[A/C/T]AAGTCCCGTCGGGCT | 1155 |
| rs773348186 | in-del | -/TTC | 1.66335e-05 | 0.00288383 | upstream-variant-2KB, cds-indel | TBCB, POLR2I | GRCh38.p7 | 19:36114678 | TAGAGCAGAATGCGG[-/TTC]TCCTTGTCTTCCTTG | 1155 |
| rs773509219 | snp | A/G | 1.64885e-05 | 0.00287123 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114749 | CAGGGGTTAGTTCTG[A/G]AGCCATTCCTCGCCC | 1155 |
| rs773511912 | snp | A/G | 1.66671e-05 | 0.00288674 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114319 | ACACCCCCGCCCCCA[A/G]CTCAGGGCCCGCCAC | 1155 |
| rs773535196 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36117393 | CTTGTTCCCCAGGCC[A/G]GAATGCAGTGGTGTG | 1155 |
| rs773706371 | snp | C/T | 1.64925e-05 | 0.00287158 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116074 | GTGGGCAGCCCTGCT[C/T]CCTGCATGGAACTGG | 1155 |
| rs773728438 | snp | C/G | 6.72778e-05 | 0.00579951 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115991 | GGTCATTGATGCAAG[C/G]GGCGGGGCCTCCGTG | 1155 |
| rs773769052 | snp | A/G | 1.65086e-05 | 0.00287298 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114210 | TCGGTCCGCGGCAAC[A/G]TGGGGTCCTGGGACA | 1155 |
| rs773819996 | snp | A/G | 1.77495e-05 | 0.002979 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125711 | CAGGCCAAGTATGGC[A/G]CCTTTGTCAAGCCAG | 1155 |
| rs773850850 | snp | G/T | 1.68247e-05 | 0.00290035 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114886 | CGCGCAGCCCTCCCA[G/T]CCTTCCGCGCTTGCT | 1155 |
| rs774047826 | snp | G/T | 1.77002e-05 | 0.00297486 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121607 | CAGGAGGCCGAGGCC[G/T]CCCAGCGCCTGGCCG | 1155 |
| rs774142386 | snp | C/T | 3.62129e-05 | 0.00425501 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125833 | AGCCACTGACTGCCC[C/T]TCCTGTGTGTGCCCA | 1155 |
| rs774181334 | snp | C/T | 0.000107118 | 0.00731762 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115525 | CGGGTGTGAGGCGGC[C/T]GGACCGCGCTGCAGG | 1155 |
| rs774219158 | snp | C/T | 1.66971e-05 | 0.00288934 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116216 | TGGGACACTCCCCCA[C/T]CCCACCTTTCATTTG | 1155 |
| rs774303696 | in-del | -/C/GC | 1.66217e-05 | 0.0028828 | intron-variant | TBCB | GRCh38.p7 | 19:36120692 | CTGATCCCCACGGAG[-/C/GC]CCCCTCCCCTCACAC | 1155 |
| rs774346042 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36123107 | CTTTCAAGTTTCATC[C/T]GTGGCATGCCTGTGT | 1155 |
| rs774457572 | in-del | -/A | | | intron-variant | TBCB | GRCh38.p7 | 19:36122754 | GGAGACCCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 1155 |
| rs774675619 | in-del | -/G | 1.66729e-05 | 0.00288724 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114319 | ACACCCCCGCCCCCA[-/G]CTCAGGGCCCGCCAC | 1155 |
| rs774697780 | snp | C/G | | | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114483 | TGGGAGGAGAGGGCA[C/G]GGTGATCCCGGAGGA | 1155 |
| rs774732833 | snp | C/T | 1.6599e-05 | 0.00288084 | intron-variant | TBCB | GRCh38.p7 | 19:36120698 | CCCCACGGAGCCCCT[C/T]CCCTCACACAGGTCA | 1155 |
| rs774777504 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115339 | ACTATGGAAGGCCCC[G/T]CTGGATTGGCTGGGC | 1155 |
| rs774835365 | snp | C/T | 1.71102e-05 | 0.00292486 | intron-variant | TBCB | GRCh38.p7 | 19:36125632 | GGAGCCATGTGAGGG[C/T]CCTCTGACCACACCC | 1155 |
| rs774884360 | snp | A/G | 1.64727e-05 | 0.00286986 | stop-gained, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125479 | CAAGCCTGGCTACTG[A/G]ATTGGTGTCCGCTAT | 1155 |
| rs774997425 | snp | C/T | 7.53055e-05 | 0.00613572 | intron-variant | TBCB | GRCh38.p7 | 19:36121489 | TCCTGTTAGGCCCGG[C/T]CGACACCCCAACTGA | 1155 |
| rs775032937 | snp | A/G | 1.64958e-05 | 0.00287187 | upstream-variant-2KB, downstream-variant-500B, synonymous-codon | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114182 | GAACGCTCACTTTTG[A/G]CACGGGTGGTCCTCG | 1155 |
| rs775102029 | snp | A/G | | | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114259 | TCAGTTCGCTGCAGG[A/G]ACGCGGGGGTGCAAA | 1155 |
| rs775136724 | in-del | -/C | 1.64931e-05 | 0.00287163 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114152 | AGCCTCACTTTACCT[-/C]CCCCAGTACCAGCTG | 1155 |
| rs775183236 | snp | A/C | 0.000100257 | 0.00707945 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114305 | AGCCTCCAGAGCCAA[A/C]ACCCCCGCCCCCAGC | 1155 |
| rs775316113 | snp | G/T | 1.86048e-05 | 0.00304993 | upstream-variant-2KB, downstream-variant-500B, missense | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113769 | GTCACTCGGTCCAGC[G/T]GTGGCCGCAGTGTGG | 1155 |
| rs775389155 | snp | C/G | 1.78493e-05 | 0.00298736 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125743 | AGTCGTGACGGTGGG[C/G]GACTTCCCGGAGGAG | 1155 |
| rs775404025 | snp | A/C/G | 4.28807e-05 | 0.00463018 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113651 | ACCGCGCCCTGCACC[A/C/G]CGCAGCCTGATACGG | 1155 |
| rs775426744 | snp | A/C/T | 1.65905e-05 | 0.0028801 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114856 | TCCCGTCGGGCTCCA[A/C/T]GGCGACGCGCAGCCC | 1155 |
| rs775648395 | snp | C/G | 8.23635e-05 | 0.00641677 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125464 | AGGTCTCACAGATTT[C/G]AAGCCTGGCTACTGG | 1155 |
| rs775766382 | snp | C/T | | | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125739 | CAGCAGTCGTGACGG[C/T]GGGGGACTTCCCGGA | 1155 |
| rs775900445 | snp | C/T | 1.80925e-05 | 0.00300764 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125821 | AGCTCCTAGCTCAGC[C/T]ACTGACTGCCCCTCC | 1155 |
| rs775931314 | snp | C/G | 4.45068e-05 | 0.00471714 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115554 | GGCATCCGCAGGGCG[C/G]GGCAAGATGGAGGTG | 1155 |
| rs776054819 | snp | G/T | 0.00020139 | 0.0100327 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121788 | ATGTTGGGGGCACAG[G/T]GGAGCCTCGGAGACC | 1155 |
| rs776063947 | in-del | -/CCAAGGCC | 4.30265e-05 | 0.00463804 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121756 | CCGGGCTCCAGGGCT[-/CCAAGGCC]CCAAGGCCGGGAGGA | 1155 |
| rs776093724 | snp | A/G | 1.74002e-05 | 0.00294954 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114627 | CCACGCTGGGAACAG[A/G]TGGACCTGCCGGGGA | 1155 |
| rs776241682 | snp | C/T | 5.30696e-05 | 0.00515092 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125689 | TGGGAAACGCTACTT[C/T]GAATGCCAGGCCAAG | 1155 |
| rs776314346 | snp | G/T | 0.000239511 | 0.0109407 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115698 | ATGGGGGCGGGGTCC[G/T]GAGGGGCGGGGCGAA | 1155 |
| rs776338331 | snp | A/G | 3.29848e-05 | 0.00406095 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114167 | TCCCCAGTACCAGCT[A/G]AACGCTCACTTTTGG | 1155 |
| rs776392320 | snp | C/T | 1.65081e-05 | 0.00287293 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114113 | TTCACACCCTTCCCT[C/T]CTCCCTTCGCCCAGT | 1155 |
| rs776429851 | snp | A/G | 1.6571e-05 | 0.0028784 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114848 | CTCGTAAGTCCCGTC[A/G]GGCTCCATGGCGACG | 1155 |
| rs776430794 | snp | A/C | 1.6486e-05 | 0.00287102 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114758 | GTTCTGGAGCCATTC[A/C]TCGCCCGCCTTCTAA | 1155 |
| rs776443765 | snp | C/T | 8.13681e-05 | 0.00637788 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115648 | GAGAAGCGATACAGC[C/T]GCAGCCTCACCATCG | 1155 |
| rs776517817 | snp | A/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113310 | GGGTGACGGTAGCAG[A/T]TGGTGGGTCATGGGC | 1155 |
| rs776548104 | snp | C/T | 3.79284e-05 | 0.00435462 | intron-variant | TBCB | GRCh38.p7 | 19:36121485 | GTCATCCTGTTAGGC[C/T]CGGCCGACACCCCAA | 1155 |
| rs776599635 | snp | C/T | 5.08496e-05 | 0.00504205 | intron-variant | TBCB | GRCh38.p7 | 19:36120822 | GTACGGGCAGGTGGG[C/T]GTCGAGGGGTGCGTG | 1155 |
| rs776704408 | snp | A/G | 2.01692e-05 | 0.00317556 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113748 | TACACTCGGGGGAGA[A/G]AGGAGGTCACTCGGT | 1155 |
| rs776711121 | snp | C/T | 0.000399093 | 0.0141205 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125816 | GCTTCAGCTCCTAGC[C/T]CAGCCACTGACTGCC | 1155 |
| rs776725596 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36118492 | TTAAGGTCAGGAGTT[C/T]GAGACGGTGAAACCC | 1155 |
| rs776845091 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124832 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCCAGTAT | 1155 |
| rs776916266 | snp | C/G | 0.000428786 | 0.0146359 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113614 | GGCTTCACCAGCTCC[C/G]GGCCCGACACCTACG | 1155 |
| rs777009283 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36117561 | TTCACCATGTTGGCC[A/G]GGCTGGTCTTGAACT | 1155 |
| rs777097604 | snp | A/G | 0.000144665 | 0.00850363 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121662 | TCCCCGTGGGCAGCC[A/G]CTGTGAGGTGCGGGC | 1155 |
| rs777147634 | snp | A/C/T | 6.64147e-05 | 0.00576225 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114331 | CCAGCTCAGGGCCCG[A/C/T]CACTCACTCCACTTC | 1155 |
| rs777165748 | snp | A/G | | | downstream-variant-500B | TBCB | GRCh38.p7 | 19:36126280 | ACAAAAAAATTAGCC[A/G]GGCATGGTGGTGGGT | 1155 |
| rs777218816 | snp | A/G | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116191 | CGCATCCACGTGAGG[A/G]CTCTCTATCTGGGAC | 1155 |
| rs777333644 | snp | C/T | 0.000161538 | 0.0089857 | upstream-variant-2KB, missense, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113467 | GGGATCCGGCCCTTC[C/T]GCTGCAGTGCTTGCG | 1155 |
| rs777407692 | snp | C/T | 1.65444e-05 | 0.00287609 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114706 | CCTTGGGGTACAGCA[C/T]GTTGTTACTGTGGGG | 1155 |
| rs777495378 | snp | A/C/G | 3.32503e-05 | 0.00407729 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114268 | TGCAGGGACGCGGGG[A/C/G]TGCAAAATTACGCTC | 1155 |
| rs777567763 | snp | C/T | 4.94425e-05 | 0.0049718 | intron-variant | TBCB | GRCh38.p7 | 19:36125437 | CTTCACAGGGATTTC[C/T]CTTCTGTTGGCAGGT | 1155 |
| rs777745092 | snp | A/G | 1.64933e-05 | 0.00287165 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114157 | TCACTTTACCTCCCC[A/G]GTACCAGCTGAACGC | 1155 |
| rs777817783 | in-del | -/AAGT | | | intron-variant | TBCB | GRCh38.p7 | 19:36117688 | TGAATTGAATCCATA[-/AAGT]AAGACCACAAGGATA | 1155 |
| rs777829443 | snp | C/T | 1.66863e-05 | 0.0028884 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116018 | CGTGGCCTCCTTCTT[C/T]TCACCCTGCCTCCTC | 1155 |
| rs777885464 | snp | C/T | 1.8946e-05 | 0.00307777 | intron-variant | TBCB | GRCh38.p7 | 19:36121476 | GGGTGGAGCGTCATC[C/T]TGTTAGGCCCGGCCG | 1155 |
| rs777890736 | snp | G/T | 5.49586e-05 | 0.00524178 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36115692 | GTGGCCATGGGGGCG[G/T]GGTCCGGAGGGGCGG | 1155 |
| rs777968979 | snp | C/G/T | 3.33063e-05 | 0.00408072 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114870 | ATGGCGACGCGCAGC[C/G/T]CGCGCAGCCCTCCCA | 1155 |
| rs778026150 | snp | C/G | 0.000124774 | 0.00789755 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121539 | CAGACACGGTCCGCT[C/G]TTTCCTGAAGCGCAG | 1155 |
| rs778057732 | snp | C/T | 1.65455e-05 | 0.00287619 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116175 | TGTAGATGACGGCTG[C/T]CGCATCCACGTGAGG | 1155 |
| rs778138181 | snp | C/T | 3.61572e-05 | 0.00425174 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125800 | CCTAAGGAATTCCCC[C/T]GCTTCAGCTCCTAGC | 1155 |
| rs778148430 | snp | C/T | 1.71167e-05 | 0.00292542 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114906 | CCGCGCTTGCTCCGC[C/T]GCGCTACAGGTCGCG | 1155 |
| rs778198391 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118169 | GTTGATTAACTGTTC[A/G]TTCCCCATCTGTGTT | 1155 |
| rs778376134 | snp | C/T | 1.69284e-05 | 0.00290928 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113856 | GGAAGGATTTGGACC[C/T]AGCAGCGCCTTACCC | 1155 |
| rs778385787 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115146 | GATGCGCATCGTAAA[C/T]CGCAAAACACTGAGC | 1155 |
| rs778392634 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36124004 | CACTGCTTCCCACAG[C/G]CGCTGCAGCAGTTTT | 1155 |
| rs778453986 | snp | C/T | 2.85026e-05 | 0.00377498 | upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113729 | CATGGAATCTGGTGT[C/T]TATTACACTCGGGGG | 1155 |
| rs778568649 | snp | A/G | 1.66732e-05 | 0.00288727 | intron-variant | TBCB | GRCh38.p7 | 19:36120674 | AGGCCTCCCTGGCCA[A/G]ACCCTGATCCCCACG | 1155 |
| rs778570928 | snp | C/T | 3.30786e-05 | 0.00406672 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114392 | GTTGTCGGCCTCCTG[C/T]TGGTAATCACAGTTC | 1155 |
| rs778600512 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36125231 | ACCCAGTGAATGGGG[A/G]ACAGGGGTGGAAGCA | 1155 |
| rs778789187 | snp | C/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116996 | CACAGTCCAGGTGAG[C/T]TCGGCCTCTGGATCC | 1155 |
| rs778882737 | snp | C/T | 5.15836e-05 | 0.0050783 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115586 | CGGGGGTGTCGGCAC[C/T]CACGGTGACCGTTTT | 1155 |
| rs779010749 | snp | C/T | 3.29848e-05 | 0.00406095 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114148 | AGACGAGCCTCACTT[C/T]ACCTCCCCAGTACCA | 1155 |
| rs779081257 | snp | A/G | 3.5977e-05 | 0.00424114 | intron-variant | TBCB | GRCh38.p7 | 19:36120851 | TGGGGGCCAGAGGGA[A/G]TATGTGCAGGTATGA | 1155 |
| rs779113019 | in-del | -/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36121201 | GGACGGATCGAGTGT[-/T]GGGGGAGACCGGGGG | 1155 |
| rs779243039 | snp | C/T | 3.31559e-05 | 0.00407147 | synonymous-codon, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120793 | CTCACAAGAAGCCTA[C/T]GACCAGAGGCAAGGT | 1155 |
| rs779260535 | snp | G/T | 1.65277e-05 | 0.00287464 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120738 | GTGGCGCCCGCCTTG[G/T]TGAGTATGAGGACGT | 1155 |
| rs779492170 | snp | A/G | 1.65323e-05 | 0.00287505 | upstream-variant-2KB, synonymous-codon | TBCB, POLR2I | GRCh38.p7 | 19:36114377 | GACATAGATGCAGCT[A/G]TTGTCGGCCTCCTGC | 1155 |
| rs779545081 | snp | A/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36117787 | TTTATTTTTTTTGAG[A/T]CAGAGTCTTGCTCTG | 1155 |
| rs779547563 | snp | C/G | 3.30535e-05 | 0.00406518 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116164 | GGCTCCTACCCTGTA[C/G]ATGACGGCTGCCGCA | 1155 |
| rs779599367 | snp | A/C | 1.65222e-05 | 0.00287417 | upstream-variant-2KB, missense | TBCB, POLR2I | GRCh38.p7 | 19:36114828 | CGAATACCCACGAAG[A/C]CCGGCTCGTAAGTCC | 1155 |
| rs779711727 | snp | C/T | 3.61148e-05 | 0.00424924 | stop-lost, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125780 | GGGTTGGACGAGATA[C/T]GACACCTAAGGAATT | 1155 |
| rs779734910 | in-del | -/AGA | 1.80856e-05 | 0.00300707 | utr-variant-3-prime, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125805 | GAATTCCCCTGCTTC[-/AGA]AGCTCCTAGCTCAGC | 1155 |
| rs779768883 | snp | C/G | 1.64972e-05 | 0.00287199 | intron-variant | TBCB | GRCh38.p7 | 19:36125406 | ATTTCATGGGGATTT[C/G]TTCTATGTCCAGAAG | 1155 |
| rs779784608 | snp | C/T | 1.65285e-05 | 0.00287471 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116047 | TCCTCACAGTGTAAA[C/T]TGGAGTTGCTGGTGG | 1155 |
| rs779877648 | snp | A/G | 1.7457e-05 | 0.00295435 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115520 | CGGAGCGGGTGTGAG[A/G]CGGCTGGACCGCGCT | 1155 |
| rs779916982 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36124101 | TTTGCTTACAGTCAT[C/G]CACTGGGTGTGAAGT | 1155 |
| rs779917914 | snp | A/C | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116778 | GGATTACAGGTGCCC[A/C]CCCAGCTAATTTTTG | 1155 |
| rs780009476 | snp | C/T | 0.000372856 | 0.0136488 | intron-variant, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121722 | TCATGTATGTAGGTG[C/T]GTGGCTCGCGGGCCC | 1155 |
| rs780030014 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36124693 | GAACTACAGGCGCCC[A/G]CCACCACACCCGGCT | 1155 |
| rs780050026 | snp | A/G | 1.6684e-05 | 0.00288821 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114449 | GGAAAGGGGGTCACG[A/G]AAGGATTCCAGACAA | 1155 |
| rs780055361 | snp | C/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36120561 | GCTACTTCTCCCTTC[C/G]GCTGGGCTCAGGAGA | 1155 |
| rs780181014 | in-del | -/CT | 1.65868e-05 | 0.00287978 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116191 | GCATCCACGTGAGGA[-/CT]CTCTCTATCTGGGAC | 1155 |
| rs780197222 | snp | A/G | 3.29897e-05 | 0.00406125 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114069 | CTTGTGGCCGCACCT[A/G]AGAGGGTAGGGGCTC | 1155 |
| rs780214303 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113920 | TAAGGGCCCGGCAGA[A/G]TTCCAAGAAGCGCAG | 1155 |
| rs780256190 | snp | A/G | 1.65162e-05 | 0.00287365 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113969 | CCCCGCCCCCAGAAA[A/G]GACCAAACAAGCCCC | 1155 |
| rs780256353 | snp | A/G | 2.75866e-05 | 0.00371383 | missense, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115576 | ATGGAGGTGACGGGG[A/G]TGTCGGCACCCACGG | 1155 |
| rs780400145 | snp | A/G | 1.65198e-05 | 0.00287395 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114729 | CTGTGGGGAGGGGGA[A/G]GTGCCAGGGGTTAGT | 1155 |
| rs780421397 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36118315 | AGATCATGAAGCTGG[A/G]AGACCCTATCCTGGG | 1155 |
| rs780561651 | in-del | -/CTT | 6.68371e-05 | 0.00578049 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116012 | GGCCTCCGTGGCCTC[-/CTT]CTTCTCACCCTGCCT | 1155 |
| rs780624085 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115097 | CGCCTCAGTTTACAG[A/C]ATAGTATGGATCTGG | 1155 |
| rs780624877 | snp | C/T | 1.65853e-05 | 0.00287964 | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116033 | CTCACCCTGCCTCCT[C/T]CTCACAGTGTAAACT | 1155 |
| rs780672372 | snp | A/G | 3.53819e-05 | 0.00420592 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36125691 | GGAAACGCTACTTCG[A/G]ATGCCAGGCCAAGTA | 1155 |
| rs780681662 | snp | A/G | 1.73276e-05 | 0.00294338 | intron-variant | TBCB | GRCh38.p7 | 19:36120839 | TCGAGGGGTGCGTGG[A/G]GGCCAGAGGGAGTAT | 1155 |
| rs780697634 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36124102 | TTGCTTACAGTCATC[C/T]ACTGGGTGTGAAGTG | 1155 |
| rs780714085 | snp | A/G | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116567 | ACAGTGAGCGACCAG[A/G]CTGGACAGCTTGGGA | 1155 |
| rs780733137 | snp | C/T | 1.65332e-05 | 0.00287512 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36120770 | TCCCGGGTGGAGAAG[C/T]ACACGATCTCACAAG | 1155 |
| rs780766762 | in-del | -/C | 0.000135934 | 0.0082431 | upstream-variant-2KB, frameshift-variant, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113623 | GCTCCCGGCCCGACA[-/C]CCTACGCACAGCACC | 1155 |
| rs780904290 | snp | A/G | 1.73012e-05 | 0.00294114 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121574 | CTCGGCCGGTACAAC[A/G]AGGAGGAGCGGGCTC | 1155 |
| rs780923992 | snp | C/T | 0.000160064 | 0.00894463 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113520 | CTCCCTGGAAGCTCA[C/T]CTTGCTAAGGTGCAT | 1155 |
| rs781190137 | snp | C/G | 1.64985e-05 | 0.0028721 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36116145 | TCAAGAGGATGCGCT[C/G]CTGGGCTCCTACCCT | 1155 |
| rs781238670 | snp | A/G | | | intron-variant | TBCB | GRCh38.p7 | 19:36119511 | CTCCCCATCTCAGCC[A/G]GAGGGAGCCTGGGAC | 1155 |
| rs781266877 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36114103 | CACCGGAGGCTTCAC[A/C]CCCTTCCCTCCTCCC | 1155 |
| rs781277299 | snp | A/C | 5.00238e-05 | 0.00500094 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114284 | TGCAAAATTACGCTC[A/C]GACCCAGCCTCCAGA | 1155 |
| rs781300531 | snp | A/G | 4.99821e-05 | 0.00499885 | upstream-variant-2KB, utr-variant-5-prime | TBCB, POLR2I | GRCh38.p7 | 19:36114872 | GGCGACGCGCAGCCC[A/G]CGCAGCCCTCCCAGC | 1155 |
| rs781369700 | snp | C/G | 1.76247e-05 | 0.00296851 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | TBCB, POLR2I | GRCh38.p7 | 19:36115515 | GGCTGCGGAGCGGGT[C/G]TGAGGCGGCTGGACC | 1155 |
| rs781397943 | snp | C/T | 1.68354e-05 | 0.00290128 | upstream-variant-2KB, downstream-variant-500B, intron-variant | TBCB, OVOL3, POLR2I | GRCh38.p7 | 19:36113864 | TTGGACCCAGCAGCG[C/T]CTTACCCCAAAAGAA | 1155 |
| rs781420693 | snp | C/T | 1.73216e-05 | 0.00294287 | missense, nc-transcript-variant | TBCB | GRCh38.p7 | 19:36121697 | GGACAATCCCCTCGC[C/T]GGGGCACCGTCATGT | 1155 |
| rs781521507 | snp | C/T | 1.66565e-05 | 0.00288583 | intron-variant | TBCB | GRCh38.p7 | 19:36120684 | GGCCAGACCCTGATC[C/T]CCACGGAGCCCCTCC | 1155 |
| rs781532529 | snp | G/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36120515 | GGGAGCTTGGATGGG[G/T]GTGAGGAAGGGGAGG | 1155 |
| rs781596314 | snp | A/G | 5.24407e-05 | 0.00512031 | upstream-variant-2KB, intron-variant | TBCB, POLR2I | GRCh38.p7 | 19:36114616 | GCAGGGCGGGGCCAC[A/G]CTGGGAACAGGTGGA | 1155 |
| rs781639404 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36125170 | GGCAAGGCAGTAGTG[C/T]CATCCCCCTTAGGTT | 1155 |
| rs796356344 | snp | A/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116830 | TTTGCCATGTTGGCC[A/T]GGCTGGTCTGGAACT | 1155 |
| rs796421045 | snp | C/T | | | intron-variant | TBCB | GRCh38.p7 | 19:36125280 | CTACCATATTAGTCC[C/T]GGCAGGAGCTGGAGG | 1155 |
| rs796809122 | in-del | -/GC | | | intron-variant | TBCB | GRCh38.p7 | 19:36120692 | CCTGATCCCCACGGA[-/GC]CCCTCCCCTCACACA | 1155 |
| rs796971074 | snp | A/T | | | intron-variant, upstream-variant-2KB | TBCB, POLR2I | GRCh38.p7 | 19:36116834 | CCATGTTGGCCAGGC[A/T]GGTCTGGAACTCCTG | 1155 |