SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs10847 | snp | A/G | 0.290201 | 0.246747 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810321 | TTTTAAATGTGATCA[A/G]GACTATAATATTGTA | 405 |
rs955156 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARNT | GRCh38.p7 | 1:150865632 | AAAAGACAGATTTAC[C/T]CTCTGGAGAGTATAA | 405 |
rs1027699 | snp | C/T | 0.477853 | 0.102875 | intron-variant | ARNT | GRCh38.p7 | 1:150839236 | GTTCTCAAATATTAA[C/T]ACTTATTAGCTTATT | 405 |
rs1268831 | snp | A/G | 0.0193405 | 0.0964168 | intron-variant | ARNT | GRCh38.p7 | 1:150841287 | TCTGTTACCACTTAA[A/G]AATTCTACTTGAACA | 405 |
rs1272965 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877235 | ccactgcacgccagt[C/T]tgggcaacaagagcg | 405 |
rs1805133 | snp | A/G | 0.0111726 | 0.0739019 | missense | ARNT | GRCh38.p7 | 1:150817408 | CAGCAAACAGAATTG[A/G]ACATGGTACCAGGAA | 405 |
rs1889740 | snp | A/G | 0.498346 | 0.0287064 | | | GRCh38.p7 | 1:150827279 | CAGTGAATGTGTTCT[A/G]AAACTGGATTGTGGT | 405 |
rs2039590 | snp | C/T | 0.447291 | 0.153545 | intron-variant | ARNT | GRCh38.p7 | 1:150840839 | GAGAAACTTAATGGG[C/T]TTTTAAAAATTCCTG | 405 |
rs2089081 | snp | A/G | 0.445987 | 0.155207 | intron-variant | ARNT | GRCh38.p7 | 1:150827641 | cacccatagatttgt[A/G]cacagttcatatctg | 405 |
rs2089082 | snp | A/C | 0.477004 | 0.104734 | intron-variant | ARNT | GRCh38.p7 | 1:150827614 | TCTGTATTATTCATA[A/C]TAGCCAAAAAAATGA | 405 |
rs2134688 | snp | A/G | 0.312348 | 0.242101 | intron-variant | ARNT | GRCh38.p7 | 1:150844410 | TACAATGCATTTTAT[A/G]TAATACCCTCTAATT | 405 |
rs2228099 | snp | C/G | 0.483541 | 0.0892109 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836413 | CAGGGTGGTGTATGT[C/G]TCTGACTCCGTGACT | 405 |
rs2229175 | snp | A/C/G/T | 1.64754e-05 | 0.00287009 | missense | ARNT | GRCh38.p7 | 1:150823299 | TCTTGGTTCTTAGAC[A/C/G/T]GGAACCGGAACATGA | 405 |
rs2256355 | snp | C/T | 0.498437 | 0.0279115 | intron-variant | ARNT | GRCh38.p7 | 1:150839318 | TGTTATAGCCAAGGA[C/T]TGAAATTCGTTTTCC | 405 |
rs2275237 | snp | C/T | 0.00267563 | 0.0364781 | missense | ARNT | GRCh38.p7 | 1:150813335 | CTGTATTTCTAGCTC[C/T]TGAGACTGGACAGAC | 405 |
rs2864873 | snp | A/G | 0.480302 | 0.0972668 | intron-variant | ARNT | GRCh38.p7 | 1:150841698 | AACAACAGTCTCCCA[A/G]GAGAATTCTAGAGTC | 405 |
rs3062353 | in-del | -/T/TT | 0 | 0 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858633 | TTTTTTTTTTTTTTT[-/T/TT]GAGACCAGGTCTCAC | 405 |
rs3062354 | in-del | -/CAGT | | | intron-variant | ARNT | GRCh38.p7 | 1:150866278 | gtgagccaccaaggt[-/CAGT]cagcctgttccaagg | 405 |
rs3215133 | in-del | -/T | 0.100231 | 0.200173 | intron-variant | ARNT | GRCh38.p7 | 1:150829797 | ATTTTGAGAGTTTTA[-/T]GGAATTCTTCATTTG | 405 |
rs3738482 | snp | A/C/G/T | 0.00915317 | 0.0671402 | intron-variant | ARNT | GRCh38.p7 | 1:150842525 | CCTTCCTCCCTCCCC[A/C/G/T]CTTCCTTCCTTCTTT | 405 |
rs3738483 | snp | A/G | 0.300421 | 0.244863 | intron-variant | ARNT | GRCh38.p7 | 1:150828990 | ATATCAACCTCAGTT[A/G]AGAAAAAGAGATCAT | 405 |
rs3768012 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | ARNT | GRCh38.p7 | 1:150875822 | GCCTACGTCGAGGCA[A/G]TTTCCAAACTCTTTC | 405 |
rs3768013 | snp | C/T | 0.498481 | 0.027514 | intron-variant | ARNT | GRCh38.p7 | 1:150842935 | CTCTGTCTTTAATTT[C/T]TTCATTATAGAATAG | 405 |
rs3768015 | snp | C/T | 0.477004 | 0.104734 | intron-variant | ARNT | GRCh38.p7 | 1:150840478 | TAAGAGAGAGGCTTA[C/T]CATATTTTATAGACC | 405 |
rs3768016 | snp | A/G | 0.47743 | 0.103805 | intron-variant | ARNT | GRCh38.p7 | 1:150837443 | GGAAAAGGGACTTGA[A/G]TTGGTAATTAGGAGG | 405 |
rs3768017 | snp | G/T | 0.173289 | 0.23794 | intron-variant | ARNT | GRCh38.p7 | 1:150826636 | AAGTATATATCTTAC[G/T]CTTCTTTCTGTATTC | 405 |
rs3820541 | snp | C/G | 0.143959 | 0.226396 | intron-variant | ARNT | GRCh38.p7 | 1:150876205 | TTTTAACCCTCTGCC[C/G]GCTGGAGCCGCTTGA | 405 |
rs3820543 | snp | A/T | 0.144969 | 0.226867 | intron-variant | ARNT | GRCh38.p7 | 1:150840382 | GGTCCTTTTATTTTC[A/T]GGCCTTTAAATAGTT | 405 |
rs3894771 | snp | A/T | 0.499526 | 0.0153875 | intron-variant | ARNT | GRCh38.p7 | 1:150817485 | AAAAAAATTTTTTTT[A/T]AAAAAGAATCTGGAG | 405 |
rs4987112 | snp | C/T | 0 | 0 | missense | ARNT | GRCh38.p7 | 1:150817409 | TCCTGGTACCATGTC[C/T]AATTCTGTTTGCTGT | 405 |
rs6587523 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | ARNT | GRCh38.p7 | 1:150813675 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 405 |
rs6656967 | snp | A/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150864769 | aagtataataaaaaa[A/T]aaataaataaataaa | 405 |
rs6660845 | snp | A/G | 0.476487 | 0.105846 | intron-variant | ARNT | GRCh38.p7 | 1:150868590 | gcaggaggatcactc[A/G]aggacagtagttcaa | 405 |
rs6671703 | snp | C/T | 0.143959 | 0.226396 | intron-variant | ARNT | GRCh38.p7 | 1:150824494 | ggagtctcgctctgt[C/T]gccaggctggagtgc | 405 |
rs6679794 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARNT | GRCh38.p7 | 1:150822188 | aagaattttctaata[C/T]atttactgaaaaaaa | 405 |
rs6689204 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARNT | GRCh38.p7 | 1:150860497 | ctaggattacaggca[C/T]gagccaccgtgccca | 405 |
rs7513824 | snp | A/G | 0.132409 | 0.220618 | intron-variant | ARNT | GRCh38.p7 | 1:150868499 | TATCAAGAACTTGTA[A/G]AGGATTCTAATAACA | 405 |
rs7514004 | snp | C/T | 0.498459 | 0.0277128 | intron-variant | ARNT | GRCh38.p7 | 1:150845758 | aatacaaaaattagc[C/T]gggcgtggtggcagg | 405 |
rs7515228 | snp | A/T | 0.0325976 | 0.123435 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877383 | AAAGAGCACCTAAAC[A/T]TCACATGGTGATTTG | 405 |
rs7517566 | snp | A/G | 0.222035 | 0.248431 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877559 | AAAATTGGAGGCAAT[A/G]GATGAAGAAAGTAAT | 405 |
rs7517945 | snp | A/G | 0.0341408 | 0.126114 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878022 | gagtcttgctccatc[A/G]cccaggctggagtgc | 405 |
rs7518440 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARNT | GRCh38.p7 | 1:150818286 | ATTCAAAACCTGGTT[A/G]TTGTGAATGTGTGTA | 405 |
rs7518546 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | ARNT | GRCh38.p7 | 1:150818353 | AAAAAATGAAAGTAC[A/G]TACACTGTACATCAA | 405 |
rs7521592 | snp | A/C | 0.472241 | 0.114494 | intron-variant | ARNT | GRCh38.p7 | 1:150849215 | tctcaaaaaaaaaga[A/C]agaaagaaaataaat | 405 |
rs7529204 | snp | C/G | 0.146532 | 0.228245 | intron-variant | ARNT | GRCh38.p7 | 1:150872904 | aaggtcaaggctgca[C/G]tgagccatgattgtg | 405 |
rs7532045 | snp | A/G | 0.498415 | 0.0281103 | intron-variant | ARNT | GRCh38.p7 | 1:150849371 | AAAAAAGCAGATTGC[A/G]GTCAAAGTTCTCTTC | 405 |
rs7533914 | snp | A/G | 0.0322494 | 0.12282 | intron-variant | ARNT | GRCh38.p7 | 1:150822580 | gtctgaaagctctgc[A/G]ctccttcctccttac | 405 |
rs9325978 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | ARNT | GRCh38.p7 | 1:150832008 | TGATTATCCTGTTTT[C/G]TAAACTCCTAAGAGC | 405 |
rs9325979 | snp | C/T | 0.0382008 | 0.13282 | intron-variant | ARNT | GRCh38.p7 | 1:150832427 | ATAAAGAGATTAAAA[C/T]CAATCAGACTGCCCT | 405 |
rs10305645 | in-del | -/T | 0.499551 | 0.0149693 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878429 | AGCGATACATGAAAA[-/T]GGAAGTACTTTGTAG | 405 |
rs10305646 | snp | A/G | 0.0894459 | 0.191631 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877889 | gcctgtaatcccaac[A/G]gtttgtgagaccgag | 405 |
rs10305647 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877225 | gcccagactggcgtg[C/T]agtggcgctatctcg | 405 |
rs10305648 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876858 | TCACTGGACTGGCTG[C/G]CGCAGTGAGTAGCCC | 405 |
rs10305649 | snp | G/T | 0.0325976 | 0.123435 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876627 | GAGGAGCCGCCGCCA[G/T]CGAACCGGGAGGGAG | 405 |
rs10305650 | snp | A/C/G/T | 0.0570107 | 0.158919 | intron-variant | ARNT | GRCh38.p7 | 1:150876501 | TTGTCAGCCCCTTCG[A/C/G/T]CCCCTCCCCTTTAGA | 405 |
rs10305651 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150876482 | AGGGGCTGACAACTA[A/T]GGAGACCCAGGGCTG | 405 |
rs10305652 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150876330 | GGGAGCGAGGGGGCA[G/T]GTGGGAGTTGAGGGG | 405 |
rs10305653 | in-del | -/AC | 0.0733688 | 0.176922 | intron-variant | ARNT | GRCh38.p7 | 1:150875501 | GATATGTGTGTGTGT[-/AC]TGCGTGGGGCGGAGA | 405 |
rs10305654 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARNT | GRCh38.p7 | 1:150868402 | TTGTTCCTTCTTTGT[C/T]CTTTTTGCTTATCTT | 405 |
rs10305655 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ARNT | GRCh38.p7 | 1:150868203 | tgtacacttgtaatc[C/T]cagctactcaggaag | 405 |
rs10305656 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150868044 | ACCTACCATAGTCCT[C/G]TTCCCTTtgtattag | 405 |
rs10305657 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150867941 | gccctgcctcccata[G/T]agcctgcggaactat | 405 |
rs10305658 | snp | C/T | 0.132409 | 0.220618 | intron-variant | ARNT | GRCh38.p7 | 1:150867870 | cagccatgtgaagac[C/T]tgcttgcttcccctt | 405 |
rs10305659 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARNT | GRCh38.p7 | 1:150867787 | tctcttgagaactct[A/G]tcatgagagagcatt | 405 |
rs10305660 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARNT | GRCh38.p7 | 1:150867608 | GGAATGAAATTTTTG[C/T]AGTCTTTTATACATA | 405 |
rs10305661 | snp | C/T | 0.0129027 | 0.0792771 | intron-variant | ARNT | GRCh38.p7 | 1:150867585 | TTCATTCCTGGCTTC[C/T]CACATAAACTACTTT | 405 |
rs10305662 | snp | A/G | 0.124491 | 0.216211 | intron-variant | ARNT | GRCh38.p7 | 1:150867574 | AAAAATATAGGAAAG[A/G]AGTTTATGTGAGAAG | 405 |
rs10305663 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | ARNT | GRCh38.p7 | 1:150867222 | AATCTGTTTTTTTTT[G/T]TTGTTGTTGTTTTTT | 405 |
rs10305664 | snp | G/T | 0.478685 | 0.10101 | intron-variant | ARNT | GRCh38.p7 | 1:150867210 | TTTGTTGTTGTTGTT[G/T]TTTTTAAAGACAGAG | 405 |
rs10305665 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | ARNT | GRCh38.p7 | 1:150866995 | tggtcttgaactccc[A/G]tcctcaagtgatcca | 405 |
rs10305666 | snp | C/T | 0.0136048 | 0.0813469 | intron-variant | ARNT | GRCh38.p7 | 1:150866962 | tgccttggcctccca[C/T]agtgctgggattaca | 405 |
rs10305667 | snp | A/G | 0.438246 | 0.16451 | intron-variant | ARNT | GRCh38.p7 | 1:150859632 | CAGTGGCTCAAACCT[A/G]TAATTCCAGTGCTCT | 405 |
rs10305668 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | ARNT | GRCh38.p7 | 1:150859618 | TGTAATTCCAGTGCT[C/T]TGGGAAGCTGAGGTG | 405 |
rs10305669 | snp | A/T | 0.0227243 | 0.104143 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858613 | aaaaaaaaaaaaTCA[A/T]GAAGAGCAATCTGGA | 405 |
rs10305670 | snp | C/G | 0.00696856 | 0.058615 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858612 | aaaaaaaaaaaTCAA[C/G]AAGAGCAATCTGGAT | 405 |
rs10305671 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857880 | aatcagcacaatgcc[A/G]taacactaattagga | 405 |
rs10305672 | snp | C/T | 0.472335 | 0.114312 | intron-variant | ARNT | GRCh38.p7 | 1:150853154 | AGCTGAGATTACAGG[C/T]ACCCGCCACCATGCC | 405 |
rs10305673 | snp | A/G | 0.477004 | 0.104734 | intron-variant | ARNT | GRCh38.p7 | 1:150853035 | CCTCAGCCTTCCAAA[A/G]TGCTGGGATTACAGG | 405 |
rs10305674 | snp | G/T | 0.00356505 | 0.0420692 | intron-variant | ARNT | GRCh38.p7 | 1:150852195 | gtgagtgtgtgaggg[G/T]gttacacaaggaagt | 405 |
rs10305675 | snp | A/G | 0.131723 | 0.220251 | intron-variant | ARNT | GRCh38.p7 | 1:150847362 | ctcactgcaacctcc[A/G]cctcccaggttcaag | 405 |
rs10305676 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ARNT | GRCh38.p7 | 1:150846748 | aaaactgaaactcta[C/T]actcatcaaacacca | 405 |
rs10305677 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150846616 | ttttttaccagaatt[A/T]aaaaaaAACCCAAAA | 405 |
rs10305678 | snp | A/G | 0.00181167 | 0.0300425 | intron-variant, synonymous-codon | ARNT | GRCh38.p7 | 1:150842447 | TCTCTCTTTATCCGC[A/G]GAGCTCTGCTCATCA | 405 |
rs10305679 | snp | C/T | 0.123105 | 0.215401 | intron-variant | ARNT | GRCh38.p7 | 1:150842326 | GCCACAGATAAGGAA[C/T]AATACAAAGAGAAAG | 405 |
rs10305680 | snp | C/T | 0.124491 | 0.216211 | intron-variant | ARNT | GRCh38.p7 | 1:150842199 | AAAAAACTTAAAACT[C/T]ATAGCAATTTCTTAA | 405 |
rs10305681 | snp | A/G | 0.0129027 | 0.0792771 | intron-variant | ARNT | GRCh38.p7 | 1:150842054 | AATAAATATATCTGT[A/G]TTTGTGATTAGTTCC | 405 |
rs10305682 | snp | C/T | 0.123452 | 0.215605 | intron-variant | ARNT | GRCh38.p7 | 1:150838962 | GCAGAAAATGTTTAC[C/T]CCTTCTTTTTTTCAT | 405 |
rs10305683 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150838864 | GCATAAAGAGAGGAA[C/T]TGTATTTTTTAATTA | 405 |
rs10305684 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150838779 | AATGGCTAGACTTGA[A/G]TGAGGATGGTTAGGG | 405 |
rs10305685 | snp | A/G | 0.108048 | 0.20579 | intron-variant | ARNT | GRCh38.p7 | 1:150838529 | TATAGCTACAAAGTA[A/G]GTAGTTTTAAGTAGA | 405 |
rs10305686 | snp | A/C/G/T | 0.0142736 | 0.0832652 | intron-variant | ARNT | GRCh38.p7 | 1:150838426 | TCTCACAGCACAACA[A/C/G/T]ACCTGGTTTGCCCAC | 405 |
rs10305687 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150838330 | CATAGAACTAGTTCT[A/G]TAATAGAAGTGCTGT | 405 |
rs10305688 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ARNT | GRCh38.p7 | 1:150837731 | CCAAGTCTATAGCCC[G/T]AGACATGACTAACGT | 405 |
rs10305689 | snp | A/C/G/T | 0.00318978 | 0.0398085 | intron-variant | ARNT | GRCh38.p7 | 1:150837647 | AAAGTTCATCTTAAG[A/C/G/T]CCTCTTTATTAATAC | 405 |
rs10305690 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150837507 | AAAGGATAAGATGGA[C/T]GACATTGTCACATTC | 405 |
rs10305691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150837381 | GCTGTTCCTGGCAGA[A/G]CAAAAACCAAACCAA | 405 |
rs10305692 | in-del | -/ATT | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150837276 | AGTGAATATAACATT[-/ATT]CTTAGTATAAGCTTG | 405 |
rs10305693 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150836912 | aaacaaaaacaaaaa[A/G]aaaactagccaggtg | 405 |
rs10305694 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARNT | GRCh38.p7 | 1:150836773 | ATTACCGGCGGGAGC[C/T]GCTGTGCCTAGCCCA | 405 |
rs10305695 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | ARNT | GRCh38.p7 | 1:150836640 | ACAGCCACAGGTTTC[A/G]ACCCTAAATGTAGTT | 405 |
rs10305696 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150836132 | TATAGTCAGTTCTTT[C/T]TATCCATATGAGATT | 405 |
rs10305697 | in-del | -/TCTGTA | 0.476833 | 0.105105 | intron-variant | ARNT | GRCh38.p7 | 1:150835815 | TTGTTGTTGTTTGTA[-/TCTGTA]CTGTTGTTCTTTTTT | 405 |
rs10305698 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | ARNT | GRCh38.p7 | 1:150835563 | gctatgatgtgccac[A/G]gtactccagcctagg | 405 |
rs10305699 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | ARNT | GRCh38.p7 | 1:150834955 | CTCTGTATGTATGTC[A/T]GTATGTGTATACAGA | 405 |
rs10305700 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150834773 | AATTCATCTCCTGCT[C/T]GGTCAGTTCTGTTAT | 405 |
rs10305701 | snp | A/G | 0.00345422 | 0.0414147 | intron-variant | ARNT | GRCh38.p7 | 1:150834494 | GGTATAGGAAGGATC[A/G]AGAGCTGAGAGTTTT | 405 |
rs10305702 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150834258 | cagatggaaaaacag[A/T]tataaagaaatgaaC | 405 |
rs10305703 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150832163 | TGGCAATATTTTCCT[A/C/G]AACTTCTAAAACTTC | 405 |
rs10305704 | snp | G/T | 0.473003 | 0.113002 | intron-variant | ARNT | GRCh38.p7 | 1:150831953 | CATTGCCCTTTGAGT[G/T]TTACGGGTAGATTTT | 405 |
rs10305705 | snp | A/C/G/T | 0.00736485 | 0.0602344 | intron-variant | ARNT | GRCh38.p7 | 1:150831800 | CAAGGGGAAATATTT[A/C/G/T]CTATTTCACTTTCTT | 405 |
rs10305706 | snp | A/T | 0.108048 | 0.20579 | intron-variant | ARNT | GRCh38.p7 | 1:150831488 | GTTAATTTGAGAAAG[A/T]TTTCTAAAGTAGGAA | 405 |
rs10305707 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150830993 | atgtaaggaaagcat[C/T]cagcccagtgcctgg | 405 |
rs10305708 | snp | C/T | 0.00335007 | 0.0407899 | intron-variant | ARNT | GRCh38.p7 | 1:150830973 | ccagtgcctggcata[C/T]ggcaggtaacccaat | 405 |
rs10305709 | snp | A/T | 0.125528 | 0.21681 | intron-variant | ARNT | GRCh38.p7 | 1:150830938 | gtAATTAATGTAATT[A/T]AAAAAAATTTAACTG | 405 |
rs10305710 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | ARNT | GRCh38.p7 | 1:150830551 | CTGGAAAATACAAGT[A/G]CTACCCAGAGTACTC | 405 |
rs10305711 | snp | A/G | 0.476918 | 0.104919 | intron-variant | ARNT | GRCh38.p7 | 1:150830520 | TTTACTATAATTAAC[A/G]TGGGTAAAATGTAGG | 405 |
rs10305712 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARNT | GRCh38.p7 | 1:150830340 | ttttttgagagggag[C/T]ctcactctgtctgtc | 405 |
rs10305713 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | ARNT | GRCh38.p7 | 1:150830277 | ctcactgcatcctcc[A/G]cctcctgggttcaag | 405 |
rs10305714 | snp | C/T | 0.477004 | 0.104734 | intron-variant | ARNT | GRCh38.p7 | 1:150828179 | acactaaaagcatga[C/T]tcacagaagaaaaaa | 405 |
rs10305717 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150826281 | TAAGGTATTTAAACT[A/G]TTGCGCCAGGCATGG | 405 |
rs10305718 | snp | C/G/T | 0.111224 | 0.207945 | intron-variant | ARNT | GRCh38.p7 | 1:150826256 | GCATGGTGGCTCATG[C/G/T]GCCCAACCTCTGTAG | 405 |
rs10305719 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150826229 | GTAGATGCTGTGAAA[A/G]TAGATGTTTTCCTCG | 405 |
rs10305720 | snp | C/G | 0.480223 | 0.0974544 | intron-variant | ARNT | GRCh38.p7 | 1:150826101 | ACAGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 405 |
rs10305721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150823073 | aaaatttagccgggc[A/G]tggtggcatgtgcct | 405 |
rs10305722 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150822976 | tgagctgggatcatg[C/G]cactgcactccagcc | 405 |
rs10305723 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | ARNT | GRCh38.p7 | 1:150822952 | tccagcctgggctac[A/G]gagcgagactccatt | 405 |
rs10305724 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | ARNT | GRCh38.p7 | 1:150822889 | aaggacacccagctg[C/T]tgtccactactgatt | 405 |
rs10305725 | snp | A/C | 0.0162565 | 0.0888194 | intron-variant | ARNT | GRCh38.p7 | 1:150822854 | ctatctccaagtaga[A/C]agtgaactgaattga | 405 |
rs10305726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150822701 | acttgggttcagtca[A/G]tttgcttgaatggct | 405 |
rs10305728 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARNT | GRCh38.p7 | 1:150822541 | acacatggagatccc[A/G]ggagggtagcccacc | 405 |
rs10305729 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | ARNT | GRCh38.p7 | 1:150822425 | ggtacctaaggttaa[A/G]ttgattaccaatggc | 405 |
rs10305730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150822379 | gggctgggactttta[A/G]ccctaaccctcaacc | 405 |
rs10305731 | snp | C/T | 0.0111728 | 0.0739025 | intron-variant | ARNT | GRCh38.p7 | 1:150822259 | aaaagacacttatca[C/T]actgaagattccaaa | 405 |
rs10305734 | in-del | -/AAAC | 0.0572261 | 0.160288 | intron-variant | ARNT | GRCh38.p7 | 1:150818752 | tttgtttgtttgttt[-/AAAC]cattgagacagtgtc | 405 |
rs10305735 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150818620 | gggactacaggagcc[C/T]gccaccacgcctgct | 405 |
rs10305737 | snp | A/C/G/T | 0.00180094 | 0.0299538 | intron-variant | ARNT | GRCh38.p7 | 1:150818082 | GAGGGAGGAAGGGGG[A/C/G/T]AGAGAGAGAGAAAGA | 405 |
rs10305738 | snp | A/C/G/T | 0.00361392 | 0.0423581 | intron-variant | ARNT | GRCh38.p7 | 1:150818078 | TCTCTCTCTCTCCCC[A/C/G/T]CTTCCTCCCTCTCCA | 405 |
rs10305739 | snp | A/T | 0.110412 | 0.207401 | intron-variant | ARNT | GRCh38.p7 | 1:150817477 | TCtttttaaaaaaaa[A/T]tttttttttCTATTT | 405 |
rs10305740 | snp | C/T | 0.0146231 | 0.0842478 | intron-variant | ARNT | GRCh38.p7 | 1:150817440 | TGCTGCTGCCTATAT[C/T]TCAAAGGCCAGTTGA | 405 |
rs10305741 | snp | G/T | 0.0146197 | 0.0842385 | missense | ARNT | GRCh38.p7 | 1:150817388 | GTAGCTGGCCAGTCC[G/T]TCTCTTCCTGGTACC | 405 |
rs10305742 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150815004 | ATTCAGAAAGTGAAG[C/T]AAAATATAAAGAAAA | 405 |
rs10305743 | in-del | -/AG | 0.106987 | 0.205054 | intron-variant | ARNT | GRCh38.p7 | 1:150814832 | gtttttttgagacag[-/AG]tctcgctgttgccca | 405 |
rs10305744 | snp | C/T | 0.0115603 | 0.0751433 | intron-variant | ARNT | GRCh38.p7 | 1:150814828 | tttgagacagagtct[C/T]gctgttgcccaggct | 405 |
rs10305745 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | ARNT | GRCh38.p7 | 1:150813562 | ATTTAATAGTATGCA[C/T]ATTTAACCTAAATGA | 405 |
rs10305746 | snp | G/T | 0.00333889 | 0.0407222 | intron-variant | ARNT | GRCh38.p7 | 1:150812556 | AATAGAACATAATGA[G/T]TATAGCCATAATGGT | 405 |
rs10305747 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150812548 | GTAAATAGACCATTA[G/T]GGCTATAATCATTAT | 405 |
rs10305748 | snp | A/G/T | 0.033641 | 0.125257 | intron-variant | ARNT | GRCh38.p7 | 1:150812144 | GTAAGAGATCAAGGT[A/G/T]TGTGACCCAAACTTA | 405 |
rs10305749 | snp | A/C/G/T | 0.00212429 | 0.0325213 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150812015 | CTTATCCTCACCCCA[A/C/G/T]TAGTTCTATTCTGAA | 405 |
rs10305750 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811349 | ACCTGGAAGATTTAA[A/G]TCCTTAGGACTCTTT | 405 |
rs10305751 | snp | A/G | 0.089084 | 0.191327 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810982 | CTTCTTGGATTAGCC[A/G]TCCCAGTGAAAATCC | 405 |
rs10305752 | in-del | -/C | 0.0170251 | 0.090679 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810763 | ATGATAGATGGGGCC[-/C]TGGACACCCATCTCA | 405 |
rs10305753 | in-del | -/TAT | 0.0138799 | 0.0821421 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810722 | TGGTAATTAACAATA[-/TAT]GCCATATAAATGCGG | 405 |
rs10305754 | snp | A/C/G/T | 0.00703391 | 0.0588853 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810663 | aaaGCTGGTATCTAC[A/C/G/T]ACTGTTACCTGAGGA | 405 |
rs10305755 | snp | A/C/G/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810566 | CTCCTCAGTCCCCTA[A/C/G/T]GACTACATTTAATAT | 405 |
rs10531895 | in-del | -/T | 0.215144 | 0.247558 | intron-variant | ARNT | GRCh38.p7 | 1:150828351 | GTGGTTTTTTTTTTG[-/T]TTTTTTTTTTTTTTG | 405 |
rs10645938 | in-del | -/AAAC | | | intron-variant | ARNT | GRCh38.p7 | 1:150818761 | TCAATGAAACAAACA[-/AAAC]AACAAACAAATCCCT | 405 |
rs11204729 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809636 | ACACACACACACACA[A/C]AAAAAAAAAAAAAAA | 405 |
rs11204730 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150835178 | aaAAAATTTTAAAAA[A/G]AAAAAAACCAAGTAA | 405 |
rs11204731 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150843917 | AAAAAAGTTAAGCAT[C/G]TAAAATTCCTATTTC | 405 |
rs11204732 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | ARNT | GRCh38.p7 | 1:150848394 | TCAGGAGGCGGAGGA[C/T]GCAATGAGCAGAGAT | 405 |
rs11204733 | snp | C/T | 0.47666 | 0.105476 | intron-variant | ARNT | GRCh38.p7 | 1:150863190 | aacacggcaaaatcc[C/T]gtctctactaaaaat | 405 |
rs11204734 | snp | A/T | 0.490007 | 0.0699769 | intron-variant | ARNT | GRCh38.p7 | 1:150864773 | ATAATAAAAAATAAA[A/T]AAATAAATAAATAAA | 405 |
rs11204735 | snp | C/T | 0.44638 | 0.154709 | intron-variant | ARNT | GRCh38.p7 | 1:150869191 | GAAAGAAATATAGAA[C/T]GTTAggctgggcgcg | 405 |
rs11204736 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150869356 | GTGGTGGATGCCTGT[A/G]GTCCCAGCTACTCGC | 405 |
rs11204737 | snp | C/T | 0.445724 | 0.155538 | intron-variant | ARNT | GRCh38.p7 | 1:150875171 | TCAGGTTTGACATAA[C/T]GGCATTTTTCCTGTT | 405 |
rs11204738 | snp | C/T | 0 | 0 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876871 | CGCCAGCCAGTCCAG[C/T]GAAGGGAGGGCGAGG | 405 |
rs11403767 | in-del | -/A | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150873306 | CAAACAAAAAAAAAA[-/A]CAAAACAAAACTTGT | 405 |
rs11459475 | in-del | -/A/AA | 0.288127 | 0.247076 | intron-variant | ARNT | GRCh38.p7 | 1:150835138 | CAAAAAAAAAAAAAA[-/A/AA]GAATAAAAAGAAAAA | 405 |
rs11552229 | snp | A/G | 0.477345 | 0.103991 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811509 | CCTCTGGAAAGAAAC[A/G]TGTGAGTAAGTGAGA | 405 |
rs11582281 | snp | C/T | 0.476918 | 0.104919 | intron-variant | ARNT | GRCh38.p7 | 1:150854355 | ttgaactcaggagtt[C/T]aagaccagcctgggc | 405 |
rs11589458 | snp | A/G | 0.472241 | 0.114494 | intron-variant | ARNT | GRCh38.p7 | 1:150820140 | ttttcatgctacagc[A/G]gagttgagtaggtgg | 405 |
rs11800855 | snp | A/G | 0.498415 | 0.0281103 | intron-variant | ARNT | GRCh38.p7 | 1:150828519 | TACACCAACACCACA[A/G]TGTCTTGGTAATAGC | 405 |
rs11807967 | snp | A/C | 0.00518131 | 0.0506341 | intron-variant | ARNT | GRCh38.p7 | 1:150852395 | acccagccatcccag[A/C]tgagtccagttctca | 405 |
rs11809393 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | ARNT | GRCh38.p7 | 1:150873268 | cactccagcctgggc[A/G]acagagtgagactct | 405 |
rs12037369 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ARNT | GRCh38.p7 | 1:150869528 | ATGTTACAGAAAAGA[G/T]TTTAGGAAACTACTC | 405 |
rs12057757 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150872943 | ctccagcctcagtga[C/T]agagcaagaccctct | 405 |
rs12059006 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150873282 | cgacagagtgagact[C/G]tgtctcaaaacaaac | 405 |
rs12060615 | snp | C/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150874586 | cagctattcgggagg[C/T]tgatcgtgagaggat | 405 |
rs12077878 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARNT | GRCh38.p7 | 1:150847514 | TGGTAAGATAAACTA[C/T]GATAGTCTTTTTTTA | 405 |
rs12082834 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845784 | gcaggggcctataat[C/T]ccagctactcaggag | 405 |
rs12094510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819974 | GAAAGAAAACTCAAA[C/T]AGAAAAGTGCAAAAG | 405 |
rs12118433 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150822015 | ttactttttataata[A/G]atttgtatatgttgt | 405 |
rs12124621 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851855 | ccaagaatgatcaat[A/T]aaaaagaaaattaat | 405 |
rs12125114 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815378 | acggtgaaatgccgt[C/T]tctactaaaaataca | 405 |
rs12125116 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815380 | ggtgaaatgccgtct[C/T]tactaaaaatacaaa | 405 |
rs12125170 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815548 | aaagtgacagtctgt[C/T]tcaagaaaaaaaaaa | 405 |
rs12125296 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851457 | gagaaatcagattgt[C/T]gctgtgtctgtgtag | 405 |
rs12125322 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851496 | agacataggagactc[C/T]attttgttctgtact | 405 |
rs12125396 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851720 | gggacacaaacactg[C/T]ggaaggccgcagggt | 405 |
rs12127856 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150851358 | ccccgtctgggaggt[A/G]tacccaacagctcat | 405 |
rs12127980 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150851729 | acactgtggaaggcc[C/G]cagggtcctctgcct | 405 |
rs12130202 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150867372 | tcatttctataaatt[A/T]aaaaaaaaaaaaact | 405 |
rs12403459 | snp | A/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150833919 | gtaacagtgggaaat[A/T]catttctttttcttt | 405 |
rs12406660 | snp | C/T | 0.355096 | 0.226837 | intron-variant | ARNT | GRCh38.p7 | 1:150863963 | taggagatttcaaca[C/T]tgtgtgaatatcatt | 405 |
rs12409021 | snp | A/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150876233 | AAAGAGGACCACATC[A/T]CAGACCAGACGCCGA | 405 |
rs12569165 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821822 | cccagctaatttttg[A/T]attttcttttttttt | 405 |
rs12726070 | snp | A/G | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150861112 | atataaataaataaa[A/G]ggttggcaaggatgt | 405 |
rs12728254 | snp | A/T | 0.308166 | 0.243139 | intron-variant | ARNT | GRCh38.p7 | 1:150847004 | actacattttctgta[A/T]ccattcatctgtcag | 405 |
rs12746950 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861121 | aataaagggttggca[A/G]ggatgtggagaaatt | 405 |
rs12755750 | snp | A/G | 0.031825 | 0.122064 | intron-variant | ARNT | GRCh38.p7 | 1:150841202 | tgatctgcctgcctc[A/G]gcctcccaaagtgct | 405 |
rs12758227 | snp | A/C | 0.44651 | 0.154543 | intron-variant | ARNT | GRCh38.p7 | 1:150872107 | GACTATAGAAGTGCA[A/C]CACAGTGCCCGGAAA | 405 |
rs13374494 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845687 | ggcgggcggatcaca[A/T]ggtcaggagttcaag | 405 |
rs16827741 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | ARNT | GRCh38.p7 | 1:150824340 | GATACTCTGACCTAG[C/T]TTTACAAGTCTATAC | 405 |
rs17660092 | snp | C/T | 0.477004 | 0.104734 | intron-variant | ARNT | GRCh38.p7 | 1:150825272 | GAAGCTAACCACTTA[C/T]TTTGTAATACTACGT | 405 |
rs17855056 | snp | G/T | 0 | 0 | missense | ARNT | GRCh38.p7 | 1:150829171 | GTTGTGTCGGGAGAT[G/T]AACTCTGTTGGTTGA | 405 |
rs17855057 | snp | G/T | 0 | 0 | missense | ARNT | GRCh38.p7 | 1:150836381 | AACCATTCAGACTGT[G/T]GCTGGTTCAAAACAG | 405 |
rs17855058 | snp | G/T | | | synonymous-codon | ARNT | GRCh38.p7 | 1:150839573 | AGCCAGGGCACTACA[G/T]GTGGGTACCATATCT | 405 |
rs17855059 | snp | G/T | 0 | 0 | intron-variant, synonymous-codon | ARNT | GRCh38.p7 | 1:150842426 | ACTGTTCTCCTACCT[G/T]GCAAGTCTCTCTTTA | 405 |
rs28409962 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | ARNT | GRCh38.p7 | 1:150851185 | CCAGCCACCCCGTCC[A/G]GGAGAGAGGCGGGGG | 405 |
rs28733210 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | ARNT | GRCh38.p7 | 1:150848857 | GTAATAAAATACACT[C/T]ATATTACTTTCCCAA | 405 |
rs34083816 | in-del | -/A | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150831926 | AGTTACAGGAGTTTG[-/A]AAAAAAAAAAAAAAA | 405 |
rs34093716 | in-del | -/A | 0.499999 | 0.000798721 | intron-variant | ARNT | GRCh38.p7 | 1:150819227 | CTAGATGGCTACAAT[-/A]AAAAAAAAAAGGCAA | 405 |
rs34096034 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150817917 | TATTTCACCCTTTTT[-/T]ACCTGGGTGCCAGCT | 405 |
rs34119041 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858807 | TTTTTTTTTTTTTTA[A/G]AGATGGGGTCTTGAT | 405 |
rs34156683 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150841136 | TTTTTATTTTTAGTA[A/G]AGACGCGGTTTCACC | 405 |
rs34223160 | in-del | -/T | 0.499713 | 0.0119774 | intron-variant | ARNT | GRCh38.p7 | 1:150823553 | TTCAGAGACTTAAGC[-/T]TTTTTTTTTTTTTTT | 405 |
rs34393818 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150868629 | GGGCAGGCCGGGCGC[-/C]GGTGGCTCACGCCTG | 405 |
rs34415707 | in-del | -/C | | | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876606 | CGCCACCCCCCCCCC[-/C]AGTGGGAGGAGCCGC | 405 |
rs34485366 | snp | G/T | 0.277778 | 0.248452 | intron-variant | ARNT | GRCh38.p7 | 1:150859160 | TTATTTTATTTATTG[G/T]GATTGGAAAATACAG | 405 |
rs34564857 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150866225 | GACCTCAGGTGATCC[-/C]ACCTGCCTCAGCCTC | 405 |
rs34606655 | in-del | -/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840212 | ACCACTGCACTTCAG[-/G]CCTGGGTGGCAGAGC | 405 |
rs34608532 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150875202 | TATAGTTTTATTCTA[-/A]TCACTCAGCACTTCC | 405 |
rs34730160 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150841138 | TTTATTTTTAGTAGA[A/G]ACGCGGTTTCACCAA | 405 |
rs34874395 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150823883 | GAGTCTCGCTCTGTC[A/G]CCAGGCTAGAGTGCA | 405 |
rs35003478 | in-del | -/A/AA | 0.499954 | 0.00479211 | intron-variant | ARNT | GRCh38.p7 | 1:150815863 | CAAGACTCTGTCTCA[-/A/AA]AAAAAAAAAAAAAAA | 405 |
rs35009537 | in-del | -/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150854469 | GGGGGGCGGGAGGGG[-/G]CTGCAGGCCTTGAGC | 405 |
rs35215658 | in-del | -/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857961 | ACATATCAATAACTT[-/T]AGAAGACAGCTATTC | 405 |
rs35231979 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150844895 | CTCACTGCAACCTCC[-/C]ACCTCCCGGGCTCAT | 405 |
rs35348500 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150830783 | ACTGCATTTCTCCCC[-/C]TGTTTTTTGCATAGT | 405 |
rs35374672 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150843661 | CAAACTTCTTTTTTT[-/T]CAAAAAGTTGAGCAA | 405 |
rs35400828 | in-del | -/G | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810503 | AGACATAAGGAAGGG[-/G]AAACTCAGCAAATGG | 405 |
rs35468275 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877848 | TGCCTGATGTCAGGA[A/G]TTCGAGACCAGCCTG | 405 |
rs35589172 | in-del | -/A/AA | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150847446 | AAAAAAAAAAAAAAA[-/A/AA]GAAGGGGGAAAGGGA | 405 |
rs35619897 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150852974 | GTTCATAGTCCCAAA[-/A]CTAGGCAAAGAAGTA | 405 |
rs35665093 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARNT | GRCh38.p7 | 1:150836557 | AGTATTTCTATTCAC[C/T]GGAAGAAGTAAGACA | 405 |
rs35672926 | in-del | -/A/AA | 0.486 | 0.0824865 | intron-variant | ARNT | GRCh38.p7 | 1:150817813 | AAAAAAAAAAAAAAA[-/A/AA]TTAACCAACCGAACA | 405 |
rs35681870 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150823885 | TCTCGCTCTGTCACC[-/C]AGGCTAGAGTGCAGT | 405 |
rs35716807 | snp | A/G | 0.0100005 | 0.0700016 | intron-variant | ARNT | GRCh38.p7 | 1:150841498 | CTGCCAGTTTAACTC[A/G]AGCTTCTTACTAACC | 405 |
rs35756904 | snp | C/G | 0.00286074 | 0.0377119 | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876600 | CCTCCCACTGGGGGG[C/G]GGGGTGGCGCGGCGG | 405 |
rs35772624 | in-del | -/A | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150860018 | CTAAAAAAAAAAAAA[-/A]GGGTGCATTTTTCTC | 405 |
rs35831938 | snp | A/G | 0.123452 | 0.215605 | intron-variant | ARNT | GRCh38.p7 | 1:150826893 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAG | 405 |
rs35883279 | snp | C/T | 0.0098471 | 0.0694736 | intron-variant | ARNT | GRCh38.p7 | 1:150839301 | CCTTGGCTATAACAT[C/T]AATTAGCATTGGGAC | 405 |
rs35906729 | snp | C/G | 0.00994498 | 0.0698111 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810198 | CTGTTTTGTTTTCTT[C/G]TTGGCCATTTCTGTA | 405 |
rs35942078 | in-del | -/AT | | | intron-variant | ARNT | GRCh38.p7 | 1:150823385 | GGAACTCATAGAAAA[-/AT]TTTTCATTACAAAAA | 405 |
rs36063967 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150852349 | TTCAGTCTGGCCTCC[-/C]TTGAGGATAAAAAAA | 405 |
rs36073656 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857353 | AGAGTAAGCTACAAA[-/A]GCTAAACCCCTAAGG | 405 |
rs36093809 | in-del | -/A | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150862587 | TCCATTAAAAAAAAA[-/A]GTTCAGGGCCAAGTG | 405 |
rs36184461 | in-del | -/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150818641 | TGTAGTCCCAGATAC[-/C]TCAGGAGACAGATGG | 405 |
rs41315561 | snp | C/T | 3.29864e-05 | 0.00406105 | intron-variant | ARNT | GRCh38.p7 | 1:150834671 | AAGAGCAGTCTGGAG[C/T]GCATTTTTGTGTGTG | 405 |
rs55979601 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ARNT | GRCh38.p7 | 1:150861734 | GGTTTCGGTAATTTT[C/T]ACCCAAAAAAAAGGG | 405 |
rs56147665 | in-del | -/AA | | | intron-variant | ARNT | GRCh38.p7 | 1:150862735 | AAAAAAAAAAAAAAA[-/AA]GTTCATACTTTTAGT | 405 |
rs56658377 | snp | A/C | 0 | 0 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809638 | ACACACACACACAAA[A/C]AAAAAAAAAAAAAAA | 405 |
rs56944688 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854262 | AACTAAATTTTTTTA[A/T]TTTAAAAAATCTCAG | 405 |
rs57465904 | in-del | -/AA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809655 | AAAAAAAAAAAAAAA[-/AA]GTTGCTAATGAACCA | 405 |
rs57927826 | in-del | -/TT | | | intron-variant | ARNT | GRCh38.p7 | 1:150828351 | GTGGTTTTTTTTTTG[-/TT]TTTTTTTTTTTTTGC | 405 |
rs57974651 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARNT | GRCh38.p7 | 1:150824032 | ATTTTTAGTATAGAC[A/G]GGGTTTCACCATGTT | 405 |
rs58112984 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | ARNT | GRCh38.p7 | 1:150872822 | TTAAAATTAGCCAGC[C/T]ACGGTGGTGCACACC | 405 |
rs58175144 | in-del | -/A | 0.46855 | 0.121392 | intron-variant | ARNT | GRCh38.p7 | 1:150867222 | AACAACAAAAAAAAA[-/A]CAGATTACTCAAATA | 405 |
rs58304714 | snp | A/T | 0.475965 | 0.106957 | intron-variant | ARNT | GRCh38.p7 | 1:150859085 | ATAATATACTAATTT[A/T]AAAAAAATACATACA | 405 |
rs58452041 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878670 | TATAAGTCACCAAAA[A/G]GAAAAAAATCATCCA | 405 |
rs58630631 | in-del | -/CACA/CACACA | 0 | 0 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811478 | ACACACACACACACA[-/CACA/CACACA]TACACACACACTCTC | 405 |
rs58707975 | in-del | -/AA | | | intron-variant | ARNT | GRCh38.p7 | 1:150874043 | AAAAAAAAAAAAAAA[-/AA]TTAGTACTCCAGCAA | 405 |
rs58859566 | in-del | -/T | 0.123105 | 0.215401 | intron-variant | ARNT | GRCh38.p7 | 1:150833725 | AAAACGTACAGTATA[-/T]AATTTATAAACACTA | 405 |
rs60202743 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150821850 | TTTTTTTTTTTTTTT[-/T]CAGTAGAGACAGGGT | 405 |
rs60782711 | in-del | -/A | 0.499295 | 0.0187567 | intron-variant | ARNT | GRCh38.p7 | 1:150848456 | AGCGAGACTCCTCTC[-/A]AAAAAAAAAAAAGGA | 405 |
rs61142030 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150840852 | AAGCCCATTAAGTTT[A/C]TCAGTGTCCTCCATG | 405 |
rs61261522 | in-del | -/CAAA | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150818771 | AAACAAACAAACAAA[-/CAAA]TCCCTAAAAGCTAAT | 405 |
rs61471196 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854273 | TTTATTTTAAAAAAT[C/T]TCAGCCAGGCATGGT | 405 |
rs61817634 | snp | A/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810630 | ACTGGCCAAAGCCAA[A/T]TTAAAAAAAAAAAAA | 405 |
rs61817635 | snp | C/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811479 | ACACACACACACACA[C/T]ACACACACACTCTCT | 405 |
rs61817636 | snp | A/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811490 | CACATACACACACAC[A/T]CTCTCTCACTTACTC | 405 |
rs61817637 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815497 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 405 |
rs61817638 | snp | G/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150818913 | AACACAAAAATGAAG[G/T]CTGTTGTGTAATATA | 405 |
rs61817639 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828338 | TTCATTTTTGGGTGT[G/T]GTTTTTTTTTTGTTT | 405 |
rs61817640 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846605 | TAAGGGGTTAGTTTT[G/T]GGTTTTTTTTTAATT | 405 |
rs61817641 | snp | C/T | 0.290201 | 0.246747 | intron-variant | ARNT | GRCh38.p7 | 1:150850765 | GGGATGTGAGGAGCC[C/T]CTCTGCCCGGCTGCC | 405 |
rs61817642 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150856624 | AAAAATTAGCTGGGC[A/G]TGGTGGCGCACGCCT | 405 |
rs61817643 | snp | C/T | 0.00195074 | 0.0311699 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858502 | TTTTTAAAAAGACAG[C/T]CCTTGCTTATCATCA | 405 |
rs61817644 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859365 | TTTTTTTTTTTTTAA[G/T]ACAGGGTCTCACTTT | 405 |
rs61817645 | snp | A/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150874045 | AAAAAAAAAAAAAAT[A/T]AGTACTCCAGCAAAA | 405 |
rs66776757 | in-del | -/C | | | utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876596 | ACCGCCGCCGCGCCA[-/C]CCCCCCCCCAGTGGG | 405 |
rs67037872 | in-del | -/A | 0.44768 | 0.153045 | intron-variant | ARNT | GRCh38.p7 | 1:150862578 | AACACTTTTTCCATT[-/A]AAAAAAAAAGTTCAG | 405 |
rs67957908 | in-del | -/GTCA | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150866276 | GCGTGAGCCACCAAG[-/GTCA]GTCAGCCTGTTCCAA | 405 |
rs71086600 | in-del | -/C | 0 | 0 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811995 | GATTTTTTCTCCCCC[-/C]ACCCCTTATCCTCAC | 405 |
rs71580328 | in-del | -/CACACA | 0.48155 | 0.0942576 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811458 | AGAAGCATGTGTGCG[-/CACACA]CACACACACACACAC | 405 |
rs71580329 | in-del | -/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150813688 | CGCTCTTGTTGCCCA[-/G]GGCTGGAGTGCAAAG | 405 |
rs71580331 | multinucleotide-polymorphism | AA/TT | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150841222 | CCCAAAGTGCTAGGG[AA/TT]ACAAGCATGAGCCAC | 405 |
rs71645814 | in-del | -/A | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810633 | GGCCAAAGCCAATTT[-/A]AAAAAAAAAAAAAAA | 405 |
rs71703142 | in-del | -/AC | | | intron-variant | ARNT | GRCh38.p7 | 1:150866699 | TACACACATACATAT[-/AC]ACACACACACACGTA | 405 |
rs72334936 | in-del | -/TA | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811474 | ACACACACACACACA[-/TA]CACATACACACACAC | 405 |
rs72549317 | snp | A/C | 1.66103e-05 | 0.00288182 | intron-variant | ARNT | GRCh38.p7 | 1:150823364 | AAAAAGTTTTCATGC[A/C]ATCAGTGGAACTCAT | 405 |
rs72704634 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815733 | AGGCGCAGTGGCGGG[C/T]GCCTGTACAAGTCCC | 405 |
rs72704639 | snp | A/C | 0.497586 | 0.0346604 | intron-variant | ARNT | GRCh38.p7 | 1:150825859 | CTAAAAAAAAAAAAA[A/C]ACTATATAAAATGAA | 405 |
rs72704643 | snp | G/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150828350 | TGTGGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 405 |
rs72704652 | snp | A/G | 0.47709 | 0.104548 | intron-variant | ARNT | GRCh38.p7 | 1:150846994 | GTATGTACATACTAC[A/G]TTTTCTGTAACCATT | 405 |
rs72704654 | snp | A/G | 0.476833 | 0.105105 | intron-variant | ARNT | GRCh38.p7 | 1:150853934 | ACCTTGATATTATGG[A/G]CCTCTAGATGGGTCG | 405 |
rs72704656 | snp | A/G | 0.480223 | 0.0974544 | intron-variant | ARNT | GRCh38.p7 | 1:150855831 | TGCTTCCTGGGCCCA[A/G]GAAGTTGAGGCTACA | 405 |
rs72704658 | snp | C/T | 0.472335 | 0.114312 | intron-variant | ARNT | GRCh38.p7 | 1:150860534 | AAAAAAATTTTCGAA[C/T]CATATATGCAACACA | 405 |
rs72704663 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150875995 | GAGACGGGGACGGGG[A/G]TTGCGGGTGGGAGGT | 405 |
rs72992007 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARNT | GRCh38.p7 | 1:150825346 | ATCTTCCCAACAACC[A/G]TCTGAATTTAGGTAC | 405 |
rs72992015 | snp | C/T | 0.186105 | 0.241697 | intron-variant | ARNT | GRCh38.p7 | 1:150870220 | AATACTTACCTAATA[C/T]GATTGTTATAAAAAT | 405 |
rs73010816 | snp | C/T | 0.000856841 | 0.0206806 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813271 | CTGGCCCTGCCACTG[C/T]GGCCAGACACCCACA | 405 |
rs74127015 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811473 | GCACACACACACACA[C/T]ACACATACACACACA | 405 |
rs74127025 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ARNT | GRCh38.p7 | 1:150820149 | TACAGCAGAGTTGAG[C/T]AGGTGGAATAAAGAC | 405 |
rs74127036 | snp | A/G | 0.132409 | 0.220618 | intron-variant | ARNT | GRCh38.p7 | 1:150870115 | CAACAATAAAATTCT[A/G]TCTCTAACTTCTAGT | 405 |
rs74127058 | snp | C/T | 0.124491 | 0.216211 | intron-variant | ARNT | GRCh38.p7 | 1:150871229 | ATAGGTGTTGTCATA[C/T]TTCCAACCTGAAGAT | 405 |
rs74228522 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150835179 | AAAAATTTTAAAAAG[A/G]AAAAAACCAAGTAAT | 405 |
rs74666085 | snp | A/G | 0.190406 | 0.242793 | intron-variant | ARNT | GRCh38.p7 | 1:150831926 | AGTTACAGGAGTTTG[A/G]AAAAAAAAAAAAAAA | 405 |
rs74777809 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | ARNT | GRCh38.p7 | 1:150839158 | TTGGTTCCATGGACA[G/T]AGTCATTTCCTCTGT | 405 |
rs74866401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822771 | GTAAAACAACCTGGG[A/G]CTTGCAACTGGCATC | 405 |
rs75007096 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150824316 | ACTTCCCTTGGGAAA[C/T]CCATTAAAGATACTC | 405 |
rs75033132 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877238 | CTGCACGCCAGTCTG[A/G]GCAACAAGAGCGAAA | 405 |
rs75067056 | snp | A/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150863068 | AAAAAAAAAAAAAAA[A/G]AGATTACCATGGAGG | 405 |
rs75156458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870433 | ACCCACTGTAAGCAC[C/T]GCAATGCTCTGGTAA | 405 |
rs75232516 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150869285 | GATCGAGATCATCCT[G/T]GCTAACACAGTGAGA | 405 |
rs75271330 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | ARNT | GRCh38.p7 | 1:150833759 | ACCTACTGAAAGACA[C/T]AGGAAGTCTCAAATT | 405 |
rs75449777 | snp | C/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150843661 | CAAACTTCTTTTTTT[C/T]CAAAAAGTTGAGCAA | 405 |
rs75467822 | snp | A/C | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150825858 | TCTAAAAAAAAAAAA[A/C]AACTATATAAAATGA | 405 |
rs75532024 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150862811 | TAATCCTAGCACTTT[G/T]AGAGGCCGAGGCAGG | 405 |
rs75567657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150874667 | CACTCCAGACTGGGC[A/G]ACAGAGCAAGGAGCA | 405 |
rs75676931 | snp | G/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150865997 | GTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTT | 405 |
rs75699144 | in-del | -/TTT | | | intron-variant | ARNT | GRCh38.p7 | 1:150828363 | TTGTTTTTTTTTTTT[-/TTT]GCATACAGATATCCA | 405 |
rs75793523 | snp | A/C | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150863355 | AATGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAG | 405 |
rs76193027 | snp | A/C | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150847429 | AGACTCCGTCTCAAA[A/C]AAAAAAAAAAAAAAA | 405 |
rs76247248 | snp | A/C | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150840241 | GCAAGACTCCATTTC[A/C]AAAAAAAACAAAAAA | 405 |
rs76262208 | snp | C/T | 0.136847 | 0.222927 | intron-variant | ARNT | GRCh38.p7 | 1:150819413 | AAACATATATCCACA[C/T]AAAAACTAGTAAACA | 405 |
rs76265459 | snp | A/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150862715 | ATCCTGCCTCTGTAA[A/G]AAAAAAAAAAAAAAA | 405 |
rs76557133 | snp | A/C | | | intron-variant, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150861378 | CATGATCCAGCAATT[A/C]CACCTCTGGGTATAT | 405 |
rs76609938 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150821546 | TATAGTTAACTTTAC[A/G]CGGTTATGATTTAAA | 405 |
rs76764447 | in-del | -/TT | | | intron-variant | ARNT | GRCh38.p7 | 1:150841124 | CAGTTTTTTTTTTTT[-/TT]ATTTTTAGTAGAGAC | 405 |
rs76783068 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150859280 | TTCCTGCCCCCCGTA[C/T]CTCTCCTCTCTCCTT | 405 |
rs76784682 | snp | A/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150862716 | TCCTGCCTCTGTAAA[A/T]AAAAAAAAAAAAAAA | 405 |
rs76820210 | snp | C/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150844826 | GTCTTTTTTTTTTTT[C/T]TCTGACACAAAATCT | 405 |
rs76929704 | snp | A/C | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150863356 | ATGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAGA | 405 |
rs76943565 | snp | A/G | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150862711 | TGAGATCCTGCCTCT[A/G]TAAAAAAAAAAAAAA | 405 |
rs77063824 | snp | A/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150831942 | AAAAAAAAAAAAAAA[A/T]CTACCCGTAAAACTC | 405 |
rs77158876 | snp | C/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150869559 | CTTTTTTTTTTTTTT[C/T]CCTAGAGACAGGGGC | 405 |
rs77212361 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150820155 | AGAGTTGAGTAGGTG[C/G]AATAAAGACCACATG | 405 |
rs77401808 | snp | A/C | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150855562 | GCGAGACTCCGTCTC[A/C]AAAAAAAATAAATAA | 405 |
rs77495541 | snp | A/C | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150871907 | AGTAAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA | 405 |
rs77523974 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858633 | TTTTTTTTTTTTTTT[G/T]GAGACCAGGTCTCAC | 405 |
rs77658209 | snp | C/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150837472 | CCTGGGTCTTCATCA[C/G]TTTATTCAACCTCTC | 405 |
rs77736775 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150836712 | TCTCTATGTCACTAT[C/T]CACCTCTTCCTCTCT | 405 |
rs77768029 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811939 | AGGGAGAGGAACTTT[C/T]ATTCTGTTTACAGAA | 405 |
rs77799725 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150876289 | CGCACTGGCTGCCGC[A/T]CCAACGGAGGTCAGG | 405 |
rs77829846 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150824206 | GCCATTTAAAAAAAT[G/T]GCAAAAAATCACAAT | 405 |
rs77832162 | snp | A/C | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150837067 | CAAGAGACCCTGTCT[A/C]AAAAAAAAAAAGGCT | 405 |
rs77917729 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809611 | GAGACTCCATCTCTC[A/T]CACACACACACACAC | 405 |
rs77969618 | snp | A/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150862712 | GAGATCCTGCCTCTG[A/T]AAAAAAAAAAAAAAA | 405 |
rs78105642 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150837077 | TGTCTCAAAAAAAAA[-/A]AGGCTTACCATGAAC | 405 |
rs78182624 | snp | C/T | 0.120326 | 0.21374 | intron-variant | ARNT | GRCh38.p7 | 1:150873937 | AAATAAAAATAAGTA[C/T]TATTTTTAAAAAGGA | 405 |
rs78193809 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150876287 | CCCGCACTGGCTGCC[C/G]CTCCAACGGAGGTCA | 405 |
rs78420733 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858634 | TTTTTTTTTTTTTTT[G/T]AGACCAGGTCTCACT | 405 |
rs78509052 | snp | C/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150869561 | TTTTTTTTTTTTTTC[C/T]TAGAGACAGGGGCTC | 405 |
rs78632670 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150861197 | CAATAGAAAACAGTA[C/T]GGAGATGCCTCCAAA | 405 |
rs78731733 | snp | A/C | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150837068 | AAGAGACCCTGTCTC[A/C]AAAAAAAAAAGGCTT | 405 |
rs78816602 | snp | A/T | 0.124491 | 0.216211 | intron-variant | ARNT | GRCh38.p7 | 1:150870781 | CCCAAAGTGCTAGGA[A/T]TACAGGTATGAGCCA | 405 |
rs78875101 | snp | G/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150871317 | TTTTTTTTTTTTTTT[G/T]TTAGACGGAGTCTCA | 405 |
rs78882070 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150861398 | TCTGGGTATATACCT[C/G]AAAGAATTGAAAGCA | 405 |
rs78903791 | snp | A/T | 0.123105 | 0.215401 | intron-variant | ARNT | GRCh38.p7 | 1:150815764 | AGCTACTTGGAAGGC[A/T]GAGGCAGGAGAATGG | 405 |
rs79015984 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878278 | TGCTATTTCCATTTT[A/G]CAATTAAGGAAACAG | 405 |
rs79054358 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150843772 | ACAGGACTAACCAGG[A/C]ATGGTGGCTATGCAT | 405 |
rs79064270 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | ARNT | GRCh38.p7 | 1:150820686 | AACAAAACAAAACAA[A/T]AAAACCTTACTCTAC | 405 |
rs79135687 | snp | C/T | 0.00841118 | 0.0643027 | intron-variant | ARNT | GRCh38.p7 | 1:150852881 | TAAAATTTCTCAACA[C/T]AAGCTACCGGAACAC | 405 |
rs79157855 | snp | A/G | 1.67083e-05 | 0.00289031 | missense | ARNT | GRCh38.p7 | 1:150816803 | CTGAAATTCTCTGCC[A/G]GCCGGGGGGTAGGAG | 405 |
rs79253161 | snp | A/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150831940 | GAAAAAAAAAAAAAA[A/T]ATCTACCCGTAAAAC | 405 |
rs79346190 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858790 | CCACACCCAGTTAAT[A/T]TTTTTTTTTTTTTTT | 405 |
rs79376152 | snp | A/C | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150837069 | AGAGACCCTGTCTCA[A/C]AAAAAAAAAGGCTTA | 405 |
rs79422017 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150862030 | TTTACAATGGGTTTA[C/T]CAAGCCATAACCCCA | 405 |
rs79640722 | snp | C/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150844813 | CTGTTTCCTTACTGT[C/T]TTTTTTTTTTTTTTC | 405 |
rs79771636 | snp | G/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150860233 | CTTTTTTTTTTTTTT[G/T]GAGTTAGAGTCTCAC | 405 |
rs79789483 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ARNT | GRCh38.p7 | 1:150839083 | TAAAACTAGAAGCTG[C/T]TTCAGGGATAAGAAA | 405 |
rs80040388 | snp | A/C | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150830362 | CTCAAAAAAAAAACC[A/C]AAAAGCAAAACAAAA | 405 |
rs80040679 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | ARNT | GRCh38.p7 | 1:150874443 | CTGTATTCCCAACTT[G/T]GAGAGACTGAGGCAA | 405 |
rs80056153 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858632 | TTTTTTTTTTTTTTT[G/T]TGAGACCAGGTCTCA | 405 |
rs80233850 | snp | A/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150840269 | AAACAAAAAACAAGA[A/G]AAAAAAAAAGATAGT | 405 |
rs80289444 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150820312 | GAAAGAGTTGATACA[C/T]AGAATTGAAACTAAA | 405 |
rs111270359 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809440 | AACCCCATCTCTACT[-/A]AAAAAAAAAAACACA | 405 |
rs111482487 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | ARNT | GRCh38.p7 | 1:150874237 | TCTCATTTCCCAAAA[A/T]GCAACAGGCTACTGA | 405 |
rs111593726 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150863500 | AACCAGCCCATGGGG[A/T]AGTTTCAAAAAGGTA | 405 |
rs111694400 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851242 | ATCCGGGAGGGTGGT[G/T]GGGGCGCCTCCGCCC | 405 |
rs111746420 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ARNT | GRCh38.p7 | 1:150832256 | GCTGAAGGAACGACT[A/G]CAGTAAGACAGGTAA | 405 |
rs111852879 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150860506 | CAGGCATGAGCCACC[A/G]TGCCCAGCAGAAAAA | 405 |
rs111881095 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809890 | TTACTCAGAATGTGT[C/T]AGGATCAGGAGGACA | 405 |
rs111898376 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150865433 | AAAACCAACTCAATT[C/T]ACGCTATGGAATTCC | 405 |
rs112079016 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150868765 | ATTAGCCAGGCGCGG[C/T]GGCACGTGCCTGTAG | 405 |
rs112087145 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863639 | TTCGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 405 |
rs112119359 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150840948 | ATCTCTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 405 |
rs112213997 | snp | A/G | 0.5 | 0 | missense | ARNT | GRCh38.p7 | 1:150814146 | CAGTTGGGGCACCAG[A/G]GAGGGACATGGAGCT | 405 |
rs112263106 | snp | C/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150850526 | TAACCGTGAGTGATC[C/T]GCCAGCCTCGGCCTC | 405 |
rs112347959 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150864712 | GCACATGTATACATA[A/T]GTAACTAACCTGCAC | 405 |
rs112350097 | snp | C/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150865642 | TTTACTCTCTGGAGA[C/G]TATAAATCAAAGGTC | 405 |
rs112417874 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | ARNT | GRCh38.p7 | 1:150869750 | TGGAGACAAGGTCTC[A/C]CTATATTGCTCAGGC | 405 |
rs112503429 | snp | A/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150833870 | TGTAGTCAGACTACT[A/G]TGAATTAAAACAAAA | 405 |
rs112591413 | snp | C/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150873666 | GCTCACACCTATAAT[C/T]CCAGCAGTTTAGGAG | 405 |
rs112702990 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840107 | TTAGCAGGGCACAGT[A/G]GCATGCATCTGTAAT | 405 |
rs112734312 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | ARNT | GRCh38.p7 | 1:150851918 | CTGGGCATGGTGGCA[C/T]GCACCTGTAGTCCCG | 405 |
rs112738761 | snp | A/G | 0.4983 | 0.0291038 | intron-variant | ARNT | GRCh38.p7 | 1:150869260 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 405 |
rs112940234 | snp | A/C | 0.129664 | 0.219133 | intron-variant | ARNT | GRCh38.p7 | 1:150854360 | CTCAGGAGTTTAAGA[A/C]CAGCCTGGGCAACAC | 405 |
rs113102646 | snp | C/T | 0.125528 | 0.21681 | intron-variant | ARNT | GRCh38.p7 | 1:150848328 | GGGCATGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 405 |
rs113151660 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ARNT | GRCh38.p7 | 1:150866996 | GGATCACTTGAGGAC[A/G]GGAGTTCAAGACCAG | 405 |
rs113151947 | snp | A/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150873582 | TGAAAAACACTGCAG[A/G]GCCACCAGCACAATT | 405 |
rs113176319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150828999 | TTTTCTTAACTGAGG[C/T]TGATATGTTTTGGCT | 405 |
rs113265287 | snp | A/G | 0.110872 | 0.20771 | intron-variant | ARNT | GRCh38.p7 | 1:150855519 | GTGAGCCAAGATCGC[A/G]TCACCGCACTCCAGC | 405 |
rs113429332 | in-del | -/A | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150842189 | CATAAAGAGAAAAAG[-/A]AAAAAAAACTTAAAA | 405 |
rs113432973 | snp | C/T | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150850014 | CCAAGACTGCAGCAC[C/T]GCACTCCAGCCTGGG | 405 |
rs113435462 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810340 | TCACATTTAAAAAGT[C/T]GATTATTAAAAAACA | 405 |
rs113701927 | snp | C/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150876119 | TCAACTAAAGAGCAG[C/T]GTGGTCCAGGGTTTA | 405 |
rs113737018 | snp | A/G | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150823155 | CTGTTGTGAGAACAG[A/G]GGAAAAACAGTTTTT | 405 |
rs113785399 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150840956 | TCTTCTTTTTTTTTT[G/T]TTTTTTTTTTGAGAT | 405 |
rs113838796 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150868763 | AAATTAGCCAGGCGC[A/G]GTGGCACGTGCCTGT | 405 |
rs113889494 | snp | A/T | 0.5 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150838080 | CCAGATCTAATACAT[A/T]TTTTATGTCTCCCCA | 405 |
rs113891064 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | ARNT | GRCh38.p7 | 1:150832173 | AAGTTTAGGAAAATA[C/T]TGCCAGAAAAAAAGT | 405 |
rs113986128 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858617 | GATTGCTCTTCTTGA[-/T]TTTTTTTTTTTTTTT | 405 |
rs114037732 | snp | A/T | 0.00938946 | 0.0678717 | missense | ARNT | GRCh38.p7 | 1:150826556 | ACCTGTTGGAAGCTG[A/T]CTCTTAGAAGCTGCT | 405 |
rs114138473 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ARNT | GRCh38.p7 | 1:150845163 | ATGGTGGCTATGCAT[A/G]TAATCCCAATATTTG | 405 |
rs114171189 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | ARNT | GRCh38.p7 | 1:150875306 | CGTGACAAATTAACC[A/G]TTTCTTAAAATAGCT | 405 |
rs114389253 | snp | C/T | 0.000415244 | 0.0144031 | missense | ARNT | GRCh38.p7 | 1:150816399 | CAGGAGGGGCTAGGC[C/T]ACTATTCCTAGGAGT | 405 |
rs114550273 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | ARNT | GRCh38.p7 | 1:150870764 | TCCACCTACATCAGC[C/T]TCCCAAAGTGCTAGG | 405 |
rs114641696 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150833108 | CAAAGCACAATGTAG[C/T]CATGTAATCATCCAA | 405 |
rs114845445 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ARNT | GRCh38.p7 | 1:150849692 | CGCTTGAGCCCTGGA[A/G]TTCGAGGCTGTAGTG | 405 |
rs114890674 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150855906 | CAAGACTCTGTCTCC[A/G]AAATGTGTGTGTGTG | 405 |
rs114897471 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARNT | GRCh38.p7 | 1:150820840 | AGAAATCCCAACATT[A/G]GAAAATGCCTATGTG | 405 |
rs115050464 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150843589 | TGAGTGATATTCAGC[A/C]GTTTAGAGTTTTACA | 405 |
rs115080725 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150815190 | ATAAATATATAGTAA[C/T]ATTAAAGAATCTTTC | 405 |
rs115308185 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | ARNT | GRCh38.p7 | 1:150849603 | CCAGCCTGGGCAACA[A/T]CATTTTAAAATTAGC | 405 |
rs115360610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854909 | GGGAAGGAGGGAGGG[A/T]AAGGTAATTGCTAAG | 405 |
rs115468728 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150821445 | TGCTCATGAAGAGAT[A/G]ATTAGCATCACACAG | 405 |
rs115472527 | snp | A/C/G/T | 0.000692354 | 0.0185936 | missense | ARNT | GRCh38.p7 | 1:150817084 | GAAAGAAACATACCC[A/C/G/T]CATTGATGTTGTGAT | 405 |
rs115569224 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810690 | AGGAAGGTAAAGGGT[A/G]AGGGTAGTAACCTGT | 405 |
rs115636467 | snp | C/T | 6.59022e-05 | 0.00573993 | synonymous-codon | ARNT | GRCh38.p7 | 1:150839459 | ATCAGTGAGGAAAGA[C/T]GGCTTATAGGAGCCA | 405 |
rs115825799 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150815242 | GCGTTATATTATATA[A/T]ATGAATATTATAAAA | 405 |
rs115950027 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150842061 | ATCACAAATACAGAT[A/G]TATTTATTGGTTTTC | 405 |
rs116075053 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857225 | CATATTTGTCGCTTA[C/T]AACTACATAGCATTC | 405 |
rs116079458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150843730 | ATAAGCCACCACTCC[C/T]GGCCTCTTACTGTCA | 405 |
rs116191890 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | ARNT | GRCh38.p7 | 1:150824208 | CATTTAAAAAAATGG[C/T]AAAAAATCACAATTT | 405 |
rs116320605 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | ARNT | GRCh38.p7 | 1:150822029 | AGATTTGTATATGTT[A/G]TATGGTAGTAAATGA | 405 |
rs116545757 | snp | C/T | 0.000197977 | 0.00994733 | synonymous-codon | ARNT | GRCh38.p7 | 1:150839597 | CATATCTGACAGTTC[C/T]GTGATGTAGGCTGTC | 405 |
rs116774603 | snp | A/G | 3.29484e-05 | 0.00405871 | missense | ARNT | GRCh38.p7 | 1:150839482 | AGGAGCCATCAGTGG[A/G]TGTGTTGCCAGTTCC | 405 |
rs116880150 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150838970 | TGTTTACGCCTTCTT[G/T]TTTTCATAGTGATCA | 405 |
rs117011333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150827903 | TGATTTTAATTTGCA[C/T]TTTCCTAATGGTAAA | 405 |
rs117582234 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150854387 | ACACGGTGAAATCCC[A/G]TCTCTACAAAACATA | 405 |
rs137869225 | snp | A/G | 0.000153988 | 0.00877328 | missense | ARNT | GRCh38.p7 | 1:150834638 | TTAGATCCAGGATAC[A/G]CCCTGAAGGAAGATG | 405 |
rs137909458 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150846363 | GTTATATCTATTTCA[C/T]TCTGAAAAGTAAACT | 405 |
rs137977500 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150850773 | AGGAGCCCCTCTGCC[C/T]GGCTGCCCAGTCTGG | 405 |
rs138036180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838835 | TATGTCTATCTAGTC[C/G]CACATAAAATTACTA | 405 |
rs138052998 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARNT | GRCh38.p7 | 1:150850304 | GTCTCCCTCTCCCTC[C/T]CTTTCCACGGTCTCC | 405 |
rs138114365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150843294 | AATGATGGGTGGCAA[C/T]TGAGGAAATAGCAAG | 405 |
rs138256279 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150874309 | CAAGAGCAAAGGGAG[A/G]AAAGAAAAAAGAAAA | 405 |
rs138276435 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809251 | TAGACTCAGTTTCTA[A/G]CTGGATTCCATGCAT | 405 |
rs138307554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816540 | ATTTGATAACAATTT[A/G]GAAAAGACAAGAAAG | 405 |
rs138385917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861972 | TCTAGGCTAAGAATA[A/G]GTTAAGTGTATTAAA | 405 |
rs138437787 | snp | A/G | 0.124837 | 0.216412 | intron-variant | ARNT | GRCh38.p7 | 1:150824063 | GGCCAGGATGGTCTC[A/G]ATTTCCCGACCTCGG | 405 |
rs138499678 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150862099 | TCCACGTAACAATAT[A/G]TTGCTATGGCAATAA | 405 |
rs138598239 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | ARNT | GRCh38.p7 | 1:150849070 | TAGCCGGGCATGGTA[G/T]TGCATGCCTGTAATC | 405 |
rs138700307 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150828879 | ATACATATTTGTACC[C/T]GCTGCTCCCACCTGG | 405 |
rs138780302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150833771 | ACATAGGAAGTCTCA[A/G]ATTTCTAACCAAAAA | 405 |
rs138932526 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | ARNT | GRCh38.p7 | 1:150817152 | TAAACCATCTGACTT[C/T]TCAAGGGGCTTGCTG | 405 |
rs138968821 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | ARNT | GRCh38.p7 | 1:150868579 | GGAGGCCAACAGCAG[A/G]AGGATCACTCGAGGA | 405 |
rs138981555 | in-del | -/A | 0.487871 | 0.076925 | intron-variant | ARNT | GRCh38.p7 | 1:150825846 | AGCTAGACTCCTTCT[-/A]AAAAAAAAAAAAAAC | 405 |
rs139158737 | snp | C/T | 1.64743e-05 | 0.00287 | missense | ARNT | GRCh38.p7 | 1:150839473 | ACGGCTTATAGGAGC[C/T]ATCAGTGGATGTGTT | 405 |
rs139273417 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150834986 | TAAATGTCATTGGTT[C/G]AAAAACAAGTACTTT | 405 |
rs139425695 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | ARNT | GRCh38.p7 | 1:150840076 | TGAAATCCTGTCTCT[A/G]CTAAAAATACAAAAA | 405 |
rs139536635 | in-del | -/A | 0.477004 | 0.104734 | intron-variant | ARNT | GRCh38.p7 | 1:150859084 | ATAATATACTAATTT[-/A]TAAAAAAATACATAC | 405 |
rs139539417 | snp | A/C | 0.00010132 | 0.00711685 | intron-variant | ARNT | GRCh38.p7 | 1:150839679 | AAGAAAGAGAAGCCC[A/C]ATCCAGGTGGTCACA | 405 |
rs139619420 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150870564 | CCAGACAGGAATGCA[A/G]TGGCACAATCATGGC | 405 |
rs139795568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865691 | GACGTAAAGGTGAAA[C/G]TGAGGGACCCGTACT | 405 |
rs139885151 | in-del | -/A | 0.306779 | 0.255436 | intron-variant | ARNT | GRCh38.p7 | 1:150861329 | ATCGCAAAAAAAAAA[-/A]TTAAATTAAAAATAG | 405 |
rs139899795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150819769 | CAGAATTTCAGAGCC[A/G]GGGGAAAGAACAGGG | 405 |
rs140023630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847021 | CATTCATCTGTCAGT[G/T]GACATTTCGGTTACT | 405 |
rs140096661 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150854328 | TTTGGGAGGCCAAGG[C/T]GAGCAGACTACTTGA | 405 |
rs140227995 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ARNT | GRCh38.p7 | 1:150837362 | TAAACTACTGTTTTC[C/T]TGTTTGGTTTGGTTT | 405 |
rs140287362 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150821362 | GTATTGCACTCAACA[C/T]GATGAAAAATATGCA | 405 |
rs140420727 | snp | C/G/T | 0.000148257 | 0.00860851 | missense | ARNT | GRCh38.p7 | 1:150816272 | ACCTGGGCAGAAAAG[C/G/T]CTGAGCGGGTAGTAG | 405 |
rs140463081 | in-del | -/CA | | | intron-variant | ARNT | GRCh38.p7 | 1:150875512 | CGCAACACACACACA[-/CA]TATCTCAAGGCCCTT | 405 |
rs140511543 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ARNT | GRCh38.p7 | 1:150841841 | GACAGATTTCTGACA[C/T]GTAAGTACAGAAACC | 405 |
rs140525728 | snp | C/T | 9.88403e-05 | 0.00702925 | missense | ARNT | GRCh38.p7 | 1:150814134 | CACCAGGCGATGCAG[C/T]TGGGGCACCAGGGAG | 405 |
rs140594843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873808 | GTCTGTAGACCCAGA[C/T]ACTCAGGAGGCTGAG | 405 |
rs140735983 | snp | C/T | | | missense | ARNT | GRCh38.p7 | 1:150834629 | TTCCAGTCTTTAGAT[C/T]CAGGATACGCCCTGA | 405 |
rs140757868 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150872806 | TGTCTCTAAAAAAAA[C/T]TTAAAATTAGCCAGC | 405 |
rs140941896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812800 | TTAGCACCATAGGAA[G/T]ATGCCAAAGAAAGTT | 405 |
rs141021749 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150837763 | TTTTCCTGAGCTTTC[A/C]GCAGACTTGAATTTC | 405 |
rs141051493 | snp | C/T | 1.66944e-05 | 0.0028891 | missense | ARNT | GRCh38.p7 | 1:150846289 | CTCCTTATCGTTAGA[C/T]ATCTGATCATCATCA | 405 |
rs141091665 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ARNT | GRCh38.p7 | 1:150815322 | GGGAGGCCGAGGAGG[A/G]CGGATCACGAGGTCA | 405 |
rs141173666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150842704 | AAAGCCATCTGTTAG[A/G]ATAAAGAAAAAGTAA | 405 |
rs141293451 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150849617 | ATCATTTTAAAATTA[A/G]CCAGGTATTATGGCT | 405 |
rs141297483 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARNT | GRCh38.p7 | 1:150848077 | TGAGGAGATAAGTGT[A/G]TGTATGCTCACACAT | 405 |
rs141351742 | snp | A/G | 0.000445688 | 0.0149213 | missense | ARNT | GRCh38.p7 | 1:150831863 | GGGGAACCTCACTTC[A/G]TGGTGGTCCACTGCA | 405 |
rs141388962 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | ARNT | GRCh38.p7 | 1:150833578 | CAAACCTTTAATATC[C/G]TACCCATAATTTCTA | 405 |
rs141428110 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857473 | AAGCTACTGAACATA[C/T]AACAAGTCTTAATAT | 405 |
rs141477218 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150863334 | GCACTCCAGCCTGGG[A/C]AACAGAATGAGACTC | 405 |
rs141736918 | snp | C/T | 0.00568792 | 0.0530246 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858450 | CAGTGATGGTACATC[C/T]GATGTCATTTCTGTC | 405 |
rs141831352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150834257 | AGTTCATTTCTTTAT[A/G]TCTGTTTTTCCATCT | 405 |
rs141872596 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150838728 | GTTATTTTAATAACC[A/G]AAACAGAACATGGCT | 405 |
rs141880487 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150869274 | CAAGGTCAGGAGATC[A/C/G]AGGCCATCCTGGCTA | 405 |
rs142085436 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150861428 | CGTGGGTATACAAAT[A/G]TTTCTTTGAGACCCT | 405 |
rs142087886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836660 | TAAATGTAGTTCATC[A/G]ATAAGAAAGTTTTTT | 405 |
rs142125101 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ARNT | GRCh38.p7 | 1:150866967 | TCCCAGCACTGTGGG[A/T]GGCCAAGGCAGGTGG | 405 |
rs142445432 | in-del | -/AAAACAAAAC | 0.354665 | 0.227036 | intron-variant | ARNT | GRCh38.p7 | 1:150820659 | GAGACCCTGTCTGAA[-/AAAACAAAAC]AAAACAAAACAAAAC | 405 |
rs142549978 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150871156 | GTGCAGCCTGGCATA[C/T]AGAAGGAACTTAATT | 405 |
rs142550962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150829032 | CTTAGGAACTACATG[A/G]TTACATAATGTCAAC | 405 |
rs142676925 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | ARNT | GRCh38.p7 | 1:150817766 | GTGAGCCTAGATCGT[C/G]CCATTGTATTCCATC | 405 |
rs143047060 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | ARNT | GRCh38.p7 | 1:150862131 | TACACACGTAGATCA[C/T]TCTTTTTAACAGTTA | 405 |
rs143051758 | in-del | -/CAAA | | | intron-variant | ARNT | GRCh38.p7 | 1:150818760 | CTCAATGAAACAAAC[-/CAAA]AAACAAACAAATCCC | 405 |
rs143086843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150868149 | GAAGGAAACTGCTTG[A/G]TTTACTATTTAGTTC | 405 |
rs143089976 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810365 | AAAACAAGGGTTCCA[C/T]TGGAAACTCAACTTT | 405 |
rs143136687 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150815944 | AATTTTCTCCTTTGC[C/T]CCTGCCTTATGGAGT | 405 |
rs143151470 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | ARNT | GRCh38.p7 | 1:150845106 | TATGCCACCACTCCC[C/G]GCCTCTTACTGTCAT | 405 |
rs143239941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150812895 | ACAGGGACAGGATCA[A/G]GCTAGTTGCTCAGCC | 405 |
rs143275383 | snp | A/C | 0.000576412 | 0.0169668 | missense | ARNT | GRCh38.p7 | 1:150832337 | TTAGGATCTCACCTG[A/C]ATCTGTTCCTCACAA | 405 |
rs143427149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826840 | TAAATAGAGACAGGG[A/T]TTCACCATGTTGGTC | 405 |
rs143466861 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150846932 | GATTCATCCATCTTG[A/C]AGCATATGACAGGTT | 405 |
rs143491065 | snp | A/G | 5.46015e-05 | 0.00522473 | missense, intron-variant | ARNT | GRCh38.p7 | 1:150818011 | TGGAGAGTGTAGGCC[A/G]TGGTTCTTGGCTAGA | 405 |
rs143635573 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARNT | GRCh38.p7 | 1:150848092 | GTGTATGCTCACACA[C/T]ACACATTTATATACA | 405 |
rs143641553 | snp | A/G | 3.32729e-05 | 0.00407864 | intron-variant, missense | ARNT | GRCh38.p7 | 1:150842445 | AGTCTCTCTTTATCC[A/G]CAGAGCTCTGCTCAT | 405 |
rs143675059 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854440 | GCGCATGTGTAGTCC[C/T]AGCTACTTGGGTTGG | 405 |
rs143880940 | in-del | -/A | 0.237882 | 0.249706 | intron-variant | ARNT | GRCh38.p7 | 1:150863051 | GCAAGATTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 405 |
rs143887202 | snp | C/T | 0.476918 | 0.104919 | intron-variant | ARNT | GRCh38.p7 | 1:150850978 | GCCCGGCAGCCGCCC[C/T]GTCTGAGAATTGAGG | 405 |
rs143921987 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150835740 | GCTCAAGAATAGATA[C/T]GACTTGTTTCCTCTA | 405 |
rs144099505 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825562 | TCATCCATAAAAGAA[C/T]AGTCTAGGCTGGGCG | 405 |
rs144260120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150842316 | GTCCTCTCTTGCCAC[A/G]GATAAGGAAAAATAC | 405 |
rs144302610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847821 | AGACTCATTAAGTCT[A/C]AAGAGACCTCTTAGA | 405 |
rs144335476 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809397 | CTAAGGTCAGGAGTT[C/T]GAGACTAGCCTGGCC | 405 |
rs144363361 | in-del | -/TTTC | 0.0107246 | 0.0724382 | intron-variant | ARNT | GRCh38.p7 | 1:150824449 | GAACATCTGTTTTCT[-/TTTC]TTTTTCTTTTTTTTT | 405 |
rs144534029 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811787 | GTTTTAACTTCACCC[A/G]GCCTCAAATTTTCAG | 405 |
rs144606334 | snp | A/G | 8.25335e-05 | 0.00642339 | missense | ARNT | GRCh38.p7 | 1:150829917 | GCCTGCAATCTGCCA[A/G]TGGCCACTAGGCAAA | 405 |
rs144780356 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150869252 | GGAGGCTGAGGTGGG[A/C/G]GGATCACAAGGTCAG | 405 |
rs144995616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812757 | TACTGTGACTTGGGT[A/G]TATGGAGCTATTTGA | 405 |
rs145021250 | in-del | -/TTAA | 0.0475351 | 0.146656 | intron-variant | ARNT | GRCh38.p7 | 1:150870315 | CATGATGTCAATGGC[-/TTAA]TTAGTTTTATCCCTT | 405 |
rs145024351 | in-del | -/A | 0.131723 | 0.220251 | intron-variant | ARNT | GRCh38.p7 | 1:150840257 | AAAAAAACAAAAAAC[-/A]AAAAAACAAGAGAAA | 405 |
rs145164839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150872825 | AAATTAGCCAGCCAC[A/G]GTGGTGCACACCTGT | 405 |
rs145179927 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150865603 | CCAAGGCAACTACCC[C/G]TCTCCATTCTGTCAA | 405 |
rs145281849 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150866139 | AGGCACACACCACCA[C/T]GTCCAACTAATCTTT | 405 |
rs145300760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869907 | ACTTGGTTCTCCAAC[A/C]AAGCAATGCCTTGCC | 405 |
rs145545051 | snp | A/G | 1.6495e-05 | 0.0028718 | missense | ARNT | GRCh38.p7 | 1:150823204 | ATCATCTGTACCAAC[A/G]CCAATGTGAA | 405 |
rs145566708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150843047 | ACACAATGACAAAAT[A/G]ACCAACCAGATTTCA | 405 |
rs145655563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838269 | CCAAAATCCACAACA[C/T]TACTCCCCAACTCAT | 405 |
rs145679570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150840384 | CTATTTAAAGGCCAG[A/G]AAATAAAAGGACCAA | 405 |
rs145720857 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | ARNT | GRCh38.p7 | 1:150854515 | TGCAGTGAGCTGAGA[C/T]TGGGCCACTGCACTC | 405 |
rs145785563 | snp | C/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 1:150837885 | ACCTGCCGTGCTCTT[C/G]CAATATTCTTAACAG | 405 |
rs145809333 | snp | A/G | 2.25675e-05 | 0.00335905 | synonymous-codon, missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858417 | AGGTCCAGAGTTTCC[A/G]GAGGCAATGGCTGGA | 405 |
rs145821643 | snp | A/G | 6.61179e-05 | 0.00574931 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836404 | CAAAACAGGAGTCAC[A/G]GAGTCAGACACATAC | 405 |
rs145897011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150815228 | AGTGTATTTATTGTG[C/T]GTTATATTATATATA | 405 |
rs145902781 | in-del | -/AAG | 0.0486741 | 0.148216 | intron-variant | ARNT | GRCh38.p7 | 1:150860969 | ACAAGCATTTCTACA[-/AAG]AAGATATACTAATGG | 405 |
rs146030272 | snp | A/G | 2.64344e-05 | 0.00363545 | missense, utr-variant-5-prime, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858457 | GGTACATCTGATGTC[A/G]TTTCTGTCAGGAAAA | 405 |
rs146121110 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150853608 | TCTAATAAACATGTA[A/C]TATATACTTCATTCA | 405 |
rs146132507 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150862861 | TTCGAGACCAGCCTG[A/G]CCAATATGGTGAAAC | 405 |
rs146538917 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon | ARNT | GRCh38.p7 | 1:150831864 | GCAGTGGACCACCAC[A/G]AAGTGAGGTTCCCCA | 405 |
rs146550901 | snp | C/G | 0.00146143 | 0.0269922 | intron-variant | ARNT | GRCh38.p7 | 1:150842398 | CATCATCTGCTTCAT[C/G]ATGCTAAAAGACACT | 405 |
rs146564009 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150847884 | TGATGGCCAAGTCAC[A/G]GTTGTTGTTTTCAAG | 405 |
rs146681310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150820730 | CCCAAATCCTATAAG[C/T]TGGAAAATGAAGAAC | 405 |
rs146813760 | snp | C/T | 3.35982e-05 | 0.00409853 | missense | ARNT | GRCh38.p7 | 1:150846272 | TATTACCTGGCAAAC[C/T]GCTCCTTATCGTTAG | 405 |
rs146992650 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857730 | CCATACACAGAAAAA[C/T]ATAGTATCAAATTTG | 405 |
rs147098894 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150832122 | GTAAAATAGCATAGC[A/G]ACTTCCTTAAACAGG | 405 |
rs147137608 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150846981 | ATAATATTCCCTTGT[A/G]TGTACATACTACATT | 405 |
rs147170059 | snp | A/G | 3.29821e-05 | 0.00406078 | synonymous-codon | ARNT | GRCh38.p7 | 1:150829135 | ACAGCGGTGATCCAC[A/G]AAAGTGAAGATACCC | 405 |
rs147260436 | snp | C/T | 0.000116421 | 0.0076287 | intron-variant | ARNT | GRCh38.p7 | 1:150876510 | CCTTCGGCCCCTCCC[C/T]TTTAGAGGCGCCCCA | 405 |
rs147313091 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150840740 | TCTCACCCAGGTAAA[C/G/T]AGACCACAGCTCCAA | 405 |
rs147359820 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | ARNT | GRCh38.p7 | 1:150840013 | TGGGAGATGGAGGCA[A/G]GTGGATTACTTGAGG | 405 |
rs147369765 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | ARNT | GRCh38.p7 | 1:150845850 | AAGGTTGCAGTGAGC[C/T]GAGATGGCGCCATTG | 405 |
rs147463981 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810816 | CTAAAGCAAAACCCA[A/G]TCTCAAGATTGGAGG | 405 |
rs147474918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816197 | CACTGATTTTACATA[C/T]GGAAAAAAGCCCAAA | 405 |
rs147618384 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150866926 | TTATTCAAATAGAGG[C/T]TGGGCGCAATGGCTC | 405 |
rs147769146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150836849 | AGTTCAAGACCAGCC[C/T]AGGCAATGGGGCGAA | 405 |
rs147781848 | in-del | -/CTCACA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809609 | CGAGACTCCATCTCT[-/CTCACA]CACACACACACACAC | 405 |
rs147945150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830422 | GCATAAAGCAATAGA[A/G]AATGATAAATAAGAA | 405 |
rs147957446 | snp | A/C | 3.30573e-05 | 0.00406541 | missense | ARNT | GRCh38.p7 | 1:150852798 | TCTCCATCATCATCA[A/C]AATCCAGCCTGAGGA | 405 |
rs148185415 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ARNT | GRCh38.p7 | 1:150851659 | AGATGCTTGAAGGCA[A/G]CATGCGCATTAAGAG | 405 |
rs148240844 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150845625 | AAAAATAAAATAGGC[C/T]GGGTGCGGTGGCTCA | 405 |
rs148301196 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150832737 | GCATGAAAATAGCCA[G/T]AGATAATATGTAAAA | 405 |
rs148355447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150822938 | TTTTCTTTTTTTGAA[A/G]TGGAGTCTCGCTCTG | 405 |
rs148499311 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | ARNT | GRCh38.p7 | 1:150854781 | AGAATTGCCTGAACC[C/T]GGGAGGCAGAGGTTG | 405 |
rs148550499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150847563 | ACGAACCTCTCTTTG[A/G]ATCTGCATGTAGTTG | 405 |
rs148700286 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878664 | TATATTTATAAGTCA[C/T]CAAAAAGAAAAAAAT | 405 |
rs148754144 | snp | C/G | 0.0138799 | 0.0821421 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809592 | CCAGCCTGGGTAACA[C/G]AGCGAGACTCCATCT | 405 |
rs148796096 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150840892 | CAAGGAGATAATCAT[C/G]CAACATGCTGCATTT | 405 |
rs148858428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150870882 | GAGGGAAAATATAAA[A/G]TGGGCCTCAGAGGGT | 405 |
rs149110232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150843844 | CCCTCTATATCCCAA[A/G]GAGGATATGTGAGGG | 405 |
rs149172717 | snp | A/C | 1.64792e-05 | 0.00287042 | intron-variant | ARNT | GRCh38.p7 | 1:150832301 | CTGCAGGTATTTGGC[A/C]ATCCCTTTGGTTTTC | 405 |
rs149242771 | in-del | -/A | 0.0803491 | 0.183626 | intron-variant | ARNT | GRCh38.p7 | 1:150842579 | AGGAAATGGAGGGAG[-/A]AAAAAAAAGAAAAGG | 405 |
rs149246648 | snp | A/G | 0.000117723 | 0.00767123 | synonymous-codon | ARNT | GRCh38.p7 | 1:150812050 | GGGGAAACATAGTTA[A/G]ATCAGGGAATTCTTC | 405 |
rs149264034 | snp | C/G | 0.000524031 | 0.0161784 | synonymous-codon, missense, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858420 | TCCAGAGTTTCCAGA[C/G]GCAATGGCTGGACCC | 405 |
rs149267370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839965 | GAAACGACAGGTCAG[A/G]CATGGTGGCTCATGC | 405 |
rs149391713 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150868893 | ACAAAGCAAGACTCC[A/G]TCTCAAAAAATAATA | 405 |
rs149487442 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150835577 | CCGTACTCCAGCCTA[C/G]GCAAGAGAGAGACCC | 405 |
rs149540396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150825558 | TCACTCATCCATAAA[A/G]GAACAGTCTAGGCTG | 405 |
rs149592617 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | ARNT | GRCh38.p7 | 1:150876349 | CCCCTCGCTCCCTTG[A/G]GTATACTCGAGTCTA | 405 |
rs149602227 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809283 | AACCCTCAAAAATAC[A/G]GGCTTATGCCTCTGG | 405 |
rs149730284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150870637 | CTCAGTCTCCCACGT[A/G]GCTGGGACTACAGGG | 405 |
rs149854802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830378 | AAAAGCAAAACAAAA[C/G]AAAATACATCTAGTT | 405 |
rs149888419 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARNT | GRCh38.p7 | 1:150821503 | GCAATAGGTGGCTAC[C/T]AAATTATTACAACAG | 405 |
rs149943809 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150812662 | ATCTTCTCTATATTC[A/G]TTCCAATTTTAGTAT | 405 |
rs149993705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865075 | TTTAAAGTTTGAAGT[A/C]ATAGAAGTAGGAAGA | 405 |
rs150104616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861556 | GGCTTACACCTGTAA[A/G]GCTAGCACTTTAAAA | 405 |
rs150106367 | snp | C/T | | | synonymous-codon | ARNT | GRCh38.p7 | 1:150834630 | TCCAGTCTTTAGATC[C/T]AGGATACGCCCTGAA | 405 |
rs150253674 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | ARNT | GRCh38.p7 | 1:150815589 | TTTCAGCCAGGCGCG[A/G]TGGCTCACGCCTGTA | 405 |
rs150306786 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150867871 | AGCCATGTGAAGACA[C/T]GCTTGCTTCCCCTTC | 405 |
rs150316463 | in-del | -/ACAC | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811466 | GTGTGCGCACACACA[-/ACAC]CACACACACACATAC | 405 |
rs150463406 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150874150 | ATGACAGTGTAGCAA[A/G]GAATTCTGACCTGAA | 405 |
rs150467759 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | ARNT | GRCh38.p7 | 1:150832353 | ATCTGTTCCTCACAA[A/G]GCTCAGCCTATTCAC | 405 |
rs150562299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839186 | TGTGATTCCACTGTT[C/G]TTCTTCCATCCTATA | 405 |
rs150570226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818440 | TTCCACATTTTCTAT[A/T]AAGAATATTTATTTA | 405 |
rs150594757 | in-del | -/AC | | | intron-variant | ARNT | GRCh38.p7 | 1:150866698 | TACACACATACATAT[-/AC]ACACACACACACACG | 405 |
rs150624358 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150824495 | GAGTCTCGCTCTGTC[G/T]CCAGGCTGGAGTGCA | 405 |
rs150893277 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150852026 | GCACTCCTGGCGACA[C/G]AGCAAGACTCCGTCT | 405 |
rs151081575 | snp | A/G | 6.68516e-05 | 0.00578112 | synonymous-codon | ARNT | GRCh38.p7 | 1:150846283 | AAACCGCTCCTTATC[A/G]TTAGACATCTGATCA | 405 |
rs151181235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867534 | AACTTTAAAAGAAAA[A/G]GAGAGAGATATCTTT | 405 |
rs151211833 | snp | C/T | 0.00365642 | 0.042601 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150812016 | TTATCCTCACCCCAA[C/T]AGTTCTATTCTGAAA | 405 |
rs151224442 | snp | A/G | 0.000527018 | 0.0162244 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814144 | TGCAGTTGGGGCACC[A/G]GGGAGGGACATGGAG | 405 |
rs151233922 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ARNT | GRCh38.p7 | 1:150856671 | GGGAGGCTGAGGCAG[A/G]AGAATCCCTTGAACC | 405 |
rs151296193 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | ARNT | GRCh38.p7 | 1:150841246 | TGAGCCACTGCGCCC[C/G]GCCTGCTTTATCTCT | 405 |
rs180798016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150815108 | GTACACAATTGAGAT[C/T]GTATTGCATATAACA | 405 |
rs180841650 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150875569 | TTGGAAAAGGATAGA[A/C]TTTATTTGGCAAGAA | 405 |
rs180843995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862966 | TGAGGCAGAAGAATC[A/G]CTTGAACACAAAAGG | 405 |
rs180853512 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150840449 | ATACAAGAATTGATA[A/G]TACAGATTTCCTTGG | 405 |
rs181033619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150853320 | GCAATAGAAACAAAA[C/G]TACCTTCTGCTACCT | 405 |
rs181040868 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150826069 | CAGGCATGCACCACC[A/G]TACCAGGCTAATTTT | 405 |
rs181059832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150873577 | CCCCTTGAAAAACAC[C/T]GCAGGGCCACCAGCA | 405 |
rs181124220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150863979 | TGTGTGAATATCATT[A/G]AGTATACTTACACAA | 405 |
rs181124844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150842157 | TTGTTCTGTGAAACT[C/T]AGTACTGACATAAAG | 405 |
rs181136591 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150816067 | AAGGTGAAAACCACA[A/G]ACTCTACTGAGATTT | 405 |
rs181333407 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811259 | CTTTACAGTTGTATA[C/T]TGGCTGGGCATGGAT | 405 |
rs181352261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150848287 | ATGGCGAAACCTTGT[C/T]GCTACTAAAAGTACA | 405 |
rs181369266 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150860088 | ATTTCAATATACATC[A/C]TGAATATCTATCTAC | 405 |
rs181375328 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ARNT | GRCh38.p7 | 1:150836960 | AGTCCCAGCTACTCC[A/G]GAGGCTGAGGTGGGA | 405 |
rs181467686 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ARNT | GRCh38.p7 | 1:150868699 | GAGGTCAGGAGATCG[A/C]GACCATCCTGGCCAA | 405 |
rs181506651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848769 | ATTCCAGAGCTTAAG[C/T]GATCCACCCACCTCA | 405 |
rs181536315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150820909 | AGGGGCACTGACCCC[C/T]GTGCCATCGAAAATT | 405 |
rs181552255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868775 | CGCGGTGGCACGTGC[C/T]TGTAGTCCCAGCTAC | 405 |
rs181672761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150833714 | TACAGAATCCTAAAA[C/T]GTACAGTATATAATT | 405 |
rs181721715 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809944 | TGATCAGAACCCTAT[A/G]ATTTCTGATTCCTGA | 405 |
rs181800295 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810767 | GATGGGTGTCCAGGC[C/T]CCATCTATCATACGG | 405 |
rs181955762 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858944 | TGAATTCTTACACTG[A/G]TACAAGATATCCCCA | 405 |
rs181961097 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | ARNT | GRCh38.p7 | 1:150839524 | TCATGTGAGAAACTG[C/T]CATGCGTAAGATGGT | 405 |
rs181965905 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150814313 | CCATGCCTATGAGAG[A/T]CAACACTGTCAATCA | 405 |
rs181974209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150874362 | CTGAACATGGGATCA[A/G]TAAGTCAGAAGAGAT | 405 |
rs182186621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150845556 | GAGGTTACAGTGAGC[C/T]GAGATTACACCACTG | 405 |
rs182197247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835448 | TCTCTACAAAAAATT[A/T]AAAAATTGGTCAAGT | 405 |
rs182198628 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854136 | TGTTACTCAGGCTGG[A/T]GTACAGTGGCATGAT | 405 |
rs182218927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865790 | TATTTCCTATATTTC[A/G]TATCTCCACTTTCTT | 405 |
rs182473180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150826878 | TCTCGAACTCCTGAC[C/T]TCAAGTGATCCACCC | 405 |
rs182481225 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150862763 | TAGTAATACGTTTAT[A/G]TAGGATATAAGAGTA | 405 |
rs182519604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828484 | CCTTATTCTGGTCTA[C/T]TGATCTATATATCTA | 405 |
rs182531033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150827090 | AAGATGAAATCTACT[A/T]AAAAAAGGCAGAATC | 405 |
rs182557230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150855369 | ACCATCCTGGCTAAT[A/G]TGGTAAAACCCCGTC | 405 |
rs182842065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150817530 | CAAATTAAACAGGCC[A/G]GGCATGGTGGCTCAT | 405 |
rs182846648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854815 | TGAGCCAAAATTGCG[C/T]CACTGCACTCCAGCC | 405 |
rs182857176 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150866648 | TAATATATGGATGTA[C/T]AGTTTTGATTTAAAT | 405 |
rs183021025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150823947 | TCCCTGGTTCAAGCG[A/G]TTCTCCTGCCTCAGC | 405 |
rs183044378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870701 | TTTTGTACAGATGGG[G/T]TTTCACCACGTTGCC | 405 |
rs183051963 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150850287 | GTCTCCCTCTCCCCA[C/T]GGTCTCCCTCTCCCT | 405 |
rs183089365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849348 | TAATATTTTCAACTC[C/T]GGAAAGAAAAAAAGC | 405 |
rs183107196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860836 | CACTCCAGCCTGAGC[A/G]ACAGAGAAAGACTCT | 405 |
rs183118427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838368 | TATTTATTTACATGT[A/C]TGTTTCCACCAGAAA | 405 |
rs183124649 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150845805 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 405 |
rs183129107 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150813064 | GTCTTCTCACATATA[A/C]CCCCAACCAAACACC | 405 |
rs183129374 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150869302 | CTAACACAGTGAAAC[C/T]CCATCTCCACTAAAA | 405 |
rs183149807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849595 | GTTTAAGACCAGCCT[C/G]GGCAACATCATTTTA | 405 |
rs183377182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150865143 | ATGAGGATGGCACAA[C/T]GAAAAGGTAGTTACT | 405 |
rs183386125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150844261 | ACTCCTTTCCTGTTA[C/T]CACTGCCACTGTAAC | 405 |
rs183413198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870384 | CATTTTTATTCCACA[A/G]ACATACATTGAACTC | 405 |
rs183654537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150860531 | GAAAAAAAAATTTTC[A/G]AATCATATATGCAAC | 405 |
rs183672646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821529 | AACAGTACAGTATAT[A/G]CTATAGTTAACTTTA | 405 |
rs183677682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812562 | ATGGCTATAATCATT[A/G]TGTTCTATTTCATTT | 405 |
rs183828772 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150868291 | AAGACCCTGTCTCAA[A/G]AAAGAGTCAAGACCC | 405 |
rs183851366 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809712 | GTCCAGACTTGAACA[C/G]TTTAAATTTCACTCA | 405 |
rs183868131 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858089 | AGGCATAGTAAAATC[C/T]CTGGGCTTAGCTACA | 405 |
rs183876904 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150833320 | GCCAGCCTGGCCAAC[A/G]TGGTGAAACACTGTT | 405 |
rs184038168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150856162 | AAAAGAAATATGGGC[C/T]GGGTGCAGTGGCTCG | 405 |
rs184110696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150838796 | CAAGTCTAGCCATTC[C/T]ATTCACTTTAGCCAT | 405 |
rs184115724 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150813840 | CATGTTGGTCAGGCT[A/G]GGGTTGAACTCCCAA | 405 |
rs184137156 | snp | C/G | 0 | 0 | intron-variant | ARNT | GRCh38.p7 | 1:150825649 | AGGTCAGGAGATCGA[C/G]ACCATCCTGGCCAAC | 405 |
rs184140186 | snp | A/G | 0.000225301 | 0.0106113 | intron-variant | ARNT | GRCh38.p7 | 1:150861328 | CAGCAAGACAACATC[A/G]CAAAAAAAAAATTAA | 405 |
rs184178847 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877282 | AAAAAAAAAAGGATA[C/T]TTTACTAAAAACCTT | 405 |
rs184190461 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150829781 | TGCCATATTCCTTCA[A/G]ATTTTGAGAGTTTTA | 405 |
rs184391767 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878627 | CATCTGTTAAAATTT[C/T]ATTTTTCTTTCATTT | 405 |
rs184400111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873870 | GGCTACAGTGAGCTG[A/T]GATTACACCATTGCA | 405 |
rs184475995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819470 | TCCTTATCCCTATTT[G/T]ACATATGGAAGCATT | 405 |
rs184486297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150856825 | TTAGGACAGGTGAAG[C/T]GGCTCACGCCTGTAA | 405 |
rs184607616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150818175 | TCCTTCATTAAAGTC[A/C]TATCCTATAGTTAAT | 405 |
rs184829745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862796 | ATGGAGTCAAACCTG[C/T]AATCCTAGCACTTTG | 405 |
rs184835935 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150839884 | ATGTAATTCCCTTCC[C/T]CCTATTTCCTGGAAA | 405 |
rs184932787 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150852249 | GGCCAATGGGACATA[A/C]GCAAATGTCATATAA | 405 |
rs185037247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873527 | TACTCTTCTTCTAAT[A/G]CAGCACCACAGTGAA | 405 |
rs185040065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150818680 | CTTGAGCCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 405 |
rs185071241 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150867692 | CATGTCAAATTGTAA[A/T]CCCCAGTGTTGAAGG | 405 |
rs185081525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150846136 | TCACATACTTCCAAA[C/T]AGGAAAGATATTAAA | 405 |
rs185133625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855045 | AAGTAATCCTCCTAC[C/T]TCAGCCTCCCAAAGT | 405 |
rs185175101 | snp | A/C | 0.000115656 | 0.00760358 | intron-variant | ARNT | GRCh38.p7 | 1:150839399 | ACTTTCAAGAGATTC[A/C]CCCAGATTCCAGACT | 405 |
rs185296119 | snp | C/G | 0.0012374 | 0.0248429 | intron-variant | ARNT | GRCh38.p7 | 1:150814278 | ATAGAACAAATACAG[C/G]ATTAACATCATTGCA | 405 |
rs185327597 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811062 | TTCTGACAGAAAAAT[A/G]CAGCATTATCTTTAT | 405 |
rs185330001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862255 | CACAGGTGCCAGTAC[C/T]TCCATATTATTTCTG | 405 |
rs185337405 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150835880 | GACCAATAACCATAT[A/C]TATAGAATAAAAAGC | 405 |
rs185379874 | snp | A/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150859027 | AACTTCATGTTAAAA[A/T]GCTTATACATACATA | 405 |
rs185433823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150872731 | TTGGGGAGTGCCCAA[C/T]GCAGGAAGATCACTT | 405 |
rs185454999 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150824644 | ATTTTTAGTAGAGAC[A/G]GGTTTTCACCATGTT | 405 |
rs185575642 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150850706 | GCCTGGCCGCCACCC[C/T]GTCTGGGAAGTGAGG | 405 |
rs185640388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860374 | GCACGCACCACCACG[C/T]CTGGCTAATTTTTGT | 405 |
rs185652020 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150837348 | CTTCACTCTCACTCT[A/G]AACTACTGTTTTCCT | 405 |
rs185688546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869183 | AACTAGGAGAAAGAA[A/G]TATAGAATGTTAGGC | 405 |
rs185738909 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150810341 | CACATTTAAAAAGTC[A/G]ATTATTAAAAAACAA | 405 |
rs185842476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150835105 | TGAAGAGTCACTGTA[C/T]TCTAGCCTCAGCAAT | 405 |
rs185875511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150827335 | TGCAGTCAATCTCTG[C/T]TCCCACTCCAACTCC | 405 |
rs185883517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150863198 | AAAATCCCGTCTCTA[C/T]TAAAAATACAAAAAT | 405 |
rs185893604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150875919 | CCCCTGCCCTCAGCA[A/G]GCAAAGACCTACAGG | 405 |
rs185897434 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150853792 | TTTCTTTAAAGGAGA[C/T]TAGGAAAGATTATAA | 405 |
rs185906000 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150826090 | GGCTAATTTTTTGTA[C/T]TTTTAGTAGACATGG | 405 |
rs186005286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849421 | TTCTTACTTGAAAAG[A/G]AGACAAGCAATTGGT | 405 |
rs186145699 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | ARNT | GRCh38.p7 | 1:150821604 | CTCTCAACTACAAAT[A/G]GTGCCATTGTACAAA | 405 |
rs186174451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869688 | AAGTAGTTGGGACTA[C/T]AGGCATCCACCACCA | 405 |
rs186186749 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150865442 | TCAATTTACGCTATG[C/G]AATTCCCCAAAGTCT | 405 |
rs186258250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150868736 | GAAACCCCGTCTCTA[C/T]TAAAAACACAAAAAT | 405 |
rs186272544 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150820517 | CAAAAATTAGCCAGG[C/T]GTCTTGGTAGATGTC | 405 |
rs186422691 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150848288 | TGGCGAAACCTTGTC[A/G]CTACTAAAAGTACAA | 405 |
rs186441310 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150848858 | TAATAAAATACACTT[A/C/T]TATTACTTTCCCAAT | 405 |
rs186447516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150820994 | CCAGAAGCCTTACCA[A/G]TAACATAAGCAGTTG | 405 |
rs186485299 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150856992 | AAAGACTTCCTTTAA[A/T]ATATTTTTCTGATTA | 405 |
rs186496166 | snp | A/T | 0.000399281 | 0.0141238 | missense | ARNT | GRCh38.p7 | 1:150831865 | CAGTGGACCACCACG[A/T]AGTGAGGTTCCCCAT | 405 |
rs186505652 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815554 | ACAGTCTGTCTCAAG[A/T]AAAAAAAAAAAAAAG | 405 |
rs186550459 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878647 | TTCTTTCATTTTGTT[G/T]TTATATTTATAAGTC | 405 |
rs186719211 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150860962 | AACTTGAACAAGCAT[C/T]TCTACAAAGAAGATA | 405 |
rs186730680 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150838495 | TGTACTGTTAGAACA[A/T]ATTAACTATTTCAAT | 405 |
rs186737810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150813078 | ACCCCCAACCAAACA[C/T]CTCAATCCAGGCATG | 405 |
rs186756541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150840552 | TTTGGCCCATTAATG[C/T]ACAAAGTCCTACCTT | 405 |
rs186817877 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARNT | GRCh38.p7 | 1:150842827 | TAGGGACCAAAGATA[C/T]ACAGAGTCTGAACAA | 405 |
rs187016351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150861443 | CATTTGTATACCCAC[A/G]TTCACAGAAGTACTA | 405 |
rs187022579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864404 | TAAGAAAATGTGGCA[A/C]ATATACACCATGGAA | 405 |
rs187038799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816205 | TTACATACGGAAAAA[A/T]GCCCAAACAAACAAA | 405 |
rs187097402 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150823741 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 405 |
rs187104415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150826924 | AGCGCTGGGATTACA[A/G]GTGTGAGCCACCGTG | 405 |
rs187132589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150875111 | TCAGTTAAAAATCTT[A/G]TTTATTTATTCCATA | 405 |
rs187336094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150854543 | CTCCAACCTCAGTGA[A/C]ATGGCAAGACCCTGT | 405 |
rs187349104 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150824305 | ACTGTTTCCCTACTT[A/C]CCTTGGGAAATCCAT | 405 |
rs187382202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150870841 | TCCATAAACTTACTT[A/G]TCCATTCAACTACAA | 405 |
rs187387999 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | ARNT | GRCh38.p7 | 1:150850642 | CGCTACAACCTCCAC[C/T]TCCCAGCCGCCTGCC | 405 |
rs187442119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150817591 | AGCAGGTGGATCACC[C/T]GAGGTCAGGAGTTCG | 405 |
rs187472871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150865914 | TTCACTAATTGATAG[C/T]TTGCCTAGCTATGGA | 405 |
rs187584228 | snp | C/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150876856 | CAGGGCTACTCACTG[C/T]GCCAGCCAGTCCAGT | 405 |
rs187589240 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150818391 | TATCTGGAGTGTGAG[A/C]ATTTTATTCCTTCTC | 405 |
rs187593675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855434 | AGACGTGGTGGTGGA[C/T]GCCTGTAGTCCCAGC | 405 |
rs187601392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150828827 | TTAATATGAGTACCT[C/T]TGAATCATCTGTATT | 405 |
rs187688242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150845631 | AAAATAGGCCGGGTG[C/T]GGTGGCTCACACCTA | 405 |
rs187699513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150844446 | CCTGAGATTGCATCT[C/T]ACCACTCCAGAATAG | 405 |
rs187707647 | snp | A/T | 0.000224928 | 0.0106025 | intron-variant | ARNT | GRCh38.p7 | 1:150817476 | CAAATAGAAAAAAAA[A/T]TTTTTTTTAAAAAAG | 405 |
rs187938786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839208 | CATCCTATATGCTAT[A/G]TTCATGAGTCAAGTT | 405 |
rs187945964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150870416 | AATCCAACATACTAG[A/G]CACCCACTGTAAGCA | 405 |
rs188183492 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150860584 | AGAGTGGCCAGGCAC[A/G]GTGGCTCACACCTGT | 405 |
rs188199949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150812632 | GTGTGTCATCCTTAC[A/G]CAGGGGCCATGCTAA | 405 |
rs188229008 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ARNT | GRCh38.p7 | 1:150813925 | GCCACCGCACCCAGC[C/T]GGTAGGTTTTAAATT | 405 |
rs188237270 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | ARNT | GRCh38.p7 | 1:150849902 | AAACCCCGTCTCTAC[G/T]AAAAATACAAAAATT | 405 |
rs188387198 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815050 | ATTCCATGGTTAACA[C/T]GTTTGGATAATTTCT | 405 |
rs188421047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150862797 | TGGAGTCAAACCTGT[A/T]ATCCTAGCACTTTGA | 405 |
rs188429286 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150840159 | GACAGGAGAATCACT[G/T]GAATCTGGGAGGTGG | 405 |
rs188479524 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838104 | CTCCCCACTGCATAA[A/G]AATTAAAATCTAAAT | 405 |
rs188499820 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ARNT | GRCh38.p7 | 1:150845863 | GCCGAGATGGCGCCA[C/T]TGCACTCCAGCCTGG | 405 |
rs188529252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150852409 | GCTGAGTCCAGTTCT[C/T]AGCTGACCAGCTGAG | 405 |
rs188537428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150825771 | GGAGAATCGCTTGAA[C/T]CTAAGAGGCAGAGGT | 405 |
rs188728406 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877891 | CGGTCTCACAAACTG[C/T]TGGGATTACAGGCGT | 405 |
rs188742655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150830442 | ATAAATAAGAATAAA[C/T]AAGTATATAAAACTT | 405 |
rs188777955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150866700 | ACACACATACATATA[C/T]ACACACACACACGTA | 405 |
rs188794665 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854046 | GTAAAATCCTATCTA[C/T]CTACCCAGTAACTCA | 405 |
rs188804521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150826128 | CTGTGTTGGCCAGGC[C/T]GGGCTTGAACTCCTG | 405 |
rs188839167 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150874007 | AATCTTGACAAAACT[A/C]ACAAGAATTGTAAAA | 405 |
rs189017402 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150856578 | GACCAGCCTGGCCAA[C/T]GTGGTGAAATCCCAT | 405 |
rs189027338 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | ARNT | GRCh38.p7 | 1:150868697 | ACGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCC | 405 |
rs189037827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858118 | CAGTCCTTTATCTTA[C/T]GGAAATTTTGGTTTA | 405 |
rs189046451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819658 | TTATACTAAGTAAAA[C/T]AGGCCAGTTACAAAG | 405 |
rs189070523 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150848291 | CGAAACCTTGTCGCT[A/C]CTAAAAGTACAAAAA | 405 |
rs189076879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150820640 | CCAGCCTGGGTGCCA[A/G]AGCGAGACCCTGTCT | 405 |
rs189320042 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ARNT | GRCh38.p7 | 1:150847628 | GTTAGAGCTAATTCA[C/T]GGGTATAAAAAAAGA | 405 |
rs189421154 | snp | A/C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150819063 | TAAACTTTACAAGTT[A/C/G]TAAAGACTGAATTGG | 405 |
rs189450272 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150867869 | CCAGCCATGTGAAGA[C/T]ATGCTTGCTTCCCCT | 405 |
rs189462702 | snp | A/G | 0.000641177 | 0.0178935 | intron-variant | ARNT | GRCh38.p7 | 1:150846351 | AGCATTACACTTGTT[A/G]TATCTATTTCACTCT | 405 |
rs189557391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873092 | GATCGAGACCACCCT[A/G]GCTAACAGGGTGAAA | 405 |
rs189578549 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824701 | CTCAAATGATCCGCC[C/T]GCCTTGGCCTCCCAA | 405 |
rs189592026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150873556 | AAAAATGCAGAAGAA[C/T]GTGGTCCCCTTGAAA | 405 |
rs189740651 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811228 | AATCGTATCAACAGC[C/T]GACTTTCTATATTTG | 405 |
rs189747500 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150836939 | GGTGTGGTGGCACAC[A/G]CCTGTAGTCCCAGCT | 405 |
rs189826916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150814294 | ATTAACATCATTGCA[C/G]ATACCATGCCTATGA | 405 |
rs189858139 | snp | A/G/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150862757 | TACTTTTAGTAATAC[A/G/T]TTTATATAGGATATA | 405 |
rs189872212 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | ARNT | GRCh38.p7 | 1:150845495 | TGCCCATATTCCCAG[C/G]TACTAGGGAGGCTGA | 405 |
rs190071544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839415 | CCCAGATTCCAGACT[C/T]TCTCAGAACTATAAG | 405 |
rs190118865 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | CTSK, ARNT | GRCh38.p7 | 1:150809767 | GGGGGAAGGCATCCA[A/G]ATGTGCCCTAGTGGT | 405 |
rs190247486 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150828298 | GCTGATTTTTGTAAA[G/T]TGTATGAGGTAAGAT | 405 |
rs190280437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150876040 | ACGTCGTATATATCA[A/C]AGAATGTCCATTTTT | 405 |
rs190286311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855278 | TTATGTTTATGGCTG[C/T]GCGCAGTGGCTCATG | 405 |
rs190345163 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150833349 | TTTTACTAAAAATAC[A/G]AAAATTAGCCAGCTG | 405 |
rs190363732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150835231 | TAGATCTGTTTGTCT[C/T]CTTTATTATACAGAA | 405 |
rs190396154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150816635 | TGCAAAGAAATAGGA[A/G]GAAGAAAAGCAGCTT | 405 |
rs190538735 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877131 | GCCGGGCGTGGTGGC[A/G]CATGCCTGTAATCCC | 405 |
rs190554511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150855567 | ACTCCGTCTCAAAAA[A/T]AAATAAATAAAAATT | 405 |
rs190599470 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810709 | GTAGTAACCTGTATC[C/T]GCATTTATATGGCTA | 405 |
rs190667944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821673 | ATTTTTTTTGAGATG[C/G]AGTCTCCCTCTGTCA | 405 |
rs190696237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150869745 | TTTTGTGGAGACAAG[A/G]TCTCCCTATATTGCT | 405 |
rs190893070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812692 | TATATGCTGCTGAAG[C/T]GAGCACTACTTTTTA | 405 |
rs190895669 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150848978 | GGAGGCCGAGGTGGG[A/C]GGATCACCTGAGGTC | 405 |
rs190904683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150821341 | CAAATGTTATTCAAG[A/G]TTTCAGTATTGCACT | 405 |
rs190913215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150849508 | GTCCATTTTCAGGCC[A/G]GGTACAGTGGCTCAT | 405 |
rs190936535 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150869225 | GCTCAAGCCTATAAT[C/T]CCAGCACTTTGGGAG | 405 |
rs190949799 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150854722 | ATTAGCTGGGTGTGG[C/T]GGCGGGCACCTGTAA | 405 |
rs191158108 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150826987 | AACTGGCCTGGTCCA[C/T]CAGCTGGGGACCTGG | 405 |
rs191183285 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150861125 | AAGGGTTGGCAAGGA[G/T]GTGGAGAAATTAAAA | 405 |
rs191191472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150838620 | ATCATTTGATTAAAT[C/T]GGTGGCATTAAGGGA | 405 |
rs191193642 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150875234 | GCAATGTAATTTTTG[C/G]GATTAATTTTACCTC | 405 |
rs191205373 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150840779 | TCCTCAAAATTAAGA[C/T]AGAAAGATATCACTG | 405 |
rs191398613 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ARNT | GRCh38.p7 | 1:150816016 | AATCTGAAAATCAGA[C/T]GTGCTCAAAACGTTC | 405 |
rs191429317 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150863770 | TGCAGTGAGCCAATC[A/G]AGCCACTGAACTCCA | 405 |
rs191597596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150819182 | AGAAAAGATTAAATG[A/G]CAAGGTGGTAACCTG | 405 |
rs191711195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150812294 | TTTTTTCCTAATCCC[G/T]TCTGTCTTCCTCCTA | 405 |
rs191720241 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ARNT | GRCh38.p7 | 1:150842851 | TGAACAAGAACCAAC[C/G]AAGGGAATTCAGGAA | 405 |
rs191740492 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150857219 | CTGAAACATATTTGT[C/T]GCTTATAACTACATA | 405 |
rs191746556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150832586 | ATTTGAAGTCAAAAT[A/G]TTCCATATGTTCTTC | 405 |
rs191747899 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150860459 | GACCTCAAGTGATCC[A/G]CCCACCTCAGCCTCC | 405 |
rs191782898 | snp | A/G | 0.0240643 | 0.107019 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878768 | AGGGCGGATCACAAA[A/G]TCAGGTGTTCGAGAC | 405 |
rs192056611 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150837608 | TTCCTTTCCTTTGTT[C/T]AAGTCTTAAATGTAG | 405 |
rs192063493 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | ARNT | GRCh38.p7 | 1:150818514 | CTGGCACTTTGGGAG[G/T]CTGAGGCAGGGTGGA | 405 |
rs192107291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150846038 | GCTTTAGTTATCACA[C/T]ACACAGAAAAACACT | 405 |
rs192248200 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150873411 | AGTGATAAGTAGAAC[C/T]AGTGAAAAATGATAG | 405 |
rs192263685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150825480 | AAAATTCACCAGATA[C/T]TTTCAGGAGCTGGAG | 405 |
rs192309979 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150823796 | ACCTTGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 405 |
rs192320711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150860653 | CTGAGGTCAGCAGTT[C/G]GAGACCAGCCTGATC | 405 |
rs192333435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150870586 | AATCATGGCTCACTG[A/C]AGCCTCAACCTCCCA | 405 |
rs192342873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150850187 | GGTCAAGAGATCGAG[A/C]CCATCCTGCCCAACA | 405 |
rs192357037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867893 | TTCCCCTTCGCCTTC[C/T]GCCATGATTCCAAGT | 405 |
rs192360588 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150846726 | ATCTAGAACTTTTTC[A/G]TCTTGCAAAACTGAA | 405 |
rs192506126 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ARNT | GRCh38.p7 | 1:150856700 | CCAGAGAGGTGGAGA[C/T]TGCAGTGAGCCAAGA | 405 |
rs192543249 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ARNT | GRCh38.p7 | 1:150862182 | ATGTATAGTTATGAC[A/G]TTCAAACCTTCACTA | 405 |
rs192564621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150872499 | ATAATAGCACAAAAA[G/T]AATTCTCTGCTAATG | 405 |
rs192567585 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | ARNT | GRCh38.p7 | 1:150850691 | AGGATTGCAGCCTCT[G/T]CCTGGCCGCCACCCC | 405 |
rs192665252 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851973 | GAATCGCTAGAACCC[A/T]GGAGGCGGAGGTTGC | 405 |
rs192724642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150845678 | GGAGGCCGAGGCGGG[C/T]GGATCACAAGGTCAG | 405 |
rs192810372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150830937 | TCAGTTAAATTTTTT[A/T]AAATTACATTAATTA | 405 |
rs192864298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150829734 | ACTTTTCAACTTTAC[C/T]TAAATCCAAGAATAG | 405 |
rs192874673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150867094 | CTGTAGTCCCAGCTA[C/T]TCGAGAGGCTGAGGC | 405 |
rs192930531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150817703 | AATCCCAGCTATTTG[A/G]GAGGCTGAGGCAGGT | 405 |
rs192948620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150866413 | CTCTATCTGATGCTG[A/G]AATTTCAGCATAATG | 405 |
rs192996355 | snp | C/T | 8.24287e-05 | 0.00641931 | missense | ARNT | GRCh38.p7 | 1:150814091 | CCAAAGTTAGATCCA[C/T]GATTGGTGAGACTAG | 405 |
rs193199531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150839333 | TTGAAATTCGTTTTC[C/T]CATTGTCTGACTTCT | 405 |
rs193209234 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878280 | CTATTTCCATTTTGC[A/T]ATTAAGGAAACAGAA | 405 |
rs193272021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150824440 | GAAACCTGAGAACAT[C/T]TGTTTTCTTTTCTTT | 405 |
rs199531175 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150813635 | TAGTTTTTTTTTTTT[-/T]ATTTTTTATTTTTTT | 405 |
rs199576139 | snp | C/G | 0.00111959 | 0.0236334 | intron-variant | ARNT | GRCh38.p7 | 1:150814036 | TCCTTTCTCTTTAGT[C/G]GTGCGATTTTCCTGT | 405 |
rs199637995 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150868918 | ATAATAATAAAATTT[-/A]AAAAAAAAAGGACCA | 405 |
rs199643789 | snp | A/G | 3.79133e-05 | 0.00435376 | intron-variant | ARNT | GRCh38.p7 | 1:150836498 | TGTTTCAGTTCCTGC[A/G]CAAGAAAAAGAAATA | 405 |
rs199669390 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809646 | ACACAAAAAAAAAAA[A/C]AAAAAAAAAAGTTGC | 405 |
rs199712372 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150828900 | AGAGAAATATGGCTT[A/C]TCAAACCAGGTGGGA | 405 |
rs199720361 | in-del | -/AC | 0.00993419 | 0.0697739 | intron-variant | ARNT | GRCh38.p7 | 1:150863898 | GGGAGATATGAAAAT[-/AC]AGTTATGTATCACTT | 405 |
rs199767293 | snp | A/T | 0.00199792 | 0.0315431 | missense | ARNT | GRCh38.p7 | 1:150829200 | GACAAACATTACTCA[A/T]GTCTGTACAGTTGGG | 405 |
rs199772061 | in-del | -/AAAAAAAAAAAAAA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809635 | CACACACACACACAC[-/AAAAAAAAAAAAAA]AAAAAAAAGTTGCTA | 405 |
rs199784498 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150866201 | TTGGCCAGGCTGGTC[C/T]CAAACTCCTGACCTC | 405 |
rs199819566 | snp | A/G | | | missense | ARNT | GRCh38.p7 | 1:150831830 | TACCTGCTGGGGGCC[A/G]GGCCTTGATGTAGCC | 405 |
rs199854652 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150865983 | GGCATTACTCCAAAG[-/T]TTTTTTTTTTTTTTT | 405 |
rs199939658 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860218 | AGAAAAAAAAAAATT[C/T]TTTTTTTTTTTTTTT | 405 |
rs200007698 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | ARNT | GRCh38.p7 | 1:150846483 | AAAGACCCACAACTA[-/T]TATTTGTCAGGTTTC | 405 |
rs200023378 | snp | A/C | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811654 | TTCAGAATTTCTTTC[A/C]AAAAACAAGCCATAC | 405 |
rs200025645 | snp | C/G | 0.00140693 | 0.0264856 | synonymous-codon | ARNT | GRCh38.p7 | 1:150813259 | ATGATGAGGCTGCTG[C/G]CCCTGCCACTGTGGC | 405 |
rs200078254 | snp | A/C/G | 0.000604143 | 0.0173699 | missense | ARNT | GRCh38.p7 | 1:150812056 | ACATAGTTAGATCAG[A/C/G]GAATTCTTCATTGTT | 405 |
rs200078710 | in-del | -/TC | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809604 | CAGAGCGAGACTCCA[-/TC]TCTCTCACACACACA | 405 |
rs200124774 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150862587 | TCCATTAAAAAAAAA[A/G]GTTCAGGGCCAAGTG | 405 |
rs200208316 | snp | A/C/G/T | 0.000448283 | 0.014966 | missense | ARNT | GRCh38.p7 | 1:150816809 | TTCTCTGCCGGCCGG[A/C/G/T]GGGTAGGAGGGAATG | 405 |
rs200224532 | in-del | -/C | 0.474903 | 0.109173 | intron-variant | ARNT | GRCh38.p7 | 1:150852051 | CGTCTCAAAAAAAAA[-/C]AAAAACAAAAACAAA | 405 |
rs200240347 | in-del | -/TCT | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858608 | TCATATCCAGATTGC[-/TCT]TCTTGATTTTTTTTT | 405 |
rs200269963 | snp | A/G | 0.000270065 | 0.0116172 | intron-variant | ARNT | GRCh38.p7 | 1:150829996 | CTTCAGAAACGTGAC[A/G]TTAAAAGGTTTAACG | 405 |
rs200291093 | snp | A/T | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878429 | CTACAAAGTACTTCC[A/T]TTTTCATGTATCGCT | 405 |
rs200315395 | in-del | -/AAAAAAAA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809635 | CACACACACACACAC[-/AAAAAAAA]AAAAAAAAAAAAAAG | 405 |
rs200317951 | snp | C/T | 0.000189995 | 0.00974481 | synonymous-codon, intron-variant | ARNT | GRCh38.p7 | 1:150817937 | GGGTGCCAGCTGTCC[C/T]GAGCCCATCTCCAGG | 405 |
rs200365033 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150866172 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 405 |
rs200394177 | snp | C/T | 0.00122218 | 0.02469 | intron-variant | ARNT | GRCh38.p7 | 1:150823379 | CATCAGTGGAACTCA[C/T]AGAAAATTTTCATTA | 405 |
rs200403781 | snp | C/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150851560 | TCTATGACCTTACCC[C/G]CAACCCAGTGCTCTC | 405 |
rs200422046 | in-del | -/TTG | 0.0134861 | 0.0810011 | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150878642 | CATTTTTCTTTCATT[-/TTG]TTGTTATATTTATAA | 405 |
rs200439860 | snp | A/C | 0.0117698 | 0.0758048 | missense | ARNT | GRCh38.p7 | 1:150836423 | TCAGACACATACACC[A/C]CCCTGCCTGTCTCAC | 405 |
rs200512038 | in-del | -/A | 0.466204 | 0.125522 | intron-variant | ARNT | GRCh38.p7 | 1:150860204 | ATAGAAAAAAAAAAA[-/A]TTCTTTTTTTTTTTT | 405 |
rs200523340 | snp | A/G | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811458 | CAGAAGCATGTGTGC[A/G]CACACACACACACAC | 405 |
rs200546248 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809648 | ACAAAAAAAAAAAAA[A/C]AAAAAAAAGTTGCTA | 405 |
rs200709838 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150856489 | AATATTAGGCCGGGC[A/G]TGGTGGCTCATGCCT | 405 |
rs200721083 | in-del | -/ATAA | | | intron-variant | ARNT | GRCh38.p7 | 1:150864772 | ATAATAAAAAATAAA[-/ATAA]TAAATAAATAAATAA | 405 |
rs200765529 | snp | C/T | 0.000494169 | 0.0157111 | intron-variant | ARNT | GRCh38.p7 | 1:150817437 | TGTTGCTGCTGCCTA[C/T]ATGTCAAAGGCCAGT | 405 |
rs200813074 | snp | C/G | 0.00199803 | 0.031544 | synonymous-codon | ARNT | GRCh38.p7 | 1:150816808 | ATTCTCTGCCGGCCG[C/G]GGGGTAGGAGGGAAT | 405 |
rs200837795 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150864769 | AAGTATAATAAAAAA[-/T]AAATAAATAAATAAA | 405 |
rs200891935 | in-del | -/A/AA/AAA | 0.492702 | 0.124768 | intron-variant | ARNT | GRCh38.p7 | 1:150831925 | AAAAAAAAAAAAAAA[-/A/AA/AAA]TCTACCCGTAAAACT | 405 |
rs201013893 | snp | A/C/G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150847447 | TTCCCTTTCCCCCTT[A/C/G/T]TTTTTTTTTTTTTTT | 405 |
rs201114247 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860219 | GAAAAAAAAAAATTC[C/T]TTTTTTTTTTTTTTG | 405 |
rs201188010 | snp | A/C/T | 1.66208e-05 | 0.00288273 | intron-variant | ARNT | GRCh38.p7 | 1:150842402 | ATCTGCTTCATCATG[A/C/T]TAAAAGACACTGTTC | 405 |
rs201248419 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150852043 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAACA | 405 |
rs201275651 | in-del | -/A | | | intron-variant | ARNT | GRCh38.p7 | 1:150867219 | AAAAAAAACAACAAC[-/A]AACAAAAAAAAACAG | 405 |
rs201288219 | snp | A/C/G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150864905 | TTTATAGGTCTTTTT[A/C/G/T]TTTCTTTTTTTTTTT | 405 |
rs201311936 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849268 | AAATCATTTTTTTTT[-/T]CATTGGGCTCCTTTA | 405 |
rs201395186 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150867225 | AAACAACAACAACAA[A/C]AAAAAACAGATTACT | 405 |
rs201406724 | in-del | -/A | 0.472147 | 0.114677 | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809439 | ACTAAAAAAAAAAAA[-/A]CACAAAAATTAGCTG | 405 |
rs201410554 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150859082 | TTAATAATATACTAA[-/T]TTTAAAAAAATACAT | 405 |
rs201448376 | in-del | -/A | 0.0221141 | 0.102801 | intron-variant | ARNT | GRCh38.p7 | 1:150844714 | ATTTAAGAATTTAAT[-/A]AAAAAAAGTATATTT | 405 |
rs201479849 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150866190 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCCCAAA | 405 |
rs201493002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150821225 | GCAGACTTCATTCTA[C/T]AGTACATATCAAGCA | 405 |
rs201499435 | snp | C/T | 0.000118998 | 0.00771264 | missense, synonymous-codon, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858383 | CCCTCTGGACAATGG[C/T]TCCTCCACCTTGAAT | 405 |
rs201515890 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150873316 | CAAACAAAAAAAAAA[A/C]AAAACAAAACTTGTC | 405 |
rs201539352 | snp | C/T | 1.67438e-05 | 0.00289338 | intron-variant | ARNT | GRCh38.p7 | 1:150829270 | AAAATGATACCATTA[C/T]TTACAGATGTATTTC | 405 |
rs201564882 | snp | A/C | 3.29886e-05 | 0.00406118 | intron-variant | ARNT | GRCh38.p7 | 1:150834521 | TACCAAATCACAATC[A/C]TCAGCTTGACACTCA | 405 |
rs201586805 | snp | A/G | 0.00299556 | 0.038585 | missense | ARNT | GRCh38.p7 | 1:150813338 | TGTCCAGTCTCAGGA[A/G]CTAGAAATACAGCAA | 405 |
rs201604664 | in-del | -/AAAT | | | intron-variant | ARNT | GRCh38.p7 | 1:150864770 | GTATAATAAAAAATA[-/AAAT]AATAAATAAATAAAT | 405 |
rs201786361 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150860216 | ATAGAAAAAAAAAAA[A/T]TCTTTTTTTTTTTTT | 405 |
rs201828588 | snp | C/G/T | 0.000181857 | 0.0095342 | missense, synonymous-codon | ARNT | GRCh38.p7 | 1:150813211 | TTGCTGTGCTGGCGG[C/G/T]TGTTGAACATGTTGC | 405 |
rs201833874 | snp | A/C/G/T | | | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811660 | TGGATAGTATGGCTT[A/C/G/T]TTTTTGGAAAGAAAT | 405 |
rs201885145 | snp | A/T | 6.59011e-05 | 0.00573988 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814192 | CTGAAAGCTGCCCAC[A/T]CCAAACTGGGAAGTA | 405 |
rs201897356 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871295 | ATTAGGCAGTCGTGG[G/T]TTTTTTTTTTTTTTT | 405 |
rs201927611 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150852051 | CCGTCTCAAAAAAAA[A/C]AAAAACAAAAACAAA | 405 |
rs201943984 | in-del | -/T | 0.00144153 | 0.0268083 | intron-variant | ARNT | GRCh38.p7 | 1:150817476 | AAATAGAAAAAAAAA[-/T]TTTTTTTTAAAAAAG | 405 |
rs201982592 | snp | C/T | 1.65356e-05 | 0.00287533 | intron-variant | ARNT | GRCh38.p7 | 1:150817248 | AAAGATTTAACATGA[C/T]AATTCAATAACCCTA | 405 |
rs202041802 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809644 | ACACACAAAAAAAAA[A/C]AAAAAAAAAAAAGTT | 405 |
rs202099674 | snp | A/C | 0.00199792 | 0.0315431 | intron-variant | ARNT | GRCh38.p7 | 1:150823190 | ACTCCTGTATAATAC[A/C]TACTTCACATTGGTG | 405 |
rs202101308 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846057 | CAGAAAAACACTGTA[A/T]AAAATATACCGCCAG | 405 |
rs202163951 | snp | A/T | 3.31104e-05 | 0.00406867 | intron-variant | ARNT | GRCh38.p7 | 1:150852746 | GACATCTAAGGAAAG[A/T]TTTTCAGTCTCTTAC | 405 |
rs202239181 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150815863 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 405 |
rs267598008 | snp | A/G | | | synonymous-codon, intron-variant | ARNT | GRCh38.p7 | 1:150829970 | TGGGTCATCATCTGG[A/G]AGGGAAACACCTTCA | 405 |
rs367558696 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150827753 | GAAACTGCCAAAATG[C/T]TTTTGCAAAGCTAGT | 405 |
rs367613113 | snp | A/G | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858001 | GCATTCTCTAAATTC[A/G]GAAAAGCAGCCTACC | 405 |
rs367614618 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150845557 | AGGTTACAGTGAGCC[C/G]AGATTACACCACTGT | 405 |
rs367615349 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150813766 | TCTCCTGCCTCAGCC[A/G/T]CCCGAGTAGCTGGAA | 405 |
rs367673581 | snp | A/G | 6.60502e-05 | 0.00574637 | intron-variant | ARNT | GRCh38.p7 | 1:150817037 | CATGCCCATCAGTAA[A/G]TGATCTAAATGAGAA | 405 |
rs367766946 | in-del | -/TTTTTT | | | intron-variant | ARNT | GRCh38.p7 | 1:150821829 | AATTTTTGTATTTTC[-/TTTTTT]TTTTTTTTTTTTTTT | 405 |
rs367810645 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150866774 | ACATAAAAAATAAAA[C/T]CCAAACACTTATAGT | 405 |
rs367823412 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ARNT | GRCh38.p7 | 1:150864472 | TTGTAGGGACATGGA[C/T]GAAATTGGAAATCAT | 405 |
rs367835231 | snp | A/G | 0.000115837 | 0.00760955 | intron-variant | ARNT | GRCh38.p7 | 1:150826499 | ATATTTATGGAGTGA[A/G]TATGACAAATATTTA | 405 |
rs367888584 | in-del | -/AAAAAA | | | upstream-variant-2KB, downstream-variant-500B | CTSK, ARNT | GRCh38.p7 | 1:150809635 | CACACACACACACAC[-/AAAAAA]AAAAAAAAAAAAAAA | 405 |
rs367909450 | snp | A/G | 1.64863e-05 | 0.00287104 | intron-variant | ARNT | GRCh38.p7 | 1:150834653 | GCCCTGAAGGAAGAT[A/G]TGAAGAGCAGTCTGG | 405 |
rs367963344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150867098 | AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCACAA | 405 |
rs368014395 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150850931 | CGCCTCTGCCCGGCC[A/G]CGACCCCGTCTGGGA | 405 |
rs368042521 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ARNT | GRCh38.p7 | 1:150817247 | TAAAGATTTAACATG[A/G]CAATTCAATAACCCT | 405 |
rs368049178 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | ARNT | GRCh38.p7 | 1:150834518 | CTATACCAAATCACA[A/G]TCCTCAGCTTGACAC | 405 |
rs368238647 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838449 | TTGCCCACAAAAGGT[A/G]CATAACTGGAGTCTG | 405 |
rs368282911 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | ARNT | GRCh38.p7 | 1:150865376 | CTATTGCCTTGGGAG[A/T]TCGACAAGAACTAAA | 405 |
rs368301723 | snp | A/G | 1.67281e-05 | 0.00289202 | intron-variant | ARNT | GRCh38.p7 | 1:150826635 | AGAATACAGAAAGAA[A/G]AGTAAGATATATACT | 405 |
rs368443588 | snp | C/T | | | intron-variant, synonymous-codon | ARNT | GRCh38.p7 | 1:150842465 | GCTCTGCTCATCATC[C/T]GACCTAAAAATAGAA | 405 |
rs368448488 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150872778 | GACCAGCCTGGGCAA[C/T]ATAGCAAGACCCTGT | 405 |
rs368465087 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150856327 | CGCCTGTAGTCCCAG[C/G]TACTCGGGAGGCTGA | 405 |
rs368471057 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150874018 | AACTAACAAGAATTG[A/T]AAAAAAAAAAAAAAA | 405 |
rs368471232 | snp | C/G | 9.91031e-05 | 0.00703859 | synonymous-codon | ARNT | GRCh38.p7 | 1:150836353 | GTGCACCTGATCATA[C/G]AGTGTGCTGCCAAAC | 405 |
rs368491308 | in-del | -/A | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877262 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 405 |
rs368505137 | snp | C/T | | | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858297 | AAATAAATTCAGCAA[C/T]TAAAGTTGGTTTATA | 405 |
rs368571689 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150841152 | AGACGCGGTTTCACC[A/G]AGTTGGCCAGGATAT | 405 |
rs368646698 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845993 | CAAAATCCATAATTT[G/T]TGCTCCTATGGAAAC | 405 |
rs368648633 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150848767 | GAATTCCAGAGCTTA[A/C]GCGATCCACCCACCT | 405 |
rs368653632 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150832642 | AGTTGGCAAGCTTTT[C/T]CTGTAAAGGACCAGA | 405 |
rs368658611 | snp | A/C/G | 1.64866e-05 | 0.00287106 | synonymous-codon, missense | ARNT | GRCh38.p7 | 1:150829153 | AGTGAAGATACCCTC[A/C/G]ATGTTGTGTCGGGAG | 405 |
rs368819686 | in-del | -/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870689 | TTTTTGTATTTTTTT[-/T]GTACAGATGGGGTTT | 405 |
rs368836195 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150830847 | TGATGCTACATAGAG[A/G]TATGAAAGATCACAT | 405 |
rs368872358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150824092 | GGGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 405 |
rs368901139 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150816959 | GTTCAGCAAGTTCCT[A/G]TTTACTCAGGTGGTA | 405 |
rs368945396 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ARNT | GRCh38.p7 | 1:150825902 | AAGCTTAGTGAAGTA[C/T]ACAATTTTCTTTTTT | 405 |
rs369016678 | snp | G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150840279 | CAAGAGAAAAAAAAA[G/T]ATAGTATTTTTAAAT | 405 |
rs369249021 | snp | A/G | 3.29533e-05 | 0.00405901 | intron-variant | ARNT | GRCh38.p7 | 1:150817436 | CTGTTGCTGCTGCCT[A/G]TATGTCAAAGGCCAG | 405 |
rs369284981 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150852037 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 405 |
rs369324967 | snp | C/G | 0.00139503 | 0.0263736 | intron-variant | ARNT | GRCh38.p7 | 1:150816736 | TAAAATTTGGATTCA[C/G]CAGCTGAATCCCTCA | 405 |
rs369391588 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150825677 | AACGTGGTGAAACCC[C/T]GCCTCTACTAAAAAT | 405 |
rs369437849 | in-del | -/C/CAAC | 0.00358923 | 0.042236 | intron-variant | ARNT | GRCh38.p7 | 1:150867224 | AAACAACAACAACAA[-/C/CAAC]AAAAAAACAGATTAC | 405 |
rs369459692 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150851567 | CCTTACCCCCAACCC[A/T]GTGCTCTCTGAAACA | 405 |
rs369482161 | snp | G/T | 1.64746e-05 | 0.00287002 | missense | ARNT | GRCh38.p7 | 1:150839478 | TTATAGGAGCCATCA[G/T]TGGATGTGTTGCCAG | 405 |
rs369494203 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ARNT | GRCh38.p7 | 1:150847634 | GCTAATTCACGGGTA[-/T]AAAAAAAGACTAGTG | 405 |
rs369510385 | snp | A/G | 0.00054368 | 0.0164786 | intron-variant | ARNT | GRCh38.p7 | 1:150832292 | TGATGATCTCTGCAG[A/G]TATTTGGCCATCCCT | 405 |
rs369510752 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon | ARNT | GRCh38.p7 | 1:150814111 | GGTGAGACTAGGGTA[C/G]GCAGCAGCACCAGGC | 405 |
rs369518059 | snp | A/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150824849 | TTTTTAAAAGTAATT[A/T]TAGTTATTTTATTTT | 405 |
rs369553658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150849141 | CTGGGAGGCAGAGGT[A/T]GCGGTGAGCCGAGAT | 405 |
rs369588647 | snp | A/G | | | upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150877198 | ACCTGGGAGGCAGAG[A/G]TTGCAGTGAGCCGAG | 405 |
rs369646827 | snp | A/C/G | 0.00036701 | 0.0135414 | intron-variant, upstream-variant-2KB | ARNT | GRCh38.p7 | 1:150858325 | ATAGGAGAGATATTC[A/C/G]TAACACACTACACTC | 405 |
rs369648560 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150845107 | ATGCCACCACTCCCC[A/G]CCTCTTACTGTCATT | 405 |
rs369693779 | snp | C/G | 4.98509e-05 | 0.00499229 | intron-variant | ARNT | GRCh38.p7 | 1:150842386 | TAGAAAAAGCAGCAT[C/G]ATCTGCTTCATCATG | 405 |
rs369839831 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150815422 | GCGTGGTGGCGAGCA[C/T]CCTGTAGTCCCAGCT | 405 |
rs369891523 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150861309 | AAGATCAGGCTGGGA[A/C]ACACAGCAAGACAAC | 405 |
rs369904882 | snp | A/G | 6.5925e-05 | 0.00574092 | intron-variant | ARNT | GRCh38.p7 | 1:150816235 | AAAATAATACACAGG[A/G]AACACACAGATGATA | 405 |
rs369972465 | in-del | -/TAATA | 0.00358779 | 0.0422022 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150810576 | CCCTATGACTACATT[-/TAATA]TATCTTCTCATTAAT | 405 |
rs370080791 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150832528 | TGCTACTAATAATGA[A/G]GGATAAAGATAGGTC | 405 |
rs370099862 | snp | C/T | 4.98318e-05 | 0.00499133 | intron-variant, missense | ARNT | GRCh38.p7 | 1:150852828 | AAAGCCAACAATAAA[C/T]ACTTTAAGCCTGCTG | 405 |
rs370147011 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150831433 | CCTCTTGATAAGTTA[C/T]TACAATAAAGGCATT | 405 |
rs370171757 | snp | C/T | 6.59348e-05 | 0.00574135 | synonymous-codon | ARNT | GRCh38.p7 | 1:150823319 | CCGGAACATGACAGA[C/T]AGCACTTGGCCTTTT | 405 |
rs370250346 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150835821 | GAACAACAGTACAGA[C/T]ACAAACAACAACAAC | 405 |
rs370308208 | snp | C/G | 0.000100693 | 0.00709482 | missense | ARNT | GRCh38.p7 | 1:150812086 | TGTAGCTGTTGCTCT[C/G]ATCTCCCAGCATGGA | 405 |
rs370425313 | snp | C/T | | | intron-variant, utr-variant-5-prime | ARNT | GRCh38.p7 | 1:150861393 | CCACCTCTGGGTATA[C/T]ACCTGAAAGAATTGA | 405 |
rs370470920 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | ARNT | GRCh38.p7 | 1:150871787 | ATGGCAGGTGCCTGT[A/C]ATCCCAGCTACTCGG | 405 |
rs370485436 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150855181 | TTCTTTTTAGCATCA[C/T]ATGTAACAGCAAAAT | 405 |
rs370486380 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150854994 | GAAAAAAAAGTCTCG[C/T]CATTTTCCCCAGGCT | 405 |
rs370493512 | snp | A/C | 3.29957e-05 | 0.00406162 | missense | ARNT | GRCh38.p7 | 1:150813288 | GCCAGACACCCACAC[A/C]CTCTGCTGTCCGTGT | 405 |
rs370497335 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150814017 | AACAACTTTAACTAC[C/T]AAATCCTTTCTCTTT | 405 |
rs370607438 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150870932 | GGCACTCTGGGAGGC[C/T]GAGGCAGGAGGATTG | 405 |
rs370611763 | snp | C/T | 1.65345e-05 | 0.00287524 | missense | ARNT | GRCh38.p7 | 1:150826554 | TTACCTGTTGGAAGC[C/T]GTCTCTTAGAAGCTG | 405 |
rs370635753 | snp | A/T | 0.000102617 | 0.00716225 | intron-variant | ARNT | GRCh38.p7 | 1:150816427 | AGTGAATAAATGAGG[A/T]AAAAGATTAAAAGGA | 405 |
rs370671525 | snp | C/T | 3.29614e-05 | 0.00405951 | missense | ARNT | GRCh38.p7 | 1:150834637 | TTTAGATCCAGGATA[C/T]GCCCTGAAGGAAGAT | 405 |
rs370736565 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150863457 | GCTCAATATGAAGAG[A/G]AAACTAAAGGAAATA | 405 |
rs370977043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ARNT | GRCh38.p7 | 1:150864489 | AAATTGGAAATCATC[A/G]TTCTCAGTAAACTAT | 405 |
rs370998493 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150849854 | TGGACCACTTAAGGC[C/T]AAGAGTTCAAGACCA | 405 |
rs371067049 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150845266 | CTCCAGCCTGGGAAA[C/T]ACAATGAAAACAATG | 405 |
rs371106151 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150872653 | GCATTACAAATGACA[C/T]ATTCAATTTAAAAAG | 405 |
rs371123667 | snp | A/T | 0.0150429 | 0.0854116 | utr-variant-3-prime | ARNT | GRCh38.p7 | 1:150811984 | AAAACAAACAGTGAT[A/T]TTTTCTCCCCCACCC | 405 |
rs371168127 | snp | A/G | 0.000153988 | 0.00877328 | missense | ARNT | GRCh38.p7 | 1:150829956 | CCCTGGCCAGCCTCT[A/G]GGTCATCATCTGGGA | 405 |
rs371216935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ARNT | GRCh38.p7 | 1:150862158 | GTTACATAGTACTCT[A/G]TACTATAAATGTATA | 405 |
rs371270390 | snp | A/C | | | intron-variant | ARNT | GRCh38.p7 | 1:150862393 | CCATACCTCCAACAG[A/C]ACTGTGTTTTGGGAA | 405 |
rs371321537 | snp | C/T | 2.07738e-05 | 0.00322281 | intron-variant | ARNT | GRCh38.p7 | 1:150818045 | CCTAGGAAACCAGAG[C/T]AGACAGTAAAGAGGG | 405 |
rs371342038 | snp | C/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150871886 | GCACTCCAGCCTGGG[C/T]GACACAGTAAGACCC | 405 |
rs371354076 | snp | A/G/T | | | intron-variant | ARNT | GRCh38.p7 | 1:150846607 | AGGGGTTAGTTTTGG[A/G/T]TTTTTTTTTAATTCT | 405 |
rs371357044 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | ARNT | GRCh38.p7 | 1:150832459 | TCAAAGAACTTTCCA[C/T]AGTAATAGCAGAATA | 405 |
rs371451848 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150838654 | CTTGATTGATACTGA[A/G]GTAAATTTTTTTCTT | 405 |
rs371477575 | snp | A/G | | | intron-variant | ARNT | GRCh38.p7 | 1:150830477 | TATATGCCAGTCATT[A/G]TTTTAAGTATTTACA | 405 |