| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs13828 | snp | C/T | 0 | 0 | utr-variant-3-prime | NUP153 | GRCh38.p7 | 6:17615739 | AATTTCAACGCGTTC[C/T]ATGAACGCTTATCAG | 9972 |
| rs727557 | snp | G/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17663342 | tcacagttcacttta[G/T]cctcgaactcctggg | 9972 |
| rs942467 | snp | A/G | 0.0838651 | 0.186813 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17629385 | TATAGACCCAGAATC[A/G]GATGACACACCTATT | 9972 |
| rs942468 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NUP153 | GRCh38.p7 | 6:17641859 | ttctttttctttctt[C/T]tttttttctgagaca | 9972 |
| rs942469 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17638479 | CTAGGCTGGATTATT[C/T]TGTGGAACTAGAAAA | 9972 |
| rs1006066 | snp | C/G | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17679884 | ttcctgaggtggact[C/G]tctgcaaccttggtt | 9972 |
| rs1065057 | snp | C/T | 0.431863 | 0.17154 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17688567 | ATTGTGCCAGGGTGG[C/T]TACAAAGATACTTCA | 9972 |
| rs1535816 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | NUP153 | GRCh38.p7 | 6:17702841 | TATTACCCTTATAAC[C/T]CTTCAGTTATTTGAG | 9972 |
| rs1830818 | snp | A/C | 0.164873 | 0.23506 | intron-variant | NUP153 | GRCh38.p7 | 6:17623829 | TTTCTAGGGATGCAT[A/C]TATTAGCCAATAAAT | 9972 |
| rs1854009 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | NUP153 | GRCh38.p7 | 6:17677090 | CCTTAAAAATAAGGA[A/G]TAAGTATATAACTAA | 9972 |
| rs1886327 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | NUP153 | GRCh38.p7 | 6:17634858 | gattggaccaccccC[A/G]CCTCCCCTGCTGATA | 9972 |
| rs1886328 | snp | A/C | 0.301681 | 0.2446 | intron-variant | NUP153 | GRCh38.p7 | 6:17634792 | GGAATGGAGGACATA[A/C]AATTAAAGACGTTGA | 9972 |
| rs1969915 | snp | A/G | 0.163564 | 0.234582 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17704174 | CTCCAGAGTAGCTGG[A/G]ACTACAGGCGCCCGC | 9972 |
| rs2006705 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17678046 | taataagattgcttc[C/T]aatgtttcaccatta | 9972 |
| rs2009377 | snp | C/T | 0.376791 | 0.215463 | intron-variant | NUP153 | GRCh38.p7 | 6:17641270 | GCCAGGCACGGGGGC[C/T]CGTGCCTGTAATCCC | 9972 |
| rs2057539 | snp | C/T | 0.172028 | 0.23753 | intron-variant | NUP153 | GRCh38.p7 | 6:17703413 | GCGCCAGACCTCTCA[C/T]TGTTTCTTACTCCAA | 9972 |
| rs2228375 | snp | A/G | 0.368983 | 0.21987 | missense | NUP153 | GRCh38.p7 | 6:17675015 | CTTGGGAATTCTTCA[A/G]TCCTTAAAACCAGTC | 9972 |
| rs2228376 | snp | A/C | 0.0142229 | 0.0831214 | synonymous-codon, intron-variant | NUP153 | GRCh38.p7 | 6:17639985 | TCCTTTTAGACCTGC[A/C]GAAATCCTGAAAGAA | 9972 |
| rs2228377 | snp | A/C | 0.00287128 | 0.0377809 | missense, intron-variant | NUP153 | GRCh38.p7 | 6:17639956 | AAGGAAGTGTTCTAG[A/C]TATTCTGAAAAGCCC | 9972 |
| rs2228378 | snp | C/T | 0.0125264 | 0.0781428 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17628941 | ATTCTCTTTTGGCAA[C/T]GTGGAGCCTGCCTCT | 9972 |
| rs2228379 | snp | A/G | 0.012541 | 0.0781871 | missense | NUP153 | GRCh38.p7 | 6:17624573 | TTTGGCTCTGGAACA[A/G]CTCCTAATTCTAGTA | 9972 |
| rs2229508 | snp | A/T | 0.0188505 | 0.095236 | synonymous-codon, intron-variant | NUP153 | GRCh38.p7 | 6:17639958 | AGAAGGAAGTGTTCT[A/T]GATATTCTGAAAAGC | 9972 |
| rs2229509 | snp | C/T | 0.0293737 | 0.117576 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17637727 | TGCTGCTCAGCCCAC[C/T]GCAACAAGCCCAGTA | 9972 |
| rs2274136 | snp | C/T | 0.330221 | 0.23678 | missense, utr-variant-3-prime, intron-variant | NUP153 | GRCh38.p7 | 6:17632830 | TGCTGCTACTTGAAG[C/T]AGGTACTGAACTTCC | 9972 |
| rs2328133 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17642380 | TCAGTAACAAAAAGA[A/C]AAACTGTTCAATGGG | 9972 |
| rs2328134 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | NUP153 | GRCh38.p7 | 6:17694223 | gtggtatgtgatcag[C/T]aagtattgattgaat | 9972 |
| rs2328135 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707097 | ACGGGGAAGGAGATC[C/T]CCGGGGCGCCGCAGA | 9972 |
| rs2876454 | snp | A/G | 0.117188 | 0.211804 | intron-variant | NUP153 | GRCh38.p7 | 6:17651676 | caaagtagatttcaa[A/G]acaaaaaatatttcc | 9972 |
| rs3076077 | in-del | -/CT | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17641844 | AGACAGAGCGAGACT[-/CT]GTCTCAGAAAAAAAG | 9972 |
| rs3076080 | snp | C/T | 0.438526 | 0.164189 | intron-variant | NUP153 | GRCh38.p7 | 6:17663260 | acacacacacacaca[C/T]aTATATATATATATA | 9972 |
| rs3777711 | snp | C/T | 0.167809 | 0.236103 | utr-variant-3-prime | NUP153 | GRCh38.p7 | 6:17616025 | CAGATAACCCCAGCA[C/T]AAAGTACAATCCAGT | 9972 |
| rs3777712 | snp | C/T | 0.498415 | 0.0281103 | intron-variant | NUP153 | GRCh38.p7 | 6:17616325 | ATACATTTTCTGCTA[C/T]ACCTAACACACACGC | 9972 |
| rs3777713 | snp | C/G | 0.303187 | 0.244277 | intron-variant | NUP153 | GRCh38.p7 | 6:17650089 | tccacttgtgctaaa[C/G]gcagagtagcttcta | 9972 |
| rs3777714 | snp | C/T | 0.172997 | 0.237846 | intron-variant | NUP153 | GRCh38.p7 | 6:17650215 | GGATGGGAGAGGACA[C/T]TTGGAAAATGGGAAG | 9972 |
| rs3777715 | snp | G/T | 0.225005 | 0.248747 | intron-variant | NUP153 | GRCh38.p7 | 6:17676970 | ACTAGACAGTGTACC[G/T]TGCTAGGGGAAAAAA | 9972 |
| rs3836949 | in-del | -/G | 0.498392 | 0.028309 | intron-variant | NUP153 | GRCh38.p7 | 6:17616282 | GTCGGGTGGGGGGGG[-/G]AGTAGACTCACATTG | 9972 |
| rs4052817 | in-del | -/TG/TGT | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17649575 | ATATACTACAGTTGT[-/TG/TGT]ACTAATATGAAACAT | 9972 |
| rs4142294 | snp | C/T | 0.259674 | 0.249813 | intron-variant | NUP153 | GRCh38.p7 | 6:17665574 | ATTCATATACCTATG[C/T]ACATAAATATACACA | 9972 |
| rs4142295 | snp | A/G | 0.499673 | 0.0127754 | intron-variant | NUP153 | GRCh38.p7 | 6:17665656 | AATGACTTTTCACAC[A/G]CATGCATGCATACAA | 9972 |
| rs4236171 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NUP153 | GRCh38.p7 | 6:17638934 | GAAAAATTGAATCCT[C/T]CTAAATCCTGTTGTA | 9972 |
| rs4236172 | snp | C/G | 0.318174 | 0.240525 | intron-variant | NUP153 | GRCh38.p7 | 6:17639232 | ACAGGTGCATGCCAG[C/G]ACGCCCAGCTAATTT | 9972 |
| rs4367384 | snp | C/G | 0.302686 | 0.244385 | intron-variant | NUP153 | GRCh38.p7 | 6:17667404 | GAGGAACTTGGTATT[C/G]CAAGAAATGTTTTCA | 9972 |
| rs4370366 | snp | A/C/T | 0.0391387 | 0.134304 | intron-variant | NUP153 | GRCh38.p7 | 6:17646293 | GCTCACTGCAACCTC[A/C/T]GCCTCCCGGGTTCAC | 9972 |
| rs4579347 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | NUP153 | GRCh38.p7 | 6:17680053 | catgtcaattcctgc[A/G]ctttgcctaataaaa | 9972 |
| rs4613811 | snp | C/T | 0.225005 | 0.248747 | intron-variant | NUP153 | GRCh38.p7 | 6:17666390 | cgtggtggcatgcgc[C/T]tgtaatcccggctat | 9972 |
| rs4712307 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NUP153 | GRCh38.p7 | 6:17686697 | AAGTTAAGAAAAAAA[A/G]ACAGTACTATAGAAA | 9972 |
| rs4716165 | snp | A/C | 0.318896 | 0.240319 | intron-variant | NUP153 | GRCh38.p7 | 6:17618292 | gtcctacactcataa[A/C]aactacaggtagcca | 9972 |
| rs4716166 | snp | A/G | 0.226484 | 0.248892 | intron-variant | NUP153 | GRCh38.p7 | 6:17623802 | TTTATATAAAAGCAG[A/G]CAAAACTACATTTTC | 9972 |
| rs4716167 | snp | C/T | 0.497959 | 0.0318836 | intron-variant | NUP153 | GRCh38.p7 | 6:17627359 | GCTCATAGCTATTTG[C/T]TGAATTCCATACTTT | 9972 |
| rs4716168 | snp | C/T | 0.303187 | 0.244277 | intron-variant | NUP153 | GRCh38.p7 | 6:17643229 | tgtaatcccagcact[C/T]tgagacgcctaggcg | 9972 |
| rs4716169 | snp | A/T | 0.498611 | 0.0263212 | intron-variant | NUP153 | GRCh38.p7 | 6:17652574 | aatattagaaaaaaa[A/T]atccagtcttcataa | 9972 |
| rs4716170 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NUP153 | GRCh38.p7 | 6:17653583 | aataaatttatttac[A/G]aaaagacctgaacaa | 9972 |
| rs4716171 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NUP153 | GRCh38.p7 | 6:17653688 | gaacaagtgaaacca[A/G]tacatggtggaaaaa | 9972 |
| rs4716172 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NUP153 | GRCh38.p7 | 6:17661512 | TTAGGTTTTCAGCAT[A/G]CATTTTGAAAGAACT | 9972 |
| rs4716173 | snp | C/T | 0.499673 | 0.0127754 | intron-variant | NUP153 | GRCh38.p7 | 6:17670865 | gcccaggctggagtg[C/T]ggtggcacaatctcg | 9972 |
| rs4716174 | snp | A/G | 0.499683 | 0.0125759 | intron-variant | NUP153 | GRCh38.p7 | 6:17670958 | tgggattacaggcac[A/G]tccaactgcaaccgg | 9972 |
| rs4716175 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | NUP153 | GRCh38.p7 | 6:17700027 | TCATCACAAACAAAA[C/G]ACCTACTTTGCATTA | 9972 |
| rs6459561 | snp | C/T | 0.316968 | 0.240864 | intron-variant | NUP153 | GRCh38.p7 | 6:17657420 | aaaaaaaaaaatagc[C/T]agccttggtggtgca | 9972 |
| rs6899967 | snp | C/T | 0.329317 | 0.237084 | upstream-variant-2KB, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17708584 | caatctcaggtgatc[C/T]gcccacggcctccca | 9972 |
| rs6901119 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17671825 | ccagcctggccaaca[C/T]ggtaaaaccctgtct | 9972 |
| rs6905654 | snp | A/G | 0.00693259 | 0.0584657 | missense | NUP153 | GRCh38.p7 | 6:17637155 | GCCAAAAACATACCT[A/G]GTTTCTCAGACATAC | 9972 |
| rs6906499 | snp | C/G | 0.405507 | 0.195748 | missense | NUP153 | GRCh38.p7 | 6:17665248 | ACTCACACTGCACTT[C/G]TTATCTATTCTTTGA | 9972 |
| rs6913539 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17657394 | ctaaaataaaaaaat[A/T]aaaaaataaaaaaaa | 9972 |
| rs6913856 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NUP153 | GRCh38.p7 | 6:17691175 | GGAAAGGTATAGGTA[A/G]CAACTGGGAAGCATG | 9972 |
| rs6913935 | snp | G/T | 0.499642 | 0.0133738 | intron-variant | NUP153 | GRCh38.p7 | 6:17644214 | CTTTTGAGGATCTAG[G/T]TTTTAAAAATTCCCA | 9972 |
| rs6914067 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17666429 | ctgaggcaggagaat[C/T]gtttgaacccggagg | 9972 |
| rs6914251 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | NUP153 | GRCh38.p7 | 6:17690708 | ATGACTCAGTAGGTA[A/C]AGAAAACAATAAAAT | 9972 |
| rs6917438 | snp | A/G | 0.227369 | 0.248974 | intron-variant | NUP153 | GRCh38.p7 | 6:17631738 | ttgggaggccgaggc[A/G]ggtggatcacgaagt | 9972 |
| rs6918123 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17657393 | actaaaataaaaaaa[A/T]aaaaaaataaaaaaa | 9972 |
| rs6919027 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NUP153 | GRCh38.p7 | 6:17696943 | ctggcaggtggtgtc[C/T]gcctgtaatcccagc | 9972 |
| rs6919957 | snp | C/T | 0.172028 | 0.23753 | intron-variant, downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17632434 | AATTTTTTTTCCCAC[C/T]TGGAGAAAAGATACC | 9972 |
| rs6926424 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NUP153 | GRCh38.p7 | 6:17646407 | gagatggggtttcac[C/T]gtgttagccaggatg | 9972 |
| rs6927877 | snp | A/C | 0.226779 | 0.248919 | intron-variant | NUP153 | GRCh38.p7 | 6:17647415 | accaacagaaataaa[A/C]cagcaattaaaggac | 9972 |
| rs6928465 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17664369 | tttaaataggagaat[A/T]gtatgatatgtgaat | 9972 |
| rs6929659 | snp | A/G | 0.499502 | 0.0157669 | intron-variant | NUP153 | GRCh38.p7 | 6:17665126 | CATCACTAATTCACA[A/G]CCTTTATGTGTTATA | 9972 |
| rs6930231 | snp | C/T | 0.225301 | 0.248777 | intron-variant | NUP153 | GRCh38.p7 | 6:17682172 | tgcatacaaaagtta[C/T]gtttacactacacta | 9972 |
| rs6933829 | snp | A/C | 0.226484 | 0.248892 | intron-variant | NUP153 | GRCh38.p7 | 6:17622141 | CAGTTATGCTGCTAC[A/C]CAGAGTCAAGAGTTT | 9972 |
| rs6935037 | snp | A/G | 0.330714 | 0.236612 | intron-variant | NUP153 | GRCh38.p7 | 6:17665771 | tgtcacccagaccac[A/G]gctcactgtaggtga | 9972 |
| rs6936033 | snp | C/T | 0.165853 | 0.235413 | intron-variant | NUP153 | GRCh38.p7 | 6:17682977 | caagaagcaactcct[C/T]atccattcgagtttg | 9972 |
| rs6936057 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17662616 | gaaaagaatataatt[A/G]ggaagtttccttccc | 9972 |
| rs6936505 | snp | A/G | 0.227074 | 0.248947 | intron-variant | NUP153 | GRCh38.p7 | 6:17635191 | ctcggctcactgcaa[A/G]ctccacctcccagat | 9972 |
| rs6938643 | snp | C/T | 0.465263 | 0.127129 | intron-variant | NUP153 | GRCh38.p7 | 6:17663258 | acacacacacacaca[C/T]acaTATATATATATA | 9972 |
| rs6938802 | snp | C/G | 0.195526 | 0.243993 | intron-variant | NUP153 | GRCh38.p7 | 6:17688193 | ACATCAGAGCTTGCA[C/G]TCTTAACTGATATAG | 9972 |
| rs6939367 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17665554 | TAATGGAACCTAAGG[C/T]ATGTATTCATATACC | 9972 |
| rs7739638 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17658648 | ggtcattcaccattt[A/G]aagaaaattggaaag | 9972 |
| rs7740055 | snp | C/T | 0.331642 | 0.236293 | intron-variant | NUP153 | GRCh38.p7 | 6:17664179 | tgaaccttgaaaaca[C/T]tatgctaagtgGCTA | 9972 |
| rs7740061 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17672065 | tagaaacaagccaat[C/T]ttagatttttataga | 9972 |
| rs7740284 | snp | A/G | | | downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17614649 | ctggggggggggggg[A/G]gtgcagttctgggaa | 9972 |
| rs7742319 | snp | A/G | 0.0452528 | 0.143452 | upstream-variant-2KB, nc-transcript-variant, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707237 | TGGTTAAGTAGGCAG[A/G]AAGTAAGCAGACAGT | 9972 |
| rs7742356 | snp | A/G | 0.17332 | 0.23795 | upstream-variant-2KB, nc-transcript-variant, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707304 | GAAAAAAAAATCTGT[A/G]GTTGAAAAATAAAGT | 9972 |
| rs7742489 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17667731 | aaaaagaaaagaaaa[A/G]aaagaaaaaTCCAAC | 9972 |
| rs7743000 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17668047 | AGATGATGATGTGCA[A/G]TGAGGACTTTAGTTT | 9972 |
| rs7745019 | snp | A/G | 0.172351 | 0.237636 | intron-variant | NUP153 | GRCh38.p7 | 6:17656084 | GTGGCGTACGCTTGT[A/G]ATCCCAGCTACTCAG | 9972 |
| rs7745148 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NUP153 | GRCh38.p7 | 6:17680073 | gcctaataaaaaaaa[A/T]tcctactggcttttt | 9972 |
| rs7745349 | snp | A/T | 0.26518 | 0.249539 | intron-variant | NUP153 | GRCh38.p7 | 6:17686329 | agaaagccatgatat[A/T]gctgatactgacttt | 9972 |
| rs7747119 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17668062 | ATGAGGACTTTAGTT[C/T]ACTGAACtttttttt | 9972 |
| rs7754076 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | NUP153 | GRCh38.p7 | 6:17693105 | CCATGATTTTCACCT[A/G]TACTGTTTTTCTCTG | 9972 |
| rs7754546 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17663233 | TAAAAAGAAAAAAAT[A/G]cacacacacacacac | 9972 |
| rs7755660 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP153 | GRCh38.p7 | 6:17657948 | attttatattatttt[A/G]gactgtggaaatgat | 9972 |
| rs7757195 | snp | C/T | 0.225005 | 0.248747 | intron-variant | NUP153 | GRCh38.p7 | 6:17684568 | tgctttcatattatc[C/T]tttgtgtgtttacta | 9972 |
| rs7758652 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17663262 | acacacacacacaca[C/T]aTATATATATATAtt | 9972 |
| rs7760533 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17668162 | ctcactgcaccctcc[A/G]cctcccgggttcaag | 9972 |
| rs7760829 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17667664 | ggttgcagtgagctg[A/C]gactgtgccactgca | 9972 |
| rs7760992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17667753 | aaaTCCAACAGTCTG[C/T]TTTCCCTGAAGGATG | 9972 |
| rs7763276 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17686020 | gggcgtggtagcaca[C/T]gcctatagtcccaac | 9972 |
| rs7765156 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NUP153 | GRCh38.p7 | 6:17616262 | TTACCATGAGCAGCA[C/G]AAGGGTAAGGGGGGT | 9972 |
| rs7768447 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17694794 | ccagcctggccaaca[C/T]agtgaaaccccgtct | 9972 |
| rs7770657 | snp | A/G | 0.426813 | 0.17674 | intron-variant | NUP153 | GRCh38.p7 | 6:17634819 | TTCCTTATTCAGTTC[A/G]ATCAGTACATTATCT | 9972 |
| rs7772277 | snp | A/T | 0.262159 | 0.249704 | intron-variant | NUP153 | GRCh38.p7 | 6:17653982 | gtactaatgtcttca[A/T]ctatctttaaaatgc | 9972 |
| rs7773218 | snp | G/T | 0.195837 | 0.244062 | intron-variant | NUP153 | GRCh38.p7 | 6:17658102 | gcagtggtggttaaa[G/T]aagttttgcaaagga | 9972 |
| rs7773655 | snp | A/G | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17671690 | tgcctattctcccca[A/G]attggtctttagact | 9972 |
| rs7773979 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17671897 | cctgtagtcccagct[A/G]cttgggaggctgagg | 9972 |
| rs7774160 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17672007 | agcaagatcccatct[A/C]aaaaataaaaaaagc | 9972 |
| rs9297042 | snp | C/T | 0.289942 | 0.246789 | intron-variant | NUP153 | GRCh38.p7 | 6:17695627 | CAGAATATGTGTTTA[C/T]GATGCACAGCCAACT | 9972 |
| rs9350050 | snp | C/G/T | | | downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17614642 | gggagaactgggggg[C/G/T]ggggggagtgcagtt | 9972 |
| rs9350051 | snp | A/C | 0.493658 | 0.0559517 | downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17614721 | TATGTATTTCCAAGA[A/C]CTTTAATAAACACTA | 9972 |
| rs9350052 | snp | A/C | 0.338296 | 0.233889 | intron-variant | NUP153 | GRCh38.p7 | 6:17663941 | ATGTCCACACACACA[A/C]ACACACAAAAAAACA | 9972 |
| rs9350054 | snp | A/G | 0.286825 | 0.247273 | intron-variant | NUP153 | GRCh38.p7 | 6:17670130 | AAAAAAGTACTACAC[A/G]CTAGCTTAAGCTTTA | 9972 |
| rs9350055 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | NUP153 | GRCh38.p7 | 6:17670208 | ATAACAGAATACTGT[C/T]CTCCACCAACACTCA | 9972 |
| rs9367956 | snp | A/G | 0.195837 | 0.244062 | intron-variant | NUP153 | GRCh38.p7 | 6:17655278 | AATTTTACATATAGA[A/G]TTCTATTAACCTGAA | 9972 |
| rs9367957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17663961 | acaaaaaaacactta[C/T]acataaatgttgaca | 9972 |
| rs9367958 | snp | A/G | 0.499663 | 0.0129749 | intron-variant | NUP153 | GRCh38.p7 | 6:17682891 | ccactgcactccaga[A/G]tgggtgacagagcaa | 9972 |
| rs9367959 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17696342 | ACTACCAAGGAAGGC[C/G]CAATGTAACCCACCT | 9972 |
| rs9371005 | snp | C/G | 0 | 0 | downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17614639 | GGCGGGAGAACTGGG[C/G]GGGGGGGGGAGTGCA | 9972 |
| rs9371006 | snp | C/T | 0.499609 | 0.0139722 | intron-variant | NUP153 | GRCh38.p7 | 6:17632031 | GAGGGAGTCTTCCTT[C/T]GTACTTATATAGTAA | 9972 |
| rs9371007 | snp | C/T | 0.49941 | 0.0171624 | intron-variant | NUP153 | GRCh38.p7 | 6:17671594 | ctgaacactacaaaa[C/T]actgatgaaaaaaat | 9972 |
| rs9371008 | snp | A/G | 0.496937 | 0.0390173 | intron-variant | NUP153 | GRCh38.p7 | 6:17683490 | aaatgcattgttaat[A/G]agcagtgttgttttg | 9972 |
| rs9383302 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17622509 | CTTTACTATCCAGGT[C/T]TACCTTGTTATAGAA | 9972 |
| rs9383303 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17622582 | AACAACAGTGTGACT[C/T]TAATTTTTAGGGCCT | 9972 |
| rs9383306 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | NUP153 | GRCh38.p7 | 6:17625708 | CAAAAGGCATTCCCA[C/T]CATTTTGTGATAACC | 9972 |
| rs9383307 | snp | C/G | 0.164546 | 0.234942 | intron-variant | NUP153 | GRCh38.p7 | 6:17656802 | GTCTGAAAAGTCCTT[C/G]GACGTGCACAGTTGT | 9972 |
| rs9383310 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17683760 | tttgatgccaggcat[C/T]gatgtctcttctctg | 9972 |
| rs9383311 | snp | C/G | 0.499354 | 0.0179596 | intron-variant | NUP153 | GRCh38.p7 | 6:17686881 | TCAGTAATGGGCAGC[C/G]GGGGGCGGGCGGCGG | 9972 |
| rs9383312 | snp | A/G | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17700941 | CCCTTTTTAAAAATA[A/G]CTAAgcagtggctca | 9972 |
| rs9396786 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17668211 | ctccggagtagctga[A/G]attacaggtgcgcac | 9972 |
| rs9396787 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | NUP153 | GRCh38.p7 | 6:17670268 | TATATGGGAGAATAA[A/T]CAGGAAAGCAAGTAC | 9972 |
| rs9396788 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | NUP153 | GRCh38.p7 | 6:17676239 | AAAGGATTCGGCTTC[A/G]CTGTTTTCCAAATGG | 9972 |
| rs9396789 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17683409 | gctgcagaatggaca[C/T]tgtattatcaagcat | 9972 |
| rs9396792 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | NUP153 | GRCh38.p7 | 6:17700807 | atttgctaaaggact[G/T]ttaaaaacaaaacaa | 9972 |
| rs9396793 | snp | C/T | 0.499575 | 0.0145705 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17705013 | CCACCCGCCTCGGCC[C/T]CCCAAAGTGCTGGGA | 9972 |
| rs9465051 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | NUP153 | GRCh38.p7 | 6:17640314 | TAAACTATAATTATC[A/G]TCCAATTAACTGACT | 9972 |
| rs9465053 | snp | C/T | 0.407674 | 0.194008 | intron-variant | NUP153 | GRCh38.p7 | 6:17699397 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGCAG | 9972 |
| rs9477494 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NUP153 | GRCh38.p7 | 6:17619513 | ACAGGTTAAAAGACC[C/T]TGTGAGAAAAGTTCT | 9972 |
| rs9477495 | snp | C/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17635273 | cgccaccacacccgg[C/G]taattttttgtattg | 9972 |
| rs9477498 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NUP153 | GRCh38.p7 | 6:17651650 | tccagtaagagtggc[C/T]gtattaataccaaag | 9972 |
| rs9477499 | snp | A/C | 0.031825 | 0.122064 | intron-variant | NUP153 | GRCh38.p7 | 6:17651694 | aaaaaatatttccaa[A/C]agttttttttaaaag | 9972 |
| rs9477500 | snp | G/T | 0.031825 | 0.122064 | intron-variant | NUP153 | GRCh38.p7 | 6:17657276 | gctaggcacagtgac[G/T]cacacctgtaatccc | 9972 |
| rs9477501 | snp | A/T | 0.388021 | 0.208447 | intron-variant | NUP153 | GRCh38.p7 | 6:17657409 | AAAAAAATAAAAAAA[A/T]AAAAAATAGCTAGCC | 9972 |
| rs9477502 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17659832 | AAGAAAATTGGTTTG[C/T]TACAAAACCTATAAA | 9972 |
| rs9477503 | snp | A/T | 0.499515 | 0.0155675 | intron-variant | NUP153 | GRCh38.p7 | 6:17664019 | TAAAACCAACCCCAA[A/T]GTCCTTCAAGTGATT | 9972 |
| rs9477504 | snp | A/G | 0.000741479 | 0.0192403 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17669496 | TGAACTGGTCACACC[A/G]TAAGATTGTGCACTG | 9972 |
| rs9477505 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17676842 | AACTGTGCAGAGAGG[G/T]TCTCCCAGAAATCCA | 9972 |
| rs9477506 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NUP153 | GRCh38.p7 | 6:17696314 | TTATGGAAGAAAAGG[C/T]TCCTTTGACCTTACT | 9972 |
| rs9800883 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17701668 | tccatctcaaaaaaa[A/T]aaaaaaaatacaaaa | 9972 |
| rs10447411 | snp | C/T | 0.275999 | 0.248644 | intron-variant | NUP153 | GRCh38.p7 | 6:17661388 | ACAAACAGACAAAAC[C/T]ATACAGTAATACCAA | 9972 |
| rs10456208 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17678353 | agaaccctctgtctc[A/C]aaaaaaaaaaaaaaa | 9972 |
| rs10456802 | snp | A/C | 0.26271 | 0.249677 | intron-variant | NUP153 | GRCh38.p7 | 6:17646345 | cccgagcagctggga[A/C]tacaggaactcgcca | 9972 |
| rs10456803 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17682878 | ggctgagattgtgcc[A/G]ctgcactccagagtg | 9972 |
| rs10527400 | in-del | -/AA/AAAAAAAAAAAAAA | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17665052 | GTGAGACTCCGTCTC[-/AA/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 9972 |
| rs10531316 | in-del | -/TATTAG | 0.285519 | 0.247464 | intron-variant | NUP153 | GRCh38.p7 | 6:17657778 | GGTATATGAATCAGA[-/TATTAG]GTTGGTGCAAACGTA | 9972 |
| rs10588743 | in-del | -/AA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17663225 | TATTATGCTAAAAAG[-/AA]AAAAATACACACACA | 9972 |
| rs10622445 | in-del | -/AAAT | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17676440 | ATTATGCTTTAGAAT[-/AAAT]TTAATGCGTGTTGAA | 9972 |
| rs10642462 | in-del | -/AATA | 0.0287284 | 0.116357 | intron-variant | NUP153 | GRCh38.p7 | 6:17676437 | AATATTATGCTTTAG[-/AATA]GAATTTAATGCGTGT | 9972 |
| rs10713867 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17704731 | AGAAAACTAGAAGAC[-/A]AAAAAAAAAAAATTC | 9972 |
| rs10719164 | in-del | -/T | 0.159292 | 0.232964 | intron-variant | NUP153 | GRCh38.p7 | 6:17677733 | TAATTTTTTTTTTCC[-/T]TTTTTTTTTTTTTTT | 9972 |
| rs10949434 | snp | A/G | 0.227074 | 0.248947 | intron-variant | NUP153 | GRCh38.p7 | 6:17628251 | TTAATGTTTGATGAG[A/G]ACTGGTTATCTGTAA | 9972 |
| rs10949435 | snp | A/G | 0.227074 | 0.248947 | intron-variant | NUP153 | GRCh38.p7 | 6:17630059 | TGATAAAATCAAAGG[A/G]GCAGAAAGGGAGTGC | 9972 |
| rs10949436 | snp | C/G | 0.371987 | 0.218218 | intron-variant | NUP153 | GRCh38.p7 | 6:17679476 | caatataacctctat[C/G]taaatcccaaagaca | 9972 |
| rs11349044 | in-del | -/A | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17634980 | AACAAATTAAAAAAT[-/A]AAAAAAAAAAATAAA | 9972 |
| rs11363028 | in-del | -/T | 0.0197687 | 0.0974348 | intron-variant | NUP153 | GRCh38.p7 | 6:17696762 | TCCATCTCAAAAAAA[-/T]AAAACAAATAAATAA | 9972 |
| rs11363029 | in-del | -/A | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17697083 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAATTA | 9972 |
| rs11417761 | in-del | -/A | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17694982 | AAGGAAAAAAAAAAA[-/A]GAGAGAGTGGGAAGT | 9972 |
| rs11418400 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17675170 | AAAAAAAAAAAAAAA[-/A]TTATAAGCAATAAAC | 9972 |
| rs11422297 | in-del | -/A/AA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17628615 | TTGTAAAAAAAAAAA[-/A/AA]TAATAATAATAATAA | 9972 |
| rs11428582 | in-del | -/AAAAAAAAAAAAAAAAAAA | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17678375 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAA]GATTCTGGCCTTTGG | 9972 |
| rs11454433 | in-del | -/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17646936 | TTTTTTTTTTTTTTT[-/T]AGTAGAGACGAGGTT | 9972 |
| rs11753865 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | NUP153 | GRCh38.p7 | 6:17682491 | tagcattctaactgc[A/G]gaattttcaaaatgg | 9972 |
| rs11753906 | snp | A/G | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17676813 | ATCAGAATTTAGGAC[A/G]CTGCAGAGTAGGGAA | 9972 |
| rs11756008 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17624039 | TAATATTATATTTCA[C/T]AATTAGAAAAAAATC | 9972 |
| rs11759047 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NUP153 | GRCh38.p7 | 6:17618756 | atttcttagtagaga[C/T]ggggtttcaccgtgt | 9972 |
| rs11963713 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NUP153 | GRCh38.p7 | 6:17680276 | aatacagaccatgga[C/T]gtgaacacagggccc | 9972 |
| rs12190799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17697033 | cccagatcacaccac[C/T]gcactccagcctggg | 9972 |
| rs12191493 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17677040 | TTAAAGATCTCATTA[C/T]TAATGGCATTCAGCT | 9972 |
| rs12192333 | snp | G/T | 0.214541 | 0.247473 | intron-variant | NUP153 | GRCh38.p7 | 6:17660024 | TAACATAATCCCAAA[G/T]CTCATTACAAGTCAA | 9972 |
| rs12192926 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17668243 | gccacacctggctaa[C/T]ttttttttgtatttt | 9972 |
| rs12194203 | snp | G/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17644202 | TTTTTAATCTATCTT[G/T]TGAGGATCTAGTTTT | 9972 |
| rs12194325 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17674682 | ggctaaggcaggaga[A/C]tcgcttgaaaccagg | 9972 |
| rs12194669 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17705319 | TACTTCTAACAATCA[A/G]TATTTTAAAAATGGA | 9972 |
| rs12194703 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17699231 | gctgggcgtggtggc[C/T]caagcctgtaatccc | 9972 |
| rs12195356 | snp | C/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17696835 | cccagcacattggga[C/G]gccgaggtgggcaga | 9972 |
| rs12195526 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17638784 | AAGACAGACTATACA[C/G]ATTTGAGGCTTGCCT | 9972 |
| rs12195779 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17674725 | cagtgtggtccgaga[C/T]tgtgccaccgcactc | 9972 |
| rs12195917 | snp | A/T | 0.226484 | 0.248892 | intron-variant | NUP153 | GRCh38.p7 | 6:17644916 | TGTTGAAACCCTGTC[A/T]CTATTAAAAATACAA | 9972 |
| rs12196207 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17627424 | TTCAAAAGTATTCAT[A/G]GATATTCAACTTTTG | 9972 |
| rs12198954 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NUP153 | GRCh38.p7 | 6:17674491 | TCAAAACTACTggcc[A/G]ggtgcagtggctcac | 9972 |
| rs12199222 | snp | G/T | 0.375996 | 0.215928 | intron-variant | NUP153 | GRCh38.p7 | 6:17699091 | TTTCTGACAGTAAAT[G/T]GTATGTGTCAGCAAG | 9972 |
| rs12199496 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NUP153 | GRCh38.p7 | 6:17641112 | TGATAATGGTTTTAT[C/T]GTTATATTTTTAAGG | 9972 |
| rs12200215 | snp | C/T | 0.195214 | 0.243923 | intron-variant | NUP153 | GRCh38.p7 | 6:17686843 | ATAAACAAGATCAAC[C/T]GTGACTTGATTATTG | 9972 |
| rs12202975 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NUP153 | GRCh38.p7 | 6:17670897 | ctcactgcaacctcc[A/G]cctcccaggttcaaa | 9972 |
| rs12203313 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17654709 | TAATCTAAGAGGAAA[A/G]AAAAGCCAAGAATTC | 9972 |
| rs12203616 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17648946 | AAGAATATCCTTCTC[G/T]ATGGTATTGCATAAG | 9972 |
| rs12204158 | snp | C/G | 0.225301 | 0.248777 | intron-variant | NUP153 | GRCh38.p7 | 6:17689055 | TAAAAATTCAGACAA[C/G]TAGAAATACAAGAGT | 9972 |
| rs12205627 | snp | A/G | 0.376394 | 0.215696 | intron-variant | NUP153 | GRCh38.p7 | 6:17652634 | tcattaagaaaatga[A/G]taggcaagcaacact | 9972 |
| rs12205920 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17689782 | cgcccacctctgcct[C/T]ccaaagtgctgggat | 9972 |
| rs12206031 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707522 | ttataaagctgttgt[A/G]aggagcagacgtgat | 9972 |
| rs12207486 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17657400 | taaaaaaataaaaaa[A/T]taaaaaaaaaaaaaa | 9972 |
| rs12207794 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17641001 | ACATCTAAAGAGTAA[C/T]GGTAGCTGCTAGCAG | 9972 |
| rs12208168 | snp | C/T | 0.225893 | 0.248835 | intron-variant | NUP153 | GRCh38.p7 | 6:17661329 | AAAAAAAGAAGAATA[C/T]GTATAGTATTAATCC | 9972 |
| rs12208315 | snp | A/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17692552 | GGGAGGATGGGAAGA[A/T]GGAAGGAAAATAATA | 9972 |
| rs12208445 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17701536 | gcgtggtggcacgtg[A/C]ctgtagtcccagcta | 9972 |
| rs12208946 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17657401 | aaaaaaataaaaaaa[A/T]aaaaaaaaaaaaaat | 9972 |
| rs12208983 | snp | A/C | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17622766 | AGAAAGTTATAGTAT[A/C]CCATATGGCTCAGCA | 9972 |
| rs12209560 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17667489 | ggaggccgaggcggg[C/T]ggatcacgaggtcaa | 9972 |
| rs12211005 | snp | C/T | 0.37778 | 0.214877 | intron-variant | NUP153 | GRCh38.p7 | 6:17697732 | GGTGGGGGCAGGCTA[C/T]TCTATAACACTAACT | 9972 |
| rs12212627 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NUP153 | GRCh38.p7 | 6:17691673 | gagaggctgaggcag[A/G]agaatcgcttgaacg | 9972 |
| rs12212710 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17659287 | tttgtgctataagaa[C/T]aagcaaatttatttc | 9972 |
| rs12213110 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17619028 | AAGAGCATGCTGCAC[C/T]CCCTACACAAACGAT | 9972 |
| rs12216500 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17626244 | CTACCCTACAATTGC[C/T]AGAATTTTCCTACCC | 9972 |
| rs12333111 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | NUP153 | GRCh38.p7 | 6:17694611 | gcagtgagccaagat[C/T]gcgccattgcactcc | 9972 |
| rs12333235 | snp | A/C | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17698370 | gccaaggcaggggtt[A/C]tgcttcagtccagga | 9972 |
| rs12523772 | snp | C/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17670960 | ggattacaggcacgt[C/G]caactgcaaccggct | 9972 |
| rs12524105 | snp | C/T | 0.227074 | 0.248947 | intron-variant | NUP153 | GRCh38.p7 | 6:17627263 | ACCCTATCATGTTTT[C/T]GTTGCTTTCCAAATA | 9972 |
| rs12662451 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17705284 | GCTTTATTAAAATAA[A/G]TTAACATTTTCCTAT | 9972 |
| rs13193842 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17659506 | tgagacaaagtctcg[A/C]tctgttgccaggctg | 9972 |
| rs13195132 | snp | A/G | 0.116138 | 0.211142 | intron-variant | NUP153 | GRCh38.p7 | 6:17694966 | CCTGAGCAACAAAGC[A/G]AGACTCTGTCTCAAG | 9972 |
| rs13196366 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | NUP153 | GRCh38.p7 | 6:17682815 | cccagctactcggga[A/G]accgaggcaggagaa | 9972 |
| rs13197197 | snp | A/T | 0.172028 | 0.23753 | intron-variant | NUP153 | GRCh38.p7 | 6:17697870 | ACGACATTCTTTTCT[A/T]ATAAACCTTTTCACA | 9972 |
| rs13199838 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17686832 | GCGAATAGAGTATAA[A/G]CAAGATCAACCGTGA | 9972 |
| rs13200169 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | NUP153 | GRCh38.p7 | 6:17680950 | caagttaaaggaaac[C/T]agtatatcaaagaga | 9972 |
| rs13202025 | snp | A/G | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17701692 | tacaaaaattagcta[A/G]gcgtggtggcctgcg | 9972 |
| rs13204459 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17623130 | gtgagattctgtctc[A/C]aaaaaaaaaaaaaaa | 9972 |
| rs13208473 | snp | C/T | 0.172028 | 0.23753 | intron-variant | NUP153 | GRCh38.p7 | 6:17697642 | GCAGTGAGCCGAGAT[C/T]ACATCACTGCACTCC | 9972 |
| rs13208760 | snp | A/G | 0.17332 | 0.23795 | intron-variant | NUP153 | GRCh38.p7 | 6:17631333 | GAAAGCTAATTACAA[A/G]GTAGATAAAGCTTGC | 9972 |
| rs13208979 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17645718 | AAACTAGAAATAAAA[C/T]CTACTACAACTATAA | 9972 |
| rs13209121 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17689400 | ctcaaaaaacaaaac[A/G]aaacaaataaacaaa | 9972 |
| rs13210077 | snp | G/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17635840 | TGCTGAAAATGATGG[G/T]TCATCATTGAAAGGA | 9972 |
| rs13210614 | snp | C/T | 0.116838 | 0.211584 | intron-variant | NUP153 | GRCh38.p7 | 6:17671137 | tatgttgagtcaacc[C/T]tgccttcccaggata | 9972 |
| rs13211045 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17686486 | ctgcaagctccgcct[A/C]ccgggttcatgccat | 9972 |
| rs13213504 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | NUP153 | GRCh38.p7 | 6:17669141 | tggagtgcagtggcg[C/T]gatcttgactcactg | 9972 |
| rs13213673 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17686895 | ccgggggcgggcggc[A/G]ggggaggggggcggg | 9972 |
| rs13217969 | snp | C/T | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17700320 | AAATCTTCACTTGTC[C/T]CATTTAACCTCCACA | 9972 |
| rs13218606 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | NUP153 | GRCh38.p7 | 6:17678888 | gagttcaaggctgca[A/G]tgagctatgatggca | 9972 |
| rs13219815 | snp | A/G | 0.171704 | 0.237423 | intron-variant, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706173 | CGGGCCTTTCCTCAG[A/G]CCCTCCTGTCTGCTC | 9972 |
| rs13219933 | snp | A/G | 0.204423 | 0.24581 | intron-variant, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706262 | CCAGGCCACCGCGGC[A/G]TCGGGGTCCCATACC | 9972 |
| rs13220654 | snp | C/T | 0.171704 | 0.237423 | intron-variant | NUP153 | GRCh38.p7 | 6:17618274 | tttaagtggtattta[C/T]gtgtcctacactcat | 9972 |
| rs13220842 | snp | A/G | | | intron-variant, downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17632461 | TACCTCACTGTTGAC[A/G]AGCAACTAATATGAC | 9972 |
| rs13362635 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | NUP153 | GRCh38.p7 | 6:17678536 | GTAAACTATATTAAA[C/T]GCTGAATGATTACTT | 9972 |
| rs13437531 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17618855 | acaggcgtgagccac[C/T]gcgcccagcAGAAGT | 9972 |
| rs16879877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17622693 | GATTGCTCTTTACAT[A/T]AAAAAAAAATAAAGA | 9972 |
| rs16879902 | snp | C/T | 0.158213 | 0.232553 | missense | NUP153 | GRCh38.p7 | 6:17688462 | TAGAGCTCTCCTCAT[C/T]GGCATATACCAGATG | 9972 |
| rs17391510 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NUP153 | GRCh38.p7 | 6:17676427 | CAAATGTTTTAAATA[C/T]TATGCTTTAGAATTT | 9972 |
| rs17857419 | snp | A/C | 0 | 0 | missense | NUP153 | GRCh38.p7 | 6:17665313 | ATGGTTTAAAATAAA[A/C]ACTTCGATTTGTTGC | 9972 |
| rs28360895 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17675163 | TGTCTCAGAAAAAAA[A/G]AAAAAAATTATAAGC | 9972 |
| rs28550474 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17623345 | CACGCAAAAGCCAAA[C/T]TGAAAAATGGCCAAA | 9972 |
| rs28576241 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17702299 | GATCACAAGGTCAGG[A/G]GATCGAGAACATCCT | 9972 |
| rs28599568 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17644969 | CAGGCGCCTGTGGTG[C/T]CAGCTACTCGGGAGG | 9972 |
| rs34018793 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17664121 | ATATTATTCAGCCAT[-/A]AAAAGGGAAAAAATG | 9972 |
| rs34031298 | snp | G/T | 0.0955749 | 0.196603 | intron-variant | NUP153 | GRCh38.p7 | 6:17686524 | CCTCAGCCTCCGGAG[G/T]AGCTGGGACTACAGG | 9972 |
| rs34093879 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | NUP153 | GRCh38.p7 | 6:17688031 | GGCTGAGGCAGGAGA[A/G]TGGCATGAATTCGGG | 9972 |
| rs34235867 | in-del | -/GTT | | | intron-variant | NUP153 | GRCh38.p7 | 6:17649571 | TACGATATACTACAG[-/GTT]TTGTACTAATATGAA | 9972 |
| rs34236407 | in-del | -/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17618563 | AAGTTAAAATCTCTC[-/T]TTTTTTTTTTTTTTT | 9972 |
| rs34277406 | snp | A/T | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17683798 | AAATCCTAGATGGTA[A/T]CTTCTTCCAACGGCG | 9972 |
| rs34317160 | in-del | -/AA | 0.40528 | 0.195929 | intron-variant | NUP153 | GRCh38.p7 | 6:17694983 | GACTCTGTCTCAAGG[-/AA]AAAAAAAAAGAGAGA | 9972 |
| rs34348749 | in-del | -/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17651551 | TTTACCTGAGACCTA[-/C]CTTTAAATATAAACA | 9972 |
| rs34394855 | in-del | -/C | 0.195837 | 0.244062 | intron-variant | NUP153 | GRCh38.p7 | 6:17656152 | GGAGGTTGCAGTGAG[-/C]CAAGATTGCGCCACT | 9972 |
| rs34403726 | in-del | -/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17658269 | GGCCTGTGGCACATG[-/C]CCTGTAATCACAGTT | 9972 |
| rs34451625 | in-del | -/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17654324 | CTGACCTTGAACCAA[-/T]TTTTTTTTTTTTTTG | 9972 |
| rs34486849 | in-del | -/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17640215 | ACAAATGACTTTACA[-/G]GGGATAATTTGCCAT | 9972 |
| rs34585342 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17639094 | CCTTTCTTTTTTTTT[A/T]AAAGACAGAGTCTTG | 9972 |
| rs34586490 | in-del | -/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17660201 | AAGACATCCAACAAC[-/T]TTCAACCAAAACATG | 9972 |
| rs34611521 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17630531 | GCCAGGCATGGTGGT[-/A]CTGTGCCTGTAGTCT | 9972 |
| rs34644936 | in-del | -/ATA | 0.225597 | 0.248806 | intron-variant | NUP153 | GRCh38.p7 | 6:17654875 | AGGGAGATATATGGC[-/ATA]ATACCATACAGCTAT | 9972 |
| rs34670606 | in-del | -/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17685305 | TAATCCCAACACTTT[-/G]GGGAGGCTGAGGAAG | 9972 |
| rs34751525 | in-del | -/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17653955 | TATGCTGACGTATTT[-/G]GGGGGTGAAGTGTAC | 9972 |
| rs34783554 | in-del | -/AT | 0.19646 | 0.2442 | intron-variant | NUP153 | GRCh38.p7 | 6:17631237 | AAACAGATTTCAATC[-/AT]ATAGACATATACGCT | 9972 |
| rs34813367 | in-del | -/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17636584 | CCATCATCCACTTCT[-/G]GGATGAGTTAAAGAT | 9972 |
| rs34872401 | in-del | -/TG | | | intron-variant | NUP153 | GRCh38.p7 | 6:17693644 | TAATCCCAGCACTTT[-/TG]GGGAGGCCGAGGCGG | 9972 |
| rs34895075 | snp | C/T | 0.116488 | 0.211364 | intron-variant | NUP153 | GRCh38.p7 | 6:17644325 | CAACCCACACTAGCA[C/T]TCACCACACTGCTAT | 9972 |
| rs34922440 | in-del | -/A | 0.33533 | 0.234987 | intron-variant | NUP153 | GRCh38.p7 | 6:17689072 | AGAAATACAAGAGTT[-/A]AAAAAAAAAAATACA | 9972 |
| rs34942113 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | NUP153 | GRCh38.p7 | 6:17685285 | GGGAGCGGTGGCTCA[C/T]GCCTGTAATCCCAAC | 9972 |
| rs34965583 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17649013 | TTTGTACATTTTTTT[-/A]AAAAAGCAAAACAGC | 9972 |
| rs34973798 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17684521 | TATCTAAACCAACTC[-/A]AAACTTTCTACACAT | 9972 |
| rs35061480 | in-del | -/AC | 0.360622 | 0.224194 | intron-variant | NUP153 | GRCh38.p7 | 6:17663233 | TAAAAAGAAAAAAAT[-/AC]ACACACACACACACA | 9972 |
| rs35205034 | in-del | -/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17684322 | GCACTTGTTGCTTCA[-/C]CCTTGCCCTTTTATG | 9972 |
| rs35211137 | in-del | -/T | 0.164546 | 0.234942 | intron-variant | NUP153 | GRCh38.p7 | 6:17681401 | CCATCCTGGCTAACA[-/T]GGTGAAACCCCGTGT | 9972 |
| rs35250197 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17681089 | TATTATTCAGCCATT[-/A]AAAAAAAAGAATTAA | 9972 |
| rs35288609 | in-del | -/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17675488 | AATTTAATGTTACTA[-/C]CCCAAATTATGTACT | 9972 |
| rs35320010 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17640952 | TTAAAAGTGTAGTTA[C/T]GGGTAAAAGCAGGTT | 9972 |
| rs35324970 | in-del | -/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17691823 | GCACTATAGCAAGAA[-/T]TTTTTTTTTTTCCAG | 9972 |
| rs35374838 | snp | A/G | 0.116138 | 0.211142 | intron-variant | NUP153 | GRCh38.p7 | 6:17698225 | GATAGGGTAAACTTC[A/G]CTGCTGAATGGCATA | 9972 |
| rs35387214 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | NUP153 | GRCh38.p7 | 6:17694710 | GGCTGGGGCCACGGT[A/G]GCTTACTCCTATAAG | 9972 |
| rs35480506 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17631840 | GCGTGGTGGCAGGTT[-/A]CCTGTAGTCCCAGCT | 9972 |
| rs35657568 | in-del | -/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17618545 | AATTAAAGAAATAGT[-/G]GGAAGTTAAAATCTC | 9972 |
| rs35659988 | in-del | -/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17641329 | TCACGAGGTCAAGAG[-/T]ATGGAGACCATCCCG | 9972 |
| rs35743574 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17688893 | GGCCATCAAATACTC[-/A]AATGTCGATTTTAGA | 9972 |
| rs35756865 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17664484 | CTCGAGTCCTGGTTC[-/A]AAAAAGCAATTATGA | 9972 |
| rs35766436 | in-del | -/T | | | downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17614656 | GGGGGGGGAGTGCAG[-/T]TCTGGGAACAATCTC | 9972 |
| rs35806277 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17698636 | CAGCTACTTGGGAGG[-/A]CTGAGGCAGGAGAAT | 9972 |
| rs35830865 | in-del | -/AATA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17676438 | ATATTATGCTTTAGA[-/AATA]ATTTAATGCGTGTTG | 9972 |
| rs35885159 | in-del | -/T | 0.117188 | 0.211804 | intron-variant | NUP153 | GRCh38.p7 | 6:17622691 | GATTGCTCTTTACAT[-/T]AAAAAAAAAATAAAG | 9972 |
| rs35910278 | in-del | -/CA/CATATATA | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17663261 | ACACACACACACACA[-/CA/CATATATA]TATATATATATATAT | 9972 |
| rs35955692 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706452 | AGGCAGAGGCGGAGG[-/C]CTTAGAGAGCCTCCC | 9972 |
| rs35988815 | in-del | -/A | 0.499928 | 0.00598999 | intron-variant | NUP153 | GRCh38.p7 | 6:17648803 | GCGAGACACCATCTC[-/A]AAAAAAAAAAAATTC | 9972 |
| rs36019644 | in-del | -/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17671094 | AGGCATGAGCCACCA[-/C]CACCTGGTCTAATCC | 9972 |
| rs36027788 | in-del | -/G | 0.673037 | 0.147312 | splice-acceptor-variant, intron-variant | NUP153 | GRCh38.p7 | 6:17632846 | GGTACTGAACTTCCT[-/G]AAAAAAAAAAAAAAA | 9972 |
| rs36106871 | in-del | -/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17700078 | TATTGAATTTAGTCA[-/C]CTAAAGGAAACAAAA | 9972 |
| rs36119233 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17642807 | CATTAATGGATGAAC[-/A]AAAATAAACTGTGGC | 9972 |
| rs36194809 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17649539 | TGGTAAAACTGAGGG[-/A]AAAAAGATAGTAATT | 9972 |
| rs45543844 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUP153 | GRCh38.p7 | 6:17616403 | GTATGGTAAATTTAT[A/G]TTGGAGAACATATTT | 9972 |
| rs55765085 | snp | C/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17701832 | AGCAAGACTCTGTCT[C/G]GGGGGGGGGGGGAAA | 9972 |
| rs55786700 | snp | A/C/T | 0.000165098 | 0.00908415 | intron-variant | NUP153 | GRCh38.p7 | 6:17669411 | CACTCCTGTATTAAT[A/C/T]GTGATTTTAAAAATT | 9972 |
| rs55834304 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NUP153 | GRCh38.p7 | 6:17648667 | AATTAGCTGGGTGTG[A/G]TGGTGTACACCTGTA | 9972 |
| rs55840325 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17633472 | ATCATAATATACTTG[G/T]GTTCTGGGGACATTA | 9972 |
| rs55935856 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17640840 | GCTGGCCAGACTGGT[C/T]TTAAACTCCTGGCCT | 9972 |
| rs55955725 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | NUP153 | GRCh38.p7 | 6:17684648 | TTGGCTAACTGGTGC[A/T]AGAGGCCTAGCTTCA | 9972 |
| rs56091523 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NUP153 | GRCh38.p7 | 6:17697547 | CAAAAATTAGCCAGG[C/G]GTGGTGGCAGGCACC | 9972 |
| rs56304086 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | NUP153 | GRCh38.p7 | 6:17696862 | CAGATCACTTGAGGT[A/C]AGGAGTTTGAGACCA | 9972 |
| rs56360376 | snp | C/T | 0.00687447 | 0.0582235 | missense | NUP153 | GRCh38.p7 | 6:17626068 | GAGGAAGAGGTGGAA[C/T]TACCAAATATGCCAC | 9972 |
| rs56781570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17655158 | AACTCATGGATTGAT[C/T]GGTAGGACAGTAAAA | 9972 |
| rs56884889 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17670717 | AATTTTTATCATGAC[C/T]AAATGTTGGATTTTT | 9972 |
| rs57010318 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NUP153 | GRCh38.p7 | 6:17634635 | AGAGACAGGGCTTTG[C/T]CATGTTGGCCAGGCT | 9972 |
| rs57177825 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | NUP153 | GRCh38.p7 | 6:17670074 | CTACTCCAGCCTGGG[A/C]AACAGAGCGAGACTC | 9972 |
| rs57316215 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17663256 | ACACACACACACACA[C/T]ACACATATATATATA | 9972 |
| rs57394467 | in-del | -/A | 0.312491 | 0.242064 | intron-variant | NUP153 | GRCh38.p7 | 6:17703656 | CTTATTTTTAAGATT[-/A]AAAAAAAAAAAAAGG | 9972 |
| rs57583116 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17689083 | GTTAAAAAAAAAAAA[-/A]TACAGGAACTAAAAC | 9972 |
| rs57737938 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NUP153 | GRCh38.p7 | 6:17643513 | CACCACTCGTACAAC[C/T]ATGCCAAAACAAACT | 9972 |
| rs57742703 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17633156 | GGTTTAAGAAAAAAA[-/A]TCATGCTCGCAAATT | 9972 |
| rs57816538 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | NUP153 | GRCh38.p7 | 6:17629964 | TTTAAAGATAAACTC[A/T]TAGACATGCAAAATG | 9972 |
| rs57961707 | in-del | -/A | 0.361474 | 0.223771 | intron-variant | NUP153 | GRCh38.p7 | 6:17698756 | AAAAAAAAAAAAAAA[-/A]GAGCTGGGAGCCTGA | 9972 |
| rs58013807 | in-del | -/AA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17620120 | AAAAAAAAAAAAAAA[-/AA]GGAAGGGAGGGAGGA | 9972 |
| rs58196936 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17682942 | AAAAAAAAAAAAAAA[-/A]CACTTTCTTTGCGCA | 9972 |
| rs58563026 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | NUP153 | GRCh38.p7 | 6:17680378 | AGTCTCTTCATTAAA[C/T]GGTTTTGGAAAACTG | 9972 |
| rs58893438 | in-del | -/AAA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17682942 | AAAAAAAAAAAAAAA[-/AAA]CACTTTCTTTGCGCA | 9972 |
| rs58921535 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17648815 | CTCAAAAAAAAAAAA[-/A]TTCAGGAGCACATTA | 9972 |
| rs58947966 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17680272 | AGGCAATACAGACCA[C/T]GGACGTGAACACAGG | 9972 |
| rs59004879 | in-del | -/AA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17634990 | AAAATAAAAAAAAAA[-/AA]TAAATCGCAAAAGAA | 9972 |
| rs59205125 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17635399 | CAGGTGTAAGCCACC[G/T]CACCCGGCCTATCAT | 9972 |
| rs59386738 | snp | C/G/T | 0.00770713 | 0.0616348 | missense | NUP153 | GRCh38.p7 | 6:17626105 | CAGAAGTGGCTGGTG[C/G/T]ACTTGAACTAGAGGA | 9972 |
| rs59416896 | snp | A/G | 0.499598 | 0.0141716 | intron-variant | NUP153 | GRCh38.p7 | 6:17641728 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 9972 |
| rs59616897 | in-del | -/AA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17623376 | AAAAAAAAAAAAAAA[-/AA]CCTTTTAAAACAATT | 9972 |
| rs59685451 | in-del | -/A/AA/AGGAA/CG/GG | | | intron-variant | NUP153 | GRCh38.p7 | 6:17701843 | TCTCGGGGGGGGGGG[-/A/AA/AGGAA/CG/GG]GAAAAAAGCTAAATG | 9972 |
| rs59700511 | in-del | -/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17635127 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 9972 |
| rs59958944 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17632073 | TTCTTTTCCTGGGAC[C/T]TACTTTGGGAAACCA | 9972 |
| rs60413776 | snp | A/G | | | missense | NUP153 | GRCh38.p7 | 6:17628814 | AAAACACTGGTTGAC[A/G]CTTTGGCTCTTCATT | 9972 |
| rs60591426 | in-del | -/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17673552 | ACCAAAGAAGATATT[-/T]CACCAAAAGATAGGC | 9972 |
| rs60645337 | in-del | -/A | 0.497241 | 0.037038 | intron-variant | NUP153 | GRCh38.p7 | 6:17701661 | ACAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 9972 |
| rs61022874 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17618564 | AGTTAAAATCTCTCT[C/T]TTTTTTTTTTTTTTT | 9972 |
| rs61174546 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17701726 | GTAATCCCAGCTACT[C/G]AAGAGCTGAGGCAGG | 9972 |
| rs61278837 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17677490 | TAAAACATTTAGCAT[G/T]ACAAGACTTTAAAGC | 9972 |
| rs61311677 | in-del | -/AAAAAAAAAAAAA/AAAAAAAAAAAAAAA | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17665065 | TCAAAAAAAAAAAAA[lengthTooLong]TTTGATCAAGGTGAC | 9972 |
| rs61553664 | in-del | -/T | 0.331874 | 0.236213 | intron-variant | NUP153 | GRCh38.p7 | 6:17699190 | AATAGCTACAAATAA[-/T]TTTTTTTTTTTTTAA | 9972 |
| rs61734900 | snp | A/G | 0.0179265 | 0.0929618 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17628860 | AAAAACTAGGGAAGT[A/G]GAAGTGACAGGCTCT | 9972 |
| rs61736681 | snp | G/T | 0.0253123 | 0.109615 | missense | NUP153 | GRCh38.p7 | 6:17688557 | TCATTCTTGTTGAAG[G/T]ATCTTTGTAGCCACC | 9972 |
| rs61744976 | snp | C/G | 0.212125 | 0.247114 | missense, utr-variant-3-prime, intron-variant | NUP153 | GRCh38.p7 | 6:17632802 | CCTCCAGAAGGCAGA[C/G]AGACAGGTACAGTGC | 9972 |
| rs61746226 | snp | C/T | 0.0104977 | 0.0716845 | missense, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706293 | TGATGCTGTTGTCGC[C/T]CCTGCTGGTAAGGCT | 9972 |
| rs61748574 | snp | A/C | 0.0096041 | 0.0686281 | missense | NUP153 | GRCh38.p7 | 6:17637748 | CTGAGCAGCAACAGA[A/C]TCTATCTTCGGCGAT | 9972 |
| rs61748575 | snp | C/T | 0.0369772 | 0.130848 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17669502 | GGTCACACCGTAAGA[C/T]TGTGCACTGAGTTGC | 9972 |
| rs61748704 | snp | C/T | 0.0374549 | 0.131623 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17675322 | AGAACGTTCAGCTTC[C/T]GGGGACCACAGAGGT | 9972 |
| rs61756010 | snp | A/G | 0.00748792 | 0.060728 | intron-variant | NUP153 | GRCh38.p7 | 6:17649153 | CTGTATTTATATAAT[A/G]GTTTTGTACCTTGTT | 9972 |
| rs61756067 | snp | A/G | 0.0128357 | 0.0790766 | missense | NUP153 | GRCh38.p7 | 6:17649263 | GAAGAACTGGTGATC[A/G]GTAGAGAGATTTTCG | 9972 |
| rs62395967 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17618527 | ATAAAAAAGAATACT[C/T]AGAAATTAAAGAAAT | 9972 |
| rs62395968 | snp | G/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17627626 | TCAGCCTCCCGACTA[G/T]TTGGGATTATAGGTG | 9972 |
| rs62395969 | snp | A/G | 0.233235 | 0.249437 | intron-variant | NUP153 | GRCh38.p7 | 6:17631860 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 9972 |
| rs62395978 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17678945 | AGCAAGACTATCTCA[A/T]TTAAAAAAAAAAAAA | 9972 |
| rs62395980 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | NUP153 | GRCh38.p7 | 6:17685033 | AAAGTGACAGACATG[C/T]TAGCGTGTGCTGGTG | 9972 |
| rs62395981 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17689727 | ACGGGGTTTCTCCAT[A/G]TTGGTCAGGCTGGCC | 9972 |
| rs62395982 | snp | A/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17699206 | TTTTTTTTTTTTTAA[A/T]TACAAGCTAGCTGGG | 9972 |
| rs62395983 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17701953 | TCTGAAGCATACTAC[A/C]CACACCACCCCACCC | 9972 |
| rs62395984 | snp | G/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17702972 | TTGGGAGGCTGTGGC[G/T]GGTGGATCACCTGAG | 9972 |
| rs62999762 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17634980 | AACAAATTAAAAAAT[A/T]AAAAAAAAAAATAAA | 9972 |
| rs66792178 | in-del | -/CT | | | intron-variant | NUP153 | GRCh38.p7 | 6:17641843 | GAGACAGAGCGAGAC[-/CT]TGTCTCAGAAAAAAA | 9972 |
| rs66939633 | in-del | -/AGAC | 0.225597 | 0.248806 | intron-variant | NUP153 | GRCh38.p7 | 6:17642377 | AACTCAGTAACAAAA[-/AGAC]AAACTGTTCAATGGG | 9972 |
| rs67348223 | in-del | -/AC/ACAC/ACACACACAC | 0.625 | 0.125 | intron-variant | NUP153 | GRCh38.p7 | 6:17693217 | CACACACACACACAC[-/AC/ACAC/ACACACACAC]TTATAAAATCACAGA | 9972 |
| rs67410781 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17699497 | AAAAAAAAAAAAAAA[-/A]GAAAATACAAGATAA | 9972 |
| rs67417559 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17657393 | CTAAAATAAAAAAAT[-/A]AAAAAAATAAAAAAA | 9972 |
| rs67493962 | in-del | -/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17681402 | CATCCTGGCTAACAG[-/T]GTGAAACCCCGTGTC | 9972 |
| rs67672270 | in-del | -/GAACCCGGGTGGCGTAGCTTGCAGTGA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17690271 | CAGGAGAATGGCGTG[-/GAACCCGGGTGGCGTAGCTTGCAGTGA]AACCCGGGTGGCGTA | 9972 |
| rs71002233 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17617466 | GATGTAGTGGGAATT[-/A]AAAAAAAAAAAAAAA | 9972 |
| rs71002235 | in-del | -/A | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17623145 | AAAAAAAAAAAAAAA[-/A]GACGATGACAACAGA | 9972 |
| rs71002237 | in-del | -/AA/AAC/AC/C | 0.00119229 | 0.024389 | intron-variant | NUP153 | GRCh38.p7 | 6:17632863 | AAAAAAAAAAAAAAA[-/AA/AAC/AC/C]CGGGGAGTGGGGGGA | 9972 |
| rs71002238 | in-del | -/T | 0.283421 | 0.247756 | intron-variant | NUP153 | GRCh38.p7 | 6:17634442 | AAGGCCTTACATACA[-/T]TTTTTTTTTTTTGAG | 9972 |
| rs71002239 | in-del | -/T | 0.43088 | 0.172575 | intron-variant | NUP153 | GRCh38.p7 | 6:17645468 | CTTTTTTTTTTTTTT[-/T]CGGTAGGGATGAGTC | 9972 |
| rs71002242 | in-del | -/A | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17657416 | TAAAAAAAAAAAAAA[-/A]TAGCCAGCCTTGGTG | 9972 |
| rs71002244 | in-del | -/A | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17670105 | AAAAAAAAAAAAAAA[-/A]GTACTACACGCTAGC | 9972 |
| rs71002249 | in-del | -/A/AA/GAA/GG | 0.460813 | 0.134379 | intron-variant | NUP153 | GRCh38.p7 | 6:17701844 | CTCGGGGGGGGGGGG[-/A/AA/GAA/GG]AAAAAAGCTAAATGC | 9972 |
| rs71002250 | in-del | -/GCCTGTAATACCAGCACTTTTGGGAGGCTGTGGCGGGTGGATCAC | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17702982 | TGGCGGGTGGATCAC[lengthTooLong]CTGAGGTCAGGAGTT | 9972 |
| rs71276887 | multinucleotide-polymorphism | CACACAC/TATATAT | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17663263 | ACACACACACACACA[CACACAC/TATATAT]ATATATATATATATT | 9972 |
| rs71536740 | in-del | -/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17618595 | TTAAAGATGGAGTCT[-/G]GGCTCTGTTGCCCAG | 9972 |
| rs71536744 | in-del | -/A | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17685548 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 9972 |
| rs71536745 | in-del | -/AC/ACAC/ACACAC/ACACACAC | 0.252444 | 0.249988 | intron-variant | NUP153 | GRCh38.p7 | 6:17693183 | ATTTAGCTTTTTCCT[-/AC/ACAC/ACACAC/ACACACAC]ACACACACACACACA | 9972 |
| rs71544310 | in-del | ACTTATCTTT/GCTTATC | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17635098 | AGGTTGCACAGCTTG[ACTTATCTTT/GCTTATC]TTTTTTTTTTTTTTT | 9972 |
| rs71556125 | snp | A/C | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17620090 | GCAACAGAGCAAGAC[A/C]CCATCAAAAAAAAAA | 9972 |
| rs71556126 | snp | A/G | 0.116838 | 0.211584 | intron-variant | NUP153 | GRCh38.p7 | 6:17644852 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 9972 |
| rs71556127 | snp | A/C | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17656175 | GCGCCACTGCACTCC[A/C]CCCTGGGAGACAGAG | 9972 |
| rs71556128 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17660568 | TATACATATACATAC[A/G]TATTTCTTAATATAC | 9972 |
| rs71556129 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17663041 | TGACAACATGTAAAT[A/G]GAATCTGTAGATTAC | 9972 |
| rs71556130 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17671245 | GTCTATAATTCATGA[A/G]AAATAATAGTCTGTT | 9972 |
| rs71556131 | snp | C/T | 0.116138 | 0.211142 | intron-variant | NUP153 | GRCh38.p7 | 6:17682800 | GCACATGCCTGTAGT[C/T]CCAGCTACTCGGGAG | 9972 |
| rs71556132 | snp | A/C | 0.0973687 | 0.197999 | intron-variant | NUP153 | GRCh38.p7 | 6:17682940 | GAAAAAAAAAAAAAA[A/C]AACACTTTCTTTGCG | 9972 |
| rs71913514 | in-del | -/TCACGCCTGTAATACCAGCACTTTTGGGAGGCTGTGGCGGGTGGA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17702934 | CCGGGCGCGGTGGCT[lengthTooLong]CACGCCTGTAATACC | 9972 |
| rs72166942 | in-del | -/AC | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17693194 | ATTTAGCTTTTTCCT[-/AC]ACACACACACACACA | 9972 |
| rs72546628 | in-del | -/TGT | | | intron-variant | NUP153 | GRCh38.p7 | 6:17649574 | GATATACTACWGTTG[-/TGT]TWSTAATATGAAACA | 9972 |
| rs72837208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17672061 | ACTGTAGAAACAAGC[C/G]AATTTTAGATTTTTA | 9972 |
| rs72837214 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NUP153 | GRCh38.p7 | 6:17685743 | GAGCAAATACATTTA[C/T]GTACTCTATAGAATA | 9972 |
| rs73367297 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NUP153 | GRCh38.p7 | 6:17630786 | GGAGAGGAGAGAAGA[A/G]AGAAGACAGGAGAGA | 9972 |
| rs73369307 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NUP153 | GRCh38.p7 | 6:17654609 | ACAGGCATGAACCAC[C/T]GCGCCCAGCTGACCT | 9972 |
| rs73369312 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NUP153 | GRCh38.p7 | 6:17662193 | TTTTTAGTTAATGAA[C/T]CCTGAAATTTGAAAT | 9972 |
| rs73369318 | snp | G/T | 0.450734 | 0.149016 | intron-variant | NUP153 | GRCh38.p7 | 6:17665724 | CTTTTACAGTTTTTT[G/T]TTTTTTTTTTTTAAG | 9972 |
| rs73369319 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | NUP153 | GRCh38.p7 | 6:17667802 | AACTAACAAAAGATA[C/T]CTCTTTAACCCAAAC | 9972 |
| rs73369325 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | NUP153 | GRCh38.p7 | 6:17684910 | GTTCATCATCTTATA[C/T]GGGTGTGGCTCGTGG | 9972 |
| rs73369331 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706648 | TCTGCGGACCCCCGC[C/T]TCTGTGTGTGTCACG | 9972 |
| rs73722990 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NUP153 | GRCh38.p7 | 6:17623332 | CTCTACAAACTTACA[C/T]GCAAAAGCCAAACTG | 9972 |
| rs73722991 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NUP153 | GRCh38.p7 | 6:17627186 | ACTTTCAACCTGGCT[A/G]ATGGAAGAATGGTTA | 9972 |
| rs73722994 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17643825 | ATATAATGAAACAAA[A/G]TTGTTGTAACAAATT | 9972 |
| rs73722995 | snp | C/T | 0.0487121 | 0.148267 | intron-variant | NUP153 | GRCh38.p7 | 6:17646025 | TACTAATCTACTGTA[C/T]GCAATTGTTTGTATG | 9972 |
| rs73722997 | snp | A/T | 0.000148496 | 0.00861546 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17647903 | CGGAGAGGTCATTTG[A/T]ACCTGGTTTTCCAAA | 9972 |
| rs73723000 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NUP153 | GRCh38.p7 | 6:17662979 | GATGAAGAGACATGA[C/T]AACTAAATGCAAGAC | 9972 |
| rs73723002 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NUP153 | GRCh38.p7 | 6:17664446 | TCTGGAAAAACAAAA[C/T]CAAAAGCAGTATCTG | 9972 |
| rs73724607 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUP153 | GRCh38.p7 | 6:17691270 | CATGAAGCCAAGTTC[C/T]AGAACACTAACTACT | 9972 |
| rs73724608 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17692478 | ATGATTGTACCACTG[A/C]GCTCCTGCCTGGGTG | 9972 |
| rs73724609 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17697185 | AGTGAATTTTAGAAT[C/G]TGAACTGGCTAAATC | 9972 |
| rs73724610 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707457 | GGATGAATCAAAACC[C/G]TCTGAGCCTTAGCTT | 9972 |
| rs74291784 | snp | C/T | 0.17332 | 0.23795 | intron-variant | NUP153 | GRCh38.p7 | 6:17621612 | GCACAAAGACACATA[C/T]TCAATGTTCTCACTC | 9972 |
| rs74291788 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | NUP153 | GRCh38.p7 | 6:17692003 | GATTTAAAAATTTTT[G/T]GGGGGACTTCAAGTA | 9972 |
| rs74291789 | snp | A/G | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17700283 | ACTCCTTACCTATAT[A/G]CATATGCCAGGTCCT | 9972 |
| rs74323776 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | NUP153 | GRCh38.p7 | 6:17649420 | GTGTTAACATTATGG[G/T]TTCTTCAATCAGAAA | 9972 |
| rs74332361 | snp | A/G | 0.046775 | 0.145601 | intron-variant | NUP153 | GRCh38.p7 | 6:17684728 | CAGCTTTTGGATAAA[A/G]GACGGGGAACTCTGA | 9972 |
| rs74367648 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | NUP153 | GRCh38.p7 | 6:17703425 | TCATTGTTTCTTACT[C/G]CAACTTTCTGCTATA | 9972 |
| rs74492210 | snp | C/T | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17699870 | AGTTTTAATTAGTGA[C/T]ATCAGACTACAATTT | 9972 |
| rs74512406 | snp | A/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17661867 | ACAAGTAAAAAAAAA[A/T]TATACAGCTGAACGT | 9972 |
| rs74594356 | snp | A/G | 3.29478e-05 | 0.00405867 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17688556 | TTCATTCTTGTTGAA[A/G]TATCTTTGTARCCAC | 9972 |
| rs74597968 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | NUP153 | GRCh38.p7 | 6:17624986 | GTTTTAAATAATGAT[C/T]GAGAATACAACGCTC | 9972 |
| rs74599670 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | NUP153 | GRCh38.p7 | 6:17643964 | TCTTGAATTAATAGT[C/T]AACATTAAAGAAAAA | 9972 |
| rs74638186 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | NUP153 | GRCh38.p7 | 6:17647628 | AAATGAATATGCATA[C/T]ATATGTACATTATGT | 9972 |
| rs74698967 | snp | C/G/T | 0.00597534 | 0.0543715 | intron-variant | NUP153 | GRCh38.p7 | 6:17659217 | AAAACACTTCCGCAA[C/G/T]AGCGGGATGCAGAAA | 9972 |
| rs74740181 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17675888 | CAATTCAAATCACTG[A/G]GGCATCCCATAATAA | 9972 |
| rs74758983 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | NUP153 | GRCh38.p7 | 6:17665614 | CTAAAATGGCTTCAC[A/G]GATACTCTATATTTC | 9972 |
| rs74761293 | snp | A/G | 0.172997 | 0.237846 | intron-variant | NUP153 | GRCh38.p7 | 6:17639147 | CAGTGGTTCGATCTC[A/G]GTTCACTGCAACCTC | 9972 |
| rs74782737 | snp | A/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17617466 | GATGTAGTGGGAATT[A/T]AAAAAAAAAAAAAAA | 9972 |
| rs74933876 | snp | C/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17665989 | GCAACTCACCTGGCT[C/T]TTTTTTTTTTTTTTA | 9972 |
| rs75036961 | snp | A/G | 0.172997 | 0.237846 | intron-variant | NUP153 | GRCh38.p7 | 6:17621474 | TCCATCAACAGATGG[A/G]TACAGAAAATGTGGT | 9972 |
| rs75076621 | snp | C/G | 0.0640965 | 0.167152 | intron-variant | NUP153 | GRCh38.p7 | 6:17640650 | GAGAGTGAGTGTCTT[C/G]TTGTCAGCAAGGCCG | 9972 |
| rs75117390 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | NUP153 | GRCh38.p7 | 6:17625705 | GACCAAAAGGCATTC[C/T]CACCATTTTGTGATA | 9972 |
| rs75138821 | snp | C/T | 0.171704 | 0.237423 | intron-variant | NUP153 | GRCh38.p7 | 6:17694706 | ATGGGGCTGGGGCCA[C/T]GGTGGCTTACTCCTA | 9972 |
| rs75170242 | snp | C/G | 0.116838 | 0.211584 | intron-variant | NUP153 | GRCh38.p7 | 6:17651245 | GAGTTCGAGGCTGTA[C/G]TGGGCCATGACTGTG | 9972 |
| rs75217959 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | NUP153 | GRCh38.p7 | 6:17618459 | ATACTTCATCCACTG[G/T]AGAGTTGGGTGGGGG | 9972 |
| rs75273932 | snp | A/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17701673 | CTCAAAAAAAAAAAA[A/T]AAATACAAAAATTAG | 9972 |
| rs75292619 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17666563 | TTTAACTCCCAAAAA[C/T]GTGACCGAATCCCTC | 9972 |
| rs75355469 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17683209 | GTTTTTCTCCCCCAA[A/G]TTAGCCTTGACTTGA | 9972 |
| rs75480416 | in-del | -/TT | | | intron-variant | NUP153 | GRCh38.p7 | 6:17665739 | TTTTTTTTTTTTAAG[-/TT]AGACGGACTCCTGCT | 9972 |
| rs75516911 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | NUP153 | GRCh38.p7 | 6:17630075 | GCAGAAAGGGAGTGC[A/G]GTATACAGACTTTTC | 9972 |
| rs75522364 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | NUP153 | GRCh38.p7 | 6:17656671 | AAAGCTTTACTTAGA[A/T]AACCAACAAGGAAGA | 9972 |
| rs75595468 | snp | C/T | 0.174288 | 0.23826 | intron-variant | NUP153 | GRCh38.p7 | 6:17664066 | TCTAGTATATCCATA[C/T]AATGAAATATCTACA | 9972 |
| rs75684024 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | NUP153 | GRCh38.p7 | 6:17658529 | GGAAGTTGACAATAA[C/T]CAGTCACTGGAAGTT | 9972 |
| rs75706996 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | NUP153 | GRCh38.p7 | 6:17674348 | TTAAAAAAAAGAATC[A/C]CATTTCTTGAGATAC | 9972 |
| rs75715398 | snp | A/G | 0.16911 | 0.236552 | intron-variant | NUP153 | GRCh38.p7 | 6:17616781 | TTGAGACGGAGTCTC[A/G]CTCTCTTGCCCAGGC | 9972 |
| rs75721030 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | NUP153 | GRCh38.p7 | 6:17659213 | AGGGAAAACACTTCC[A/G]CAACAGCGGGATGCA | 9972 |
| rs75748560 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17665990 | CAACTCACCTGGCTT[C/T]TTTTTTTTTTTTTAA | 9972 |
| rs75752227 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707592 | ATGCGATGAATGATT[A/G]CAATTATAACCCATG | 9972 |
| rs75796477 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | NUP153 | GRCh38.p7 | 6:17650838 | TCTCCAGATGTAATA[C/T]AAGTAAGTACAGCAT | 9972 |
| rs75863477 | snp | A/G | 0.116838 | 0.211584 | intron-variant | NUP153 | GRCh38.p7 | 6:17653807 | TCAATCTCTTGATAG[A/G]GCTTGCATTACACAG | 9972 |
| rs75896782 | snp | A/G | 0.174288 | 0.23826 | intron-variant | NUP153 | GRCh38.p7 | 6:17660165 | CCTGCAGAGCAAAAT[A/G]CCAATAGGCATGAAG | 9972 |
| rs75939490 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17657923 | GCTGATGACTTACTA[C/T]TTGCTATTTATTTTA | 9972 |
| rs75952474 | snp | A/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17661868 | CAAGTAAAAAAAAAA[A/T]ATACAGCTGAACGTG | 9972 |
| rs76072554 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17633716 | GTAAGGCCCAAAATA[C/T]AGTGCTGACAGTGAA | 9972 |
| rs76097316 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NUP153 | GRCh38.p7 | 6:17635611 | TTCACCATGCTGCTC[A/G]GGCTGGTCTTAAACT | 9972 |
| rs76122329 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17622240 | GGACTGCTTGAGCTC[A/G]GGAGTTAGAGACCAG | 9972 |
| rs76134277 | snp | A/C | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17698738 | GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA | 9972 |
| rs76192542 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17650400 | ACATATAAGCCACCC[A/G]AATCTCTGGTGGACC | 9972 |
| rs76204717 | snp | A/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17685862 | CATTAAAAAAAAAAA[A/T]TTGACTCACAGGTGG | 9972 |
| rs76232907 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NUP153 | GRCh38.p7 | 6:17655074 | TCAAGTCTTCTTATA[C/T]ACTGCTACATGTTTT | 9972 |
| rs76328297 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17630221 | AGGGAAGGTGGAAAA[A/T]GAGACAATGGAGAGA | 9972 |
| rs76339429 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17665460 | AAATTTTGACAATAG[C/T]TAACATGACCTAAAG | 9972 |
| rs76354537 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17664353 | CCACTGAATTGAAAA[C/T]TTTAAATAGGAGAAT | 9972 |
| rs76429953 | snp | A/T | 0.15665 | 0.231917 | intron-variant | NUP153 | GRCh38.p7 | 6:17650321 | ACGTGTTAACTGAAC[A/T]ATCAGCCAGAAAAGG | 9972 |
| rs76430044 | snp | A/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17699203 | AATTTTTTTTTTTTT[A/T]AAATACAAGCTAGCT | 9972 |
| rs76517776 | snp | A/T | 0.173965 | 0.238157 | intron-variant | NUP153 | GRCh38.p7 | 6:17661511 | ATTAGGTTTTCAGCA[A/T]GCATTTTGAAAGAAC | 9972 |
| rs76573419 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17640392 | AGGGCAAGCCCATCC[A/C]CTGCATGAAATATCT | 9972 |
| rs76591770 | snp | A/C | 0.00993419 | 0.0697739 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706682 | TCTATGGAGATCTCC[A/C]GCAGAGGACAGCACG | 9972 |
| rs76592223 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | NUP153 | GRCh38.p7 | 6:17658698 | GGGTGTCTCACAAGC[C/T]GAGTGAAAATTTAAA | 9972 |
| rs76597246 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | NUP153 | GRCh38.p7 | 6:17646727 | GTTCCAATTTCTGAA[G/T]GCCATTTTCTTTCCT | 9972 |
| rs76601967 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NUP153 | GRCh38.p7 | 6:17630211 | TGGAAGTGGGAGGGA[A/G]GGTGGAAAAAGAGAC | 9972 |
| rs76606316 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17621135 | AACATAACTAATCAT[A/C]AGGGAAATCAAATCA | 9972 |
| rs76643622 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | NUP153 | GRCh38.p7 | 6:17657192 | GTGTGACTTTGCTGT[A/G]CTGAACAGTTTATTA | 9972 |
| rs76656502 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NUP153 | GRCh38.p7 | 6:17639655 | ACATGTCTATGTGTA[C/T]CATCAGGTTTACTTA | 9972 |
| rs76665434 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17689417 | AACAAATAAACAAAC[-/A]AAAAAAAACAATCCA | 9972 |
| rs76736580 | snp | A/C/T | 0.0315239 | 0.122042 | intron-variant | NUP153 | GRCh38.p7 | 6:17668776 | TGAACCTGGGAGCCA[A/C/T]AGGTCGCAGTGAGTC | 9972 |
| rs76798160 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17626935 | TGGCATGTTACAAGT[A/T]CTGCTGCTTTTATAA | 9972 |
| rs76802122 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17691434 | CCATTTCCATACTTC[A/C]AGACTTGAAAGTGTT | 9972 |
| rs76852012 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | NUP153 | GRCh38.p7 | 6:17684324 | CACTTGTTGCTTCAC[C/T]TTGCCCTTTTATGTT | 9972 |
| rs76865694 | snp | C/T | 0.16911 | 0.236552 | intron-variant | NUP153 | GRCh38.p7 | 6:17703331 | CACATGCAGAAGTCA[C/T]AGGTACTGGGTGACT | 9972 |
| rs76905413 | snp | C/G | 0.00159617 | 0.0282053 | downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17614640 | GCGGGAGAACTGGGG[C/G]GGGGGGGGAGTGCAG | 9972 |
| rs76907216 | snp | C/T | 0.173643 | 0.238054 | intron-variant | NUP153 | GRCh38.p7 | 6:17627601 | CCCAGGTTCAAGAGA[C/T]TCTTGTGCTTCAGCC | 9972 |
| rs76940290 | in-del | -/AAAA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17623373 | AAAAAAAAAAAAAAA[-/AAAA]CCTTTTAAAACAATT | 9972 |
| rs77013859 | snp | A/C | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17634114 | TTCATGAACCCCCCC[A/C]ATTACTCCCACCACT | 9972 |
| rs77018004 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | NUP153 | GRCh38.p7 | 6:17681737 | GAAATGTTTCCCAGG[A/G]TATCAAGTATTCCAA | 9972 |
| rs77046899 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17633685 | GTGGGAGAGGTGGCA[A/C]AGGAAGAACGGCTTG | 9972 |
| rs77079186 | snp | C/T | 0.174932 | 0.238463 | intron-variant | NUP153 | GRCh38.p7 | 6:17658710 | AGCTGAGTGAAAATT[C/T]AAAAAATTGTTTTGA | 9972 |
| rs77082364 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17692954 | TATACATGTGGAGCA[C/T]TAGTCAGACAATATT | 9972 |
| rs77141145 | snp | C/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17665988 | GGCAACTCACCTGGC[C/T]TTTTTTTTTTTTTTT | 9972 |
| rs77146855 | snp | A/G | 0.030665 | 0.119967 | intron-variant | NUP153 | GRCh38.p7 | 6:17664343 | CATGCTAAAACCACT[A/G]AATTGAAAACTTTAA | 9972 |
| rs77242493 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17634860 | TCAGCAGGGGAGGCG[C/G]GGGTGGTCCAATCTT | 9972 |
| rs77246007 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NUP153 | GRCh38.p7 | 6:17675147 | AACAGCAAAAGACTC[C/T]TGTCTCAGAAAAAAA | 9972 |
| rs77275907 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17682928 | CTCAAAAAAGAAGAA[A/G]AAAAAAAAAAAAAAC | 9972 |
| rs77276901 | snp | A/C | 0.00112532 | 0.0236938 | missense | NUP153 | GRCh38.p7 | 6:17625836 | TGTGGTTGTGGCTCC[A/C]AAGCCGAAACCAGAG | 9972 |
| rs77284943 | snp | A/G | 0.000932981 | 0.0215782 | intron-variant | NUP153 | GRCh38.p7 | 6:17637776 | GATGCGAAACCTACA[A/G]TGAACGAAGGAGAGA | 9972 |
| rs77408899 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17635104 | CACAGCTTGGCTTAT[C/T]TTTTTTTTTTTTTTT | 9972 |
| rs77416157 | snp | C/T | 0.173965 | 0.238157 | intron-variant | NUP153 | GRCh38.p7 | 6:17674265 | TTATATACATAATAA[C/T]ATGTTTTGTTAAAGC | 9972 |
| rs77425298 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17626932 | ATTTGGCATGTTACA[A/G]GTTCTGCTGCTTTTA | 9972 |
| rs77437282 | snp | C/G | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17617384 | GCAGTAGGGAAAGAA[C/G]AGAAGCAATTGCATT | 9972 |
| rs77458411 | snp | A/G | 0.172028 | 0.23753 | intron-variant | NUP153 | GRCh38.p7 | 6:17657491 | ATCACTTGAACTCAG[A/G]AGGTGGAGGGTGCCA | 9972 |
| rs77463409 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | NUP153 | GRCh38.p7 | 6:17697160 | TAAATTTAAGTTCAA[A/G]GATTAAAGGAGTGAA | 9972 |
| rs77498387 | snp | A/C | 0.0715223 | 0.175059 | intron-variant | NUP153 | GRCh38.p7 | 6:17702812 | TCATATTTGCTTCTA[A/C]AATTCTTAAGAGTTA | 9972 |
| rs77508340 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NUP153 | GRCh38.p7 | 6:17694075 | TTTATTGATAGCACT[A/G]AATCACCATATTATA | 9972 |
| rs77678701 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | NUP153 | GRCh38.p7 | 6:17645658 | ACAATCTACATGGGC[A/C]TGCATAACCTTTATA | 9972 |
| rs77790355 | snp | C/T | 0.0329622 | 0.124075 | upstream-variant-2KB, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707966 | ACTATAAATCTTTTT[C/T]TTTCTTTCTTTCTTT | 9972 |
| rs77801592 | snp | A/G | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17618954 | AGGAAAGGAAGGATT[A/G]GGGGACAAAATCTTC | 9972 |
| rs77845359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17635073 | CCATCCTAAGCCACA[C/T]GCAGCCCACAGGTTG | 9972 |
| rs77917493 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17686211 | AGCCTTAGGTAAGTC[C/T]TTCTGGAAGTATTCC | 9972 |
| rs77941672 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17683485 | TGACCAAATGCATTG[C/T]TAATGAGCAGTGTTG | 9972 |
| rs77945401 | snp | C/T | 0.172028 | 0.23753 | intron-variant | NUP153 | GRCh38.p7 | 6:17630619 | AGTGAGCCAAGATTG[C/T]GCCACAGCACTCCAG | 9972 |
| rs77948096 | snp | A/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17697083 | CTCAAAAAAAAAAAA[A/T]TTAATCTTAAAAAAT | 9972 |
| rs77999365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17663037 | CAAGTGACAACATGT[A/G]AATAGAATCTGTAGA | 9972 |
| rs78026797 | snp | C/T | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17700003 | TAATATAATACCACA[C/T]AAAACCTCTCATCAC | 9972 |
| rs78030216 | snp | C/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17665987 | AGGCAACTCACCTGG[C/T]TTTTTTTTTTTTTTT | 9972 |
| rs78074635 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17640740 | TCCCACCTTAGCCTC[G/T]CAAGTAGCCAGGAAC | 9972 |
| rs78111257 | snp | A/C | 0.000906413 | 0.0212693 | intron-variant, downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17632324 | AAACAAACAAACAAA[A/C]AAACAAACAAACAAA | 9972 |
| rs78111458 | snp | G/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17640395 | GCAAGCCCATCCACT[G/T]CATGAAATATCTGAT | 9972 |
| rs78190612 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | NUP153 | GRCh38.p7 | 6:17666862 | CAGCTGTGAACAACA[C/T]TGGTTTCCAGGGCAA | 9972 |
| rs78256790 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17649570 | CTTACGATATACTAC[A/T]GTTGTWSTAATATGA | 9972 |
| rs78260507 | snp | G/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17677748 | TTTTTTTTTTTTTTT[G/T]TGAGACAGTCTCACT | 9972 |
| rs78321985 | snp | A/C/T | 0.0118342 | 0.0760079 | intron-variant | NUP153 | GRCh38.p7 | 6:17640086 | TTTTTTTAAATTTAA[A/C/T]AACATTATGCCAAAT | 9972 |
| rs78329297 | snp | A/G | 0.173643 | 0.238054 | intron-variant | NUP153 | GRCh38.p7 | 6:17623062 | TTGAACCCGGGAAGC[A/G]GAGGTTGCAGTGAGC | 9972 |
| rs78329450 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17683593 | ATAGATGTGTTGTCA[C/T]CCAGGTTTTGTTGTT | 9972 |
| rs78331228 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | NUP153 | GRCh38.p7 | 6:17635646 | TCAAGCAATATACCC[A/G]CCTTGGCTTCTCCCA | 9972 |
| rs78339042 | snp | G/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17660590 | TTAATATACATATAA[G/T]AAATTATATATATAT | 9972 |
| rs78377903 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NUP153 | GRCh38.p7 | 6:17648244 | TGATCCCAGCACTTT[A/G]GGAAGCCATGACAGA | 9972 |
| rs78424454 | snp | C/G | 0.0718919 | 0.175435 | intron-variant | NUP153 | GRCh38.p7 | 6:17635740 | CCTAATCTATCTTCC[C/G]GTCTCCAAATTTTTT | 9972 |
| rs78425522 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | NUP153 | GRCh38.p7 | 6:17676872 | ACAAGGGAGTGTCCA[C/G]TGAGCAGAGAGGCTG | 9972 |
| rs78429165 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17629543 | ATGTGTCAAAGCCTA[A/C]AAAAATATAAAAGAC | 9972 |
| rs78430158 | snp | A/C | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17636334 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 9972 |
| rs78432376 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17663741 | TTGTTAGAAATGAGA[C/T]AAAATATAACTAAAG | 9972 |
| rs78439469 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17704306 | CAAAAAAAAAAAAAA[A/G]AGCTGTGATAACTTC | 9972 |
| rs78442076 | snp | A/G | 0.172674 | 0.237741 | intron-variant | NUP153 | GRCh38.p7 | 6:17617784 | TAGGAGGTCGAGGAC[A/G]CAGTGTGCCCTGACT | 9972 |
| rs78464598 | snp | A/G | 0.173965 | 0.238157 | intron-variant | NUP153 | GRCh38.p7 | 6:17675889 | AATTCAAATCACTGG[A/G]GCATCCCATAATAAG | 9972 |
| rs78470470 | snp | A/G | 0.172997 | 0.237846 | intron-variant | NUP153 | GRCh38.p7 | 6:17702052 | CTGGTTTGCCCATGG[A/G]CTCAAGTTTTTTGTA | 9972 |
| rs78486364 | snp | A/G | 0.174288 | 0.23826 | intron-variant | NUP153 | GRCh38.p7 | 6:17658417 | AAACAAAACAAAACA[A/G]AACAAAACACCCAAA | 9972 |
| rs78512215 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17694324 | CCCTTTTCTGGTCCA[C/T]TTATGTACTGTTTTA | 9972 |
| rs78539506 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NUP153 | GRCh38.p7 | 6:17683812 | ATCTTCTTCCAACGG[C/T]GGGCCATGTTTCATC | 9972 |
| rs78541395 | snp | C/T | 0.0142359 | 0.0831582 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17628773 | TGAAGAATTCTCATC[C/T]TTGGTTTGCTCTGAA | 9972 |
| rs78649343 | snp | A/C | 0.168785 | 0.236441 | intron-variant | NUP153 | GRCh38.p7 | 6:17700200 | AAAAAAAAAGATCCT[A/C]AATCAAACAGTTCTA | 9972 |
| rs78670558 | in-del | -/AGA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17678375 | AAAAAAAAAAAAAAA[-/AGA]TTCTGGCCTTTGGTT | 9972 |
| rs78697785 | snp | C/T | 0.168785 | 0.236441 | intron-variant | NUP153 | GRCh38.p7 | 6:17619088 | GATGTATCAGAACAA[C/T]GGAGGCAAAAGAGGA | 9972 |
| rs78726608 | snp | A/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17678962 | TAAAAAAAAAAAAAA[A/T]ATAAGTCTTAACAAA | 9972 |
| rs78734391 | in-del | -/T | 0.173965 | 0.238157 | intron-variant | NUP153 | GRCh38.p7 | 6:17670741 | GATTTTTAAAAAATA[-/T]TTTATGTATCTATAG | 9972 |
| rs78741611 | snp | A/G | 0.173965 | 0.238157 | intron-variant | NUP153 | GRCh38.p7 | 6:17669853 | AATCCCAGCACTTTG[A/G]GAGGTGTGAGGAGGG | 9972 |
| rs78784624 | snp | A/G | 0.02016 | 0.0983543 | downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17614810 | ACTTTTAAAAAAGGT[A/G]CCTAAGTCGATATGC | 9972 |
| rs78792225 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17657052 | GCCACTGATTTCTTT[A/C]ATTCTTTGGAGCATG | 9972 |
| rs78817738 | snp | C/T | 0.174288 | 0.23826 | intron-variant | NUP153 | GRCh38.p7 | 6:17672658 | ATAACACTAGAACAA[C/T]TGCACACCCATATGT | 9972 |
| rs78976710 | snp | A/C | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17698737 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 9972 |
| rs79019804 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP153 | GRCh38.p7 | 6:17698302 | TCAGATTATTGAAAC[C/T]AGATTCAGGTCCAAG | 9972 |
| rs79237983 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NUP153 | GRCh38.p7 | 6:17660656 | TCAAGAGAAAACTCA[A/G]ATGTCCAAAAAACAC | 9972 |
| rs79240416 | snp | A/G | 0.174288 | 0.23826 | intron-variant | NUP153 | GRCh38.p7 | 6:17660596 | TACATATAAGAAATT[A/G]TATATATATCCCTAC | 9972 |
| rs79278031 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | NUP153 | GRCh38.p7 | 6:17655040 | CAAGACAAGAGCAAG[A/C]AATTAAGTCTCTCCA | 9972 |
| rs79295215 | snp | A/C | 0.173965 | 0.238157 | intron-variant | NUP153 | GRCh38.p7 | 6:17679914 | AGGAATGCGAAATAA[A/C]TGATTTACAGCATTG | 9972 |
| rs79319306 | in-del | -/TTTT | | | intron-variant | NUP153 | GRCh38.p7 | 6:17677746 | CCTTTTTTTTTTTTT[-/TTTT]GAGACAGTCTCACTC | 9972 |
| rs79340119 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17708363 | TTTTTTTTTTTTTTT[G/T]AGACGAAGTTTTTTC | 9972 |
| rs79354825 | snp | A/G | 0.170557 | 0.237469 | intron-variant | NUP153 | GRCh38.p7 | 6:17618011 | AATTAAGTGTAGCTC[A/G]ATATTCACAAAATAC | 9972 |
| rs79376042 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | NUP153 | GRCh38.p7 | 6:17693156 | AAGTTTTTCTTTACT[A/C]ACTTTTCTTAAAATT | 9972 |
| rs79385238 | snp | A/C | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17662510 | CAGGAAATGCATGTG[A/C]TGAGCCTGAATTATC | 9972 |
| rs79386133 | snp | A/C/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17634115 | TCATGAACCCCCCCC[A/C/T]TTACTCCCACCACTA | 9972 |
| rs79400240 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17643494 | CATCCCCACCAAAAA[A/T]AACCACCACTCGTAC | 9972 |
| rs79437413 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17701974 | CACCCCACCCCACCC[C/T]CATCCCGGGACAAAA | 9972 |
| rs79470665 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NUP153 | GRCh38.p7 | 6:17697876 | TTCTTTTCTTATAAA[A/C]CTTTTCACAGGAATA | 9972 |
| rs79483981 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NUP153 | GRCh38.p7 | 6:17658951 | TTTCAGAATCCCAGC[A/G]AAACCACTACATCTG | 9972 |
| rs79553128 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NUP153 | GRCh38.p7 | 6:17672248 | GGGGGAGGGATGGTC[A/G]AAAGTCCAGAAATAA | 9972 |
| rs79668409 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | NUP153 | GRCh38.p7 | 6:17648871 | TAAAAACATGAAACA[C/T]TGAGTGCACTCCTAC | 9972 |
| rs79715649 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17704291 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 9972 |
| rs79841096 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | NUP153 | GRCh38.p7 | 6:17689323 | ATCCAGGAGACAGAG[G/T]TTACAGGGAGCCCAG | 9972 |
| rs79996658 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | NUP153 | GRCh38.p7 | 6:17648603 | GCCTGGGTGACAGGG[A/C]GAGACTCAAGCTGAA | 9972 |
| rs80043733 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17701844 | TCTCGGGGGGGGGGG[A/G]AAAAAAGCTAAATGC | 9972 |
| rs80068577 | snp | C/T | 0.173643 | 0.238054 | intron-variant | NUP153 | GRCh38.p7 | 6:17670935 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 9972 |
| rs80084912 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | NUP153 | GRCh38.p7 | 6:17627654 | GTGTGAGCTACGGCA[C/T]CCGGATTGTCTTTAT | 9972 |
| rs80114459 | snp | C/T | 0.174932 | 0.238463 | intron-variant | NUP153 | GRCh38.p7 | 6:17620231 | ATCATACTATCTGAC[C/T]TCAAAATATACTACA | 9972 |
| rs80132069 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NUP153 | GRCh38.p7 | 6:17678569 | ATTCCTTGATTAATG[C/T]TCTCCTCAGTAAGTA | 9972 |
| rs80161593 | snp | G/T | 0.030665 | 0.119967 | intron-variant | NUP153 | GRCh38.p7 | 6:17619153 | AAGAGCAAAGATCAA[G/T]ACTTCAGGCAACTCT | 9972 |
| rs80190785 | in-del | -/AA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17701238 | CTAAAAAAAAAAAAA[-/AA]GCTAAATGCGCCAGG | 9972 |
| rs80294097 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NUP153 | GRCh38.p7 | 6:17642492 | AGGGAAATGCAAATC[A/G]AAACTACAACAAAGT | 9972 |
| rs80307851 | snp | C/T | 0.174288 | 0.23826 | intron-variant | NUP153 | GRCh38.p7 | 6:17640761 | AGCCAGGAACACAGG[C/T]GCATGCCACCACATC | 9972 |
| rs80322027 | snp | A/G | 0.00120251 | 0.024491 | intron-variant | NUP153 | GRCh38.p7 | 6:17662098 | TACACACATATTTAC[A/G]TTTGCTTATTTGTTG | 9972 |
| rs80322909 | snp | G/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17665869 | TTTTTGGTTTTTTTT[G/T]GTAGAGACAGGGTCT | 9972 |
| rs111144833 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17660591 | TAATATACATATAAG[A/G]AATTATATATATATC | 9972 |
| rs111266316 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | NUP153 | GRCh38.p7 | 6:17622289 | ACCCTGTCTCTACAA[A/C]CCACGCCCCCCTCCA | 9972 |
| rs111270697 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17623628 | GTAGTTAAAAACAAC[C/T]GAAACATATGTCAAC | 9972 |
| rs111367229 | in-del | -/A | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17619670 | AATTAAAGAGAACAC[-/A]AAACAAATGTAAAGA | 9972 |
| rs111369102 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NUP153 | GRCh38.p7 | 6:17630280 | ATTTTTAAATCTTGT[A/G]AATAAATGTGTTATT | 9972 |
| rs111380757 | in-del | -/AG | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17687308 | TCATAACCAGGAAAC[-/AG]AGGGGGGAAAACAGA | 9972 |
| rs111408858 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706829 | CTGTGCGCACAGCGC[C/G]CGCCCCGCCGCCGTC | 9972 |
| rs111475035 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NUP153 | GRCh38.p7 | 6:17643244 | CTGAGACGCCTAGGC[A/G]GCCAGATCACCTGAG | 9972 |
| rs111525686 | snp | C/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17626452 | TCTAACTGGATACTG[C/T]AGTTGAATAGCAAGC | 9972 |
| rs111530122 | snp | A/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17648161 | TAAGAATATGTTCAG[A/T]AGAAGTGAAAGCAAG | 9972 |
| rs111613792 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17674365 | ATTTCTTGAGATACA[C/T]GCACATATCTAATAC | 9972 |
| rs111630805 | in-del | -/TC | 0.0209421 | 0.100162 | intron-variant | NUP153 | GRCh38.p7 | 6:17649038 | AACAGCATTTCCATT[-/TC]TCTGTTTACTATGTT | 9972 |
| rs111640267 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17658159 | AATCCCAGCACTCTG[A/G]GAGGCTGAGGCAGGC | 9972 |
| rs111660832 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | NUP153 | GRCh38.p7 | 6:17642241 | GACTTCATCAAAATT[A/T]AATACCTCTGTCCAT | 9972 |
| rs111690421 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | NUP153 | GRCh38.p7 | 6:17646965 | TTCCACTATGTTGGT[C/T]AGGCTGGTCTCGAAC | 9972 |
| rs111712045 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17648643 | AAATATTTAAAAAAA[A/T]ATTTTTTTAATTAGC | 9972 |
| rs111779990 | snp | G/T | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17704995 | TCTCCTGACCTCGGT[G/T]ATCCACCCGCCTCGG | 9972 |
| rs111852985 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17683920 | TCAATGTTGGAAGTG[A/G]GGTCATGGGAAGTCT | 9972 |
| rs111897352 | snp | A/G | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17647391 | TCCTAGTCTTTAATT[A/G]GCTCTAGGACCAACA | 9972 |
| rs111918776 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17676597 | TCCAGTTAGAACGGA[A/G]TAAGTGGGACCAGAC | 9972 |
| rs111950827 | snp | C/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17641251 | CAATAAGAAACAAGA[C/T]GCGGCCAGGCACGGG | 9972 |
| rs111962295 | snp | C/T | 0.5 | 0 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17661752 | ACCATTGGCTGCAGG[C/T]AAACTGAAATTTGGA | 9972 |
| rs111966122 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | NUP153 | GRCh38.p7 | 6:17696003 | GACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 9972 |
| rs111998748 | in-del | -/A | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17693793 | GGAAGGCTGAGGCAG[-/A]AAAAAACGCTTGAAC | 9972 |
| rs112031543 | snp | C/T | 0.5 | 0 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17637664 | TAAACTCTCCCCAAA[C/T]CCAATTCCACTAGAA | 9972 |
| rs112052068 | in-del | -/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17640784 | CTCATTTTTTTTTTT[-/T]ACTTTTTTGTAGACA | 9972 |
| rs112101308 | snp | A/G/T | 0.000153988 | 0.00877328 | missense | NUP153 | GRCh38.p7 | 6:17637165 | TACCTGGTTTCTCAG[A/G/T]CATACAGGACACACA | 9972 |
| rs112105653 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17701845 | CTCGGGGGGGGGGGG[A/G]AAAAAGCTAAATGCA | 9972 |
| rs112239759 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706601 | AAGGGGGTGGCGGCC[C/G]CAGAGGCCGAGGAGG | 9972 |
| rs112336964 | snp | C/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17642932 | CTGTACGAAGCCACA[C/T]TGTATGATTCTACTT | 9972 |
| rs112376483 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | NUP153 | GRCh38.p7 | 6:17655513 | GGCAGGAGTGCAGTG[A/G]TACGATCTCAGCTCA | 9972 |
| rs112413803 | snp | C/T | 0.5 | 0 | missense | NUP153 | GRCh38.p7 | 6:17688615 | TAACCCTGCTAAGAA[C/T]GCCCTGTTGAGAGAA | 9972 |
| rs112445506 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NUP153 | GRCh38.p7 | 6:17646373 | CCACCACACCCGGCT[A/G]ATTTTTTGTATTTTA | 9972 |
| rs112496979 | in-del | -/T | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17655458 | ACTTTTTTTTTTTTT[-/T]AAGACAAAGTCTCAA | 9972 |
| rs112507485 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706076 | GCGGCCCAAACCACA[A/C]GTGTGCGCCGCAAGG | 9972 |
| rs112521393 | in-del | -/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17628619 | ACTTGTAAAAAAAAA[-/T]AATAATAATAATAAT | 9972 |
| rs112534108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17691457 | AAAGTGTTTAAAAGC[C/T]ATAATACAGTTTAAG | 9972 |
| rs112595829 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17624204 | GAGAGAGCACTGGAC[C/G]TGGGGGTAACTTCCT | 9972 |
| rs112629783 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17618562 | GAAGTTAAAATCTCT[C/T]TTTTTTTTTTTTTTT | 9972 |
| rs112688487 | in-del | -/AAAAATACAA | 0.0452528 | 0.143452 | intron-variant | NUP153 | GRCh38.p7 | 6:17689223 | AACCCCATCTCTACT[-/AAAAATACAA]AAAAATACAAAAAAT | 9972 |
| rs112785312 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17665608 | ATAATTCTAAAATGG[C/T]TTCACGGATACTCTA | 9972 |
| rs112802398 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NUP153 | GRCh38.p7 | 6:17701078 | TAAAAATACAAAATT[A/G]GCTGGGAGTGGTGGC | 9972 |
| rs112855971 | in-del | -/GTT/TGT | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17649573 | CGATATACTACAGTT[-/GTT/TGT]GTACTAATATGAAAC | 9972 |
| rs112857469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17618405 | CAGCAAAGAAACAAA[A/C]TTTTAAGGAGAAAAA | 9972 |
| rs112862041 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | NUP153 | GRCh38.p7 | 6:17687744 | AAACATGTAGTGAAA[C/G]AAAAAATGTATATAC | 9972 |
| rs112864618 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706828 | CCTGTGCGCACAGCG[C/G]CCGCCCCGCCGCCGT | 9972 |
| rs112931496 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17631244 | TTTCAATCATATAGA[C/T]ATATACGCTGTGCAG | 9972 |
| rs112957894 | snp | C/T | 9.88696e-05 | 0.00703029 | missense | NUP153 | GRCh38.p7 | 6:17665325 | AAACACTTCGATTTG[C/T]TGCTATGGAAACTGG | 9972 |
| rs112989746 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17629661 | GCCTACTTTGAAGAG[G/T]ATTACCAGCAGCTGT | 9972 |
| rs113067519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17634329 | TTCATTTCAGGCCAT[C/G]TTGAGTGAACACACT | 9972 |
| rs113118202 | in-del | -/A | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17696019 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAACAGAA | 9972 |
| rs113164641 | in-del | -/GGAAAA | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17701843 | GTCTCGGGGGGGGGG[-/GGAAAA]AAGCTAAATGCAGGA | 9972 |
| rs113259635 | snp | C/T | 0.5 | 0 | missense, intron-variant | NUP153 | GRCh38.p7 | 6:17639939 | TTTTAATTATCTTAC[C/T]AGGGCTTTTCAGAAT | 9972 |
| rs113272846 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | NUP153 | GRCh38.p7 | 6:17620713 | TCAGTTCATCAGCTA[C/T]TGTTAGTGTTAATGT | 9972 |
| rs113486869 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17676789 | TCAAGTAAAACAGAG[C/T]GGGAAGAAATCAGAA | 9972 |
| rs113513410 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17691742 | CACAGCGAGACTCCA[A/G]CTCAGAAAAACAAAA | 9972 |
| rs113681374 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17703515 | ATAAAACATGCCATG[C/T]CATGAAGCTTGCTTC | 9972 |
| rs113681670 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17631944 | GCACTCCGGCCTGGG[C/T]GACAGAGCAAGACAC | 9972 |
| rs113691932 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17634478 | GTCTCACTCTGTTGC[A/C]CAGGGTGGAGTAGAG | 9972 |
| rs113716582 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | NUP153 | GRCh38.p7 | 6:17634944 | AATATACTAACACTA[A/G]CAACAGCTGATGAGC | 9972 |
| rs113730559 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NUP153 | GRCh38.p7 | 6:17699476 | TGACAGGGCGAGACT[A/C]GTCTCAAAAAAAAAA | 9972 |
| rs113794477 | in-del | -/C | 0.0722614 | 0.17581 | intron-variant | NUP153 | GRCh38.p7 | 6:17683718 | CACCAGTTGCATTAA[-/C]CCCCTAATAAGAGAG | 9972 |
| rs113797231 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | NUP153 | GRCh38.p7 | 6:17671460 | GCTGGAACGTATTTT[A/C]AATTATGAACTCAAT | 9972 |
| rs113825225 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NUP153 | GRCh38.p7 | 6:17620071 | CCATTATACTCCAGC[C/T]TGGGCAACAGAGCAA | 9972 |
| rs113852994 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | NUP153 | GRCh38.p7 | 6:17631862 | GTCCCAGCTACTCGG[C/G]AGGCTGAAGCAGGAG | 9972 |
| rs113876976 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | NUP153 | GRCh38.p7 | 6:17677155 | ACAGGGGAGACAGAG[C/G]TTGGAGGCTAAGGCC | 9972 |
| rs113878152 | snp | A/G | 0.5 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17676334 | CCACTGTTACCACAT[A/G]CTAAACCATACTAAA | 9972 |
| rs113888954 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | NUP153 | GRCh38.p7 | 6:17655022 | GTAAGTGGCAGGATT[A/C]TACAAGACAAGAGCA | 9972 |
| rs113902198 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NUP153 | GRCh38.p7 | 6:17666190 | TCCCTGAATTACTGT[C/T]CATATTTTTTGAGCT | 9972 |
| rs113930368 | snp | A/T | 0.121353 | 0.21436 | intron-variant | NUP153 | GRCh38.p7 | 6:17669243 | ACCACCACACCCGGC[A/T]AATTTTTGTATGAAC | 9972 |
| rs113993443 | snp | A/T | 0.054767 | 0.156154 | intron-variant | NUP153 | GRCh38.p7 | 6:17648644 | AATATTTAAAAAAAA[A/T]TTTTTTTAATTAGCT | 9972 |
| rs114009444 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17634979 | AAACAAATTAAAAAA[A/T]AAAAAAAAAAAATAA | 9972 |
| rs114017367 | snp | A/C | 0.0532157 | 0.154195 | intron-variant | NUP153 | GRCh38.p7 | 6:17680731 | AACATAAAAAGTACT[A/C]CAACCCCCAGTGAAA | 9972 |
| rs114055481 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NUP153 | GRCh38.p7 | 6:17691205 | GTAATTATTCTTCCA[C/T]GTATTGTGCAAATTT | 9972 |
| rs114176609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17626691 | TTATCACTAGACTGT[A/T]TTAATTATTATAACT | 9972 |
| rs114178430 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NUP153 | GRCh38.p7 | 6:17657977 | ATGTTAGACAAAAGA[C/T]AAGTTCGAGCGATTT | 9972 |
| rs114178562 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | NUP153 | GRCh38.p7 | 6:17636056 | TGAAGATTCTAGGCC[A/G]GGCATGGTGGCTCAC | 9972 |
| rs114182919 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17676959 | AAAACAGAGATACTA[A/G]ACAGTGTACCGTGCT | 9972 |
| rs114190006 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NUP153 | GRCh38.p7 | 6:17683588 | TGTAAATAGATGTGT[C/T]GTCATCCAGGTTTTG | 9972 |
| rs114193832 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NUP153 | GRCh38.p7 | 6:17660453 | AAAAGAGCAATATAT[A/G]GACAGAAAGGTTAAT | 9972 |
| rs114254315 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | NUP153 | GRCh38.p7 | 6:17663095 | CTGGGTTTGACCACT[A/G/T]CTATGCATTATGTAA | 9972 |
| rs114322474 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | NUP153 | GRCh38.p7 | 6:17627203 | TGGAAGAATGGTTAA[A/G]AGTGTCTACCATAGC | 9972 |
| rs114434841 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17667999 | ACACACAATAGATTT[C/G]ACAAAATTTTGGTTA | 9972 |
| rs114474650 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | NUP153 | GRCh38.p7 | 6:17670363 | TGTATATAAATACAA[A/C]AGACTTTTGTATATT | 9972 |
| rs114476312 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17643487 | CCCCAACCATCCCCA[C/T]CAAAAATAACCACCA | 9972 |
| rs114498339 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NUP153 | GRCh38.p7 | 6:17685815 | ATGTACTTACTATAC[C/T]TTTTATCACTAGAGT | 9972 |
| rs114563011 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17673495 | TATTAATAAGAAAAT[A/G]ACCCAATTTTTAAAT | 9972 |
| rs114565079 | snp | A/C | 0.179744 | 0.239925 | intron-variant | NUP153 | GRCh38.p7 | 6:17701957 | AAGCATACTACCCAC[A/C]CCACCCCACCCCACC | 9972 |
| rs114571095 | snp | A/C/G | 0.0162488 | 0.0887351 | intron-variant | NUP153 | GRCh38.p7 | 6:17645646 | AAATTATGTATCACA[A/C/G]TCTACATGGGCCTGC | 9972 |
| rs114577588 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | NUP153 | GRCh38.p7 | 6:17628161 | TTAAGGTGCTATGTC[A/G]TTTTTTTCCCCAGGA | 9972 |
| rs114582845 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17619510 | GGAACAGGTTAAAAG[A/T]CCCTGTGAGAAAAGT | 9972 |
| rs114639595 | snp | A/G | 0.17332 | 0.23795 | intron-variant | NUP153 | GRCh38.p7 | 6:17635098 | AGGTTGCACAGCTTG[A/G]CTTATCTTTTTTTTT | 9972 |
| rs114688263 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17678539 | AACTATATTAAACGC[C/T]GAATGATTACTTGCA | 9972 |
| rs114710818 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NUP153 | GRCh38.p7 | 6:17673138 | CTTTGGGAGGCCAAC[A/G]CGGGTGAATCACAAG | 9972 |
| rs114731679 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUP153 | GRCh38.p7 | 6:17626897 | CCAGCAACAAGTATG[C/T]CTTTTGTGTTCTTTT | 9972 |
| rs114812432 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NUP153 | GRCh38.p7 | 6:17657801 | TGGTGCAAACGTAAT[C/T]GCAGTTTTGCATTAT | 9972 |
| rs114817846 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NUP153 | GRCh38.p7 | 6:17670971 | ACGTCCAACTGCAAC[C/T]GGCTAATTTTTGTAT | 9972 |
| rs114828656 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NUP153 | GRCh38.p7 | 6:17649502 | TGGGGAACCTAACTG[C/T]CTTCTGTACCAATTT | 9972 |
| rs114885624 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17630831 | AGAGAAAAGAGAAGA[C/G]AGCAAGCATTATACT | 9972 |
| rs114904693 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NUP153 | GRCh38.p7 | 6:17638802 | TTGAGGCTTGCCTAC[C/T]ACTTGGTTAATTCCA | 9972 |
| rs114937587 | snp | A/G | 0.0119135 | 0.0762987 | intron-variant | NUP153 | GRCh38.p7 | 6:17667665 | GTTGCAGTGAGCTGC[A/G]ACTGTGCCACTGCAC | 9972 |
| rs114940914 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17705213 | CCTTTTGCTACACTT[C/T]TGTTTTTCAACAAAT | 9972 |
| rs114980523 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17654276 | ATGCCAACTCCTTAA[A/G]GCACACACTTGTCCA | 9972 |
| rs114996770 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NUP153 | GRCh38.p7 | 6:17641130 | TATATTTTTAAGGGG[C/T]GATTTCTATTTACAG | 9972 |
| rs115075587 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NUP153 | GRCh38.p7 | 6:17669801 | GCATGCACCATTTTA[A/G]AGAAAGTATGGGCCG | 9972 |
| rs115093410 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17668607 | CGGCACTTTGGGAGG[C/T]CACGGCAGGCAGATC | 9972 |
| rs115095834 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17643243 | TCTGAGACGCCTAGG[C/T]GGCCAGATCACCTGA | 9972 |
| rs115215328 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17622797 | ATAATCAGCATTTCC[A/G]TAATCAGAATCCTGA | 9972 |
| rs115314054 | snp | A/G | 0.039522 | 0.134904 | intron-variant | NUP153 | GRCh38.p7 | 6:17646511 | GCGCCTGGCCCAAAT[A/G]TAGAGGTTATTTTTA | 9972 |
| rs115324600 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NUP153 | GRCh38.p7 | 6:17618022 | GCTCGATATTCACAA[A/G]ATACCGAGCGCTCCA | 9972 |
| rs115341329 | snp | C/G | 0.0722614 | 0.17581 | intron-variant | NUP153 | GRCh38.p7 | 6:17685272 | CAGTCAACTAGTTGG[C/G]AGCGGTGGCTCACGC | 9972 |
| rs115372719 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17630996 | CTACAGGTAGAGAAC[A/C]GTATAAAAAGGGGAG | 9972 |
| rs115381017 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17644031 | ATTAATTTCTATTAC[A/G]TAAGGCTGTGTTAGC | 9972 |
| rs115394314 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17692586 | TGGACCTGGAACCAG[C/T]ATGAAGGAACAAACA | 9972 |
| rs115418136 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NUP153 | GRCh38.p7 | 6:17674437 | TAAATGAAAAAAATA[C/T]AACCCATAGCTGTTG | 9972 |
| rs115462246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17698975 | TAACATGTTTGAAAA[C/T]TGGGAGTAAGAGTTT | 9972 |
| rs115491643 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NUP153 | GRCh38.p7 | 6:17657259 | CTAAAAATTATTTTC[C/T]GGCTAGGCACAGTGA | 9972 |
| rs115521311 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17670507 | ATTACAGGAATAATA[A/C]CCTTTCCAATCTGCA | 9972 |
| rs115661537 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17704493 | TCTACAGACGGATTA[G/T]GTTAAATGGCCAGGC | 9972 |
| rs115695916 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17634278 | ATTAACTGTTCAAAA[C/G]CTTTATTCCTGCCAC | 9972 |
| rs115842483 | snp | A/G | 0.491157 | 0.065903 | intron-variant | NUP153 | GRCh38.p7 | 6:17682925 | TGTCTCAAAAAAGAA[A/G]AAAAAAAAAAAAAAA | 9972 |
| rs115897149 | snp | C/G | 0.0418186 | 0.138422 | upstream-variant-2KB, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17708399 | GTTTTGCCCAGGCTG[C/G]AGTGCAATGGCGCAA | 9972 |
| rs115898399 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NUP153 | GRCh38.p7 | 6:17656346 | GGGTGAAGAATCCTG[C/T]GACACAAAATTGGCA | 9972 |
| rs115900163 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17699190 | AATAGCTACAAATAA[A/T]TTTTTTTTTTTTTAA | 9972 |
| rs115918610 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | NUP153 | GRCh38.p7 | 6:17668829 | GTCTGGATGACAGAG[C/T]GAGACTGAGACTCAA | 9972 |
| rs115920718 | snp | C/T | 0.00459988 | 0.0477366 | intron-variant | NUP153 | GRCh38.p7 | 6:17616702 | AAGCCGAACCTGCAA[C/T]AGTTAAAGCAGAAAT | 9972 |
| rs115927757 | snp | G/T | 0.02016 | 0.0983543 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706545 | CAGGAACCGCGAGGT[G/T]GCGAGCAGGAGCGGA | 9972 |
| rs115934249 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17668550 | TCCAAGTAGAAGAAT[A/G]CTATTTTTCAGGGTC | 9972 |
| rs115995308 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NUP153 | GRCh38.p7 | 6:17645448 | ACAGGCTCACACCAC[C/T]ACCTGGTTATTTCTT | 9972 |
| rs116024316 | snp | A/G | 0.039522 | 0.134904 | intron-variant | NUP153 | GRCh38.p7 | 6:17641582 | AAAAGGCCAGGCAGC[A/G]GTGGCTCACGCCTGT | 9972 |
| rs116024884 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NUP153 | GRCh38.p7 | 6:17682253 | CTTAAAAAAAAATTG[C/T]TAACAAATAACAATC | 9972 |
| rs116059938 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NUP153 | GRCh38.p7 | 6:17688147 | AGAAAGAAAAAAAGA[A/G]AAAGAAAAGAAAATT | 9972 |
| rs116186524 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17686312 | CGACAAGATGTGGGG[A/G]TAGAAAGCCATGATA | 9972 |
| rs116220253 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707011 | GCTGGTCGAGTCCAC[C/G]CTCTCGGCCGCGCGG | 9972 |
| rs116247141 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NUP153 | GRCh38.p7 | 6:17689475 | AAATCTTTTCTGATG[C/T]TGACATTTCACTACA | 9972 |
| rs116278792 | snp | A/C | 0.00420499 | 0.0456598 | intron-variant | NUP153 | GRCh38.p7 | 6:17637775 | CGATGCGAAACCTAC[A/C]ATGAACGAAGGAGAG | 9972 |
| rs116303927 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NUP153 | GRCh38.p7 | 6:17660922 | TGGCAGAATGGATTA[C/T]GGTAAATCTTCAAAC | 9972 |
| rs116341619 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17632990 | AGAATGTGCCAGAAA[C/T]AGACAACTGTTCATA | 9972 |
| rs116417845 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17682922 | GACTGTCTCAAAAAA[A/G]AAGAAAAAAAAAAAA | 9972 |
| rs116418264 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17645452 | GCTCACACCACCACC[C/T]GGTTATTTCTTTTTC | 9972 |
| rs116476821 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | NUP153 | GRCh38.p7 | 6:17668782 | TGGGAGCCATAGGTC[A/G]CAGTGAGTCAAGATG | 9972 |
| rs116524062 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | NUP153 | GRCh38.p7 | 6:17700883 | CCTTTCAGAAAAAGT[A/T]TACTGACCCCTGATC | 9972 |
| rs116588261 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NUP153 | GRCh38.p7 | 6:17634956 | CTAGCAACAGCTGAT[A/G]AGCTTTAAAACAAAT | 9972 |
| rs116590042 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NUP153 | GRCh38.p7 | 6:17657975 | TGATGTTAGACAAAA[A/G]ACAAGTTCGAGCGAT | 9972 |
| rs116612749 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NUP153 | GRCh38.p7 | 6:17657519 | CCATGAGCCAAGATC[A/G]TGCACTCCAGCCTGG | 9972 |
| rs116619672 | snp | A/C | 0.030665 | 0.119967 | intron-variant | NUP153 | GRCh38.p7 | 6:17620777 | AAAGTAGCCCCTGGA[A/C]GCCAAAAGATAGGAC | 9972 |
| rs116646203 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NUP153 | GRCh38.p7 | 6:17686400 | CAAACCTTTTTTTTA[C/T]TTCTTTTTTTTTTTT | 9972 |
| rs116697968 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NUP153 | GRCh38.p7 | 6:17659418 | CCCAATTACTTTTGT[A/G]CCAACCTAATAAATT | 9972 |
| rs116739115 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17698418 | GGAATATGGCGAAAC[C/T]CTGTCTCTACCGAAA | 9972 |
| rs116739909 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17628153 | TTTAACCTTTAAGGT[A/G]CTATGTCATTTTTTT | 9972 |
| rs116758840 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NUP153 | GRCh38.p7 | 6:17665834 | TGTACACAGGCGTGC[A/G]CCACCACACCCGGCT | 9972 |
| rs116759139 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NUP153 | GRCh38.p7 | 6:17617549 | CAACACCAACACAAA[C/G]ATGGTAATTATCAGT | 9972 |
| rs116820863 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | NUP153 | GRCh38.p7 | 6:17657433 | GCTAGCCTTGGTGGT[G/T]CATGCCTGTAATCCC | 9972 |
| rs116855919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17677992 | ACATTCTTAATATCT[A/G]GAAGTGGTGGTGATG | 9972 |
| rs116994251 | snp | A/G | 6.58946e-05 | 0.0057396 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17688466 | GCTCTCCTCATCGGC[A/G]TATACCAGATGGTCC | 9972 |
| rs117042400 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUP153 | GRCh38.p7 | 6:17665623 | CTTCACGGATACTCT[A/G]TATTTCATTCCAGAC | 9972 |
| rs117088663 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NUP153 | GRCh38.p7 | 6:17659528 | GCCAGGCTGGAGTAC[A/G]CTGGTGCAATCTTGG | 9972 |
| rs117232327 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NUP153 | GRCh38.p7 | 6:17653949 | CGCTATGTATGCTGA[C/T]GTATTTGGGGGTGAA | 9972 |
| rs117297819 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | NUP153 | GRCh38.p7 | 6:17658230 | GGTGAAACCCTGTCT[C/T]GCTAAAAATACAAAA | 9972 |
| rs117455901 | snp | C/G | 0.0547245 | 0.156101 | intron-variant | NUP153 | GRCh38.p7 | 6:17648608 | GGTGACAGGGCGAGA[C/G]TCAAGCTGAAAAAAT | 9972 |
| rs117725822 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17646918 | CTAATTCTGTATTTT[C/T]TTTTTTTTTTTTTTT | 9972 |
| rs117754623 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NUP153 | GRCh38.p7 | 6:17685706 | TGTAAATAAACTCAG[C/T]GTTACCAGTCATGTA | 9972 |
| rs117930902 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17691135 | CAACAGAGCAAAAGC[A/G]AGACTCCGTCTCAAG | 9972 |
| rs118024406 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NUP153 | GRCh38.p7 | 6:17632980 | ATTAAAACACAGAAT[A/G]TGCCAGAAATAGACA | 9972 |
| rs118071331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17640573 | ATATGGTTACATAAA[A/T]TACATAACAGTGACA | 9972 |
| rs118130109 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | NUP153 | GRCh38.p7 | 6:17677936 | TGTCAATTGCTAGAG[C/T]TTTCTTATTCTAACA | 9972 |
| rs118161512 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | NUP153 | GRCh38.p7 | 6:17658772 | AAACCATTTCTCAGA[C/T]TGAGACATGGGACAA | 9972 |
| rs137894438 | snp | C/T | 1.64855e-05 | 0.00287097 | missense | NUP153 | GRCh38.p7 | 6:17675701 | ATGGAAAAATTCAGA[C/T]GGCTCCGATGAAGAG | 9972 |
| rs137915465 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NUP153 | GRCh38.p7 | 6:17668610 | CACTTTGGGAGGCCA[C/T]GGCAGGCAGATCACC | 9972 |
| rs137982296 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17625566 | ACAAAGCTTAGAAAA[A/G]TTAAGTATTACACTC | 9972 |
| rs138007010 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17670863 | TTGCCCAGGCTGGAG[C/T]GCGGTGGCACAATCT | 9972 |
| rs138014616 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NUP153 | GRCh38.p7 | 6:17684913 | CATCATCTTATATGG[A/G]TGTGGCTCGTGGCAC | 9972 |
| rs138037804 | snp | A/C/G | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17645230 | CCTGGGCAACAGAGC[A/C/G]AGACTCTGTCTCAAA | 9972 |
| rs138040866 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17671105 | CACCACACCTGGTCT[A/C/G]ATCCCATTAATTTTC | 9972 |
| rs138049037 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17631164 | TCTCTTTTAAAATAA[A/G]ATAAAACAGAAAATA | 9972 |
| rs138050745 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | NUP153 | GRCh38.p7 | 6:17637543 | TTCCAGTCTGTTTAG[C/T]AGTATCTCTGGGTGA | 9972 |
| rs138123680 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUP153 | GRCh38.p7 | 6:17653740 | GGGGTAGGAGGTGAC[A/G]GCAACTGACTGAGAA | 9972 |
| rs138125720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17676014 | GATACGATACAACAG[C/T]TGAAATACAACTATT | 9972 |
| rs138191132 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17701927 | CTTAGCTCTAAACCA[C/G]AAGATAAATGTCTGA | 9972 |
| rs138192099 | snp | C/T | 0.000153988 | 0.00877328 | missense | NUP153 | GRCh38.p7 | 6:17688522 | CCTCGCTTGTGTCTG[C/T]TGAACAGCTGCATAC | 9972 |
| rs138311573 | in-del | -/GAGAGAA | 0.0387552 | 0.1337 | intron-variant | NUP153 | GRCh38.p7 | 6:17630810 | GGAGAGAAGAGAGAG[-/GAGAGAA]GAGAAAAGAGAAGAG | 9972 |
| rs138315420 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NUP153 | GRCh38.p7 | 6:17693895 | AGTGCACCACCACCG[C/T]GCCTGGCCTAATACT | 9972 |
| rs138382230 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | NUP153 | GRCh38.p7 | 6:17637644 | TGCCATGATGACCCA[A/G]CTTTTAAACTCTCCC | 9972 |
| rs138384275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17675114 | TAAGATCATGCTGCT[A/G]CACACTCAAGCCTGG | 9972 |
| rs138387850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17617366 | AGAGTTGATACTAAA[C/T]GAGCAGTAGGGAAAG | 9972 |
| rs138388837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17658169 | CTCTGGGAGGCTGAG[A/G]CAGGCAGATCATTTG | 9972 |
| rs138392855 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NUP153 | GRCh38.p7 | 6:17689280 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 9972 |
| rs138449761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17663662 | CTGGTGAATCAACAT[A/G]AAGAAATACATGGCA | 9972 |
| rs138466995 | snp | A/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17634991 | AAATAAAAAAAAAAA[A/T]TAAATCGCAAAAGAA | 9972 |
| rs138472520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17621459 | GAATCAATCTAAGTG[C/T]CCATCAACAGATGGA | 9972 |
| rs138480194 | snp | A/T | 4.9498e-05 | 0.00497459 | missense | NUP153 | GRCh38.p7 | 6:17629150 | AACCTGCAGAGGAAG[A/T]TTTGGGCAGTTCCTC | 9972 |
| rs138493266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17624910 | ATTTCTGTAAACCCA[C/T]AAGCAAATGTCAAGC | 9972 |
| rs138544307 | in-del | -/AAAACA | 0.0718919 | 0.175435 | intron-variant | NUP153 | GRCh38.p7 | 6:17621015 | AAAGAACTCAACAGC[-/AAAACA]AAAACAACCAAATAA | 9972 |
| rs138546875 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17621931 | GTAACAAAATAACAC[A/G]TCAGTTTTTAAAAAT | 9972 |
| rs138595290 | snp | G/T | 1.65056e-05 | 0.00287272 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17665259 | ACTTGTTATCTATTC[G/T]TTGATTAGTCTTCCT | 9972 |
| rs138611135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17704465 | AAAGAAAGCATGCAT[A/G]TGTAACTTCCATTCT | 9972 |
| rs138648653 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17676405 | CTTTATACTTCTGCA[A/C]GAGTACCAAATGTTT | 9972 |
| rs138661034 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NUP153 | GRCh38.p7 | 6:17631688 | ATCTGGCCTCCAGAC[C/T]AGGCGTGTTGGCTCA | 9972 |
| rs138680206 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NUP153 | GRCh38.p7 | 6:17681181 | AGGCACAAAAAGACA[A/G]CTATCACATGTTCTC | 9972 |
| rs138680691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17636264 | TGCATGCATCTGGGA[A/G]ATGGAGGTCTCAGTG | 9972 |
| rs138709791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17703301 | GTCAAAACAGGAAAT[C/T]ACAAGTCAAATGAAC | 9972 |
| rs138716490 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NUP153 | GRCh38.p7 | 6:17635281 | CACCCGGCTAATTTT[C/T]TGTATTGTTAGTAGA | 9972 |
| rs138736948 | snp | A/G | 0.225597 | 0.248806 | intron-variant | NUP153 | GRCh38.p7 | 6:17668315 | GAACTCCTGACCTCA[A/G]GTGATCCACTGGCCT | 9972 |
| rs138758002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17640459 | TAATTTTCAACTGAG[A/C]AATTATTTCATTTTT | 9972 |
| rs138778067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17644811 | TAGCCAGGGGCAGGG[C/T]GCGGTGGTTCACGCC | 9972 |
| rs138887090 | snp | A/G | 3.31104e-05 | 0.00406867 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17624769 | AAATGTTGGGGTCTG[A/G]TTAGCACCAAATGCT | 9972 |
| rs138936266 | snp | C/T | | | intron-variant | NUP153 | GRCh38.p7 | 6:17694139 | CCTTGTCTTCCTAAC[C/T]TAGAACATAAGCTCC | 9972 |
| rs138964143 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NUP153 | GRCh38.p7 | 6:17617716 | CAGGCGTAGTGGCGT[A/G]CACCTGTAATCCCAG | 9972 |
| rs138967553 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | NUP153 | GRCh38.p7 | 6:17696140 | TCAAAACAAACAAAC[A/C]AACCAACCCCAAAAA | 9972 |
| rs138969831 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17654106 | ATACGCTGCACAGTT[A/C]TTTCAACATTTCATG | 9972 |
| rs138985396 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17691838 | TTTTTTTTTTTCCAG[A/G]GACCTGTGTCATACC | 9972 |
| rs139012111 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17657931 | CTTACTACTTGCTAT[A/T]TATTTTATATTATTT | 9972 |
| rs139052300 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17682982 | AGCAACTCCTTATCC[A/G]TTCGAGTTTGAGCAT | 9972 |
| rs139092694 | in-del | -/CT | 0.0352966 | 0.128072 | intron-variant | NUP153 | GRCh38.p7 | 6:17641842 | GGAGACAGAGCGAGA[-/CT]CTGTCTCAGAAAAAA | 9972 |
| rs139122342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17705061 | CGCGCCCGACCCAAA[A/T]CTTTACTTTTAAAAA | 9972 |
| rs139137833 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17652985 | AGTGAGCTGAGACCA[C/T]GCCATTGTACTCCAG | 9972 |
| rs139138885 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | NUP153 | GRCh38.p7 | 6:17652103 | CAAATTCACCAAATA[A/T]AAGTTGGCAATTTTA | 9972 |
| rs139146297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17622897 | GCACTGTGGGAGGCC[A/G]AGGTGGGTGGATCAT | 9972 |
| rs139165043 | in-del | -/ACTA | 0.02016 | 0.0983543 | intron-variant | NUP153 | GRCh38.p7 | 6:17697829 | AGGCTATTCTATAAC[-/ACTA]ACTCAGAACTCACTT | 9972 |
| rs139174374 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NUP153 | GRCh38.p7 | 6:17654367 | GATCTTGTTGCCCGG[A/G]CCGGACTGCAGTGGT | 9972 |
| rs139182201 | in-del | -/CT | 0.0154538 | 0.0865337 | intron-variant | NUP153 | GRCh38.p7 | 6:17633893 | CACTGTCCTCACAAA[-/CT]CTCATTTACTCCAGT | 9972 |
| rs139229972 | in-del | -/C | | | frameshift-variant | NUP153 | GRCh38.p7 | 6:17625833 | GATGTGGTTGTGGCT[-/C]CCAAAGCCGAAACCA | 9972 |
| rs139274964 | snp | C/T | 0.000978842 | 0.0221012 | missense | NUP153 | GRCh38.p7 | 6:17646082 | CTGAACTACTTATAA[C/T]TGGTTCTAAAGTACT | 9972 |
| rs139301277 | snp | A/T | 9.93608e-05 | 0.00704773 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17637721 | ATAAACTACTGGGCT[A/T]GTTGCGGTGGGCTGA | 9972 |
| rs139313273 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NUP153 | GRCh38.p7 | 6:17699310 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 9972 |
| rs139344519 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NUP153 | GRCh38.p7 | 6:17686298 | AAGAGTATCCAGTGC[A/G]ACAAGATGTGGGGGT | 9972 |
| rs139423501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17664513 | GAAAAACGTTTCAAT[A/G]TGGACTGGATATTAG | 9972 |
| rs139465537 | snp | G/T | 6.59489e-05 | 0.00574196 | missense | NUP153 | GRCh38.p7 | 6:17626020 | ACAGGATTGCTGGAC[G/T]GTCCAAACACAAAGG | 9972 |
| rs139560129 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | NUP153 | GRCh38.p7 | 6:17670045 | AGGTTGTGGTGAGCC[G/T]AGACTGCACCACTCT | 9972 |
| rs139599178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17671596 | GAACACTACAAAACA[C/T]TGATGAAAAAAATTT | 9972 |
| rs139659236 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime | NUP153 | GRCh38.p7 | 6:17615572 | CATTCTTTAATCAGG[A/C]TTCCTCTATCAGAAA | 9972 |
| rs139696811 | snp | A/G | 0.195214 | 0.243923 | intron-variant | NUP153 | GRCh38.p7 | 6:17618667 | ACCTCCCGAGTTCAC[A/G]CCATTCTCCTGCCTC | 9972 |
| rs139710622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17698417 | GGGAATATGGCGAAA[C/T]CCTGTCTCTACCGAA | 9972 |
| rs139713378 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17677415 | GATCCATGCACGGGG[A/G]TAGGGGGTGGGGGAG | 9972 |
| rs139751821 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17659305 | GCAAATTTATTTCTC[A/G]TTGGCAAAAATGTGT | 9972 |
| rs139836964 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17686676 | CTGGGATTAACAAAG[C/T]TTTAAAAGTTAAGAA | 9972 |
| rs139899864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17633069 | TGATTTCTTTTAACC[C/T]TATAAATGAGCAGCT | 9972 |
| rs139958213 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | NUP153 | GRCh38.p7 | 6:17675963 | TAAAATTAATTTAAA[-/T]AAGAGCTAATTTTTT | 9972 |
| rs139990509 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | NUP153 | GRCh38.p7 | 6:17639725 | CCATTTCCTCCTCCT[A/C]CACTTGCCTATTAGA | 9972 |
| rs140045489 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17634587 | GATTACGGGCATCCA[C/T]GACCACGCCCAGCTA | 9972 |
| rs140049385 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | NUP153 | GRCh38.p7 | 6:17702599 | GAGAATAGCTTGAAC[C/G]CAGGAGGCAGAGGTT | 9972 |
| rs140065471 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17636655 | GAAACAGAAAAAACT[C/G]AAAACTAACTCCATG | 9972 |
| rs140070600 | snp | A/G | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17705026 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 9972 |
| rs140141850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17680140 | CCACTGTTTCCCTTG[C/T]GCTCAAGCACAAGCC | 9972 |
| rs140172330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17678629 | CCATTCTGTAGTGTT[C/G]TTCTATGTGCTATCT | 9972 |
| rs140178850 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NUP153 | GRCh38.p7 | 6:17639222 | AGCTGGAACTACAGG[C/T]GCATGCCAGGACGCC | 9972 |
| rs140210628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17647606 | AACTTTCAAATGGTA[C/T]AGAAGAAAATGAATA | 9972 |
| rs140217238 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17657402 | AAAAAATAAAAAAAT[-/A]AAAAAAAAAAAAATA | 9972 |
| rs140264940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17627160 | TTACAGAAAATGGAA[C/T]ATGTTGGCTTACTTT | 9972 |
| rs140265964 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17623457 | GTGGTAGGATATGAA[C/T]TGGCAGAATCCATCA | 9972 |
| rs140325264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17684732 | TTTTGGATAAAAGAC[A/G]GGGAACTCTGATTTC | 9972 |
| rs140420650 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | NUP153 | GRCh38.p7 | 6:17620740 | ATGTATCTTGTGTTT[C/G]GCCGAAGACAATAAT | 9972 |
| rs140431622 | in-del | -/AT | 0.0722614 | 0.17581 | intron-variant | NUP153 | GRCh38.p7 | 6:17700237 | TCAAATTTCAATTGC[-/AT]ATATATATAATAAGG | 9972 |
| rs140440980 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | NUP153 | GRCh38.p7 | 6:17693723 | AAACCCCAGCACTAC[C/T]AAAAATACAAAAATT | 9972 |
| rs140462471 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NUP153 | GRCh38.p7 | 6:17666458 | GGCAGAGCTTTCAAT[A/G]GGCCGAGATTGTGCC | 9972 |
| rs140496420 | snp | C/G | 0.000364226 | 0.01349 | missense | NUP153 | GRCh38.p7 | 6:17616695 | AACTGGAAAGCCGAA[C/G]CTGCAATAGTTAAAG | 9972 |
| rs140542389 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17629034 | CACTGAAGCACTCTT[A/G]GTTTCTATGGTTCCA | 9972 |
| rs140553157 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NUP153 | GRCh38.p7 | 6:17624420 | TGTTTATATATAAAT[A/C]CAACCATATTACCTC | 9972 |
| rs140571428 | snp | G/T | 0.00112006 | 0.0236384 | missense | NUP153 | GRCh38.p7 | 6:17675267 | ACAAGTTGAATGCTG[G/T]TTTTTTTGAGCTGGT | 9972 |
| rs140583083 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17628806 | CCCAAAGGAAAACAC[C/T]GGTTGACACTTTGGC | 9972 |
| rs140596634 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | NUP153 | GRCh38.p7 | 6:17634900 | CTAGTCCACACTGGA[C/T]AAAAAGAATTGTCTT | 9972 |
| rs140621235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17702856 | TCTTCAGTTATTTGA[A/G]CAAGACAATGAATTT | 9972 |
| rs140676985 | snp | A/G | 0.000349401 | 0.0132128 | intron-variant | NUP153 | GRCh38.p7 | 6:17646046 | TGTTTGTATGTTAAA[A/G]TGTAAGAAATTTTTA | 9972 |
| rs140727277 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17662788 | AGCACACTCCCTCAA[C/T]GGTCTTCACTGCCAA | 9972 |
| rs140748720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17644253 | AGATCATTGAAGAAA[C/T]GCTTTTCGATAAGGT | 9972 |
| rs140757649 | snp | A/G | | | intron-variant | NUP153 | GRCh38.p7 | 6:17684122 | CTTGAGACCACACTA[A/G]AAGCCAAGCAGATGC | 9972 |
| rs140788804 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NUP153 | GRCh38.p7 | 6:17701397 | GGCCGAGTGTGGTAG[C/T]TCACACCCATAATCC | 9972 |
| rs140804016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17661208 | AGTCCCAGCTACTTG[C/T]GTGGCTGAGGCACAG | 9972 |
| rs140809404 | snp | C/T | 0.00330874 | 0.0405391 | intron-variant | NUP153 | GRCh38.p7 | 6:17688366 | CATGAAAACCTATCA[C/T]TCATGACAAAATATT | 9972 |
| rs140853655 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NUP153 | GRCh38.p7 | 6:17648488 | CGGGCATGGTGGTGC[A/G]CACCTGTAATCCCAG | 9972 |
| rs140875591 | snp | A/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17679341 | TAAAAGATGTGCACA[A/T]GGAAACTACAAAACA | 9972 |
| rs140912965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17656950 | TAGTTCCAGCCAATT[C/T]CAGTCAGTTTTGTTA | 9972 |
| rs140998716 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17642803 | TGTCCATTAATGGAT[A/G]AACAAAAATAAACTG | 9972 |
| rs141058527 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, nc-transcript-variant, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707190 | TAACATAAAAACAGT[A/G]ACCTCTTCCCATTCT | 9972 |
| rs141073145 | snp | A/G | 0.000264266 | 0.0114919 | missense | NUP153 | GRCh38.p7 | 6:17675749 | TCTGGATAATTTGAA[A/G]CAGTACTAGTTGTTG | 9972 |
| rs141106240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17670457 | CTTTGGATTTTTCTA[C/T]GTAGATAAGCATGTT | 9972 |
| rs141130610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17680974 | AAAGAGATAATCTGC[A/G]CTCGCAGCACTATTC | 9972 |
| rs141146652 | in-del | -/ATA | 0.02016 | 0.0983543 | intron-variant | NUP153 | GRCh38.p7 | 6:17624023 | TACACCCCTTTCTAC[-/ATA]ATATTATATTTCACA | 9972 |
| rs141160476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17703854 | AGTATTTTAGATAAG[A/G]GGCAATGATAAATTA | 9972 |
| rs141169660 | snp | A/G | 0.00464149 | 0.04795 | missense | NUP153 | GRCh38.p7 | 6:17629398 | TCGGATGACACACCT[A/G]TTTTGAATCCTCCCT | 9972 |
| rs141215228 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUP153 | GRCh38.p7 | 6:17668450 | GATCCTCAAGATGGA[A/G]ATGCTGAATAGCCCA | 9972 |
| rs141259717 | snp | C/T | 0.000181212 | 0.00951698 | missense | NUP153 | GRCh38.p7 | 6:17628910 | TTCCCAAAACAAACA[C/T]TGAGGCAGATGGCAG | 9972 |
| rs141283559 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | NUP153 | GRCh38.p7 | 6:17652937 | GGGAGACTGAGGTAG[A/G]AGAATCACTTGAACC | 9972 |
| rs141373572 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NUP153 | GRCh38.p7 | 6:17670999 | TATTTTTAGTAGAGA[C/T]AGGGTTTCACCATGT | 9972 |
| rs141410680 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUP153 | GRCh38.p7 | 6:17624928 | GCAAATGTCAAGCTT[C/T]GTTTCAGACTCTTAC | 9972 |
| rs141431613 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17681972 | AGCACTTTTAGGAGG[C/G]TGAGGCAGGAGGATC | 9972 |
| rs141446931 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | NUP153 | GRCh38.p7 | 6:17695996 | CCTGGGTGACAGAGT[A/G]AGACTCCGTCTCAAA | 9972 |
| rs141481884 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | NUP153 | GRCh38.p7 | 6:17641365 | CATAGTGAAACCCCA[A/T]CTCCACTAAAAATAC | 9972 |
| rs141500733 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NUP153 | GRCh38.p7 | 6:17625434 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATTGCTTG | 9972 |
| rs141541131 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NUP153 | GRCh38.p7 | 6:17685974 | ACAGAGTTTGACCTC[A/G]TCTCCACAAAAAAAT | 9972 |
| rs141574342 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NUP153 | GRCh38.p7 | 6:17653010 | CTCCAGCCTAGCATT[C/T]GGTAGGCCGAGGCGG | 9972 |
| rs141639082 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NUP153 | GRCh38.p7 | 6:17694397 | GGCCCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 9972 |
| rs141691713 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17637553 | TTTAGCAGTATCTCT[A/G]GGTGACAATTTTGCT | 9972 |
| rs141708403 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | NUP153 | GRCh38.p7 | 6:17670749 | AAAAATATTTTATGT[A/T]TCTATAGAGATGTTC | 9972 |
| rs141735437 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NUP153 | GRCh38.p7 | 6:17636296 | GCCAAGATTGTGCCA[C/T]TGCACTCCAGCCTGG | 9972 |
| rs141787223 | snp | C/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17704197 | CTCTGGAGGCTGAGG[C/T]AGGAGAATGGCATTA | 9972 |
| rs141795377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17635778 | AAATCCATTATCTAA[A/C]AAGCCAGTGACTCAT | 9972 |
| rs141799420 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NUP153 | GRCh38.p7 | 6:17673272 | TACTCAGGAGGCTGA[C/T]GCAGAGAATTGCTTG | 9972 |
| rs141823244 | in-del | -/C | 0.170084 | 0.236883 | intron-variant | NUP153 | GRCh38.p7 | 6:17648795 | CAATACAGCGAGACA[-/C]CCATCTCAAAAAAAA | 9972 |
| rs141866112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17617421 | AAACATACCCAAAAT[A/G]TTTAGGTTCCAGATA | 9972 |
| rs141893200 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUP153 | GRCh38.p7 | 6:17676719 | CAAGGTGAGCCCTAC[A/G]ATTACCCAGCTCTCT | 9972 |
| rs141965188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17650122 | TGATAAACGTTTAGA[C/T]ATATGATAAACTCTG | 9972 |
| rs141972554 | in-del | -/CCC | 0.02016 | 0.0983543 | intron-variant | NUP153 | GRCh38.p7 | 6:17644363 | CTCACATCCATCTCA[-/CCC]CCAAGTAAAAATCAT | 9972 |
| rs142048960 | in-del | -/TTTC | 0.16911 | 0.236552 | intron-variant | NUP153 | GRCh38.p7 | 6:17652248 | AACTACAGAATATAT[-/TTTC]TTTAAGAATTATCAA | 9972 |
| rs142056238 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | NUP153 | GRCh38.p7 | 6:17659006 | AGATGCACCAAAAAC[C/T]GCAATGTCTGCAGCT | 9972 |
| rs142075762 | snp | A/G/T | 0.00677088 | 0.0578511 | intron-variant | NUP153 | GRCh38.p7 | 6:17618846 | GCTGGGATTACAGGC[A/G/T]TGAGCCACTGCGCCC | 9972 |
| rs142085298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17674067 | GCTAAGTAGAATAAG[A/C]CAGACTCAAAAGGTT | 9972 |
| rs142119689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUP153 | GRCh38.p7 | 6:17679358 | GAAACTACAAAACAG[C/T]ACCGAAAGAAAGAAA | 9972 |
| rs142121080 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NUP153 | GRCh38.p7 | 6:17617083 | AATTAAAGACTCTGA[A/C]CTTTACATATAAAAA | 9972 |
| rs142159248 | in-del | -/A | | | intron-variant | NUP153 | GRCh38.p7 | 6:17653098 | TCTCTAATGAAATAT[-/A]AAAAATTAGCCGGGC | 9972 |
| rs142163375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17665880 | TTTTTGTAGAGACAG[A/G]GTCTCGCCATGTTGC | 9972 |
| rs142177210 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NUP153 | GRCh38.p7 | 6:17658136 | TGGGCGTGATGGCTC[A/G]CGCCTATAATCCCAG | 9972 |
| rs142212006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17619749 | ACTACTCAAAGCAAT[C/T]TATGGATTCAATGCA | 9972 |
| rs142342732 | snp | A/G | 0.000675692 | 0.0183682 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17616586 | CGAGCCTGAAGGCTG[A/G]GCTGAGGCTGCAGGT | 9972 |
| rs142452167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17692873 | CATTTTAGAGAAGCC[C/T]CTCCAAAACAGATGA | 9972 |
| rs142461728 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17672712 | AAAAAACCTTGGCCA[A/G]GCACACCTGTAATCT | 9972 |
| rs142486947 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUP153 | GRCh38.p7 | 6:17635078 | CTAAGCCACATGCAG[C/T]CCACAGGTTGCACAG | 9972 |
| rs142527597 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | NUP153 | GRCh38.p7 | 6:17654520 | ACAGACAGGGTTTCA[A/C]CATGTTGGCCAGGCT | 9972 |
| rs142545731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17683821 | CAACGGCGGGCCATG[C/T]TTCATCTGAAAATAT | 9972 |
| rs142554775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17671149 | ACCTTGCCTTCCCAG[A/G]ATAAACCCCACTTGA | 9972 |
| rs142564542 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NUP153 | GRCh38.p7 | 6:17644028 | CTTATTAATTTCTAT[C/T]ACGTAAGGCTGTGTT | 9972 |
| rs142568303 | snp | A/G | 0.261884 | 0.249717 | intron-variant | NUP153 | GRCh38.p7 | 6:17693653 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 9972 |
| rs142576733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17638603 | GATTGGCAAGATATT[A/G]ACAGTAACCATCTCA | 9972 |
| rs142585759 | snp | C/G | 3.29473e-05 | 0.00405864 | missense | NUP153 | GRCh38.p7 | 6:17637495 | TCCCTGATGCAGAAA[C/G]AGTTGTTTTGCCACT | 9972 |
| rs142587240 | in-del | -/GTT | 0.0592355 | 0.161582 | intron-variant | NUP153 | GRCh38.p7 | 6:17649570 | TTACGATATACTACA[-/GTT]GTTGTACTAATATGA | 9972 |
| rs142592966 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | NUP153 | GRCh38.p7 | 6:17676178 | TTTATTTCAATATGT[C/G]TAATCTTGACTCCCA | 9972 |
| rs142610692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17627872 | AGTGATCTTTGCCAA[C/T]AGGTAATTTCCATTT | 9972 |
| rs142660367 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NUP153 | GRCh38.p7 | 6:17688105 | CCTGGGCCACAGAGC[A/G]AGACTCCGTCTCAAA | 9972 |
| rs142677873 | snp | G/T | 0.000576658 | 0.0169705 | missense | NUP153 | GRCh38.p7 | 6:17662030 | TACCTTTCTCGTTGT[G/T]CTCTATTTTGTCCGG | 9972 |
| rs142695466 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NUP153 | GRCh38.p7 | 6:17701652 | GGTGACAGAACAAGA[C/T]TCCATCTCAAAAAAA | 9972 |
| rs142730251 | snp | A/C | 0.000307953 | 0.0124049 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17629376 | CATGGGGTTTATAGA[A/C]CCAGAATCGGATGAC | 9972 |
| rs142756581 | in-del | -/GAAA | | | intron-variant | NUP153 | GRCh38.p7 | 6:17686165 | AAAAAAAGAAAGAAA[-/GAAA]GAAAGAAAGAAAAAG | 9972 |
| rs142764283 | snp | C/T | 0.00458724 | 0.0476716 | missense | NUP153 | GRCh38.p7 | 6:17625913 | TGACAGCTGTACCTG[C/T]GCTGGATGTGGTTGC | 9972 |
| rs142875095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17702229 | GACACCATTTCTGGC[C/T]GGGCGAGGTAGCTCA | 9972 |
| rs142896907 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | NUP153 | GRCh38.p7 | 6:17697731 | GGGTGGGGGCAGGCT[A/C]CTCTATAACACTAAC | 9972 |
| rs142913025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17627257 | GATTAGACCCTATCA[C/T]GTTTTTGTTGCTTTC | 9972 |
| rs142913960 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NUP153 | GRCh38.p7 | 6:17618670 | TCCCGAGTTCACGCC[A/G]TTCTCCTGCCTCAGT | 9972 |
| rs142951913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17690904 | CAGCACTTTGGGAGG[C/T]CGAGGTGGGTGGATC | 9972 |
| rs142956913 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | NUP153 | GRCh38.p7 | 6:17648948 | GAATATCCTTCTCTA[A/T]GGTATTGCATAAGAG | 9972 |
| rs142978088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17638049 | TTCAATGGTACTAAT[C/T]TACTGATATGTATTA | 9972 |
| rs142980784 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707074 | CGGCTTCTCGGAAAG[A/G]AAGAGGGACGGGGAA | 9972 |
| rs142989255 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17693987 | ACCCATCTCATTTTG[C/T]TTCCCAGCTTTATTT | 9972 |
| rs143003640 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17621584 | GGACATTATGTTAGG[G/T]GAAATAAGCCAGGCA | 9972 |
| rs143083233 | snp | A/G | 0.00074121 | 0.0192368 | missense | NUP153 | GRCh38.p7 | 6:17649242 | CTAAAATTAAAGGTA[A/G]GCAGTGAAGAACTGG | 9972 |
| rs143139766 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUP153 | GRCh38.p7 | 6:17686707 | AAAAAAACAGTACTA[C/T]AGAAAAAAAAAATTT | 9972 |
| rs143157905 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17632585 | TTCTCAAATACTTCA[-/T]TTTTTAAATGGCCTT | 9972 |
| rs143165674 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NUP153 | GRCh38.p7 | 6:17652344 | CTCAATCTTTTTCTA[A/C]TCACAATGAAATTAT | 9972 |
| rs143208971 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17708097 | CTATTCTCCTGCCTC[A/G]GCTTCCTAAGTAGCT | 9972 |
| rs143231903 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17691626 | AAAAATTAGCCAGGC[A/G]TGATGGTGCATGCCT | 9972 |
| rs143235890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17647118 | GATGGATTTCAGCAT[A/G]TGGCAAGGAAATTAC | 9972 |
| rs143270303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUP153 | GRCh38.p7 | 6:17620317 | ACCAATGGAATAGAA[C/T]AGAGAATTCAGAAAC | 9972 |
| rs143274864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUP153 | GRCh38.p7 | 6:17651481 | CTATAAATGGATTTG[A/G]TGTTCCAATTAAAAC | 9972 |
| rs143313125 | snp | A/C/T | 0.0197763 | 0.0975112 | intron-variant | NUP153 | GRCh38.p7 | 6:17681382 | ACGAGGTCAGGAGAT[A/C/T]GAGACCATCCTGGCT | 9972 |
| rs143338076 | snp | C/T | 6.12776e-05 | 0.0055349 | intron-variant | NUP153 | GRCh38.p7 | 6:17646179 | GAAAGAATATCCTTA[C/T]ACTTCGTTTTCAATA | 9972 |
| rs143406335 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17668816 | CCACTGCACACCAGT[A/C]TGGATGACAGAGCGA | 9972 |
| rs143433747 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NUP153 | GRCh38.p7 | 6:17635398 | ACAGGTGTAAGCCAC[C/T]GCACCCGGCCTATCA | 9972 |
| rs143450371 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NUP153 | GRCh38.p7 | 6:17625613 | AATTGCTCCCAAGAG[G/T]TAAATATGTTAAAGT | 9972 |
| rs143450543 | snp | A/C/G | 3.43626e-05 | 0.00414492 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17629526 | GTTCGAAGATGAGGA[A/C/G]GATGTGTCAAAGCCT | 9972 |
| rs143510632 | snp | A/G | 0.195837 | 0.244062 | intron-variant | NUP153 | GRCh38.p7 | 6:17701556 | AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCAGAG | 9972 |
| rs143536422 | in-del | -/GAGTT | 0.0422008 | 0.138995 | intron-variant | NUP153 | GRCh38.p7 | 6:17621786 | TTTGAGAGCACAGTA[-/GAGTT]AACAATAATTTATTG | 9972 |
| rs143543771 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NUP153 | GRCh38.p7 | 6:17631166 | TCTTTTAAAATAAAA[C/T]AAAACAGAAAATACC | 9972 |
| rs143566917 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17702624 | GAGGTTGCACTGAGC[C/G/T]GAGATTGCACCATTG | 9972 |
| rs143586296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17617044 | GTAAGCCACTGCACC[C/T]GGCCGCAACATGATA | 9972 |
| rs143624938 | snp | C/T | 0 | 0 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17675670 | TGGCTGACAGTGTAA[C/T]GCAGGGGATTCCAAC | 9972 |
| rs143647331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17695692 | GAAAAGAAATATGCA[C/T]AGTATTGGAAAGGAG | 9972 |
| rs143662961 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17666218 | GCTGCAAATAAGATA[C/T]TTTAAAACTAGCTAT | 9972 |
| rs143662967 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17705169 | ATCTAGGAAGTCTAC[C/T]TTTAACAGTAGGCAA | 9972 |
| rs143695815 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NUP153 | GRCh38.p7 | 6:17656517 | GTAGCTGGGACCACA[A/G]GCGCTAACCACCATG | 9972 |
| rs143732552 | snp | A/G | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17664668 | CAACACCACCACATG[A/G]AAGAAACAGATAAAG | 9972 |
| rs143753409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17630614 | GTTGCAGTGAGCCAA[A/G]ATTGCGCCACAGCAC | 9972 |
| rs143797364 | in-del | -/TCT | | | intron-variant | NUP153 | GRCh38.p7 | 6:17618561 | GGAAGTTAAAATCTC[-/TCT]TTTTTTTTTTTTTTT | 9972 |
| rs143824475 | snp | C/G | 0.00255011 | 0.0356168 | missense | NUP153 | GRCh38.p7 | 6:17637466 | CACTGGTTTAAATTT[C/G]TCTCCAAAGCCTGTC | 9972 |
| rs143827062 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | NUP153 | GRCh38.p7 | 6:17685503 | GCAATGAGCCGAGAT[C/T]GAGCCACTGCACTCC | 9972 |
| rs143849141 | in-del | -/AAG | 0.168785 | 0.236441 | intron-variant | NUP153 | GRCh38.p7 | 6:17702077 | TTTGTAGTGGTTACT[-/AAG]AAAAGCAAGCAGCCT | 9972 |
| rs143860526 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17645983 | GAAGGCATTTATAAG[A/T]ATTACCAAAGGTGAA | 9972 |
| rs143915531 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17658732 | TTGTTTTGAAGTGTC[A/G]TCTTCTCCTATTCTA | 9972 |
| rs143939878 | snp | A/G | 4.94336e-05 | 0.00497135 | missense | NUP153 | GRCh38.p7 | 6:17625879 | TTACTGCTGGCTCCT[A/G]GACCAAAGACAAATG | 9972 |
| rs143985779 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17652157 | CAGGCTAACCATACC[C/T]TCCCTCCCCATGAAA | 9972 |
| rs144021950 | snp | C/T | 3.4747e-05 | 0.00416801 | intron-variant, downstream-variant-500B | NUP153 | GRCh38.p7 | 6:17632621 | AAGGCGCTTTACCAT[C/T]ACCTTTATTTTTATT | 9972 |
| rs144046887 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NUP153 | GRCh38.p7 | 6:17686389 | TTAATTGTTAACAAA[C/T]CTTTTTTTTATTTCT | 9972 |
| rs144052168 | snp | A/C | 0.00478085 | 0.0486577 | utr-variant-3-prime | NUP153 | GRCh38.p7 | 6:17615630 | CTCACTTCACACATA[A/C]ACCAGCACAAACTCA | 9972 |
| rs144058614 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NUP153 | GRCh38.p7 | 6:17702115 | CTCCAAAGAGCTGAC[A/T]TTCTGTGCCTGACAA | 9972 |
| rs144128421 | snp | C/G | 3.47005e-05 | 0.00416522 | missense | NUP153 | GRCh38.p7 | 6:17629532 | AGATGAGGAAGATGT[C/G]TCAAAGCCTACAAAA | 9972 |
| rs144245176 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUP153 | GRCh38.p7 | 6:17671911 | TACTTGGGAGGCTGA[A/G]GCAGGAAAATTGTGT | 9972 |
| rs144280411 | snp | C/T | 1.65007e-05 | 0.00287229 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17637193 | ACACTTATTGTCTTC[C/T]GCATTATTAGAAACA | 9972 |
| rs144294630 | snp | C/T | 0.00635571 | 0.056013 | missense | NUP153 | GRCh38.p7 | 6:17628828 | CACTTTGGCTCTTCA[C/T]TGTCAGCTTTCTTCC | 9972 |
| rs144298434 | snp | C/T | 0 | 0 | intron-variant | NUP153 | GRCh38.p7 | 6:17633255 | GACATAAGATGTAAA[C/T]TGTAGGCAATATCCT | 9972 |
| rs144366531 | snp | A/C | | | intron-variant | NUP153 | GRCh38.p7 | 6:17654046 | TTTCTTTTTTGATAA[A/C]GCAAATGTAACACAA | 9972 |
| rs144389087 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17692312 | GTGAGACAGAGACAT[A/T]ACTAGTGGCACAGTG | 9972 |
| rs144408253 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NUP153 | GRCh38.p7 | 6:17619824 | CATATCCGGCCAGGC[A/G]CTGTGGCTCACACCT | 9972 |
| rs144451644 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | NUP153 | GRCh38.p7 | 6:17623309 | AATATCCAGAATACA[A/T]AAAGAACCTCTACAA | 9972 |
| rs144475380 | snp | A/G/T | 0.00875054 | 0.0656008 | intron-variant | NUP153 | GRCh38.p7 | 6:17694418 | AATCCCAGCACTTCC[A/G/T]GAGGCCGACGCGGGC | 9972 |
| rs144481878 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NUP153 | GRCh38.p7 | 6:17694889 | AAGGCTGAGGTAGGA[A/G]AATCGCTTGAACCCA | 9972 |
| rs144557785 | snp | G/T | 1.67125e-05 | 0.00289067 | intron-variant | NUP153 | GRCh38.p7 | 6:17669586 | TGTTGCAACATAAAA[G/T]CTAAGGCACATATTT | 9972 |
| rs144593136 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NUP153 | GRCh38.p7 | 6:17644585 | CTCAAAATTCTTGAC[C/T]TGAGTAACTCAGCTC | 9972 |
| rs144688186 | snp | C/G | 0.00172815 | 0.0293443 | missense | NUP153 | GRCh38.p7 | 6:17637335 | CTTTCCGAAACCACT[C/G]TCAATGTAAGGGCTC | 9972 |
| rs144758578 | snp | A/C/T | 6.61336e-05 | 0.00575005 | missense | NUP153 | GRCh38.p7 | 6:17665382 | GAGGATATTGAGAAT[A/C/T]CACCTTACAGGTAAA | 9972 |
| rs144817609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17639030 | TAAATTCTTTCTGAG[C/G]TATTAGATTATCTCA | 9972 |
| rs144834845 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NUP153 | GRCh38.p7 | 6:17681045 | CAAATGAATGGACAA[A/G]GAAACTGTGCTACAT | 9972 |
| rs144865117 | snp | A/G | 0.000994167 | 0.0222732 | intron-variant | NUP153 | GRCh38.p7 | 6:17649159 | TTATATAATGGTTTT[A/G]TACCTTGTTTGTTAA | 9972 |
| rs144896647 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NUP153, LOC105374952 | GRCh38.p7 | 6:17707804 | CAACCAACCAGACAA[A/G]ATGTCCAGAGAAATT | 9972 |
| rs144916497 | snp | C/G | 0.000493897 | 0.0157068 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | NUP153, LOC105374952 | GRCh38.p7 | 6:17706379 | GACTCCTCCGGCTCC[C/G]GAGGCCATGGCGGAG | 9972 |
| rs144921881 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUP153 | GRCh38.p7 | 6:17684412 | TTCTCCTGCAGCTTT[A/G]TCATCTCCCTCAGAC | 9972 |
| rs144924021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUP153 | GRCh38.p7 | 6:17640162 | ATCTTTTGGATTAAT[C/T]TCTAAAAGTTCATGA | 9972 |
| rs144924068 | snp | C/T | 0.000364009 | 0.013486 | synonymous-codon | NUP153 | GRCh38.p7 | 6:17675763 | AGCAGTACTAGTTGT[C/T]GAAGGTTCTTAAAAG | 9972 |
| rs144967346 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NUP153 | GRCh38.p7 | 6:17661866 | AACAAGTAAAAAAAA[A/T]ATATACAGCTGAACG | 9972 |
| rs144981009 | snp | A/C | 0.000477921 | 0.015451 | missense | NUP153 | GRCh38.p7 | 6:17616174 | AGAACACATTTTTCC[A/C]ATTTGACCTGTGAAA | 9972 |
| rs145018406 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | NUP153 | GRCh38.p7 | 6:17622614 | TGTAGCCTTTTCTCA[A/C]TTCTTTAACTGGAAG | 9972 |
| rs145033226 | in-del | -/AAC | 0.173965 | 0.238157 | intron-variant | NUP153 | GRCh38.p7 | 6:17678972 | AAAAAAATAAGTCTT[-/AAC]AAATATTTTACAGCT | 9972 |