| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs2705 | snp | C/T | 0.48978 | 0.0707512 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445076 | AACGGCAGGAGGGGA[C/T]GCTGGCCTTCCTGCA | 80700 |
| rs11909 | snp | C/T | 0.47109 | 0.116702 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454003 | GATGGCAGCCGCTGC[C/T]GCCCTAGCCCGGCTG | 80700 |
| rs243385 | snp | G/T | 0.445064 | 0.156365 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444953 | CAAGCCATCCGCTCT[G/T]CAGCAGGTGGGCCTG | 80700 |
| rs243387 | snp | C/T | 0.489722 | 0.0709447 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445159 | CTGCAGCATGGGTCC[C/T]GTTCCCGTGTGCCGT | 80700 |
| rs243388 | snp | A/G | 0.0230416 | 0.104839 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446435 | CCCCGGCCAGCCCTC[A/G]TGACCTGGCCCGCGT | 80700 |
| rs243389 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446998 | CAATAGCGAGAGCCG[A/G]GCCCCTGGACTGGGT | 80700 |
| rs243390 | snp | A/G | 0.489201 | 0.0726845 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449255 | TGTTCACCCGCCCTC[A/G]TCTGGGCAGCCCAGG | 80700 |
| rs243391 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449811 | TAGATCTTGGCTCAG[C/T]TTTCTTCTCAGCCCC | 80700 |
| rs243392 | snp | C/T | 0.488302 | 0.0755777 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450182 | gctggagtgcagtgg[C/T]gcaatctcagctcac | 80700 |
| rs243393 | snp | A/G | 0.482757 | 0.0912364 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450745 | ttgagacagagtctc[A/G]ctctgtcgcccaggc | 80700 |
| rs243394 | snp | A/T | 0.48155 | 0.0942576 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451563 | acttcggctttagcc[A/T]gggcaacatggcaaa | 80700 |
| rs243395 | snp | C/T | 0.464033 | 0.12919 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452500 | CTTGGACGCTTTCAC[C/T]GCCCCAGGTATCTGA | 80700 |
| rs243396 | snp | A/G | 0.480697 | 0.0963277 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453232 | GGGCCTCAGGTACAC[A/G]AGCCCATCGCTCCCT | 80700 |
| rs243397 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454830 | CTCCCAGCAGGGTCC[C/T]GGCACACAGTAGGTG | 80700 |
| rs376965 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453327 | CCTTGCAAGGTGGAC[A/G]CAGGTTGTGGTGGAA | 80700 |
| rs411833 | snp | C/G | 0.488905 | 0.0736498 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453328 | TCCACCACAACCTGT[C/G]TCCACCTTGCAAGGC | 80700 |
| rs741923 | snp | A/G | 0.422315 | 0.181128 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448846 | TCTGGAACCACTCCC[A/G]GGCCTCATGTTTACA | 80700 |
| rs760369 | snp | C/T | 0.282632 | 0.247861 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449290 | GGCAGCCCAGGGCCA[C/T]GTGTCAGGATTCGGG | 80700 |
| rs1044477 | snp | A/G | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445083 | GGGTGACAACGGCAG[A/G]AGGGGATGCTGGCCT | 80700 |
| rs1044510 | snp | A/G | 0.460898 | 0.134246 | synonymous-codon, intron-variant | UBXN6 | GRCh38.p7 | 19:4457653 | CGACATCAAGTTCAA[A/G]AGCGCGGGACCCGGT | 80700 |
| rs1127888 | snp | A/G | 0.344869 | 0.2313 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454086 | GTTCCCAGGGAAAAG[A/G]CCCACAAAGAGAAGC | 80700 |
| rs2077444 | snp | A/G | 0.424037 | 0.179474 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449413 | CATGAGCCCCGGCTC[A/G]GTGTGTAGGTCATTG | 80700 |
| rs2272639 | snp | C/T | | | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447614 | GGGTGCAGGTGGATG[C/T]TGTCCAGGTACCTGG | 80700 |
| rs2293930 | snp | C/T | 0.422473 | 0.180978 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444859 | AGGTGGGTGGCTCAT[C/T]GGGCACTTGTGGCCA | 80700 |
| rs3830686 | in-del | -/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445205 | AGGGAGATGCCACGT[-/T]GTGTCTGTCCGGCAG | 80700 |
| rs4806983 | snp | A/G | 0.111928 | 0.208413 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459782 | caggaggcagagctt[A/G]cagtgagccgagatc | 80700 |
| rs4807589 | snp | A/G | 0.105569 | 0.204058 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444686 | GCCAGGTGAAGTTGC[A/G]CATCTGCAGGTTCCA | 80700 |
| rs6510808 | snp | A/T | 0.488485 | 0.0749998 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458914 | ACCCAATGCACCCAA[A/T]TGGGACCTGGGGATT | 80700 |
| rs7253478 | snp | A/G | 0.482008 | 0.0931261 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456190 | CCCTGCATCCTTCCT[A/G]TCATGCCCAGTCCCA | 80700 |
| rs7257129 | snp | C/T | 0.482008 | 0.0931261 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456385 | CCCACTGCCCCGTGA[C/T]TCCTGACCCCCACTT | 80700 |
| rs8101961 | snp | A/G | 5.11967e-05 | 0.00505922 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446632 | GCGCGCACGGGCTCC[A/G]CAGCCAGCAGCTGTT | 80700 |
| rs8110072 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448703 | TGACGCGACAGAACT[G/T]TGCCTCACACTCTGG | 80700 |
| rs10423797 | snp | C/G | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457461 | CCTCGGCCCGACTTC[C/G]TCCGCCCCCGGCGCC | 80700 |
| rs10423822 | snp | C/G | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457500 | TCCCCTGACCCTCGC[C/G]TGCCGCTCCCAGCCC | 80700 |
| rs10425294 | snp | C/G | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457460 | CCCTCGGCCCGACTT[C/G]GTCCGCCCCCGGCGC | 80700 |
| rs10425328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457499 | CTCCCCTGACCCTCG[C/G]GTGCCGCTCCCAGCC | 80700 |
| rs10432304 | snp | A/T | 0.459233 | 0.136827 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458245 | CTCTATAAAAAAAAA[A/T]AAAATAAAATAAAAT | 80700 |
| rs11085075 | snp | A/G | 0.482683 | 0.0914256 | upstream-variant-2KB, missense | UBXN6 | GRCh38.p7 | 19:4457847 | GCCGCCGGAAGTCCC[A/G]CCTTCCCCTGGCCTG | 80700 |
| rs11558242 | snp | C/G/T | 0.000107549 | 0.0073324 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453494 | TCAAGCCGAAGCCAC[C/G/T]GTCAGCGGGAGCCCC | 80700 |
| rs11670503 | snp | A/G | 0.259951 | 0.249802 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458066 | GACAGGGACAGGCCA[A/G]CTGAACCTCGCAGAG | 80700 |
| rs12459922 | snp | A/G | 0.27893 | 0.24832 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455865 | TTCCCAAACCACCTG[A/G]CGGCCCCTGCTCACC | 80700 |
| rs12608655 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458556 | TCACCACGTACCCTA[A/G]GTAGGAGCTGTTTAA | 80700 |
| rs12609703 | snp | C/T | 0.48692 | 0.0798058 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456156 | CAGGCTCTGGGCTGA[C/T]CCAGCCATCACCCCG | 80700 |
| rs12977256 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457795 | CCACCGGAAGAAAAT[A/T]AAAAAAAAAAAAAAA | 80700 |
| rs12985005 | snp | C/T | | | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457726 | ccggcggcggggggc[C/T]gcgggggcggggggg | 80700 |
| rs12985963 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457799 | CGGAAGAAAATTaaa[A/T]aaaaaaaaaaaaaaa | 80700 |
| rs34179017 | snp | C/T | 0.00404235 | 0.0447754 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446167 | GGGAGCGGCTGGGGG[C/T]GGTGTACGGGTTCGT | 80700 |
| rs34822893 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445778 | CCTCCTGCCCTCTCC[C/T]TCCGGGACTCCAGGA | 80700 |
| rs35081974 | in-del | -/C | | | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448255 | GGGGGTGACAGCCCC[-/C]AGTGGGAGGGGTGCT | 80700 |
| rs35111635 | in-del | -/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444750 | CCTCTGGCCACAGGG[-/G]AAGCCAGGCCTGTGA | 80700 |
| rs35137279 | snp | A/G | 0.0452528 | 0.143452 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459654 | CATCCCGGCTAATAC[A/G]GTGAAACCCTGTCTT | 80700 |
| rs35208178 | multinucleotide-polymorphism | CG/GC | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4457460 | CCCTCGGCCCGACTT[CG/GC]TCCGCCCCCGGCGCC | 80700 |
| rs35436704 | snp | C/T | 0.0145626 | 0.0840787 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445550 | CCGCGGGGGCCGAGC[C/T]GGACTCCATCCTGAA | 80700 |
| rs35539786 | multinucleotide-polymorphism | CG/GC | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4457499 | CTCCCCTGACCCTCG[CG/GC]TGCCGCTCCCAGCCC | 80700 |
| rs35708976 | in-del | -/C | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455476 | AGGGCACCTCACCCC[-/C]AACCAGCCATGGACC | 80700 |
| rs45464495 | snp | A/G | 0.0399052 | 0.1355 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455465 | ATGCCATTTCCCAGG[A/G]CACCTCACCCCAACC | 80700 |
| rs45503199 | snp | C/T | 0.0548986 | 0.156324 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446243 | GCCCAGGGCCCCCTA[C/T]CAACCCGAGCCGCCC | 80700 |
| rs55661974 | snp | C/G | 0.438386 | 0.164349 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459150 | GCCAACATGGTGAAA[C/G]CCTGTCTCTATGGGC | 80700 |
| rs55674497 | snp | A/G | 0.421526 | 0.181876 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459218 | GAATCGCTTGAACCC[A/G]GCAGGTGGAGGTTGC | 80700 |
| rs55940498 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451970 | CCTGGCCAACATGGT[A/G]AAACCCCATCTCTAC | 80700 |
| rs56153949 | snp | C/G | 0.251578 | 0.249995 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457521 | CTCCCAGCCCCTCAT[C/G]CTCTCCGATCTCCCG | 80700 |
| rs56156435 | in-del | -/GCC | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444659 | CCTTTCATCATACCC[-/GCC]AAGCCCCTCTTGCCA | 80700 |
| rs56254866 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457801 | GAAGAAAATTAAAAA[A/T]AAAAAAAAAAAAAAA | 80700 |
| rs57787685 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457802 | AAGAAAATTAAAAAA[A/T]AAAAAAAAAAAAAAA | 80700 |
| rs58895127 | in-del | -/TAA | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457795 | CCACCGGAAGAAAAT[-/TAA]AAAAAAAAAAAAAAA | 80700 |
| rs58900477 | in-del | -/AAA | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450786 | AAAAAAAAAAAAAAA[-/AAA]GAGTGCCTACAAATC | 80700 |
| rs59106361 | snp | C/G | 0.0562307 | 0.157967 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448185 | TGGGTGGAGCTGCCT[C/G]ACTCTCGGCCTATGC | 80700 |
| rs59121637 | snp | A/G | 0.175897 | 0.238765 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452186 | AGTTGGGAGAGAGGA[A/G]ATACAGATGCATACA | 80700 |
| rs59258359 | snp | C/T | 0.02016 | 0.0983543 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445368 | CAGCTCCACGGCTGG[C/T]GCCCCTCCCGTGCCC | 80700 |
| rs60079641 | snp | C/G | 0.0182019 | 0.0936463 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457193 | AGAGCTCTCCCTCAC[C/G]ACCCGGCTCAGGACT | 80700 |
| rs60087438 | in-del | -/AG | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448488 | CGCTGCCCAGGTAAC[-/AG]GGGCAGGAAAAGGAA | 80700 |
| rs60981683 | snp | C/T | 0.0433974 | 0.140767 | upstream-variant-2KB, missense | UBXN6 | GRCh38.p7 | 19:4457925 | CTGGCCCAGGGCGGC[C/T]GCTCTGTACGCTGGA | 80700 |
| rs61729794 | snp | A/G/T | 0.000231089 | 0.010747 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445555 | GATGGAGTCCGGCTC[A/G/T]GCCCCCGCGGCCTTG | 80700 |
| rs62130982 | snp | A/G | 0.0596104 | 0.162024 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448483 | CCCTCCGCTGCCCAG[A/G]TAACAGGGGCAGGAA | 80700 |
| rs62130983 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450094 | CCCGGGTGTGGTGGC[C/G]TGCACCTGTAGTCCC | 80700 |
| rs62130984 | snp | C/T | 0.423413 | 0.180077 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450328 | CCAAAAGCCATGAAC[C/T]AAAACTGACACATTT | 80700 |
| rs62130985 | snp | A/C | 0.422944 | 0.180528 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450333 | AGCCATGAACTAAAA[A/C]TGACACATTTAATTA | 80700 |
| rs62130993 | snp | C/T | 0.438386 | 0.164349 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459153 | AACATGGTGAAAGCC[C/T]GTCTCTATGGGCACC | 80700 |
| rs67614381 | in-del | -/T | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450786 | GATTTGTAGGCACTC[-/T]TTTTTTTTTTTTTTT | 80700 |
| rs70947751 | multinucleotide-polymorphism | CC/TG | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453327 | TTCCACCACAACCTG[CC/TG]TCCACCTTGCAAGGC | 80700 |
| rs71166999 | in-del | -/TT | 0 | 0 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458889 | ATTGGGTGCATCCTC[-/TT]TTTTTTTTTTTTTTT | 80700 |
| rs72990638 | snp | C/T | 0.423257 | 0.180228 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453238 | CGATGGGCTCGTGTA[C/T]CTGAGGCCCACTTCT | 80700 |
| rs72990643 | snp | C/T | 0.273856 | 0.248859 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454739 | CAGGAATTGAGGAGA[C/T]TCAAGGGGTGTCACA | 80700 |
| rs72990646 | snp | A/C | 0.0252325 | 0.109451 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458519 | GGCCTGTTTTGGTGC[A/C]TGAAGCACCCCCCCG | 80700 |
| rs73541319 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448228 | CACCTCAGCAGGTAA[C/T]GAGGGGGCCAGAGGG | 80700 |
| rs74788480 | snp | C/T | 0.000137611 | 0.00829376 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446060 | TCACCAGCCCGCACT[C/T]GTTCAAGGCCAGGTT | 80700 |
| rs74938087 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445308 | GCTTGGGCGCATCCC[A/C]ACAGCCCCCAAGGGA | 80700 |
| rs74995992 | snp | C/G | 0.0333695 | 0.124785 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445286 | TCCCCAGGCCTCTCC[C/G]TCGGGGGCTTGGGCG | 80700 |
| rs75122921 | snp | A/C | | | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446164 | CGGACGAACCCGTAC[A/C]CCGCCCCCAGCCGCT | 80700 |
| rs75475637 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447058 | CAGCCCTGGGGGTGC[C/T]TCAGTGCTGGATGCA | 80700 |
| rs75762432 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458244 | TCTCTATAAAAAAAA[A/T]AAAAATAAAATAAAA | 80700 |
| rs77077573 | snp | A/G | 0.000577639 | 0.0169849 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445562 | TCCGGCTCGGCCCCC[A/G]CGGCCTTGATGTCCT | 80700 |
| rs77324462 | snp | A/C | 0.5 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450221 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 80700 |
| rs77562484 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448693 | GAAGCCAGTGTGACG[C/T]GACAGAACTGTGCCT | 80700 |
| rs77571267 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444962 | CGCTCTTCAGCAGGT[A/G]GGCCTGCCCTGTGTC | 80700 |
| rs77767396 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450992 | GGGACACGGGTGCTT[C/T]TGCACACACTGCTGG | 80700 |
| rs78035520 | snp | A/C/T | 0.000115848 | 0.00761005 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446848 | TACCCTGATCCTGGG[A/C/T]GGGAAGCAACACCTT | 80700 |
| rs78869060 | snp | A/G | 0.277067 | 0.24853 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444745 | CCTGTCCCTCTGGCC[A/G]CAGGGAAGCCAGGCC | 80700 |
| rs79412879 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448994 | GCCCCTGCCCCTCCC[C/T]GAGGTCCCACCTATC | 80700 |
| rs79703899 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452298 | TACCACCTGGGCTTC[C/T]GATGGAGGGTGGCTC | 80700 |
| rs79719998 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452961 | TAGAACTCCTTTCAG[C/T]GGAGCTCTGAAGGCC | 80700 |
| rs111246916 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450738 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 80700 |
| rs111389080 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451700 | TGGAGTGCAATGGCG[C/T]TATCTCGGCTCACCA | 80700 |
| rs111603296 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450632 | GCGTGGTGGCGGTTC[A/G]CCTGTGGTCCCAGCT | 80700 |
| rs111715463 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453277 | GAGCCGGCATCCTCA[A/G]CTGCCGAGCCCCGAA | 80700 |
| rs111828265 | snp | C/G | 0.5 | 0 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446556 | GAAGAAGTCCCCAGG[C/G]AGTTCGAACTGCGAG | 80700 |
| rs111889558 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459653 | CCATCCCGGCTAATA[C/T]GGTGAAACCCTGTCT | 80700 |
| rs111939571 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4457376 | CTCGCCTCCCCCGCC[C/G]CGCCCCCGGGTCATA | 80700 |
| rs111988541 | snp | A/C | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445145 | AGCCACTGCCACCCA[A/C]GGCACACGGGAACAG | 80700 |
| rs112061040 | snp | C/G | 0.5 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449653 | CGACTGGCTGCCAGG[C/G]TTAGGTCAGGAGCTG | 80700 |
| rs112457954 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455655 | TGGCCTGTCTCCCCT[G/T]GGCTCCCCGCAGTTC | 80700 |
| rs112497201 | snp | C/T | 5.19773e-05 | 0.00509764 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446568 | AGGCAGTTCGAACTG[C/T]GAGGCCAGGGGCGAG | 80700 |
| rs112498876 | snp | C/T | | | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447519 | GCCCCCACCCCCAGC[C/T]TGGGCCCCGGGGGCC | 80700 |
| rs112621848 | snp | C/G | 0 | 0 | splice-donor-variant | UBXN6 | GRCh38.p7 | 19:4452363 | ACAGGGTGCCACTCA[C/G]CAAGAGAATGGCCTC | 80700 |
| rs112788696 | snp | A/C/G | 0 | 0 | missense | UBXN6 | GRCh38.p7 | 19:4452419 | TTCCTCAGGGTGGCC[A/C/G]CAGTGAGCGGACAGG | 80700 |
| rs112913612 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4457319 | CGGCCCCGCCCCCGA[C/G]ACCTCCCCTCCCGCC | 80700 |
| rs113114260 | snp | A/C/T | 0 | 0 | splice-acceptor-variant | UBXN6 | GRCh38.p7 | 19:4454095 | TGTGGGCCTTTTCCC[A/C/T]GGGAACAGACCGAGG | 80700 |
| rs113231772 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447190 | TGCTGGGGCCTGATG[C/T]GAGGCTAACACCGCC | 80700 |
| rs113246379 | snp | C/T | 0.0126979 | 0.078662 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457002 | CTAGTCTCCCATCAG[C/T]CTCCCACGTGCTCCA | 80700 |
| rs113377816 | snp | C/T | 0.5 | 0 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446738 | CAGCGTGGCAGGACA[C/T]GGGTGTCACTGTGCA | 80700 |
| rs113388522 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454202 | GCACCATCAGCCAGA[C/T]GTGTCCCTGCCTATG | 80700 |
| rs113422482 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451919 | CTTTGGGAGGCTGAG[C/G]CGGGTTGATCACTTG | 80700 |
| rs113460946 | snp | A/C/T | 1.92328e-05 | 0.00310097 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445981 | TCCCTCCTGGGGGTG[A/C/T]CTGTGCCGGTCCCAG | 80700 |
| rs113474646 | snp | C/T | | | splice-acceptor-variant, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447626 | ATGTTGTCCAGGTAC[C/T]TGGGGTAGGTGGAGA | 80700 |
| rs113832155 | snp | A/G | 0.0391387 | 0.134304 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458534 | CTGAAGCACCCCCCC[A/G]CCACCATCACCACGT | 80700 |
| rs113855338 | snp | A/G/T | 0.000239952 | 0.0109512 | synonymous-codon, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448335 | GGCAATGGTGTCCAC[A/G/T]CCCAGCTTCACCCGG | 80700 |
| rs113872945 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452904 | CCATCTCTAAGGTCC[C/T]TGCGTGCTAAAATTC | 80700 |
| rs114110189 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449553 | GTCCCCAAGACAACA[A/G]CTTCCTTGGGATCAG | 80700 |
| rs114545086 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454705 | ATAGGCATGAGCCAC[A/G]GCACCCAGCCCGCAT | 80700 |
| rs115616812 | snp | C/G/T | 0.00661732 | 0.0571391 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447644 | GGGTAGGTGGAGAAG[C/G/T]TGAGTGGGGCACAGC | 80700 |
| rs115648743 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456454 | ACAATCCCTTCCACT[A/C]TTGCTTACAGACCCG | 80700 |
| rs116059819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454613 | ATCGAGACAGGGTCT[C/T]GCTATGTAGCTCAGG | 80700 |
| rs116062482 | snp | C/G | 0.00356328 | 0.0420588 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446438 | CGGGCCAGGTCACGA[C/G]GGCTGGCCGGGGTTC | 80700 |
| rs116735639 | snp | C/T | 0.431643 | 0.171772 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457276 | GCCCCGTCGCCCTAA[C/T]CCCCCGCCACTGCAT | 80700 |
| rs117152435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453803 | GCACCTGCCCTTGAT[A/G]AGCCGCTCCCAAGGG | 80700 |
| rs117404916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451812 | CTGGCTAATTTTGTA[A/G]GAAGTTCTTTCTGTA | 80700 |
| rs117607603 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449131 | ACAGTACGTACCCTA[A/T]GACCTGGAAAAGATT | 80700 |
| rs117803167 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453266 | TCTCCAGGCCTGAGC[C/T]GGCATCCTCAGCTGC | 80700 |
| rs117885408 | snp | G/T | 0.0390633 | 0.134203 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454107 | CCCTGGGAACAGACC[G/T]AGGGAGAGTGAGTGT | 80700 |
| rs138129036 | snp | C/G/T | 0.000329934 | 0.0128403 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445530 | TGGCTGACAGGAGCT[C/G/T]GGGTTTCAGGATGGA | 80700 |
| rs138342613 | snp | A/G | 0.000596323 | 0.017257 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446874 | ACCTTCTGGAACCCA[A/G]TGGCCTCAAAAAACT | 80700 |
| rs138428778 | snp | A/C/T | 0.000231469 | 0.0107557 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445597 | CACAGCCATGTCCCA[A/C/T]GAGAAGGTCAGGAGG | 80700 |
| rs138817781 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455519 | GCAGCCACAGGGACC[C/T]TTCTGGAACCTCAGC | 80700 |
| rs138897797 | snp | A/G/T | 5.05884e-05 | 0.00502912 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454009 | GGCTAGGGCGGCAGC[A/G/T]GCTGCCATCTGTGCC | 80700 |
| rs139000330 | in-del | -/CCG | 0.275999 | 0.248644 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444657 | GACCTTTCATCATAC[-/CCG]CCAAGCCCCTCTTGC | 80700 |
| rs139000566 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445719 | CGGGGATGCCCCGGC[C/G]TGGAAGCCATCTCAG | 80700 |
| rs139020875 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449761 | AAAGGTGGGATTTCA[C/T]AGCTGTAAGCAAAAG | 80700 |
| rs139475353 | snp | C/T | 6.60055e-05 | 0.00574442 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447619 | CAGGTGGATGTTGTC[C/T]AGGTACCTGGGGTAG | 80700 |
| rs139535362 | snp | A/G | 5.06684e-05 | 0.00503305 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446085 | CAGGTTCTCGTCCTC[A/G]GACAGCTTCTGCCCT | 80700 |
| rs139656461 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448365 | GTCCTGGTCTTTGTT[A/G]AACGTGTAGATCTTC | 80700 |
| rs139712027 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447222 | AGGACCCCAGTCCCT[G/T]CCCTTTCCCCCAGAA | 80700 |
| rs139717823 | snp | C/G/T | 0.000360765 | 0.0134263 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446515 | CTGAGCCTCTGCTCC[C/G/T]GCTTGATCTCCTCTG | 80700 |
| rs139865144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451507 | GCAGGTGCACGCCAC[C/T]ATGCCCAGCTATTTT | 80700 |
| rs139905537 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456381 | CCACCCCACTGCCCC[A/G]TGATTCCTGACCCCC | 80700 |
| rs140113334 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448869 | TGTTTACAAAGAGAC[C/G]GAGAGGCCCATCGTC | 80700 |
| rs140486278 | snp | A/C/G | 0.000198951 | 0.00997187 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453479 | GGTCCCTGGGGCCTC[A/C/G]GGGCTCCCGCTGACG | 80700 |
| rs140698840 | snp | A/G | 0.000473117 | 0.0153732 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446691 | GGCCAAGGTGGTCTC[A/G]CTCAGCACGTAGAAC | 80700 |
| rs140778307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452872 | CAAGGCATGACTTCT[G/T]GGCCTCCATTTCTAG | 80700 |
| rs140818399 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459354 | AAGCCTCCAGGTGAG[C/G]AAACAGCCCACCCCA | 80700 |
| rs140949456 | snp | C/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447762 | GGCCCAGTGACGCGA[C/G]GGCAGCAGACCATCT | 80700 |
| rs141014666 | snp | C/T | 0.00276601 | 0.0370858 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446624 | CCAGCTTGGCGCGCA[C/T]GGGCTCCGCAGCCAG | 80700 |
| rs141123683 | snp | C/T | 3.32973e-05 | 0.00408014 | missense | UBXN6 | GRCh38.p7 | 19:4453938 | ATCTCACCCTGGTTT[C/T]GGATGGTGTCCTGCG | 80700 |
| rs141391502 | snp | C/T | 0.000214452 | 0.0103528 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447597 | GGTACTTCTCCTCCT[C/T]GGGGTGCAGGTGGAT | 80700 |
| rs141667104 | snp | A/G | 0.000311937 | 0.0124848 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446055 | GACACTCACCAGCCC[A/G]CACTCGTTCAAGGCC | 80700 |
| rs141788493 | in-del | -/GC | 0.039522 | 0.134904 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449628 | AAAAGCGGGCCTCGG[-/GC]GTTTTGGGCGACTGG | 80700 |
| rs141958598 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454951 | GGCGATGTGCCCCAT[C/G]CCACGCCACCCTCGT | 80700 |
| rs142289397 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449996 | GCACTTTGGGAGGCC[G/T]AGGCGGTCGGATCAC | 80700 |
| rs142735003 | snp | A/C/G | 0.00187795 | 0.0305869 | utr-variant-5-prime, synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454033 | CTGTGCCTCATTGGT[A/C/G]GGTCCCTGGCGGGGC | 80700 |
| rs142895800 | snp | C/T | 0.00530081 | 0.0512101 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446423 | TCGGACCTGCACACG[C/T]GGGCCAGGTCACGAG | 80700 |
| rs143155703 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455926 | CACTCATCGCCTGAG[C/T]GCTCATCCAAGGTCT | 80700 |
| rs143191932 | snp | A/G | 0.212728 | 0.247206 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459788 | GCAGAGCTTACAGTG[A/G]GCCGAGATCATGCCA | 80700 |
| rs143363747 | snp | A/G | 1.64996e-05 | 0.0028722 | stop-gained, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447567 | GAAACACCTTGTTCT[A/G]CAGCTTGATCTTCCG | 80700 |
| rs143390041 | snp | G/T | 0.183568 | 0.241012 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459751 | GGGAGGCTGAGGCAG[G/T]AGAATGGCGTGAACC | 80700 |
| rs143704241 | snp | A/G | 2.43775e-05 | 0.00349115 | synonymous-codon, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448350 | ACCCAGCTTCACCCG[A/G]TCCTGGTCTTTGTTG | 80700 |
| rs143712546 | snp | C/T | 0.000153988 | 0.00877328 | missense | UBXN6 | GRCh38.p7 | 19:4452395 | TTGATGCAGGCGTCC[C/T]GCTGGTCCTTCCTCA | 80700 |
| rs143798123 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456404 | TGACCCCCACTTCCT[A/G]CCACCTCCCTGCCTC | 80700 |
| rs144059317 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459160 | TGAAAGCCTGTCTCT[A/G]TGGGCACCGGTAATC | 80700 |
| rs144165012 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456791 | AGAGAAGCTCTTTCT[C/T]CCAGCCTGCTAAGAC | 80700 |
| rs144275315 | in-del | -/CCAGGGCCAGGCA | 0.480697 | 0.0963277 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453860 | ATGTGACTTCTGCAT[-/CCAGGGCCAGGCA]CCAGGGCCGAGAACC | 80700 |
| rs144587110 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459644 | AGATTGAGACCATCC[C/T]GGCTAATACGGTGAA | 80700 |
| rs144624172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451083 | AGATGAAGTTTCGCT[A/C]TTGTCACCCAGTGTC | 80700 |
| rs144934048 | snp | C/T | 1.70638e-05 | 0.00292089 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446631 | GGCGCGCACGGGCTC[C/T]GCAGCCAGCAGCTGT | 80700 |
| rs145191302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448962 | GAAACTCAATAGCTG[A/G]AAGACGGATACCCCC | 80700 |
| rs145290718 | snp | C/G | 0.000115484 | 0.00759794 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447603 | TCTCCTCCTCGGGGT[C/G]CAGGTGGATGTTGTC | 80700 |
| rs145303168 | snp | A/G/T | 0.000592502 | 0.017202 | synonymous-codon, missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446516 | TGAGCCTCTGCTCCC[A/G/T]CTTGATCTCCTCTGC | 80700 |
| rs145338031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452584 | GTGTGGCCCGTAGAA[C/G]CAGACATCTCCAGCC | 80700 |
| rs145410565 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459645 | GATTGAGACCATCCC[A/G]GCTAATACGGTGAAA | 80700 |
| rs145514331 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452030 | GGCAGGTGCCTGTAA[G/T]CCCAGCTACTTGAGA | 80700 |
| rs145565148 | snp | C/T | 4.98004e-05 | 0.00498976 | missense | UBXN6 | GRCh38.p7 | 19:4452378 | CCAAGAGAATGGCCT[C/T]CTTGATGCAGGCGTC | 80700 |
| rs145656576 | snp | A/T | 0.000153988 | 0.00877328 | missense | UBXN6 | GRCh38.p7 | 19:4453484 | CTGGGGCCTCGGGGC[A/T]CCCGCTGACGGTGGC | 80700 |
| rs145906971 | snp | A/G | 0.000219682 | 0.0104782 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446700 | GGTCTCGCTCAGCAC[A/G]TAGAACTCCTCGGGG | 80700 |
| rs145914769 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453267 | CTCCAGGCCTGAGCC[A/G]GCATCCTCAGCTGCC | 80700 |
| rs146350492 | snp | A/C/G | 0.00110636 | 0.023494 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445586 | ATGTCCTCCAGCACA[A/C/G]CCATGTCCCACGAGA | 80700 |
| rs146438565 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452634 | CTGGTGGCCGTGGGA[A/G]ACACCCTGGCCAAGT | 80700 |
| rs146778894 | snp | C/T | 0.00298509 | 0.038518 | missense | UBXN6 | GRCh38.p7 | 19:4453478 | TGGTCCCTGGGGCCT[C/T]GGGGCTCCCGCTGAC | 80700 |
| rs146789207 | snp | C/G/T | 3.38457e-05 | 0.00411362 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446666 | TGTGCCTCTCCAGGC[C/G/T]CTGGGGCTGGGCCAA | 80700 |
| rs146963914 | snp | A/G | 0.000381587 | 0.0138075 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454049 | GGTCCCTGGCGGGGC[A/G]GCCTGGGGGCTGGCT | 80700 |
| rs147213791 | snp | A/C | 7.15931e-05 | 0.00598259 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448358 | TCACCCGGTCCTGGT[A/C]TTTGTTGAACGTGTA | 80700 |
| rs147341905 | snp | A/G | 0.000197984 | 0.0099475 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447609 | CCTCGGGGTGCAGGT[A/G]GATGTTGTCCAGGTA | 80700 |
| rs147364683 | snp | A/G | 0.000429738 | 0.0146521 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446349 | ACTTGCGCAGCCCCC[A/G]CTGCTCCTCCTTCTC | 80700 |
| rs147447369 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451128 | ATGGCGTGATCTGGG[C/T]TCACTGCAACCTCCA | 80700 |
| rs147563273 | snp | A/G | 0.029116 | 0.117091 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450074 | CTCTAAAATACAAAA[A/G]TTAGCCCGGGTGTGG | 80700 |
| rs147606668 | snp | G/T | 0.000259837 | 0.0113952 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446567 | CAGGCAGTTCGAACT[G/T]CGAGGCCAGGGGCGA | 80700 |
| rs147636603 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451638 | GGAAAAAAATGCTGT[A/G]GACGTTTTTATTTTT | 80700 |
| rs147856824 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447307 | ACAAGCCCAGCTGAA[A/G]AGGAGGAAAAGGATG | 80700 |
| rs148210917 | snp | A/G | 0.0287284 | 0.116357 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448730 | CTGGCTTTAGAACTC[A/G]ACCTCAGTGCTGAGA | 80700 |
| rs148219784 | snp | C/T | 0.000577258 | 0.0169793 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447581 | TGCAGCTTGATCTTC[C/T]GGTACTTCTCCTCCT | 80700 |
| rs148557515 | snp | A/G | 0.000686609 | 0.0185157 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446405 | CTCAGCCGCTCCACC[A/G]CCTCGGACCTGCACA | 80700 |
| rs148678034 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456907 | ACACCTTCCTCAGCC[C/T]CTCCCTCTCAATTCG | 80700 |
| rs148732278 | snp | A/G | 0.00104668 | 0.0228526 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4452391 | CTCCTTGATGCAGGC[A/G]TCCCGCTGGTCCTTC | 80700 |
| rs148736820 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450846 | TAATGTAGAAAGGAC[A/G]CATTCTCATATGAAA | 80700 |
| rs148839817 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452081 | TTGAATCCAGGAGGC[A/G]GAGGTTGTAGTGAGC | 80700 |
| rs148878855 | in-del | -/C | 0.0535932 | 0.154675 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457245 | AGGTCGTTCCACTGA[-/C]CCCCAACTGCCTACA | 80700 |
| rs149091880 | snp | A/G | 0.000242248 | 0.011003 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446571 | CAGTTCGAACTGCGA[A/G]GCCAGGGGCGAGGGC | 80700 |
| rs149133767 | snp | C/G | 0.00108843 | 0.023303 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445544 | TCGGGTTTCAGGATG[C/G]AGTCCGGCTCGGCCC | 80700 |
| rs149240636 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445152 | GCCACCCACGGCACA[C/T]GGGAACAGGACCCAT | 80700 |
| rs149591009 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448540 | CGGCCCCAGCTGTGC[A/G]CTCATCACAGAAAGG | 80700 |
| rs149610347 | snp | A/G | 0.00400154 | 0.0445506 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446891 | GGCCTCAAAAAACTC[A/G]TGGGTCCCTTCCAGG | 80700 |
| rs149717969 | snp | C/T | 4.7372e-05 | 0.0048666 | synonymous-codon, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448368 | CTGGTCTTTGTTGAA[C/T]GTGTAGATCTTCATG | 80700 |
| rs149835255 | in-del | -/TA | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457795 | CCACCGGAAGAAAAT[-/TA]AAAAAAAAAAAAAAA | 80700 |
| rs150112726 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444999 | TTTCAACGGAGAACC[A/G]AGAAACTATATTCAA | 80700 |
| rs150233844 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4455050 | CTGTGCAAGTACGAA[C/G]AGCTCATGGACTCGT | 80700 |
| rs150530113 | snp | A/C | 0.000358573 | 0.013385 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446065 | AGCCCGCACTCGTTC[A/C]AGGCCAGGTTCTCGT | 80700 |
| rs150635571 | snp | C/T | 4.96775e-05 | 0.0049836 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446829 | CAGCCAGGCCCTGTC[C/T]ACTTACCCTGATCCT | 80700 |
| rs151060057 | snp | C/T | 6.85295e-05 | 0.00585321 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446618 | GCCTGTCCAGCTTGG[C/T]GCGCACGGGCTCCGC | 80700 |
| rs151114260 | snp | A/G | 1.66579e-05 | 0.00288595 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453934 | CCATATCTCACCCTG[A/G]TTTCGGATGGTGTCC | 80700 |
| rs151206289 | snp | C/G | 0.0232847 | 0.105357 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458533 | CCTGAAGCACCCCCC[C/G]GCCACCATCACCACG | 80700 |
| rs180818666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452784 | CAGATGGCAGCTGGG[C/T]TCCTGCTGGTCCTGT | 80700 |
| rs180886926 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445891 | ACTTGCTCGAGGCCC[G/T]GCTGCCAGTAAGTGG | 80700 |
| rs180916285 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455417 | ATGAAGACCCACCCC[A/G]GCCTCATCCGATATC | 80700 |
| rs180938866 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450593 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAGAA | 80700 |
| rs181160213 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456220 | AGTGGCCCCAGCACC[C/T]CCCACCCACTATTGG | 80700 |
| rs181368786 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449902 | CAAAGCTTCAACCAT[A/G]GAAACAAGCAAGCAG | 80700 |
| rs181653820 | snp | A/G | 0.000100766 | 0.00709738 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445663 | CTGAGACCGAGAGTC[A/G]GCCCTTGCCGCGGCA | 80700 |
| rs181714755 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456099 | GGGACCTCCGCACCG[A/C]TTCCTTTCCCAACCT | 80700 |
| rs181978838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452898 | TCTAGGCCATCTCTA[A/G]GGTCCCTGCGTGCTA | 80700 |
| rs182021672 | snp | A/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453174 | GGTTCTCTTTTTGAA[A/T]AGTGGAAACTGTAAC | 80700 |
| rs182269512 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454228 | CTATGTGGGCCAGGA[C/G]ACCTGGTTCCCAGGG | 80700 |
| rs182272623 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445054 | ATTTACTAACTGCAG[A/G]TCTATGTGCAGGAAG | 80700 |
| rs182314507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451889 | GCGTGGTGGCTCACG[C/T]CTGTAATCCTAGCAC | 80700 |
| rs182781263 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448621 | GCGACGCAGCCAAGA[C/G]CCAGCAGAACTCAAG | 80700 |
| rs182845700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451023 | AGTGGGTGTGAGTCT[G/T]GAGAGTCTATGGAAC | 80700 |
| rs182866566 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451291 | TGGAACTTCTGACCT[A/C]AGGTGATCCACCTGC | 80700 |
| rs182890664 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, stop-gained, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447128 | AGCTCTGCACAGAGG[A/T]AAGAGTCACAACCAG | 80700 |
| rs183262169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454601 | GCTAATTTTTCTATC[A/G]AGACAGGGTCTCGCT | 80700 |
| rs183356732 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458659 | ATCACAAGGTCAGGA[A/G]ATCGAGACCATCCTG | 80700 |
| rs183565495 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4455242 | TGTCAATTTCTGTGC[C/T]GTAGGTCTATTAAAA | 80700 |
| rs183725976 | snp | A/G | 0.000210959 | 0.0102682 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446187 | CAGCCGCTCCCGAGC[A/G]TAGAAAGTGCCTGGG | 80700 |
| rs183861781 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459217 | AGAATCGCTTGAACC[C/T]GGCAGGTGGAGGTTG | 80700 |
| rs184448060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452237 | GGGTATCAGAGGAGG[A/G]GCTTCACTACTAGCA | 80700 |
| rs184527329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444718 | GAATAGGATGTGGCC[A/G]TCTCAGGACACCCTG | 80700 |
| rs184581650 | snp | C/T | 0.00638509 | 0.0561407 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452523 | CGTCCAAGTCTGGAC[C/T]GTGGACAGAGGCCAC | 80700 |
| rs184671857 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459687 | CTGAAAATAATTTTT[A/T]AAAAAATTAGCCAGC | 80700 |
| rs184715735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449825 | AGCTGAGCCAAGATC[C/T]AAAAAAAAAATTACA | 80700 |
| rs184782133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449293 | AGCCCAGGGCCATGT[A/G]TCAGGATTCGGGCCA | 80700 |
| rs185204211 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445214 | GCCACGTGTGTCTGT[C/T]CGGCAGCTTCATGAC | 80700 |
| rs185223028 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452840 | TGTGTGGGTGTCTGC[A/G]GGCACAGTGCGCTGG | 80700 |
| rs185411512 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455432 | GGCCTCATCCGATAT[C/T]TGGGTCTTTCCAACA | 80700 |
| rs185464027 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454815 | GCTTCGTTTGCTGAG[C/T]ACCTACTGTGTGCCA | 80700 |
| rs185758658 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457195 | AGCTCTCCCTCACCA[C/G]CCGGCTCAGGACTCA | 80700 |
| rs186009738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451035 | TCTGGAGAGTCTATG[A/G]AACTATTACTATTTT | 80700 |
| rs186087815 | snp | C/G/T | 0.000813635 | 0.0201555 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445975 | GGAGGCTCCCTCCTG[C/G/T]GGGTGTCTGTGCCGG | 80700 |
| rs186322973 | snp | C/T | 0.000153598 | 0.00876216 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446313 | CATCGGGGAGGCGCA[C/T]GCGCAGCAGCGTGTA | 80700 |
| rs186362606 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452920 | TGCGTGCTAAAATTC[A/C]CTGAATCCTCGAGGG | 80700 |
| rs186652496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449957 | TCTGGAGGCCGGGCA[C/T]GGTGGCTCATGCCTG | 80700 |
| rs186928207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454500 | CGATCATGGCTTACT[A/G]CAATCCTGAGCTCCC | 80700 |
| rs187059352 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459315 | AAGGAGTTGGAATGA[A/G]ATACACAGAGACTGA | 80700 |
| rs187138254 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456114 | CTTCCTTTCCCAACC[C/T]TCCCCTCCAACCTTC | 80700 |
| rs187703047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449093 | CTGACTGCGAACAGC[A/G]TCCCAGCATGGAGAG | 80700 |
| rs187936889 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454840 | GTGCCAGGACCCTGC[C/T]GGGAGCTGGTCGGCT | 80700 |
| rs188048657 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4455289 | GCTCTCAGTTCAAGC[C/T]CTATACTCCTCTGGC | 80700 |
| rs188332691 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451324 | CAGCCTCCCAAAGCA[C/T]TGGAATTACAGGCAA | 80700 |
| rs188762921 | snp | A/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458964 | CACCAGTTAATAGTG[A/G]CGTACTTTGGTCTGT | 80700 |
| rs188969463 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445484 | ACAGGGCTGAGGCCA[A/G]CCCTGCTTTTATTTC | 80700 |
| rs189030396 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450307 | TTTCTAAGAATGACC[C/T]CAAACCCAAAAGCCA | 80700 |
| rs189091879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454684 | GCCTCCCAAACTGCT[A/G]GGATTATAGGCATGA | 80700 |
| rs189254349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452850 | TCTGCGGGCACAGTG[C/T]GCTGGACAAGGCATG | 80700 |
| rs189507126 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449461 | CCCGGCCCAGTCTGC[C/T]GGTTTAGTTGCTGAG | 80700 |
| rs189812028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449827 | CTGAGCCAAGATCTA[A/G]AAAAAAAATTACATC | 80700 |
| rs189848059 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452600 | CAGACATCTCCAGCC[C/G]CCATGCTGTCCCTTC | 80700 |
| rs189877336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452299 | ACCACCTGGGCTTCC[A/G]ATGGAGGGTGGCTCA | 80700 |
| rs189930963 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454520 | CCTGAGCTCCCAGGC[C/T]CAAGGAATCCTCCCG | 80700 |
| rs190188654 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456187 | ATACCCTGCATCCTT[C/T]CTATCATGCCCAGTC | 80700 |
| rs190257660 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445823 | TACTGCACTAGCTAA[C/T]GCACGTCACCGCTCC | 80700 |
| rs190331849 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446944 | GGAGATGGGCGTCAC[G/T]GGGGGCCCCTGGCTT | 80700 |
| rs190609688 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445035 | CTGTTTATTTGGGCT[C/T]ATGATTTACTAACTG | 80700 |
| rs190652552 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455473 | TCCCAGGGCACCTCA[C/G]CCCAACCAGCCATGG | 80700 |
| rs191061033 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450651 | GTGGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 80700 |
| rs191109013 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459608 | TTTGGAAGGCCGAGG[C/T]GGGTGGATCACGAGG | 80700 |
| rs191346832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451214 | GGCGCCTGTCACCAC[A/G]CCTGGCTAATTTTTG | 80700 |
| rs191455839 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452953 | AAGCTGCTTAGAACT[A/C]CTTTCAGCGGAGCTC | 80700 |
| rs191612298 | snp | A/G | 9.10423e-05 | 0.00674632 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454140 | CCTCCCGAGGTGGCC[A/G]GCAAAGCTGACGTGC | 80700 |
| rs191816351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4455177 | AACCTGCTCGGACGC[A/G]TCTGTCTCACCCGTC | 80700 |
| rs191973140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449789 | AAGACAGGTGCTCTC[A/G]ACAGGTGGGGCTGAG | 80700 |
| rs192174502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451568 | CATGTTGCCCAGGCT[A/G]AAGCCGAAGTTTCTG | 80700 |
| rs192195006 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459100 | GAGGCCGAGGCCGGC[A/G]GATCACTTGAGGTCA | 80700 |
| rs192197761 | snp | A/G | 0.000163289 | 0.00903425 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446160 | CTCCCGGACGAACCC[A/G]TACACCGCCCCCAGC | 80700 |
| rs192457462 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458605 | GGCGCGGTGGCTCAT[G/T]CCTGTAATCCCAGCA | 80700 |
| rs192516175 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444701 | GCATCTGCAGGTTCC[A/C]GGAATAGGATGTGGC | 80700 |
| rs192661521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451946 | CTTGAGGCAAAAGTT[C/T]GAGACCAGCCTGGCC | 80700 |
| rs192763149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449183 | CACAGCCATCACACA[C/T]GGCCACACCCAGAGA | 80700 |
| rs192780984 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447233 | CCCTGCCCTTTCCCC[C/T]AGAAGAACCAGACAT | 80700 |
| rs192808812 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454717 | CACAGCACCCAGCCC[A/G]CATCCTCAGGAATTG | 80700 |
| rs193168940 | snp | C/T | 0.000399281 | 0.0141238 | missense | UBXN6 | GRCh38.p7 | 19:4452390 | CCTCCTTGATGCAGG[C/T]GTCCCGCTGGTCCTT | 80700 |
| rs199526691 | snp | C/G | 0.00299544 | 0.0385843 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452520 | AAGCGTCCAAGTCTG[C/G]ACCGTGGACAGAGGC | 80700 |
| rs199552431 | snp | C/G | 0.000947891 | 0.0217496 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446792 | CCTCCTGCCCCGAGG[C/G]CCCTCGTCCCCATTC | 80700 |
| rs199562374 | snp | C/G/T | 0.000399281 | 0.0141238 | UBXN6, MIR4746, CHAF1A | 19 | allele_origin=T(somatic)/C(germline) | 19:4446365 | CTGCTCCTCCTTCTC[C/G/T]CGCATGGCCTTGGTC | 80700 |
| rs199661814 | snp | A/C | 1.96566e-05 | 0.00313495 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457597 | GCAGGGCCTCAAGCC[A/C]CTGCGTTCCTCACGC | 80700 |
| rs199694508 | snp | A/G | 0.000376888 | 0.0137223 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453503 | GCTGACGGTGGCTTC[A/G]GCTTGAAGTTCCTTT | 80700 |
| rs199794846 | snp | C/G | 1.73966e-05 | 0.00294924 | missense | UBXN6 | GRCh38.p7 | 19:4452464 | GGCACAGCCAGGTGG[C/G]CAGAGCCTTCCTCTC | 80700 |
| rs199967454 | snp | C/G | 0.00174439 | 0.0294814 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448278 | GGGGTGCTGGGATGA[C/G]CTGGAGGGGCCAGGC | 80700 |
| rs200009861 | in-del | -/A | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449825 | GCTGAGCCAAGATCT[-/A]AAAAAAAAAATTACA | 80700 |
| rs200014531 | snp | A/G | 0.000173058 | 0.00930049 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454044 | TGGTGGGTCCCTGGC[A/G]GGGCGGCCTGGGGGC | 80700 |
| rs200047802 | snp | C/T | 0.00100961 | 0.0224451 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446620 | CTGTCCAGCTTGGCG[C/T]GCACGGGCTCCGCAG | 80700 |
| rs200183933 | snp | A/G/T | 0.000760567 | 0.0194869 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447528 | CCCAGCCTGGGCCCC[A/G/T]GGGGCCAGAAGGCAC | 80700 |
| rs200267132 | snp | C/T | 5.09992e-05 | 0.00504945 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446755 | GGTGTCACTGTGCAA[C/T]GGAGAGACCCCCAAG | 80700 |
| rs200291730 | snp | A/G | 0.000116207 | 0.00762167 | missense | UBXN6 | GRCh38.p7 | 19:4453972 | TGGGGCCCCAGGCCC[A/G]GGACTGCTTCTGCTC | 80700 |
| rs200383476 | snp | C/G | 0.000413044 | 0.0143649 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457585 | CGTCCCCGCCCCGCA[C/G]GGCCTCAAGCCCCTG | 80700 |
| rs200528029 | snp | C/T | 0.00256162 | 0.0356966 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446787 | CGGGCCCTCCTGCCC[C/T]GAGGCCCCTCGTCCC | 80700 |
| rs200531988 | snp | C/G | | | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446952 | GCGTCACTGGGGGCC[C/G]CTGGCTTCCTCCATG | 80700 |
| rs200532411 | snp | A/G | 0.000457701 | 0.0151209 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446314 | ATCGGGGAGGCGCAC[A/G]CGCAGCAGCGTGTAG | 80700 |
| rs200555890 | snp | C/T | 0.000528541 | 0.0162478 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445584 | TGATGTCCTCCAGCA[C/T]AGCCATGTCCCACGA | 80700 |
| rs200629234 | in-del | -/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453872 | ATCCAGGGCCAGGCA[-/T]CCAGGGCCGAGAACC | 80700 |
| rs200629893 | snp | A/C/G | 8.44382e-05 | 0.00649717 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446686 | GGCTGGGCCAAGGTG[A/C/G]TCTCGCTCAGCACGT | 80700 |
| rs200646154 | snp | C/T | 0.000561927 | 0.0167525 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452541 | GGACAGAGGCCACCC[C/T]GACCCTCGCCGAGCA | 80700 |
| rs200662399 | snp | C/T | 0.00121191 | 0.0245863 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446421 | CCTCGGACCTGCACA[C/T]GCGGGCCAGGTCACG | 80700 |
| rs200738828 | snp | A/G | 0.000166611 | 0.00912567 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457746 | GGGCGGGGGGGCACG[A/G]GGCCCAGTCGGGGAC | 80700 |
| rs200744680 | snp | C/T | 9.90066e-05 | 0.00703516 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445549 | TTTCAGGATGGAGTC[C/T]GGCTCGGCCCCCGCG | 80700 |
| rs200775962 | snp | C/T | 0.00013643 | 0.00825812 | missense | UBXN6 | GRCh38.p7 | 19:4452444 | GACAGGTGAAGTACA[C/T]GCCAGGCACAGCCAG | 80700 |
| rs200865875 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447634 | CAGGTACCTGGGGTA[A/G]GTGGAGAAGGTGAGT | 80700 |
| rs200880137 | snp | C/T | 1.76058e-05 | 0.00296692 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454067 | CTGGGGGCTGGCTGG[C/T]TGGGCTTCTCTTTGT | 80700 |
| rs200898701 | snp | C/G | 0.00011824 | 0.00768805 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446683 | TGGGGCTGGGCCAAG[C/G]TGGTCTCGCTCAGCA | 80700 |
| rs200974035 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452151 | GAGACTCCATCTCAA[A/G]AAAAAAAAAAAAGAC | 80700 |
| rs201011300 | snp | C/T | 8.40018e-05 | 0.00648027 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445662 | TCTGAGACCGAGAGT[C/T]GGCCCTTGCCGCGGC | 80700 |
| rs201076191 | snp | A/G/T | 0.00139332 | 0.026358 | synonymous-codon, missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446183 | CCCCCAGCCGCTCCC[A/G/T]AGCGTAGAAAGTGCC | 80700 |
| rs201109123 | snp | A/G | 0.00149365 | 0.0272873 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446737 | ACAGCGTGGCAGGAC[A/G]TGGGTGTCACTGTGC | 80700 |
| rs201286440 | snp | A/G | 8.95568e-05 | 0.00669107 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453881 | CCAGGCACCAGGGCC[A/G]AGAACCTCAAACAGC | 80700 |
| rs201302959 | snp | A/G | 0.00261346 | 0.0360541 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457722 | TGGCCCGGCGGCGGG[A/G]GGCCGCGGGGGCGGG | 80700 |
| rs201322182 | snp | C/T | 0.000417188 | 0.0144368 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446361 | CCCGCTGCTCCTCCT[C/T]CTCCCGCATGGCCTT | 80700 |
| rs201394926 | snp | A/G | 0.00017111 | 0.00924801 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446621 | TGTCCAGCTTGGCGC[A/G]CACGGGCTCCGCAGC | 80700 |
| rs201431319 | snp | C/T | 8.75664e-05 | 0.00661631 | missense | UBXN6 | GRCh38.p7 | 19:4452471 | CCAGGTGGGCAGAGC[C/T]TTCCTCTCTGGGCTC | 80700 |
| rs201517666 | snp | A/C/T | 0.000141707 | 0.00841625 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446396 | CGCAGCACGCTCAGC[A/C/T]GCTCCACCGCCTCGG | 80700 |
| rs201600986 | in-del | -/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457795 | CCACCGGAAGAAAAT[-/T]AAAAAAAAAAAAAAA | 80700 |
| rs201671391 | snp | C/T | 5.13641e-05 | 0.00506749 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453880 | GCCAGGCACCAGGGC[C/T]GAGAACCTCAAACAG | 80700 |
| rs201700000 | snp | C/T | 0.000132107 | 0.00812626 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447543 | GGGGGCCAGAAGGCA[C/T]GCCCACCTGAAACAC | 80700 |
| rs201783696 | snp | C/T | 0.000453347 | 0.0150489 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446176 | TACACCGCCCCCAGC[C/T]GCTCCCGAGCGTAGA | 80700 |
| rs201865786 | snp | A/G/T | 0.000484593 | 0.0155585 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445656 | CGTCACTCTGAGACC[A/G/T]AGAGTCGGCCCTTGC | 80700 |
| rs202019475 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453871 | GCATCCAGGGCCAGG[C/T]ACCAGGGCCGAGAAC | 80700 |
| rs202166922 | snp | C/G | 5.02071e-05 | 0.00501009 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448282 | TGCTGGGATGAGCTG[C/G]AGGGGCCAGGCAGGG | 80700 |
| rs202169732 | snp | C/G/T | 3.3865e-05 | 0.00411477 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446660 | GTTCCTTGTGCCTCT[C/G/T]CAGGCTCTGGGGCTG | 80700 |
| rs202229402 | snp | C/T | 1.73411e-05 | 0.00294453 | utr-variant-5-prime, synonymous-codon | UBXN6 | GRCh38.p7 | 19:4454048 | GGGTCCCTGGCGGGG[C/T]GGCCTGGGGGCTGGC | 80700 |
| rs267605469 | snp | C/T | 5.18847e-05 | 0.0050931 | UBXN6, MIR4746, CHAF1A | 19 | allele_origin=T(somatic)/C(germline) | 19:4446366 | TGCTCCTCCTTCTCC[C/T]GCATGGCCTTGGTCC | 80700 |
| rs367564016 | snp | A/G | 4.21985e-05 | 0.0045932 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446424 | CGGACCTGCACACGC[A/G]GGCCAGGTCACGAGG | 80700 |
| rs367564505 | snp | C/T | 6.80793e-05 | 0.00583395 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446752 | ATGGGTGTCACTGTG[C/T]AATGGAGAGACCCCC | 80700 |
| rs367618040 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453299 | AGCCCCGAAGGTCCC[A/G]GACAACACCGTGTTC | 80700 |
| rs367682939 | in-del | -/AG | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449498 | TGGGGAGCGGGACAG[-/AG]CACGTGGATGCAGAG | 80700 |
| rs367738297 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449086 | AGCCCTGCTGACTGC[A/G]AACAGCGTCCCAGCA | 80700 |
| rs367786829 | snp | C/T | 0.000115484 | 0.00759794 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447591 | TCTTCCGGTACTTCT[C/T]CTCCTCGGGGTGCAG | 80700 |
| rs367970662 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445781 | CCTGCCCTCTCCCTC[C/T]GGGACTCCAGGACCT | 80700 |
| rs367993303 | snp | A/G | 0.00013293 | 0.00815153 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446798 | GCCCCGAGGCCCCTC[A/G]TCCCCATTCCCTACT | 80700 |
| rs367999996 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447638 | TACCTGGGGTAGGTG[A/G]AGAAGGTGAGTGGGG | 80700 |
| rs368092631 | snp | C/T | 0.000202071 | 0.0100496 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448465 | AGAGCCCGGGCCGCA[C/T]GGCCCTCCGCTGCCC | 80700 |
| rs368127059 | snp | A/C | 3.61618e-05 | 0.00425201 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446514 | CCTGAGCCTCTGCTC[A/C]CGCTTGATCTCCTCT | 80700 |
| rs368206089 | snp | G/T | 4.94988e-05 | 0.00497463 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445542 | GCTCGGGTTTCAGGA[G/T]GGAGTCCGGCTCGGC | 80700 |
| rs368344029 | snp | A/C/T | 0.000214349 | 0.0103507 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453555 | AAAGAGAGGCAGAGA[A/C/T]GGGATAGTGAGCACG | 80700 |
| rs368345593 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458521 | CCTGTTTTGGTGCCT[A/G]AAGCACCCCCCCGCC | 80700 |
| rs368371362 | snp | C/G/T | 6.3713e-05 | 0.00564387 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446207 | AAGTGCCTGGGGAGT[C/G/T]GGGGAGTCAGAGCGG | 80700 |
| rs368501215 | snp | A/G | 3.34627e-05 | 0.00409026 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452350 | GGGGCAGGAGCACAC[A/G]GGGTGCCACTCACCA | 80700 |
| rs368537262 | snp | C/G/T | 8.34528e-05 | 0.00645912 | missense | UBXN6 | GRCh38.p7 | 19:4454002 | CCAGCCGGGCTAGGG[C/G/T]GGCAGCGGCTGCCAT | 80700 |
| rs368543843 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456641 | CGGCCCTCCCAGCTG[A/G]CTCAGCCCTGCTCAG | 80700 |
| rs368641996 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456491 | GGCTGCCTGGCTGAC[C/T]TCCTCAGTCCCTCTC | 80700 |
| rs368642665 | snp | C/T | 0.000340015 | 0.0130343 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446726 | CGGGGTCCTCTACAG[C/T]GTGGCAGGACATGGG | 80700 |
| rs368648392 | snp | C/T | 3.30267e-05 | 0.00406353 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445575 | CCGCGGCCTTGATGT[C/T]CTCCAGCACAGCCAT | 80700 |
| rs368693394 | snp | A/G | 1.75829e-05 | 0.00296498 | utr-variant-5-prime, stop-gained | UBXN6 | GRCh38.p7 | 19:4454065 | GCCTGGGGGCTGGCT[A/G]GTTGGGCTTCTCTTT | 80700 |
| rs368709318 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445248 | GTTACCAAGCAGCTA[A/G]GGAGGGCTTAGATTT | 80700 |
| rs368745334 | snp | A/C/T | 0.000561838 | 0.0167528 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446484 | CCCCACTCTGCTCCG[A/C/T]GGACGTCAGGCCCAC | 80700 |
| rs368753562 | snp | A/C/T | 2.59994e-05 | 0.00360541 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446186 | CCAGCCGCTCCCGAG[A/C/T]GTAGAAAGTGCCTGG | 80700 |
| rs368841367 | snp | A/C/T | 0.000362542 | 0.0134596 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446580 | CTGCGAGGCCAGGGG[A/C/T]GAGGGCTGGAAGACG | 80700 |
| rs369022235 | snp | A/G | 3.29984e-05 | 0.00406179 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445531 | GGCTGACAGGAGCTC[A/G]GGTTTCAGGATGGAG | 80700 |
| rs369043795 | snp | A/C/T | 0.000112594 | 0.00750227 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446006 | TCCCAGGAGAACCTG[A/C/T]AGAGGCATCGGGTCA | 80700 |
| rs369055580 | snp | C/G | 1.67002e-05 | 0.00288961 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4452412 | CTGGTCCTTCCTCAG[C/G]GTGGCCCCAGTGAGC | 80700 |
| rs369227829 | snp | A/G | 0.000182672 | 0.00955523 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454131 | TGAGTGTATCCTCCC[A/G]AGGTGGCCGGCAAAG | 80700 |
| rs369231229 | snp | A/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454372 | CAGCGTCCTCATCTG[A/T]AAAATGGGGTGACAG | 80700 |
| rs369250495 | snp | A/G | 0.000116203 | 0.00762154 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445628 | GCAGAGGGCACCTGC[A/G]GTAGGGGTAGGCCGT | 80700 |
| rs369261662 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454910 | TCACCATCCCATTCC[C/T]AAACCCAAGAGGGAC | 80700 |
| rs369277545 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458727 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGCGTCT | 80700 |
| rs369377758 | snp | A/G | 0.000185743 | 0.00963521 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445673 | GAGTCGGCCCTTGCC[A/G]CGGCAGGGAACTCAG | 80700 |
| rs369387765 | snp | A/G | 0.00012097 | 0.00777628 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446226 | GAGTCAGAGCGGGTG[A/G]GGCCCAGGGCCCCCT | 80700 |
| rs369394770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451656 | CGTTTTTATTTTTTG[A/C]GATGGAGTTTTGCTC | 80700 |
| rs369398559 | snp | C/T | 9.87191e-05 | 0.00702494 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448391 | TCTTCATGATGGAGG[C/T]GGCCACTGGGTCGGT | 80700 |
| rs369416771 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444695 | AGTTGCGCATCTGCA[A/G]GTTCCAGGAATAGGA | 80700 |
| rs369580764 | snp | C/G | 1.67447e-05 | 0.00289345 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452349 | TGGGGCAGGAGCACA[C/G]AGGGTGCCACTCACC | 80700 |
| rs369581272 | snp | C/T | 8.43832e-05 | 0.00649496 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445672 | AGAGTCGGCCCTTGC[C/T]GCGGCAGGGAACTCA | 80700 |
| rs369583372 | snp | C/T | 0.000334487 | 0.0129279 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453922 | GCCCGAGGAGGGCCA[C/T]ATCTCACCCTGGTTT | 80700 |
| rs369595122 | snp | A/G/T | 0.000130591 | 0.00807969 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457611 | CCCTGCGTTCCTCAC[A/G/T]CACCCCACGGACTCT | 80700 |
| rs369643959 | snp | C/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459647 | TTGAGACCATCCCGG[C/G]TAATACGGTGAAACC | 80700 |
| rs369689234 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455488 | CCCCAACCAGCCATG[G/T]ACCCTGCCCCCCTGG | 80700 |
| rs369845863 | snp | C/T | 8.68742e-05 | 0.00659011 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446054 | CGACACTCACCAGCC[C/T]GCACTCGTTCAAGGC | 80700 |
| rs369996640 | snp | C/T | | | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4455263 | TCTATTAAAACCTTC[C/T]GGGAGGCCAGGCTCT | 80700 |
| rs370002824 | snp | C/T | 0.000505652 | 0.0158925 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446446 | GTCACGAGGGCTGGC[C/T]GGGGTTCTTCCACCC | 80700 |
| rs370082053 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458016 | GGAGACAGGGCATTC[C/T]GTGGCGCTCCCCAAA | 80700 |
| rs370108620 | snp | A/G | 0.000985923 | 0.0221808 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446340 | TGTAGTTGTACTTGC[A/G]CAGCCCCCGCTGCTC | 80700 |
| rs370207460 | snp | A/G | 2.40053e-05 | 0.0034644 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446177 | ACACCGCCCCCAGCC[A/G]CTCCCGAGCGTAGAA | 80700 |
| rs370224035 | in-del | -/A | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458235 | AAACCTCGTCTCTAT[-/A]AAAAAAAAAAAAAAT | 80700 |
| rs370261331 | snp | A/G | 0.000107718 | 0.00733808 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452524 | GTCCAAGTCTGGACC[A/G]TGGACAGAGGCCACC | 80700 |
| rs370308244 | snp | A/G | | | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448527 | CAGCGGCTTGGAGCG[A/G]CCCCAGCTGTGCGCT | 80700 |
| rs370440061 | snp | C/G | 3.3094e-05 | 0.00406766 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445473 | GAGACAGACCCACAG[C/G]GCTGAGGCCAACCCT | 80700 |
| rs370648980 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445338 | ATGGGGGCTCTGCCA[A/C/T]GGGGCCCAATTCCAC | 80700 |
| rs370654543 | snp | A/G | 4.22502e-05 | 0.00459601 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453570 | CGGGATAGTGAGCAC[A/G]CCGCTGTCCTGGCCC | 80700 |
| rs370706235 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452338 | AAGCTACAGGTTGGG[G/T]CAGGAGCACACAGGG | 80700 |
| rs370743500 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453157 | TCACCTCTCTCAACC[C/T]CGGTTCTCTTTTTGA | 80700 |
| rs370750754 | snp | C/T | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459099 | GGAGGCCGAGGCCGG[C/T]GGATCACTTGAGGTC | 80700 |
| rs370962024 | snp | A/G/T | 5.65492e-05 | 0.00531714 | synonymous-codon, missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446150 | TCTGCAGGGCCTCCC[A/G/T]GACGAACCCGTACAC | 80700 |
| rs371036878 | snp | G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452832 | AGGAGCTCTGTGTGG[G/T]TGTCTGCGGGCACAG | 80700 |
| rs371042638 | snp | C/T | 6.82338e-05 | 0.00584057 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448441 | GGAAGCAGGGAAAGC[C/T]ACTCACTGAGAGCCC | 80700 |
| rs371133685 | snp | A/G | 3.30387e-05 | 0.00406427 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447540 | CCCGGGGGCCAGAAG[A/G]CACGCCCACCTGAAA | 80700 |
| rs371157853 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452241 | ATCAGAGGAGGGGCT[C/T]CACTACTAGCAGTGG | 80700 |
| rs371480940 | snp | A/G | 5.27505e-05 | 0.00513541 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446924 | GTTAATGCGCTCCTG[A/G]GGGTGGAGATGGGCG | 80700 |
| rs371513236 | snp | A/G | 3.44039e-05 | 0.00414738 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446598 | GGGCTGGAAGACGCG[A/G]CGCTGCCTGTCCAGC | 80700 |
| rs371604650 | snp | A/C/G | 1.80036e-05 | 0.00300024 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454096 | GTGGGCCTTTTCCCT[A/C/G]GGAACAGACCGAGGG | 80700 |
| rs371620601 | in-del | -/CT | | | intron-variant, upstream-variant-2KB, frameshift-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444571 | TCTTCCAGTCTCTCT[-/CT]GATTCACCCTCCTGC | 80700 |
| rs371626143 | snp | A/G | 0.000133134 | 0.00815776 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445642 | CGGTAGGGGTAGGCC[A/G]TCACTCTGAGACCGA | 80700 |
| rs371728558 | snp | C/G | 1.66048e-05 | 0.00288134 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446802 | CGAGGCCCCTCGTCC[C/G]CATTCCCTACTCAGC | 80700 |
| rs371759678 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454190 | TGCCCCTCCCCAGCA[C/G]CATCAGCCAGACGTG | 80700 |
| rs371899421 | snp | A/G | 2.05666e-05 | 0.00320669 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457586 | GTCCCCGCCCCGCAG[A/G]GCCTCAAGCCCCTGC | 80700 |
| rs371983225 | snp | C/T | 3.36757e-05 | 0.00410326 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4452427 | GGTGGCCCCAGTGAG[C/T]GGACAGGTGAAGTAC | 80700 |
| rs372052682 | snp | A/G/T | 0.000312199 | 0.0124902 | missense, synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446562 | GTCCCCAGGCAGTTC[A/G/T]AACTGCGAGGCCAGG | 80700 |
| rs372079802 | snp | A/G | 0.000131744 | 0.00811508 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446485 | CCCACTCTGCTCCGC[A/G]GACGTCAGGCCCACC | 80700 |
| rs372118660 | snp | A/G | 0.000102246 | 0.00714932 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452509 | TGGGGCGGTGAAAGC[A/G]TCCAAGTCTGGACCG | 80700 |
| rs372222159 | snp | A/G | 0.000259241 | 0.0113821 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457567 | CAGATCTCTCTCCCC[A/G]GCCGTCCCCGCCCCG | 80700 |
| rs372256170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445863 | GGGAAACTGAGGCGT[A/G]GAGTAGTTATGAACT | 80700 |
| rs372294631 | in-del | -/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455501 | TGGACCCTGCCCCCC[-/T]GGGCAGCCACAGGGA | 80700 |
| rs372305065 | snp | C/T | 0.00018879 | 0.00971387 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446220 | GTGGGGGAGTCAGAG[C/T]GGGTGGGGCCCAGGG | 80700 |
| rs372467383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451873 | AAAACAACCAGGCCA[C/T]GCGTGGTGGCTCACG | 80700 |
| rs372573234 | snp | G/T | | | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448692 | GGAAGCCAGTGTGAC[G/T]CGACAGAACTGTGCC | 80700 |
| rs372577339 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454928 | ACCCAAGAGGGACAG[A/G]AAGTCCGGGCGATGT | 80700 |
| rs372577786 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454861 | CTGGTCGGCTCGCTT[A/G]GTTTACTCCTCCTAA | 80700 |
| rs372645367 | snp | C/T | 8.43533e-05 | 0.00649381 | missense | UBXN6 | GRCh38.p7 | 19:4454008 | GGGCTAGGGCGGCAG[C/T]GGCTGCCATCTGTGC | 80700 |
| rs372855117 | snp | C/T | 1.6906e-05 | 0.00290736 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445674 | AGTCGGCCCTTGCCG[C/T]GGCAGGGAACTCAGC | 80700 |
| rs372866203 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458250 | TAAAAAAAAAAAAAA[A/T]AAAATAAAATAAATT | 80700 |
| rs372941405 | snp | A/G | 1.68576e-05 | 0.00290319 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452316 | TGGAGGGTGGCTCAG[A/G]CACAGGAAGCTACAG | 80700 |
| rs373118368 | snp | A/G | 3.66146e-05 | 0.00427855 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446024 | AGGCATCGGGTCAGC[A/G]GTGCTCCTGCGGGCC | 80700 |
| rs373206871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451360 | ACCGCGCCCAGCCAC[C/T]TACTATTTTCTGAGA | 80700 |
| rs373243636 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448192 | AGCTGCCTCACTCTC[A/G]GCCTATGCTCCTTCC | 80700 |
| rs373282942 | snp | C/G | 0.000307953 | 0.0124049 | missense, intron-variant | UBXN6 | GRCh38.p7 | 19:4457643 | TGAGCTTCTGACCGG[C/G]TCCCGCGCTCTTGAA | 80700 |
| rs373300757 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452601 | AGACATCTCCAGCCC[C/T]CATGCTGTCCCTTCC | 80700 |
| rs373328636 | snp | C/T | 0.000260601 | 0.0114119 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446938 | GGGGGTGGAGATGGG[C/T]GTCACTGGGGGCCCC | 80700 |
| rs373444038 | snp | C/T | 0.000109226 | 0.00738925 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454139 | TCCTCCCGAGGTGGC[C/T]GGCAAAGCTGACGTG | 80700 |
| rs373495789 | snp | C/T | 2.11338e-05 | 0.00325061 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453569 | ACGGGATAGTGAGCA[C/T]GCCGCTGTCCTGGCC | 80700 |
| rs373535033 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453453 | CCACCAGTGGCTGTT[A/C]TTACCACGTTGGTCC | 80700 |
| rs373552202 | snp | C/T | 0.000140519 | 0.0083809 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446398 | CAGCACGCTCAGCCG[C/T]TCCACCGCCTCGGAC | 80700 |
| rs373573268 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455617 | CCAGAGAGCCCTTCC[C/T]AGCCTGGCCCACTGC | 80700 |
| rs373605033 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447695 | CTCTGTGCCTCCTGC[C/T]CCAGGTAACAGCAGC | 80700 |
| rs373680105 | snp | A/G | 0.000165123 | 0.00908483 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447544 | GGGGCCAGAAGGCAC[A/G]CCCACCTGAAACACC | 80700 |
| rs373839704 | snp | A/G | 3.30136e-05 | 0.00406273 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447631 | GTCCAGGTACCTGGG[A/G]TAGGTGGAGAAGGTG | 80700 |
| rs373953023 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447681 | TGCCCACCCGGCCCC[G/T]CTGTGCCTCCTGCTC | 80700 |
| rs374004284 | snp | A/G | 3.34499e-05 | 0.00408948 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452351 | GGGCAGGAGCACACA[A/G]GGTGCCACTCACCAA | 80700 |
| rs374004344 | snp | C/T | 6.7579e-05 | 0.00581248 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446084 | CCAGGTTCTCGTCCT[C/T]GGACAGCTTCTGCCC | 80700 |
| rs374021818 | snp | C/T | 3.85431e-05 | 0.00438977 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446153 | GCAGGGCCTCCCGGA[C/T]GAACCCGTACACCGC | 80700 |
| rs374043001 | snp | A/T | | | intron-variant, upstream-variant-2KB, missense, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444582 | CTCTCTGATTCACCC[A/T]CCTGCCACCTCTTGT | 80700 |
| rs374105434 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450688 | GGTGTGAACCTCGTA[C/G]GCGGAGCTTGCAGTG | 80700 |
| rs374388919 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445702 | AGCGGGCAACCTGGG[C/T]GCGGGGATGCCCCGG | 80700 |
| rs374415048 | snp | C/T | 3.31868e-05 | 0.00407336 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446806 | GCCCCTCGTCCCCAT[C/T]CCCTACTCAGCCAGG | 80700 |
| rs374415680 | snp | A/G | 0.000554409 | 0.0166402 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446204 | AGAAAGTGCCTGGGG[A/G]GTGGGGGAGTCAGAG | 80700 |
| rs374422509 | snp | A/C | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459389 | TGAAATTGAAATATC[A/C]TGGGTTGGACGGGTG | 80700 |
| rs374440724 | snp | C/T | 0.000107558 | 0.00733263 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457570 | ATCTCTCTCCCCGGC[C/T]GTCCCCGCCCCGCAG | 80700 |
| rs374519026 | in-del | -/C | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454769 | ATCCTCCCTCCCTCC[-/C]TGCCATAAGACTCTC | 80700 |
| rs374622332 | snp | C/T | 2.34601e-05 | 0.00342484 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446482 | CGCCCCACTCTGCTC[C/T]GCGGACGTCAGGCCC | 80700 |
| rs374783993 | snp | C/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445189 | GGCCTGCTCTCCTGC[C/G]CAGGGAGATGCCACG | 80700 |
| rs374837108 | snp | A/G | 0.00113775 | 0.0238239 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453556 | AAGAGAGGCAGAGAC[A/G]GGATAGTGAGCACGC | 80700 |
| rs374894185 | snp | C/G | 1.65825e-05 | 0.00287941 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445623 | GGAGGGCAGAGGGCA[C/G]CTGCGGTAGGGGTAG | 80700 |
| rs375058270 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455911 | GGGCACTCATCCAAG[C/G]ACTCATCGCCTGAGC | 80700 |
| rs375116712 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447650 | GTGGAGAAGGTGAGT[A/G]GGGCACAGCCCAGGC | 80700 |
| rs375118398 | snp | C/G | 3.70453e-05 | 0.00430363 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446506 | CAGGCCCACCTGAGC[C/G]TCTGCTCCCGCTTGA | 80700 |
| rs375144112 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456992 | CAGACTCTTTCTAGT[C/T]TCCCATCAGCCTCCC | 80700 |
| rs375328300 | snp | A/G | 6.59935e-05 | 0.0057439 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445513 | TCACAAGAGCTTCTC[A/G]ATGGCTGACAGGAGC | 80700 |
| rs375328388 | snp | A/G/T | 7.52078e-05 | 0.00613174 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446221 | TGGGGGAGTCAGAGC[A/G/T]GGTGGGGCCCAGGGC | 80700 |
| rs375483349 | snp | A/C/G | 3.31919e-05 | 0.0040737 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446807 | CCCCTCGTCCCCATT[A/C/G]CCTACTCAGCCAGGC | 80700 |
| rs375533590 | snp | C/G/T | 0.000730367 | 0.0190984 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446388 | CCTTGGTCCGCAGCA[C/G/T]GCTCAGCCGCTCCAC | 80700 |
| rs375566477 | snp | A/G | 0.000827593 | 0.0203251 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448462 | CTGAGAGCCCGGGCC[A/G]CACGGCCCTCCGCTG | 80700 |
| rs375587069 | in-del | -/A | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450719 | GCAGAGATGGCGCCA[-/A]CTGCACTCCAGCCTG | 80700 |
| rs375594132 | snp | A/G | 3.59299e-05 | 0.00423835 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453488 | GGCCTCGGGGCTCCC[A/G]CTGACGGTGGCTTCG | 80700 |
| rs375597089 | snp | A/G | 1.69971e-05 | 0.00291518 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446749 | GACATGGGTGTCACT[A/G]TGCAATGGAGAGACC | 80700 |
| rs375603947 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4455175 | CCAACCTGCTCGGAC[A/G]CGTCTGTCTCACCCG | 80700 |
| rs375737439 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458162 | TCACAGCACTTTGGA[A/G]GCTCAAGCGGAAGGA | 80700 |
| rs375785683 | snp | G/T | 1.66219e-05 | 0.00288283 | missense | UBXN6 | GRCh38.p7 | 19:4452369 | TGCCACTCACCAAGA[G/T]AATGGCCTCCTTGAT | 80700 |
| rs375913154 | snp | A/G | 0.00013207 | 0.00812512 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445564 | CGGCTCGGCCCCCGC[A/G]GCCTTGATGTCCTCC | 80700 |
| rs375914270 | snp | C/T | 1.72044e-05 | 0.0029329 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446599 | GGCTGGAAGACGCGG[C/T]GCTGCCTGTCCAGCT | 80700 |
| rs375980769 | snp | G/T | 0.000112659 | 0.00750446 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446005 | GTCCCAGGAGAACCT[G/T]CAGAGGCATCGGGTC | 80700 |
| rs376078592 | snp | A/G | 1.69453e-05 | 0.00291073 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446111 | GCCCTCCCGAGGCCA[A/G]CAGCTCAAAAGGCAG | 80700 |
| rs376146426 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456075 | TGGATATGCAGTCTC[A/G]CTCCACAAGGGACCT | 80700 |
| rs376155335 | snp | A/G | 1.67756e-05 | 0.00289612 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452342 | TACAGGTTGGGGCAG[A/G]AGCACACAGGGTGCC | 80700 |
| rs376182636 | snp | G/T | 0.000247445 | 0.0111203 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447601 | CTTCTCCTCCTCGGG[G/T]TGCAGGTGGATGTTG | 80700 |
| rs376266080 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458575 | GGAGCTGTTTAAGAG[C/G]ATGCACCTGGGCCGG | 80700 |
| rs376306553 | snp | A/G | 5.40283e-05 | 0.00519723 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446035 | CAGCGGTGCTCCTGC[A/G]GGCCGACACTCACCA | 80700 |
| rs376394271 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459223 | GCTTGAACCCGGCAG[A/G]TGGAGGTTGCAGTGA | 80700 |
| rs376449016 | snp | A/G | 5.30602e-05 | 0.00515047 | synonymous-codon, intron-variant | UBXN6 | GRCh38.p7 | 19:4457650 | CTGACCGGGTCCCGC[A/G]CTCTTGAACTTGATG | 80700 |
| rs376520962 | snp | A/G/T | 9.98951e-05 | 0.00706665 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448466 | GAGCCCGGGCCGCAC[A/G/T]GCCCTCCGCTGCCCA | 80700 |
| rs376539898 | snp | A/G | 0.000101321 | 0.00711688 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453911 | CCCCAACCTGGGCCC[A/G]AGGAGGGCCATATCT | 80700 |
| rs376542939 | snp | A/G | 9.28678e-05 | 0.00681361 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446250 | GCCCCCTACCAACCC[A/G]AGCCGCCCTCCACGG | 80700 |
| rs376663846 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450284 | TCAGCATGGAAATGG[A/G]GAAGGCATTTCTAAG | 80700 |
| rs376666525 | snp | A/C | 0.000153988 | 0.00877327 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457595 | CCGCAGGGCCTCAAG[A/C]CCCTGCGTTCCTCAC | 80700 |
| rs376724268 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446566 | CCAGGCAGTTCGAAC[C/T]GCGAGGCCAGGGGCG | 80700 |
| rs376743195 | snp | A/G | 3.39755e-05 | 0.00412148 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446072 | ACTCGTTCAAGGCCA[A/G]GTTCTCGTCCTCGGA | 80700 |
| rs376843627 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455670 | GGGCTCCCCGCAGTT[C/G]TTCCCACACCCCAGC | 80700 |
| rs376962408 | snp | G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452828 | AGGAAGGAGCTCTGT[G/T]TGGGTGTCTGCGGGC | 80700 |
| rs377061785 | snp | A/G | 3.3112e-05 | 0.00406877 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445464 | GGAGAGCATGAGACA[A/G]ACCCACAGGGCTGAG | 80700 |
| rs377074858 | snp | C/T | | | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448539 | GCGGCCCCAGCTGTG[C/T]GCTCATCACAGAAAG | 80700 |
| rs377116965 | snp | C/T | 2.22165e-05 | 0.00333283 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446165 | GGACGAACCCGTACA[C/T]CGCCCCCAGCCGCTC | 80700 |
| rs377124839 | snp | A/G | 0.00158371 | 0.0280953 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447637 | GTACCTGGGGTAGGT[A/G]GAGAAGGTGAGTGGG | 80700 |
| rs377150021 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453088 | CTGAAACCACAGACT[A/G]GCTCTGGTCCTGCCT | 80700 |
| rs377202278 | in-del | -/AGGCACCAGGGCC | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453868 | TCTGCATCCAGGGCC[-/AGGCACCAGGGCC]GAGAACCTCAAACAG | 80700 |
| rs377246147 | snp | C/G | 6.87297e-05 | 0.00586175 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454039 | CTCATTGGTGGGTCC[C/G]TGGCGGGGCGGCCTG | 80700 |
| rs377275281 | snp | A/G | 0.000112803 | 0.00750925 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446939 | GGGGTGGAGATGGGC[A/G]TCACTGGGGGCCCCT | 80700 |
| rs377437234 | snp | A/G | 0.000247274 | 0.0111165 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446382 | GCATGGCCTTGGTCC[A/G]CAGCACGCTCAGCCG | 80700 |
| rs377439468 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454935 | AGGGACAGGAAGTCC[A/G]GGCGATGTGCCCCAT | 80700 |
| rs377499507 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444773 | GCCTGTGACAGCACT[C/T]GCCTCCCCTGCAGGG | 80700 |
| rs377504263 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458134 | AACTAGGCGCGGTGG[C/T]TCACGCCTGCAATCA | 80700 |
| rs377563623 | snp | A/G | 5.12527e-05 | 0.00506199 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446625 | CAGCTTGGCGCGCAC[A/G]GGCTCCGCAGCCAGC | 80700 |
| rs377566456 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453455 | ACCAGTGGCTGTTCT[C/T]ACCACGTTGGTCCCT | 80700 |
| rs377568188 | snp | C/T | | | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4455298 | TCAAGCCCTATACTC[C/T]TCTGGCTCTGCTTAC | 80700 |
| rs386806125 | multinucleotide-polymorphism | AG/GA | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450012 | AGGCGGTCGGATCAC[AG/GA]GATTAGGAGAGCGAG | 80700 |
| rs397859534 | in-del | -/A | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457823 | AAAAAAAAAAAAAAA[-/A]TTTACCTCGCCGCCG | 80700 |
| rs527443187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4455191 | CGTCTGTCTCACCCG[C/T]CTCCTCTCAGGCCCC | 80700 |
| rs527527324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450631 | GGCGTGGTGGCGGTT[C/T]GCCTGTGGTCCCAGC | 80700 |
| rs527573846 | snp | A/G | 0.000142455 | 0.00843844 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446447 | TCACGAGGGCTGGCC[A/G]GGGTTCTTCCACCCC | 80700 |
| rs527661186 | snp | G/T | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459407 | GGTTGGACGGGTGGC[G/T]CAGGCCTGCAGTCCC | 80700 |
| rs527679878 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459776 | TGAACCCAGGAGGCA[A/G]AGCTTACAGTGAGCC | 80700 |
| rs527857170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445767 | TCGCACCCAGGCCTC[C/T]TGCCCTCTCCCTCCG | 80700 |
| rs528130435 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458121 | GCTGCTCAACCTAAA[C/T]TAGGCGCGGTGGCTC | 80700 |
| rs528154365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452549 | GCCACCCCGACCCTC[A/G]CCGAGCACCACAGTC | 80700 |
| rs528154874 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458585 | AAGAGGATGCACCTG[C/G]GCCGGGCGCGGTGGC | 80700 |
| rs528276221 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452871 | ACAAGGCATGACTTC[C/T]GGGCCTCCATTTCTA | 80700 |
| rs528541722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447279 | AACCTCCCCAGAGTC[G/T]ACATGTTCCCAAACA | 80700 |
| rs528653883 | in-del | -/AAAA | 0.478603 | 0.101197 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450758 | GCGAGACTCTGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 80700 |
| rs528774635 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453703 | GCCACCCCTCAGCCT[A/G]AGCAAGCACCCCACT | 80700 |
| rs528775410 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451219 | CTGTCACCACGCCTG[A/C/G]CTAATTTTTGTATAT | 80700 |
| rs528801695 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456692 | CCTAGACAATCCGGA[A/G]GCCTGCCCGGCATCT | 80700 |
| rs528860858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449572 | CCTTGGGATCAGAGC[A/G]CCCGGGACAGCACAC | 80700 |
| rs529057526 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447216 | CCGCCCAGGACCCCA[C/G]TCCCTGCCCTTTCCC | 80700 |
| rs529266625 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456074 | CTGGATATGCAGTCT[C/T]GCTCCACAAGGGACC | 80700 |
| rs529317347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451202 | GCTGGGATTACAGGC[A/G]CCTGTCACCACGCCT | 80700 |
| rs529374397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451631 | CTGTATTGGAAAAAA[A/T]TGCTGTGGACGTTTT | 80700 |
| rs529445386 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456549 | CCAGCTCCCTGCAGC[A/G]GCCCCAGCTCTCCAG | 80700 |
| rs529635861 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455320 | TCTGCTTACATACCC[A/G]GGCAGCCCTCCCTCC | 80700 |
| rs529672396 | snp | C/T | 6.44822e-05 | 0.00567776 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453572 | GGATAGTGAGCACGC[C/T]GCTGTCCTGGCCCAA | 80700 |
| rs529738525 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449023 | TCCACCTATGTTACC[A/G]GGGGAGGGGAGAAGT | 80700 |
| rs529801124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449411 | ACCAATGACCTACAC[A/G]CTGAGCCGGGGCTCA | 80700 |
| rs529947921 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458735 | GCCGGGCATGGTGGC[A/G]GGCGTCTGTACTCAC | 80700 |
| rs530013442 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451113 | CCACGCTGGAGCTCA[A/G]TGGCGTGATCTGGGC | 80700 |
| rs530079999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444685 | TGCCAGGTGAAGTTG[A/C]GCATCTGCAGGTTCC | 80700 |
| rs530193189 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458022 | AGGGCATTCCGTGGC[G/T]CTCCCCAAACGGTGA | 80700 |
| rs530193331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452209 | TGCATACACAATGGT[A/G]TGCCTGGATTTGGGG | 80700 |
| rs530406927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448113 | TCCTTCAACACCTTC[A/C]TTTTGCACACGGGTA | 80700 |
| rs530468648 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458668 | TCAGGAGATCGAGAC[A/C]ATCCTGGCTAACACG | 80700 |
| rs530565369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452930 | AATTCACTGAATCCT[C/T]GAGGGTCAAGCTGCT | 80700 |
| rs530606447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448611 | CAGGGCAGAGGCGAC[A/G]CAGCCAAGACCCAGC | 80700 |
| rs530661437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444863 | GGGTGGCTCATCGGG[C/T]ACTTGTGGCCAGGTG | 80700 |
| rs530839845 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458228 | ACATGGCAAAACCTC[C/G]TCTCTATAAAAAAAA | 80700 |
| rs530929730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448030 | CCGATCCTGAGACCC[A/G]GGGAGTGGGGTGGGA | 80700 |
| rs530960928 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456866 | AGAGTCCATCTGTCA[A/G]AATCCCTCACCTCCA | 80700 |
| rs531020029 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB, missense, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444585 | TCTGATTCACCCTCC[G/T]GCCACCTCTTGTGAG | 80700 |
| rs531049172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451856 | TACTTAACCTTTTAT[A/G]AAAAACAACCAGGCC | 80700 |
| rs531175438 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457483 | CCCGGCGCCTCTCCC[C/G]CTCCCCTGACCCTCG | 80700 |
| rs531211220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452098 | AGGTTGTAGTGAGCC[A/G]AGAATGCGCCACTGC | 80700 |
| rs531440612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454550 | GCCTCAGCCTCCCAA[G/T]TCGCTGGGACTTAGA | 80700 |
| rs531484684 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450005 | GAGGCCGAGGCGGTC[A/G]GATCACGAGATTAGG | 80700 |
| rs531716371 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459757 | CTGAGGCAGGAGAAT[A/G]GCGTGAACCCAGGAG | 80700 |
| rs531775192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448996 | CCCTGCCCCTCCCCG[A/C]GGTCCCACCTATCCA | 80700 |
| rs532149017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449958 | CTGGAGGCCGGGCAC[A/G]GTGGCTCATGCCTGG | 80700 |
| rs532149477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445861 | TGGGGAAACTGAGGC[A/G]TGGAGTAGTTATGAA | 80700 |
| rs532236289 | snp | C/T | 0.0001434 | 0.00846637 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446178 | CACCGCCCCCAGCCG[C/T]TCCCGAGCGTAGAAA | 80700 |
| rs532248771 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459698 | TTTTAAAAAAATTAG[C/T]CAGCCTTGGTGGCGG | 80700 |
| rs532343400 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445339 | TGGGGGCTCTGCCAC[A/G]GGGCCCAATTCCACA | 80700 |
| rs532377611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453629 | GGGGCCACGCACACC[A/G]CCCCAGCCTGCTTCT | 80700 |
| rs532571413 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448532 | GCTTGGAGCGGCCCC[A/C]GCTGTGCGCTCATCA | 80700 |
| rs532601401 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444717 | GGAATAGGATGTGGC[C/T]GTCTCAGGACACCCT | 80700 |
| rs532831103 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445040 | TATTTGGGCTTATGA[A/T]TTACTAACTGCAGGT | 80700 |
| rs532929768 | snp | C/T | 0.000157281 | 0.00886655 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446539 | TCCTCTGCTGTGAGG[C/T]TGAAGAAGTCCCCAG | 80700 |
| rs532967129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446781 | CCAAGCCGGGCCCTC[C/T]TGCCCCGAGGCCCCT | 80700 |
| rs533211000 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4455248 | TTTCTGTGCCGTAGG[C/T]CTATTAAAACCTTCT | 80700 |
| rs533445637 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455867 | CCCAAACCACCTGAC[A/G]GCCCCTGCTCACCCT | 80700 |
| rs533512298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450480 | TGTAAAGAGTGCTGC[C/T]GGGCACGGTGGCTCC | 80700 |
| rs533661161 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447915 | AGCCACAGTGCCGGA[-/AG]AGTGGAGAGCCAGAG | 80700 |
| rs533707283 | snp | A/C/G | 0.000305564 | 0.012357 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445952 | CAGGCCCCCTGCTCT[A/C/G]AGAACAAGGAGGCTC | 80700 |
| rs533850408 | in-del | -/AG | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454606 | TTTTTCTATCGAGAC[-/AG]GGTCTCGCTATGTAG | 80700 |
| rs533893085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454969 | ACGCCACCCTCGTGG[C/T]GGGACCCTGGGGAGA | 80700 |
| rs533927912 | snp | A/G | 0.000232581 | 0.0107813 | missense | UBXN6 | GRCh38.p7 | 19:4453953 | CGGATGGTGTCCTGC[A/G]ATGTGGGGCCCCAGG | 80700 |
| rs533963897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454203 | CACCATCAGCCAGAC[A/G]TGTCCCTGCCTATGT | 80700 |
| rs534048492 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449621 | CAGCTCCAAAAGCGG[G/T]CCTCGGGCGTTTTGG | 80700 |
| rs534182652 | snp | C/T | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459399 | ATATCATGGGTTGGA[C/T]GGGTGGCTCAGGCCT | 80700 |
| rs534231590 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459565 | AAAAAAGGCCAGGCA[C/T]GGTGGCTCATGCCTG | 80700 |
| rs534275993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451887 | ACGCGTGGTGGCTCA[C/T]GTCTGTAATCCTAGC | 80700 |
| rs534356809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452259 | CTACTAGCAGTGGCC[C/T]CTGGGGACTCTGGGA | 80700 |
| rs534358767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447485 | GGTGTGGGCCACCAC[C/T]GGCTCCTGCAGGCCA | 80700 |
| rs534393347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447752 | GGGAAGAAGCGGCCC[A/G]GTGACGCGAGGGCAG | 80700 |
| rs534435804 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459070 | TGGCTCATGCCTCTA[A/T]TCCCAGCACTTTGGG | 80700 |
| rs534545654 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456335 | CTCCCCCAGGAACCC[C/T]GACGTCCTCACTATG | 80700 |
| rs534866083 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451574 | GCCCAGGCTAAAGCC[A/G]AAGTTTCTGAGAACC | 80700 |
| rs534925331 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450025 | ACGAGATTAGGAGAG[C/T]GAGACCATCCCGGCC | 80700 |
| rs534932768 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457048 | ACCCCTCTTCCCATG[C/G]ATACCTCAAAACAAC | 80700 |
| rs534975080 | snp | C/T | 4.96602e-05 | 0.00498274 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446860 | GGGCGGGAAGCAACA[C/T]CTTCTGGAACCCAAT | 80700 |
| rs534985329 | snp | A/G | 0.000103263 | 0.00718477 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446597 | AGGGCTGGAAGACGC[A/G]GCGCTGCCTGTCCAG | 80700 |
| rs535113860 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456972 | CCCCGGCCTCCCTGG[C/G]CTTCCAGACTCTTTC | 80700 |
| rs535137314 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451385 | CTGAGAAAGGGTCTC[A/T]CTTGTCACCCAGGCT | 80700 |
| rs535181388 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450267 | GCCACAAAAGAATTC[C/T]CTCAGCATGGAAATG | 80700 |
| rs535194799 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451876 | ACAACCAGGCCACGC[A/G]TGGTGGCTCACGTCT | 80700 |
| rs535216693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447000 | CCAGTCCAGGGGCCC[A/G]GCTCTCGCTATTGGG | 80700 |
| rs535276421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450746 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 80700 |
| rs535618127 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458323 | AGAGGCGGGAGGATC[A/G]CTTGAACCCAAGAGG | 80700 |
| rs535804378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450725 | GATGGCGCCACTGCA[C/T]TCCAGCCTGGGCGAC | 80700 |
| rs536092386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454843 | CCAGGACCCTGCTGG[A/G]AGCTGGTCGGCTCGC | 80700 |
| rs536202517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444830 | CCTCCCCTAGCGCAC[A/G]GGACTTCCTCCCCAG | 80700 |
| rs536447554 | snp | C/T | 5.06385e-05 | 0.00503157 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452319 | AGGGTGGCTCAGGCA[C/T]AGGAAGCTACAGGTT | 80700 |
| rs536482409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452624 | TCCCTTCCACCTGGT[C/G]GCCGTGGGAGACACC | 80700 |
| rs536687016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448207 | GGCCTATGCTCCTTC[C/T]CAACCCACCTCAGCA | 80700 |
| rs536751442 | snp | C/G | 0.000749157 | 0.0193395 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457715 | TGGCGGCTGGCCCGG[C/G]GGCGGGGGGCCGCGG | 80700 |
| rs536810627 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447402 | CTTGTCCTGCTACCT[C/G/T]CTACTGGCCGAACCC | 80700 |
| rs536956200 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445832 | AGCTAACGCACGTCA[C/T]CGCTCCCATTTGATG | 80700 |
| rs537010792 | snp | A/T | 0 | 0 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447775 | GAGGGCAGCAGACCA[A/T]CTCCGGGTGGAAGGC | 80700 |
| rs537279197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457606 | CAAGCCCCTGCGTTC[C/G]TCACGCACCCCACGG | 80700 |
| rs537360529 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449708 | AGGAACAGCAGCCAG[A/G]AAGGGGTCCAAATCC | 80700 |
| rs537492750 | in-del | -/AGG | 0.00398564 | 0.0444627 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458558 | CCACGTACCCTAGGT[-/AGG]AGGAGCTGTTTAAGA | 80700 |
| rs537603583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449165 | GCACAAATCCACGCT[C/T]GGCACAGCCATCACA | 80700 |
| rs537604218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451344 | ATTACAGGCAAGAGC[C/G]ACCGCGCCCAGCCAC | 80700 |
| rs537622437 | in-del | -/A | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450221 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 80700 |
| rs537715794 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447323 | AGGAGGAAAAGGATG[C/T]AGGTGAGGAGAGGCA | 80700 |
| rs537846566 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458931 | GGGACCTGGGGATTG[A/G]GGATCCACTTTGGTG | 80700 |
| rs537885294 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459497 | AAGCTAGGATCACGC[C/G]ACTGCACTCCAGCCT | 80700 |
| rs537979518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453857 | CTCATGTGACTTCTG[C/T]ATCCAGGGCCAGGCA | 80700 |
| rs538086106 | snp | C/T | 4.95716e-05 | 0.00497829 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445587 | TGTCCTCCAGCACAG[C/T]CATGTCCCACGAGAA | 80700 |
| rs538122751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445874 | GCGTGGAGTAGTTAT[G/T]AACTTGCTCGAGGCC | 80700 |
| rs538789592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448426 | AAGTGCTGGGAGGAG[G/T]GAAGCAGGGAAAGCC | 80700 |
| rs538879430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448779 | ACTTACAGAACCTCC[C/T]GCCACCATGGACGCC | 80700 |
| rs538915568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449095 | GACTGCGAACAGCGT[A/C]CCAGCATGGAGAGGC | 80700 |
| rs538915573 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445227 | GTCCGGCAGCTTCAT[C/G]ACACAGTTACCAAGC | 80700 |
| rs539050906 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458378 | AAGCCACTGCATTCC[A/G]GCCTGGGCGACAGAG | 80700 |
| rs539088184 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455499 | CATGGACCCTGCCCC[C/G]CTGGGCAGCCACAGG | 80700 |
| rs539137260 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452716 | TGCTCAGAACTAAAC[A/G]AGGTAAGGAACGGAA | 80700 |
| rs539142110 | snp | G/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445027 | CAAACAACCTGTTTA[G/T]TTGGGCTTATGATTT | 80700 |
| rs539173632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450904 | CAAATTAACTCTATC[C/G]TGAGATGTTATTTTC | 80700 |
| rs539179171 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456097 | AAGGGACCTCCGCAC[C/T]GCTTCCTTTCCCAAC | 80700 |
| rs539487043 | snp | A/C/G | 5.54937e-05 | 0.00526729 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446016 | ACCTGCAGAGGCATC[A/C/G]GGTCAGCGGTGCTCC | 80700 |
| rs539523761 | snp | A/C/G/T | 0.00019368 | 0.00983909 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446271 | CCCTCCACGGGCATC[A/C/G/T]TTGGTGCCCACCCTG | 80700 |
| rs539532262 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456144 | CCCCTCTCCGCCCAG[A/G]CTCTGGGCTGATCCA | 80700 |
| rs539760386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454270 | CCACCAGATGGTTCT[A/G]CTGCAGGCGGAAGAG | 80700 |
| rs540011628 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459620 | AGGCGGGTGGATCAC[A/G]AGGTCAGGAGATTGA | 80700 |
| rs540189753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448915 | GGCAGGTGGCAGAGA[A/G]GACACAAATGAGTCT | 80700 |
| rs540260591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454350 | AAGTCCTGCCCCCAC[C/T]GGCCCTCAGCGTCCT | 80700 |
| rs540309030 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445323 | CACAGCCCCCAAGGG[A/G]TGGGGGCTCTGCCAC | 80700 |
| rs540389796 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453159 | ACCTCTCTCAACCCC[A/G]GTTCTCTTTTTGAAT | 80700 |
| rs540456493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452870 | GACAAGGCATGACTT[A/C]TGGGCCTCCATTTCT | 80700 |
| rs540463477 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458540 | CACCCCCCCGCCACC[A/G]TCACCACGTACCCTA | 80700 |
| rs540722278 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450707 | GAGCTTGCAGTGAGC[A/C]GAGATGGCGCCACTG | 80700 |
| rs540937353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448503 | AGGGGCAGGAAAAGG[A/C]AGGCAGAACAGCGGC | 80700 |
| rs541209422 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455803 | CAGGGAGAGAAGGAG[A/G]GGCAGATTTCCCCAC | 80700 |
| rs541689701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4455120 | TAACCCACGTGGCAC[A/G]GTGACCTGGCAGAGA | 80700 |
| rs541730523 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455672 | GCTCCCCGCAGTTCT[A/T]CCCACACCCCAGCTG | 80700 |
| rs541766807 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450533 | GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG | 80700 |
| rs541801311 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451501 | GGGACTGCAGGTGCA[C/T]GCCACCATGCCCAGC | 80700 |
| rs541889645 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4448870 | GTTTACAAAGAGACC[A/G]AGAGGCCCATCGTCC | 80700 |
| rs542052960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449342 | AGCTCCACCCACCAC[A/C]CCCCACCCTCAACTG | 80700 |
| rs542143097 | snp | A/G | 1.65482e-05 | 0.00287643 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446851 | CCTGATCCTGGGCGG[A/G]AAGCAACACCTTCTG | 80700 |
| rs542318199 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458029 | TCCGTGGCGCTCCCC[A/G]AACGGTGACAAACGG | 80700 |
| rs542490638 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447911 | GGGAAGCCACAGTGC[C/T]GGAAGAGTGGAGAGC | 80700 |
| rs543113445 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457234 | TTTTTCCCCAAAGGT[C/T]GTTCCACTGACCCCC | 80700 |
| rs543151700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451986 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAATT | 80700 |
| rs543288261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451921 | TTGGGAGGCTGAGGC[A/G]GGTTGATCACTTGAG | 80700 |
| rs543600287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451592 | GTTTCTGAGAACCTA[C/T]TGATGGTGTTAAGTG | 80700 |
| rs543909659 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456398 | GATTCCTGACCCCCA[C/G]TTCCTGCCACCTCCC | 80700 |
| rs543987334 | snp | A/G | 0.000119844 | 0.00773999 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446619 | CCTGTCCAGCTTGGC[A/G]CGCACGGGCTCCGCA | 80700 |
| rs544239843 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447760 | GCGGCCCAGTGACGC[A/G]AGGGCAGCAGACCAT | 80700 |
| rs544277504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452839 | CTGTGTGGGTGTCTG[C/T]GGGCACAGTGCGCTG | 80700 |
| rs544427368 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4455046 | AGGGCTGTGCAAGTA[C/T]GAAGAGCTCATGGAC | 80700 |
| rs544593126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448062 | CCTGCCTCCTCCACA[A/T]GTTCCCCAAGGAAGC | 80700 |
| rs544704312 | in-del | -/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455660 | TGTCTCCCCTGGGCT[-/C]CCCGCAGTTCTTCCC | 80700 |
| rs544742622 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444930 | GACAGGGAGCCACAC[C/G]CAGCCCCCAAGCCAT | 80700 |
| rs544777997 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459112 | GGCGGATCACTTGAG[C/G]TCAGGAGTTTGAGAC | 80700 |
| rs545063702 | snp | A/G | 0.0023084 | 0.033895 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457736 | GGGGCCGCGGGGGCG[A/G]GGGGGCACGGGGCCC | 80700 |
| rs545261441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444904 | AACAGGTATCCACAT[G/T]GTCCCACCTTGACAG | 80700 |
| rs545480216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449983 | GCCTGGAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 80700 |
| rs545531999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448017 | TCCAGGCCTGCCCCC[A/G]ATCCTGAGACCCGGG | 80700 |
| rs545580299 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459711 | AGCCAGCCTTGGTGG[C/T]GGGCGCCTGTAGTCC | 80700 |
| rs545783555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4455037 | GCCAGGCCTAGGGCT[A/G]TGCAAGTACGAAGAG | 80700 |
| rs546456568 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458759 | TACTCACAGCTACTC[G/T]GGAGGCTGAGGCAGG | 80700 |
| rs546572942 | snp | C/G | | | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447013 | CCGGCTCTCGCTATT[C/G]GGAGCAGCTGTCGAC | 80700 |
| rs546611562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449092 | GCTGACTGCGAACAG[C/T]GTCCCAGCATGGAGA | 80700 |
| rs546709574 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449419 | CCTACACACTGAGCC[A/G]GGGCTCATGCCAACT | 80700 |
| rs546780421 | snp | A/G | 0.000430832 | 0.0146707 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452542 | GACAGAGGCCACCCC[A/G]ACCCTCGCCGAGCAC | 80700 |
| rs546880955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453214 | CCTTAAGGGGTTAAG[A/G]GGAGGGAGCGATGGG | 80700 |
| rs546908536 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448124 | CTTCATTTTGCACAC[A/G]GGTAAACTGAGGCCC | 80700 |
| rs546921503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453621 | TGGGCCTGGGGGCCA[C/T]GCACACCGCCCCAGC | 80700 |
| rs547362689 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454220 | GTCCCTGCCTATGTG[A/G]GCCAGGACACCTGGT | 80700 |
| rs547486827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450037 | GAGCGAGACCATCCC[A/G]GCCAACATGGTGAAA | 80700 |
| rs547814911 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459777 | GAACCCAGGAGGCAG[A/C]GCTTACAGTGAGCCG | 80700 |
| rs548159084 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459500 | CTAGGATCACGCCAC[C/T]GCACTCCAGCCTGGG | 80700 |
| rs548245190 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459767 | AGAATGGCGTGAACC[C/T]AGGAGGCAGAGCTTA | 80700 |
| rs548281448 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454194 | CCTCCCCAGCACCAT[C/T]AGCCAGACGTGTCCC | 80700 |
| rs548434981 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450012 | AGGCGGTCGGATCAC[A/G]AGATTAGGAGAGCGA | 80700 |
| rs548528181 | snp | C/G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453018 | TTCCACCCGTCTCCA[C/G/T]AGAGCCTCTTGACCT | 80700 |
| rs548548425 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456975 | CGGCCTCCCTGGCCT[C/T]CCAGACTCTTTCTAG | 80700 |
| rs549316399 | snp | A/G | | | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4453464 | TGTTCTTACCACGTT[A/G]GTCCCTGGGGCCTCG | 80700 |
| rs549378428 | snp | A/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459610 | TGGAAGGCCGAGGCG[A/G]GTGGATCACGAGGTC | 80700 |
| rs549389822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451208 | ATTACAGGCGCCTGT[A/C]ACCACGCCTGGCTAA | 80700 |
| rs549563323 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446783 | AAGCCGGGCCCTCCT[A/G]CCCCGAGGCCCCTCG | 80700 |
| rs549666379 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455338 | CAGCCCTCCCTCCTC[A/G]TCCCACCCCTGCCTA | 80700 |
| rs549874491 | snp | C/T | 0.000190861 | 0.00976699 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446561 | AGTCCCCAGGCAGTT[C/T]GAACTGCGAGGCCAG | 80700 |
| rs549889287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450093 | GCCCGGGTGTGGTGG[C/T]GTGCACCTGTAGTCC | 80700 |
| rs550018065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451114 | CACGCTGGAGCTCAA[C/T]GGCGTGATCTGGGCT | 80700 |
| rs550133938 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4455268 | TAAAACCTTCTGGGA[A/G]GCCAGGCTCTCAGTT | 80700 |
| rs550223564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450672 | GCTGAGGCAGGAGAA[C/T]GGTGTGAACCTCGTA | 80700 |
| rs550253402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454805 | TCAGGTCACAGCTTC[A/G]TTTGCTGAGCACCTA | 80700 |
| rs550349075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454293 | CGGAAGAGCCCCTGG[A/G]GGAAGGAGATGCTGG | 80700 |
| rs550511741 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450863 | ATTCTCATATGAAAC[A/G]TGGCCAATCCAAAAT | 80700 |
| rs550657921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449015 | CCCACCTATCCACCT[A/G]TGTTACCGGGGGAGG | 80700 |
| rs550745113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457484 | CCGGCGCCTCTCCCC[C/T]TCCCCTGACCCTCGC | 80700 |
| rs550850024 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458240 | CTCGTCTCTATAAAA[A/T]AAAAAAAAATAAAAT | 80700 |
| rs550897169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452602 | GACATCTCCAGCCCC[A/C]ATGCTGTCCCTTCCA | 80700 |
| rs550963041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452105 | AGTGAGCCGAGAATG[C/T]GCCACTGCACTCCAG | 80700 |
| rs550986501 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454607 | TTTTCTATCGAGACA[-/G]GGTCTCGCTATGTAG | 80700 |
| rs551025774 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, synonymous-codon, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444590 | TTCACCCTCCTGCCA[C/T]CTCTTGTGAGGACAC | 80700 |
| rs551072102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448191 | GAGCTGCCTCACTCT[C/T]GGCCTATGCTCCTTC | 80700 |
| rs551136421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451858 | CTTAACCTTTTATGA[A/G]AAACAACCAGGCCAC | 80700 |
| rs551136545 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458614 | GCTCATGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 80700 |
| rs551163582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452567 | GAGCACCACAGTCCT[A/G]AGTGTGGCCCGTAGA | 80700 |
| rs551220018 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456807 | CCAGCCTGCTAAGAC[A/G]CGTCTGTCTCACCCG | 80700 |
| rs551227182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447333 | GGATGCAGGTGAGGA[A/G]AGGCAGAATTTGTTG | 80700 |
| rs551341853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452260 | TACTAGCAGTGGCCT[C/T]TGGGGACTCTGGGAG | 80700 |
| rs552071112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453731 | ACTGCCTGGGCAGCC[C/G]GTTTCTGCTCCAAGT | 80700 |
| rs552343246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448537 | GAGCGGCCCCAGCTG[C/T]GCGCTCATCACAGAA | 80700 |
| rs552428226 | snp | A/G | | | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446773 | AGAGACCCCCAAGCC[A/G]GGCCCTCCTGCCCCG | 80700 |
| rs552438981 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459342 | CTGATGGAGGAGAAG[A/C]CTCCAGGTGAGGAAA | 80700 |
| rs552441520 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451155 | TCCACCTCCCAGGTT[C/G]AAGCGATTCTCCTGC | 80700 |
| rs552510595 | snp | C/G | 0.000214711 | 0.010359 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445578 | CGGCCTTGATGTCCT[C/G]CAGCACAGCCATGTC | 80700 |
| rs552600452 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458844 | GCACTCCAGCCTGGG[A/C]GACAGAGCGAGACTC | 80700 |
| rs552628326 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, synonymous-codon | UBXN6 | GRCh38.p7 | 19:4457969 | GGTTCTTCCGGACTC[C/T]GTTGCCAGGGCGACG | 80700 |
| rs553181402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447934 | TGGAGAGCCAGAGCT[A/G]AAGGGCCGCAGTGCC | 80700 |
| rs553181583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452654 | CCTGGCCAAGTGACC[A/G]GATCCCCGAGTCTTT | 80700 |
| rs553188876 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445166 | ACGGGAACAGGACCC[A/G]TGCTGCAGGCCTGCT | 80700 |
| rs553414754 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450028 | AGATTAGGAGAGCGA[C/G]ACCATCCCGGCCAAC | 80700 |
| rs553472057 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458251 | AAAAAAAAAAAAAAT[A/G]AAATAAAATAAATTA | 80700 |
| rs553544793 | snp | A/G | 1.66158e-05 | 0.0028823 | missense | UBXN6 | GRCh38.p7 | 19:4452389 | GCCTCCTTGATGCAG[A/G]CGTCCCGCTGGTCCT | 80700 |
| rs553792629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4455009 | AGAACCAGCCTCGCC[C/G]TGGCCACTCCATGCC | 80700 |
| rs553814581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449635 | GGCCTCGGGCGTTTT[A/G]GGCGACTGGCTGCCA | 80700 |
| rs554082014 | snp | G/T | 1.66103e-05 | 0.00288182 | missense | UBXN6 | GRCh38.p7 | 19:4453981 | AGGCCCGGGACTGCT[G/T]CTGCTCCAGCCGGGC | 80700 |
| rs554095711 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459091 | GCACTTTGGGAGGCC[A/G]AGGCCGGCGGATCAC | 80700 |
| rs554395187 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459603 | AGCCCTTTGGAAGGC[C/T]GAGGCGGGTGGATCA | 80700 |
| rs554732719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448880 | AGACCGAGAGGCCCA[A/T]CGTCCAGGGTCACAG | 80700 |
| rs554769753 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445289 | CCAGGCCTCTCCCTC[A/G]GGGGCTTGGGCGCAT | 80700 |
| rs554862257 | snp | C/T | 1.7224e-05 | 0.00293457 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446596 | GAGGGCTGGAAGACG[C/T]GGCGCTGCCTGTCCA | 80700 |
| rs554885392 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458951 | CCACTTTGGTGGACA[C/T]CAGTTAATAGTGGCG | 80700 |
| rs555010325 | snp | C/T | | | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445992 | GGTGTCTGTGCCGGT[C/T]CCAGGAGAACCTGCA | 80700 |
| rs555011583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451884 | GCCACGCGTGGTGGC[C/T]CACGTCTGTAATCCT | 80700 |
| rs555050142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449166 | CACAAATCCACGCTC[A/G]GCACAGCCATCACAC | 80700 |
| rs555176300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447434 | TCACTGCTTGTGGCT[C/G]AACTCTCGCTAGCTC | 80700 |
| rs555196154 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455716 | GCCCCTGCACTGTCT[A/G]CACCTTCTGCCCAGA | 80700 |
| rs555355665 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | UBXN6 | GRCh38.p7 | 19:4457909 | AGCGCTCGGTGCCTT[A/G]CTGGCCCAGGGCGGC | 80700 |
| rs555403874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447006 | CAGGGGCCCGGCTCT[C/T]GCTATTGGGAGCAGC | 80700 |
| rs555755881 | snp | G/T | | | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446989 | CCACACCCCACCCAG[G/T]CCAGGGGCCCGGCTC | 80700 |
| rs555994784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450231 | TGTCTCAAAAAAAAA[A/G]AAAAAAAAAGCACTG | 80700 |
| rs556031529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451347 | ACAGGCAAGAGCCAC[C/T]GCGCCCAGCCACTTA | 80700 |
| rs556034103 | snp | A/G | 0.0182019 | 0.0936463 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458791 | GAATGGCGTGAACCC[A/G]CGAGGCGGAGCTTGC | 80700 |
| rs556183469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450940 | CCAACAGGCGTAAAG[A/C]TCAAAGTTTGGTGAT | 80700 |
| rs556207850 | snp | C/T | 0.000149361 | 0.00864051 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446301 | GCAGGAGGCAGCCAT[C/T]GGGGAGGCGCACGCG | 80700 |
| rs556610361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444803 | GACTGGGCCTTTGTG[A/G]GCACAGCACAGCCTC | 80700 |
| rs556774965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454285 | ACTGCAGGCGGAAGA[A/G]CCCCTGGAGGAAGGA | 80700 |
| rs556860761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449804 | GACAGGTGGGGCTGA[A/G]AAGAAAGCTGAGCCA | 80700 |
| rs557020882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447802 | AGGCACACCTCGGAC[A/G]CCCCATGGAGCCCAC | 80700 |
| rs557317932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447486 | GTGTGGGCCACCACC[A/G]GCTCCTGCAGGCCAG | 80700 |
| rs557333177 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449791 | GACAGGTGCTCTCGA[C/T]AGGTGGGGCTGAGAA | 80700 |
| rs557404513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447757 | GAAGCGGCCCAGTGA[C/T]GCGAGGGCAGCAGAC | 80700 |
| rs557532672 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457215 | CTCAGGACTCATGAT[A/C]CCGTTTTTCCCCAAA | 80700 |
| rs557727960 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457148 | TGCCCCAAATCATCC[C/T]GGCCTCTTCGGCCAG | 80700 |
| rs558063845 | snp | C/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452661 | AAGTGACCGGATCCC[C/G]GAGTCTTTTCCCTGG | 80700 |
| rs558401926 | in-del | -/G | 0.00244748 | 0.0348963 | upstream-variant-2KB, frameshift-variant | UBXN6 | GRCh38.p7 | 19:4457926 | TGGCCCAGGGCGGCC[-/G]CTCTGTACGCTGGAG | 80700 |
| rs558461737 | snp | A/G/T | 6.88082e-05 | 0.00586515 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446600 | GCTGGAAGACGCGGC[A/G/T]CTGCCTGTCCAGCTT | 80700 |
| rs558702659 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458480 | TCCCAATTCAATGTT[A/G]GGTATTGGAGGCCCC | 80700 |
| rs558743566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452756 | CAGCTTCTGACACGC[A/G]GGAAACACCCAGCAG | 80700 |
| rs558771328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448832 | CCCATGATGGACGTT[C/T]TGGAACCACTCCCGG | 80700 |
| rs558773178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444911 | ATCCACATGGTCCCA[C/T]CTTGACAGGGAGCCA | 80700 |
| rs558865532 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445253 | CAAGCAGCTAGGGAG[A/G]GCTTAGATTTGTTGG | 80700 |
| rs558870909 | in-del | -/A | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452149 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 80700 |
| rs559059829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452548 | GGCCACCCCGACCCT[C/T]GCCGAGCACCACAGT | 80700 |
| rs559142839 | snp | A/C | 3.78022e-05 | 0.00434737 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448447 | AGGGAAAGCCACTCA[A/C]TGAGAGCCCGGGCCG | 80700 |
| rs559197386 | snp | G/T | | | intron-variant, upstream-variant-2KB, missense, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444596 | CTCCTGCCACCTCTT[G/T]TGAGGACACTGGGTC | 80700 |
| rs559236008 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457744 | GGGGGCGGGGGGGCA[C/T]GGGGCCCAGTCGGGG | 80700 |
| rs559623473 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452671 | ATCCCCGAGTCTTTT[C/T]CCTGGTATGTCAAAT | 80700 |
| rs559715340 | snp | G/T | | | intron-variant, missense, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447127 | CAGCTCTGCACAGAG[G/T]AAAGAGTCACAACCA | 80700 |
| rs559799399 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457445 | TCCCCCTGACGCCCA[A/C]CCTCGGCCCGACTTC | 80700 |
| rs559917487 | snp | C/T | 0 | 0 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454360 | CCCACTGGCCCTCAG[C/T]GTCCTCATCTGTAAA | 80700 |
| rs560115585 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456689 | CTCCCTAGACAATCC[A/G]GAAGCCTGCCCGGCA | 80700 |
| rs560215795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449414 | AATGACCTACACACT[A/G]AGCCGGGGCTCATGC | 80700 |
| rs560375677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448525 | AACAGCGGCTTGGAG[C/T]GGCCCCAGCTGTGCG | 80700 |
| rs560393829 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459694 | TAATTTTTAAAAAAA[C/T]TAGCCAGCCTTGGTG | 80700 |
| rs560497264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448916 | GCAGGTGGCAGAGAG[G/T]ACACAAATGAGTCTG | 80700 |
| rs560614219 | snp | A/G/T | 8.24891e-05 | 0.00642172 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447598 | GTACTTCTCCTCCTC[A/G/T]GGGTGCAGGTGGATG | 80700 |
| rs560667513 | snp | C/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459264 | CGCCATTGCACTTCA[C/G]CCTGGGCAACAGAGG | 80700 |
| rs560773811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449022 | ATCCACCTATGTTAC[C/T]GGGGGAGGGGAGAAG | 80700 |
| rs561077752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449356 | CCCCCCACCCTCAAC[C/T]GCACAGCAGGGTCCC | 80700 |
| rs561156585 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458728 | AAAATTAGCCGGGCA[C/T]GGTGGCAGGCGTCTG | 80700 |
| rs561193559 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459181 | ACCGGTAATCCCAGC[G/T]ACTCGGGAGGCTGAG | 80700 |
| rs561242510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444621 | TGGGTCCCGGACCAC[C/T]CAGGATCATCTCCCA | 80700 |
| rs561316501 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448473 | GGCCGCACGGCCCTC[A/C]GCTGCCCAGGTAACA | 80700 |
| rs561330039 | in-del | -/A | 0.245346 | 0.249957 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450222 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 80700 |
| rs561468162 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448091 | GCCAGGGTGGGAAAC[A/C]CCTGATTCCTTCAAC | 80700 |
| rs561599251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450555 | CGAGGTCAGGAGATC[C/G]AGACCATCCTGGCTA | 80700 |
| rs561668056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449469 | AGTCTGCCGGTTTAG[G/T]TGCTGAGATGATGTG | 80700 |
| rs561795935 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450805 | TGCCTACAAATCACT[A/G]ATAAAAAGACAAACT | 80700 |
| rs562216669 | snp | A/G/T | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459051 | AGTTGGGGGTCAGAC[A/G/T]TGGTGGCTCATGCCT | 80700 |
| rs562283092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445744 | TCTCAGCTGGTGGAG[A/G]CTGTGGCTCGCACCC | 80700 |
| rs562350799 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451045 | CTATGGAACTATTAC[C/T]ATTTTGTTTTGTTTT | 80700 |
| rs562365055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450417 | AGAAGCAACTAGAGG[A/G]AAACATGTGCAACTC | 80700 |
| rs562800440 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445378 | GCTGGCGCCCCTCCC[A/G]TGCCCATGGGGCAGA | 80700 |
| rs562890252 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445703 | GCGGGCAACCTGGGC[G/T]CGGGGATGCCCCGGC | 80700 |
| rs563318125 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447211 | TAACACCGCCCAGGA[C/T]CCCAGTCCCTGCCCT | 80700 |
| rs563472721 | snp | C/T | 3.38312e-05 | 0.00411272 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446699 | TGGTCTCGCTCAGCA[C/T]GTAGAACTCCTCGGG | 80700 |
| rs563598242 | snp | A/C | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451511 | GTGCACGCCACCATG[A/C]CCAGCTATTTTTTTT | 80700 |
| rs563672036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451618 | AAGTGAGGACTTGCT[A/G]TATTGGAAAAAAATG | 80700 |
| rs563688711 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455961 | GTTTATTTGTCCATC[A/G]GCTCCCTCTAGAAGG | 80700 |
| rs563729300 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456448 | TCCCTCACAATCCCT[C/T]CCACTATTGCTTACA | 80700 |
| rs563963463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451064 | TTGTTTTGTTTTGTT[C/T]TTAAGATGAAGTTTC | 80700 |
| rs564272889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450636 | GGTGGCGGTTCGCCT[A/G]TGGTCCCAGCTACTC | 80700 |
| rs564413900 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4450525 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 80700 |
| rs564599494 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4455243 | GTCAATTTCTGTGCC[A/G]TAGGTCTATTAAAAC | 80700 |
| rs564609260 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448902 | GGGTCACAGGGATGG[C/T]AGGTGGCAGAGAGGA | 80700 |
| rs564672174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448578 | AGACCCTCCAAGACC[A/G]CAGCCCTGCCCACGC | 80700 |
| rs565334741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448023 | CCTGCCCCCGATCCT[C/G]AGACCCGGGGAGTGG | 80700 |
| rs565348066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451885 | CCACGCGTGGTGGCT[C/T]ACGTCTGTAATCCTA | 80700 |
| rs565429007 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, synonymous-codon, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444581 | TCTCTCTGATTCACC[A/C]TCCTGCCACCTCTTG | 80700 |
| rs565436436 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452258 | ACTACTAGCAGTGGC[A/C]TCTGGGGACTCTGGG | 80700 |
| rs565471129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452097 | GAGGTTGTAGTGAGC[C/T]GAGAATGCGCCACTG | 80700 |
| rs565482157 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456857 | TCCCGGGTAAGAGTC[C/T]ATCTGTCAGAATCCC | 80700 |
| rs565679157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457548 | CCCGAGCCGCCCAAG[A/G]CCCCAGATCTCTCTC | 80700 |
| rs566250145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454962 | CCATGCCACGCCACC[C/T]TCGTGGCGGGACCCT | 80700 |
| rs566375016 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456085 | GTCTCGCTCCACAAG[A/G]GACCTCCGCACCGCT | 80700 |
| rs566398192 | snp | A/G/T | 0.00024107 | 0.0109763 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446595 | CGAGGGCTGGAAGAC[A/G/T]CGGCGCTGCCTGTCC | 80700 |
| rs566631836 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458764 | ACAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT | 80700 |
| rs566680639 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453226 | AAGGGGAGGGAGCGA[C/T]GGGCTCGTGTACCTG | 80700 |
| rs566685419 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445216 | CACGTGTGTCTGTCC[A/G]GCAGCTTCATGACAC | 80700 |
| rs566734316 | snp | A/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454384 | CTGTAAAATGGGGTG[A/T]CAGCACCCCTCCTGA | 80700 |
| rs566745512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448134 | CACACGGGTAAACTG[A/C]GGCCCAAGGAGGCCC | 80700 |
| rs566770883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453628 | GGGGGCCACGCACAC[C/T]GCCCCAGCCTGCTTC | 80700 |
| rs566835357 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458278 | ATTAGCCGAGGGTGG[C/T]GGCGCGCGCCTCTCA | 80700 |
| rs567164635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444829 | GCCTCCCCTAGCGCA[C/T]GGGACTTCCTCCCCA | 80700 |
| rs567266330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448670 | CAAGGCTAGATCCAT[A/G]GGACTTGGAAGCCAG | 80700 |
| rs567432678 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | UBXN6 | GRCh38.p7 | 19:4457685 | CCTTGAACTCCTGAA[A/G]GAATTTCTTCATGGT | 80700 |
| rs567470191 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458242 | CGTCTCTATAAAAAA[A/T]AAAAAAATAAAATAA | 80700 |
| rs567555757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452611 | AGCCCCCATGCTGTC[C/T]CTTCCACCTGGTGGC | 80700 |
| rs567775740 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447364 | ATTTGGGGTGACCGG[C/T]GCATAAAAGTCTTGC | 80700 |
| rs567929463 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450013 | GGCGGTCGGATCACG[A/G]GATTAGGAGAGCGAG | 80700 |
| rs568045343 | snp | G/T | | | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447020 | TCGCTATTGGGAGCA[G/T]CTGTCGACCCCTGGA | 80700 |
| rs568087970 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459555 | TAAAAAAAGAAAAAA[A/C]GGCCAGGCACGGTGG | 80700 |
| rs568114552 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459768 | GAATGGCGTGAACCC[A/G]GGAGGCAGAGCTTAC | 80700 |
| rs568143087 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458247 | CTATAAAAAAAAAAA[A/T]AATAAAATAAAATAA | 80700 |
| rs568232630 | snp | C/T | 0.000789379 | 0.0198511 | missense | UBXN6 | GRCh38.p7 | 19:4453502 | CGCTGACGGTGGCTT[C/T]GGCTTGAAGTTCCTT | 80700 |
| rs568260682 | snp | C/T | 0.000102364 | 0.00715341 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445950 | CCCAGGCCCCCTGCT[C/T]TGAGAACAAGGAGGC | 80700 |
| rs568459408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449175 | ACGCTCGGCACAGCC[A/G]TCACACACGGCCACA | 80700 |
| rs568568117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449575 | TGGGATCAGAGCGCC[C/T]GGGACAGCACACCAG | 80700 |
| rs569009890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449544 | GATGGGCATGTCCCC[A/C]AGACAACAGCTTCCT | 80700 |
| rs569049967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449135 | TACGTACCCTAAGAC[C/G]TGGAAAAGATTGGGG | 80700 |
| rs569128972 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445058 | ACTAACTGCAGGTCT[A/G]TGTGCAGGAAGGCCA | 80700 |
| rs569214812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445873 | GGCGTGGAGTAGTTA[C/T]GAACTTGCTCGAGGC | 80700 |
| rs569340013 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456983 | CTGGCCTTCCAGACT[C/G]TTTCTAGTCTCCCAT | 80700 |
| rs569401116 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456952 | GTCACTGACGACGCT[A/G]CCCACCCCGGCCTCC | 80700 |
| rs569509159 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4454378 | CCTCATCTGTAAAAT[A/G]GGGTGACAGCACCCC | 80700 |
| rs569734108 | snp | C/T | 0.000956095 | 0.0218434 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446309 | CAGCCATCGGGGAGG[C/T]GCACGCGCAGCAGCG | 80700 |
| rs570285035 | snp | C/T | 4.95798e-05 | 0.0049787 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447656 | AAGGTGAGTGGGGCA[C/T]AGCCCAGGCTGCCCA | 80700 |
| rs570297464 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449639 | TCGGGCGTTTTGGGC[A/G]ACTGGCTGCCAGGCT | 80700 |
| rs570356872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450149 | TGAATTGCTTGAACC[C/T]GGGAAGCAGAGGTTG | 80700 |
| rs570416019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454304 | CTGGAGGAAGGAGAT[A/G]CTGGTTCCACTCAGC | 80700 |
| rs570606846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450053 | GCCAACATGGTGAAA[C/T]CTCATCTCTAAAATA | 80700 |
| rs570643547 | snp | C/T | 0.000242972 | 0.0110194 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446263 | CCGAGCCGCCCTCCA[C/T]GGGCATCGTTGGTGC | 80700 |
| rs570705283 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449967 | GGGCACGGTGGCTCA[C/T]GCCTGGAATCCCAGC | 80700 |
| rs570926880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447765 | CCAGTGACGCGAGGG[C/T]AGCAGACCATCTCCG | 80700 |
| rs571044044 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444721 | TAGGATGTGGCCGTC[C/T]CAGGACACCCTGTCC | 80700 |
| rs571107111 | snp | G/T | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459787 | GGCAGAGCTTACAGT[G/T]AGCCGAGATCATGCC | 80700 |
| rs571480723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452265 | GCAGTGGCCTCTGGG[G/T]ACTCTGGGAGGGATC | 80700 |
| rs571681600 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451526 | CCCAGCTATTTTTTT[G/T]TGTTTTTGGCAGAGA | 80700 |
| rs571718613 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456121 | TCCCAACCTTCCCCT[C/T]CAACCTTCCCCTCTC | 80700 |
| rs571808725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447468 | CAGGGAGCCCACCGC[C/G]TGGTGTGGGCCACCA | 80700 |
| rs571905141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451855 | ATACTTAACCTTTTA[C/T]GAAAAACAACCAGGC | 80700 |
| rs571931916 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458707 | CCGTCTCTACTAAAA[A/C]TACAAAAAATTAGCC | 80700 |
| rs571955580 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455763 | TGGGAGGAGGATGGG[A/G]GTCTGGAAAGGGCTA | 80700 |
| rs571965440 | snp | A/G | 1.70752e-05 | 0.00292187 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446913 | CCTTCCAGGCAGTTA[A/G]TGCGCTCCTGGGGGT | 80700 |
| rs571990594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4451029 | TGTGAGTCTGGAGAG[C/T]CTATGGAACTATTAC | 80700 |
| rs571992428 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4456227 | CCAGCACCCCCCACC[A/C]ACTATTGGTTGAATC | 80700 |
| rs572004073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447309 | AAGCCCAGCTGAAGA[A/G]GAGGAAAAGGATGCA | 80700 |
| rs572612568 | snp | C/T | 6.6261e-05 | 0.00575553 | synonymous-codon, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446166 | GACGAACCCGTACAC[C/T]GCCCCCAGCCGCTCC | 80700 |
| rs572649360 | snp | C/T | 0.000101456 | 0.00712163 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446315 | TCGGGGAGGCGCACG[C/T]GCAGCAGCGTGTAGT | 80700 |
| rs572651248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449851 | TTACATCAGCTCCAT[C/T]CCACCATGTTACATA | 80700 |
| rs572690080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450244 | AAAAAAAAAAAAGCA[C/T]TGGAGAGGCCACAAA | 80700 |
| rs573045333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447988 | TCCCTCGGCGTTGGC[A/G]GGCAGCGTGGACCTC | 80700 |
| rs573084795 | snp | A/G | | | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446639 | CGGGCTCCGCAGCCA[A/G]CAGCTGTTCCTTGTG | 80700 |
| rs573112304 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBXN6 | GRCh38.p7 | 19:4457448 | CCCTGACGCCCACCC[C/T]CGGCCCGACTTCGTC | 80700 |
| rs573197853 | snp | A/G/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4452687 | CCTGGTATGTCAAAT[A/G/T]TCCCTGTGGGGCCTG | 80700 |
| rs573235961 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457735 | GGGGGCCGCGGGGGC[C/G]GGGGGGCACGGGGCC | 80700 |
| rs573320661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452038 | CCTGTAATCCCAGCT[A/G]CTTGAGAGGCTGAGG | 80700 |
| rs573756478 | snp | C/G | 1.65029e-05 | 0.00287248 | missense, downstream-variant-500B, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447558 | CGCCCACCTGAAACA[C/G]CTTGTTCTGCAGCTT | 80700 |
| rs573870624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447819 | CCCATGGAGCCCACC[C/T]CTGGTGCCAGCAGGA | 80700 |
| rs573882213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452310 | TTCCGATGGAGGGTG[C/G]CTCAGGCACAGGAAG | 80700 |
| rs574051260 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | UBXN6 | GRCh38.p7 | 19:4458612 | GGCTCATGCCTGTAA[-/T]TCCCAGCACTTTGGG | 80700 |
| rs574168708 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4457225 | ATGATCCCGTTTTTC[C/T]CCAAAGGTCGTTCCA | 80700 |
| rs574292403 | snp | A/G | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459069 | GTGGCTCATGCCTCT[A/G]ATCCCAGCACTTTGG | 80700 |
| rs574335249 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459665 | ATACGGTGAAACCCT[A/G]TCTTTACTGAAAATA | 80700 |
| rs574466280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453294 | TGCCGAGCCCCGAAG[G/T]TCCCAGACAACACCG | 80700 |
| rs574568541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454331 | CAGCTCTGCACCATC[A/G]GGCAAGTCCTGCCCC | 80700 |
| rs574739480 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4458535 | TGAAGCACCCCCCCG[C/T]CACCATCACCACGTA | 80700 |
| rs574778746 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459011 | ATACACAAAGTGACA[A/G]TTAAAACAAGCCTCA | 80700 |
| rs574779120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452859 | ACAGTGCGCTGGACA[A/G]GGCATGACTTCTGGG | 80700 |
| rs574873146 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445300 | CCTCGGGGGCTTGGG[C/T]GCATCCCCACAGCCC | 80700 |
| rs575528306 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445280 | TTGGTGTCCCCAGGC[C/T]TCTCCCTCGGGGGCT | 80700 |
| rs575595162 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455543 | CCTCAGCCAGGGAGC[A/G]TCAGCATCACTCCAC | 80700 |
| rs575609882 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, synonymous-codon, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447148 | GTCACAACCAGGCAC[A/G]AAGAGTGAGGCTGAG | 80700 |
| rs575685119 | snp | C/T | 9.35148e-05 | 0.0068373 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448456 | CACTCACTGAGAGCC[C/T]GGGCCGCACGGCCCT | 80700 |
| rs575801874 | snp | C/T | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4459312 | AAGAAGGAGTTGGAA[C/T]GAGATACACAGAGAC | 80700 |
| rs575838391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444929 | TGACAGGGAGCCACA[C/T]CCAGCCCCCAAGCCA | 80700 |
| rs575908506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4455076 | CTCGTGGCTCCACCC[C/T]GTTGAGCCCTACACC | 80700 |
| rs575951941 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBXN6 | GRCh38.p7 | 19:4450961 | GTTTGGTGATTTACA[A/G]TATGGTGAGAGGATG | 80700 |
| rs576317051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445715 | GGCGCGGGGATGCCC[C/T]GGCCTGGAAGCCATC | 80700 |
| rs576544561 | snp | C/T | 0.000327538 | 0.012793 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454043 | TTGGTGGGTCCCTGG[C/T]GGGGCGGCCTGGGGG | 80700 |
| rs576564069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454286 | CTGCAGGCGGAAGAG[C/G]CCCTGGAGGAAGGAG | 80700 |
| rs576574588 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448093 | CAGGGTGGGAAACCC[-/CT]GATTCCTTCAACACC | 80700 |
| rs576579241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449308 | GTCAGGATTCGGGCC[A/G]CCTGCCCAGGCAGCC | 80700 |
| rs576740311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454394 | GGGTGACAGCACCCC[C/T]CCTGAGGTGAAGGCA | 80700 |
| rs576767309 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBXN6 | GRCh38.p7 | 19:4455016 | GCCTCGCCCTGGCCA[C/T]TCCATGCCAGGCCTA | 80700 |
| rs576797971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBXN6 | GRCh38.p7 | 19:4449266 | CAGACGAGGGCGGGT[A/G]AACAGAAGGGCAGCC | 80700 |
| rs576835241 | snp | C/T | 0.000100976 | 0.00710478 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445667 | GACCGAGAGTCGGCC[C/T]TTGCCGCGGCAGGGA | 80700 |
| rs576921068 | snp | G/T | 0.00125341 | 0.0250027 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445979 | GCTCCCTCCTGGGGG[G/T]GTCTGTGCCGGTCCC | 80700 |
| rs577105032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4448943 | TCTGCAACCCTCAAT[A/G]TCTGAAACTCAATAG | 80700 |
| rs577412084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453331 | ACCACAACCTGTGTC[C/T]ACCTTGCAAGGCAAG | 80700 |
| rs577449025 | snp | G/T | 1.66288e-05 | 0.00288343 | missense | UBXN6 | GRCh38.p7 | 19:4453990 | ACTGCTTCTGCTCCA[G/T]CCGGGCTAGGGCGGC | 80700 |
| rs577508990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4447184 | AGACACTGCTGGGGC[C/T]TGATGCGAGGCTAAC | 80700 |
| rs578223416 | snp | G/T | 6.86318e-05 | 0.00585758 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446606 | AGACGCGGCGCTGCC[G/T]GTCCAGCTTGGCGCG | 80700 |
| rs745431736 | snp | A/G | 1.92528e-05 | 0.00310258 | intron-variant, nc-transcript-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445980 | CTCCCTCCTGGGGGT[A/G]TCTGTGCCGGTCCCA | 80700 |
| rs745444748 | in-del | -/CACGCTCAGCCGCTC | 4.88079e-05 | 0.00493979 | cds-indel, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446386 | GGCCTTGGTCCGCAG[-/CACGCTCAGCCGCTC]CACCGCCTCGGACCT | 80700 |
| rs745536160 | snp | C/T | 5.15849e-05 | 0.00507837 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448403 | AGGCGGCCACTGGGT[C/T]GGTGGAGAAGTGCTG | 80700 |
| rs745590188 | snp | C/G | 8.28439e-05 | 0.00643545 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445448 | GCGGGGAGAGGAACA[C/G]GGAGAGCATGAGACA | 80700 |
| rs745627789 | in-del | -/TC | | | intron-variant, upstream-variant-2KB, frameshift-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444566 | CAGCCTCTTCCAGTC[-/TC]TCTCTGATTCACCCT | 80700 |
| rs745757731 | snp | A/C | 9.9681e-05 | 0.00705908 | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447510 | AGGCCAGCTGCCCCC[A/C]CCCCCAGCCTGGGCC | 80700 |
| rs745818837 | snp | C/T | 3.71278e-05 | 0.00430842 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453531 | TTTCTCACTGGAAGG[C/T]AGCCCAAGAAAGAGA | 80700 |
| rs745970805 | snp | A/G | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4449626 | CCAAAAGCGGGCCTC[A/G]GGCGTTTTGGGCGAC | 80700 |
| rs745992034 | snp | C/T | 1.70217e-05 | 0.00291729 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446763 | TGTGCAATGGAGAGA[C/T]CCCCAAGCCGGGCCC | 80700 |
| rs746019034 | snp | A/G | 6.00198e-05 | 0.0054778 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453444 | GGGACAGTGCCACCA[A/G]TGGCTGTTCTTACCA | 80700 |
| rs746126107 | snp | C/T | 6.81594e-05 | 0.00583738 | synonymous-codon | UBXN6 | GRCh38.p7 | 19:4452442 | CGGACAGGTGAAGTA[C/T]ACGCCAGGCACAGCC | 80700 |
| rs746288583 | snp | C/T | 1.82864e-05 | 0.00302372 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454130 | GTGAGTGTATCCTCC[C/T]GAGGTGGCCGGCAAA | 80700 |
| rs746295954 | snp | C/T | 1.64928e-05 | 0.00287161 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448315 | AAGGGGCCACACGCT[C/T]ACTTGGCAATGGTGT | 80700 |
| rs746369025 | snp | A/G/T | 3.49084e-05 | 0.00417771 | utr-variant-5-prime, missense | UBXN6 | GRCh38.p7 | 19:4454055 | TGGCGGGGCGGCCTG[A/G/T]GGGCTGGCTGGTTGG | 80700 |
| rs746389889 | snp | A/G | 3.31044e-05 | 0.0040683 | stop-gained, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446845 | ACTTACCCTGATCCT[A/G]GGCGGGAAGCAACAC | 80700 |
| rs746456850 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4455003 | GACAGCAGAACCAGC[C/T]TCGCCCTGGCCACTC | 80700 |
| rs746463913 | in-del | -/G | | | upstream-variant-2KB, intron-variant | UBXN6 | GRCh38.p7 | 19:4455566 | ACTCCACTGCACAAC[-/G]GCCCTCCCACTGCAA | 80700 |
| rs746572072 | snp | C/T | 1.71422e-05 | 0.0029276 | stop-gained, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446128 | AGCTCAAAAGGCAGC[C/T]AGTCGCTCTGCAGGG | 80700 |
| rs746596029 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445896 | CTCGAGGCCCTGCTG[-/C]CAGTAAGTGGGAAAG | 80700 |
| rs746713566 | snp | A/C | | | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445931 | ATTCAAACCCAGGGA[A/C]CTGCCCAGGCCCCCT | 80700 |
| rs746812859 | snp | A/G | 1.65272e-05 | 0.0028746 | synonymous-codon, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445591 | CTCCAGCACAGCCAT[A/G]TCCCACGAGAAGGTC | 80700 |
| rs746942604 | in-del | -/CC | 1.8276e-05 | 0.00302286 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452498 | CTCAGATACCTGGGG[-/CC]CGGTGAAAGCGTCCA | 80700 |
| rs746957370 | snp | A/C/T | 0.000116511 | 0.00763173 | missense | UBXN6 | GRCh38.p7 | 19:4453992 | TGCTTCTGCTCCAGC[A/C/T]GGGCTAGGGCGGCAG | 80700 |
| rs747169318 | snp | A/G | 0.000132396 | 0.00813512 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446849 | ACCCTGATCCTGGGC[A/G]GGAAGCAACACCTTC | 80700 |
| rs747172947 | snp | C/T | 1.78506e-05 | 0.00298747 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446928 | ATGCGCTCCTGGGGG[C/T]GGAGATGGGCGTCAC | 80700 |
| rs747254265 | snp | G/T | 0.00393028 | 0.0441553 | intron-variant | UBXN6 | GRCh38.p7 | 19:4453451 | TGCCACCAGTGGCTG[G/T]TCTTACCACGTTGGT | 80700 |
| rs747431889 | snp | C/G | 1.72371e-05 | 0.00293568 | synonymous-codon, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446583 | CGAGGCCAGGGGCGA[C/G]GGCTGGAAGACGCGG | 80700 |
| rs747449598 | snp | C/T | 0.000159528 | 0.00892964 | missense, intron-variant | UBXN6 | GRCh38.p7 | 19:4457640 | CTTTGAGCTTCTGAC[C/T]GGGTCCCGCGCTCTT | 80700 |
| rs747474407 | snp | A/T | 3.31192e-05 | 0.00406921 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445456 | AGGAACAGGGAGAGC[A/T]TGAGACAGACCCACA | 80700 |
| rs747520058 | snp | C/T | 2.61407e-05 | 0.0036152 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448406 | CGGCCACTGGGTCGG[C/T]GGAGAAGTGCTGGGA | 80700 |
| rs747575242 | snp | A/G | 0.000109254 | 0.00739019 | intron-variant | UBXN6 | GRCh38.p7 | 19:4454137 | TATCCTCCCGAGGTG[A/G]CCGGCAAAGCTGACG | 80700 |
| rs747762509 | snp | A/C/T | 9.92189e-05 | 0.00704282 | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4447659 | GTGAGTGGGGCACAG[A/C/T]CCAGGCTGCCCACCC | 80700 |
| rs747763788 | snp | C/T | 5.42942e-05 | 0.00521001 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446144 | AGTCGCTCTGCAGGG[C/T]CTCCCGGACGAACCC | 80700 |
| rs747786324 | snp | G/T | 0.000332414 | 0.0128878 | missense | UBXN6 | GRCh38.p7 | 19:4453946 | CTGGTTTCGGATGGT[G/T]TCCTGCGATGTGGGG | 80700 |
| rs747808102 | snp | A/C | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4451681 | TTGCTCTTGTTGCCC[A/C]GGTTGGAGTGCAATG | 80700 |
| rs747811859 | snp | G/T | 1.66457e-05 | 0.00288489 | missense | UBXN6 | GRCh38.p7 | 19:4453995 | TTCTGCTCCAGCCGG[G/T]CTAGGGCGGCAGCGG | 80700 |
| rs747946051 | snp | A/G | | | intron-variant, utr-variant-3-prime | UBXN6, CHAF1A | GRCh38.p7 | 19:4447442 | TGTGGCTCAACTCTC[A/G]CTAGCTCCTCCAGGG | 80700 |
| rs748050606 | snp | C/T | 3.74763e-05 | 0.0043286 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448307 | GCAGGGCAAAGGGGC[C/T]ACACGCTCACTTGGC | 80700 |
| rs748075251 | in-del | -/CT | 7.76287e-05 | 0.00622963 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446474 | CCCCGCCCCGCCCCA[-/CT]CTGCTCCGCGGACGT | 80700 |
| rs748096436 | in-del | -/CCAGGGCCAGGCA | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453859 | ATGTGACTTCTGCAT[-/CCAGGGCCAGGCA]CCAGGGCCAGGCACC | 80700 |
| rs748110180 | snp | A/G | 0.000348142 | 0.013189 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446436 | CGCGGGCCAGGTCAC[A/G]AGGGCTGGCCGGGGT | 80700 |
| rs748171502 | snp | C/T | 1.77008e-05 | 0.00297491 | synonymous-codon, intron-variant | UBXN6 | GRCh38.p7 | 19:4457647 | CTTCTGACCGGGTCC[C/T]GCGCTCTTGAACTTG | 80700 |
| rs748226345 | snp | C/T | 1.65548e-05 | 0.002877 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445470 | CATGAGACAGACCCA[C/T]AGGGCTGAGGCCAAC | 80700 |
| rs748257663 | snp | C/T | 3.30017e-05 | 0.00406199 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445548 | GTTTCAGGATGGAGT[C/T]CGGCTCGGCCCCCGC | 80700 |
| rs748332018 | snp | A/G | 5.16943e-05 | 0.00508375 | missense, downstream-variant-500B, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446316 | CGGGGAGGCGCACGC[A/G]CAGCAGCGTGTAGTT | 80700 |
| rs748387045 | snp | G/T | 5.81356e-05 | 0.00539114 | intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446946 | AGATGGGCGTCACTG[G/T]GGGCCCCTGGCTTCC | 80700 |
| rs748686351 | snp | C/G | 1.67697e-05 | 0.00289561 | intron-variant | UBXN6 | GRCh38.p7 | 19:4452345 | AGGTTGGGGCAGGAG[C/G]ACACAGGGTGCCACT | 80700 |
| rs748695421 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4455103 | CACCAAGGAGAGTTC[C/T]GTAACCCACGTGGCA | 80700 |
| rs748780485 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445421 | CAGAGGTGGCTTGGA[A/G]GCCCTGGGGTGGCGG | 80700 |
| rs748791464 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4444678 | CCCCTCTTGCCAGGT[C/G]AAGTTGCGCATCTGC | 80700 |
| rs748810938 | snp | A/G | 2.40145e-05 | 0.00346507 | missense, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448381 | AACGTGTAGATCTTC[A/G]TGATGGAGGCGGCCA | 80700 |
| rs748889534 | snp | A/G | 0.000269494 | 0.0116049 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446489 | CTCTGCTCCGCGGAC[A/G]TCAGGCCCACCTGAG | 80700 |
| rs748890345 | snp | C/T | | | intron-variant | UBXN6 | GRCh38.p7 | 19:4453163 | CTCTCAACCCCGGTT[C/T]TCTTTTTGAATAGTG | 80700 |
| rs748911150 | in-del | -/GCGGCGCTGCCTGTCCAGCTTGGCGCGCA | 3.66428e-05 | 0.00428019 | intron-variant, downstream-variant-500B | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4446445 | GTCACGAGGGCTGGC[lengthTooLong]CGGGGTTCTTCCACC | 80700 |
| rs748942813 | snp | A/G | 0.000103984 | 0.00720981 | intron-variant, nc-transcript-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4448312 | GCAAAGGGGCCACAC[A/G]CTCACTTGGCAATGG | 80700 |
| rs749115552 | in-del | -/AAA | | | upstream-variant-2KB | UBXN6 | GRCh38.p7 | 19:4458866 | GCGAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 80700 |
| rs749150607 | snp | G/T | 1.65616e-05 | 0.00287759 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446867 | AAGCAACACCTTCTG[G/T]AACCCAATGGCCTCA | 80700 |
| rs749155322 | snp | A/G/T | 3.74688e-05 | 0.00432819 | synonymous-codon, missense | UBXN6 | GRCh38.p7 | 19:4453461 | GGCTGTTCTTACCAC[A/G/T]TTGGTCCCTGGGGCC | 80700 |
| rs749171894 | snp | C/G | 1.81952e-05 | 0.00301617 | missense | UBXN6 | GRCh38.p7 | 19:4453519 | GCTTGAAGTTCCTTT[C/G]TCACTGGAAGGCAGC | 80700 |
| rs749182866 | snp | A/G | 1.73198e-05 | 0.00294272 | missense, intron-variant | UBXN6, CHAF1A | GRCh38.p7 | 19:4446569 | GGCAGTTCGAACTGC[A/G]AGGCCAGGGGCGAGG | 80700 |
| rs749243018 | snp | C/T | | | intron-variant, downstream-variant-500B | UBXN6, CHAF1A | GRCh38.p7 | 19:4448610 | CCAGGGCAGAGGCGA[C/T]GCAGCCAAGACCCAG | 80700 |
| rs749244855 | snp | A/G | 6.35923e-05 | 0.00563845 | intron-variant, upstream-variant-2KB | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445934 | CAAACCCAGGGACCT[A/G]CCCAGGCCCCCTGCT | 80700 |
| rs749380240 | snp | A/T | | | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4455286 | CAGGCTCTCAGTTCA[A/T]GCCCTATACTCCTCT | 80700 |
| rs749445536 | snp | A/G | 0.000403796 | 0.0142033 | utr-variant-5-prime, intron-variant | UBXN6 | GRCh38.p7 | 19:4457740 | CCGCGGGGGCGGGGG[A/G]GCACGGGGCCCAGTC | 80700 |
| rs749450032 | snp | C/G | 1.69077e-05 | 0.00290751 | missense | UBXN6 | GRCh38.p7 | 19:4452434 | CCAGTGAGCGGACAG[C/G]TGAAGTACACGCCAG | 80700 |
| rs749462877 | snp | C/T | 6.60273e-05 | 0.00574537 | missense, upstream-variant-2KB, intron-variant | UBXN6, MIR4746, CHAF1A | GRCh38.p7 | 19:4445554 | GGATGGAGTCCGGCT[C/T]GGCCCCCGCGGCCTT | 80700 |
| rs749553327 | snp | G/T | 1.78768e-05 | 0.00298966 | missense, intron-variant | UBXN6 | GRCh38.p7 | 19:4457660 | CCCGCGCTCTTGAAC[G/T]TGATGTCGGCCTTGA | 80700 |