SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs142736822 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75658004 | AAGTCATGATTTTTA[A/G]CTAGATCACTTTTTC | 26054 |
rs142775585 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615106 | ATGTTGGCCAAGCTG[C/G]TCTTGAATGCCTGAC | 26054 |
rs142791556 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SENP6 | GRCh38.p7 | 6:75686653 | TTTCTCCTTCACTTA[C/T]GAAGCTTAGTTTGGC | 26054 |
rs142800105 | in-del | -/TTTCTTTTC | 0.151001 | 0.229563 | intron-variant | SENP6 | GRCh38.p7 | 6:75653026 | TTTTTCTGTTACTTT[-/TTTCTTTTC]TTTTTTTTCTTTTTT | 26054 |
rs142806373 | in-del | -/ACTTA | 0.367503 | 0.220665 | intron-variant | SENP6 | GRCh38.p7 | 6:75608680 | GATCTTGGATAGATT[-/ACTTA]ACTTCTCTGTTTTCT | 26054 |
rs142888347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679386 | ACTCCAGCCTGGTCA[A/G]CAAAGCAAAACTCTA | 26054 |
rs142903910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619404 | TGTATCCTGTATCCA[A/G]TTCGTATCCCTTTAA | 26054 |
rs142927810 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621032 | AATGAGCACATTTAG[C/T]GTTCTGATCTAGAGT | 26054 |
rs142945540 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75603582 | TAACTTCTTTTAGTA[C/T]GTTTCGGAAAGATTA | 26054 |
rs142990924 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75683114 | TAACTGGCATGAGAT[A/G]GTTATCTCATTGTGG | 26054 |
rs143078316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75655832 | ATGTCTTCTATTTAT[A/G]TCGAACCTGTATATA | 26054 |
rs143087285 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75714972 | ATTGTTGAATTACCT[A/G]TCTTTCTAAACTGGA | 26054 |
rs143147892 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75684364 | ACAGTTTGACTTCCC[C/T]ATTTCCTAATTGAAT | 26054 |
rs143183180 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75659784 | CTCTATGCCTTTTTC[C/T]CTCCTTCCTCCTGCC | 26054 |
rs143187747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672515 | ATGTAGAAATTTGCA[A/G]TGTGGTATTAACCTT | 26054 |
rs143212068 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SENP6 | GRCh38.p7 | 6:75703180 | CAGGTTAATGACTGG[A/G]TGTGGTGGCTCACGC | 26054 |
rs143219181 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SENP6 | GRCh38.p7 | 6:75632730 | TGGATTTAAAGTTTT[A/G]GGGACTTCCAGACTG | 26054 |
rs143221748 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75677786 | GAAGCAAAGGCCACA[A/G]TACTACTAAACACAT | 26054 |
rs143223098 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75602921 | GCATTCACATCTTGT[C/T]TGGTGTTCATGAAAA | 26054 |
rs143227035 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75627661 | GGCATTGGTCTTCAT[A/G]TACACATATGTAGCT | 26054 |
rs143257255 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693106 | TTAAGTTTTATAAAA[-/C]CAGCCATTGTAGGCC | 26054 |
rs143321532 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | SENP6 | GRCh38.p7 | 6:75640597 | ACAGTATAATTTTGC[C/G]TTAATGACTATAGTT | 26054 |
rs143377348 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75630730 | CAGTTTCACTGTGCT[G/T]CTTTTAAGGGATTTA | 26054 |
rs143455508 | in-del | -/ATC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628116 | TTCTGATATGATAGT[-/ATC]ATCTATTTTAAGTAT | 26054 |
rs143481800 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | SENP6 | GRCh38.p7 | 6:75702007 | GGCAAAGGGGAATGA[C/T]GAGTTGCAAAGTGAC | 26054 |
rs143511046 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75681076 | AAGACACAAATGTCA[A/G]AATTATTTGACAAAG | 26054 |
rs143512346 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SENP6 | GRCh38.p7 | 6:75705279 | TGGCCAGGTGTGGTG[A/G]CTCACGCCTGTAATC | 26054 |
rs143513202 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | SENP6 | GRCh38.p7 | 6:75652140 | CACAATCGCGCCACT[C/G]TCCTCCAACCTGGGC | 26054 |
rs143522761 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75635776 | GCAAAAACATGAGAA[A/T]AAACAATAAAAGGAG | 26054 |
rs143567916 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75667571 | ATTGTTAAAAAATCA[A/C]TTAATATGTGCTGTT | 26054 |
rs143601514 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75622662 | CAGAGATCCACAAAT[A/G]TACACACAAAGTTCT | 26054 |
rs143633223 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671420 | CTTTTTACATAAAGC[A/C]CTTGTCTTTAAGAGA | 26054 |
rs143684011 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SENP6 | GRCh38.p7 | 6:75614089 | TATGATTCAAGTCAG[G/T]TTATGCATTTTTTAA | 26054 |
rs143706464 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SENP6 | GRCh38.p7 | 6:75626673 | AATTGAAGTTGCTAT[G/T]TCAGAGGTGAAATTC | 26054 |
rs143739363 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75677805 | TACTAAACACATAGT[A/G]TAATGGTAAATAATA | 26054 |
rs143773230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75686437 | ATTTGATCCTGTCAT[C/T]ATGATGTTCGCTGGT | 26054 |
rs143805012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75611618 | GAACATTTGGAACTA[C/T]TTATCTCATGCAGTC | 26054 |
rs143852662 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SENP6 | GRCh38.p7 | 6:75604452 | GCCTGGCCAACATGG[C/T]GAAACCCCACTCTAC | 26054 |
rs143894280 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | SENP6 | GRCh38.p7 | 6:75685013 | GTAGAATTAGGCTGT[A/G]AATCCATCTGGTCCT | 26054 |
rs143907517 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SENP6 | GRCh38.p7 | 6:75704787 | TGCGGCTTTCTGCAG[C/T]GCATTGTGCCCCTGG | 26054 |
rs143942232 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75615370 | TTTTTAGTAGAGACG[A/G]GGTTTCGCAGCATTG | 26054 |
rs143943738 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SENP6 | GRCh38.p7 | 6:75667633 | AATTTGCTGATGGAA[A/G]AGAAAGTTACTATGA | 26054 |
rs144066090 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690730 | GAGAGTCTCGCTCTG[-/T]TCACCCAGGCTCTGG | 26054 |
rs144074697 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | SENP6 | GRCh38.p7 | 6:75705530 | GTCTGGGCAACAGAG[C/T]GAGACTCCATCTCAA | 26054 |
rs144077299 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75711187 | AAGTAACATACCACA[C/T]CTCTAGTGTCTAATC | 26054 |
rs144145485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671538 | ACCAGCCTGGCTAAT[A/G]TGCTAAAACCCCATC | 26054 |
rs144146954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75711156 | GTCAGTGTTGTAGCA[C/T]TGGATAATTGGAATT | 26054 |
rs144149117 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75669596 | TATAATTACTTGTAA[A/T]TAAAATTACATACCT | 26054 |
rs144157747 | in-del | -/AAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674170 | TTTTTTTTTTTTTTT[-/AAA]AAAAACGATAAGGTC | 26054 |
rs144166196 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617263 | AGAATTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 26054 |
rs144167094 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75649049 | TGGTGGCTCACACCT[A/C]TAATCCCAGCACTTT | 26054 |
rs144168600 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75674447 | CTGCCTCAGCCTCCT[C/G]AGTAGCTGGGATTAC | 26054 |
rs144276996 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SENP6 | GRCh38.p7 | 6:75690684 | TATATGTTTGTTTTG[G/T]TTTTTTTGTTTTTTG | 26054 |
rs144296360 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653475 | CAAAAGTCCTTGTAG[A/G]TTTATTTTTATTTAT | 26054 |
rs144365000 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75688477 | CCCATCTTCTGCATC[A/G]GTCATGCTGAGAGCT | 26054 |
rs144378828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696287 | ATATCTAGAATAGTG[C/T]TTCCCAAATGTGACT | 26054 |
rs144380352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646145 | TTCTCTTTAGTGTGA[A/C]AGTGTATGGAATTTG | 26054 |
rs144384844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624703 | CCTTTGCCCATTTTT[C/G]TATCTGGTCTTTAGA | 26054 |
rs144467550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673726 | TCTTATGCAACAATT[G/T]TATTTAAATGCTTTA | 26054 |
rs144522637 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617259 | TTGGAGAATTTCTTT[C/T]TTTCTTTTTTTTTTT | 26054 |
rs144579119 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75679974 | ATCAGAGAAATGATA[C/T]CATAATTGAATTTCT | 26054 |
rs144700593 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75685382 | TTTTGTCTCTATCTC[C/T]TTCAGTTCTGCTTTG | 26054 |
rs144719252 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SENP6 | GRCh38.p7 | 6:75682888 | CATGTGTCTTTATAG[C/T]AGCATGATTTATAAT | 26054 |
rs144738596 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717289 | GATTCTGACAAAATA[A/G]AGTTCATTAAAAAAA | 26054 |
rs144742538 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | SENP6 | GRCh38.p7 | 6:75686794 | TGGGCTTCCCTTTGT[A/G]GGTAATCAACCTTTC | 26054 |
rs144742933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626516 | TTGGATGGATATACT[A/G]TAGATATTCAGTTTG | 26054 |
rs144756449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642510 | AATCCAGGAATGAGT[C/T]TGGCATGTCAAAGAA | 26054 |
rs144801209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75625060 | GGTATTTTGGAGAAA[C/T]TGGCCCTTTGCTGTG | 26054 |
rs144868217 | snp | C/G | 0.35809 | 0.225425 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601636 | CGCCAGGTCTGCCAT[C/G]GGGCCCTGGGCGGTG | 26054 |
rs144933671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693710 | GTGATAAAAGTAACA[A/G]ATCTCAAGAATGTGC | 26054 |
rs144953456 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SENP6 | GRCh38.p7 | 6:75655684 | AACAAGTTATTTATC[A/G]ATTTTCCTGATAATC | 26054 |
rs144988901 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SENP6 | GRCh38.p7 | 6:75659476 | TAGTTTCAGTACTTA[C/T]TAAATTCTAGGTGAT | 26054 |
rs145031402 | snp | A/G | 0.00805556 | 0.0629515 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663290 | TTATTAAGAACGTCA[A/G]TTCATCAGAATTCTG | 26054 |
rs145036916 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SENP6 | GRCh38.p7 | 6:75642314 | TGAAATAATAATTTC[C/T]ATGTAGAGAAGTGTA | 26054 |
rs145062141 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SENP6 | GRCh38.p7 | 6:75698572 | ACTCTTGGCCTCAAG[C/T]CATCCCCCAACCTCA | 26054 |
rs145070909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624219 | CCTTTAACTTAATAT[A/G]TTATCTTGGAGACCA | 26054 |
rs145070997 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75670322 | TACTATTCCTGAATG[C/T]CATACTATTACTCAA | 26054 |
rs145072598 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75626230 | TTGGATGGTTTCAGC[A/G]TCATATCTCAAAAGA | 26054 |
rs145085536 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75683541 | TTAGGTCTAACATTT[A/C]AGTCTTTAATCCATC | 26054 |
rs145091638 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75607326 | AAGGTCATCAGCTGC[C/T]ACATGGAGAGAGCTT | 26054 |
rs145235594 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75632653 | ATTCATCTATTCACA[A/G]TAGTTCTCTTGATGC | 26054 |
rs145329416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75712756 | AAAAAGTTCTAAACT[A/G]ATTATTTCATGTGAT | 26054 |
rs145330589 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637868 | TGAGAGGTTTTTTGT[G/T]TTTGTTTGAGACTGA | 26054 |
rs145378963 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SENP6 | GRCh38.p7 | 6:75603740 | CACAGTAGGTACTCA[C/G]TGTTAGTCTAGTGAA | 26054 |
rs145411095 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75664575 | TCTCAAATGCTATAT[A/G]TGTAAATCTGTTTAG | 26054 |
rs145446210 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718436 | ATAACTGTAAGGACA[A/G]AAGGAGAGGGAGATT | 26054 |
rs145489439 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75649882 | AATACAGAGACATAC[A/G]TTTATTTTTTCACAC | 26054 |
rs145493469 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601417 | ATTTAAAGCTGACTG[A/G]TAGGATCTTCCCTGC | 26054 |
rs145522366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75661653 | GGAGATAAAGAATTG[C/T]AGCCAGCCTCTATGT | 26054 |
rs145603486 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664236 | TTGAAGTGTAGCCAG[A/G]GCAATATAGTAGGAC | 26054 |
rs145636094 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75622507 | GAGGTTGCAGTGAAC[A/C]CAGATCATGCCATTG | 26054 |
rs145666497 | in-del | -/CTGTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640479 | TGTGTATTCATCTTC[-/CTGTT]TGTTTATTTTGTATA | 26054 |
rs145676643 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605707 | GATCTTTCATGCAGG[A/T]TCATGAATAATTTTT | 26054 |
rs145683169 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SENP6 | GRCh38.p7 | 6:75699722 | CTCAAACTCCAGAGC[C/T]GAAGCGGTCCACCTG | 26054 |
rs145686437 | in-del | -/GTTTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623715 | TATTGTTTATGGCTG[-/GTTTT]TTTTCATACAACATA | 26054 |
rs145715623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660512 | TGTCCCAGATTCCAT[A/G]TGAGTCCCTTCAAGC | 26054 |
rs145725617 | snp | C/G | 0.349452 | 0.229367 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601637 | GCCAGGTCTGCCATG[C/G]GGCCCTGGGCGGTGG | 26054 |
rs145728379 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75706256 | TCTTTTTGAGATGAT[C/G]AAAAGGTTTAAAAAT | 26054 |
rs145745521 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75670373 | ATAGCTAAATAAGAT[A/G]CAAGGATTTACTGTT | 26054 |
rs145760348 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SENP6 | GRCh38.p7 | 6:75647202 | GGTTTTTGCTTTTTT[C/T]CCCCCCAAATTTTGC | 26054 |
rs145873754 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SENP6 | GRCh38.p7 | 6:75650962 | CTTTATTTTGAATTT[C/G]AGGCACTTAGTATAT | 26054 |
rs145922628 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75681663 | AGTGAGAGAACGGAC[G/T]GATACAGCATCCATC | 26054 |
rs145922927 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SENP6 | GRCh38.p7 | 6:75635282 | TTCTCATTGATCTTG[A/C]AAGTACTGCTTGAGT | 26054 |
rs145965599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75641251 | TGTACATTTTTCTAT[A/G]ATGGTTATATATATT | 26054 |
rs146034420 | snp | A/G/T | 0.0036806 | 0.0427411 | intron-variant | SENP6 | GRCh38.p7 | 6:75678807 | CCTTCTAATTTTGTT[A/G/T]CAGGTTGATAGTATA | 26054 |
rs146046753 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SENP6 | GRCh38.p7 | 6:75660782 | GACTACAGGCATCTG[A/C]CACCATACCCGGCTT | 26054 |
rs146046791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615222 | GTCTTGCTGTGTCGC[A/G]CAGGCTGAAGTGCAG | 26054 |
rs146047951 | in-del | -/TTG | 0.265622 | 0.249511 | intron-variant | SENP6 | GRCh38.p7 | 6:75626125 | AATAGAGAGTTAGGT[-/TTG]TTGTTGTTGTTGTTG | 26054 |
rs146074479 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617255 | TGGTTTGGAGAATTT[C/T]TTTCTTTCTTTTTTT | 26054 |
rs146088954 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619747 | CAATGCACAAGAGTT[C/G]CAGTTTCTCCCACAT | 26054 |
rs146120116 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | SENP6 | GRCh38.p7 | 6:75686476 | CCATTAATTGATGCA[C/G]TTTCTTCATAGCATC | 26054 |
rs146207739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689370 | CAGCATCAAAACAAT[A/G]TAACACAGTGTCATC | 26054 |
rs146223299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75617846 | CTTAATCTTTCCTTG[C/T]TTTTCATAACCTTGA | 26054 |
rs146264208 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | SENP6 | GRCh38.p7 | 6:75705285 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 26054 |
rs146275475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75710702 | TGCTTTATTATTACT[A/G]TTATTCCTACTATTG | 26054 |
rs146279488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641742 | TAGTACTTTGGGAGG[A/G]CAAAGCGGGAGTATC | 26054 |
rs146329989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75657840 | CATAGGCAGAGCTTC[A/G]CTTGTGAAAAGAACA | 26054 |
rs146397987 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75692146 | CAGGCGTGAGCCACC[G/T]CGCCTGGCCTCCCAT | 26054 |
rs146499090 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670190 | GACCTCAGATGATCC[A/G]CCCATCTCGGCCTCC | 26054 |
rs146551731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637413 | AGTCTTTGGGTCATA[A/G]TTAAGATTCCAATCT | 26054 |
rs146566386 | snp | A/G | 4.9783e-05 | 0.00498889 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702982 | AATGAAGAATTCAAT[A/G]AAGGAGAATCTACAT | 26054 |
rs146620024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75651752 | TTTTTAAATTGATAC[A/G]TAATATTCATACTGT | 26054 |
rs146629737 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SENP6 | GRCh38.p7 | 6:75655040 | ACTAGAGTTCAATAT[G/T]TGTTTACAGTTTATT | 26054 |
rs146630551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606674 | CCAAAATCCTCCAGA[A/G]TTTGAAGCAACATGA | 26054 |
rs146669831 | snp | C/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75708404 | TAACTAAAAGTCATG[C/T]TTTTCAAATTTTTGA | 26054 |
rs146736382 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | SENP6 | GRCh38.p7 | 6:75702456 | CTGCTGACCTCAGGT[A/G]ATCCACCCACCTCAG | 26054 |
rs146739590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631774 | TACTTACTTTTAGCC[C/T]TTGGCAGAAAAAGTT | 26054 |
rs146750900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75636116 | TAGGTCTCAACACCT[A/G]TAACATTTTGCATGT | 26054 |
rs146859116 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SENP6 | GRCh38.p7 | 6:75685074 | ATTACCTCAATTTCA[A/G]AGCCTGTTACTGGTC | 26054 |
rs146861958 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SENP6 | GRCh38.p7 | 6:75612306 | AAAATTGCTTTTCGA[A/G]CATACACATTTAATT | 26054 |
rs146871538 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SENP6 | GRCh38.p7 | 6:75687436 | CGTCCAGCTTTGTTC[C/T]GTTGCTGGCAAGAAG | 26054 |
rs146873754 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SENP6 | GRCh38.p7 | 6:75615980 | TTGGTCAACTATACT[A/G]GTTCCTATTCATCCA | 26054 |
rs146901155 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671683 | GCCGAGACGGCGCCA[C/T]TGCACTCCAGTCTGG | 26054 |
rs146911771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75676772 | TAAATTAGTTACATA[C/T]GTGAATAGATTTGTT | 26054 |
rs146921731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613374 | ACGTTGAGTAACTGA[C/G]AGGGACTGTATGGAC | 26054 |
rs146931729 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75616975 | CTCAATTGATCCTCC[A/G]TCCAATCCTCCTATC | 26054 |
rs147016958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656389 | AAGTACTTCTCTGGA[A/G]TAATCTGTTGAGGAT | 26054 |
rs147108126 | in-del | -/GTGTGTGTGT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638556 | GTCTTTGTGTGTGTA[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 26054 |
rs147110952 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75704404 | TGCCTGGATGTGCAC[A/G]TAGGCCAGATTTATG | 26054 |
rs147111901 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75633363 | GATTCACATGAAAAG[A/T]AAGTAATACAATAAA | 26054 |
rs147120415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75707465 | ACCTCCTGGACTCAA[A/G]CAGTCCTCCCAGCTC | 26054 |
rs147169534 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | SENP6 | GRCh38.p7 | 6:75696626 | GGGACTAAGGCACAC[A/G]CCACTCCACCCAGCT | 26054 |
rs147171917 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75625307 | TTTATTAGAGACCGG[C/G]TTTCACCATTTTGGC | 26054 |
rs147182060 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610077 | AGAAGTGTGAGTCAC[C/T]GCACCTGGCCTTAGT | 26054 |
rs147285994 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666810 | TGTTCTTCCCCTGCA[C/T]CATCCACTGGAAAAG | 26054 |
rs147373435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701317 | TGTACAGCTTCTTGC[C/T]TGTGTCCTATACTCT | 26054 |
rs147381882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75661666 | TGTAGCCAGCCTCTA[C/T]GTAAACTTTAATTCC | 26054 |
rs147392950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75649748 | TCTCAAACTCCTGAC[C/T]TCGTGATCCACCCAC | 26054 |
rs147438218 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75609275 | CTCCCCCCAAAGGAA[C/G]GGGCGACTGAACAAG | 26054 |
rs147478198 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SENP6 | GRCh38.p7 | 6:75684365 | CAGTTTGACTTCCCC[A/G]TTTCCTAATTGAATA | 26054 |
rs147488158 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75646207 | GGAACTAAAAACCTA[C/T]CTTCTTTCTTATAAG | 26054 |
rs147497595 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SENP6 | GRCh38.p7 | 6:75627783 | TGGGTTCAAGGGATT[C/T]TCCTGCCTCAGTCTC | 26054 |
rs147497669 | in-del | -/AGG | 0.111928 | 0.208413 | intron-variant | SENP6 | GRCh38.p7 | 6:75605830 | TTTGTGGAATTAATT[-/AGG]GGGCAAGATTAAAAG | 26054 |
rs147523286 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75701054 | CTGGATGCTGTTTGA[G/T]GAAGAGATAGATAGT | 26054 |
rs147555561 | in-del | -/A | 0.0766824 | 0.180169 | intron-variant | SENP6 | GRCh38.p7 | 6:75636046 | AATGTTAAAAAAAAA[-/A]CAACCCGTTAATAGT | 26054 |
rs147573925 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75617630 | CACTAATGTTGCCAC[A/C]AAATATAGCCAGTGT | 26054 |
rs147643622 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659529 | GACTTGGAAAACTTA[C/T]TTAGGCAGCTTTTTC | 26054 |
rs147677777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75675631 | GTAATTTCATTCAGA[A/G]ATATCACAGAACCTA | 26054 |
rs147678153 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718490 | GTCTAGTCAAGTGGA[C/T]GTAAGTAAATAGTTG | 26054 |
rs147687800 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679502 | TGTTAGAAGTTTATG[G/T]TCTTGTAGGAAGCAC | 26054 |
rs147781437 | snp | A/G | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697471 | ACATGGACCCGGCAC[A/G]TAGATATTTTTGAGA | 26054 |
rs147851894 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75694115 | TACAAAATTAGCCTG[G/T]CATGGTGGTCCATGC | 26054 |
rs147887866 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SENP6 | GRCh38.p7 | 6:75683067 | TCCTCTCCAGCATCT[A/G]TTGTTTCCTGACTTT | 26054 |
rs147887899 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75638834 | AGGGCAAAATAGGAG[C/G]ATAGCCTGAGCCCAG | 26054 |
rs147897642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642898 | AGCAAGGTCTAGGAG[C/T]TGGGGAGGTAGAAAG | 26054 |
rs147957854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680308 | GATAAGTTCCCTTTT[A/G]GAGGTCTGTGATATA | 26054 |
rs148042549 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SENP6 | GRCh38.p7 | 6:75694989 | AAGTGATTCTCCCAC[C/T]TCAGCCTCCCAAGTA | 26054 |
rs148044769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75623337 | TATTAACATGAACCT[A/G]TTAATAGATACATTA | 26054 |
rs148051354 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SENP6 | GRCh38.p7 | 6:75684113 | GAAGAGGTCCTTCAC[A/G]TCCCTTGTAAGTTGG | 26054 |
rs148060973 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75645577 | AGCCAAGATTGCGCA[C/T]GCTACTGTTCTCCAG | 26054 |
rs148096914 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75626796 | AATCTTGCAAAATAT[A/G]TAGTCATACTTGAAT | 26054 |
rs148139549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678020 | GTTGAGAAAAGAACA[A/C]AAGAAGAAAGGGAAA | 26054 |
rs148167257 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SENP6 | GRCh38.p7 | 6:75671449 | GAACTTATTGCCGGG[C/T]GCGGTGTCTCACGCC | 26054 |
rs148214854 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SENP6 | GRCh38.p7 | 6:75613029 | TGAGGCACGAGAATC[A/G]CTTGAACCCAGGAGG | 26054 |
rs148244702 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SENP6 | GRCh38.p7 | 6:75609932 | AGCTGGGATTACAGG[C/T]GCATACCACCATGCC | 26054 |
rs148266723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75617988 | CAGTGCTGAAGTGCT[A/G]TTTTCATCATACCAT | 26054 |
rs148297485 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75703182 | GGTTAATGACTGGGT[A/G]TGGTGGCTCACGCTT | 26054 |
rs148308644 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SENP6 | GRCh38.p7 | 6:75665902 | TGTAGTGGTGCACAC[A/G]TGTAATCCCAGGTGC | 26054 |
rs148411084 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | SENP6 | GRCh38.p7 | 6:75628832 | TCAAGCGATCCTACC[A/G]CCTCAGCCTCCCAAG | 26054 |
rs148452684 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679361 | CACTGAGCCATGATG[G/T]CGCCACTGCACTCCA | 26054 |
rs148462844 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75636323 | GACAGATTCTACTTA[C/T]ATTTGTCTTTTATTT | 26054 |
rs148525590 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75614606 | AATATTGTGTGGAGA[C/G]ATACTTTGAAACCTG | 26054 |
rs148566722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661275 | CCCCTGGTGTATTTA[A/C]CTGTTAGCTTAGTTT | 26054 |
rs148576632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620878 | CCTGGGTTCTAGGAC[A/T]TCAGGTTTTTGGTCA | 26054 |
rs148597023 | in-del | -/TATTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618311 | CGGGAATGTTTATTT[-/TATTT]AGGAGTTATAACCCA | 26054 |
rs148607837 | in-del | -/T | 0.0554779 | 0.157039 | intron-variant | SENP6 | GRCh38.p7 | 6:75712569 | AAAAAATAACCTAGA[-/T]TTTTTTTTAACATTT | 26054 |
rs148609348 | in-del | -/ATAC | 0.0711525 | 0.174681 | intron-variant | SENP6 | GRCh38.p7 | 6:75664376 | TTTTAAAAAATCTAT[-/ATAC]ATGTACACACATACG | 26054 |
rs148617603 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | SENP6 | GRCh38.p7 | 6:75668307 | AAAAGATGAATATAT[A/T]TGATTAAATGAAAAG | 26054 |
rs148659604 | snp | C/T | | | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711342 | GGATGATAGCAGTGA[C/T]GATGGATTCCTCGCT | 26054 |
rs148662199 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75642333 | TAGAGAAGTGTAATG[A/G]GTTGATGTGATAGAC | 26054 |
rs148733599 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716708 | CAGAAACTTCATTAT[A/T]TTTCAAATGAAATGG | 26054 |
rs148734448 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653834 | TGTAAACATACTGTT[A/G]TAGAGTCAGAAAGTA | 26054 |
rs148776718 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75696374 | TCCTAGATGTTCATC[C/T]ATAATATCTAAGAAA | 26054 |
rs148786561 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75658124 | GGTTTGGAGAAGACA[C/G]AGTGAACTTAAGAGC | 26054 |
rs148862648 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SENP6 | GRCh38.p7 | 6:75688623 | TTTTGGTGTGTTTCA[A/G]AGTTCTTCATAGCTG | 26054 |
rs148880883 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664424 | TATATACATCTATAT[A/G]TGTCAGGTACTGTGC | 26054 |
rs148924022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707257 | TTTTGGACAAATGTT[A/C]TTCAAATATAGGTGT | 26054 |
rs148925475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75683106 | TGCCATTCTAACTGG[C/T]ATGAGATGGTTATCT | 26054 |
rs148927554 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | SENP6 | GRCh38.p7 | 6:75606156 | TTTGACATTTTTGCT[C/G]TGAAGTATGTTTTAT | 26054 |
rs148932342 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SENP6 | GRCh38.p7 | 6:75670960 | TGCATGAAACTTTCA[A/G]TGAGTTAGAAAACCT | 26054 |
rs148973756 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75714726 | AATACAACAGCCAGC[C/T]ACCTGAATGCCATTG | 26054 |
rs148978860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75612637 | ATAACCCCATGAGAC[A/G]TAGAAATTAAAACAT | 26054 |
rs149047600 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75655690 | TTATTTATCGATTTT[C/T]CTGATAATCGATAAT | 26054 |
rs149089495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698831 | ACCTGGCGAACATGG[C/T]GAAACCTCGTCTCTA | 26054 |
rs149099461 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75659568 | GTAGACCATTTTTAT[G/T]CTTGTTCAAAATATA | 26054 |
rs149140428 | snp | A/G | 1.68721e-05 | 0.00290444 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703046 | ATGGCCTACAGAATG[A/G]AAGTTTAAGTTCCAC | 26054 |
rs149143930 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632692 | CATTACCTGGAAAAC[C/T]GTCTTAGGCTGGGGT | 26054 |
rs149186237 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SENP6 | GRCh38.p7 | 6:75680968 | TAGTACTCAAAATGT[C/G]CAGATTTCAAAATGA | 26054 |
rs149241268 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | SENP6 | GRCh38.p7 | 6:75609190 | CTTCAGCATTTCCTT[A/C]CTCTCCCTTTCTCCC | 26054 |
rs149246201 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | SENP6 | GRCh38.p7 | 6:75673600 | AAGTGCTGGGATTAC[A/G]GGTGTGAGCCACTGT | 26054 |
rs149389350 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75657767 | AAACTCTAGGGATTA[A/C]TTGTGCCTAGAGTGG | 26054 |
rs149405371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700899 | GAAGTGATGAAATGA[A/G]GAGGTTGGTGTGTTA | 26054 |
rs149458677 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75704775 | GGCAGAGGTCCCTGC[A/G]GCTTTCTGCAGCGCA | 26054 |
rs149460546 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75635159 | AAATTACAGTTAATA[C/T]CGTACTTTCTTTATA | 26054 |
rs149462486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604361 | TCTGGGCACGGTGGC[A/G]GCACGCCCTTAATCA | 26054 |
rs149598584 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75690573 | AGACATATGTTCAGT[A/T]TTGCAAAACAAAGTT | 26054 |
rs149619423 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SENP6 | GRCh38.p7 | 6:75639967 | GTAGTCTCCTCCTTA[C/T]TTGTGGTTTGATTTA | 26054 |
rs149649623 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75696285 | AAATATCTAGAATAG[G/T]GTTTCCCAAATGTGA | 26054 |
rs149651964 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75624524 | TCGATATCTGAACGT[A/G]TCTGTTTCCCCACAC | 26054 |
rs149695094 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | SENP6 | GRCh38.p7 | 6:75693947 | AGATGTATAAAAAAA[-/T]AACTAAGGCAATAAA | 26054 |
rs149702575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75658417 | ACTAGAAGTATTTAA[C/T]AAAGCTGTGTTTGTG | 26054 |
rs149703747 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | SENP6 | GRCh38.p7 | 6:75627952 | GCTGAGATTACAGGC[A/G]TGAGCCACCACGCCT | 26054 |
rs149719559 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679186 | TGGGAGGTCAAGGTG[A/G]GAGGATCGCTTGAGC | 26054 |
rs149721851 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600558 | TCAGCCTCCTGAGTA[G/T]CTGAGATTACAGGCA | 26054 |
rs149754318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664153 | TTCTTCTAAAAAATA[A/G]AAATTGGGCACAGTG | 26054 |
rs149763760 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SENP6 | GRCh38.p7 | 6:75650379 | ATATACTCTGAAACT[A/G]TGCAAATACCCTGTT | 26054 |
rs149774336 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75605521 | GGAAGCCATTTTACA[C/T]AGCATTGAAGTCAAG | 26054 |
rs149795249 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75706226 | AAGAGAGTGATAGCT[A/C]AGTGGTATGGGGTTT | 26054 |
rs149816048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655255 | CCAGTTACCCCTGGC[C/G]ATCAATGGGGTGACA | 26054 |
rs149912559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75693486 | TGGTTCACTCATTAC[A/G]GTATAGTCCCTGGAC | 26054 |
rs149923483 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75682140 | AAATTACCAGGGATC[A/T]AGAAGGATGTTATGT | 26054 |
rs149976547 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75611190 | CTTCTGTGGAAACCA[A/G]TAACTTCTCTTTCTT | 26054 |
rs150028097 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | SENP6 | GRCh38.p7 | 6:75616516 | TGCTTTGGGAGGCCG[A/G]GGCGGGTGGATCACA | 26054 |
rs150077768 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75652253 | TTTGACCTCGTGATC[C/T]GCCTGCCTCAGCCTC | 26054 |
rs150113628 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | SENP6 | GRCh38.p7 | 6:75608276 | GACCAGCCTGGGCAA[A/C]ATAACGAGGCCCCAT | 26054 |
rs150129675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657170 | CAAATTTAGTAAGGC[C/T]AAAAAAGCTTGTAGG | 26054 |
rs150268834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75713616 | CGTATTCTGATGGGG[A/T]TGAAGAACTATGTAT | 26054 |
rs150269840 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75643605 | CATGCGCCTGTAATC[C/G]CAGCTACTCGGGAGG | 26054 |
rs150275580 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SENP6 | GRCh38.p7 | 6:75700546 | GACTGGAGTGCAGTG[A/G]CACCATCTCGGCTCA | 26054 |
rs150284962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685579 | ATTTAAATGTGTCCA[A/G]GAGATTCTGGTACGT | 26054 |
rs150321455 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75648452 | CTCTTACTTCCAAAA[C/T]AGAATAATTTTTAAA | 26054 |
rs150339880 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619290 | TGTCTCTATGAATTT[A/T]CCTATTCTGGGTACT | 26054 |
rs150427800 | snp | G/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675465 | ATCAAGATACAGCTA[G/T]ACGGTAAGCTATTTT | 26054 |
rs150438345 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75632381 | CCAGTCAGAATAGCA[A/G]ACTCTAGGCTTGCCA | 26054 |
rs150456176 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75603269 | TAGACTAAGCCAGCC[C/T]CAAGAAAAGCTGTAT | 26054 |
rs150480741 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75680822 | GGTCTAGTAGAGAAC[A/G]TGTACTTTTAGTCCC | 26054 |
rs150530350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709416 | ACTAAGGCAGATTTT[A/G]TGTTCTTGACTACTG | 26054 |
rs150583979 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716361 | GTGTTACCTTTCTCT[A/G]TTACAGCTTAAAGTA | 26054 |
rs150585195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75645796 | TATAATTTTTAAAAA[A/G]CAGAACTTTAATTTG | 26054 |
rs150595255 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600179 | CAAATTTTTTTCTGA[C/T]AGTTCTGCAGGGTCA | 26054 |
rs150626651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75687339 | CCTTGCGATGGGTTC[A/G]AACATCCTCCTTTAG | 26054 |
rs150636540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650017 | AGCTTTTCACTAATA[C/T]CCTTTTTCTGTTCCA | 26054 |
rs150677670 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | SENP6 | GRCh38.p7 | 6:75693130 | GTAGGCCAGGCACAG[G/T]GGCTCACGCCTATAA | 26054 |
rs150699943 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | SENP6 | GRCh38.p7 | 6:75627535 | TTGGTAGGATGAAGC[A/G/T]GGAGGATCGTTCGAA | 26054 |
rs150751620 | snp | A/G/T | 0.000819562 | 0.0202267 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634788 | TCATGCACAGATACC[A/G/T]GTAGTAAAAACAGCA | 26054 |
rs150793730 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75682114 | CTGACAAATAAACTT[C/G]TGAGGAAAGAAAATT | 26054 |
rs150795807 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75604811 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAACA | 26054 |
rs150811818 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75654230 | GCTACAGAGTGAGAC[C/T]CTATCTCAAAAACAA | 26054 |
rs150813293 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624506 | AGATTTACACTTGTT[C/G]CATCGATATCTGAAC | 26054 |
rs150848149 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75610505 | GATAATCTGTGCCAT[A/C]TCCATTTGACACTAA | 26054 |
rs150891342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658351 | TGATTTTTATGTCTA[C/T]ATAATCTTATTTTTA | 26054 |
rs150909980 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | SENP6 | GRCh38.p7 | 6:75666108 | ATGATATATATAAAA[C/T]GTATATATGATATAT | 26054 |
rs150940548 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SENP6 | GRCh38.p7 | 6:75688806 | GGCGTGGTGGCTCAC[A/G]CCTATAATCCCAGCA | 26054 |
rs150950216 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75652162 | AACCTGGGCAACAGA[A/G]TGAGACCATATCTCA | 26054 |
rs151063471 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75705587 | ATTAAAAACTAGTTT[A/C]TGTTCAAATTCTTAA | 26054 |
rs151067115 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75636850 | TTACAGCTTCTCCTA[A/G]ATTTTCTTATTTTCT | 26054 |
rs151077210 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621123 | CTGTTAAAAGGCAGG[G/T]ATCGTTGAGTTTAAG | 26054 |
rs151109676 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | SENP6 | GRCh38.p7 | 6:75683123 | TGAGATGGTTATCTC[A/C]TTGTGGTTTTTGATT | 26054 |
rs151119607 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75643367 | AAAGCCACAAGAGAT[A/G]CAAACAAAAAGAAAG | 26054 |
rs151155671 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | SENP6 | GRCh38.p7 | 6:75625855 | GCCTGGGTGACAGAG[A/C]GAGACTCAGTCTCCA | 26054 |
rs151161750 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75685404 | TCTGCTTTGATCTTA[A/G]TTATTTCTTGCCTTC | 26054 |
rs151224925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668671 | TGGCAGTAATTCTAA[A/G]TGTGTACCACAACTG | 26054 |
rs151267647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75712585 | TTTTTTTTAACATTT[A/G]AGGAGTTTGGGCTCT | 26054 |
rs151319773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75646878 | ACTATCTCCACCCAT[A/G]TTACTTTTTCTTTTG | 26054 |
rs151330135 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603096 | CTGGCCTTGTCTGAT[A/G]TTCTTTCGGAATGTG | 26054 |
rs180678931 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SENP6 | GRCh38.p7 | 6:75665914 | CACATGTAATCCCAG[A/G]TGCTGGGGAGGCTGA | 26054 |
rs180686492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696158 | ATTTTTTTTAACAAC[A/T]TATTTATATTGAGGC | 26054 |
rs180692144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681043 | GAGAAAAGAATATCA[A/G]TAGACATTAACACCA | 26054 |
rs180702801 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715970 | GGTGTGACATATTTC[A/C]TGGGAATATTCAAAT | 26054 |
rs180798714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624603 | ATCTCAGTGTAGTTT[C/T]AATTTCCATTTTATT | 26054 |
rs180812400 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75609945 | GGCGCATACCACCAT[A/G]CCTGACTAATTTTTG | 26054 |
rs180846702 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75649263 | GAGGTTGCAGTGAGC[C/T]GAGATCGCATCACTA | 26054 |
rs180850767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75617466 | TAGTAGAGACAGGGT[C/T]TCTCCACGTTGGTCA | 26054 |
rs180851544 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75602874 | GACATTTAAAAAATT[A/T]TGGGGTGGTGGCCTA | 26054 |
rs180868719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75633300 | TTACTCTCTGGAGAA[A/G]GCTATCCTAAGATCC | 26054 |
rs180946651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606632 | GGTGGATTGTTTATA[C/T]AAGTTGAACATCCCA | 26054 |
rs180951199 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SENP6 | GRCh38.p7 | 6:75636062 | AAAAAAAAACAACCC[A/G]TTAATAGTCTGGAAA | 26054 |
rs180958685 | snp | A/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620858 | TTGAGGTTAACCTAA[A/T]AAAGCCTGGGTTCTA | 26054 |
rs181013071 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75678309 | TTTACCAGCATTATT[G/T]AATTTCATGTAGATA | 26054 |
rs181017541 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75684908 | CAGGATGATTCTGGC[C/G]TCATAAAATGAGTTA | 26054 |
rs181037212 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75670067 | GCCTCCTGAGTAGCC[G/T]CCTGAGTAGCCGGGA | 26054 |
rs181046705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692812 | AAAAAAATCTGTAAT[C/G]CTAGCACTTGGGACG | 26054 |
rs181053476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75701497 | ATAAAACATTACTTA[C/T]ATACATATTTTTGAT | 26054 |
rs181057585 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | SENP6 | GRCh38.p7 | 6:75711496 | GACAGTTTTTTTTTT[A/T]AATAAATACTTAAGC | 26054 |
rs181213914 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75717137 | GATATCTTAATTAGC[C/T]CATATGAAAAACAAG | 26054 |
rs181242507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658334 | TAAATATTATATAAT[A/G]TTGATTTTTATGTCT | 26054 |
rs181244343 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75633456 | CTTAAATCCATGCCA[A/G]TGCTATCCACCATCA | 26054 |
rs181250010 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SENP6 | GRCh38.p7 | 6:75673028 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 26054 |
rs181266438 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75687184 | TTCTTCCTCTTGATC[G/T]AATTGGCTATTGAAG | 26054 |
rs181321774 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75611023 | AATTCTCCTAGGCTT[C/G]GAGAATTTAAACTGT | 26054 |
rs181329586 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75639452 | TTTTTTTCTTCATTT[A/G]CTAGGATTAAATTGG | 26054 |
rs181343502 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | SENP6 | GRCh38.p7 | 6:75666126 | ATATATGATATATAT[A/G]AAACGTATATATGAT | 26054 |
rs181373600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636128 | CCTATAACATTTTGC[A/G]TGTGTATTATTGCTC | 26054 |
rs181379752 | snp | A/G | 0.00526774 | 0.0510502 | intron-variant | SENP6 | GRCh38.p7 | 6:75670752 | CTCTTTACTATACCA[A/G]TTATAACATTAAAAA | 26054 |
rs181384371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75702287 | CTGTGGCACAATCTC[A/G]GCTCACTGCAACCTC | 26054 |
rs181393702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685182 | TTTTCTAGATTATTT[A/G]CATAGAGGTGTTTAT | 26054 |
rs181399956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75625093 | ACTAGTTGCTAATAT[A/G]TATACGTGTGTGTGT | 26054 |
rs181473855 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677189 | ATGGCAGACTTGTTG[C/T]CTGTACAAGAACCTA | 26054 |
rs181479487 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75681783 | CCTGTAATCCTAGCA[A/G]TTTTGGAGGCCAAGG | 26054 |
rs181490203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75709869 | AAAGCAATTTCTTCA[A/G]CTAGTAATTTATCAT | 26054 |
rs181555530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75613411 | GTGTAAGATATTTAC[C/T]GTCTGGCCTTTTACA | 26054 |
rs181607968 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SENP6 | GRCh38.p7 | 6:75691837 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 26054 |
rs181695474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632644 | AACAAATGGATTCAT[C/T]TATTCACAGTAGTTC | 26054 |
rs181695629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75648628 | TAATGAACAGTCTTT[A/G]TAGATGTGAATTATT | 26054 |
rs181702939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680354 | CAATAAGCAGTTGAG[C/T]AAATGGCGCTAGAGT | 26054 |
rs181706292 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75665057 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACGAGG | 26054 |
rs181706733 | snp | A/G | 1.78258e-05 | 0.00298539 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621664 | ATGTTTTATAAGAAT[A/G]AAACTTCTCATTAGA | 26054 |
rs181719244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75695447 | GTTTTTAATACAAAG[C/T]GAACTGTGGCCGGGC | 26054 |
rs181722673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715170 | GCAGAATTTGGTCCA[C/T]TGGCAAACCCTGATC | 26054 |
rs181831097 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602132 | GAAGGGAGGCGTGTT[G/T]GTGTGCTCGCTTTCA | 26054 |
rs181833240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616520 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACAAGGT | 26054 |
rs181841875 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75625617 | CTTATGCCAGTAATC[C/G/T]CAACACTTTGGGAGG | 26054 |
rs181865635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628588 | CTTTCTTAAAAATTG[A/G]CACATAACAATTGTA | 26054 |
rs181865894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75658941 | CATGCCACTGAACTC[C/T]GGCCTAGGTGACAGA | 26054 |
rs181870749 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75687711 | TTGCTGGAGTTCCAC[G/T]CCAGACCAGCAGAGG | 26054 |
rs181879144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75606961 | TAAAATAGGGGAGCA[C/T]GGCATGTTTGGGGAA | 26054 |
rs181879166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661076 | TGGGTATTATTGTTT[C/G]TCGGCCTTCTCAGTG | 26054 |
rs181949033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75613670 | TAGCTTTTTTTTTTT[C/T]CTTTAACTCTTTGAA | 26054 |
rs181969526 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75661880 | AATATGGTGAAATCC[C/T]GTCTCTACTAAAAAA | 26054 |
rs181973828 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75629060 | TAAATGCCAAAAATG[A/G]CATAGTAATCAAACA | 26054 |
rs181976296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644813 | GGCTAGAATTTAGTT[A/C]GTAATAGTGTACCAG | 26054 |
rs181979487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75677563 | TCCAACATATATATG[C/T]ACACACTGCTACATT | 26054 |
rs181995473 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75692006 | GGATTACAGGCATGT[A/G]CTACCACACCCGGCT | 26054 |
rs182078437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75611641 | ATGCAGTCATTTCTC[A/G]GTTTAATTTCTGGCT | 26054 |
rs182092360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640853 | ATGTAATAATTGTAC[A/G]TATTTATAGGATACA | 26054 |
rs182102379 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718061 | TTTAGTCAATTAAAT[A/G]TAGGAGGTTTTATTT | 26054 |
rs182106143 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626012 | GTTTTTGATGACACT[A/G]GCAGGTATATGTATA | 26054 |
rs182107571 | snp | A/G | 0.000532597 | 0.01631 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659352 | GACACTGTAGTACCT[A/G]TCAGCCTACTCCTCC | 26054 |
rs182114183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640506 | TTTGTATATTGACAG[A/G]AATCGAAAAACAATT | 26054 |
rs182120690 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75675167 | CCTGCACATGTACCC[C/G]TGAACCTAAAATAAA | 26054 |
rs182122442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673873 | TAAGACTACAAAAAT[C/T]AGTGGGGTGTGGTGG | 26054 |
rs182129940 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75688397 | CACCCTCCATGGGCT[A/G]CATCCCCTGTCCAAC | 26054 |
rs182136618 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75606010 | TACATTGAGTGTCAG[A/G]ATAAGAGGAATCAAA | 26054 |
rs182165815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75706317 | AAAACATTAGACTGT[A/C]TGCTTTAAATGGCTG | 26054 |
rs182169352 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75635808 | GTAATTAGGGGAGAG[A/T]AAAAGAGTAGACACA | 26054 |
rs182175917 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SENP6 | GRCh38.p7 | 6:75669148 | TGAGGTCAGGAGTTC[A/G]AGACCAGTCTGGCCA | 26054 |
rs182282743 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75612364 | ATATTTCTAAGTTAC[A/G]TTTTTCTCATATTCG | 26054 |
rs182353681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618692 | ACCTGTACATCTGTG[C/T]ATGTATTAAATAAAT | 26054 |
rs182373416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75651253 | AGAGAACAGACATAT[A/G]TTGTCCCTGAATGTA | 26054 |
rs182401022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707708 | TGTTCTTTTTTGAGA[C/T]AGTCTCACTTTCATA | 26054 |
rs182413789 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75607918 | ACTAGAGCACAGCTT[C/G]TCCCAAACGATTGGC | 26054 |
rs182428862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653764 | TGGCCTTGTGCCCCT[A/G]TAAAATGACAGTGTC | 26054 |
rs182432313 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636729 | GAAACTGCATGCAGT[A/G]GGAATCACGTCTTCA | 26054 |
rs182433757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75682412 | ATTATATTCTTTTTT[C/T]TTTTTAATTATACTT | 26054 |
rs182434480 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620049 | AGTGAGCCATGATGG[C/T]ACCACTGCACTCCAG | 26054 |
rs182451653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622679 | ACACACAAAGTTCTA[C/G]CAAAACTATAAATAT | 26054 |
rs182460739 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75684729 | ATGTTGAACCAGCCT[G/T]GCATCCCAGGGATGA | 26054 |
rs182463310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75656290 | TCTTCATGTTCCTAC[C/T]GCAGGGTCTTTGGTA | 26054 |
rs182471862 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671615 | TAGTCCCAGCTGCTC[A/G]GGAGGCTGAGGCAGG | 26054 |
rs182481397 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75710750 | GTTGCCAGAAGCTTT[C/T]TCAAAGAACAACAAT | 26054 |
rs182583705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75603120 | GAATGTGTTTTTATA[A/G]AAATATTCTGTAAAA | 26054 |
rs182589608 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617559 | CTGGGATTACAGGCA[A/G]GAGCCACTGTGCCCG | 26054 |
rs182591986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75675272 | AGTTAGTGGGTTTAG[A/G]TAAGCAATGTTTAGG | 26054 |
rs182605061 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75689234 | GCAAGACACTATATC[C/T]AAGAAAAAAATAAAA | 26054 |
rs182611381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707919 | TCCTTCTGAACTCAG[G/T]TGATCCTCCTGCCTC | 26054 |
rs182632505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75604016 | GCTATGTGTGTTGTT[C/T]TTGTTTTGAAATTGG | 26054 |
rs182649202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634055 | TGTCTCCTTTAGGAA[A/G]TACTAATCAGGATTG | 26054 |
rs182649650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667649 | AGAAAGTTACTATGA[G/T]CTTTTGGGAAAGAAA | 26054 |
rs182682028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699188 | GATTATACACGATTT[A/G]GGAATAGAGGCGCAT | 26054 |
rs182715272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75630499 | GTCTCTCTGGGCCTG[A/G]TAAATTTTGCATATC | 26054 |
rs182717613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630013 | GTTCTTTGTATCACA[A/G]ATTCCTGGAACATGA | 26054 |
rs182724891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75662335 | AGATTGGATGTCGCT[A/G]TGTTGCCCAGGCTGG | 26054 |
rs182728478 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614661 | TTCACCCACTGGTTC[A/C]GCATCCATTGATGAT | 26054 |
rs182748062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685667 | ATTTACCCGTCATTC[A/G]GGAGCAAGTTGTTCA | 26054 |
rs182872555 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599631 | GATAATCAGGAAGGA[C/G]ATTTGATTTAAAAAA | 26054 |
rs182888778 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656441 | AAAAATCACTTCTGT[C/G/T]ATCAGTTAGCTAGTA | 26054 |
rs182898943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671837 | GTTCATGGTTCTAGG[A/G]TACAATATGATCAAA | 26054 |
rs182918771 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75704250 | TCTTTGAGTTCTCTC[A/T]GTTTTGGTTGATTAC | 26054 |
rs182923193 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75686200 | AAAGTCTGTTTTATC[C/T]GAGACTAGGATTGCA | 26054 |
rs182990595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75614416 | GATTACAGGTGTGCA[C/T]CACCACGCCAGGCAA | 26054 |
rs182994179 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75645802 | TTTTAAAAAACAGAA[A/C]TTTAATTTGCCCTGC | 26054 |
rs183001807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633792 | GACACCAAAAACTTA[A/G]AAGCTAATAGGCCCA | 26054 |
rs183013189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626561 | TAGAGATTTTTTTCC[C/G]CCAGTCTTTTGCTAT | 26054 |
rs183017439 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650249 | ACATGATGTTGAATA[C/T]GTCTTAGGATTGGTA | 26054 |
rs183030915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681949 | GAAATAATGACTTCA[G/T]GGGCTGGGCTCAATA | 26054 |
rs183033465 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75612626 | TGAGCTGTCTGATAA[A/C/T]CCCATGAGACGTAGA | 26054 |
rs183035703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703444 | TGTATACATAGAGTC[A/G]TGTAATCACTACTGC | 26054 |
rs183038302 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666413 | ACTGTTCTTCTTGTA[A/G]CTTGCTGATATTGCT | 26054 |
rs183039587 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | SENP6 | GRCh38.p7 | 6:75698785 | AGAGGCTGAGGTGGG[C/T]GGATTACTTGAGGTC | 26054 |
rs183054603 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717637 | GAATCTTTCGTGTAT[A/G]TGCACATTCACTTGA | 26054 |
rs183062945 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75612531 | AGACAGAGTGTCACT[A/G]TGCTGCTCAGGCTGC | 26054 |
rs183102850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75641404 | TATGCTTTAATAGAC[C/T]GGGGGAGGGAGAGGG | 26054 |
rs183161316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646687 | TAAAAATACAAAAAA[G/T]TAGCTGGGCGTGGTG | 26054 |
rs183163244 | snp | C/T | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75678997 | TATGTCTTTGTTTTC[C/T]AGAGTCAGGCTTTTT | 26054 |
rs183171591 | snp | C/T | 0.00165584 | 0.0287259 | intron-variant | SENP6 | GRCh38.p7 | 6:75663216 | GTGGTGTTCTTTTTT[C/T]TAAGGATTTGCAAAG | 26054 |
rs183181573 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75659842 | TTTTGTACTATTTGA[G/T]TTGAAGTTGCAAGCA | 26054 |
rs183182586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75693907 | CCTTTGTGATATAAA[C/T]GACTATTGTTACTTG | 26054 |
rs183185641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75714199 | AATTCTACAGATTCT[A/G]CTTCTCAAATCTCTA | 26054 |
rs183240318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646450 | ATGTATAAAGTATTA[A/C]TATGTTATATAAGTT | 26054 |
rs183289253 | snp | G/T | 4.97459e-05 | 0.00498703 | intron-variant | SENP6 | GRCh38.p7 | 6:75678699 | AGTAGAAAAGTGAGA[G/T]AATTCCTTTATATTT | 26054 |
rs183297074 | snp | A/G | 0.000481244 | 0.0155045 | intron-variant | SENP6 | GRCh38.p7 | 6:75713473 | TTATGCATTTGTAAT[A/G]TTATGAAGTATTCGA | 26054 |
rs183355423 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631227 | TTATCTGATATTCTT[C/G/T]GGTGCTAAACTTCCT | 26054 |
rs183365887 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626447 | ATGTAGATCACTCTA[A/C]AGCAAAGTATTTACA | 26054 |
rs183368710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75615219 | TGAGTCTTGCTGTGT[C/T]GCGCAGGCTGAAGTG | 26054 |
rs183481396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627900 | GGCTGGTCTCGAACT[C/G]TGACCTCGTGATCTG | 26054 |
rs183484406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606163 | TTTTTGCTCTGAAGT[A/G]TGTTTTATATCTTTA | 26054 |
rs183490623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662668 | CAAGATAAATGTTTC[C/T]TAGCTGATGGAAGGC | 26054 |
rs183492418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612981 | CAGCCGGGCATCGTG[G/T]CATATGCCTGTAATC | 26054 |
rs183495815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660904 | CCAAAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAC | 26054 |
rs183506014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643177 | GAAACAAAATGAAAT[A/C]ATAAACATAAATAGA | 26054 |
rs183510314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676336 | TTAACTAACACTGTA[A/G]TCTGAGTAAAATAAA | 26054 |
rs183513211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693569 | GCAATTAATATAAAC[C/T]GTGTCTTGATCTGAC | 26054 |
rs183522032 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75708580 | GGGCAAAAGAGTGAG[A/C]GAAATCCTGTCTCTT | 26054 |
rs183522315 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690765 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAAGCTC | 26054 |
rs183580167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75603805 | TCTTCTTACTTGAGT[A/G]TAGTAAAGTGAAAAA | 26054 |
rs183623993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660775 | TATCTGGGACTACAG[A/G]CATCTGCCACCATAC | 26054 |
rs183624503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75694290 | ACCAATGTAAGATCA[C/T]TTTACAGAGTCATTG | 26054 |
rs183627304 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75658179 | CAAGGAGTAGTCATC[A/G]ATTATTTAAATTTCT | 26054 |
rs183630011 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SENP6 | GRCh38.p7 | 6:75689733 | GTACGGTAACATACT[A/G]TACAGGTGTATAGTG | 26054 |
rs183638786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75672927 | CCGCCTCCTGGGTTC[A/G]TGCCATTCTCCTGCC | 26054 |
rs183644444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687071 | TTCACATAGTCCCAT[A/G]TTTCTTGGAGGCTTT | 26054 |
rs183692768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708430 | TTTGAGAGGAAAATA[A/G]ATAAATAAAAATCAG | 26054 |
rs183775787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75624605 | CTCAGTGTAGTTTTA[A/G]TTTCCATTTTATTTT | 26054 |
rs183792140 | snp | C/T | 0.00173929 | 0.0294384 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702872 | TAGCTGTAATTGATT[C/T]CAATCCTGGGCAGGA | 26054 |
rs183793273 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75638732 | CCTCTGTTTTTCTAC[C/T]TATTTCCTTTCCTCT | 26054 |
rs183794980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75618131 | TTTATGTCTGTGTTT[C/T]TGACGTAAGTTACCA | 26054 |
rs183801124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75610401 | TTACTTAGAATGATG[C/T]AACAATGGATAATCC | 26054 |
rs183823522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642099 | TTTCTACAATTGTTT[A/G]AAATGGTAAATATAT | 26054 |
rs183854367 | snp | A/G | 0.000318866 | 0.0126227 | intron-variant | SENP6 | GRCh38.p7 | 6:75675515 | AGCTTTCTTTACACC[A/G]AAGCACTTTACAGGA | 26054 |
rs183934912 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | SENP6 | GRCh38.p7 | 6:75607302 | GAGACCCTGCCACCC[A/C]AAAAAAAAAAGGTCA | 26054 |
rs183943794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691660 | TTTGGAGTGCAGTGG[C/T]GCGATCTCAGCTCAC | 26054 |
rs183954876 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75709403 | TGTGATATTACACAC[A/T]AAGGCAGATTTTGTG | 26054 |
rs183955357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75685453 | TTTGCTCTTGCTTCT[C/T]TAGTTTTTTAAATTG | 26054 |
rs183964839 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75636296 | AAGAAAACTGTATAA[A/T]CAAGTCAGCAGGACA | 26054 |
rs183969758 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75671385 | TTTGTTTCCATCTCT[G/T]CTTTCAAACTGATAT | 26054 |
rs184075807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635238 | TGTTGGAGAAAATGT[A/T]ATTTTGTAGTTGTAG | 26054 |
rs184083552 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75668055 | AAATATGGGAACATA[C/T]ATACTTGGTTATTAA | 26054 |
rs184088027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75652045 | AGCCGGGTATAGTGG[C/T]GTGTGCCTGTAGTCC | 26054 |
rs184106375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622211 | TAAAAATTTTAAATG[A/G]TAGTTTTAATAGAAC | 26054 |
rs184148873 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600079 | AAAAACAAACAAACA[A/G]AAATCTTCTACACAC | 26054 |
rs184151837 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75655660 | TTTAACATTGCATTG[C/T]ATGAGTATAACAAGT | 26054 |
rs184174347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620162 | TATGGTTTTGATTTG[C/T]ATTTTTTAATGGTTA | 26054 |
rs184198614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654059 | TGAGACCCTGTCTCT[A/G]TAAAATAAAAAAAAA | 26054 |
rs184209602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684828 | AGGATTTTCACATCA[A/G]TGTTCATCAGGGATA | 26054 |
rs184247664 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604732 | TAATACTAATGTTTT[C/T]TGCTTATTTCCCATG | 26054 |
rs184257181 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619516 | GTTTATTAATCTGTT[A/G]ATAGAAATTTGGGTT | 26054 |
rs184321257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635962 | CAACCAAAATTATTA[C/T]ATTATTTTTGCTTTT | 26054 |
rs184326541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669334 | GCACTCCAGCCTGTG[C/T]GACAGAGCGAGACTC | 26054 |
rs184370608 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601574 | AGAAATGACATTTTC[A/C]CATTTCTTAGGCATC | 26054 |
rs184373736 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75616345 | GGTTGCCCCCAAACT[C/T]TTAAAAATCTCTTTT | 26054 |
rs184406520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632246 | GCTACTAATAGAGGA[A/G]TGGTTAAATTAAAAT | 26054 |
rs184484620 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75679882 | ATGCTGGAATCTGCT[C/G]AATTGATTTTATAGC | 26054 |
rs184504230 | snp | G/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75704729 | AGACTATCACATGGG[G/T]AGAAACCTTGGACAA | 26054 |
rs184523801 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601069 | TGTCGGTTTTCTGCA[A/T]CATTTTAATTGCTGT | 26054 |
rs184537061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631825 | TTTATTTTGTATAAA[G/T]GTATTTCATAGATTG | 26054 |
rs184542736 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668534 | GAAAATGAAATTAAA[A/G]TACCTTTTGTGAACT | 26054 |
rs184545186 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663897 | CAATATCCTTACCAC[A/T]TTTGTTCCTAACTCT | 26054 |
rs184550755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75700781 | ACAGGTGTGAGCCAC[C/T]GTGCCCGGCATCATC | 26054 |
rs184555163 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75683926 | TAGTTTTTTCTAATT[C/T]TGTGAAGAAAGTCAC | 26054 |
rs184624751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75608916 | TCTATTTGAATTTTA[A/G]TTTGCATTGTTTTTC | 26054 |
rs184637450 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75615997 | TTCCTATTCATCCAC[C/T]GAATGTTTATCTTTT | 26054 |
rs184646634 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613286 | AATTCAAATGTCACT[G/T]CCCTTAAATAAAGTT | 26054 |
rs184662122 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75647163 | TTCCCCTTCTGTGAT[A/G]CGCTTTTATACAATT | 26054 |
rs184689081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75676857 | ATTGGCATGTAACAC[A/G]TACTGGTCTTTCCAG | 26054 |
rs184696466 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700251 | GCTGTTAAAGTTAAC[A/G]TAGCTGTTATTAAAA | 26054 |
rs184716858 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75653092 | CTGGTGTGCAATGGC[G/T]CAATCTCAGCTCACC | 26054 |
rs184803958 | snp | C/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75628420 | TAAAAAGTATTATTA[C/T]AGATATTTATAATTA | 26054 |
rs184814891 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75682643 | TGCCACCTATGAGTG[A/C]GAACATGCTGTGTTT | 26054 |
rs184837931 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75660963 | TCTCAGCCCTAGAGT[C/T]ATTCATTTCTCTGAG | 26054 |
rs184862062 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649089 | ATGCAGGCAATCACC[A/T]GAGGTCAGGAATTCG | 26054 |
rs184877556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665568 | ATATAGAGATAGATT[G/T]GCTACGATTCAGTAA | 26054 |
rs184879244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75695692 | CAGTGAGTTGAGATC[A/G]CTCCACTGCACTCCA | 26054 |
rs184895201 | snp | A/C | 1.65836e-05 | 0.0028795 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715469 | AAAAGAGAAGAAATC[A/C]GAAACATAATTCTGA | 26054 |
rs185049817 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75680193 | GGAGGAGAGGAAAGG[A/G]TACCAGGTAGCTCCT | 26054 |
rs185066393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75715038 | AGGCTTTGCAACTGT[A/G]CAGTCTCTATTGCCT | 26054 |
rs185094440 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75608195 | GTTTAGTGGGTCATA[C/T]CTGTTATCCTGAGAT | 26054 |
rs185129914 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75637133 | GTCCTGCCTCAGCAC[C/T]GTAAAGTGCTGGAAT | 26054 |
rs185144739 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75664767 | AAATTAAGCATTTAT[A/G]TTTGAAATACTAATA | 26054 |
rs185178951 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75694891 | TATTTTTATTTTCTT[A/G]AGACCAAGTCTTGGT | 26054 |
rs185209497 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75629731 | CTTACAGGTAATGTA[A/T]AGGTCTGTCAAGCTA | 26054 |
rs185209687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75645405 | CAGATCACTTGAGGC[C/T]AGGAGTTCGAGGCCA | 26054 |
rs185214749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75691845 | GTGATCCGCCCGCCT[C/T]GGCCTCCCATTGTTT | 26054 |
rs185326082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605213 | CTTTCTTTACTTTCC[A/G]GTCGAGTCCTTGAAA | 26054 |
rs185342422 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75635559 | CTGTTTACATAGATG[G/T]GCTATCAGATCTTTT | 26054 |
rs185352431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75659761 | ACATTTGCTTTATTG[G/T]CCTCACTCTCTATGC | 26054 |
rs185363165 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640915 | TATGATCAGATCAGG[G/T]TAATTAGTATATCCA | 26054 |
rs185365586 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75675196 | AAAGTTAAAAAAAGA[A/T]AAAAAAAAGAGGAAA | 26054 |
rs185381938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707747 | GAGTACAGCAATACA[A/G]TCACAGTTCACCGCA | 26054 |
rs185383681 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75689014 | GAGGTTGCGGGGAGC[C/T]GAGATCATGCCATTG | 26054 |
rs185394019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621092 | GCCAAAACCGAAAAC[A/G]TTGTTTGTTTTTCTT | 26054 |
rs185409304 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75636100 | GCGATTTGTTTTACT[C/G]TAGGTCTCAACACCT | 26054 |
rs185411951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606876 | ATGAGAATTGGATCT[A/G]ATCAGGGTGGTTTGA | 26054 |
rs185430611 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SENP6 | GRCh38.p7 | 6:75654708 | TATTCTATCACTGTC[A/G]TCTGGGTACTTATTT | 26054 |
rs185440801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684965 | TTGAAATAGTTTCAG[A/G]AGGAATGATACCAGC | 26054 |
rs185445149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75670166 | TGGGCAGGCTAGTCT[C/T]GAACTCCTGACCTCA | 26054 |
rs185474484 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75637678 | ATAAGAACCTTATAA[C/G]AAATTCTTGTAATTC | 26054 |
rs185477887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619757 | GAGTTCCAGTTTCTC[C/T]CACATCCTAGCCAAT | 26054 |
rs185485935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672649 | TTCTTCTTGAACATA[A/G]CTTCCTTATATTTTG | 26054 |
rs185507157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75711974 | CATCGCGCCCGGCCA[C/T]AAGTTTTGATAGTGA | 26054 |
rs185517950 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75704504 | CTCCTGCCATAGGGC[A/G]GTTTTTCTCCTATCT | 26054 |
rs185574103 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SENP6 | GRCh38.p7 | 6:75666255 | TATAAAATATATATA[C/T]GATATATATAAAATA | 26054 |
rs185579371 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649959 | AACTAAGAAATTGGT[A/G]TAAGATTCTTAACTA | 26054 |
rs185583406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687242 | GCAATGGTTATCAGC[C/T]CCATCAGGTCATTTA | 26054 |
rs185592196 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75705570 | AATAAATTAATTAAT[A/T]AATTAAAAACTAGTT | 26054 |
rs185610196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75624174 | ATGTTACACAATTGG[C/T]AATATACTGTGCATG | 26054 |
rs185620906 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657924 | AAAGTTTAAGTGGAA[A/G]TAAGATTGAAACAGG | 26054 |
rs185626873 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75686729 | GAATATTGGCCCCCA[A/C]TCTCTTCTGGCTTGT | 26054 |
rs185750588 | snp | A/G | 0.000337484 | 0.0129857 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633599 | AATCGTCGATCTGAA[A/G]TTGTTGCTAATAGCT | 26054 |
rs185757134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75673345 | TTTTTTTTTTGAGAC[C/T]GAGTCTCACTGTTGT | 26054 |
rs185757315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75603297 | TATGTTTTTGTTGGG[A/G]AAGGTGGTAATGGGG | 26054 |
rs185765498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617609 | ATATAACTTTTACTC[C/T]GCCTCCACTAATGTT | 26054 |
rs185794475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75701209 | AGGACAAATATTATT[A/G]TGCTTGACCAATAAG | 26054 |
rs185908104 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SENP6 | GRCh38.p7 | 6:75670928 | ATATGTTATTGTTTA[G/T]TATCATGCCAGCTTC | 26054 |
rs185921391 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75702461 | GACCTCAGGTGATCC[A/C]CCCACCTCAGCCTCC | 26054 |
rs185923350 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685185 | TCTAGATTATTTGCA[G/T]AGAGGTGTTTATTCT | 26054 |
rs185944321 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75614387 | TCTTCTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA | 26054 |
rs185958074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633317 | CTATCCTAAGATCCT[C/G]TACCCTAATTGTCTC | 26054 |
rs185985240 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SENP6 | GRCh38.p7 | 6:75665930 | TGCTGGGGAGGCTGA[A/G]GCAGGAGAATCACTT | 26054 |
rs186093658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75644459 | ATTAGTAAATAGCTG[A/G]TAAATTTCTTTCTTT | 26054 |
rs186098634 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SENP6 | GRCh38.p7 | 6:75649598 | TCTCAGCTCATTGCA[A/G]CCTCCGCCTCCCGGG | 26054 |
rs186102697 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SENP6 | GRCh38.p7 | 6:75617514 | CGACCTCAGGTGATC[C/T]GCCCGCCTCCGCCTC | 26054 |
rs186108613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628937 | TGTTGGCCACCAGGC[A/T]GGTCTTGGAACTCCT | 26054 |
rs186133098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681069 | CACCAAGAAGACACA[A/T]ATGTCAGAATTATTT | 26054 |
rs186140130 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75602974 | TGCAACTGGGGACCA[A/C]TCTAAGTAGGGAGGG | 26054 |
rs186145775 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716112 | AGGAACAAAGTAACA[A/G]CCTTTCAATTCATAT | 26054 |
rs186272791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613560 | GTAATAGTAAAAAGG[C/T]GGATATAACCTAAAT | 26054 |
rs186320411 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75646034 | GTTTCATCAATCTCT[A/G]TACATGCATGTATGA | 26054 |
rs186320595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75614489 | GCCAGACTGGTCTCA[A/G]ACTCCTGACCTTGTG | 26054 |
rs186326550 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701568 | AAAGAACAAAACTAT[A/G]TATGCAATTCTTAGA | 26054 |
rs186344268 | snp | C/T | 0.00184338 | 0.0303033 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678608 | AATCTAAAATACAAC[C/T]TAGAAGCAAACAAGA | 26054 |
rs186383766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611662 | ATTTCTGGCTTTAGA[A/G]GTTTGTGTGCTTCAG | 26054 |
rs186396977 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632676 | CTTGATGCTGTGCTT[C/G]CATTACCTGGAAAAC | 26054 |
rs186412295 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75625728 | AGAAAAATTAGCCAG[G/T]CATGGTAGTGGGCTC | 26054 |
rs186478953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681817 | GAGGATCACTTGAGG[C/T]CAGGAGTTTGAGACC | 26054 |
rs186499025 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717468 | AAAATATAGATTAAT[A/G]TATGTCAGCTTTCTA | 26054 |
rs186511711 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75630031 | TCCTGGAACATGAAG[A/C]TAATGAATGAGGGCC | 26054 |
rs186515877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75677630 | AAATTGTGGTCCGTG[A/G]TGTACATTTGTATGT | 26054 |
rs186524506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662113 | AATGGGATTAACATC[C/T]TTAGGATATTTAGTA | 26054 |
rs186530232 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75662400 | TCAGCCTCCCAATGT[G/T]TTGGGCTTACAGACC | 26054 |
rs186533093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692098 | CGACCTCAGGTGATC[A/C]GCCTGCCTCGGCCTC | 26054 |
rs186535958 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75710895 | AGTGTTTCCAAAAAC[C/T]CTTTAAATATTTCTG | 26054 |
rs186542103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693249 | TACTAAAAAAAAAAT[A/C]CAGAAATTAGCTGGG | 26054 |
rs186584819 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708760 | ATGCCAGGCATGGTG[A/G]TATGTACCTGTAATC | 26054 |
rs186597243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75625491 | GCCATGGGGAAAATA[C/T]ATTTCCTTATGTCAT | 26054 |
rs186645683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658352 | GATTTTTATGTCTAC[A/C]TAATCTTATTTTTAA | 26054 |
rs186669206 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607529 | GTACTGCACTTGTTC[A/G]TATCTAGTTTTCTTT | 26054 |
rs186676376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622418 | CAAAAGATTAGCTGG[A/T]TGTGGTGGCATACAC | 26054 |
rs186705770 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SENP6 | GRCh38.p7 | 6:75698573 | CTCTTGGCCTCAAGC[A/C]ATCCCCCAACCTCAG | 26054 |
rs186772072 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75661232 | TTGTAACTCCCTTCT[C/T]CAGAGGTAAGTAACT | 26054 |
rs186774836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607107 | AATCCCAGCATTTTG[A/G]GAGGCCAAGTTGAGA | 26054 |
rs186792233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636170 | AGATTAGATTCAGTT[A/C]ATATGAACTAGTTTA | 26054 |
rs186801277 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75612388 | ATATTCGTAATTGTT[C/G]TGGTGCGCTTATGGC | 26054 |
rs186832105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604037 | TTGAAATTGGAAACA[A/G]AAGATGGCTTACTCG | 26054 |
rs186846663 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75611059 | AACCTTGTTGTTTCA[C/T]ATATTCAAAAATCTA | 26054 |
rs186852644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640337 | ATTGGATTCGGTACT[A/C]TCATCAGTTTCAGGC | 26054 |
rs186973716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621802 | ATAAATAATTTTACT[A/G]TTATTTTCTCCATCT | 26054 |
rs186991637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75671800 | AATGTAATGAATAAT[A/G]ACTGTTTCTTTTCTG | 26054 |
rs186992501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655315 | TTTCTTTTGAAATAA[A/G]ATTTACTACAATGAA | 26054 |
rs186994487 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75703875 | CAATTTTGAAATTGC[A/G]GTACAAAGTTTATAT | 26054 |
rs186998961 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75685670 | TACCCGTCATTCAGG[A/C]GCAAGTTGTTCAGTT | 26054 |
rs187002814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75677329 | ATATGTTTTATTTTA[A/C]TACTGTTCATTTCAG | 26054 |
rs187122676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75608028 | TTTGGAAACTACATC[A/G]TGGTGTCATTCCTTA | 26054 |
rs187133485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636747 | AATCACGTCTTCAAA[A/G]GCACAAAGAAAGGCT | 26054 |
rs187134138 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75616819 | AATATTACGACGTCT[C/T]TTTTGACTTTTGAAA | 26054 |
rs187145099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SENP6 | GRCh38.p7 | 6:75622795 | CGTTCATCATTACCA[C/G]TTTATGTGCCTTCAC | 26054 |
rs187145336 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656291 | CTTCATGTTCCTACC[A/G/T]CAGGGTCTTTGGTAA | 26054 |
rs187147134 | snp | C/T | 0.000342386 | 0.0130796 | intron-variant | SENP6 | GRCh38.p7 | 6:75640650 | AACAATGAGGTCTTG[C/T]CTCTTATATTTTTTT | 26054 |
rs187168677 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673916 | ACCCCAGCTACTAGG[A/G]AGGCTGAGGCAGAAG | 26054 |
rs187171895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75706330 | GTATGCTTTAAATGG[C/G]TGTATATGGTATGTG | 26054 |
rs187274485 | snp | A/G | 0.000203625 | 0.0100882 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602477 | CCCGGCGAGCACGGC[A/G]GCGGTGTGGGCCATG | 26054 |
rs187292221 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75635422 | ATTATAAACAGTTCC[A/T]TATAACTAGTAACAT | 26054 |
rs187302716 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689323 | AAAAAGCATATGAAA[G/T]ATGCTCAACATCAGT | 26054 |
rs187304031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619663 | TCGTAGGGTAATTCT[A/G]TGTTTAACTTTTTGA | 26054 |
rs187307969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75652134 | GTGAGCCACAATCGC[A/G]CCACTGTCCTCCAAC | 26054 |
rs187313045 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75708101 | GTCTTGCTCTATCAC[C/G/T]CAGGTCGGAGTACAG | 26054 |
rs187315439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75683178 | GGTGAGCATTTTTTC[A/C]TGTGTCTGTTCGCTG | 26054 |
rs187319766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75668163 | CTTACTTATTTAAAG[A/G]GGGGATCTTGCTCTG | 26054 |
rs187321298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75700694 | ACGGGGTTTTGCCAC[A/G]TTGCCCAGGCCAGTC | 26054 |
rs187332523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685507 | ATCTTTCCTGCTTTC[C/T]CTTGTGGGCATTTAG | 26054 |
rs187363181 | snp | A/G | 0.000249181 | 0.0111592 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659287 | GAAGAAAACAGAAGA[A/G]TCCGAATCACAAGTG | 26054 |
rs187369033 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SENP6 | GRCh38.p7 | 6:75687770 | TCCTTCCTCTGGAAG[C/T]TTCGTCCCAGAGGGG | 26054 |
rs187370997 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599669 | AAGAGGAGAGAGAAG[G/T]AGCGAGAAAGAGAGA | 26054 |
rs187400238 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75630862 | TTAAAAAAAAAAATC[C/T]GTAACCTATATTTTA | 26054 |
rs187418054 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75614713 | ATTAATATAATGGTT[C/T]CCAAGTGATTTTTCT | 26054 |
rs187422685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663106 | AATGCCAAAATCTTT[C/T]ATTTCTTTTGTTCTT | 26054 |
rs187432197 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646513 | AAGCACACATGGCAC[A/G/T]TGATGCTATTTTCTG | 26054 |
rs187442736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75704395 | GAGGTACTATGCCTG[C/G]ATGTGCACGTAGGCC | 26054 |
rs187541485 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75698926 | TGAGGCAGGAGGATC[A/G]CCTGAACCCGGGAGG | 26054 |
rs187545594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682177 | AAAGGAATGATCCAC[C/T]AAGAAAACATACTAA | 26054 |
rs187548713 | snp | A/C | 0.00835141 | 0.0640778 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717805 | ACTAATTAGATAGAT[A/C]TGTTGTATTGGTTTT | 26054 |
rs187590179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671451 | ACTTATTGCCGGGCG[C/T]GGTGTCTCACGCCTG | 26054 |
rs187599802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686287 | TTTGAGCCTGTGTGT[C/G]TCTCTGCATGTGAGA | 26054 |
rs187628440 | snp | A/T | 0.00712914 | 0.0592776 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703030 | AGGACTAAAAGTGAG[A/T]ATGGCCTACAGAATG | 26054 |
rs187652360 | snp | C/T | 0.00183637 | 0.0302459 | intron-variant | SENP6 | GRCh38.p7 | 6:75634671 | TGTATATAATTTTTC[C/T]GTGTTCAAGTTATTT | 26054 |
rs187653836 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75667686 | AATGACCATTAAAAA[A/T]TTTTTAATGTGTACT | 26054 |
rs187677026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75699978 | TACAGTGGTGCAATC[A/G]TAGCTCACTGAAGCT | 26054 |
rs187739573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626580 | GTCTTTTGCTATTAC[A/G]TATAAGACTTCACTA | 26054 |
rs187740494 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650327 | CACTGTAAAATTACC[A/G]TTTTTCCCTTGGTGC | 26054 |
rs187749115 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75642262 | CCTGTAGTTTACATT[C/T]TTATGGGACAAAGAC | 26054 |
rs187750429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612630 | CTGTCTGATAACCCC[A/T]TGAGACGTAGAAATT | 26054 |
rs187753330 | snp | C/G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667258 | CAGAGATATATTTTA[C/G/T]TGTAATACTATGTTT | 26054 |
rs187786512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647916 | ATAGATATATATGTA[A/G]AAAACCATTTTTTTG | 26054 |
rs187815928 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75679911 | GCCTATTGGTGGTTG[A/C]AACTCAGTTTGGTGG | 26054 |
rs187886346 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75647031 | AGCTATGATTTACAT[C/T]ACTAGATCACCAGTG | 26054 |
rs187897072 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679043 | TCTCTGCCACTTACT[A/G]TGTGACATTTGGGGA | 26054 |
rs187899887 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618726 | AGTTCAGGCTGGTAT[A/G]TCTGACTCTAACCTA | 26054 |
rs187903068 | snp | A/G | 0.000714007 | 0.018881 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663328 | GAAGTCACAAAACAC[A/G]GGATTAACAACCAAG | 26054 |
rs187905288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75694170 | CTGAGGCAAGAGAAT[C/T]GCTTGAACCCGGGAG | 26054 |
rs187919384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75714421 | TAGGTTCTGTGAATT[A/G]TGTCATTTAATGTCA | 26054 |
rs187940873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651268 | ATTGTCCCTGAATGT[A/G]CATTTAATTATATTC | 26054 |
rs187952966 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75682550 | CCTAATGCTATCCCT[A/C]CCCCAGCCCTCCATC | 26054 |
rs187963345 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718309 | TTTGGTGGAGCAAAG[C/T]GACTGGAATATAACA | 26054 |
rs188063516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690903 | GGATTTCACCTTGTT[A/G]GCCACGCTGGTCTTG | 26054 |
rs188092347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694509 | AGTGTGTTTCATTGC[C/T]CCATAAAGAAGCCTA | 26054 |
rs188101004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626500 | GTTATATAGTACTTC[A/C]TTGGATGGATATACT | 26054 |
rs188114737 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75660696 | GGAGTTGAGTGGAGC[C/G]ATCTCGGCTCACTGT | 26054 |
rs188212059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75628152 | TGGACCATCTCTTAA[C/T]AGTTAGAAATTTTAT | 26054 |
rs188236788 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75643649 | ATTGCTTGAACCTGG[A/G]AGGCGAAGGTTGCAG | 26054 |
rs188242658 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75676687 | TCACATGGCAATTTT[C/G]TATTTGTGTTTGACA | 26054 |
rs188242853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606529 | ACCATGTTTTTTTCA[A/T]AGAGTGTTCAGTCTA | 26054 |
rs188250055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620546 | GAGAGCTGTGCCCTC[A/G]TGATCTAATCAGCTC | 26054 |
rs188356040 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75624853 | AAAAAATGTTTTTGG[C/T]CAAGTGTAGTGGCTC | 26054 |
rs188377116 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75658192 | TCGATTATTTAAATT[C/T]CTAGCTTTGGTGTCT | 26054 |
rs188378412 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612535 | AGAGTGTCACTATGC[G/T]GCTCAGGCTGCTCTC | 26054 |
rs188382526 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641522 | GTGATCAGTCTTCTA[C/T]CATTATTTGTTCTCT | 26054 |
rs188385507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75638778 | AAAAACAACAGAGGC[C/T]GGACATGGTTGACTT | 26054 |
rs188392670 | snp | A/G | 0.0005922 | 0.0171974 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675454 | GTTTAGATTTTATCA[A/G]GATACAGCTAGACGG | 26054 |
rs188395860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75673018 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 26054 |
rs188403916 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705325 | GCTGAGGCGGGTGGA[C/T]CAGTAGGTCAGGAGT | 26054 |
rs188407945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687167 | TCAATCACTGATACT[C/G]TTTCTTCCTCTTGAT | 26054 |
rs188412385 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75608712 | TCTCAGCTATATAAC[A/C]AGGGTAATAATTGTC | 26054 |
rs188446686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637512 | GATAGAGAAGTATGG[A/G]AAAAAATGCAGAAAT | 26054 |
rs188450778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75672127 | CATACTGCAGACTGT[C/T]TTTCCTGGTTTCTGT | 26054 |
rs188460011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75693859 | CCTATGAGAAAGTTT[A/G]GATCATAAATAAATT | 26054 |
rs188547564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75702184 | TGATTACATAAAACA[A/G]GCAGATTAATTTGAG | 26054 |
rs188602177 | snp | A/G | 0.000136308 | 0.00825443 | intron-variant | SENP6 | GRCh38.p7 | 6:75676089 | TTATAATAGATAATA[A/G]TAGATACTGTATTTA | 26054 |
rs188612369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708485 | AATCCCAGCACTCTG[G/T]GAGGCCAAAGCAGGA | 26054 |
rs188670250 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601095 | GCTGTTGACTTTTCA[C/T]TGACATTTAGCATAG | 26054 |
rs188729571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75623233 | AAAAACTGTCTTTAC[A/G]GTGCTAGCTGTCCTG | 26054 |
rs188730241 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75618169 | CCCATACTCAAGGGA[A/G]GGAAAATTCATTTTT | 26054 |
rs188731803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678756 | TTTTATTACATTTCA[A/G]TTGTGTATATATATA | 26054 |
rs188734828 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75685062 | AGGCTATTAATTATT[A/G]CCTCAATTTCAGAGC | 26054 |
rs188742138 | snp | G/T | 0.00164322 | 0.0286166 | intron-variant | SENP6 | GRCh38.p7 | 6:75713844 | GGTTTCAATTTGTTG[G/T]ATCTGCTATAATAAA | 26054 |
rs188744280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75656540 | TTTTATGTTTCTGCT[A/G]TAATTTTAGACTAGT | 26054 |
rs188874422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690126 | TTGTTGGCCAGGCTG[G/T]TCTTGAGCTCCTGCC | 26054 |
rs188885509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631516 | TGAAGTCTATTGTCT[A/G]TTAGCTACAGTGGTT | 26054 |
rs188886731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75705847 | AAAGAACCTATCAAA[A/G]ATTGTGAATATGGAA | 26054 |
rs188890143 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600355 | AAAGCCAGCATATAT[A/G]CATTTTAAAAGCAAA | 26054 |
rs189017359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633843 | ATTTGTCTATAGGGC[C/G]AAGAGGTAGCATGGT | 26054 |
rs189026278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75603905 | AGTAAGAAAAGCTTC[A/T]GAGTTTTTCTGGGTT | 26054 |
rs189073361 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75669605 | TTGTAATTAAAATTA[C/T]ATACCTATATGAAGT | 26054 |
rs189107097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701220 | TATTGTGCTTGACCA[A/G]TAAGCTCCCTGACAT | 26054 |
rs189124093 | snp | G/T | 0.0718919 | 0.175435 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602033 | CGGCGGCTGCAGAAC[G/T]AGCTAGGGGCCTGGG | 26054 |
rs189158893 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615369 | ATTTTTAGTAGAGAC[A/G]GGGTTTCGCAGCATT | 26054 |
rs189159970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75664924 | CAAGTGAACATCCGC[A/G]ACAAGGAACAACAGA | 26054 |
rs189161180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636313 | AAGTCAGCAGGACAG[A/G]TTCTACTTACATTTG | 26054 |
rs189163292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632415 | ACTGTCCACTTTCTA[A/G]AATTGTCATGAGATT | 26054 |
rs189167252 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75648344 | AAAAAATATATCATC[A/T]TAAAATCAGTTTTCA | 26054 |
rs189245893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75613087 | CCACTGCACTCCAGC[C/T]TGCGTGACAGAGTGA | 26054 |
rs189265443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75636005 | TAGTTTGGAATTACT[A/G]GTGACCTATTTTCCA | 26054 |
rs189276610 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75613606 | GATGTATAAATAAGC[A/G]ATTATATTTATACTG | 26054 |
rs189297800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75669071 | TAAGGGAAAATAGGC[C/T]GGATGCGGTGGCTCA | 26054 |
rs189310674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75628975 | AGTGATCCACCCACC[C/T]TGGCCTCCCAAAGTG | 26054 |
rs189310883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75701068 | ATGAAGAGATAGATA[A/G]TGCTGTTTCTTAGTA | 26054 |
rs189311059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661771 | CAAGATCTGTGGGCC[A/G]GGCACAGTGGCTCAT | 26054 |
rs189312970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684692 | TCTGTTTATACGATG[G/T]ATTATGTTTATTGAT | 26054 |
rs189317020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644682 | TAGAGACGGTGTTTC[G/T]CCATGTTGGCCAGTC | 26054 |
rs189329026 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75677524 | ATCATTTTCTCTGTC[A/G]TCCTTTTTTCTTTAT | 26054 |
rs189366940 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654083 | AAAAAAATTAGCCAG[G/T]TGTGGTTATGAGCAC | 26054 |
rs189371210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75684874 | CTTTTTTTGTTGTGT[A/G]TCTCCCAGGCTTTGG | 26054 |
rs189461668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75638046 | TGTGTGTTTTTAGTA[A/G]AGATGCGGTGTCACT | 26054 |
rs189465449 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75609918 | TCAGCCTCCCTAGTA[G/T]CTGGGATTACAGGCG | 26054 |
rs189468622 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715674 | AATAAAGAACTGAAG[C/T]GCTCACTACTCAGTG | 26054 |
rs189469846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75624208 | TTTCTGATCTTCCTT[C/T]AACTTAATATATTAT | 26054 |
rs189550439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75616167 | ATATTTAACTGGGAT[C/T]TCTCCTTAACCTTTT | 26054 |
rs189632385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75665756 | CTACAGCCAGGTGCG[A/G]TGGCTCACGCCTGTA | 26054 |
rs189640266 | snp | A/G | 3.36157e-05 | 0.0040996 | intron-variant | SENP6 | GRCh38.p7 | 6:75695932 | ATCTGTCGTAAGTCA[A/G]ACTCTGAAAATATTT | 26054 |
rs189646883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680893 | TGTGGTGCTAGAGGA[A/G]GTCTGCTAAAACACA | 26054 |
rs189667712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75631912 | TGGATATATATCCTC[A/G]GATGAAGCATTGATG | 26054 |
rs189673824 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610596 | GAATCTTCTGCATCC[A/G]TTGGCAAAAATTATT | 26054 |
rs189728506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75628459 | ATTATGCAAAATAAT[A/G]TTGGAAATTTATCTT | 26054 |
rs189753795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75607622 | ACTTTTTTCTGCCTT[C/T]CTTTCTAATATACAT | 26054 |
rs189758089 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75622660 | TTCAGAGATCCACAA[A/T]TATACACACAAAGTT | 26054 |
rs189762481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661070 | TTCACATGGGTATTA[C/T]TGTTTCTCGGCCTTC | 26054 |
rs189766170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75645553 | ACCCGGGAGGCAGAG[A/G]TTGCAGTGAGCCAAG | 26054 |
rs189772660 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75691686 | CTCACTGCAAGCTCC[A/G]CCTCCCTGAGGCATT | 26054 |
rs189776350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636622 | GCAGCAGTAGAGCTA[C/T]ACAAAATACGTGTAG | 26054 |
rs189776599 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75678227 | CTGCCCCTACATCTT[A/C]TAGATTGCCTAGCCA | 26054 |
rs189784414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662265 | TCTACTGACCAAAGC[A/G]GGGAATGAGATTTTA | 26054 |
rs189786325 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75692561 | AGCCCAGGAGTTTGA[C/G]GTTGCAGTGAGCTGT | 26054 |
rs189790761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655935 | AAAAAGACATTGAGC[A/T]AGGCTGGGCGTGGTG | 26054 |
rs189801316 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711084 | GATTTATTCTAGATT[A/G]AGTAAATAGATGTAA | 26054 |
rs189896065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640409 | GGAATATTGTATTCT[A/G]ACATATCTTCAAGTA | 26054 |
rs189905835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673716 | AATTCCTTTATCTTA[C/T]GCAACAATTTTATTT | 26054 |
rs189911142 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75695347 | CATTGCCTGAAGATA[A/G]TCGGATAGTTATCAA | 26054 |
rs189920160 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SENP6 | GRCh38.p7 | 6:75603047 | GTTTCTCAGAGTTTC[A/G]GGCTTGCTTTTGCAG | 26054 |
rs189954453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75707903 | TATGTTGCCCAGGTG[A/G]TCCTTCTGAACTCAG | 26054 |
rs189956234 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75617553 | AAAGTGCTGGGATTA[C/T]AGGCAGGAGCCACTG | 26054 |
rs189973841 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613313 | AGTTTTATTGCAACA[A/C]AGCAATACCTATTTG | 26054 |
rs189997931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643921 | ATCATTAAAGCAAGG[C/G]AAACAACAATAACAA | 26054 |
rs190027477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75676940 | GGATTTCTGATTATC[C/T]TCCTGGAAAGAATTA | 26054 |
rs190032057 | snp | A/C/G | 5.04862e-05 | 0.00502404 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709625 | TCAGAAGATCAGGAT[A/C/G]ACCAGGTAAAACTTA | 26054 |
rs190110116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75659810 | CTGCCTACCCATAAA[C/T]GTGTGTATATGTATT | 26054 |
rs190118260 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641270 | GTTATATATATTTAT[G/T]CTAATAAGTGACTCC | 26054 |
rs190122282 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75675239 | GAAGGGATGTGACAA[G/T]AATGTTAACAGTTTA | 26054 |
rs190143379 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75689205 | CACCACTGTACTCCA[A/G]CCTGGGTGACAGAGC | 26054 |
rs190165836 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75658614 | TTATTAAATTTACAT[A/T]AAAAATATCGAGAAA | 26054 |
rs190167757 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75687388 | TACTGACCTCCTGAA[G/T]CCTGCTTCTGTCAAC | 26054 |
rs190174174 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SENP6 | GRCh38.p7 | 6:75715141 | TAAAACTTTATTACA[A/G]AAACAGGTGGTGGGC | 26054 |
rs190201627 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75653354 | TTCTAATGTTGTCAA[A/G]TAGTACATTGTAGTT | 26054 |
rs190205454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619999 | TCCATAGGCTGAGGC[A/G]GGAAGATCATTTGGG | 26054 |
rs190255976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621409 | ATGTTTACAAAAAAT[A/C]GACAAAGGCAACCAA | 26054 |
rs190256890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75710584 | GCAACTAAATATAGC[C/T]TTTCAATCCAACATA | 26054 |
rs190267092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636126 | CACCTATAACATTTT[C/G]CATGTGTATTATTGC | 26054 |
rs190269166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606943 | CTTTCTAGGTAGAGA[C/G]AGTAAAATAGGGGAG | 26054 |
rs190298113 | snp | C/T | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670623 | AACCTCCAGATGCTT[C/T]AGCTTTAAGCTGCCA | 26054 |
rs190407996 | snp | A/G | 0.000450778 | 0.0150062 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633641 | ATCTTGAAGACATAT[A/G]TAAGACGAAACAAGT | 26054 |
rs190417949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75603519 | TCTTTGGATAATTTT[A/G]CAAAGATGATTTTCA | 26054 |
rs190422914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617905 | TTTTATACAGTGTCC[C/T]TCAGGTTGGGTTTGT | 26054 |
rs190430433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650033 | CCTTTTTCTGTTCCA[C/G]GATTCATTCTGTGAT | 26054 |
rs190441360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681928 | TAGAACTCAAAATAC[A/G]AAACTGAAATAATGA | 26054 |
rs190447298 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75666404 | AATAGACCTACTGTT[C/G]TTCTTGTAACTTGCT | 26054 |
rs190457902 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75635653 | GTATTATTGTATCAA[A/G]TAGTGTTCACCTGAG | 26054 |
rs190461532 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75698767 | TGTAATCCCAACACT[C/T]TGAGAGGCTGAGGTG | 26054 |
rs190507002 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691901 | CACTCTCGTTGTCCA[A/G]GCTGGAGTGCAATGG | 26054 |
rs190518951 | snp | A/T | 0.000102717 | 0.00716574 | intron-variant | SENP6 | GRCh38.p7 | 6:75602607 | CCCTTGACGGGGAGA[A/T]GGGAGGGTATACTGG | 26054 |
rs190544639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657981 | TTAATTAGAGTATTA[A/G]AATGACAAAGTCATG | 26054 |
rs190553875 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75686800 | TCCCTTTGTGGGTAA[C/T]CAACCTTTCTCTCTG | 26054 |
rs190560001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75632776 | TTTTATTAATGGGAG[C/T]ACTCTAATCTGTGAG | 26054 |
rs190608120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693879 | ATAAATAAATTTAAT[A/T]TATCATAATTTCCCT | 26054 |
rs190619175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605295 | CAGTCAGTGTACCAC[A/G]GTGAAGTGCATAAGA | 26054 |
rs190698111 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75614404 | CCGAGTAGCTGGGAT[G/T]ACAGGTGTGCACCAC | 26054 |
rs190741882 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75671598 | GCAGTGGCATGTGCC[C/T]GTAGTCCCAGCTGCT | 26054 |
rs190756161 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75703243 | GGAGGATCACTTGAG[A/G]CCAGGAGTTTGAGAC | 26054 |
rs190771455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75663157 | ACACCGTGAATGTTC[A/G]AAATGTGGAAAGGAA | 26054 |
rs190783749 | snp | A/G | 0.00144086 | 0.0268021 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678820 | TTACAGGTTGATAGT[A/G]TATCCACCACCTCCA | 26054 |
rs190789619 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75702498 | GCTGGGATTACTGGC[A/G]TGAGCTACTGCGCCC | 26054 |
rs190798402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617344 | AATGGCGTGATCTTG[A/G]CTCACTGCGACCTCC | 26054 |
rs190803174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75649208 | TAATCCCAGCTACTC[A/G]GAAGGCTGAGACACA | 26054 |
rs190807347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672771 | TTGCTTATTATTAGA[A/T]AATTTAATCATTTTA | 26054 |
rs190823670 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75704628 | AAGAGGCTTTCCTCT[C/T]TCACTAATCCTTCTC | 26054 |
rs190921069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75699148 | CAGAAATGAGTTATA[A/C]AAATTTTAAATAGAA | 26054 |
rs190922906 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75682199 | ACATACTAATCCTAT[A/G]TACTAAACAACAGAA | 26054 |
rs190936309 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717924 | AGGAGCAGAAGTGGT[A/G]TTTAGTCCCTTCCCG | 26054 |
rs190956844 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SENP6 | GRCh38.p7 | 6:75629893 | CTTTGATTAGCAGCA[A/G]ATATGAGTGAGTTTT | 26054 |
rs191051272 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75626188 | ATTGCATTTTATTTT[A/C]ATTTTAATTTTTATT | 26054 |
rs191053850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75681657 | TAGAGCAGTGAGAGA[A/G]CGGACTGATACAGCA | 26054 |
rs191065514 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716579 | ATGTAAAAGTACTGT[A/T]TTCAACCAGTTGCAT | 26054 |
rs191184313 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75662555 | TTTTTAGAGAGTTAG[A/G]TTAATAAAATGTTAA | 26054 |
rs191188821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75612034 | TTTGTCTTCTATACC[A/G]AGAGATACAGGTTTT | 26054 |
rs191205408 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75693456 | CCATTATAGTTTGGG[A/C]CAGCAAAAGTCTCAT | 26054 |
rs191206742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640781 | ATGTTTTGAAAAATA[C/T]TGGTTGAATTAGAGT | 26054 |
rs191218077 | snp | C/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75625751 | GTGGGCTCCTGTAGT[C/T]CCAGCTACGTGGGAG | 26054 |
rs191220062 | snp | A/G | 0.00170523 | 0.0291497 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659328 | TTAAGAGGAAAGTAC[A/G]ACAGAAACGACACTG | 26054 |
rs191247724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679433 | CGAAAACAGGAGTTG[G/T]GAGAATTAAATGAGA | 26054 |
rs191254934 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75633374 | AAAGAAAGTAATACA[A/T]TAAACCTCCATGTTC | 26054 |
rs191257964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694171 | TGAGGCAAGAGAATC[A/G]CTTGAACCCGGGAGG | 26054 |
rs191261726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658178 | ACAAGGAGTAGTCAT[C/T]GATTATTTAAATTTC | 26054 |
rs191263113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75612436 | TCCTGGGCTCAAGGG[A/G]TCCTCCTGCCTCAGC | 26054 |
rs191270048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714585 | CCTGCTTTAAATCTT[A/G]TAGTGGCTTCCTGTG | 26054 |
rs191276507 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75672897 | CAGTGGCGCAATCTC[C/G]GCTCACTGCAAGCTC | 26054 |
rs191281621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75666002 | TGTACTCCAGCCTGG[A/G]TGACAGAATGAGATT | 26054 |
rs191307000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698016 | TATTATTCTCTCCCA[A/G]TGACTAGATAGTAGT | 26054 |
rs191359247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75630321 | GTGATCCATCAGCCT[C/T]GACCTCCCAAAGTGC | 26054 |
rs191399090 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75676775 | ATTAGTTACATACGT[G/T]AATAGATTTGTTCTT | 26054 |
rs191402077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75660949 | ATTTTGTATTTCTGT[C/T]TCAGCCCTAGAGTCA | 26054 |
rs191416723 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691625 | TTTTTTTTGAGACGG[A/C]GCCTCGCTCTGTTGC | 26054 |
rs191422584 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75708786 | TAATCCCAGCTACTC[A/G]GTAGGCTGAGGCAGG | 26054 |
rs191456889 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75712747 | CTTGAAAAAAAAAAG[G/T]TCTAAACTAATTATT | 26054 |
rs191614536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75646219 | CTACCTTCTTTCTTA[C/T]AAGACTGTTACTACT | 26054 |
rs191616774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614638 | AAATAACTTGTTTCT[C/T]GTCAGATTTCACCCA | 26054 |
rs191654491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604556 | AGAATCGCTTGGAAA[C/T]GGGAGGCAGAGGTTG | 26054 |
rs191661133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619487 | TGTACATATGTACAC[A/C]CATACTGTATTTTGT | 26054 |
rs191665072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611305 | TTCATTTTTTAACCA[C/T]AGGAGATATAAAAGA | 26054 |
rs191685973 | snp | A/G | 4.99555e-05 | 0.00499752 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634716 | CTGCAGTGAAAATAC[A/G]CAAAATACGTCATTA | 26054 |
rs191708755 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75713878 | TAAAATAGTGCATTT[A/G]ACTTTACCTTAGTAA | 26054 |
rs191789171 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75616335 | CCCCACTCCAGGTTG[C/T]CCCCAAACTTTTAAA | 26054 |
rs191797159 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75622891 | AGTCAGTATTTTATG[A/G]TTTTCTTTCTTTCAT | 26054 |
rs191797384 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SENP6 | GRCh38.p7 | 6:75656295 | ATGTTCCTACCGCAG[A/G]GTCTTTGGTAAATAC | 26054 |
rs191800695 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601525 | CTACCTTTTCTCTTC[G/T]GTTGGCTGTAGTTTA | 26054 |
rs191803774 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | SENP6 | GRCh38.p7 | 6:75637059 | CTAACTTTAAAAAAA[A/T]TTTTTTTGTAGAGAC | 26054 |
rs191804329 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717586 | TATATTGAAATCTTC[A/G]GAGGCTGCCAGGTTG | 26054 |
rs191812953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75671826 | TTCTGGTAAAGGTTC[A/G]TGGTTCTAGGATACA | 26054 |
rs191818632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622041 | GTATCTTTCTTCCCC[A/G]GTTGTGACCACCACC | 26054 |
rs191819279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703887 | TGCAGTACAAAGTTT[A/G]TATTTTCCATTTATT | 26054 |
rs191820885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75686104 | TGCATATATATTTAG[A/G]ATAGTTAGTTCTTCT | 26054 |
rs191835354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655341 | ATGAAATACATAAAT[C/T]TTAAGTATATAAAAT | 26054 |
rs191869076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75685222 | GTAGTTTGTACTTCT[A/G]TGGGATCAGTGGTGA | 26054 |
rs191965860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75625604 | CTGGGCACAGTGGCT[C/T]ATGCCAGTAATCCCA | 26054 |
rs191969246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75688269 | GCACAGTATTTGGGC[A/G]GGAGTGTCCCATTTT | 26054 |
rs191975357 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75633930 | CTTGTTTCTGAATAA[A/G]ACATTGCAAGAAATA | 26054 |
rs191981461 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75667576 | TAAAAAATCAATTAA[C/T]ATGTGCTGTTGTCAA | 26054 |
rs192110421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635496 | AAAAATGTAATATCT[A/C]GACTGCTCGTCATTT | 26054 |
rs192122880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619701 | CCAAATTATTTTCTA[C/T]AGTGCCTGAACTGTT | 26054 |
rs192125063 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SENP6 | GRCh38.p7 | 6:75652386 | CTATGTTTATGTGGC[A/G]TAATTTGTTTTCAAT | 26054 |
rs192133666 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75607191 | TGTCTGTACAAAAAC[A/G]TAAAAAAATGATATG | 26054 |
rs192136254 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704694 | GGTCAGGTCCTTCCC[A/G]TCCCACGAGGCCATA | 26054 |
rs192137093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75683806 | TTACTGTAGCTTTGT[A/G]GTATAGTTTGAAGTC | 26054 |
rs192139134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668236 | TGGATTAATATTTTT[A/G]TATAATCTTACAGAA | 26054 |
rs192145678 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75636245 | GTATTTAAGAAATAA[A/T]CCTAATTGAAAAATT | 26054 |
rs192147262 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75700768 | AAGTGTTGGGATTAC[A/G]GGTGTGAGCCACCGT | 26054 |
rs192153946 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SENP6 | GRCh38.p7 | 6:75670935 | ATTGTTTATTATCAT[C/G]CCAGCTTCGTGCATG | 26054 |
rs192245074 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75615984 | TCAACTATACTAGTT[C/G]CTATTCATCCACCGA | 26054 |
rs192274070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647103 | GGTTTATTTAGAGTA[A/G]GAAAGTAGCTATTGT | 26054 |
rs192295366 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75650756 | CTATAATAATACTGT[A/G]TATATTGTTATATGA | 26054 |
rs192306510 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75674249 | GTAACCTTGAACTCC[C/T]AGGCACAAGCAATCC | 26054 |
rs192309083 | snp | A/C | 0.0479149 | 0.147179 | intron-variant | SENP6 | GRCh38.p7 | 6:75707023 | CACTGATTGAGAGAA[A/C]CACTGATCAAGTCAT | 26054 |
rs192311964 | snp | A/G | | | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718762 | AGGAATAGTGCTAGC[A/G]TTTCCTAAAATACCA | 26054 |
rs192354454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630938 | AGTATATCTCTGTAC[C/T]GTATTCTGAATAATT | 26054 |
rs192364166 | snp | A/C | 0.0146672 | 0.084371 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599773 | ACCAGGCTAAAAAAA[A/C]CAGGAAAGGGGCCGG | 26054 |
rs192371584 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614951 | GGAGTGCAGTGGTGG[C/T]CTGATCTCGGCTCAC | 26054 |
rs192382676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646607 | TTTGGGAGGCTGAGA[A/C]AGGCAGATCACGAGG | 26054 |
rs192439135 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718636 | TTATGAACACTGCTA[C/T]TCCAAAACTTATTAC | 26054 |
rs192492851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75618240 | TCTTCTGTAAGGAAC[A/C]TGTGTCCCTTCTTTC | 26054 |
rs192497766 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75626847 | CACCTTCACATATTT[C/T]CTGTATTTACAGTGT | 26054 |
rs192519266 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612904 | AGATCACTTGAGGCC[A/G]GGAGTTCAAAACCAG | 26054 |
rs192527928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660867 | AACTCCTGACCTCAC[A/G]TGGTCCACCCACCTC | 26054 |
rs192535336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642392 | TTCAGGGAAACTCTT[A/T]ACTATGAAGCTAACA | 26054 |
rs192547789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75676146 | AGTGCACTTTGACAG[A/G]TGCCTTAGGTGTATA | 26054 |
rs192581693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701168 | TTGTTTTTCATCCAG[C/T]AAATATTTATTGAAC | 26054 |
rs192606864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75628217 | CTGTTCAGTTTTCCC[A/G]TAGAATCTTAATATG | 26054 |
rs192620775 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652034 | ATATAAAAATTAGCC[A/G]GGTATAGTGGCGTGT | 26054 |
rs192665013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631678 | TGTCTATGGCCACTT[C/T]TGTGCTACAACAACA | 26054 |
rs192667670 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600653 | GCTGATCTTGAACTC[A/C]TCCCGACCTCAGGTG | 26054 |
rs192697183 | snp | A/C/G | 6.70392e-05 | 0.00578928 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663450 | AAGTCATTTTACCTG[A/C/G]GGCAAAAATACCCAA | 26054 |
rs192710194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686972 | GGGAAGTTCTCCTGG[A/G]TAATATCCTGCAGAG | 26054 |
rs192730216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664299 | ATTATAAACAGAACA[C/T]TAGGCTTTCCTTTTA | 26054 |
rs192739330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694871 | GCCCTTGGTTTTTTT[A/T]AATTTATTTTTATTT | 26054 |
rs192769204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643708 | GCCTGGGTGACAGCA[A/G]GGCGCCATCTCAAAA | 26054 |
rs192776434 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75700203 | GGCATGAGCCACTGC[A/G]CCTGGCCAAAAGTCT | 26054 |
rs192795389 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SENP6 | GRCh38.p7 | 6:75608119 | TGTTTATCATGTGAG[C/T]TCATGTACTTGAAAC | 26054 |
rs192852519 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75613166 | AAATTTGTCCAGCTG[A/C]CTGTTTTTAAGAGGC | 26054 |
rs192857931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667939 | TAAGGAAATATGTGT[A/G]TATTACTTTAGTATG | 26054 |
rs192872786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75612600 | CACCCAAAACGCTAG[A/G]ATTATAGGTGTGAGC | 26054 |
rs192874538 | snp | A/C | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75641548 | TCTCTTTGTAAGAAC[A/C]CTGGCAGACACATGT | 26054 |
rs192889113 | snp | A/G | 3.47687e-05 | 0.00416931 | intron-variant | SENP6 | GRCh38.p7 | 6:75675476 | GCTAGACGGTAAGCT[A/G]TTTTATGTCTTTTTA | 26054 |
rs192891140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708270 | TTTCACCATGTTAGC[C/T]AGTCTGGATTATATA | 26054 |
rs192926005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648103 | GAGTTTTATTGAACT[A/G]TGTTATAATGTATTA | 26054 |
rs192942640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75679973 | GATCAGAGAAATGAT[A/G]TCATAATTGAATTTC | 26054 |
rs192947954 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75714829 | TATACCTTGTCTGTC[A/T]AACATGTATTCATTC | 26054 |
rs192958593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656745 | ACATTGGTTTCAAAA[C/G]TCTCAGCTTAACTTT | 26054 |
rs192959659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75686350 | TTGACTCTTTATCCA[A/G]TTTGCCAGTCTGTGT | 26054 |
rs193049868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75623479 | TTTTCATTAGCTAAG[G/T]CTTTCTTTCCTTTCA | 26054 |
rs193073617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75604942 | GTCTGGCGTGGTGGC[A/G]CGCGCCTGTAATCCC | 26054 |
rs193083713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75626532 | TAGATATTCAGTTTG[C/T]CCCTACTGATGAATA | 26054 |
rs193087734 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75660744 | TCAAGCAGTTCTTCT[C/G]TCTCAGCCTCCTGAG | 26054 |
rs193093161 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75689613 | AGTCAATTATGGACC[A/G]TATGTGATAGTGAGC | 26054 |
rs193113068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690490 | TAAAGTAGTCAAATT[C/G]ATAGAAACAGAAAAT | 26054 |
rs193151319 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75603972 | GTACCTGTCGAGGCT[C/G]AGAGGGTGCAGCTTG | 26054 |
rs193180802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75672568 | CAAAGGGCATTCTTC[A/G]TTGAAGAATAATTAG | 26054 |
rs193188039 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75704465 | AAAGAATAACAAAGG[A/G]GCATTGCTGCCAACA | 26054 |
rs193226480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75608862 | TTATTAGCAGATAGA[A/G]AAAAGAAAAAGAGCT | 26054 |
rs193227601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637547 | AAGTCTGTAGTTCAT[A/G]CCATCCCTGCCCCTA | 26054 |
rs193268032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75708514 | GAGGATGGCTTGAGC[A/G]TAGGAGTTCAAGGTT | 26054 |
rs199528219 | snp | C/T | 6.65358e-05 | 0.00576745 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670636 | TTTAGCTTTAAGCTG[C/T]CAAAGTTCCTTTGAC | 26054 |
rs199538730 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662286 | TGAGATTTTAATCAG[-/T]TTTTTTTTTCTCTTC | 26054 |
rs199545912 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75640478 | TTGTGTATTCATCTT[-/C]CTGTTTGTTTATTTT | 26054 |
rs199612622 | in-del | -/AA/AAACAGA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610994 | AATAAAGAGTGGACG[-/AA/AAACAGA]ACGAGGAACTAGAAA | 26054 |
rs199617972 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634678 | AATTTTTCCGTGTTC[A/G]AGTTATTTTTTGTTT | 26054 |
rs199660674 | snp | C/T | 0.000347846 | 0.0131834 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666835 | GAAAAGTAGAAGCAG[C/T]GCTAAATGAAAATAC | 26054 |
rs199666669 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75708812 | GCAGGAGAAATCACT[C/T]GAACCTGGGAGGCAG | 26054 |
rs199670923 | in-del | -/TAGC | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75656448 | ACTTCTGTGATCAGT[-/TAGC]TAGTAAAACTTCCAC | 26054 |
rs199673146 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708352 | CTTAACACCTTTTTA[C/T]TAACTTATACCAAAA | 26054 |
rs199676354 | snp | C/T | 0.000116093 | 0.00761794 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715481 | ATCCGAAACATAATT[C/T]TGAAGCTACAGGAAG | 26054 |
rs199689914 | in-del | -/TAAGTTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699222 | CTTAGTCACTATACC[-/TAAGTTA]TCTGCATGGAAGTTA | 26054 |
rs199697956 | snp | C/T | 0.000375471 | 0.0136965 | intron-variant | SENP6 | GRCh38.p7 | 6:75713850 | AATTTGTTGGATCTG[C/T]TATAATAAATAATAA | 26054 |
rs199710933 | in-del | -/AAAA | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75643373 | ACAAGAGATGCAAAC[-/AAAA]AGAAAGCATGAGTGG | 26054 |
rs199794830 | snp | A/C | 0.000133382 | 0.00816537 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634774 | CGTTTTCATCATGCT[A/C]ATGCACAGATACCAG | 26054 |
rs199816111 | in-del | -/ATG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666234 | TGATATATATAAAAT[-/ATG]ATATATAAAATATAT | 26054 |
rs199819513 | in-del | -/A | 0.0748431 | 0.178382 | intron-variant | SENP6 | GRCh38.p7 | 6:75703293 | TCCAACAAAAAAAAA[-/A]TAAATAGAAAATTTT | 26054 |
rs199819742 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613493 | AACTTAAAAAAAAAA[-/A]GTTCTTAATAGCAAT | 26054 |
rs199864221 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664403 | ACATACGTCTGTATG[C/T]ATATATATATACATC | 26054 |
rs199880096 | in-del | -/TG | 0.0283406 | 0.115616 | intron-variant | SENP6 | GRCh38.p7 | 6:75693569 | GCAATTAATATAAAC[-/TG]TGTCTTGATCTGACT | 26054 |
rs199925258 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699353 | CTTGTTTTTGTTTTT[G/T]CTTTTTTTTTTTTTT | 26054 |
rs199928355 | snp | C/G | 0.00043316 | 0.0147103 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659367 | ATCAGCCTACTCCTC[C/G]TCTATCTCCTGCTTC | 26054 |
rs199947145 | in-del | -/AGT | 0.0283406 | 0.115616 | intron-variant | SENP6 | GRCh38.p7 | 6:75712102 | CTTTGAAGGCTGTGG[-/AGT]AGTAACCCAAGGCAG | 26054 |
rs199976746 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653034 | TTACTTTTTTCTTTT[C/T]TTTTTTTTCTTTTTT | 26054 |
rs200012624 | snp | A/T | 1.89806e-05 | 0.00308057 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659270 | CCTTTAGAACGTATA[A/T]TGAAGAAAACAGAAG | 26054 |
rs200024592 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625476 | CTTATGGTGGCTATT[G/T]CCATGGGGAAAATAT | 26054 |
rs200034085 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662859 | TAGATACTAAAGTAA[G/T]GGAGCCAGTCAGTAC | 26054 |
rs200035614 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619474 | GTGTGTGTGTGTGTG[C/T]ACATATGTACACACA | 26054 |
rs200039328 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699224 | TTAGTCACTATACCT[A/C]TGCATGGAAGTTATT | 26054 |
rs200061055 | snp | A/G | 0.000621993 | 0.0176241 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678842 | CCACCTCCAGCTAAG[A/G]GAGGCATCTCTGTTA | 26054 |
rs200144591 | snp | A/G | 0.000265057 | 0.0115091 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677107 | GTATTTGAAAGTATC[A/G]TTAATGAAATTGGTA | 26054 |
rs200170034 | in-del | -/AT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666160 | TATAAAACATATATG[-/AT]ATATATATAAAACGT | 26054 |
rs200232003 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701596 | AGAATGTTGAAAAAA[-/T]CATATGACCTAATTA | 26054 |
rs200233021 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75626335 | ATTATGTGGCTTAGC[-/TT]TTTTTATATATATAT | 26054 |
rs200245008 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716281 | TCATCAAATGCATTT[C/T]TGAAGACATCAAAGA | 26054 |
rs200273746 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | SENP6 | GRCh38.p7 | 6:75693398 | GACAGAGTGATACTC[-/A]GTCTGAAATTTAAAA | 26054 |
rs200305776 | snp | A/G | 0.000403959 | 0.0142062 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602485 | GCACGGCGGCGGTGT[A/G]GGCCATGGATTAAGA | 26054 |
rs200342690 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687698 | GGTCTTTTGGAGTTT[-/G]CTGGAGTTCCACTCC | 26054 |
rs200379468 | snp | G/T | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718108 | TCTCTAAATTACATC[G/T]TGTTTTAAGCCACCA | 26054 |
rs200397872 | snp | A/C | 0.000469145 | 0.0153086 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670681 | CTGTCGAAGTATACG[A/C]GTAGGAACACTCTTC | 26054 |
rs200405708 | snp | C/G | 1.67725e-05 | 0.00289585 | intron-variant | SENP6 | GRCh38.p7 | 6:75663201 | CCAAATGCCAAAGTT[C/G]TGGTGTTCTTTTTTC | 26054 |
rs200427934 | in-del | -/T | 0.0138799 | 0.0821421 | intron-variant | SENP6 | GRCh38.p7 | 6:75639382 | TTTTCCTTTTGAAAA[-/T]TTTTTTTAAATTTGT | 26054 |
rs200471319 | snp | C/T | 3.33862e-05 | 0.00408558 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697470 | AACATGGACCCGGCA[C/T]GTAGATATTTTTGAG | 26054 |
rs200483413 | snp | A/G | 5.04579e-05 | 0.00502259 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633689 | TTGAAAGGCAACCCA[A/G]TTGGACTTAACATGT | 26054 |
rs200513593 | snp | A/G | 0.000735351 | 0.0191608 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703060 | GAAAGTTTAAGTTCC[A/G]CACATCATACAGGTA | 26054 |
rs200515881 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708353 | TTAACACCTTTTTAT[A/T]AACTTATACCAAAAT | 26054 |
rs200517533 | snp | A/C | 1.65833e-05 | 0.00287948 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678657 | AGAAGAAGAAACTGG[A/C]GAAAACCACACCATC | 26054 |
rs200528364 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75698557 | CAGGCTGGTCTTGAA[-/C]CTCTTGGCCTCAAGC | 26054 |
rs200531593 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702219 | AAAAAAAAAATAGGC[-/T]TTTTTTTTTTTTTTG | 26054 |
rs200565081 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652696 | CTCAAAAAAAAAAAA[A/G]AAAAAAAGAAAAAGA | 26054 |
rs200576938 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602482 | CGAGCACGGCGGCGG[A/C]GTGGGCCATGGATTA | 26054 |
rs200589767 | snp | C/T | 1.66551e-05 | 0.00288571 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659361 | GTACCTATCAGCCTA[C/T]TCCTCCTCTATCTCC | 26054 |
rs200633509 | snp | A/G | 5.247e-05 | 0.00512174 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711403 | TGGCATTTAAAGCCT[A/G]CTATCTGTAAACAGT | 26054 |
rs200650537 | snp | A/G | 0.000101123 | 0.00710996 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670718 | TTAATAGAGCCTGTA[A/G]TTGTAAGTACATCTT | 26054 |
rs200669353 | in-del | -/AT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666183 | TAAAACGTATATATG[-/AT]ATATATATAAAACGT | 26054 |
rs200687808 | in-del | -/C | 0.448836 | 0.15154 | intron-variant | SENP6 | GRCh38.p7 | 6:75658971 | AATGAGACCTTGTCT[-/C]CCCAAAAAAAAAAAA | 26054 |
rs200752159 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694255 | ACAAGAGTGAAACTC[C/T]TATCTCAAAAAAAAT | 26054 |
rs200756525 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689217 | CCAACCTGGGTGACA[C/G]AGCAAGACACTATAT | 26054 |
rs200764192 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625261 | GGATTACAGGCATAC[A/G]CCACCATGCCTGGCT | 26054 |
rs200891828 | snp | C/G/T | 8.28192e-05 | 0.00643449 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666864 | ACTTGCAGAGCAGAG[C/G/T]GTGAACTACGAAGCA | 26054 |
rs200942344 | snp | G/T | 1.65957e-05 | 0.00288055 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623930 | CAGTGTGGATGAAGA[G/T]GAGGATTCTGAAACC | 26054 |
rs200948028 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659004 | AAAAAAAAAAAAGGG[C/T]AATTGTGAGTATGTG | 26054 |
rs200950678 | in-del | -/GT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663808 | TCCTGCTGATAGTGG[-/GT]TTTTTTTTTTGTGGG | 26054 |
rs200971151 | in-del | -/ATTAACTTATA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708351 | TCTTAACACCTTTTT[-/ATTAACTTATA]CCAAAATTTATTTTA | 26054 |
rs200985174 | in-del | -/TTC | 0.177182 | 0.23916 | intron-variant | SENP6 | GRCh38.p7 | 6:75683667 | GAATCCTTTCCCCGT[-/TTC]TTGTTTTTGTCAGGT | 26054 |
rs201042466 | snp | A/G | 1.72886e-05 | 0.00294007 | intron-variant | SENP6 | GRCh38.p7 | 6:75659440 | TCTTTGTTGCTAATC[A/G]GATTGTGTTTTGATT | 26054 |
rs201057204 | snp | A/G | 0.000795822 | 0.0199318 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702739 | AATGCTGTCATACAG[A/G]AATGTTCAACTGTAG | 26054 |
rs201073122 | in-del | -/TTT | 0.0146344 | 0.0842973 | intron-variant | SENP6 | GRCh38.p7 | 6:75675710 | AGGCAGTTATAAAGA[-/TTT]TTTTTTTTATTACCC | 26054 |
rs201084715 | in-del | -/TCCTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640477 | TTTGTGTATTCATCT[-/TCCTG]TTTGTTTATTTTGTA | 26054 |
rs201195000 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643553 | ATGGTAAAACCCCGC[C/G]TCTATTAAAAATACA | 26054 |
rs201196530 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708351 | TCTTAACACCTTTTT[A/G]TTAACTTATACCAAA | 26054 |
rs201200562 | snp | A/G | 0.000196312 | 0.00990543 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75678973 | AATCTTTAACATTCC[A/G]TCATATCTTATGTCT | 26054 |
rs201202035 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641255 | CATTTTTCTATAATG[C/G/T]TTATATATATTTATG | 26054 |
rs201204874 | in-del | -/AAATA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705554 | ATCTCAAAAATAAAT[-/AAATA]AATTAATTAATTAAT | 26054 |
rs201222975 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706865 | ATGTGTGGAATCACT[A/G]CTTTCACTTGCTGTT | 26054 |
rs201263879 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619447 | TTCCGTTGTGTCTAT[A/G]TGTGTGTGTGTGTGT | 26054 |
rs201264695 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631033 | GGATTTTTTTTTTTT[-/T]ACTTTTAAAAGATTT | 26054 |
rs201289254 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708362 | TTTTATTAACTTATA[C/G]CAAAATTTATTTTAT | 26054 |
rs201300347 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685184 | TTCTAGATTATTTGC[A/T]TAGAGGTGTTTATTC | 26054 |
rs201325347 | in-del | -/A | 0.0322114 | 0.122752 | intron-variant | SENP6 | GRCh38.p7 | 6:75662467 | TCCAAAAGAAACTAC[-/A]CTTAACATAAAATTT | 26054 |
rs201325696 | in-del | -/AA | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75713279 | AGCTAAGATATGGTT[-/AA]GTTAATATTCTATAA | 26054 |
rs201326500 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636892 | TTTTTTTTTTTTTTT[A/T]ATTATAGAGATAGGG | 26054 |
rs201327201 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664379 | TAAAAAATCTATATA[C/T]ATGTACACACATACG | 26054 |
rs201344205 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602586 | TGGAAGGTACGTCTG[C/T]TTCTGCCCTTGACGG | 26054 |
rs201379212 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693428 | AAAAAAAAAAAAAAA[-/C]ACACCAAAGTAGCCA | 26054 |
rs201398729 | snp | A/G | 0.00018232 | 0.00954603 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702778 | TGTATTTCTTCTTCA[A/G]CCAGTGAAATGGAGA | 26054 |
rs201401262 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698507 | GAATTTTTTTTTTTT[-/T]AACTTTTGTAGAGGT | 26054 |
rs201418276 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626911 | TTCCGTCTTTCTGGG[-/T]TTTTTTTTTCCCTCT | 26054 |
rs201451056 | in-del | -/G | 0.0663309 | 0.169604 | intron-variant | SENP6 | GRCh38.p7 | 6:75664260 | TAGGACCCTGTTGCT[-/G]AAAAAAAAAAAACAA | 26054 |
rs201458110 | in-del | -/TAAGTGA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699221 | TCTTAGTCACTATAC[-/TAAGTGA]CTCTGCATGGAAGTT | 26054 |
rs201470021 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619030 | AGGCTTTTTTTTTTT[C/T]CCTTTTAAAAGCAGT | 26054 |
rs201553957 | in-del | -/GTT | 0.0479149 | 0.147179 | intron-variant | SENP6 | GRCh38.p7 | 6:75623167 | GTTGTCTTCGAAAAC[-/GTT]GTATTTGACTTTCTT | 26054 |
rs201561791 | snp | A/G | 1.66493e-05 | 0.0028852 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670639 | AGCTTTAAGCTGCCA[A/G]AGTTCCTTTGACAGT | 26054 |
rs201563185 | snp | A/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718109 | CTCTAAATTACATCT[A/G]GTTTTAAGCCACCAA | 26054 |
rs201637447 | snp | C/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619443 | AACATTCCGTTGTGT[C/G]TATGTGTGTGTGTGT | 26054 |
rs201645101 | snp | A/C | 0.00087924 | 0.0209487 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663491 | TTGAAAGAAAGGAAA[A/C]CAAGTTTGTCAGACC | 26054 |
rs201658545 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | SENP6 | GRCh38.p7 | 6:75627945 | CCGAAGTGCTGAGAT[A/G/T]ACAGGCGTGAGCCAC | 26054 |
rs201663177 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | SENP6 | GRCh38.p7 | 6:75605397 | TGAAAAAGTAATGAC[-/T]TTTTTTTCACCATCA | 26054 |
rs201673325 | snp | G/T | | | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702671 | TTTTGGCTGTTGTTT[G/T]TTTCCCCGGTTTGGA | 26054 |
rs201707953 | snp | A/T | 0.000116933 | 0.00764543 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663236 | GATTTGCAAAGAAAT[A/T]GCAGACAAGCTATTA | 26054 |
rs201757519 | snp | C/G | 0.00199795 | 0.0315433 | intron-variant | SENP6 | GRCh38.p7 | 6:75647825 | GCAGTTTTGTTACAC[C/G]TGTGAAGGATTTCAA | 26054 |
rs201758987 | in-del | -/TGTG | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619446 | ATTCCGTTGTGTCTA[-/TGTG]TGTGTGTGTGTGTGT | 26054 |
rs201762586 | snp | A/T | 0.00018167 | 0.009529 | intron-variant | SENP6 | GRCh38.p7 | 6:75666683 | ACTATAGTTTTAATA[A/T]AAATTATAAATTATT | 26054 |
rs201769886 | snp | A/G | 0.000139261 | 0.00834333 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670682 | TGTCGAAGTATACGA[A/G]TAGGAACACTCTTCC | 26054 |
rs201807563 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SENP6 | GRCh38.p7 | 6:75614055 | TTTAATCCCAATTTG[C/T]GTTTATCTGATGTTT | 26054 |
rs201826577 | snp | A/G | 3.15025e-05 | 0.00396866 | intron-variant | SENP6 | GRCh38.p7 | 6:75640639 | AGTGATATATCAACA[A/G]TGAGGTCTTGCCTCT | 26054 |
rs201827129 | in-del | -/T | 0.0137245 | 0.0816939 | intron-variant | SENP6 | GRCh38.p7 | 6:75703122 | TCAGAATAATCTGGA[-/T]TTTTTTAATAAACAG | 26054 |
rs201832020 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619473 | TGTGTGTGTGTGTGT[A/G]TACATATGTACACAC | 26054 |
rs201849278 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608684 | TTGGATAGATTACTT[A/T]ACTTCTCTGTTTTCT | 26054 |
rs201855743 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655374 | GAAAACTACATATCC[C/T]TTTCTAACCAAAATC | 26054 |
rs201983251 | in-del | -/TA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706677 | CATTTTTGTTTTGTT[-/TA]TTTAGTATGTGTATA | 26054 |
rs202009517 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638584 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATATATAT | 26054 |
rs202019332 | snp | C/T | 0.000421869 | 0.014518 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677112 | TGAAAGTATCATTAA[C/T]GAAATTGGTATAAAG | 26054 |
rs202024204 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SENP6 | GRCh38.p7 | 6:75625566 | TTGTTCCTAATGATG[G/T]TAATTTAATAACTTA | 26054 |
rs202062729 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649321 | TTGGTCTCAAAAGTG[-/A]AAAAAAAAAGCATTT | 26054 |
rs202079296 | snp | G/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663254 | AGACAAGCTATTACT[G/T]TGAATGAGTCTACTG | 26054 |
rs202089228 | snp | A/G | 0.00168206 | 0.0289517 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659371 | GCCTACTCCTCCTCT[A/G]TCTCCTGCTTCAAAA | 26054 |
rs202125150 | snp | G/T | 0.000100356 | 0.00708294 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602550 | GCAAGAGCGGCGGTA[G/T]CGCAGGGGAGATTAC | 26054 |
rs202191578 | in-del | -/AA/CA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658974 | AGACCTTGTCTCCCC[-/AA/CA]AAAAAAAAAAAAAAA | 26054 |
rs202208481 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691139 | TTACCATTCCCAGCT[-/A]AAAATTTTTTTTTTT | 26054 |
rs367578951 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75670844 | ATCAGTTAGTTCAAG[A/T]TTTCACATTGCTTTA | 26054 |
rs367595448 | snp | C/T | 1.68083e-05 | 0.00289894 | intron-variant | SENP6 | GRCh38.p7 | 6:75715351 | AAAGGTTATTTATTA[C/T]AGTTTTCTAATACGC | 26054 |
rs367597650 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608030 | TGGAAACTACATCAT[-/G]GTGTCATTCCTTATT | 26054 |
rs367668144 | snp | A/G | 3.32989e-05 | 0.00408024 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623956 | AAACCTCAAAAGGAA[A/G]AAAGGCAAGTGTTGC | 26054 |
rs367714149 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606796 | AATCCAAAAAAAAAA[A/T]CTGAAATCTGAAACA | 26054 |
rs367784277 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75717048 | TCACCATTAGTGATA[C/T]CAACTGTAGTTTGTT | 26054 |
rs367828851 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628161 | TCTTAACAGTTAGAA[A/G]TTTTATATTGTGCCT | 26054 |
rs367883729 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715712 | AATTTTGATGCTTGT[A/G]TAAATGTCAGATAAT | 26054 |
rs367915598 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617863 | TTTCATAACCTTGAC[A/G]GTTGTACAAAATACT | 26054 |
rs367917057 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699354 | TGTTTTTGTTTTTGC[-/T]TTTTTTTTTTTTTTT | 26054 |
rs367933982 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678510 | TTGAAAAGCATTCTT[A/G]CCTTGTGCTTACCCT | 26054 |
rs367938140 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659070 | GTAGAACAAAATAAA[C/G]TGAAGAGGATATTGA | 26054 |
rs367965753 | snp | A/C | 1.65883e-05 | 0.00287991 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702955 | AAAAAAATAAATCAT[A/C]CTGCGAGTGAAAATG | 26054 |
rs368013516 | snp | A/T | 1.66593e-05 | 0.00288607 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663274 | TGAGTCTACTGGACC[A/T]TTATTAAGAACGTCA | 26054 |
rs368016745 | snp | A/G | 1.75557e-05 | 0.00296269 | intron-variant | SENP6 | GRCh38.p7 | 6:75670526 | TTTTAGTAAATTATT[A/G]AGTGAACATTTTCTT | 26054 |
rs368030969 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615556 | TTACTTTTGCTTTTT[-/T]AGAATAAACCCTGCT | 26054 |
rs368035412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645493 | ATGGTGGCGCACACG[G/T]GTAATCCCAGCTACT | 26054 |
rs368042829 | in-del | -/GTTTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691580 | TTGTTATTGTGTTTT[-/GTTTT]TTGTTTTTTGTTTTT | 26054 |
rs368066186 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666595 | GGAGGAGGTCCAAAG[A/C]AAATTTAGGATATTT | 26054 |
rs368069882 | snp | A/G/T | 6.63398e-05 | 0.005759 | intron-variant | SENP6 | GRCh38.p7 | 6:75678718 | TCCTTTATATTTGCA[A/G/T]TGATCTTAAATGTCT | 26054 |
rs368105862 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653179 | GGGATTACAGGCCTG[C/G]GCCAGTCTGCCTGGC | 26054 |
rs368121660 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633516 | TTAAATGGTTTTCAA[A/G]TAGTTGTTGATAGAT | 26054 |
rs368126880 | in-del | -/TA | 0.000341504 | 0.0130627 | intron-variant | SENP6 | GRCh38.p7 | 6:75678761 | TACATTTCAGTTGTG[-/TA]TATATATATATAGAT | 26054 |
rs368137519 | snp | C/T | 0.000171985 | 0.00927163 | synonymous-codon, utr-variant-5-prime, intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621614 | AGAAAGTGAAGGAGA[C/T]ACAGATAAAGAGTAA | 26054 |
rs368141100 | in-del | -/AAGTT | 0.00676609 | 0.0577691 | intron-variant | SENP6 | GRCh38.p7 | 6:75707725 | GTCTCACTTTCATAG[-/AAGTT]AAGAGTACAGCAATA | 26054 |
rs368151542 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653176 | GCTGGGATTACAGGC[C/T]TGGGCCAGTCTGCCT | 26054 |
rs368173869 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671506 | AGGCGGCTGGATCAC[A/G]AGGTCAGGAGTTTGA | 26054 |
rs368207965 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655835 | TCTTCTATTTATATC[A/G]AACCTGTATATAGAT | 26054 |
rs368259401 | in-del | -/GTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612391 | TTCGTAATTGTTGTG[-/GTG]CGCTTATGGCTCATT | 26054 |
rs368308579 | in-del | -/AT | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75631585 | ATTCTATTTCATGAC[-/AT]GTGAGCATAATATAA | 26054 |
rs368349895 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692707 | CTAGTGCCTGAGCCC[C/T]ACATCCCTCGCCCCC | 26054 |
rs368386697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75674186 | AAAAACGATAAGGTC[C/T]CTCTTCGTTGCTCAG | 26054 |
rs368395989 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660917 | ATTACAGGCGTGAGC[C/G]ACCGCGCCTGGCCAT | 26054 |
rs368441950 | snp | A/C/T | 1.82734e-05 | 0.00302264 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621671 | ATAAGAATAAAACTT[A/C/T]TCATTAGAAAAACAA | 26054 |
rs368478592 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664980 | TGTGTGTGCTTACTT[C/T]ATTGGGTTATCAAAG | 26054 |
rs368555146 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716592 | GTATTCAACCAGTTG[A/C]ATAATACAGCAAAAA | 26054 |
rs368581636 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659912 | TTTGGTTTTTTATAA[-/T]CAGAATACATCTGTC | 26054 |
rs368615527 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709507 | CCTTTTTTATTATGT[A/G]ATGTTTCTTATTGAT | 26054 |
rs368644116 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653150 | ATTTTCCTGCCTCAC[C/T]CTCCCGAATAGCTGG | 26054 |
rs368652337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75675808 | CAATTTCCCCCATTC[A/G]TGATATTACCCTCTT | 26054 |
rs368659489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75642754 | AGTCTTTTGCATGTG[A/G]TTTATAATTTGGCAT | 26054 |
rs368673069 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667977 | TTATAAAATAATAAA[C/G]TTGTATGTTAAATTC | 26054 |
rs368684914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682975 | AGATCCTTGAGGAAT[C/T]GCCACACTGTCTTCC | 26054 |
rs368687851 | snp | C/T | 1.66857e-05 | 0.00288835 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663414 | ATGACAGTAAACACA[C/T]TTATTTACAGACTAA | 26054 |
rs368698860 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647854 | AAATTGCTGTATGAA[A/G]AGTACAATGGAGATA | 26054 |
rs368707586 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75627894 | ATGTGAGGCTGGTCT[C/T]GAACTCTGACCTCGT | 26054 |
rs368720464 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700549 | TGGAGTGCAGTGGCA[A/C]CATCTCGGCTCACTG | 26054 |
rs368722627 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638582 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTATATAT | 26054 |
rs368759740 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631751 | TATATGATCAAGAAA[A/G]CCTACAATACTTACT | 26054 |
rs368792602 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688528 | TTGGCCATCTTGGAA[-/C]CCGCCACCCCACCCC | 26054 |
rs368870806 | snp | C/T | 0.000151557 | 0.00870377 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711354 | TGACGATGGATTCCT[C/T]GCTGATGACAACTGC | 26054 |
rs368899568 | in-del | -/ACCCC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688543 | CCGCCACCCCACCCC[-/ACCCC]CCCGTCCAGGATTAT | 26054 |
rs368907825 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621047 | TGTTCTGATCTAGAG[C/T]TTTTCAGGTTGTCAA | 26054 |
rs368927758 | in-del | -/AAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666194 | ATATGATATATATAA[-/AAC]GTATATATGATATAT | 26054 |
rs368932775 | in-del | -/GT | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75711195 | CATACCACATCTCTA[-/GT]GTCTAATCACCTAAA | 26054 |
rs368965164 | snp | C/T | | | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713816 | GCAGTATGTAGAGAG[C/T]TTTTTTGAGGTGGGT | 26054 |
rs368978820 | snp | A/C | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675867 | TCCTCCAGAACCAGA[A/C]CATGATCCTGTAGAG | 26054 |
rs369030925 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653187 | AGGCCTGGGCCAGTC[C/T]GCCTGGCTAATTTTG | 26054 |
rs369068184 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697776 | AAATAATACCATTTT[C/T]AAAAATATGGTGCTT | 26054 |
rs369078810 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618361 | ATTTTTGCTAAAATT[A/G]TTCCAACTTTGGCCG | 26054 |
rs369079545 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630633 | GGAATTAAGAGAAAT[A/C/T]CTTTATTAAATTTAG | 26054 |
rs369080228 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599964 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATCG | 26054 |
rs369118745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75640138 | TTAAACATGAAAGGA[C/T]AAGCTAACTCTTCTG | 26054 |
rs369122577 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660654 | TTTTTTTTCCCCGAG[A/T]TGGAGTCTTGCTCTG | 26054 |
rs369142823 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697913 | CCAGAAAGGAGAAAC[A/G]ATGGTTGGATTTATG | 26054 |
rs369154009 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690198 | TTACAGGCATAAGCC[A/C]CTGCTCCCAACCAGA | 26054 |
rs369170652 | snp | A/T | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715395 | TTCAGAATCCAATTC[A/T]CAGTTTTGAACTACC | 26054 |
rs369199183 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605720 | GGATCATGAATAATT[G/T]TTATATCTTTCTCAG | 26054 |
rs369219835 | snp | A/G | 8.5873e-05 | 0.00655203 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676025 | AGGATAAAGTTTGGA[A/G]TGATTGTAAAGGAGT | 26054 |
rs369249387 | snp | C/T | 5.46363e-05 | 0.00522639 | intron-variant | SENP6 | GRCh38.p7 | 6:75633537 | GTTGATAGATTGTCA[C/T]ATTATAGCATTTTTG | 26054 |
rs369296130 | snp | A/G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611607 | TAAAGCATAAGGAAC[A/G/T]TTTGGAACTACTTAT | 26054 |
rs369307665 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604799 | ATATTCCGGCCAGGC[A/G]TGGTGGCTCACGCCT | 26054 |
rs369317335 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75707924 | CTGAACTCAGGTGAT[C/T]CTCCTGCCTCAGCCT | 26054 |
rs369318056 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611123 | ATCAAGAACTAAATT[C/T]TGGAGACAAGATGAA | 26054 |
rs369356671 | snp | A/C | 0.000292451 | 0.0120888 | intron-variant | SENP6 | GRCh38.p7 | 6:75697381 | CATATAAGCTGGAGC[A/C]CTAGAAATATTTCAG | 26054 |
rs369403204 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653232 | GGCAGGGTTTCTCCA[C/T]GTTGGTCAGTCTGGT | 26054 |
rs369405641 | snp | C/T | 1.68457e-05 | 0.00290216 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75703044 | GAATGGCCTACAGAA[C/T]GAAAGTTTAAGTTCC | 26054 |
rs369429111 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699230 | ACTATACCTCTGCAT[G/T]GAAGTTATTATCAGT | 26054 |
rs369445637 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75692618 | GCGAGAGAGTGAGAC[-/T]TTATCTCAAAGAAAT | 26054 |
rs369559897 | snp | A/T | 0.000642192 | 0.0179076 | intron-variant | SENP6 | GRCh38.p7 | 6:75640657 | AGGTCTTGCCTCTTA[A/T]ATTTTTTTTCTTTTT | 26054 |
rs369588082 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661452 | CCTCTGTTTGTTTGT[C/T]TTTAAAGTTCAGGGG | 26054 |
rs369601032 | snp | A/G | 0.000150239 | 0.00866585 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697467 | AAAAACATGGACCCG[A/G]CACGTAGATATTTTT | 26054 |
rs369617806 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658298 | ATTATAGGTTTCTTA[A/G]GATGGTGTTGTATAT | 26054 |
rs369628360 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693973 | ATAAAAACTTAGAAC[A/C]AGGCCAGGCACGGTG | 26054 |
rs369639429 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676583 | TTCAGCTTAATTATG[A/C]AAAAATGTTAGCTAC | 26054 |
rs369643822 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655848 | TCGAACCTGTATATA[A/G]ATCACTCTTACCCAG | 26054 |
rs369679388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75604827 | CCTGTAATCCCAACA[A/G]TTTGGGAGGCCGAGA | 26054 |
rs369748108 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662912 | TTCTTGGAGACAGAA[G/T]TATTTTATATATAGC | 26054 |
rs369793549 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625697 | AACATGTTGAAACCT[C/T]GTCTCTACTAAAAAT | 26054 |
rs369803268 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684282 | AAGTTGCTTATCAGC[A/T]TAAGGAGATTTTGGG | 26054 |
rs369819665 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667332 | ATGGAAAAAGGTAAT[A/G]TGAACGATGTCAATA | 26054 |
rs369833944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693126 | CATTGTAGGCCAGGC[A/G]CAGTGGCTCACGCCT | 26054 |
rs369841989 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615300 | TTCTCCTGTGTCAGC[C/T]TCCCGAGTAGCTGGG | 26054 |
rs369860148 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684160 | TTCTCTTTGTAGCAA[C/T]TGTGAATGGGAGTTC | 26054 |
rs369878566 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645991 | AGTACACAAGTTCAA[A/T]TTGCAAGAGCACTGC | 26054 |
rs369918693 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629896 | TGATTAGCAGCAGAT[A/T]TGAGTGAGTTTTTTA | 26054 |
rs369920056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75640851 | ACATGTAATAATTGT[A/G]CATATTTATAGGATA | 26054 |
rs370016028 | snp | C/G | 3.33195e-05 | 0.0040815 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709603 | TGAAGATGAACTCGT[C/G]GACTTCTCAGAAGAT | 26054 |
rs370060982 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624391 | GTAAATTAGCCTTCT[A/G]TATGGGTTATTTTGC | 26054 |
rs370154406 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653144 | CAAGCGATTTTCCTG[C/T]CTCACCCTCCCGAAT | 26054 |
rs370179620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75616544 | ACAAGGTCAGGGGTT[C/T]GAGACCAGCCTGACC | 26054 |
rs370212328 | in-del | -/TG | 0.00874735 | 0.0655527 | intron-variant | SENP6 | GRCh38.p7 | 6:75650378 | GATATACTCTGAAAC[-/TG]TGCAAATACCCTGTT | 26054 |
rs370233754 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644495 | TTTTTTTTTTGTTTT[C/T]TTTTTCTTTGAGACA | 26054 |
rs370244586 | snp | C/T | 1.72311e-05 | 0.00293518 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75702678 | TGTTGTTTGTTTCCC[C/T]GGTTTGGAAAAACCA | 26054 |
rs370298246 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684721 | ATTTGCATATGTTGA[A/C]CCAGCCTTGCATCCC | 26054 |
rs370298337 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75638158 | TGTGCCACCACACCT[G/T]TCCCATTTTGAGAGA | 26054 |
rs370328442 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695027 | TTACAGGCACTCGCC[A/G]CCACACCCGGCTAAA | 26054 |
rs370360870 | in-del | -/CCCCCCCC | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601634 | ACGCCAGGTCTGCCA[-/CCCCCCCC]TGGGGCCCTGGGCGG | 26054 |
rs370361295 | in-del | -/ACT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641154 | AGTATCCACAGTTCT[-/ACT]CTCTATAATAAAAGG | 26054 |
rs370379424 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627006 | GTCTCACTCTGTTGC[C/T]CAGGTTGGAGTGCAT | 26054 |
rs370430119 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613285 | AAATTCAAATGTCAC[C/T]GCCCTTAAATAAAGT | 26054 |
rs370528274 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75607137 | AGGATTGCTTGAGCC[C/G]AGGAGTTGGAGACCA | 26054 |
rs370647143 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602967 | GGTTGGGTGCAACTG[C/G]GGACCAATCTAAGTA | 26054 |
rs370702962 | snp | A/G | 3.42912e-05 | 0.00414058 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633714 | ACATGTTGAGCAACA[A/G]TAAGAAATTGAGGTA | 26054 |
rs370713823 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652129 | TTGCAGTGAGCCACA[A/G]TCGCGCCACTGTCCT | 26054 |
rs370719224 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631537 | TACAGTGGTTTTTAC[A/G]TTTTTAAATGCTTGG | 26054 |
rs370731226 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691001 | GAGCCACTGTGCTCA[A/G]CCTAATTTTTTTTTT | 26054 |
rs370743086 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75683000 | TCTTCCACAATGGTT[A/G]AACTAATTTACACTC | 26054 |
rs370759063 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653138 | CGGGTTCAAGCGATT[C/T]TCCTGCCTCACCCTC | 26054 |
rs370794979 | snp | C/T | 0.000515914 | 0.0160528 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659344 | ACAGAAACGACACTG[C/T]AGTACCTATCAGCCT | 26054 |
rs370813391 | in-del | -/AAATAAATAAAT | 0.0505635 | 0.150748 | intron-variant | SENP6 | GRCh38.p7 | 6:75662054 | TGAATCTCCTTCTCA[-/AAATAAATAAAT]AAATAAATAAATAAA | 26054 |
rs370825373 | snp | A/G | 1.66696e-05 | 0.00288696 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621619 | GTGAAGGAGATACAG[A/G]TAAAGAGTAAGGATT | 26054 |
rs370858820 | snp | C/T | 2.05797e-05 | 0.00320772 | intron-variant | SENP6 | GRCh38.p7 | 6:75663561 | CTTATATCAATCCAG[C/T]ATTTTTCAGATATAT | 26054 |
rs370872779 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623515 | TTTCTTTGTTTCTCT[A/T]TCTTTCTACCCTTAA | 26054 |
rs370896374 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75627908 | TCGAACTCTGACCTC[A/G]TGATCTGCCCGCCTT | 26054 |
rs370909523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686803 | CTTTGTGGGTAATCA[A/G]CCTTTCTCTCTGGCT | 26054 |
rs370910395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627833 | GGCATGGTGCCACCA[C/T]GCCCGGCTAATTTTT | 26054 |
rs370918127 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75713450 | ATAATATGCCACTTT[A/T]AATCCTTTTATGCAT | 26054 |
rs370921527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75714542 | TCATGGTTGTTTCCC[A/G]AAAACATAAATCTAA | 26054 |
rs370942848 | in-del | -/TGTGTGTGTGTATATATATATA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638581 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTATATATATATA]TATATATATATATAT | 26054 |
rs370962421 | snp | A/G | 0.000169986 | 0.00921758 | intron-variant | SENP6 | GRCh38.p7 | 6:75678767 | TTCAGTTGTGTATAT[A/G]TATATAGATTTGTTT | 26054 |
rs370968423 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657395 | TCTGTAACCTCAGAT[G/T]TTAGATCTCGGGAGA | 26054 |
rs371021968 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660601 | CTTCTCTGCTTTTTA[A/G]TATAACAAGATGGTC | 26054 |
rs371078321 | in-del | -/CTTTTCTTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653029 | TTCTGTTACTTTTTT[-/CTTTTCTTT]TTTTTCTTTTTTGAC | 26054 |
rs371123845 | snp | A/G | 1.69132e-05 | 0.00290797 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677204 | CCTGTACAAGAACCT[A/G]TGAAGAGAGCATCAA | 26054 |
rs371167576 | in-del | -/C | 0.0119091 | 0.0762411 | intron-variant | SENP6 | GRCh38.p7 | 6:75701771 | CAGCCTCCCAAGTAG[-/C]TGGGACTACAGGCGC | 26054 |
rs371174203 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665005 | TCAAAGTGATATTTA[G/T]GCTGGGCGCATTGGG | 26054 |
rs371184543 | snp | A/T | 6.65657e-05 | 0.00576875 | intron-variant | SENP6 | GRCh38.p7 | 6:75713661 | GTATTCTTAATATAT[A/T]TGAATTATTGCAGGT | 26054 |
rs371189996 | snp | A/C/T | 6.63625e-05 | 0.00575993 | intron-variant | SENP6 | GRCh38.p7 | 6:75713486 | ATATTATGAAGTATT[A/C/T]GACTTTTGGTCATTT | 26054 |
rs371248793 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75639950 | CTATTTCTGTAACAA[C/T]AGTAGTCTCCTCCTT | 26054 |
rs371284427 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607939 | AACGATTGGCATTCC[A/G]TGGAATATGAACAGG | 26054 |
rs371301417 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600378 | AAAGCAAAGATTTAT[C/T]TTTAATTAAAAAAAC | 26054 |
rs371315357 | snp | C/T | 3.32745e-05 | 0.00407875 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634730 | CGCAAAATACGTCAT[C/T]ATGTTCTGGAACTGT | 26054 |
rs371350441 | snp | A/G | 1.66646e-05 | 0.00288652 | intron-variant | SENP6 | GRCh38.p7 | 6:75715377 | TACGCATTTAATTGT[A/G]TTTTCAGAATCCAAT | 26054 |
rs371355492 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680229 | TCTGGCTCACAAGAC[C/T]TGCTAAATGATGTTG | 26054 |
rs371368432 | in-del | -/TC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648723 | CTCTTCAGCATTTAT[-/TC]TGTTATACCTTAAAT | 26054 |
rs371369893 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623642 | AAACTATGATCCATG[A/G]GCTAATCTTGCGTGC | 26054 |
rs371378041 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604312 | TTTATAAAGCAAGCA[A/C]ACGGTAACTTCTTTA | 26054 |
rs371400035 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653182 | ATTACAGGCCTGGGC[C/T]AGTCTGCCTGGCTAA | 26054 |
rs371417211 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636856 | CTTCTCCTAAATTTT[A/C]TTATTTTCTGAAGTC | 26054 |
rs371421182 | snp | A/G | 0.000100005 | 0.00707054 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695813 | AAATAGATACTTGGT[A/G]CTTGAAAAACTGAAG | 26054 |
rs371436730 | snp | A/G | 1.66988e-05 | 0.00288949 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663241 | GCAAAGAAATTGCAG[A/G]CAAGCTATTACTTTG | 26054 |
rs371444018 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641922 | TCAATTAAAAAAAAA[A/G]ACGAGTCTATAGTGC | 26054 |
rs371452994 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606797 | ATCCAAAAAAAAAAT[A/C]TGAAATCTGAAACAT | 26054 |
rs371470340 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700556 | CAGTGGCACCATCTC[A/G]GCTCACTGCAATCTC | 26054 |
rs371549895 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619004 | TATGTTTGCTTGTGT[C/T]AGTCACTTTCAGGCT | 26054 |
rs371550363 | snp | A/G | 3.5536e-05 | 0.00421506 | intron-variant | SENP6 | GRCh38.p7 | 6:75634840 | TTGTCTTTGGTTAGT[A/G]TATACATGGCATCTT | 26054 |
rs371557491 | snp | A/G | 6.78081e-05 | 0.00582232 | intron-variant | SENP6 | GRCh38.p7 | 6:75659412 | CCCATTTAGAGGTAA[A/G]TAGAGAAATTATTCT | 26054 |
rs371571007 | in-del | -/TA | 0.0903818 | 0.195857 | intron-variant | SENP6 | GRCh38.p7 | 6:75626339 | TGTGGCTTAGCTTTT[-/TA]TATATATATATATAT | 26054 |
rs371593970 | snp | A/G | 0.000169986 | 0.00921758 | intron-variant | SENP6 | GRCh38.p7 | 6:75675826 | ATATTACCCTCTTAA[A/G]AATTATTTTTCCATT | 26054 |
rs371609709 | in-del | -/GT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693572 | ATTAATATAAACTGT[-/GT]CTTGATCTGACTCAC | 26054 |
rs371621555 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653155 | CCTGCCTCACCCTCC[C/T]GAATAGCTGGGATTA | 26054 |
rs371748608 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684045 | AATGGAATATTCTTC[C/G]ATTTGTTTGTGTCCT | 26054 |
rs371776397 | snp | C/G | 1.65853e-05 | 0.00287964 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702901 | GAAGAAAGTGACCCT[C/G]GTTATAAGAGAAACA | 26054 |
rs371784002 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75628795 | GGCAATCTCGGCTCA[C/G]TGCAGCCTCTTCCTC | 26054 |
rs371860547 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654323 | AAAAGCTTTGCACCT[A/G]ATGAGGATGGAATGC | 26054 |
rs371874764 | snp | C/T | 3.33039e-05 | 0.00408055 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663285 | GACCATTATTAAGAA[C/T]GTCAATTCATCAGAA | 26054 |
rs371879898 | snp | A/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620112 | AAAAAAAGAGGAAAA[A/T]AAGCTTTCCTAATGG | 26054 |
rs371916884 | snp | A/G | 1.83538e-05 | 0.00302929 | intron-variant | SENP6 | GRCh38.p7 | 6:75623997 | TTCTTCTTTTACATT[A/G]TATACAAAAAAATTG | 26054 |
rs371941676 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634023 | ATTTGAAGAAGCACA[A/G]TAGAGTGGTGTGGTC | 26054 |
rs372036898 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75629791 | GTTAATAAGTTAATA[A/G]AGTAAAAATTAATAT | 26054 |
rs372050433 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636500 | AGATGAGGTGCATAA[A/G]GATGAATATGATAAA | 26054 |
rs372058034 | in-del | -/CAA | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75708984 | ATTAGCTTCTTTCAG[-/CAA]AATAGTTGCTTATTA | 26054 |
rs372060537 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669297 | GGAGGTGGAGGTTGC[A/G]GTGAGCTGAGATCAT | 26054 |
rs372094515 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75639546 | GTAAATTATGCTTTG[C/T]TTACAGTTAGTTCCA | 26054 |
rs372098916 | in-del | -/AACTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608684 | TTGGATAGATTACTT[-/AACTT]CTCTGTTTTCTCAGC | 26054 |
rs372111371 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677596 | AATGGATTGGTTACC[C/T]TGTGTCTTACGTTTG | 26054 |
rs372131851 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663833 | TTGTGGGGGGGGGGG[-/T]GCCTAAAATAACATA | 26054 |
rs372184903 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618259 | GTCCCTTCTTTCCAT[G/T]TATTTATTTATTCAT | 26054 |
rs372207525 | snp | C/T | 0.000596797 | 0.0172639 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715498 | GAAGCTACAGGAAGA[C/T]CAGAGCAAAGAGAAA | 26054 |
rs372278833 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75665967 | AGGAGGCGGAGTTGC[A/G]GTGAGACAAGATCGC | 26054 |
rs372321074 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634340 | CAACCTCCGCCTCCC[A/G]GGTTCAAGTGATTCT | 26054 |
rs372343924 | in-del | -/ATTATA | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75658574 | TCAAATCATTTAAAC[-/ATTATA]ATTATATTTGTAATG | 26054 |
rs372365575 | snp | C/G/T | 4.97701e-05 | 0.00498828 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623911 | GTAGTGGGACAAATC[C/G/T]GCTCAGTGTGGATGA | 26054 |
rs372371869 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615217 | TTTGAGTCTTGCTGT[C/G]TCGCGCAGGCTGAAG | 26054 |
rs372409080 | snp | A/G | 0.000167986 | 0.00916322 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715473 | GAGAAGAAATCCGAA[A/G]CATAATTCTGAAGCT | 26054 |
rs372437973 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622577 | AAAACAAAAACAAAC[A/C]AAAAAACATTGTTTT | 26054 |
rs372446212 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610761 | AGTAGTATGAAAACA[C/G]CTATGTTCTGATCTT | 26054 |
rs372450606 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639220 | GATAGGACAGACTAG[A/T]TTTAAACTTTTATGT | 26054 |
rs372461131 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653177 | CTGGGATTACAGGCC[C/T]GGGCCAGTCTGCCTG | 26054 |
rs372461786 | in-del | -/TATA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666198 | GATATATATAAAACG[-/TATA]TATGATATATATAAG | 26054 |
rs372464987 | in-del | -/GTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712106 | GAAGGCTGTGGAGTA[-/GTA]ACCCAAGGCAGACGT | 26054 |
rs372502636 | snp | C/T | 0.00172671 | 0.0293321 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647740 | TTTTAGGAAAGAATA[C/T]CCACCTCATGTCCAA | 26054 |
rs372524294 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648487 | AGGTTTTTCTGATAG[C/T]TTAGAATGTGCTTTT | 26054 |
rs372547197 | snp | A/G | 0.000175984 | 0.00937876 | intron-variant | SENP6 | GRCh38.p7 | 6:75677283 | TTTTAATTTAAAAAT[A/G]TTCTTAAATTGTGGG | 26054 |
rs372560560 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650274 | TTGGTAGTGTTAACC[A/G]TGATCATTTGGTTAA | 26054 |
rs372594339 | snp | A/G | 0.000171985 | 0.00927162 | intron-variant | SENP6 | GRCh38.p7 | 6:75640735 | AAGAAATTAGAGCAT[A/G]GATATAGTGGTAAAA | 26054 |
rs372602888 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701965 | TCTTTAAGATGGATA[A/G]CTTTCCATCTTTTTA | 26054 |
rs372661703 | snp | A/G | 1.66147e-05 | 0.0028822 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663324 | GACAGAAGTCACAAA[A/G]CACAGGATTAACAAC | 26054 |
rs372678397 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | SENP6 | GRCh38.p7 | 6:75604482 | CTAAAAATACAAAAA[G/T]TAGCCGTGTGTGGTT | 26054 |
rs372757071 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653140 | GGTTCAAGCGATTTT[C/G]CTGCCTCACCCTCCC | 26054 |
rs372759562 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638395 | TTCCCCGGTTTTATG[C/T]TTTATTTTAACATGA | 26054 |
rs372765480 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692710 | GTGCCTGAGCCCCAC[A/G]TCCCTCGCCCCCCAT | 26054 |
rs372951963 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655611 | TATTTTGAGACTCAT[C/T]CATCCTGGTGCTTGC | 26054 |
rs372955991 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75635696 | CTTAAAAGGACAAAT[G/T]ACTGTGCAGACCAAA | 26054 |
rs372986825 | snp | A/G/T | 0.000218146 | 0.0104417 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621492 | TTTATATTGAATAGC[A/G/T]CTATTAATGAATACT | 26054 |
rs372988415 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667464 | GAACAAAGGATAAGA[A/G]TGGACAAAAAGAAAA | 26054 |
rs373000177 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627027 | TGGAGTGCATGGTGC[A/G]ATATCGGCTCACTGC | 26054 |
rs373002100 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698736 | AAGGTTTTGGCTGGG[C/T]GTGGTGGCTCACGCC | 26054 |
rs373018161 | snp | G/T | 1.77881e-05 | 0.00298223 | intron-variant | SENP6 | GRCh38.p7 | 6:75633566 | TGACTCATATTTCTG[G/T]ATCTTTTTTTACAGT | 26054 |
rs373023768 | snp | C/T | 1.70411e-05 | 0.00291895 | intron-variant | SENP6 | GRCh38.p7 | 6:75709638 | ATAACCAGGTAAAAC[C/T]TAATGCTTGGCAAAA | 26054 |
rs373023926 | snp | A/G | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670653 | AAAGTTCCTTTGACA[A/G]TGTCATTTTAAACTG | 26054 |
rs373031139 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630741 | TGCTTCTTTTAAGGG[A/T]TTTATATCTTTTGTT | 26054 |
rs373034380 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656715 | ACTATCAATCATTTA[C/T]CATTTCTCCTCATGA | 26054 |
rs373088891 | snp | C/G/T | 6.8921e-05 | 0.00586998 | intron-variant | SENP6 | GRCh38.p7 | 6:75697412 | AAGCTTATAATTTAT[C/G/T]TCTTTCTTACAGAAT | 26054 |
rs373092067 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684207 | TCTGTTTATCTGTTA[A/T]TGGTGTATAGGAATG | 26054 |
rs373092766 | snp | A/T | 3.73343e-05 | 0.00432039 | intron-variant | SENP6 | GRCh38.p7 | 6:75663554 | AATATTGCTTATATC[A/T]ATCCAGTATTTTTCA | 26054 |
rs373124699 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652710 | AAAAAAAAAGAAAAA[A/G]AAAAAAAATGCCTTG | 26054 |
rs373138316 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681327 | TGGCCATGTAAGATG[G/T]ATGTCCTTCCTCTTC | 26054 |
rs373139824 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698211 | AAGGATGTTTCAAAG[A/G]ACCTGTGACAGAATC | 26054 |
rs373143615 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631012 | GCTGCTATTTAATCC[A/G]TACATTGGATTTTTT | 26054 |
rs373150600 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661331 | TGCCAACCTAAGTTT[G/T]GCTCAGGCCATGCTG | 26054 |
rs373177804 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601146 | TTTAAAGAACGATAC[C/T]GAAAGACAAGAAAAA | 26054 |
rs373194096 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616383 | TAATTTATTTTTTCT[C/T]TCACTGGAAATTATC | 26054 |
rs373236548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75653289 | CCCCGCCTCGGCCTC[C/T]CAAAGTGGCGGGATT | 26054 |
rs373237452 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699347 | AGAGAGCTTGTTTTT[G/T]TTTTTGCTTTTTTTT | 26054 |
rs373240602 | snp | C/T | 0.000169986 | 0.00921759 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663444 | ATGGAAAAGTCATTT[C/T]ACCTGGGGCAAAAAT | 26054 |
rs373242974 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667338 | AAAGGTAATATGAAC[A/G]ATGTCAATAGACAGT | 26054 |
rs373268066 | snp | A/T | 7.89962e-05 | 0.00628426 | intron-variant | SENP6 | GRCh38.p7 | 6:75676081 | AAAACAGATTATAAT[A/T]GATAATAATAGATAC | 26054 |
rs373276113 | snp | A/C | 3.50453e-05 | 0.00418586 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677116 | AGTATCATTAATGAA[A/C]TTGGTATAAAGAATA | 26054 |
rs373289254 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653188 | GGCCTGGGCCAGTCT[A/G]CCTGGCTAATTTTGT | 26054 |
rs373338643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606296 | GATTTCATTAAGCCA[C/T]AGCTTGTGTTAAAAT | 26054 |
rs373396523 | snp | A/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679331 | AGATTACCTGAGCCC[A/G]TGAGTTCGAAGTTGC | 26054 |
rs373435139 | in-del | -/TT/TTT | 0.375399 | 0.216275 | intron-variant | SENP6 | GRCh38.p7 | 6:75673319 | TAGACCAATGTCTAC[-/TT/TTT]TTTTTTTTTTTTTTT | 26054 |
rs373476931 | snp | C/T | 3.33795e-05 | 0.00408517 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715595 | AGTATCTCAGATTGA[C/T]CATTTCTGTTACTTG | 26054 |
rs373530532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620637 | TTGAGAACATTCAGA[C/T]CATAGCACTGACCAT | 26054 |
rs373538199 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | SENP6 | GRCh38.p7 | 6:75713460 | ACTTTTAATCCTTTT[A/G]TGCATTTGTAATATT | 26054 |
rs373598331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667268 | TTTTACTGTAATACT[A/G]TGTTTCATTATGTTT | 26054 |
rs373627243 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688546 | CCACCCCACCCCCCC[-/C]GTCCAGGATTATATT | 26054 |
rs373658810 | snp | C/T | 3.39426e-05 | 0.00411948 | intron-variant | SENP6 | GRCh38.p7 | 6:75659413 | CCATTTAGAGGTAAG[C/T]AGAGAAATTATTCTT | 26054 |
rs373667868 | snp | A/G | 0.00057241 | 0.0169079 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659335 | GAAAGTACAACAGAA[A/G]CGACACTGTAGTACC | 26054 |
rs373690987 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637028 | TAGGACTGCAGGCAT[G/T]CACCACCGCACCAGG | 26054 |
rs373692800 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659195 | TTATGTTCTGATTAT[-/T]TTTTTTGCTGAAACA | 26054 |
rs373755219 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628154 | GACCATCTCTTAACA[A/G]TTAGAAATTTTATAT | 26054 |
rs373761729 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664642 | AAAGACCAGTGTTGA[A/G]AGAGAAACCATGCTC | 26054 |
rs373788740 | snp | A/G | 1.6588e-05 | 0.00287988 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702953 | TGAAAAAAATAAATC[A/G]TACTGCGAGTGAAAA | 26054 |
rs373815149 | snp | C/T | 3.37815e-05 | 0.0041097 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697517 | TACCCCTTAATGAAG[C/T]GTGAGTAAGAATTTC | 26054 |
rs373881663 | snp | A/G | 0.000265988 | 0.0115292 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715391 | TATTTTCAGAATCCA[A/G]TTCTCAGTTTTGAAC | 26054 |
rs373909253 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684915 | ATTCTGGCCTCATAA[A/G]ATGAGTTAGGGAGGA | 26054 |
rs373949306 | snp | G/T | 1.66239e-05 | 0.00288299 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621612 | GAAGAAAGTGAAGGA[G/T]ATACAGATAAAGAGT | 26054 |
rs373956925 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673778 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCAG | 26054 |
rs373999163 | snp | C/T | 1.6691e-05 | 0.00288881 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663247 | AAATTGCAGACAAGC[C/T]ATTACTTTGAATGAG | 26054 |
rs374046095 | snp | C/T | 1.68732e-05 | 0.00290454 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670662 | TTGACAGTGTCATTT[C/T]AAACTGTCGAAGTAT | 26054 |
rs374052845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75705418 | GGTGTGGTGGTGCCC[A/G]CCTGTAATCCTAGCT | 26054 |
rs374087556 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601941 | CAGAGGAGACCCACC[C/G]CTGTCCACATGGACA | 26054 |
rs374091491 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681983 | GAATGGAAAAGACAG[A/C]GGAAAGAATCAGTGA | 26054 |
rs374100771 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717334 | AACTATTCTAAAATG[C/G]CTACTTGTTTTTGCA | 26054 |
rs374174807 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632821 | AATTTTAAAAACTTA[C/T]TTACACCTTATTTCC | 26054 |
rs374276670 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75697912 | GCCAGAAAGGAGAAA[C/T]GATGGTTGGATTTAT | 26054 |
rs374280396 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603008 | AGACAGTTTCATTGA[A/G]GTGTGTTTTATACCC | 26054 |
rs374302110 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642706 | AGATAGGGAAGTATT[G/T]TTACCTGATAAATAT | 26054 |
rs374368413 | in-del | -/TGT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623169 | TGTCTTCGAAAACGT[-/TGT]ATTTGACTTTCTTTG | 26054 |
rs374396189 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699965 | GCCCAAGCTGGAGTA[C/G]AGTGGTGCAATCATA | 26054 |
rs374400367 | snp | C/G/T | 6.62691e-05 | 0.00575588 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713540 | ACTTATGGACTCACT[C/G/T]CGAGGCCCTTCTCGG | 26054 |
rs374419568 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652704 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAAAAT | 26054 |
rs374434862 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653149 | GATTTTCCTGCCTCA[C/G]CCTCCCGAATAGCTG | 26054 |
rs374443853 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660421 | TTATATCAGCATGTA[C/T]ATATGAATACTTTAC | 26054 |
rs374458449 | snp | G/T | 1.65814e-05 | 0.00287931 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666773 | AAGAGAAAGCATATC[G/T]CCTCAGCCTGCTGAT | 26054 |
rs374466768 | in-del | -/AT/TG | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619445 | ATTCCGTTGTGTCTA[-/AT/TG]TGTGTGTGTGTGTGT | 26054 |
rs374556603 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624967 | TGAGACTCCATCTCT[A/T]AAAAATAAAAAATTT | 26054 |
rs374561849 | snp | A/G | 8.31801e-05 | 0.0064485 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634731 | GCAAAATACGTCATT[A/G]TGTTCTGGAACTGTA | 26054 |
rs374587970 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75691065 | CCCAGGCTGGTCTCA[A/G]ATTTCTGGGCTGAAG | 26054 |
rs374587986 | in-del | -/AAGAG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659147 | AAAAATAAATAAGAG[-/AAGAG]TAATCCAGGATATAA | 26054 |
rs374608675 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708442 | ATAAATAAATAAAAA[C/T]CAGCTGGGCATAGTG | 26054 |
rs374615578 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75670242 | GTGAGCCACTGCTCC[C/T]GGCCAAGATCACATC | 26054 |
rs374629238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75603322 | ATGGGGAACAATATT[A/G]ATTTTTTTGGCCTAT | 26054 |
rs374631692 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631586 | TTCTATTTCATGACA[C/T]GTGAGCATAATATAA | 26054 |
rs374660252 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689391 | CAGTGTCATCTCACA[C/T]CCATTAGGATGGCTA | 26054 |
rs374680735 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665033 | GGGTCATGCCTGTAA[G/T]CCCAGCACTTTGGGA | 26054 |
rs374690407 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604326 | AAACGGTAACTTCTT[C/T]AGAGCATAAGCATAA | 26054 |
rs374711561 | in-del | -/CAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658974 | GAGACCTTGTCTCCC[-/CAA]AAAAAAAAAAAAAAA | 26054 |
rs374744474 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75708889 | ACAGAGCAAGACCCC[A/G]TCTCAAAAAATAAAA | 26054 |
rs374767322 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655276 | TGGGGTGACAGATGT[C/T]GCAGCCAGATCACCC | 26054 |
rs374768053 | snp | C/G | 1.69896e-05 | 0.00291454 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634807 | GTAAAAACAGCAGCC[C/G]AAAGGTAAGAATTCT | 26054 |
rs374768767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691913 | CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCGGC | 26054 |
rs374775701 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701590 | ATTCTTAGAATGTTG[A/G]AAAAATCATATGACC | 26054 |
rs374899955 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715662 | TTGGGTATAGACAAT[A/G]AAGAACTGAAGTGCT | 26054 |
rs374944444 | snp | A/G | 1.94498e-05 | 0.00311841 | intron-variant | SENP6 | GRCh38.p7 | 6:75624009 | ATTATATACAAAAAA[A/G]TTGTTACCTCAAAAG | 26054 |
rs375002155 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600505 | CGATCTCCGTTCATC[A/G]CAACCTCCGCCTCCC | 26054 |
rs375017619 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651224 | TTCAGCCTGTTTTTT[-/T]GTATCCTTGTTAGAG | 26054 |
rs375017719 | snp | A/G | 0.000377858 | 0.0137399 | intron-variant | SENP6 | GRCh38.p7 | 6:75640638 | CAGTGATATATCAAC[A/G]ATGAGGTCTTGCCTC | 26054 |
rs375048001 | in-del | -/CT | 0.00755907 | 0.0610114 | intron-variant | SENP6 | GRCh38.p7 | 6:75678155 | TCCTCCAAGGAACCC[-/CT]GTTTCACTTAGCTTT | 26054 |
rs375072039 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698390 | TTATGATATGGCCCT[A/G]CTTTGTCTCATTCTA | 26054 |
rs375152334 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75691419 | GTTTAACTTCATCTT[A/T]TAGTTAAAGGAGTTC | 26054 |
rs375205740 | snp | A/G | 3.40205e-05 | 0.00412421 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633591 | TACAGTTAAATCGTC[A/G]ATCTGAAATTGTTGC | 26054 |
rs375223441 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645647 | AAATTAATGTAAATT[G/T]TCATTTTAGATCATC | 26054 |
rs375229450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605037 | GAGATCGCACCATTC[A/G]CACTCCAGCCTGGGC | 26054 |
rs375230509 | snp | A/G | 0.000184879 | 0.00961276 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697430 | TTTCTTACAGAATAC[A/G]GCAAAAACGGCATGG | 26054 |
rs375242004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653528 | CATTTTTATTTAACA[A/G]CATTATTTTATTAAT | 26054 |
rs375299224 | snp | A/G | 0.000169985 | 0.00921758 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677089 | GATCCTCCGGCAAAT[A/G]TGGTATTTGAAAGTA | 26054 |
rs375353979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75658898 | GATCACTTGAGCTAA[A/G]GTGTTTGAGATTAGA | 26054 |
rs375361033 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75638769 | GTGAGTATAAAAAAC[A/G]ACAGAGGCCGGACAT | 26054 |
rs375364687 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668617 | TTTGGAGAAGTGGAA[C/T]GTTGAATGTATAAGT | 26054 |
rs375379427 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613389 | CAGGGACTGTATGGA[C/T]TACACAGTGTAAGAT | 26054 |
rs375391977 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606798 | TCCAAAAAAAAAATC[A/T]GAAATCTGAAACATT | 26054 |
rs375397460 | snp | A/G | 0.000169986 | 0.00921759 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702851 | TGCTAAACAAAAAAC[A/G]TTGCATAGCTGTAAT | 26054 |
rs375412427 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75688577 | CTATTTAGTTTAAAC[-/TG]TGCCCCCATTTCAAG | 26054 |
rs375413449 | snp | A/C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688541 | GAACCGCCACCCCAC[A/C/G]CCCCCGTCCAGGATT | 26054 |
rs375461519 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716104 | TGTGTAACAGGAACA[A/G]AGTAACAGCCTTTCA | 26054 |
rs375490878 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666183 | ATAAAACGTATATAT[G/T]ATATATATAAAACGT | 26054 |
rs375535795 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610409 | AATGATGCAACAATG[C/G]ATAATCCATTATTGT | 26054 |
rs375546238 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661048 | ATTTGGGCACTAGTT[A/G]TGTTCATTCACATGG | 26054 |
rs375569038 | snp | C/G | 1.65781e-05 | 0.00287902 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702757 | TGTTCAACTGTAGAG[C/G]ACAGTTGTATTTCTT | 26054 |
rs375585667 | in-del | -/AAAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705546 | GAGACTCCATCTCAA[-/AAAT]AAATAAATAAATTAA | 26054 |
rs375606706 | snp | A/G | 0.000104803 | 0.00723811 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677049 | AGAAGAACAATATAT[A/G]ATTTTAATTTTTCAA | 26054 |
rs375646908 | snp | A/T | 0.000167986 | 0.00916322 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715475 | GAAGAAATCCGAAAC[A/T]TAATTCTGAAGCTAC | 26054 |
rs375684798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664879 | CCCTGTTCTCTTATA[A/G]TTTATGTGTAGCAGG | 26054 |
rs375689983 | snp | A/G | 0.000171985 | 0.00927163 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621649 | TTTTTTTTCCCTCAG[A/G]TGTTTTATAAGAATA | 26054 |
rs375710393 | snp | A/G | 1.73516e-05 | 0.00294542 | intron-variant | SENP6 | GRCh38.p7 | 6:75647691 | CATTTTGAAAACTGT[A/G]TTTCCTGTTAGAATA | 26054 |
rs375730723 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711706 | GAGACAGAGTCTTGC[A/T]CTGTCGCCCAGGCTG | 26054 |
rs375775760 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638937 | GTGGTGCACACTTGT[A/G]GTCCCAGCTGCTCAA | 26054 |
rs375780685 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666213 | ATATATGATATATAT[-/A]AAGTATGATATATAT | 26054 |
rs375800571 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644490 | CTTTTTTTTTTTTTT[G/T]TTTTCTTTTTCTTTG | 26054 |
rs375823933 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611536 | TGTTTCTCAAATTTC[A/G]TTGGTCTGTCTCACA | 26054 |
rs375825922 | snp | C/T | 0.000169986 | 0.00921759 | intron-variant | SENP6 | GRCh38.p7 | 6:75678788 | AGATTTGTTTATTTG[C/T]TTGCCTTCTAATTTT | 26054 |
rs375839662 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693264 | ACAGAAATTAGCTGG[G/T]TGTGGTGGAGGGTGC | 26054 |
rs375842271 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716982 | AACCAAAAAATATCT[A/G]TTGAGACACAGTAGA | 26054 |
rs375901068 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707342 | GGTCATTATTTTTTT[C/T]TTTCTTCTTCTTCTT | 26054 |
rs375932789 | snp | A/G/T | 0.000188375 | 0.00970351 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675871 | CCAGAACCAGACCAT[A/G/T]ATCCTGTAGAGATTA | 26054 |
rs375962622 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636158 | CATTTACATAAAAGA[G/T]TAGATTCAGTTCATA | 26054 |
rs375964199 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653184 | TACAGGCCTGGGCCA[C/G]TCTGCCTGGCTAATT | 26054 |
rs376016271 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653141 | GTTCAAGCGATTTTC[C/G]TGCCTCACCCTCCCG | 26054 |
rs376086972 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75625532 | ATTTTTCTTTTAAAG[C/G]CTTTTGAGTCTACTG | 26054 |
rs376091484 | snp | G/T | 0.000169985 | 0.00921758 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621537 | TTTATTTCAGCTTTG[G/T]CTAGATCAGAGTCTA | 26054 |
rs376121292 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651856 | AGACATGGAACCAGC[A/G]TGGAAAACACAATTA | 26054 |
rs376129013 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653134 | CTCCCGGGTTCAAGC[A/G]ATTTTCCTGCCTCAC | 26054 |
rs376129622 | snp | C/T | 4.99197e-05 | 0.00499573 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695823 | TTGGTGCTTGAAAAA[C/T]TGAAGAAGGAAGACG | 26054 |
rs376133355 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613940 | TGTATTGCATTGATT[A/G]TTATGTCCCATTTGT | 26054 |
rs376142312 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653158 | GCCTCACCCTCCCGA[A/G]TAGCTGGGATTACAG | 26054 |
rs376226928 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610264 | GCTCTTAGAAATGGT[C/T]ATACTATTCACGATA | 26054 |
rs376235220 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688181 | GTGAGCAAGGCTCCA[C/T]GGGCGTGGGAGCCGC | 26054 |
rs376254398 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648418 | CTGAGGCCTTTGTTT[A/G]TTTAAATAGCTCTGA | 26054 |
rs376275083 | in-del | -/AG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614909 | GTTGTTTTGAGACAG[-/AG]TCTCACACACTTTTT | 26054 |
rs376309996 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669335 | CACTCCAGCCTGTGC[A/G]ACAGAGCGAGACTCC | 26054 |
rs376373316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630369 | GCTGCTCGGCCAACA[A/T]TTTAGGTAATTTATC | 26054 |
rs376404897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691472 | TTATGGAATAGCAAC[C/T]AAACAGCTTCACCAG | 26054 |
rs376420938 | snp | C/T | 8.57832e-05 | 0.0065486 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677150 | TCTCCAATTTTTTTG[C/T]GAAAATTCCCTTTGA | 26054 |
rs376443438 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75713909 | AAAACACAATAAGCA[A/C]ATATTTTAAAGAGTT | 26054 |
rs376455496 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684941 | GAGGATTTCCTCTTT[C/T]TCTGTTGATTGAAAT | 26054 |
rs376458295 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711963 | CAGGCGTGACCCATC[A/G]CGCCCGGCCACAAGT | 26054 |
rs376490134 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75607758 | TGTTCTCTACAGATA[C/G]CAGCAAAAATGCTTC | 26054 |
rs376496246 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75675160 | TAACAAACCTGCACA[C/T]GTACCCCTGAACCTA | 26054 |
rs376503042 | snp | A/G | 6.66056e-05 | 0.00577047 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709601 | CTTGAAGATGAACTC[A/G]TCGACTTCTCAGAAG | 26054 |
rs376506154 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714942 | GTCATAATACTTGCC[A/G]TATTTCTTGTTTTAA | 26054 |
rs376558598 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630792 | CATTATCTCTGTGGA[C/T]TTTACCTTTCTACAT | 26054 |
rs376601021 | snp | C/T | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679827 | TTTTCTAGTTTCTTA[C/T]ACTGTGTTTCATTAA | 26054 |
rs376640031 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619557 | TTTAGCTTACTGTGA[A/G]TAATGCTGCTATGAA | 26054 |
rs376653986 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710140 | ACCTTCAGTTATATG[A/G]TACATGAGTACCAAA | 26054 |
rs376660436 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661695 | CCTAGACAAGGTTAG[C/T]GGTTTTTTCTTTCCA | 26054 |
rs376716656 | snp | A/G | 3.62937e-05 | 0.00425976 | intron-variant | SENP6 | GRCh38.p7 | 6:75703116 | AAAAAATTCAGAATA[A/G]TCTGGATTTTTTAAT | 26054 |
rs376722027 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664797 | AAAGTCAACGCATGA[C/T]TTTTGAATGCTTTTT | 26054 |
rs376746616 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653178 | TGGGATTACAGGCCT[A/G]GGCCAGTCTGCCTGG | 26054 |
rs376762689 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684250 | GCACATTGATTTTGT[A/T]TCCTGAGACTTTGCT | 26054 |
rs376799237 | snp | A/C/G | 1.65894e-05 | 0.00288 | synonymous-codon, utr-variant-5-prime, missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623912 | TAGTGGGACAAATCT[A/C/G]CTCAGTGTGGATGAA | 26054 |
rs376842832 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630939 | GTATATCTCTGTACC[A/G]TATTCTGAATAATTT | 26054 |
rs376914581 | snp | A/G | 0.000315745 | 0.0125608 | intron-variant | SENP6 | GRCh38.p7 | 6:75678546 | TTGAAACTTTTCCTA[A/G]TTGACTGTAAATTGC | 26054 |
rs376915194 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641135 | CCTACCCTTCCCAGC[C/T]TACAGTATCCACAGT | 26054 |
rs376953659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663843 | GGGGGTGCCTAAAAT[A/T]ACATAAAGTATGCAT | 26054 |
rs376969370 | in-del | -/AATAAAGAGTGGAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610906 | TGCATTACAGTTTTT[-/AATAAAGAGTGGAC]GAAACAGAACGGGAG | 26054 |
rs376978858 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631641 | AGTTTTCTTGGAAAA[-/C]CAGCCATGCTTATTT | 26054 |
rs376980734 | snp | C/G/T | 0.000144477 | 0.00849811 | intron-variant | SENP6 | GRCh38.p7 | 6:75697566 | AAATCATGTAAATGA[C/G/T]GGCAATTTTTAAATA | 26054 |
rs377015557 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610867 | TAGTTTTTGAAGATG[C/T]GTTTTTTCCCCCTCC | 26054 |
rs377040490 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674384 | TGGAGTGCAGTGGCA[C/T]AATCTTGGCTCATTG | 26054 |
rs377093294 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75715220 | TAGAAACTGTGTCTT[A/G]TATCTCCAATACCTA | 26054 |
rs377163914 | snp | C/G | 0.000371501 | 0.013624 | intron-variant | SENP6 | GRCh38.p7 | 6:75675514 | AAGCTTTCTTTACAC[C/G]AAAGCACTTTACAGG | 26054 |
rs377182405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672631 | AAAAGATGATTTGAT[A/G]TTTTCTTCTTGAACA | 26054 |
rs377202036 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75706501 | GATTTCTAGTGCCCT[A/C]ACCTACAAATTAATT | 26054 |
rs377205416 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689394 | TGTCATCTCACATCC[A/C]TTAGGATGGCTACTA | 26054 |
rs377235145 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649662 | GCTGGGATTACAGGC[A/G]CCTGCCACCAAGCCC | 26054 |
rs377259726 | snp | C/T | 1.65866e-05 | 0.00287976 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715555 | AGAAGCACCTTTAGG[C/T]GAAGGAACAGAACAA | 26054 |
rs377290043 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674354 | GAGATGATGTCTCAC[A/T]ATTTTTGCCCAGGCT | 26054 |
rs377321896 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606709 | CCTAAGAAATGCTCA[C/T]TGAATCAATTCAGAT | 26054 |
rs377338156 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626892 | CTTTTAACATTTACT[A/T]TTTTTTCCGTCTTTC | 26054 |
rs377365832 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615819 | TAGTGGCGAAGCCTT[C/G]TGAGCCTGAGTTTTG | 26054 |
rs377476270 | snp | A/G | 3.33056e-05 | 0.00408065 | intron-variant | SENP6 | GRCh38.p7 | 6:75713636 | GAACTATGTATATTT[A/G]TATATGTGTGTATTC | 26054 |
rs377489649 | snp | A/G | 1.67091e-05 | 0.00289038 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633651 | CATATGTAAGACGAA[A/G]CAAGTCTGAAAGTTT | 26054 |
rs377539784 | snp | C/T | 0.00018255 | 0.00955205 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75702729 | TTACCATGAAAATGC[C/T]GTCATACAGAAATGT | 26054 |
rs377559844 | snp | C/G | 5.00864e-05 | 0.00500407 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633634 | TGAATTCATCTTGAA[C/G]ACATATGTAAGACGA | 26054 |
rs377565481 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698829 | CAACCTGGCGAACAT[A/G]GCGAAACCTCGTCTC | 26054 |
rs377577840 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622283 | AGTTTTTTGGCCGGG[C/T]ACAGTGGCTCATGCC | 26054 |
rs377598819 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617690 | TTGTGTGATAGTGTT[A/G]TTACTATTACCTGAA | 26054 |
rs377641813 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673428 | TCACGGGTTCCGGCA[A/G]TTCTCCTACCTCAGC | 26054 |
rs377662361 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616988 | CCGTCCAATCCTCCT[A/G]TCCCAGTCTCCTGAG | 26054 |
rs377710101 | in-del | -/CT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630932 | TGAAGAAGTATATCT[-/CT]GTACCGTATTCTGAA | 26054 |
rs386407596 | in-del | -/GTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626143 | TTGTTGTTGTTGTTG[-/GTT]TTTTTTAATTTTGTT | 26054 |
rs386407597 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663808 | TCCTGCTGATAGTGG[-/G]TTTTTTTTTTTGTGG | 26054 |
rs386702798 | multinucleotide-polymorphism | CTGTTGCACTTTTTGT/GTGTTGCACTTTTTGC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647130 | TTGTAGCTCCCTGGT[lengthTooLong]AGTTCCCCTTCTGTG | 26054 |
rs386702799 | multinucleotide-polymorphism | CG/TC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674107 | CCAAAACATATAATG[CG/TC]AACATCCACGTATGC | 26054 |
rs397705606 | in-del | -/AT | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75666157 | ATATATAAAACATAT[-/AT]GATATATATATAAAA | 26054 |
rs397707194 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700172 | ACCTCAGCCTCCCAT[-/T]AGCACCAGGATTACA | 26054 |
rs397719795 | in-del | -/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75632675 | CTTGATGCTGTGCTT[-/T]GCATTACCTGGAAAA | 26054 |
rs397775597 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619030 | GGCTTTTTTTTTTTT[-/T]CCTTTTAAAAGCAGT | 26054 |
rs397787547 | in-del | -/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75625131 | TTTTTTTTTTTTTTT[-/T]CAGACGGAGTCTGGC | 26054 |
rs397796265 | in-del | -/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75644489 | CTTTTTTTTTTTTTT[-/T]GTTTTCTTTTTCTTT | 26054 |
rs397821253 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692477 | CATACAAAAAAAAAA[-/A]TTAGTTGGGCATGGT | 26054 |
rs397826346 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653671 | TTGTGTTTTTTTTTT[-/T]TAACTAGTTTATTTT | 26054 |
rs397834526 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638624 | tatatatatatatat[A/T]ttttttttttttttt | 26054 |
rs397885916 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630859 | CATTTAAAAAAAAAA[-/A]TCCGTAACCTATATT | 26054 |
rs397886050 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681475 | TTCTTTTTTTTTTTT[-/T]GGAGATGGAGTCTTG | 26054 |
rs397887004 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677005 | TTTTGTGTTTTTTTT[-/T]GGACTTATATTTATT | 26054 |
rs397887386 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653672 | GTGTTTTTTTTTTTT[-/T]AACTAGTTTATTTTG | 26054 |
rs397888024 | in-del | -/TTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691158 | TTTTTTTTTTTTTTT[-/TTT]CAAAGACAGATTCTT | 26054 |
rs397888163 | in-del | -/A | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601313 | AGTTAAAAAAAAAAA[-/A]GGCCTCACTTGTAAG | 26054 |
rs397953392 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636891 | TTTTTTTTTTTTTTT[-/T]AATTATAGAGATAGG | 26054 |
rs397954915 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682417 | TTCTTTTTTTTTTTT[-/T]AATTATACTTTAAGA | 26054 |
rs397956526 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607314 | CCAAAAAAAAAAAGG[-/G]TCATCAGCTGCTACA | 26054 |
rs397958016 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638256 | GTTTTTTTTTTTTTT[-/T]AATTTTAAGGCCACA | 26054 |
rs398002003 | in-del | -/A | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75613127 | TTAAAAAAAAAAAAA[-/A]GAAAAGAAAACTATG | 26054 |
rs398002004 | in-del | -/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75617290 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCGC | 26054 |
rs398002005 | in-del | -/AAAAAAAAAAA | 0 | 0 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620093 | GCCTCAAAAAAAAAA[-/AAAAAAAAAAA]GAGGAAAATAAGCTT | 26054 |
rs398002006 | in-del | -/A | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75652703 | AAAAAAAAAAAAAAA[-/A]GAAAAAGAAAAAAAA | 26054 |
rs398002007 | in-del | -/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75669950 | CAGATTTTTTTTTTT[-/T]AAGAAGGAATTTCGA | 26054 |
rs398002008 | in-del | -/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75707381 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC | 26054 |
rs398065964 | in-del | -/TTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638254 | TTTGTTTTTTTTTTT[-/TTT]AATTTTAAGGCCACA | 26054 |
rs398085037 | in-del | -/A | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601312 | AAGTTAAAAAAAAAA[-/A]AGGCCTCACTTGTAA | 26054 |
rs398085038 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669949 | TCAGATTTTTTTTTT[-/T]TAAGAAGGAATTTCG | 26054 |
rs398085039 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677004 | CTTTTGTGTTTTTTT[-/T]TGGACTTATATTTAT | 26054 |
rs398094319 | in-del | -/AG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689218 | CAACCTGGGTGACAG[-/AG]CAAGACACTATATCC | 26054 |
rs398110305 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607913 | TTGAACTAGAGCACA[-/A]GCTTCTCCCAAACGA | 26054 |
rs527239677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75661240 | CCCTTCTCCAGAGGT[A/G]AGTAACTTGACTCCC | 26054 |
rs527278076 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611613 | ATAAGGAACATTTGG[A/T]ACTACTTATCTCATG | 26054 |
rs527289765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708620 | ATAAGTGAGGCCAGG[C/T]ACGGTGGCTCATGCC | 26054 |
rs527291752 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75700855 | TTGAGATGTGACTTT[A/T]TAAATAAAATAAAAT | 26054 |
rs527328371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654723 | GTCTGGGTACTTATT[G/T]TTCAGCGTATTAGTA | 26054 |
rs527354520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612363 | TATATTTCTAAGTTA[C/T]GTTTTTCTCATATTC | 26054 |
rs527428616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694525 | CCATAAAGAAGCCTA[G/T]TACCCATTAGCAATC | 26054 |
rs527468821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674261 | TCCTAGGCACAAGCA[A/G]TCCTTCCACCTCAGG | 26054 |
rs527498358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624871 | AGTGTAGTGGCTCAC[A/G]CCTATAATCCTAGCA | 26054 |
rs527504998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633292 | CTTACTTTTTACTCT[C/T]TGGAGAAAGCTATCC | 26054 |
rs527528864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674932 | CTTGTTTTTTAATAC[A/G]TTTCAAAATACTTGC | 26054 |
rs527542241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75617573 | AGGAGCCACTGTGCC[C/T]GGCCGGTTTAGAGAA | 26054 |
rs527600231 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75668875 | GTACTGTCTTTGATG[A/T]TGCTCCATGGAGGGT | 26054 |
rs527664571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676771 | GTAAATTAGTTACAT[A/T]CGTGAATAGATTTGT | 26054 |
rs527668277 | snp | C/G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616784 | TTGTGTGTAAAGAAC[C/G/T]CCAGTTCCTTTAGTG | 26054 |
rs527670154 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651419 | GAGTACAGTGACATG[A/G]TTATGGCTCACTGCA | 26054 |
rs527691992 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718722 | TAGCCCAGCCCTACC[A/G]TCTTAATTCTTAGAA | 26054 |
rs527702766 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75626920 | TTCTGGGTTTTTTTT[C/T]CCCTCTGCAACAGCT | 26054 |
rs527731738 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648546 | TTGGGTGAAAATCTT[C/T]TGTGCATGTATTGAA | 26054 |
rs527732371 | snp | A/G | 0.000315167 | 0.0125493 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670606 | TAAAGTGTTTTCTCA[A/G]GAACCTCCAGATGCT | 26054 |
rs527737262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619868 | GGCTGAGGCAGGGAG[A/G]ATGGATTGAGGCTGG | 26054 |
rs527792427 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75613833 | ACAATACTATAATCT[A/G]CAAACATTTTTCCAC | 26054 |
rs527796348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671051 | CTGTAGTGAGTGAAT[G/T]AAGATTCCAGAAGTT | 26054 |
rs527809150 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619799 | TCCATTTTTAAAAGT[A/G]AATAATAGCAGCCAG | 26054 |
rs527809755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75702497 | TGCTGGGATTACTGG[C/T]GTGAGCTACTGCGCC | 26054 |
rs527816827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710417 | ATCCTACAGCATACC[A/G]TTTTGTTAATTCTCT | 26054 |
rs527854393 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698919 | AGGAGGCTGAGGCAG[A/G]AGGATCGCCTGAACC | 26054 |
rs527885130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641512 | AGAGAATTTTGTGAT[C/T]AGTCTTCTATCATTA | 26054 |
rs527940746 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75682669 | TGTTTGGTTTTCTGT[A/C]CTTGTGATAGTTTGC | 26054 |
rs527947424 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689079 | CTCAAGAAAAAAATT[A/C/T]AGCTGGGCATGGTGG | 26054 |
rs527968220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634246 | GCTCAGTAACTTTCA[A/G]GTCAGTGGCAAAATC | 26054 |
rs528000027 | snp | A/G | 1.74995e-05 | 0.00295795 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676038 | GAATGATTGTAAAGG[A/G]GTAAATAAATTAACA | 26054 |
rs528052661 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627405 | ATTTCCTGAAGTGCT[A/G]TTTTTTAGGTGTTTT | 26054 |
rs528058285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679802 | TCAGTATGCATAGTT[C/T]TCTGTAATATTTTCT | 26054 |
rs528070356 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663552 | TTAATATTGCTTATA[G/T]CAATCCAGTATTTTT | 26054 |
rs528134469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673049 | AGCCAGGATGGTCTC[A/G]ATCTCTTGACCTTGT | 26054 |
rs528147300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75623104 | AAACAGTAATACAAC[A/G]TTTTACATTTTTGTG | 26054 |
rs528180315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673662 | GTGTGACTTACTTAG[A/T]TATTTCTAAATGACA | 26054 |
rs528198505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75666480 | TTATATTTGTATCAT[A/G]TTTTTTAAAAGATAC | 26054 |
rs528204436 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75706757 | ATACAGTGATTTCAC[-/AT]AGAGTCAACAAGTGT | 26054 |
rs528213368 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603252 | TAAACATTTGCTGTA[A/G]GTAGACTAAGCCAGC | 26054 |
rs528218048 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635750 | TATACAAGCTCTCTG[G/T]CCTACATATGGCAAA | 26054 |
rs528237905 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711832 | TGCGTGCCACCATGC[A/C]TGGCTAAGTTTTGAA | 26054 |
rs528238754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615807 | TTTGAAAGAAATTAG[C/T]GGCGAAGCCTTCTGA | 26054 |
rs528242272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75638515 | ATGCATTTTTTCTCA[A/G]GGATAAGAAAAATGA | 26054 |
rs528259024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650971 | GAATTTGAGGCACTT[A/C]GTATATTTTTTTATA | 26054 |
rs528288221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691571 | GGCTTTTTTTTGTTA[C/T]TGTGTTTTGTTTTTT | 26054 |
rs528296503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75644253 | TACATCAAAGGGAAA[C/T]GGGAGCCAACTAAAA | 26054 |
rs528318762 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708220 | GTGCATGCCACCATG[C/T]CCAGCTAGTTTTTGT | 26054 |
rs528326485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685021 | AGGCTGTGAATCCAT[C/T]TGGTCCTGGACTTTT | 26054 |
rs528336115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691888 | TGAGATGGAGTTTCA[C/T]TCTCGTTGTCCAGGC | 26054 |
rs528371124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644969 | TACTACAAAAAATAG[A/T]CTTTCACCACTGAGG | 26054 |
rs528377129 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75684611 | TTTTAGCATGAAGGG[A/T]TGTTGAATTTTGTCA | 26054 |
rs528389783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685563 | GCTTTAAATTAAGGT[A/G]ATTTAAATGTGTCCA | 26054 |
rs528408664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75638081 | TGGTCAGGCTGGTCT[C/T]GAACTCTTTACCTCA | 26054 |
rs528430613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629367 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 26054 |
rs528441608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691082 | TTTCTGGGCTGAAGC[A/G]ATCCTCCCACCTTGG | 26054 |
rs528453490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646049 | ATACATGCATGTATG[A/G]TTTACTGTCTCAGAT | 26054 |
rs528462704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653585 | GGGTGAATGTCAGGA[A/C]TGCCTACTGAAGTAT | 26054 |
rs528479907 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75646600 | CCAGCACTTTGGGAG[G/T]CTGAGACAGGCAGAT | 26054 |
rs528486677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686444 | CCTGTCATTATGATG[A/T]TCGCTGGTTATTTTG | 26054 |
rs528490780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639435 | AAAACAAGTTACTAT[A/G]TTTTTTTTCTTCATT | 26054 |
rs528590793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632324 | AAAACCATCGATAAA[A/G]GGGGACTACTATGTA | 26054 |
rs528621111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681332 | ATGTAAGATGTATGT[C/G]CTTCCTCTTCACCTT | 26054 |
rs528647468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667386 | TTGTAATGCAGATGA[A/C]ATAGTATTTTAATGT | 26054 |
rs528670296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705997 | GCTGGAGTGCAGTGG[C/T]GTAATCTTGTCTCAC | 26054 |
rs528729623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699259 | GTGCTTCCAGTCATC[C/T]TAGTGAGAGGTAGAA | 26054 |
rs528738691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75659849 | CTATTTGAGTTGAAG[G/T]TGCAAGCATGATGCC | 26054 |
rs528762213 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602443 | GCGGCGTCTACCCTC[C/T]TCCGGCGCGGCCCCT | 26054 |
rs528783667 | snp | A/C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681287 | TGTGTAGCACCTCCC[A/C/T]CTTTGCTCTCTGTTA | 26054 |
rs528792841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699844 | TTGTTATAGTAATTT[C/T]CAGAAACACAAATTT | 26054 |
rs528793889 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674891 | GCTTTCCATATATCT[A/G]TTCATCCCTGTATAT | 26054 |
rs528802220 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75709475 | TCAGCCTCATATACT[A/G]TGAGTGATAGACATG | 26054 |
rs528888548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649051 | GTGGCTCACACCTAT[A/C]ATCCCAGCACTTTAC | 26054 |
rs528890405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642241 | AGCAGACAAGATCCC[C/T]GCAGTCCTGTAGTTT | 26054 |
rs528957428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689729 | TTCAGTACGGTAACA[C/T]ACTATACAGGTGTAT | 26054 |
rs528977993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642714 | AAGTATTGTTACCTG[A/C]TAAATATTTGAGATT | 26054 |
rs528990454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635664 | TCAAATAGTGTTCAC[C/T]TGAGATGCTTGAGAA | 26054 |
rs529056069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662398 | CGTCAGCCTCCCAAT[A/G]TGTTGGGCTTACAGA | 26054 |
rs529155360 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609924 | TCCCTAGTAGCTGGG[A/G]TTACAGGCGCATACC | 26054 |
rs529155721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605060 | GCCTGGGCGAGGAGC[A/G]AAACTACATCTCAAA | 26054 |
rs529184356 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75656208 | GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 26054 |
rs529219474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664914 | AACAGATAAACAAGT[A/G]AACATCCGCAACAAG | 26054 |
rs529224263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703168 | TTAAAAAAAAATCAG[G/T]TTAATGACTGGGTGT | 26054 |
rs529236751 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611659 | TTAATTTCTGGCTTT[A/G]GAAGTTTGTGTGCTT | 26054 |
rs529238506 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75673119 | AGTGTGAGCCACTGC[A/C]CCCGGCCAATTGGCA | 26054 |
rs529272416 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75614299 | GAGACAGAGTCTGGC[C/T]CTGTCACCCAGGCTG | 26054 |
rs529272673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75652848 | TCAAAATGTTTTTCT[C/T]ATATTTTCTTCATAA | 26054 |
rs529291259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657978 | AATTTAATTAGAGTA[C/T]TAGAATGACAAAGTC | 26054 |
rs529312763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703864 | CCCCTAGGGTGCAAT[C/T]TTGAAATTGCAGTAC | 26054 |
rs529329829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658355 | TTTTATGTCTACATA[A/G]TCTTATTTTTAAAAA | 26054 |
rs529338817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696853 | TTGATCAAAAGATAC[A/G]CTTAAGAATTGGTAC | 26054 |
rs529340621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614806 | TTGCTGGGGAGAAAT[C/T]AGATGTTTGCTGAAG | 26054 |
rs529410013 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599966 | CTACTCGGGAGGCTG[A/G]GGCAGGAGAATCGCT | 26054 |
rs529423157 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654185 | GCACAGGTTGAGGCA[C/G]TGTGATCACGCCTCT | 26054 |
rs529449659 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75677749 | TAACTATTCATATAG[A/G]TAGGTAACTCTGAAG | 26054 |
rs529469612 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75636234 | TGAGTTAATTTGTAT[A/T]TAAGAAATAATCCTA | 26054 |
rs529469701 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627834 | GCATGGTGCCACCAC[G/T]CCCGGCTAATTTTTT | 26054 |
rs529492928 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652149 | GCCACTGTCCTCCAA[C/T]CTGGGCAACAGAGTG | 26054 |
rs529495366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684381 | TTTCCTAATTGAATA[C/T]GCTTTATTTCTTTCT | 26054 |
rs529505438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628391 | TCATTATAATTATTA[A/G]TGAACACTTGATCTA | 26054 |
rs529508740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671336 | ATGTGTTCTGTAAGC[C/T]TTTGTTTTATAATGC | 26054 |
rs529536572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678323 | TTAATTTCATGTAGA[C/T]AGTAGAGAGAGAAGT | 26054 |
rs529594889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645486 | GCACAGCATGGTGGC[A/G]CACACGTGTAATCCC | 26054 |
rs529598734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671926 | CAGCTCTATGAGAAT[C/T]CGGCAAATTTTTCTT | 26054 |
rs529609177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668104 | TGAAAAACAACAAAA[A/G]CAATCATAAGGATAA | 26054 |
rs529660279 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75711495 | GGACAGTTTTTTTTT[A/T]AAATAAATACTTAAG | 26054 |
rs529669357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668724 | TGAAGAATAGTTTGC[A/T]ATCGCAAGAGATTGG | 26054 |
rs529682224 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610969 | AGATGGTAAATTCAC[-/T]TTTCATTTTTAATAA | 26054 |
rs529768130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75700056 | GCTAGAACTACAGGC[A/G]CATGCCACAGGCCCA | 26054 |
rs529780172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653982 | TAATCCCAGCACTTT[A/G]GGAGGCCAGGGTGGG | 26054 |
rs529787206 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75700721 | AGTCTCCAACTCCTG[A/C]GCTCAAGCGATATGC | 26054 |
rs529788726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707968 | AGGATTACAGGTGCT[A/T]GGCCACTGTGCCCGG | 26054 |
rs529821560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611531 | TAAAGTGTTTCTCAA[A/G]TTTCATTGGTCTGTC | 26054 |
rs529873358 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636778 | TTAACTAAGATTGTT[C/G]CTTCCAGGGATTTAG | 26054 |
rs529877190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680572 | GAAGAGAAATTGAAG[A/G]GAAGTGAGAGCTTTA | 26054 |
rs529888832 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690424 | TTGAGGTCATTGTGC[C/G]AAGCACAGTAAGTCA | 26054 |
rs529890612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681259 | TCTCACAAGTTCTGG[C/T]TGTTTATAAAAGTGT | 26054 |
rs529942429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667547 | AACTGTATTCAATGG[A/T]CTTTAAAAATTGTTA | 26054 |
rs529951147 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75641456 | CTTAGAGTTAAAACT[G/T]TAAACATCAAGTGTA | 26054 |
rs529958917 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639437 | AACAAGTTACTATAT[A/T]TTTTTTCTTCATTTG | 26054 |
rs529991052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624827 | TAGCATGATATGCTT[C/T]AATTATTTAAAAAAA | 26054 |
rs530062420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616592 | TCTTTACTAAAAATA[A/C]AAAATTAGCCGGGCG | 26054 |
rs530103676 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674022 | TGAGACTCATTCTCA[A/G]ATAAATAAATGAATG | 26054 |
rs530132105 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75625680 | TCGAGACCAGCCTGG[C/T]CAACATGTTGAAACC | 26054 |
rs530142236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669870 | AGTTGAGTGGGTACT[C/G]TTACTCTGCATATTT | 26054 |
rs530155177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672007 | AGTACCCTGGAGATT[C/G]GAAGCAAATTATATA | 26054 |
rs530181421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708888 | GACAGAGCAAGACCC[C/T]GTCTCAAAAAATAAA | 26054 |
rs530204271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654676 | AAATACATAATCATT[A/G]TAAAGATAACAGTTT | 26054 |
rs530218071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75676732 | TATATCTTTAAGACT[A/G]TAGATTTAGATTTAT | 26054 |
rs530230862 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647974 | TAACCTGATACCTGG[A/C]ACAGTTGCACAGTTA | 26054 |
rs530257486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626832 | CTGATCTGAACATAG[C/G]ACCTTCACATATTTC | 26054 |
rs530283978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646664 | ACACAGTGAAAGCCC[A/G]TCTCTACTAAAAATA | 26054 |
rs530308980 | in-del | -/GA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685338 | AAAAACCAGCTCCTG[-/GA]GATTCATTGATTTTT | 26054 |
rs530311442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75603732 | GCCTGGAACACAGTA[A/G]GTACTCAGTGTTAGT | 26054 |
rs530371854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694439 | ATAATGATAACAGCT[C/T]TACTTAGATATAATA | 26054 |
rs530407003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678531 | TGCTTACCCTTTTTA[A/T]TGAAACTTTTCCTAA | 26054 |
rs530419617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647601 | TTTTGTTATTTTATA[A/G]TATCACTTTTTATAT | 26054 |
rs530423370 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696257 | TACCTGGAATTTATA[A/G]ATGTTCTGGGTCAAA | 26054 |
rs530454402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633402 | TTCCTACAAATTTGC[A/G]TTGTCTTTAGGAAAA | 26054 |
rs530512370 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658065 | ATTGGGATAGAGGAC[A/T]TCAGTTTAGGCAAGA | 26054 |
rs530535360 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75613484 | CAAGGAAACAAACTT[-/A]AAAAAAAAAGTTCTT | 26054 |
rs530538305 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633496 | GCTGTATGTTTTTAC[C/T]ACTTTTAAATGGTTT | 26054 |
rs530542974 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660735 | CCTCCCGGTTCAAGC[A/G]GTTCTTCTGTCTCAG | 26054 |
rs530543481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75636929 | TCTGTTGCCCAGGCT[A/G]TAGTGTAGTGTCTCA | 26054 |
rs530555613 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714456 | GATTTACTTGTTTAT[C/T]GTCGAGTGTCGCTAT | 26054 |
rs530568673 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75682648 | CTATGAGTGAGAACA[-/T]TGCTGTGTTTGGTTT | 26054 |
rs530571120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679036 | AATTCCATCTCTGCC[A/G]CTTACTGTGTGACAT | 26054 |
rs530607127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75696664 | GTATTTTTTGTGGAG[A/G]CAGGGTTTCACCATG | 26054 |
rs530644839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75627683 | TATGTAGCTTTCAGA[C/T]TGCTTTTTTTTTGAG | 26054 |
rs530668914 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75690831 | CTCCTGAGTAGCTGG[A/G]ACTACAGGCGCTCAC | 26054 |
rs530676059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622342 | GCAGGTGGTTCATTT[A/G]AGGTCAGGAGTTCAA | 26054 |
rs530706100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657942 | AGATTGAAACAGGAA[C/T]TTCTGCTTGCCAAAA | 26054 |
rs530732489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684540 | GCTGTGGGTTTGTCA[C/T]AAATAGCTCTTATTA | 26054 |
rs530745774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649858 | GACTTAGAGAAAATT[G/T]GCAAATTTAATACAG | 26054 |
rs530795001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609279 | CCCCAAAGGAAGGGG[C/T]GACTGAACAAGAGAA | 26054 |
rs530820282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75652707 | AAAAAAAAAAAAGAA[A/G]AAGAAAAAAAATGCC | 26054 |
rs530823688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643653 | CTTGAACCTGGGAGG[C/T]GAAGGTTGCAGTAAG | 26054 |
rs530838137 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708032 | TAAATAGTGTGCTTC[G/T]GAACACAAGAGTTAG | 26054 |
rs530873941 | in-del | -/AT | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75667248 | GTCATTTTGACAGAG[-/AT]ATATTTTACTGTAAT | 26054 |
rs530878593 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602363 | GCCTGGCCTGCCTTT[G/T]TATAGGCCCGTCTGA | 26054 |
rs530911650 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SENP6 | GRCh38.p7 | 6:75638537 | GAAAAATGAGCATTG[A/T]TGTGTCTTTGTGTGT | 26054 |
rs530917781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75692043 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCTCCATG | 26054 |
rs530978986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692733 | CCCCCCATCCTCCCC[G/T]CATCCCACTCCTCCC | 26054 |
rs530998590 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75602953 | TTTCAAATTGCTAAG[A/G]TTGGGTGCAACTGGG | 26054 |
rs531059007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658465 | CAGATTCTTCACTTA[C/T]GTTTTAGAAACATGT | 26054 |
rs531065682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615707 | GTTTAGGATCAAGTA[C/T]TCTGACTTCATAAAA | 26054 |
rs531078403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607812 | CCATTTCGCCTTAGC[C/G]AGTCTTTTATGTTAT | 26054 |
rs531089589 | snp | C/T | | | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718500 | GTGGACGTAAGTAAA[C/T]AGTTGAAGACCAAGT | 26054 |
rs531138113 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605750 | GCGGGAAGCCATTGA[C/T]GAGTTTGGCGCAAGG | 26054 |
rs531146327 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603144 | TGTAAAATAATTTAT[C/T]TGGAAAAAGAGTAAG | 26054 |
rs531156815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75666397 | ACTCTGAAATAGACC[C/T]ACTGTTCTTCTTGTA | 26054 |
rs531217505 | snp | A/G | 1.66449e-05 | 0.00288482 | intron-variant | SENP6 | GRCh38.p7 | 6:75647849 | ATTTCAAATTGCTGT[A/G]TGAAAAGTACAATGG | 26054 |
rs531262632 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SENP6 | GRCh38.p7 | 6:75698578 | GGCCTCAAGCCATCC[C/G]CCAACCTCAGCCTCC | 26054 |
rs531266381 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687852 | TTAGGCTACACAGGG[G/T]TCAGGGACCCACTTC | 26054 |
rs531303803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641653 | ACATTTCAAAGTAAA[A/G]TGATCATAATTGTTC | 26054 |
rs531320873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694736 | TTTCTATTTCAGATA[C/T]TTCATTGTATAAATG | 26054 |
rs531376350 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75656169 | GAGTGAGCCGAGATT[A/G]CGCCACTGCACTCCA | 26054 |
rs531390409 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75688547 | CCACCCCACCCCCCC[A/G]TCCAGGATTATATTC | 26054 |
rs531396023 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614225 | TCACTTAGTTAAGGT[A/C/G]GTGTTCACCAGATTT | 26054 |
rs531397749 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75655384 | TATCCCTTTCTAACC[-/A]AAATCCCCATGAAGA | 26054 |
rs531407467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604996 | GAGAATCACCTGAAC[C/T]CAGGAGCTGGAGGTT | 26054 |
rs531427977 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696077 | ACACTAAATAAATCA[C/G]TTCCATTTTCATTCT | 26054 |
rs531447471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689149 | GGAGGATCACTTGAG[C/G]CCATGACAAGAGTTT | 26054 |
rs531496896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75668970 | TTTTATTAGTGAGCT[A/G]AATAACCTCTCATTT | 26054 |
rs531534444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701378 | CTGTATCATAAGCAC[C/T]TACTTGATAGCTGGA | 26054 |
rs531562280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75671168 | TACTTTATCTTACCC[A/G]TCATACCTGTGTACT | 26054 |
rs531582626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661382 | TAGGTAAAGGAGGAG[C/G]AAAGCTCCTCCCTAA | 26054 |
rs531604146 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615629 | TAAGATTTTGTTTAG[A/G]TTTTATATCTGTCTT | 26054 |
rs531638286 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75681752 | ATATAAAGAAGAAAC[-/A]AATGGATGGGTCATG | 26054 |
rs531688724 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658461 | TTTACAGATTCTTCA[A/C]TTATGTTTTAGAAAC | 26054 |
rs531756037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642171 | TTCCAAGTATTTATC[A/G]AACCTGCTGTTACAG | 26054 |
rs531772227 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676892 | TGTTGTGTATCCACT[G/T]TATGTCAGACATTGT | 26054 |
rs531793311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613862 | ACTTTCATTAGTTGA[C/T]CTAAAAATGTTCCTT | 26054 |
rs531796574 | snp | C/T | 0.000586409 | 0.0171132 | intron-variant | SENP6 | GRCh38.p7 | 6:75711282 | TTAGGTTATTAGTTA[C/T]TTAGATTATATATTT | 26054 |
rs531832415 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75674469 | GGGATTACAGGCATG[-/C]CATTACCACGCCTGG | 26054 |
rs531860966 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75703738 | CTGCAGTCCAGCCTG[A/G]GTGACAGAGTGAAAC | 26054 |
rs531867517 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698882 | TGGGCGTGGTGGTGC[A/G]TGCCTGTAATCCCAG | 26054 |
rs531883803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75614269 | TACTATCTTTTTTTT[G/T]TTTTTTTTTTGTTTG | 26054 |
rs531948031 | in-del | -/AAAAT | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75643167 | GAGAAAAGAGGAAAC[-/AAAAT]GAAATAATAAACATA | 26054 |
rs531966562 | snp | A/G | 8.32452e-05 | 0.00645102 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634760 | TAGTTCATGGTAGAC[A/G]TTTTCATCATGCTCA | 26054 |
rs531986633 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620658 | CACTGACCATGGGGT[A/G]GATGTACTTTATTTG | 26054 |
rs532028646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667442 | AATTACAGGATAAAA[A/C]CAAAATGAACAAAGG | 26054 |
rs532059767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75627762 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 26054 |
rs532089150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668022 | TATACATGTCAGTGT[C/T]CATAGGAGTACAGAT | 26054 |
rs532105828 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75699337 | CTATAAATCAAGAGA[G/T]CTTGTTTTTGTTTTT | 26054 |
rs532135679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707074 | ATCACTTGTTTATGG[C/G]GGAATTGACTGCATC | 26054 |
rs532139894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645332 | AAATTAATGTAAATG[C/T]TGGCCAGGTGTGGTG | 26054 |
rs532159318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624183 | AATTGGTAATATACT[A/G]TGCATGGTTTTTCTG | 26054 |
rs532188808 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687986 | TGCCTATTTTTCAGC[C/T]ATGCCCTGCCCACAG | 26054 |
rs532199757 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75706099 | GGTGCGCACCACCTC[A/C]CCCGACCTGTTGAGC | 26054 |
rs532214460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75679932 | AGTTTGGTGGGAAAA[C/T]ACATTGTTATAAAGA | 26054 |
rs532220706 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75715313 | CTTATTTTTAACTTC[A/G]GAATGTTTCTGTGAT | 26054 |
rs532246904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686237 | GCCTTTTTTTGTTTT[A/C]CATTTGCTTGGTAGA | 26054 |
rs532274366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609791 | TTTTTGTTTTTTGAG[A/G]TGGAGTAGATGGAGT | 26054 |
rs532275464 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608821 | GGCATATAATAAGCA[C/T]TCCGTGTTACTTGAT | 26054 |
rs532285419 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75617330 | CCAGGCTGGAGTGCA[A/G]TGGCGTGATCTTGGC | 26054 |
rs532292973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639298 | GTTTTTCTGTCATTT[A/G]TCTAACCTATGTGTT | 26054 |
rs532312273 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75685636 | AGAACATCTTTATTT[C/T]TGTCTTCATTTCGTT | 26054 |
rs532316555 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661020 | TATCTTCTCCTTTAA[A/G]TGGAGGGAACATATT | 26054 |
rs532324883 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663670 | CCATCTTAAATAGTT[-/A]AAAAAAAACAAAAAA | 26054 |
rs532327247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680499 | GATTACATTTTAAGA[G/T]ATAGACCGGGAATAA | 26054 |
rs532386157 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669109 | AATCCCAGCACTTTC[A/G]GAGACTGAGGTGGGC | 26054 |
rs532429901 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75630360 | CAGGTTTGAGCTGCT[C/T]GGCCAACATTTTAGG | 26054 |
rs532509763 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716734 | AATGGTGTATACTTC[C/T]TTCAAATGAACTTTG | 26054 |
rs532513708 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75640318 | CAATGCTTCATTTTG[A/G]TATATTGGATTCGGT | 26054 |
rs532535579 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634468 | GGCTGGGCTGGTCTC[A/G]ATCTCCTGACCTCAG | 26054 |
rs532560936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75699959 | TCTGTTGCCCAAGCT[A/G]GAGTACAGTGGTGCA | 26054 |
rs532604138 | in-del | -/GAA | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75630918 | AATGGCTAATGGAAT[-/GAA]GAAGTATATCTCTGT | 26054 |
rs532622044 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75693267 | GAAATTAGCTGGGTG[A/T]GGTGGAGGGTGCCTG | 26054 |
rs532658901 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671262 | CTAGCCTTCTTAGTC[A/G]TTATTTTTTTCTCTA | 26054 |
rs532667105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75603006 | ACAGACAGTTTCATT[A/G]AGGTGTGTTTTATAC | 26054 |
rs532724223 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711776 | CTCCCAGGTTCAAGC[A/G]ATTCTCATGCCTCAG | 26054 |
rs532738796 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601166 | GACAAGAAAAATGCT[A/G]TCAGAGGACTACAAA | 26054 |
rs532754995 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599684 | GAGCGAGAAAGAGAG[A/G]TGAGAGATTCCTAGT | 26054 |
rs532759979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75642798 | AATCAGTGGCAATCA[A/G]TTAAGGCTGGGCAAG | 26054 |
rs532788005 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75684071 | GTCCTCTTTTATTTC[A/G]TTGAGCAGTGGTTTG | 26054 |
rs532853522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687041 | GGTACACCAATCAAA[C/T]GTAGATTTGGTCTTT | 26054 |
rs532863930 | in-del | -/TTTTTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691588 | TGTTTTGTTTTTTGT[-/TTTTTG]TTTTTGTTTTTGTTT | 26054 |
rs532889451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628440 | ATTTATAATTATTAA[A/G]TTTATTATGCAAAAT | 26054 |
rs532922537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649807 | CGCGTCAGCCACCGC[G/T]CCTGGCCCTTAACCT | 26054 |
rs532938196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690718 | TTTTTTTTGAGATGA[A/G]AGTCTCGCTCTGTCA | 26054 |
rs532948294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75643614 | GTAATCCCAGCTACT[C/T]GGGAGGTTGAGACAT | 26054 |
rs532953549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703226 | TTTGGGAGGCCAAGG[C/T]AGGAGGATCACTTGA | 26054 |
rs532994132 | in-del | -/ATATG | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75666155 | ATATATATAAAACAT[-/ATATG]ATATATATATAAAAC | 26054 |
rs533005410 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75684433 | GAACTTCCAACACTA[A/T]GTTGAATAGGAGTGG | 26054 |
rs533028744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696045 | TACTTTTTAAATTCT[C/G]CAGCCAGGAAGAGAA | 26054 |
rs533035194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636300 | AAACTGTATAATCAA[A/G]TCAGCAGGACAGATT | 26054 |
rs533053150 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654900 | TAACACTTTTCTGTT[C/G]TTGTTTTATGACATG | 26054 |
rs533089627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696619 | AGTAGCTGGGACTAA[A/G]GCACACGCCACTCCA | 26054 |
rs533101449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663899 | ATATCCTTACCACAT[C/T]TGTTCCTAACTCTAT | 26054 |
rs533202367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656966 | GATGTTATAGGTATG[A/G]TGAAGAGAAGAGTGT | 26054 |
rs533227689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644319 | TATAACTTAGACCGA[A/G]GGACACTCTATGAAA | 26054 |
rs533229187 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75641014 | ACATAAAATAAATTA[C/T]AGTTAACCATATTCA | 26054 |
rs533232602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608553 | GGAAAGAAAGGAAGA[A/C]AGAAAGGAAGGAGAA | 26054 |
rs533262502 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671014 | ATCCCAGCTAAGTGC[A/G]TGAAAAGAATATATT | 26054 |
rs533274763 | snp | A/G | 0.000168047 | 0.00916491 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703040 | GTGAGAATGGCCTAC[A/G]GAATGAAAGTTTAAG | 26054 |
rs533336284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607739 | AAACTGTTGCATGCA[A/G]TGTTGTTCTCTACAG | 26054 |
rs533356531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697950 | TTCAATTAAAAACCA[C/T]GTGGACTACTTGAAG | 26054 |
rs533363441 | snp | C/T | 8.53774e-05 | 0.0065331 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621641 | GTAAGGATTTTTTTT[C/T]CCCTCAGATGTTTTA | 26054 |
rs533392220 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624999 | GCACTGTAGTACATA[A/C]AATAATGGTGTATTG | 26054 |
rs533397188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622217 | TTTTAAATGATAGTT[A/T]TAATAGAACTTTTTG | 26054 |
rs533402933 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602778 | CTCGGCTGCGAGCCG[A/G]TTCGGCCCAGGGGGC | 26054 |
rs533403218 | in-del | -/TA | 0.00835141 | 0.0640778 | intron-variant | SENP6 | GRCh38.p7 | 6:75653676 | TTTTTTTTTTTTAAC[-/TA]GTTTATTTTGCAAAT | 26054 |
rs533403999 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75657960 | CTGCTTGCCAAAAGA[A/T]GGAATTTAATTAGAG | 26054 |
rs533408533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664998 | TGGGTTATCAAAGTG[A/G]TATTTAGGCTGGGCG | 26054 |
rs533419387 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75698559 | AGGCTGGTCTTGAAC[C/T]CTTGGCCTCAAGCCA | 26054 |
rs533476695 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601610 | TGCCAGAGGAGCAAA[C/G]CCATCGCACACGCCA | 26054 |
rs533480993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691963 | CCGGGTTCAAGCTAT[C/T]CTCCTGCCTCAGCCT | 26054 |
rs533550072 | snp | C/T | 2.7541e-05 | 0.00371076 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75678969 | ATTAAATCTTTAACA[C/T]TCCGTCATATCTTAT | 26054 |
rs533561273 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75693429 | AAAAAAAAAAAAAAA[A/C]CACCAAAGTAGCCAT | 26054 |
rs533594861 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75646709 | GGCGTGGTGGTGGGC[A/G]CCTGTAGTCCTAGCT | 26054 |
rs533608202 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610484 | CTACAGTTACAGAAA[A/G]TGATAGATAATCTGT | 26054 |
rs533688951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665725 | GTAGCTTCCTGTGTG[A/C]GATAAAATTACTTGG | 26054 |
rs533700388 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75704701 | TCCTTCCCGTCCCAC[A/C/G]AGGCCATATTTCAGA | 26054 |
rs533718614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614913 | TTTTGAGACAGAGTC[C/T]CACACACTTTTTTAC | 26054 |
rs533732872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667591 | TATGTGCTGTTGTCA[A/G]GAATCCAAGGGAAAG | 26054 |
rs533761142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616798 | CCCCAGTTCCTTTAG[C/T]GCATAAATATTACGA | 26054 |
rs533824809 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608859 | ATTTTATTAGCAGAT[A/G]GAGAAAAGAAAAAGA | 26054 |
rs533850623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653330 | GCCACTGTGCCTGGC[C/T]TTACTTTTTTCTAAT | 26054 |
rs533879336 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693990 | GGCCAGGCACGGTGG[C/T]TCACGCCTGTAATCC | 26054 |
rs533923381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687802 | AGCTGCCTATGTGAG[G/T]TGTCTGTCGGCCCCT | 26054 |
rs533929236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661736 | CTGAAATTCTACACT[A/G]TGTACCACTTGTAAG | 26054 |
rs533955086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612014 | AAGTAGTAGTGATCT[A/G]TTAGTTTGTCTTCTA | 26054 |
rs533972102 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609658 | AAACCCAAAATCCAA[A/C]TTTTGGACAGTTTGG | 26054 |
rs533989837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604051 | AAAAGATGGCTTACT[A/C]GTGCTTATTATCTTC | 26054 |
rs534056771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694907 | AGACCAAGTCTTGGT[C/T]TGTCATGCCCAGGCT | 26054 |
rs534110406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75660897 | CAGCCTTCCAAAGTG[C/T]TGGGATTACAGGCGT | 26054 |
rs534122868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692995 | AGGATGGCTTCAGCC[A/C]AGGAGGCGGAGGCTG | 26054 |
rs534131626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75602657 | CCCGGATATTCAGTT[A/G]TCTGCGCTGGGTGGG | 26054 |
rs534145928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75610671 | GGATAGTCCCAGGCA[C/T]ACTGGGATGTTTGGA | 26054 |
rs534183865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669964 | TTAAGAAGGAATTTC[A/G]ATCTTGTTGCCCAGG | 26054 |
rs534184916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75675279 | GGGTTTAGATAAGCA[A/G]TGTTTAGGTGTTCAT | 26054 |
rs534197384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619426 | TCCCTTTAAGGCTGA[A/G]TAACATTCCGTTGTG | 26054 |
rs534204837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708988 | GCTTCTTTCAGCAAA[A/G]TAGTTGCTTATTATT | 26054 |
rs534205943 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75717121 | TAGAGCTGTTAGCTC[A/C]GATATCTTAATTAGC | 26054 |
rs534209792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75655045 | AGTTCAATATTTGTT[C/T]ACAGTTTATTTTCTT | 26054 |
rs534225802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662618 | CTTATTCAGCATAGT[C/G]TATCTGCATTTTGTT | 26054 |
rs534248085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75669108 | TAATCCCAGCACTTT[C/T]GGAGACTGAGGTGGG | 26054 |
rs534252078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618705 | TGTATGTATTAAATA[A/C]ATGTGAGTTCAGGCT | 26054 |
rs534266177 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75708359 | CCTTTTTATTAACTT[A/T]TACCAAAATTTATTT | 26054 |
rs534309186 | snp | C/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600023 | GAACCGAGATCATGC[C/G]ATTGCACTCCAGCCT | 26054 |
rs534336869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75713091 | GGTGACAGAGTGAGA[A/C]CCTGCCTGAAAAAAA | 26054 |
rs534341760 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693411 | CAGTCTGAAATTTAA[-/A]AAAAAAAAAAAAAAA | 26054 |
rs534358521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643831 | CTGTAAAATAAATAA[C/G]ACTTGATTCATTTTC | 26054 |
rs534367368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665913 | ACACATGTAATCCCA[A/G]GTGCTGGGGAGGCTG | 26054 |
rs534370133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640924 | ATCAGGGTAATTAGT[A/G]TATCCATCACCTCAA | 26054 |
rs534383290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615174 | GGGATTATCTCGCCT[A/G]TCCTGCTAAGAGGTT | 26054 |
rs534392708 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75625137 | TTTTTTTTTTCAGAC[A/G]GAGTCTGGCTCTTGC | 26054 |
rs534392733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633461 | ATCCATGCCAATGCT[A/G]TCCACCATCATTCCC | 26054 |
rs534485335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643712 | GGGTGACAGCAAGGC[A/G]CCATCTCAAAAAAAT | 26054 |
rs534502968 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646506 | AAATACAAAGCACAC[A/G]TGGCACATGATGCTA | 26054 |
rs534502977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612744 | AGTTTGGCAATACCT[A/G]TTGAACTTGAAAATG | 26054 |
rs534508561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678099 | AGAAAAGAGCAGCAT[A/G]ATGCCACTGGGATGG | 26054 |
rs534595021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665119 | GTGAAACCCCGTCTC[C/T]ACTAAAAATATAAAA | 26054 |
rs534650761 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627964 | GGCGTGAGCCACCAC[A/G]CCTGGCCTGCTTTCA | 26054 |
rs534699156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630528 | TCTCACAGAGCTCAG[A/G]CTGCTCTGAGCTATT | 26054 |
rs534727677 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662002 | GGTTGCAGTGAGCCA[A/G]GATTGCGCCATTGCA | 26054 |
rs534729508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622398 | CCTCATCTCTACTAA[A/G]AATACAAAAGATTAG | 26054 |
rs534762098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698077 | TGTTTTATTCTTTCG[C/G]TTTTCTATGCCCTCA | 26054 |
rs534775879 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656084 | GCCAGGCATGGTGAC[A/G]CATGCCTGTAATCCC | 26054 |
rs534800529 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636857 | TTCTCCTAAATTTTC[G/T]TATTTTCTGAAGTCT | 26054 |
rs534820753 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75636418 | ATGTTCAAAGACAAG[A/T]CATTGAGAGTTCTTC | 26054 |
rs534830446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673945 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 26054 |
rs534913399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75628590 | TTCTTAAAAATTGAC[A/G]CATAACAATTGTACA | 26054 |
rs534939093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672214 | CCCTGTAACTTTTAC[A/G]GCTTTCTCCCACATT | 26054 |
rs534951383 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601640 | AGGTCTGCCATGGGG[C/G]CCTGGGCGGTGGGGA | 26054 |
rs534954068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621859 | AGTACATGTAACCTT[A/G]CAATTAAAAATTGAC | 26054 |
rs534977560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692145 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCTCCCA | 26054 |
rs535000949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686134 | TTATTGAATTGATCC[C/T]TTTACCATTATGTAA | 26054 |
rs535016869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680088 | AGCCTATTTAAGATA[C/T]TTTAGTTGAAATGAT | 26054 |
rs535049440 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674986 | GTAAAATAATTAATT[A/C]AGGCTATAATAGGCT | 26054 |
rs535070881 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75711964 | AGGCGTGACCCATCG[C/T]GCCCGGCCACAAGTT | 26054 |
rs535076937 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75673350 | TTTTTGAGACCGAGT[C/G]TCACTGTTGTCAGCC | 26054 |
rs535098261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75714467 | TTATCGTCGAGTGTC[A/G]CTATTCTGAACTGCT | 26054 |
rs535108360 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673220 | GGAATACCACATATG[C/T]ACAAATTCATTTTTC | 26054 |
rs535131979 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75699740 | AGCGGTCCACCTGCC[A/G]TAGCCTCTCAAAGTG | 26054 |
rs535174558 | snp | A/G | 0.00028641 | 0.0119634 | intron-variant | SENP6 | GRCh38.p7 | 6:75635001 | GAGTAATCAGATTCT[A/G]TAAATAGAGAATTTT | 26054 |
rs535174909 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708803 | TAGGCTGAGGCAGGA[A/G]AAATCACTCGAACCT | 26054 |
rs535181485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651701 | TTAATATTTTAATAT[A/G]TAACTCTCCAGATCT | 26054 |
rs535193913 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718067 | CAATTAAATGTAGGA[A/G]GTTTTATTTGAAAAC | 26054 |
rs535210213 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75627133 | CAAACCAGCTAACTT[A/T]TGTATTTTAGTAGAG | 26054 |
rs535229060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691785 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 26054 |
rs535250861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604003 | TGTTACAGGTAGTGC[C/T]ATGTGTGTTGTTTTT | 26054 |
rs535253816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654989 | CGATTGTAGACGCCT[A/G]GTATACTTCTAAACA | 26054 |
rs535265228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644608 | TTGTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT | 26054 |
rs535269553 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653233 | GCAGGGTTTCTCCAT[C/G]TTGGTCAGTCTGGTC | 26054 |
rs535305311 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75668318 | ATATTTGATTAAATG[-/A]AAAGTAGAACAGTGT | 26054 |
rs535309256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685320 | AATTTTGTTGATCTT[G/T]TCAAAAAACCAGCTC | 26054 |
rs535330919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604619 | AACTGAGCGAGATTC[C/T]GTCTCCAAAAAAAAA | 26054 |
rs535377163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685724 | GTGAGTTTCTTAATC[C/T]TAAGTTCTAATTTGA | 26054 |
rs535412718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657237 | TTTTTCAAATAATTG[C/G]TTGTGTGTTTCAGAC | 26054 |
rs535435178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648790 | CAGTGCTTTGCATTC[A/G]TTATTTACTTTTATC | 26054 |
rs535437848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75682900 | TAGTAGCATGATTTA[C/T]AATCCTTTGGGTATA | 26054 |
rs535444395 | in-del | -/TGA | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75691435 | TAGTTAAAGGAGTTC[-/TGA]TGATGTTAGATTTTC | 26054 |
rs535499577 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75683382 | GTTTCTTTTGCCATG[C/T]GGAAGTTCTTTAGTT | 26054 |
rs535591090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684210 | GTTTATCTGTTAATG[A/G]TGTATAGGAATGCTT | 26054 |
rs535607013 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75690851 | CAGGCGCTCACCACC[A/G]CACCTGGCTAATTGT | 26054 |
rs535645101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75662964 | TTGAAAATTTCTTCC[A/G]GCATTTTGATATTAA | 26054 |
rs535693403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655667 | TTGCATTGTATGAGT[A/G]TAACAAGTTATTTAT | 26054 |
rs535717288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75688070 | TTTGAGCTTCCTGGC[C/T]GCTTTGTTTACCTAC | 26054 |
rs535765969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | SENP6 | GRCh38.p7 | 6:75620316 | TGTCTTAGTTCATTC[G/T]GGCTGCTGTATTGAA | 26054 |
rs535780076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75682437 | ATACTTTAAGATCTA[C/T]GGTACATGTGCACAA | 26054 |
rs535798238 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75703739 | TGCAGTCCAGCCTGG[A/G]TGACAGAGTGAAACT | 26054 |
rs535816391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75695512 | GAGGCTGAGGCGGGC[A/G]GATTACTTGAGGTCA | 26054 |
rs535820460 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75613952 | ATTGTTATGTCCCAT[A/T]TGTCTTCTTTAATCT | 26054 |
rs535824255 | snp | A/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717810 | TTAGATAGATCTGTT[A/G]TATTGGTTTTCTTGT | 26054 |
rs535881580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699431 | GATTGGCTGCCATAT[A/G]TTTGTCATCTGTTTT | 26054 |
rs535902149 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75693334 | CACTTGAACCTGGAG[A/G]TGGAGATTGCAGTGA | 26054 |
rs535916724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75692960 | CCTGTAGTTCCAGCT[A/G]CTCTGGAGGAAGAGG | 26054 |
rs535921663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642943 | AATCTTTTTGGTGGG[A/G]GAGGTGGGGATTGGA | 26054 |
rs535975104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686540 | GGCTGGTACCAGTTG[C/T]TTCTTTCCATGTTTA | 26054 |
rs536014249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709231 | AAGTACTTATTTGTT[C/T]ACACATATACATATG | 26054 |
rs536045965 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604316 | TAAAGCAAGCAAACG[A/G]TAACTTCTTTAGAGC | 26054 |
rs536076455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709925 | AAAAAACAAATTCAG[C/T]TTTCAAGTCAGAAGT | 26054 |
rs536077643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75623378 | CTAGAATTTCAGGCC[A/G]GTGATTTCTCAATGA | 26054 |
rs536079014 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599830 | GCACTTTGGGATGCC[A/G]AGGCGGGTGGATCAC | 26054 |
rs536093178 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617706 | TTACTATTACCTGAA[C/T]TACAAACTTTATTTT | 26054 |
rs536139457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710721 | TTCCTACTATTGATT[A/G]TTCCATTCGTAAAGT | 26054 |
rs536199661 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75703337 | GAATTTACTTATAAC[A/C]ATATAGTAACACAAC | 26054 |
rs536202253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75652426 | TTTAAAATATTATTA[C/T]TGTACTGGTACGTGC | 26054 |
rs536224337 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602011 | GGTGGGCGGACGGCC[A/G]TAGCGGCGGCGGCTG | 26054 |
rs536238016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609879 | TGCAACCTCTGCCTT[C/G]CAGGTTCAAGCAATT | 26054 |
rs536268843 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716806 | ATTTTTAAATACACA[A/T]ATATCAAAAATAGTT | 26054 |
rs536274741 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655185 | CAGCTTTGGAAGGGA[C/T]GCGCATGGAGCGATG | 26054 |
rs536298698 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610111 | ACTTCTAGTTGATTG[A/G]GAATGGATTCAGGAA | 26054 |
rs536315058 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75673776 | CTGTAATCCCAGCAC[-/T]TTGGGAGGCTGAGGC | 26054 |
rs536395040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611833 | AACTGCTGCCTGACT[A/G]ACGAACTGAACTGAC | 26054 |
rs536412330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75713455 | ATGCCACTTTTAATC[C/T]TTTTATGCATTTGTA | 26054 |
rs536466513 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621814 | ACTGTTATTTTCTCC[A/G]TCTTTTGAAATGTAT | 26054 |
rs536471336 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669255 | TACTTGGGAGGCTGA[C/T]GCAGGAGAATTGCTT | 26054 |
rs536472190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615307 | GTGTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG | 26054 |
rs536476652 | in-del | -/A/AA | 0.301177 | 0.244706 | intron-variant | SENP6 | GRCh38.p7 | 6:75604625 | CGAGATTCTGTCTCC[-/A/AA]AAAAAAAAAAAGCAT | 26054 |
rs536564185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674562 | TCTTGGGCTCAAGCC[A/G]TCCTCCCAAAATGCT | 26054 |
rs536618455 | in-del | -/ATG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625560 | CTGTCTTTGTTCCTA[-/ATG]ATGTTAATTTAATAA | 26054 |
rs536629221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668410 | GACAAAGTGTAAAGT[A/G]GTCCTTTATATATTT | 26054 |
rs536676040 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75660992 | AGGAGCCATGCATAC[A/G]AGGAGAAGGAAATAT | 26054 |
rs536695386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669036 | CACTTTTAAACCTCT[C/T]TAACAGGTTTCTTTA | 26054 |
rs536705084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621738 | TTCTTAAGAAAACAT[A/G]TAACTCTTTCACAGT | 26054 |
rs536711862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618530 | TCAGTCATTTCTTCT[A/G]GGAACCCTGGCTCCT | 26054 |
rs536733195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700560 | GGCACCATCTCGGCT[C/T]ACTGCAATCTCCGCC | 26054 |
rs536734627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75703624 | AAACTTAGCCAGATA[C/T]GGTGGTGCCCATCGG | 26054 |
rs536735724 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75711968 | GTGACCCATCGCGCC[C/T]GGCCACAAGTTTTGA | 26054 |
rs536759729 | in-del | -/CT | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75668996 | CATTTGAAGATATAA[-/CT]CTACAGCTAAAAACA | 26054 |
rs536768221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75654199 | ACTGTGATCACGCCT[C/T]TGCACTCCAGCCTGG | 26054 |
rs536768585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657626 | TCCAGGAAACATTTA[C/T]TAAGCCCTTGTGTAG | 26054 |
rs536792616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606350 | TGACTTGTTTCTTTC[A/G]CTTCTCTTCACTAAC | 26054 |
rs536837563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690046 | CTTCCTAAGTAGCTG[C/G]GACTACAGGTGCACA | 26054 |
rs536846622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75683576 | ATTAGTTTTTGTATA[A/G]GGTGTAAGGAGGGGA | 26054 |
rs536864318 | in-del | -/AATC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664369 | TGGGCCTTTTTAAAA[-/AATC]TATATACATGTACAC | 26054 |
rs536875737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691631 | TTGAGACGGAGCCTC[A/G]CTCTGTTGCCCAGTT | 26054 |
rs536908438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674099 | ACATTTTTCCAAAAC[A/G]TATAATGTCAACATC | 26054 |
rs536941207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627383 | TAGCTTTTATTTTGA[C/T]ATCTGGATTTCCTGA | 26054 |
rs536944505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632541 | TTGTAAACTGATGTT[C/T]CTTTGCAAATAATGT | 26054 |
rs536952151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75624584 | TTTGCAAATGAAAAC[C/T]AGTATCTCAGTGTAG | 26054 |
rs537011665 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685508 | TCTTTCCTGCTTTCT[C/T]TTGTGGGCATTTAGT | 26054 |
rs537085936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664402 | CACATACGTCTGTAT[A/G]TATATATATATACAT | 26054 |
rs537095452 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75715048 | ACTGTGCAGTCTCTA[-/TT]GCCTCTTAGTTCTGC | 26054 |
rs537132404 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659951 | AAAGTTAACATTGAT[C/T]TAAAATTACCATTTA | 26054 |
rs537144763 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685918 | TATTAGGTCTGCTTG[G/T]TGCAGAGCTGAGTTC | 26054 |
rs537146990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665062 | GAGGCTGAGGCGGGC[A/G]GATCACGAGGTCAGG | 26054 |
rs537149106 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75661697 | TAGACAAGGTTAGTG[C/G]TTTTTTCTTTCCATG | 26054 |
rs537166122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75679997 | GAATTTCTGTTAAGA[C/T]CATTTTGATAGGCAT | 26054 |
rs537180482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630404 | AGTCAGGAAACTACC[A/G]GCAAGAAAAAGCACA | 26054 |
rs537199353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75704078 | TAGTTGTGAACAGTC[C/T]TGAAGGGGTGGCCTG | 26054 |
rs537216024 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677972 | AGTTGAGCAAGGACT[C/T]CCCAGAGAAGAGCTG | 26054 |
rs537228495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607114 | GCATTTTGGGAGGCC[A/G]AGTTGAGAGGATTGC | 26054 |
rs537250531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635269 | TTAGATTTAGGAGTT[C/G]TCATTGATCTTGAAA | 26054 |
rs537254657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642873 | GTCTGTAAGTACTCA[A/G]AACTATCTCAGCAAG | 26054 |
rs537273295 | in-del | -/A | 0.00199561 | 0.0315249 | intron-variant | SENP6 | GRCh38.p7 | 6:75668494 | AAATGAATAGAATTC[-/A]AAAAAAAATAGTAAT | 26054 |
rs537335195 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709841 | AAAAGAAAAAGACTT[C/T]ATAAAGTCTTGTAAA | 26054 |
rs537338363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635891 | ATATTCTGATAATGT[A/G]GTCTAAGTTTGAAAT | 26054 |
rs537349766 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601018 | ATAGCACAACTGAAT[C/T]AGAACAGTCCATTCC | 26054 |
rs537382911 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75702559 | TGGCAAGAACTTTAG[-/A]AAAAAAACATTTTAA | 26054 |
rs537383805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627920 | CTCGTGATCTGCCCG[C/T]CTTGGCCTCCCGAAG | 26054 |
rs537420367 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697262 | GTCCCATGCCTTCCT[A/G]GTTTCCATCCAACAA | 26054 |
rs537422300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75640456 | CTTTTAAGATTTTTT[C/T]ATATTTTTGTGTATT | 26054 |
rs537439404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685247 | TGGTGATATCCCCTT[C/T]ATCATTTTTTATGGC | 26054 |
rs537499894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682357 | GGATATAGAAGAACT[C/T]GACAACACCATCAAC | 26054 |
rs537540654 | snp | A/G | 5.4546e-05 | 0.00522207 | intron-variant | SENP6 | GRCh38.p7 | 6:75633538 | TTGATAGATTGTCAC[A/G]TTATAGCATTTTTGA | 26054 |
rs537545065 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644322 | AACTTAGACCGAGGG[A/G]CACTCTATGAAATAC | 26054 |
rs537547399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629728 | TAGCTTACAGGTAAT[A/G]TATAGGTCTGTCAAG | 26054 |
rs537565620 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629958 | TTACCAAGAATTTAC[A/G]TTAAAATAGCTAACA | 26054 |
rs537569969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75672889 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 26054 |
rs537696482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75650339 | ACCGTTTTTCCCTTG[A/G]TGCTTAATAAAGATT | 26054 |
rs537735177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646811 | ACTGCACTCCAGCCT[A/G]GGCGACAGAGCGAGA | 26054 |
rs537774592 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640542 | ATGACTCAAAACATA[A/G]TATATTATATATATA | 26054 |
rs537775014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684696 | TTTATACGATGGATT[A/G]TGTTTATTGATTTGC | 26054 |
rs537776661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75691734 | CGAGTAGCTGGGACC[A/G]CAGGCGCCTGCCACC | 26054 |
rs537833156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687811 | TGTGAGGTGTCTGTC[G/T]GCCCCTACTGGGAGG | 26054 |
rs537838017 | in-del | -/GAAAACA | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75631637 | AGTAAAGTTTTCTTG[-/GAAAACA]GCCATGCTTATTTAT | 26054 |
rs537875071 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620081 | TTGGGCTACCTTGCC[-/T]CAAAAAAAAAAAAAA | 26054 |
rs537913961 | snp | C/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75695462 | CGAACTGTGGCCGGG[C/T]GCCATGGCTCACGCC | 26054 |
rs537964221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682854 | TATTGTGAATAGTGC[C/T]GCAATAAACATACAT | 26054 |
rs537978967 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634371 | CCTGCTTCATCCTCC[C/G/T]GAGTAGCTGGGATTA | 26054 |
rs538027346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669200 | ACTAAAAATACAAAA[A/T]AATTAGCCAGGCGTG | 26054 |
rs538041138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700480 | GTATTATACTATATT[A/T]CATCAATTTTATTTT | 26054 |
rs538106195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700930 | GCCTGATCTAAATCC[A/G]TAGGGTACTAAGGAA | 26054 |
rs538130613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75654859 | ACAGTGAACATGTGT[A/G]TATCTATGTGGTAGA | 26054 |
rs538168368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75694074 | CCAGCCTGAGCAACA[C/T]GGAGAAACCCCGTCT | 26054 |
rs538219477 | snp | A/G | 1.66687e-05 | 0.00288688 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666736 | CCAGTGATGATGATG[A/G]TGACAACGACAGAAC | 26054 |
rs538247181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698247 | TTTCCTTGAGTGATA[C/T]GGGGGAGGGTCTAAA | 26054 |
rs538286599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656434 | GCCTAGCAAAAATCA[C/T]TTCTGTGATCAGTTA | 26054 |
rs538310330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698839 | AACATGGCGAAACCT[C/T]GTCTCTACTGAAAAT | 26054 |
rs538332132 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700994 | ATCCATCTGGACTTC[A/G]CAATACAGAAGATGA | 26054 |
rs538371682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692313 | ATCAGAAAAACGAAA[C/T]TAGTTACTTTAAAAG | 26054 |
rs538401494 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601896 | GCGGCGGCGGCTGGA[A/G]CTGCTGTGGCGACCG | 26054 |
rs538413289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75676157 | ACAGATGCCTTAGGT[A/G]TATATTATCTACAAT | 26054 |
rs538419583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637232 | CTGGTAATTCATACA[C/T]AGTGTATTCTTGGGG | 26054 |
rs538424790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679215 | GCCCAAGAGTTCACG[A/T]CCAGCCTGGGAAACA | 26054 |
rs538460589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75629602 | ACCATGCCCAGCCAG[A/G]TTGAGGATTTAAAAG | 26054 |
rs538461097 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618769 | TCATTCTGTCTTTCC[C/T]CTCTTGCTTATTTGT | 26054 |
rs538553029 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617315 | TTTCGCTCTTGTTGC[A/C]CAGGCTGGAGTGCAA | 26054 |
rs538590196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658725 | GTTTGAATTCAGATT[C/T]TTCTCATTACTACTC | 26054 |
rs538596937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75714284 | CCTTTGACAGTGTCA[A/G]CCATTTCTTCCTCAC | 26054 |
rs538621601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631755 | TGATCAAGAAAGCCT[A/G]CAATACTTACTTTTA | 26054 |
rs538625937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607596 | TATTTTCTCCCGTTT[C/T]TCCTGAAGTAACTTT | 26054 |
rs538645424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608215 | TATCCTGAGATAACA[C/G]TTCGGGAGGCCAAGG | 26054 |
rs538652151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624511 | TACACTTGTTCCATC[A/G]ATATCTGAACGTATC | 26054 |
rs538655267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615963 | TTAGGTTTTTGCTTT[A/C]TTTGGTCAACTATAC | 26054 |
rs538659293 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617058 | TTTTTTTGTATTTTT[A/T]TGTAGAGACAGGATT | 26054 |
rs538697199 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637746 | TTTTAAGTCTTCCCC[C/T]GCAACTTAGGGGGAT | 26054 |
rs538721321 | in-del | -/T | 0.498253 | 0.0294992 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619019 | AGTCACTTTCAGGCT[-/T]TTTTTTTTTTTCCTT | 26054 |
rs538723353 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715825 | TTTCACTTGTTAGGA[A/G]GCTTTTGTTATGTAT | 26054 |
rs538729898 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660599 | CACTTCTCTGCTTTT[C/T]AGTATAACAAGATGG | 26054 |
rs538737636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624989 | AAAAAATTTTGCACT[A/G]TAGTACATACAATAA | 26054 |
rs538778814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617695 | TGATAGTGTTATTAC[G/T]ATTACCTGAACTACA | 26054 |
rs538840351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692849 | CAAGCAGACCACCTG[A/G]GCCCAGAAGTTCGAG | 26054 |
rs538841986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621898 | GGAAGGCTTCAAAAT[A/G]AGGAAATTGTTTTTT | 26054 |
rs538901990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75713215 | TTTGACTTTTTACTA[A/G]TTTTGAAGTACTTTT | 26054 |
rs538914358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686489 | CAGTTTCTTCATAGC[A/C]TCGATGGTCTTTACA | 26054 |
rs538927837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622465 | TCAGGAGGCTGAGGC[A/G]GGAGAATCACTTGAA | 26054 |
rs538951886 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632170 | CCTTGCCTGAGCATT[A/G]TTCATAATCTCTGAA | 26054 |
rs538963676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615221 | AGTCTTGCTGTGTCG[C/T]GCAGGCTGAAGTGCA | 26054 |
rs538977555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680831 | GAGAACATGTACTTT[C/T]AGTCCCACCTCACAA | 26054 |
rs539011108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674020 | AGTGAGACTCATTCT[C/T]AAATAAATAAATGAA | 26054 |
rs539052201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627224 | ACCTTGGCCTCCCAA[A/C]GTGCTGAGATTACAG | 26054 |
rs539069241 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667021 | TTAGAAGGCAGTTTG[A/G]TAGTGCCAAGAAAAA | 26054 |
rs539074188 | in-del | -/TT | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75658257 | ATCACTTAGTGAAAC[-/TT]TTTGTGATTGCACTA | 26054 |
rs539088656 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649333 | AGTGAAAAAAAAAGC[A/T]TTTCAAAGATGTTAA | 26054 |
rs539099707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75706562 | AGTAAATAGCCTCAA[A/G]AATCCTAATGGAGAC | 26054 |
rs539106605 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677558 | CTACTTCCAACATAT[A/T]TATGCACACACTGCT | 26054 |
rs539138325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620278 | CCCTAGTTAATTGTC[A/G]TCTCTTATGATTAGG | 26054 |
rs539153613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609977 | ATTTTTAGTAGAGAT[A/G]GGGTTTCTCCATGTT | 26054 |
rs539173156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620790 | TCACCAAGTCAGAGC[A/G]TTGCCCTTCAGCTTG | 26054 |
rs539187309 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613464 | CCTAGAGAAATATAC[A/C]TGCACAAGGAAACAA | 26054 |
rs539216681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685846 | TGAATAAGTGCGATG[C/T]GGTGCTGAGAAGAAT | 26054 |
rs539245722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75688757 | GAAGCCCTGTGTCTA[C/T]AAAAAAGAAAATTTT | 26054 |
rs539289425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75698289 | CCTAGGTAAAGAAGT[A/G]GCATTCACTCATTAA | 26054 |
rs539413446 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618904 | TGGTTTGCTCATTAA[C/G]ACTTATTTCCTCCTG | 26054 |
rs539477589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75670850 | TAGTTCAAGATTTCA[C/T]ATTGCTTTAAGAGTA | 26054 |
rs539480966 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706438 | TTAAGGTACTTGACT[G/T]AAAGCAATGGGACAA | 26054 |
rs539500616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75677855 | CTAAGTTTATTTCCT[A/G]TTACAGCAACTTAGC | 26054 |
rs539560506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710766 | TCAAAGAACAACAAT[A/G]ACCAAAAAAGCCTTG | 26054 |
rs539563959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671405 | CAAACTGATATTGTC[C/G]TTTTTACATAAAGCA | 26054 |
rs539577441 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75690939 | CTGTCCTCAAGTGAT[-/C]CCCCCTGCCCCCCAT | 26054 |
rs539588457 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700250 | TGCTGTTAAAGTTAA[C/T]GTAGCTGTTATTAAA | 26054 |
rs539592092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647999 | CAGTTAGGTGATTAC[A/G]GTTTGAAATCTTTTG | 26054 |
rs539672612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75689439 | AAAAAAAACAGAAAA[C/T]AAGTGTTGATGAGGA | 26054 |
rs539694381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642266 | TAGTTTACATTCTTA[C/T]GGGACAAAGACTAAT | 26054 |
rs539697235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682950 | TGGGTCAAATGGTAA[C/T]TCTAGTTCTAGATCC | 26054 |
rs539726984 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675339 | TTTTAAGAGATAAAC[A/G]AGTAATATAAGAAAC | 26054 |
rs539734977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75683545 | GTCTAACATTTAAGT[C/T]TTTAATCCATCTTGA | 26054 |
rs539758447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658000 | GACAAAGTCATGATT[G/T]TTAACTAGATCACTT | 26054 |
rs539775816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690335 | ATGTGGTGTATACAT[A/G]TAATGCAATATGTAT | 26054 |
rs539873761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684661 | TTGAGATAATCATGT[A/G]GTTTTTGTCATTGGT | 26054 |
rs539892420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673691 | CAAATACTTAGATAT[C/T]ACTTCCTTCAATTCC | 26054 |
rs539898251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636476 | GATTTTATGCTACAT[A/G]CCAGGCATAGATGAG | 26054 |
rs539952950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674118 | AATGTCAACATCCAC[A/G]TATGCTAGAATGTTT | 26054 |
rs540010411 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75715285 | ATACATATTGAATGC[A/G]TTGTTGGGTTTTCTT | 26054 |
rs540011492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664226 | AGTCCAGGAGTTGAA[A/G]TGTAGCCAGGGCAAT | 26054 |
rs540027478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75659609 | TTCTGTAAAGAATTT[A/G]TCAGTGCTTCCCTGC | 26054 |
rs540042598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703366 | ACTTACTTTTAATTT[A/T]TACTGAGGTATAATT | 26054 |
rs540065561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75652492 | CCCTAGAAATAAAAT[C/T]TGGGGGACAAATGAT | 26054 |
rs540104024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703899 | TTTATATTTTCCATT[C/T]ATTGGAACTTGGATC | 26054 |
rs540105874 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75696316 | CTAGTAGGTTTTTTT[A/T]AAATTACTTAGATAC | 26054 |
rs540133545 | snp | A/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718259 | CTGAACAGGAATAAT[A/G]AAGAACATATTTTAA | 26054 |
rs540153289 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75687746 | AGAACAGCAAATATT[A/G]CTGCCTGATCCTTCC | 26054 |
rs540162169 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605413 | TTTTTTTCACCATCA[C/T]ATTTCTTGCACCTGA | 26054 |
rs540166516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697057 | ATCAGATAATGCTCA[C/G]TTTTCCTACTGTCTT | 26054 |
rs540184456 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599519 | GAGATTAAGGAATAA[C/G]CTGTTTGAAGCTATT | 26054 |
rs540214408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686641 | TAAAGTATTTTATTT[C/T]TCCTTCACTTATGAA | 26054 |
rs540254000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75603475 | TGCTGCTCAGAGACT[C/T]ATTCTTCTTGTTAAA | 26054 |
rs540272805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631105 | TCAAAGTTGTATTTT[C/T]GATAGTGTGTCTAAT | 26054 |
rs540273739 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75693757 | TGTTTTAAGCATTTG[C/G]TCTTTCTGTGTAAGA | 26054 |
rs540311372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624166 | CACCTCCCATGTTAC[A/G]CAATTGGTAATATAC | 26054 |
rs540311506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632004 | AGATATTTTTTGTTT[C/T]TGTTTCTGGGAGCGT | 26054 |
rs540331577 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75687457 | TGGCAAGAAGCTGCA[A/G]TCCTTTGGAGAAGAA | 26054 |
rs540335851 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639151 | TAATGCCTAACTGTT[G/T]GTTTTCATTTTGCTT | 26054 |
rs540424905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715229 | TGTCTTGTATCTCCA[A/G]TACCTAACACAGTAC | 26054 |
rs540426106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691892 | ATGGAGTTTCACTCT[C/T]GTTGTCCAGGCTGGA | 26054 |
rs540430728 | snp | A/C | 0.0741063 | 0.177655 | intron-variant | SENP6 | GRCh38.p7 | 6:75699010 | AGTGAGACTCCATCT[A/C]AAAAAAAAAAAAAGG | 26054 |
rs540446409 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75667887 | ATCAGTGACTTTTAG[A/G]AGTTCTGCATGGTAC | 26054 |
rs540447231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75645080 | TTTTAAACAGCTTGT[A/G]AAAATCTTGGGTTTA | 26054 |
rs540474109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617112 | TCAAACTCCTGGGCT[A/T]AAGTGATCTGCCCAC | 26054 |
rs540485660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75685578 | GATTTAAATGTGTCC[A/G]AGAGATTCTGGTACG | 26054 |
rs540494828 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602170 | TTCTTGGGAACCCAC[A/G]GCTGGGGGAAGTTTC | 26054 |
rs540505492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699885 | TCTAATCTATCTTAA[A/G]TGAAATTGCCTAGGT | 26054 |
rs540544264 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75684044 | GAATGGAATATTCTT[-/C]CATTTGTTTGTGTCC | 26054 |
rs540567056 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75700611 | CCCACCTCAGCCTCC[A/C]ACCCCAGTAGCTTGG | 26054 |
rs540649872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606505 | AGGCATAACAGTGAG[A/G]GAGAAGAAACCATGT | 26054 |
rs540657508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75647039 | TTTACATTACTAGAT[C/T]ACCAGTGTGAATAGA | 26054 |
rs540686619 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599652 | ATTTAAAAAAGAGGG[G/T]AAAGAGGAGAGAGAA | 26054 |
rs540717167 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695376 | AAACTTTGCTAATAA[A/C]TTCCTTGGTTCTAAA | 26054 |
rs540729397 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603334 | ATTGATTTTTTTGGC[C/T]TATGAATATATAAGG | 26054 |
rs540746633 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75647463 | TAACGTTTTTTGTTC[C/T]GATTTTGGAATTGTC | 26054 |
rs540766494 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600316 | ACACACATTCCTTGA[A/C]TCCTGGCACCTTCTT | 26054 |
rs540797803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624657 | CATATGTATAGTCTC[A/G]TTCTTTTTTAGAATA | 26054 |
rs540815223 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75691158 | ATTTTTTTTTTTTTT[C/T]CAAAGACAGATTCTT | 26054 |
rs540833739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619763 | CAGTTTCTCCCACAT[C/T]CTAGCCAATACTTGT | 26054 |
rs540839690 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622584 | AAACAAACAAAAAAA[-/C]ATTGTTTTTAGTTTT | 26054 |
rs540884189 | snp | A/C | 0.000799201 | 0.019974 | intron-variant | SENP6 | GRCh38.p7 | 6:75668494 | GAAATGAATAGAATT[A/C]AAAAAAAATAGTAAT | 26054 |
rs540911783 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75669753 | TAAATTGCTTGCTTT[-/C]TAAAGAATTACTGAT | 26054 |
rs540922868 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661060 | GTTATGTTCATTCAC[A/T]TGGGTATTATTGTTT | 26054 |
rs540928904 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75653653 | TCTCATGTTTTTGGA[A/G]TGTTGTGTTTTTTTT | 26054 |
rs540963120 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75605929 | GATGTCAGTGGAGAC[G/T]GGGGAAGAGAAGTTG | 26054 |
rs540991367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629805 | AGAGTAAAAATTAAT[A/G]TAGTGAGTTTATGTG | 26054 |
rs541007520 | snp | A/T | 1.7081e-05 | 0.00292237 | intron-variant | SENP6 | GRCh38.p7 | 6:75695975 | TCACTCACATTTAAC[A/T]AAGTGAAAAATCACG | 26054 |
rs541036215 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602609 | CTTGACGGGGAGAAG[A/G]GAGGGTATACTGGAA | 26054 |
rs541047797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649792 | AGTGCTGGGATTACA[C/T]GCGTCAGCCACCGCG | 26054 |
rs541083120 | snp | C/T | 3.31614e-05 | 0.00407181 | intron-variant | SENP6 | GRCh38.p7 | 6:75713596 | AGTAAGTTCACACTT[C/T]ATTTCGTATTCTGAT | 26054 |
rs541089358 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625677 | AGTTCGAGACCAGCC[C/T]GGCCAACATGTTGAA | 26054 |
rs541091478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658395 | AAAAGAATATTAAAT[A/G]TAGGAAACTAGAAGT | 26054 |
rs541128050 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670843 | TATCAGTTAGTTCAA[A/G]ATTTCACATTGCTTT | 26054 |
rs541142893 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638594 | TGTGTGTGTGTGTAT[A/G]TATATATATATATAT | 26054 |
rs541143585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650420 | CTTTCACCCACTGAT[G/T]TTAGCATCCATTGGT | 26054 |
rs541155449 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75684416 | CCTGATTGCCCTAGC[A/C]AGAACTTCCAACACT | 26054 |
rs541193860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608536 | AGAAGGAAAGAGAGG[A/G]AGGAAAGAAAGGAAG | 26054 |
rs541218650 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75671005 | TTTAGTATCATCCCA[G/T]CTAAGTGCATGAAAA | 26054 |
rs541220726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620520 | TTGATAAGGGCACCA[A/G]TCCCATTCGTGAGAG | 26054 |
rs541252509 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618960 | TTTTTCAGGCTTGCA[C/T]TGAAGTTTTATATTT | 26054 |
rs541257605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653159 | CCTCACCCTCCCGAA[C/T]AGCTGGGATTACAGG | 26054 |
rs541265501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628411 | CACTTGATCTAAAAA[C/G]TATTATTACAGATAT | 26054 |
rs541295206 | in-del | -/T | 0.366885 | 0.220993 | intron-variant | SENP6 | GRCh38.p7 | 6:75682405 | ATCAGGATTATATTC[-/T]TTTTTTTTTTTTAAT | 26054 |
rs541307152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636735 | GCATGCAGTAGGAAT[C/T]ACGTCTTCAAAGGCA | 26054 |
rs541370087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75712678 | AATCTTCAGCCATCA[A/G]TATTTATATACAGAG | 26054 |
rs541380209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622202 | ACTGTTGTGTAAAAA[A/T]TTTAAATGATAGTTT | 26054 |
rs541410620 | snp | A/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718157 | TTCTTTAAAAAAATG[A/G]TCTCTGAAAACTGTG | 26054 |
rs541415235 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75665600 | GAGTACAAGGTATAA[C/G]AGCAAATTACCATCA | 26054 |
rs541419176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614807 | TGCTGGGGAGAAATT[A/C]GATGTTTGCTGAAGG | 26054 |
rs541476389 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622451 | GTAATCCCAGCTACT[C/G]AGGAGGCTGAGGCAG | 26054 |
rs541516334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75705417 | GGGTGTGGTGGTGCC[C/T]GCCTGTAATCCTAGC | 26054 |
rs541528947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662070 | AATAAATAAATAAAT[A/T]AATAAATAAAACAAG | 26054 |
rs541563772 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667556 | CAATGGACTTTAAAA[A/T]TTGTTAAAAAATCAA | 26054 |
rs541569765 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75683973 | ATGACATTGAATCTA[C/T]ACATTACTTTGGGCA | 26054 |
rs541578288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640034 | GAATTTGCTATGATA[A/T]CATTATTGAATTTTT | 26054 |
rs541581734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705769 | CCTTGCTCATGGAAC[C/T]AATGAATCTTATTTG | 26054 |
rs541581805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698521 | TTAACTTTTGTAGAG[G/T]TGAGGGTCTCACTGT | 26054 |
rs541661972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632273 | AAATTTTTTTTGGAA[C/T]GCAATTGACTGTTAG | 26054 |
rs541664027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640511 | ATATTGACAGAAATC[A/G]AAAAACAATTTAGAC | 26054 |
rs541697973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633164 | CTGTACAGAAACTTT[G/T]ATACTAAGGCAAAAG | 26054 |
rs541721664 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638779 | AAAACAACAGAGGCC[A/G]GACATGGTTGACTTA | 26054 |
rs541754401 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641490 | TCTTCTGACTGAAAG[A/G]TTTGTAAGAGAATTT | 26054 |
rs541780102 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613184 | GTTTTTAAGAGGCTC[A/G]TGAGCTCAGAATGGC | 26054 |
rs541795127 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674844 | TTATATAACTCCCCG[C/G/T]TAAATTTTACTATTA | 26054 |
rs541868161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669296 | GGGAGGTGGAGGTTG[C/T]GGTGAGCTGAGATCA | 26054 |
rs541878694 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717378 | CTTACATTTTGCACC[C/T]TTAGATAATGTTTGA | 26054 |
rs541934148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676751 | ATTTAGATTTATTAG[A/G]TGAAGTAAATTAGTT | 26054 |
rs541952927 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718621 | GAAGAAGAAAATGGG[G/T]TATGAACACTGCTAT | 26054 |
rs541983079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612260 | GATAGTTCTTAAGAA[A/G]GACTTGGGCTGTAGC | 26054 |
rs542016120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701259 | TGTTCCTTGTATCCC[A/G]GCACAGCCCTGTGTC | 26054 |
rs542047249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655986 | CACTTAGGCCGAGGT[A/G]GGTGGATCACCTGAA | 26054 |
rs542058468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681293 | GCACCTCCCCCTTTG[C/T]TCTCTGTTACTCCTG | 26054 |
rs542087754 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647632 | GGCAAAGAAGCTATG[A/T]TTTGCTTTTAATAGG | 26054 |
rs542119739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681816 | GGAGGATCACTTGAG[A/G]CCAGGAGTTTGAGAC | 26054 |
rs542156119 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633199 | TATACATAAGCACAA[G/T]TTGAAATGACAGCCG | 26054 |
rs542162303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642056 | TTTGACAGCATTACC[A/T]TCCTTGGTGATGACA | 26054 |
rs542165203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689015 | AGGTTGCGGGGAGCC[A/G]AGATCATGCCATTGA | 26054 |
rs542201794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75648025 | TTTTGATTATTTTAG[C/T]ATTTTTGCTATGTTA | 26054 |
rs542205736 | in-del | -/T | 0.0325976 | 0.123435 | intron-variant | SENP6 | GRCh38.p7 | 6:75685348 | TCCTGGATTCATTGA[-/T]TTTTTTTTGAAGGGT | 26054 |
rs542262407 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674060 | GCTTTATGTCATCAT[C/T]ATTGACACTTTTTGC | 26054 |
rs542282733 | snp | C/G | 3.33801e-05 | 0.00408521 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634780 | CATCATGCTCATGCA[C/G]AGATACCAGTAGTAA | 26054 |
rs542285391 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75685954 | CTGGGTATCCTTCTT[A/C]ACTTTCTGTCTCGTT | 26054 |
rs542338024 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651398 | TTGCTCTATTACCCA[A/G]GCTTGGAGTACAGTG | 26054 |
rs542345227 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600056 | GCGACAAGTGAAACT[C/T]CGTCTCAAAAAACAA | 26054 |
rs542390491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680339 | ACAAAAGGACAGTGC[C/T]AATAAGCAGTTGAGC | 26054 |
rs542430896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701892 | CAATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 26054 |
rs542454754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75604338 | CTTTAGAGCATAAGC[A/G]TAAGGGTTCTGGGCA | 26054 |
rs542492429 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75695051 | GGCTAAATTTTTGTA[A/T]TTTTAGTAGAGACAG | 26054 |
rs542515173 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75631787 | CCCTTGGCAGAAAAA[A/G]TTTGCTGATCCCTGT | 26054 |
rs542528960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648196 | CAATTAAAAAGAGAC[C/G]ACACCTGCTAAAACT | 26054 |
rs542544497 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75698452 | GGTATTCTATGAGAT[G/T]GTTTATGTCTAATAA | 26054 |
rs542571657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75706871 | GGAATCACTACTTTC[A/C]CTTGCTGTTTTTTCA | 26054 |
rs542577329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651830 | TTTTTACACTCTCAT[G/T]AAAAGATGACAGACA | 26054 |
rs542597458 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601445 | TGCTAAATTATTTTG[C/G]AAACTTCTTTAAAAA | 26054 |
rs542597916 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687213 | AGCTTGTGCATGTGT[C/T]GTGAAGTTCTTGTGC | 26054 |
rs542601748 | in-del | -/TA | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75630840 | TAATAGACATAAAAC[-/TA]CATCATTTAAAAAAA | 26054 |
rs542621635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75715103 | AGACCATATGTAAAT[A/G]AGTTAGTGTGGCTGT | 26054 |
rs542625302 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602378 | GTATAGGCCCGTCTG[A/C]ACGTGGGAGCGCAGC | 26054 |
rs542664073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75602929 | ATCTTGTCTGGTGTT[C/T]ATGAAAAGTTTCAAA | 26054 |
rs542676822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679768 | TGGACATGTATATGA[A/G]ATAAAACAGAACTTA | 26054 |
rs542685746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653558 | TTAACCTTGTTTTCC[C/T]TCAATGCGTTTGGGT | 26054 |
rs542703985 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75708320 | TCCTTTTCATCCCAT[C/G]TTGTTTATATTAATA | 26054 |
rs542726089 | in-del | -/AGCCTCCTGAGT | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75670051 | CAGTTCTCCTGCCTC[-/AGCCTCCTGAGT]AGCCTCCTGAGTAGC | 26054 |
rs542740269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673041 | ACTGTGTTAGCCAGG[A/T]TGGTCTCGATCTCTT | 26054 |
rs542838095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650900 | GATATCATGGTCTTT[C/G]TATAGTTAACACTCA | 26054 |
rs542849050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673620 | TGAGCCACTGTGCCC[A/G]GCCCAGTGTCTACTT | 26054 |
rs542859626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607511 | ATACATTTCTTCATT[G/T]TTGTACTGCACTTGT | 26054 |
rs542861543 | snp | A/G | 7.44241e-05 | 0.00609972 | intron-variant | SENP6 | GRCh38.p7 | 6:75623999 | CTTCTTTTACATTAT[A/G]TACAAAAAAATTGTT | 26054 |
rs542892511 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602009 | GGGGTGGGCGGACGG[A/C]CGTAGCGGCGGCGGC | 26054 |
rs542909315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715192 | ACCCTGATCTAGACT[A/G]TAAGATCTATGATAG | 26054 |
rs542926447 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75665280 | GACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 26054 |
rs542950279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609472 | CTGATTGAAGGGGAG[A/C]GGGAGTAGATTCCAC | 26054 |
rs542951295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616486 | AGGTGTGGTGGCACA[C/T]GCCTGTAATCCTAGT | 26054 |
rs542959966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644220 | AAAAAGAAAAAAAAA[A/G]CACCAAAAGGATGTA | 26054 |
rs542974780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710133 | TGTTTAAACCTTCAG[C/T]TATATGGTACATGAG | 26054 |
rs542999634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75652739 | TGTGTAAAGATGGTT[A/G]GCTCCCAACACAGTA | 26054 |
rs543012610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75702194 | AAACAAGCAGATTAA[C/T]TTGAGAACTAAAAAA | 26054 |
rs543045474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656180 | GATTGCGCCACTGCA[C/T]TCCAGCCTGGGCGAC | 26054 |
rs543091144 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702012 | AGGGGAATGACGAGT[A/T]GCAAAGTGACATTAC | 26054 |
rs543151125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693592 | GATCTGACTCACTGT[C/T]TTGTATTATCTTCTG | 26054 |
rs543178900 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638090 | TGGTCTCGAACTCTT[A/T]ACCTCAAATAGTCCA | 26054 |
rs543214964 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650553 | ATCTGTACCTTCCTG[-/A]ATATATTTATTGATG | 26054 |
rs543216627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630870 | AAAAATCCGTAACCT[A/C]TATTTTATGTTTAAA | 26054 |
rs543280626 | in-del | -/T | 0.0744748 | 0.178019 | intron-variant | SENP6 | GRCh38.p7 | 6:75607547 | CTAGTTTTCTTTTCC[-/T]TTTTTTTTTTAACCA | 26054 |
rs543307635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619720 | GCCTGAACTGTTTTG[C/T]GTTCCCACTAGCAAT | 26054 |
rs543340656 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617002 | TATCCCAGTCTCCTG[A/C]GTAGCTGGTACTACA | 26054 |
rs543346211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620453 | CACAAATGGTGCCTT[C/T]TGGCTGTCTCCTCAC | 26054 |
rs543346364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612986 | GGGCATCGTGGCATA[G/T]GCCTGTAATCCCAGC | 26054 |
rs543427207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703137 | ATTTTTTAATAAACA[A/G]GATTAAGATCCTGTT | 26054 |
rs543436782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663739 | CTAGTTATAACCAGC[A/G]TTCTGACTTCGGCCA | 26054 |
rs543437098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656670 | TTTGTGTTTTTTTCT[G/T]AACTCTCTATAGATC | 26054 |
rs543448073 | snp | G/T | 1.7246e-05 | 0.00293644 | intron-variant | SENP6 | GRCh38.p7 | 6:75678782 | ATATATAGATTTGTT[G/T]ATTTGCTTGCCTTCT | 26054 |
rs543464483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628904 | TTTGTATTTTTAGTA[A/G]TTTTAGTGGTTTTGC | 26054 |
rs543473300 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625028 | TGTATAATAATGTTA[C/T]AGGTTTGATGAAATA | 26054 |
rs543478230 | in-del | -/TTCAGAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657246 | TAATTGGTTGTGTGT[-/TTCAGAC]AACTGTGTTTATTTT | 26054 |
rs543506580 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671486 | CCCAGCACTTTGGGA[G/T]GCCAAGGCGGCTGGA | 26054 |
rs543508960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672414 | TGTAAATTTAGTTAA[A/G]AAAATAAAAGGCAGT | 26054 |
rs543526427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649036 | TTCTGGCCTGGTATG[G/T]TGGCTCACACCTATA | 26054 |
rs543529604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665520 | AGTTTGTATTTGACT[C/T]AAATACAATGTGAGT | 26054 |
rs543530364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75695717 | ACTCCAGCCTGGGCA[A/G]CAGAGTGAGACTCTG | 26054 |
rs543551617 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75622042 | TATCTTTCTTCCCCA[A/G]TTGTGACCACCACCC | 26054 |
rs543562889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679162 | CTTATGTCTATAATC[C/T]TGACACTTTGGGAGG | 26054 |
rs543568892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75642613 | ACTGGCTGGGACCTA[C/T]GTCATAAAAGGTTTT | 26054 |
rs543591124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689655 | TAATAACGTATTTTT[A/C]CTGTACCTTTTCTCT | 26054 |
rs543596129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676645 | AAAAGCTGTTTTGCA[A/G]TTAGATTCTCTTGAG | 26054 |
rs543610433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626795 | TAATCTTGCAAAATA[C/T]GTAGTCATACTTGAA | 26054 |
rs543621739 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704388 | TCAAGTGGAGGTACT[A/G]TGCCTGGATGTGCAC | 26054 |
rs543634980 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599573 | AGTGGCTAAGATTGA[G/T]GGGGAGACACCGGAA | 26054 |
rs543638742 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647892 | GGCTTTAGAATATTC[C/T]CAGGTATAATAGATA | 26054 |
rs543655824 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75610869 | GTTTTTGAAGATGCG[-/T]TTTTTCCCCCTCCCA | 26054 |
rs543656564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635590 | ACTTAAAAATGTTAA[A/G]TAACCTCATACTTTA | 26054 |
rs543696577 | in-del | -/AAGG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681890 | AAAAATATAAAAAAC[-/AAGG]AAGAAACAAATGGAA | 26054 |
rs543758421 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75608958 | ACCTTTTTCTAGATA[C/T]TAGCTGATTTTGACC | 26054 |
rs543774528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628336 | TTAACATTAAGTAGA[A/G]CTCCTGCTACTAAAG | 26054 |
rs543834735 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624259 | GTTCATAAAAAGCAC[C/G]TCATTGTTTTCAGTG | 26054 |
rs543858458 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668045 | GTACAGATACAAATA[C/G/T]GGGAACATATATACT | 26054 |
rs543860079 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680404 | CAGAGATGGTAAGAT[A/G]TTGTTTAATTGTGAG | 26054 |
rs543870788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624745 | AGGAATTATTTTTAT[A/G]TTTAGTCTAAGACAC | 26054 |
rs543879919 | in-del | -/TACTT | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75660429 | GCATGTACATATGAA[-/TACTT]TACTTAAAAGGGTTA | 26054 |
rs543912187 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75703781 | TTAAAAAACAAAAAA[A/T]TTGAGAACTTTCCAT | 26054 |
rs543930491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75712465 | GAGGACCGCATGAGG[C/T]CAGGAGTGCAAGACC | 26054 |
rs543964516 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690063 | ACTACAGGTGCACAC[C/T]GTCACACCCTGCTAA | 26054 |
rs543964638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645975 | TTAGCAAAGATGGCT[C/T]AGTACACAAGTTCAA | 26054 |
rs543969000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614741 | TCTCCCTTTACTGCA[C/G]CAACAATAGGACCTT | 26054 |
rs543979543 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626558 | GAATAGAGATTTTTT[C/T]CCCCCAGTCTTTTGC | 26054 |
rs544051495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639325 | TGTTTTTTAGTAGCA[A/G]AGATAAAATTTCAGA | 26054 |
rs544099994 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692092 | AACTCCCGACCTCAG[A/G]TGATCCGCCTGCCTC | 26054 |
rs544128768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75678296 | AGGTTATTTGAATTT[C/T]ACCAGCATTATTTAA | 26054 |
rs544158719 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641370 | TATCATTATATTTTA[G/T]TGATAATACCCTTGT | 26054 |
rs544177877 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665142 | ATATAAAAAATTAGC[C/T]GGGCATGGTGGTGGG | 26054 |
rs544189266 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75681679 | GATACAGCATCCATC[A/C]TAAAAATGTTTTAAT | 26054 |
rs544230522 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667982 | AAATAATAAACTTGT[A/G]TGTTAAATTCTATAT | 26054 |
rs544292059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75625205 | CCACCTCTGTCTCCC[A/G]GGTTCAAACAATTCT | 26054 |
rs544323181 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716120 | AGTAACAGCCTTTCA[A/G]TTCATATACTGCCTT | 26054 |
rs544325167 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610868 | AGTTTTTGAAGATGC[A/G]TTTTTTCCCCCTCCC | 26054 |
rs544412090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75675735 | TTACCCACAAGAGTA[A/G]TGATTTATAGAGCAT | 26054 |
rs544422183 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75693102 | TTCAGTTAAGTTTTA[A/T]AAAACAGCCATTGTA | 26054 |
rs544535145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75603589 | TTTTAGTATGTTTCG[A/G]AAAGATTACTGAATC | 26054 |
rs544551353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694352 | CTTTATTTTCTATTT[C/T]CATAAAAAATACTAT | 26054 |
rs544606363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691290 | TGGGACTACATGTGC[A/G]AGCTACCACACTCTG | 26054 |
rs544624991 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600409 | AATTTTTCCAAATGG[A/T]ATCAAGCTGCTGAAA | 26054 |
rs544630390 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695662 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 26054 |
rs544667736 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75691816 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 26054 |
rs544721761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75683041 | TGTAAAAGCATTCCT[A/G]TTTCTCCACATCCTC | 26054 |
rs544752152 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75711695 | TATATTTTTTGAGAC[-/A]AGAGTCTTGCTCTGT | 26054 |
rs544776241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684236 | TGCTTGTGATTTTTG[C/T]ACATTGATTTTGTAT | 26054 |
rs544816930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703698 | GCTCAGGGTGCTGAA[A/G]TTGCAGTGAGTGGAG | 26054 |
rs544823745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661923 | TGAGCATGGTGGTGG[A/G]CACCTGTAGTCCCAG | 26054 |
rs544831127 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667986 | AATAAACTTGTATGT[G/T]AAATTCTATATGTAT | 26054 |
rs544840225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75611383 | GCTTCTCCTTCACAA[A/G]TTTGGGTATCAGCTC | 26054 |
rs544857022 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612886 | TGGGAGGCCAAAACA[C/G]GCAGATCACTTGAGG | 26054 |
rs544873140 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648785 | TAGTCCAGTGCTTTG[C/T]ATTCATTATTTACTT | 26054 |
rs544877005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612070 | TCAGGGACTTGAGAA[A/G]GGCTTAGCTAGGTGA | 26054 |
rs544892128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701797 | GGCGCACACTACCAC[A/G]CCCAGCTAATTTTCT | 26054 |
rs544909982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655197 | GGATGCGCATGGAGC[A/G]ATGAGGGAGGAAGTG | 26054 |
rs544913691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665339 | GTGGCCAAAATGCAT[A/G]ATATTGAGGGAAGTA | 26054 |
rs544932428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604256 | AGGGTCTTTGAATGT[A/G]TAGGTATGATAAATT | 26054 |
rs544941407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647104 | GTTTATTTAGAGTAG[C/G]AAAGTAGCTATTGTA | 26054 |
rs544984325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650555 | TCTGTACCTTCCTGA[G/T]ATATTTATTGATGAT | 26054 |
rs545007648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607423 | GGCTAGCTTGTTCCT[A/G]TAAACTTTCTTTTGA | 26054 |
rs545018782 | snp | G/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618761 | CATAGGGTTCATTCT[G/T]TCTTTCCTCTCTTGC | 26054 |
rs545045661 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SENP6 | GRCh38.p7 | 6:75707677 | GTGCTTTTTTGTTGT[G/T]GTGGTGGTGGATTTT | 26054 |
rs545054828 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663623 | ATTTTTAATATAAAT[A/G]TGAGCTTAAAACTAA | 26054 |
rs545071723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644085 | TCAAAAAATTAAGAG[C/T]GCCCACTTCAAAAGC | 26054 |
rs545076401 | snp | A/G | | | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715510 | AGATCAGAGCAAAGA[A/G]AAAAGAAAGCATAAG | 26054 |
rs545089769 | in-del | -/GTAC | 0.00835141 | 0.0640778 | intron-variant | SENP6 | GRCh38.p7 | 6:75624992 | AAATTTTGCACTGTA[-/GTAC]ATACAATAATGGTGT | 26054 |
rs545139946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75711220 | CTAAATAGAGAAAAA[G/T]TTTTGACAATCATTA | 26054 |
rs545162676 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75630580 | GGATCATTGGTTTAA[A/G]CTATTATAGACTGGT | 26054 |
rs545165845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609266 | TTCCTGTACCTCCCC[C/G]CAAAGGAAGGGGCGA | 26054 |
rs545166233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664634 | TGCTAATAAAAGACC[A/G]GTGTTGAAAGAGAAA | 26054 |
rs545168354 | in-del | -/ATATA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638618 | TATATATATATATAT[-/ATATA]TTTTTTTTTTTTTTT | 26054 |
rs545193118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614234 | TAAGGTGGTGTTCAC[C/T]AGATTTTTCCACAGA | 26054 |
rs545194664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75652563 | CTTGTGTGGCCAGGC[A/G]CGGTGGCTCACGCCT | 26054 |
rs545202908 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602314 | TCGGGCCGCGGGCCT[A/C]GCTGCCCGCCAGCCC | 26054 |
rs545223803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75657844 | GGCAGAGCTTCACTT[A/G]TGAAAAGAACAGCAT | 26054 |
rs545264232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679561 | CATTAACATGGTACA[A/G]TCCTAGCAGATGAGA | 26054 |
rs545282921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606628 | CAGTGGTGGATTGTT[G/T]ATACAAGTTGAACAT | 26054 |
rs545297820 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634934 | GTCTGTAGAGAGATA[C/T]ATCTCTGAAATAATT | 26054 |
rs545299583 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602872 | TTGACATTTAAAAAA[G/T]TTTGGGGTGGTGGCC | 26054 |
rs545308805 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660510 | ATTGTCCCAGATTCC[A/T]TGTGAGTCCCTTCAA | 26054 |
rs545315089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614639 | AATAACTTGTTTCTC[A/G]TCAGATTTCACCCAC | 26054 |
rs545326813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615555 | GTTTACTTTTGCTTT[G/T]TAGAATAAACCCTGC | 26054 |
rs545343991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649808 | GCGTCAGCCACCGCG[C/T]CTGGCCCTTAACCTA | 26054 |
rs545348641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705476 | CTTGAACCTGGGGGC[A/G]GAGGTTGCAGTGAGC | 26054 |
rs545359052 | in-del | -/TTTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644463 | TAAATAGCTGGTAAA[-/TTTC]TTTCTTTCTTTCTTT | 26054 |
rs545361817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626704 | ACATGTAGTTTTGCT[A/G]GATACTGCCAAATTC | 26054 |
rs545382936 | snp | A/C | 0.00100833 | 0.0224309 | intron-variant | SENP6 | GRCh38.p7 | 6:75659230 | CTTATTTTAACTAAA[A/C]CTTAAAGTTTATTTT | 26054 |
rs545399325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619655 | TTGCTAGCTCGTAGG[G/T]TAATTCTATGTTTAA | 26054 |
rs545404878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75608554 | GAAAGAAAGGAAGAA[A/G]GAAAGGAAGGAGAAA | 26054 |
rs545435085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708630 | CCAGGCACGGTGGCT[C/T]ATGCCTGTAATCCCA | 26054 |
rs545480375 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75662239 | TTTAATTTTGTAAAA[C/T]GCCTTCCACTTCTAC | 26054 |
rs545517115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75656119 | ACTCAGGAGGCAGAG[A/G]CAGGAGAATTGCTTG | 26054 |
rs545554748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629064 | TGCCAAAAATGACAT[A/G]GTAATCAAACATTTA | 26054 |
rs545558518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699645 | GGTGCATGCTACCAC[A/G]CCCAGCTAATTTTTG | 26054 |
rs545559959 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645907 | TAGTTTAATGTTACA[A/G]TACTTGGTAAGATTG | 26054 |
rs545651177 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75673889 | GTGGGGTGTGGTGGC[-/G]GTGCACCCGTAACCC | 26054 |
rs545670964 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75672965 | CCCGAGTAGCTGGGA[C/T]TACAGGCACCGGCCA | 26054 |
rs545674156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626116 | CTACCAACTAAATAG[A/G]GAGTTAGGTTTGTTG | 26054 |
rs545732180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75666257 | TAAAATATATATACG[A/G]TATATATAAAATATA | 26054 |
rs545736571 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718405 | AAGAGATACAGATAA[C/G]AAGGCTGCTCTTTAG | 26054 |
rs545761244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709261 | GTATATGTATTTAAG[C/T]ATATGTATACTTAAT | 26054 |
rs545768064 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717508 | TACTCAGCTATTTGA[C/T]GGCATTTTTCCCACC | 26054 |
rs545782527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75677487 | GTTCCTCCACATTCT[A/G]TCCTTATCTTTACTT | 26054 |
rs545799902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709283 | ATACTTAATCATATA[A/G]CTGATAACTAGTTTT | 26054 |
rs545819015 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75713103 | AGACCCTGCCTGAAA[A/G]AAATGGGCCGAGGTT | 26054 |
rs545820497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663008 | TTACTTATTTAGGCT[C/G]TCATGGTAGCCATGA | 26054 |
rs545846339 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75671102 | TATTATAGCATCAAG[A/C]CTCCTAGAAATAGAT | 26054 |
rs545849790 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653799 | CTTGGGAAACTCCAC[A/G]GCTAGATAGACTACA | 26054 |
rs545875591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612824 | AGGTATCAGAAAACT[A/G]TGCCCCAGACCAGGC | 26054 |
rs545908082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671773 | GGAAAGTTGTAAGGT[A/T]TTTTATTATTTAATG | 26054 |
rs545913070 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678501 | CCTTTTGCATTGAAA[A/G]GCATTCTTGCCTTGT | 26054 |
rs545935140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75641258 | TTTTCTATAATGGTT[A/G]TATATATTTATGCTA | 26054 |
rs545950808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656606 | TTTTTCTCTTCTTTC[C/G]CTAGAAAATGGAATC | 26054 |
rs545958457 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75695125 | AGGTGATCTGCCCAC[C/T]TCAGCCTCCCAAAGT | 26054 |
rs546009393 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75682578 | ATCCCACAACAGGCC[C/T]TGGTGTGTGATGTTC | 26054 |
rs546012385 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671145 | ATGGCTGCCCAAAGG[A/T]CTTTGTGTACTTTAT | 26054 |
rs546034255 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632274 | AATTTTTTTTGGAAC[A/G]CAATTGACTGTTAGT | 26054 |
rs546036967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648969 | ACAAAGAAGGTTACT[A/G]CTAATCCTCAGAACT | 26054 |
rs546132625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635520 | GTCATTTAGAAGACA[C/T]GTCCTGAACCTTGCT | 26054 |
rs546133016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75676543 | ACTGCTTAGAAGATA[C/T]ACACATTTCAGCAGT | 26054 |
rs546244343 | in-del | -/ACTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603735 | TGGAACACAGTAGGT[-/ACTC]AGTGTTAGTCTAGTG | 26054 |
rs546279938 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75705554 | ATCTCAAAAATAAAT[A/T]AATAAATTAATTAAT | 26054 |
rs546298997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620589 | CCTCTTAATACCATC[G/T]GTATCTTGGGGTTAG | 26054 |
rs546305630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714229 | AAAATCTGGCTTTAT[A/C]CTTAACCTTATGTTA | 26054 |
rs546330023 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75666580 | ATTAATTTTAGATCT[A/G]GAGGAGGTCCAAAGC | 26054 |
rs546390493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685041 | CCTGGACTTTTTTTG[A/G]TTGGTAGGCTATTAA | 26054 |
rs546438965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689621 | ATGGACCATATGTGA[C/T]AGTGAGCCCATAAGA | 26054 |
rs546468849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644304 | TGATAACAATTGGAT[G/T]ATAACTTAGACCGAG | 26054 |
rs546491755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642531 | TGTCAAAGAACAGAA[A/G]AAAGGGGCCACTAAG | 26054 |
rs546502196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75683815 | CTTTGTAGTATAGTT[C/T]GAAGTCAGGTAGCGT | 26054 |
rs546505558 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637140 | CTCAGCACCGTAAAG[G/T]GCTGGAATTACAGGC | 26054 |
rs546538957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75713147 | TCTTTATACTTTTTC[A/G]TGGTCCTTTTGTTGA | 26054 |
rs546612111 | in-del | -/TTTG | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75687084 | ATATTTCTTGGAGGC[-/TTTG]TTTGTTTCTTTTTAC | 26054 |
rs546618484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615182 | CTCGCCTATCCTGCT[A/G]AGAGGTTTGTTTTGG | 26054 |
rs546635571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631605 | AGCATAATATAAAAC[G/T]CAAATCTGTGTCCAT | 26054 |
rs546648324 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631553 | TTTTTAAATGCTTGG[A/G]AGAAAGAATCAAATG | 26054 |
rs546662424 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75623217 | TAGTTATACATTTTT[A/T]AAAAACTGTCTTTAC | 26054 |
rs546678633 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639753 | CCAAGATTTTAAATT[A/G]TAGGCTTTTCCTTGT | 26054 |
rs546740137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698822 | TCAAGACCAACCTGG[A/C]GAACATGGCGAAACC | 26054 |
rs546742141 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75706080 | CCTAGTAGCTGGGAT[A/T]ACGGGTGCGCACCAC | 26054 |
rs546775420 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668993 | TCTCATTTGAAGATA[C/T]AACTCTACAGCTAAA | 26054 |
rs546776629 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658328 | TCAAATTAAATATTA[C/T]ATAATATTGATTTTT | 26054 |
rs546789971 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688545 | CGCCACCCCACCCCC[A/C]CGTCCAGGATTATAT | 26054 |
rs546838861 | in-del | -/CTA | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618825 | CCTTGTTTCCATCAT[-/CTA]CTATTTATTTACTTA | 26054 |
rs546907472 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628074 | CCTACAGGACACATT[A/G]ATTTATTTAGTGAAC | 26054 |
rs546933769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629385 | CTCACTGCAACCTTC[A/G]CCTTCCCAGGTTCAA | 26054 |
rs546953344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75692827 | CCTAGCACTTGGGAC[A/G]CCAAGGCAAGCAGAC | 26054 |
rs546963502 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688882 | AACCAACCTGACCAA[C/G]ATGGAGAAACCCCAA | 26054 |
rs546995153 | snp | A/C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691207 | GAGAGCAGTGACGCA[A/C/G]TCACGACTCACTGAA | 26054 |
rs546999601 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75640205 | GGTGTAGTATACAGA[A/G]CAAAAAACCCATGTG | 26054 |
rs547000646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646065 | TTTACTGTCTCAGAT[G/T]ATTTATGTCAATTGT | 26054 |
rs547001840 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603933 | GTTCGTTTCGTATTA[C/T]CTCCATTCCAGTTTG | 26054 |
rs547014908 | in-del | -/AGTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685659 | TTTCGTTATTTACCC[-/AGTA]GTCATTCAGGAGCAA | 26054 |
rs547019296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75635022 | AGAGAATTTTTCACT[A/G]AGACCTGTTGTATTG | 26054 |
rs547067590 | in-del | -/AAAT | 0.0460113 | 0.144529 | intron-variant | SENP6 | GRCh38.p7 | 6:75662065 | TCAAAATAAATAAAT[-/AAAT]AAATAAATAAATAAA | 26054 |
rs547083023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75673946 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 26054 |
rs547108353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627185 | CAGGCTGGTCTTGAA[C/T]TCCTGACCTCAGATG | 26054 |
rs547142509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674405 | TGGCTCATTGCAACT[G/T]CTGCCTCCTGGGTTC | 26054 |
rs547145180 | snp | C/T | 6.65613e-05 | 0.00576855 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709558 | CAGACTAAACTATAG[C/T]GATGAATCACCTGAA | 26054 |
rs547154106 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75712312 | TTGAAAATGCAGCAT[-/C]ATTCTACAGAAAAAT | 26054 |
rs547172396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660000 | AATTTCAGCTAAATA[A/G]TGTCCTTTATGCTTA | 26054 |
rs547200100 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75604622 | TGAGCGAGATTCTGT[C/T]TCCAAAAAAAAAAAG | 26054 |
rs547206695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75645515 | CCAGCTACTCAGGAG[A/G]CTGAGGCATGGGAAT | 26054 |
rs547214253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75652295 | GGATTACAGGCATGA[A/G]CCACCACGCCCAGCT | 26054 |
rs547252634 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75652981 | GCAACTCTTTGTTAT[C/G]TTTGATGTATATATC | 26054 |
rs547276168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613062 | GAGGTTGCAGTGAGC[C/G]GAGATTGTGCCACTG | 26054 |
rs547292473 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694881 | TTTTTTAATTTATTT[G/T]TATTTTCTTGAGACC | 26054 |
rs547314251 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75693248 | CTACTAAAAAAAAAA[A/T]ACAGAAATTAGCTGG | 26054 |
rs547357297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642245 | GACAAGATCCCCGCA[A/G]TCCTGTAGTTTACAT | 26054 |
rs547366052 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606679 | ATCCTCCAGAATTTG[A/C]AGCAACATGACCCCC | 26054 |
rs547366534 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716669 | ACAGATTTATAGCAC[A/G]TATAGGGATCTTGCA | 26054 |
rs547412997 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696644 | ACTCCACCCAGCTAA[A/T]TTTTGTATTTTTTGT | 26054 |
rs547418949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75683484 | CCCATGCCTATGACC[C/T]GAATGGTATTGCCTA | 26054 |
rs547436449 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75615024 | GCCTCCCAATTAGCT[A/G]GGATTACAAGCATGC | 26054 |
rs547439748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614327 | CTGGAGTGCTGTGGC[A/G]CATTCTCAGCTCACT | 26054 |
rs547481566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684059 | CCATTTGTTTGTGTC[C/T]TCTTTTATTTCGTTG | 26054 |
rs547523120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684645 | GCCTTTTCTGCATCT[A/G]TTGAGATAATCATGT | 26054 |
rs547533714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612542 | CACTATGCTGCTCAG[G/T]CTGCTCTCGACTTCT | 26054 |
rs547591627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663111 | CAAAATCTTTTATTT[C/T]TTTTGTTCTTTTGGA | 26054 |
rs547616270 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654321 | GGAAAAGCTTTGCAC[C/T]TAATGAGGATGGAAT | 26054 |
rs547618646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691610 | TTTTTGTTTTTTGTT[C/T]TTTTTTTGAGACGGA | 26054 |
rs547653998 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700123 | GCTGTGTTGCCCAGA[C/T]TGGTCTCAAACTTCT | 26054 |
rs547708356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75689377 | AAAACAATATAACAC[A/G]GTGTCATCTCACATC | 26054 |
rs547825587 | in-del | -/GAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702067 | TCATTCCAAAAACAA[-/GAA]AGCGTTCAGGGATTG | 26054 |
rs547849922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75690853 | GGCGCTCACCACCAC[A/G]CCTGGCTAATTGTTT | 26054 |
rs547891485 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710913 | TTAAATATTTCTGAT[A/G]TGAAAACATTATTCA | 26054 |
rs547909566 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599970 | TCGGGAGGCTGAGGC[A/G]GGAGAATCGCTTGAA | 26054 |
rs547934092 | in-del | -/T | 0.489177 | 0.0727629 | intron-variant | SENP6 | GRCh38.p7 | 6:75653661 | TTTGGAATGTTGTGT[-/T]TTTTTTTTTTTAACT | 26054 |
rs547934380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631355 | CATTGATGCAGCAAA[C/T]ACATATTGAGCACAG | 26054 |
rs547950271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672751 | TGTTTTATAAAATTC[C/T]ACACTTGCTTATTAT | 26054 |
rs547954691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693422 | TTTAAAAAAAAAAAA[A/C]AAAAAAACACCAAAG | 26054 |
rs548011203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620725 | AGACATCAGAATTAT[C/T]CCCACTGCCTCTTCA | 26054 |
rs548037031 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606834 | TAGTTTCAAGCATTT[C/T]GGATAAGGGACACTT | 26054 |
rs548047645 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75613954 | TGTTATGTCCCATTT[G/T]TCTTCTTTAATCTGG | 26054 |
rs548092561 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75673875 | AGACTACAAAAATTA[A/G]TGGGGTGTGGTGGCG | 26054 |
rs548099153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703345 | TTATAACAATATAGT[A/G]ACACAACTTACTTTT | 26054 |
rs548104364 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636813 | ATTGTTAGACTTCAG[G/T]TGAGGGTAAACACAT | 26054 |
rs548118067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660330 | GCAATGTCAGTTAAT[A/G]GGTATTTGACTAATT | 26054 |
rs548163084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707259 | TTGGACAAATGTTAT[A/T]CAAATATAGGTGTTT | 26054 |
rs548164320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616603 | AATACAAAATTAGCC[A/G]GGCGTGGTAGCATGC | 26054 |
rs548209202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75610632 | TTATCTTCAGAGTAT[A/G]TGGGGCTTTCAGTGC | 26054 |
rs548254610 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716870 | ATTTTATTTTTAATT[G/T]GGCCATCTCTGACAT | 26054 |
rs548274992 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668762 | TTAGATGTCCAGCAT[A/G]TGAGTTCAGTTAAAT | 26054 |
rs548332593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618662 | AGCTCTCTATACTAA[C/T]CCGTGTTACAACATA | 26054 |
rs548434387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715088 | AGTGAAAGCATCTGC[A/G]GACCATATGTAAATG | 26054 |
rs548459272 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609394 | CTCTTGAGGCCCAAC[A/T]TCAGAAATTTACAGT | 26054 |
rs548496220 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715653 | CTTTCAAATTTGGGT[A/G]TAGACAATAAAGAAC | 26054 |
rs548499117 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75668151 | TTTACTTATTTACTT[A/C]CTTATTTAAAGGGGG | 26054 |
rs548521672 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614301 | GACAGAGTCTGGCTC[A/T]GTCACCCAGGCTGGA | 26054 |
rs548554774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634113 | ATTCCTCCTTTTTAC[A/G]ATAGTGAACCACCAT | 26054 |
rs548592718 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717733 | AAGTTGTAAAACAGA[A/G]CTTATAGAGGTTTGT | 26054 |
rs548621826 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646286 | CTTCACAAATTTCAA[A/C]TTTTTCAGTGTGGAA | 26054 |
rs548637499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669910 | GGGAACCAAAACTTA[C/T]GTAAGTTATTAAGTT | 26054 |
rs548675449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75713027 | TGGGAGGATCACCTG[C/T]GCTCAGGACATTGAA | 26054 |
rs548743048 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75629353 | CCCCAGGCAGGAGTG[C/T]AGTGGCGCAATCTTG | 26054 |
rs548757500 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669761 | TTGCTTTCTAAAGAA[C/T]TACTGATTTAATTCA | 26054 |
rs548786132 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75690843 | TGGGACTACAGGCGC[C/T]CACCACCACACCTGG | 26054 |
rs548788896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640371 | CATTGGGGGTCTTGG[A/G]AAGGATCGTTAGAGA | 26054 |
rs548790021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622369 | TCAAGATCAGCTTGG[C/T]CAACATGGTGAGACC | 26054 |
rs548800289 | snp | A/C | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599900 | GAAACCCCGTCTCCA[A/C]TAAAAATACAAAAAT | 26054 |
rs548853620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684566 | TATTATTTTGAGATA[C/T]TTTCCATCAATACCT | 26054 |
rs548861423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696703 | GCTGGTTTCAAACTC[C/T]TGGGCTCAAGGAATC | 26054 |
rs548892611 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75643322 | TTGTTTACAAGCATC[A/T]TACTAAAATAACAAT | 26054 |
rs548911278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633418 | TTGTCTTTAGGAAAA[A/G]AAAAGTAGGCAGTTG | 26054 |
rs548920814 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599956 | GCAATCCCAGCTACT[A/C]GGGAGGCTGAGGCAG | 26054 |
rs548952164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636975 | AGCCTCAAACTTCTG[C/G]TCTCAAGCAATCCTT | 26054 |
rs548973592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672167 | AAAATGTCACTGTGT[A/G]TCACTTAGCACCTCA | 26054 |
rs549001829 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621739 | TCTTAAGAAAACATA[C/T]AACTCTTTCACAGTC | 26054 |
rs549072968 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649639 | TCTCTGCCTCAGCCT[A/C]CCGAGTAGCTGGGAT | 26054 |
rs549083187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75639398 | TTTTTTTAAATTTGT[A/G]TATTTTTAATGTGTT | 26054 |
rs549133816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665856 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 26054 |
rs549140408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615119 | TGGTCTTGAATGCCT[C/G]ACCTCAAGTGATTCA | 26054 |
rs549177117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615766 | TCTGCAAAAGTTCAG[A/G]TAAGATTGATGCTAT | 26054 |
rs549190968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642893 | ATCTCAGCAAGGTCT[A/G]GGAGTTGGGGAGGTA | 26054 |
rs549197785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705498 | GCAGTGAGCTGGGAT[C/T]GCGCAACTGCACTTC | 26054 |
rs549204981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75610628 | ACTATTATCTTCAGA[A/G]TATATGGGGCTTTCA | 26054 |
rs549227766 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75643670 | AAGGTTGCAGTAAGC[C/G]AAGATAGTGCCACTG | 26054 |
rs549265193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608755 | AATTGTAGTTACCTT[A/G]TAAGATTGCCATGAG | 26054 |
rs549308938 | snp | C/T | 1.68975e-05 | 0.00290662 | intron-variant | SENP6 | GRCh38.p7 | 6:75678574 | TGCTAATTTAATTTC[C/T]TTTACCAGGTATCAT | 26054 |
rs549342042 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611663 | TTTCTGGCTTTAGAA[G/T]TTTGTGTGCTTCAGC | 26054 |
rs549345915 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SENP6 | GRCh38.p7 | 6:75674478 | AGGCATGCATTACCA[C/T]GCCTGGCTAATTTTT | 26054 |
rs549369548 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697702 | GAAGCATGTAAGATA[C/T]TGAATTTTAGAGACA | 26054 |
rs549378247 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75713110 | GCCTGAAAAAAATGG[A/G]CCGAGGTTGGGGGGA | 26054 |
rs549384094 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647438 | GTTCCACGATTGCTG[A/T]TCTTGTACGTAACGT | 26054 |
rs549399609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641672 | TCATAATTGTTCTAA[A/C]GTGGGTATCCATAAG | 26054 |
rs549484401 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75686401 | CCCATTTACATTTAA[A/C]GTTAACATTGTTATG | 26054 |
rs549487384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642217 | GCATAAGGATACAGT[A/G]ATGAACAAAGCAGAC | 26054 |
rs549525572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75704862 | GCTTGTAAACATTTT[A/G]TTAACAAAGCACATC | 26054 |
rs549536545 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717631 | ACTTGAGAATCTTTC[A/G]TGTATATGCACATTC | 26054 |
rs549536685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75618383 | CTTTGGCCGTTGGGA[A/G]TTCTTTCAAGTTGGC | 26054 |
rs549545116 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75648472 | TAATTTTTAAAAGCT[A/C]GGTTTTTCTGATAGC | 26054 |
rs549547980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75680750 | TATCAGTGGAAGCCT[A/G]TTGGAGGAGTCCCAC | 26054 |
rs549575502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611666 | CTGGCTTTAGAAGTT[G/T]GTGTGCTTCAGCTTG | 26054 |
rs549575559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619300 | AATTTACCTATTCTG[G/T]GTACTTCATATATGT | 26054 |
rs549578265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658479 | ATGTTTTAGAAACAT[A/G]TTTGGCCTCTTGGAT | 26054 |
rs549587146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698034 | ACTAGATAGTAGTAT[G/T]TTACAATGGAGACTT | 26054 |
rs549640228 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601032 | TTAGAACAGTCCATT[C/T]CCCAAAGACTGCACT | 26054 |
rs549661407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612432 | AAACTCCTGGGCTCA[A/G]GGGATCCTCCTGCCT | 26054 |
rs549664208 | snp | C/T | 5.30274e-05 | 0.00514887 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659290 | GAAAACAGAAGAGTC[C/T]GAATCACAAGTGGAG | 26054 |
rs549741981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75700993 | CATCCATCTGGACTT[C/T]GCAATACAGAAGATG | 26054 |
rs549747295 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619729 | GTTTTGCGTTCCCAC[C/T]AGCAATGCACAAGAG | 26054 |
rs549753912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694829 | GAATAATGTGGGGAC[A/G]TATGCTCTACTCTAG | 26054 |
rs549774722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654885 | GTAGATAGATATAAT[G/T]AACACTTTTCTGTTC | 26054 |
rs549797280 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75603951 | CCATTCCAGTTTGCG[A/G]AATGGGTACCTGTCG | 26054 |
rs549808895 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75641840 | AATAATTGGCCTGGA[G/T]TAGGTAGTAAGACAG | 26054 |
rs549820802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75688588 | AAACTGTGCCCCCAT[C/T]TCAAGGACACCATTT | 26054 |
rs549893566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75683246 | CTTTGCCCATTTTTT[C/G]ATGGGGTTTTTTTTT | 26054 |
rs549923112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75634968 | GACATGAAATTATAC[C/T]ATTTTATATCTGCTT | 26054 |
rs549982081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661584 | TGTTTTTTAATAGAA[A/G]TCTTCCTTCTTTTAC | 26054 |
rs550031341 | snp | C/T | 0.0011332 | 0.0237764 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670644 | TAAGCTGCCAAAGTT[C/T]CTTTGACAGTGTCAT | 26054 |
rs550054275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75655651 | TTGTTTCTTTTTAAC[A/G]TTGCATTGTATGAGT | 26054 |
rs550066916 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652019 | TAACTCTCCAAAAAA[A/G]TATAAAAATTAGCCG | 26054 |
rs550076708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604540 | CGGAGGCTGAGGCAG[G/T]AGAATCGCTTGGAAA | 26054 |
rs550102590 | snp | C/T | 3.33461e-05 | 0.00408313 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663264 | TTACTTTGAATGAGT[C/T]TACTGGACCATTATT | 26054 |
rs550153791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75667500 | GTAGTAAACTACCAC[A/G]TGAAAAGTGCAAATT | 26054 |
rs550173124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613348 | ATCCCTGCCTTCTCA[C/T]TGAAATGGCAACGTT | 26054 |
rs550179640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75677627 | AAGAAATTGTGGTCC[A/G]TGGTGTACATTTGTA | 26054 |
rs550180671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703285 | ACATAGCGAGACCCA[A/G]TCTCCAACAAAAAAA | 26054 |
rs550206200 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620702 | TCAGAAAGCCAGAGC[C/T]AAGCTTAAGACATCA | 26054 |
rs550210134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613922 | GGATCTGATACAGAA[C/T]GATGTATTGCATTGA | 26054 |
rs550217434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657210 | TTTAAGACTGCTTTA[C/T]TGTAAATTAAGTTTT | 26054 |
rs550243990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696221 | ATTAATATAATTCAT[A/G]ATATTCTAATACTTT | 26054 |
rs550252262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649238 | AAGAATCGCTTGAAC[C/T]CAGGAGGCAGAGGTT | 26054 |
rs550260188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75699395 | GACAAAGCTACAAAT[A/G]CTTATACACTAATTA | 26054 |
rs550287180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606106 | GAATGAGAAGGAAAT[C/T]AACAACACTGGTCAT | 26054 |
rs550304958 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628450 | ATTAAATTTATTATG[C/T]AAAATAATATTGGAA | 26054 |
rs550325849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606693 | GAAGCAACATGACCC[C/T]CCTAAGAAATGCTCA | 26054 |
rs550371805 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648915 | TTGATGCCAAATCCC[A/T]CTCTTAAACACTGTA | 26054 |
rs550374709 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75688071 | TTGAGCTTCCTGGCC[A/G/T]CTTTGTTTACCTACT | 26054 |
rs550398431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627108 | AGCTGGGATTACACA[C/T]GGACACCAACAAACC | 26054 |
rs550400116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609815 | ATGGAGTCTCGGCTC[C/T]GTTGCCCAGGCTGGA | 26054 |
rs550432567 | snp | C/G | 0.000201086 | 0.0100251 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602539 | GATGGCGGCCGGCAA[C/G]AGCGGCGGTAGCGCA | 26054 |
rs550491491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673831 | TTTCAGACCAGCCTG[C/G]TCAACATGGTAAAAC | 26054 |
rs550493481 | snp | G/T | 1.65773e-05 | 0.00287895 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666776 | AGAAAGCATATCTCC[G/T]CAGCCTGCTGATTCA | 26054 |
rs550502911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709873 | CAATTTCTTCAACTA[G/T]TAATTTATCATGGCT | 26054 |
rs550514722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661069 | ATTCACATGGGTATT[A/G]TTGTTTCTCGGCCTT | 26054 |
rs550568110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714974 | TGTTGAATTACCTGT[C/T]TTTCTAAACTGGAGC | 26054 |
rs550632073 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606528 | AACCATGTTTTTTTC[A/G]TAGAGTGTTCAGTCT | 26054 |
rs550648008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707098 | CTGCATCATTTAGGT[C/T]ATTTTTCTCCTGTTT | 26054 |
rs550658990 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612188 | ACCTCTTCAGATGGC[C/T]TCTGCAGCAGGGTAC | 26054 |
rs550661619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632423 | CTTTCTAGAATTGTC[A/C]TGAGATTTATATGAG | 26054 |
rs550669362 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716747 | TCTTTCAAATGAACT[C/T]TGAGACTTGAAACAT | 26054 |
rs550748419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75625012 | TACAATAATGGTGTA[C/T]TGTATAATAATGTTA | 26054 |
rs550785984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693298 | CAGTCCTAGCTACTC[A/G]GGAGGCTGAGGCAGG | 26054 |
rs550819383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680525 | AATAAAAAGGCTCCC[A/G]TGAATAATTTCCAAA | 26054 |
rs550860624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714376 | CTGATCTTGGCTCCT[A/G]TCTTCATCCACCATA | 26054 |
rs550908505 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75687567 | TTTGATGTTGGTGAC[C/T]GACAGATGGGGTTTT | 26054 |
rs550913556 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642345 | ATGGGTTGATGTGAT[A/G]GACTGACAGTATGAT | 26054 |
rs550951969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75640759 | GGTAAAATATAAAAT[C/T]ATTTATATGTTTTGA | 26054 |
rs550962578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681985 | ATGGAAAAGACAGAG[A/G]AAAGAATCAGTGAAC | 26054 |
rs550967028 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669256 | ACTTGGGAGGCTGAC[A/G]CAGGAGAATTGCTTG | 26054 |
rs550969535 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667082 | CACATGGGAGATTAT[C/T]TGGAAGAACATTAAG | 26054 |
rs550974319 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640918 | GATCAGATCAGGGTA[A/G]TTAGTATATCCATCA | 26054 |
rs551034723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681386 | AGGCCTCCACAGCTA[C/T]GCTTCCTGTATAGCC | 26054 |
rs551040544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75625619 | TATGCCAGTAATCCC[A/G]ACACTTTGGGAGGCC | 26054 |
rs551052946 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655219 | GAGGAAGTGGACACC[C/T]ACCTAGCCAGCCAGA | 26054 |
rs551114390 | in-del | -/T | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679728 | TTATCAATTTGTATG[-/T]TTTTTACTGGTTTGT | 26054 |
rs551121155 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75695449 | TTTTAATACAAAGCG[A/T]ACTGTGGCCGGGCGC | 26054 |
rs551134973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636311 | TCAAGTCAGCAGGAC[A/G]GATTCTACTTACATT | 26054 |
rs551148621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653800 | TTGGGAAACTCCACG[G/T]CTAGATAGACTACAA | 26054 |
rs551176725 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75696091 | AGTTCCATTTTCATT[C/G]TTCATGGGTTCATAT | 26054 |
rs551191668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646206 | AGGAACTAAAAACCT[A/G]CCTTCTTTCTTATAA | 26054 |
rs551230362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646651 | ACCATCCTGGCTAAC[A/C]CAGTGAAAGCCCATC | 26054 |
rs551275438 | in-del | -/TACTAT | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75616036 | TGTTAATCTCTCTTC[-/TACTAT]TATCTCCTCTCTGGT | 26054 |
rs551278322 | in-del | -/T | 0.00247862 | 0.0351165 | intron-variant | SENP6 | GRCh38.p7 | 6:75675423 | CAATACTAATTCATC[-/T]TTTTTTTTTAGTTTT | 26054 |
rs551292533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605983 | GTAGAGCTTACAGGA[C/T]TTGATGAACTGTACA | 26054 |
rs551313387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635781 | AACATGAGAATAAAC[A/G]ATAAAAGGAGAGTAA | 26054 |
rs551316244 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75603815 | GAGTATAGTAAAGTG[-/A]AAAAAAAAGTCTTAC | 26054 |
rs551357244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643629 | CGGGAGGTTGAGACA[G/T]GAGAATTGCTTGAAC | 26054 |
rs551358566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651343 | AGCACTGCTTAACAC[A/G]TGTTAACTTTTGCTT | 26054 |
rs551393343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644334 | GGGACACTCTATGAA[A/G]TACCTGACGAGTTCT | 26054 |
rs551400255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75677887 | TTGCTGACCTAATTT[A/G]TTGGGAACAGATCTC | 26054 |
rs551426967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690725 | TGAGATGAGAGTCTC[A/G]CTCTGTCACCCAGGC | 26054 |
rs551479752 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75645348 | TGGCCAGGTGTGGTG[G/T]TTTATGCCTGTAATC | 26054 |
rs551500209 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712589 | TTTTAACATTTGAGG[A/C]GTTTGGGCTCTACAT | 26054 |
rs551501799 | in-del | -/CTGA | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75611827 | GCACTAAACTGCTGC[-/CTGA]CTAACGAACTGAACT | 26054 |
rs551532295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672079 | TGTCAGTGTTTTTAG[G/T]GATTTATGAAATTTG | 26054 |
rs551558572 | snp | G/T | 0.5 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75683024 | TACACTCCCACCAAC[G/T]GTGTAAAAGCATTCC | 26054 |
rs551567771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622268 | TAAAGTTCAACATCT[A/G]GTTTTTTGGCCGGGC | 26054 |
rs551586393 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627443 | GACAAGAAAAAAGTA[C/G]AAAAAAAGGAGTGAA | 26054 |
rs551629858 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677720 | ATTGTCAAAACATGT[A/G]TCTAGTACTAAAATA | 26054 |
rs551651717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614959 | GTGGTGGCCTGATCT[C/T]GGCTCACTGCAATTT | 26054 |
rs551694541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684101 | GTAATTGTCCTTGAA[G/T]AGGTCCTTCACATCC | 26054 |
rs551724643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642823 | GGCAAGTTCCTCTCT[A/G]AATGGAGGTGTGTTA | 26054 |
rs551739039 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75703272 | ACCAGCGTGGGCAAC[A/G]TAGCGAGACCCAATC | 26054 |
rs551742362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75665754 | GGCTACAGCCAGGTG[C/T]GGTGGCTCACGCCTG | 26054 |
rs551753648 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75654729 | GTACTTATTTTTCAG[C/T]GTATTAGTAGTATCA | 26054 |
rs551759366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697967 | TGGACTACTTGAAGC[A/C]GTTTCTGAGTAAATG | 26054 |
rs551792546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655514 | TTTCCTAGCATAGAT[G/T]AATTTTACCTGTTCT | 26054 |
rs551792735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647171 | CTGTGATGCGCTTTT[A/G]TACAATTAGCTATAA | 26054 |
rs551795647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658439 | GTGTTTGTGCAGGTT[A/G]TTTTGGTTTACAGAT | 26054 |
rs551872148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637256 | CTTGGGGTGAGTGGT[A/G]TATCTTGTCTTTTAA | 26054 |
rs551890432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691982 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 26054 |
rs551908415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624957 | GACAACATAGTGAGA[C/T]TCCATCTCTAAAAAA | 26054 |
rs551920622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611145 | CAAGATGAAGGTACT[A/G]CTTAACTACCATGAC | 26054 |
rs551943019 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75665025 | GGCGCATTGGGTCAT[A/G]CCTGTAATCCCAGCA | 26054 |
rs551966588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687804 | CTGCCTATGTGAGGT[A/G]TCTGTCGGCCCCTAC | 26054 |
rs551981271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604413 | GAGGCAGGCGGATCA[C/T]TTGAGGCCAGGAATT | 26054 |
rs551982031 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641935 | AAAACGAGTCTATAG[C/T]GCCTTTCAAATGCCT | 26054 |
rs551983369 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75713657 | GTGTGTATTCTTAAT[A/G]TATATGAATTATTGC | 26054 |
rs551985614 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75703973 | TAGTTGTGCAGTCTT[A/C]GATGTATAAGACAAA | 26054 |
rs551995019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672572 | GGGCATTCTTCATTG[A/G]AGAATAATTAGTGGA | 26054 |
rs552009975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640970 | TTGTGTTGTCAGCAT[C/T]CAAAGTCCCTTTTTC | 26054 |
rs552035086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75618335 | GTTATAACCCAATGC[C/T]GATGTTATTTATTTT | 26054 |
rs552043053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607095 | GCTCACGCCTGTAAT[C/T]CCAGCATTTTGGGAG | 26054 |
rs552046148 | snp | C/T | 0.0059267 | 0.0541131 | intron-variant | SENP6 | GRCh38.p7 | 6:75677282 | TTTTTAATTTAAAAA[C/T]ATTCTTAAATTGTGG | 26054 |
rs552048798 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715706 | TTTGGAAATTTTGAT[A/G]CTTGTATAAATGTCA | 26054 |
rs552054439 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SENP6 | GRCh38.p7 | 6:75710996 | ACAAACTAAATTTTT[A/G]TAAAAATAAACTAAA | 26054 |
rs552113969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75707579 | CCCAGGCTGGTCTCA[A/G]ACTTCTGTGTTCAAG | 26054 |
rs552168972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75610764 | AGTATGAAAACAGCT[A/G]TGTTCTGATCTTGCC | 26054 |
rs552217530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75693995 | GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 26054 |
rs552375016 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716671 | AGATTTATAGCACAT[A/G]TAGGGATCTTGCATG | 26054 |
rs552376014 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699120 | CTAGGTGAAAGGGAG[A/G]AAAGCGATTTGTCAG | 26054 |
rs552377821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75710439 | TAATTCTCTGACCTT[C/T]CATTAGTTGTTAGGA | 26054 |
rs552400175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663917 | TTCCTAACTCTATAT[C/G]CTGTCTTTTTACTCT | 26054 |
rs552435694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708071 | ATCTTTTCTCTTCTC[C/T]TTTTTTGAGACAGAG | 26054 |
rs552480921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669967 | AGAAGGAATTTCGAT[C/G]TTGTTGCCCAGGCTG | 26054 |
rs552490050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700231 | TCTGTGTAACCCTCT[C/G]TCTTGCTGTTAAAGT | 26054 |
rs552542808 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623439 | ATAACTATTTTACCA[A/T]GGTAATACCACTGGA | 26054 |
rs552562165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75683168 | GACCAGTGGTGGTGA[A/G]CATTTTTTCATGTGT | 26054 |
rs552569255 | snp | A/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620398 | CTGGGAAGTTAGATC[A/G]AGAGGTCCAGATTCA | 26054 |
rs552574813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75705128 | GGTTCTTCATTCCTC[A/G]CTCTCCTTCACTGTT | 26054 |
rs552578045 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75709716 | GGTGCACACCTGTAG[A/T]CCCAGTGACTTGGGA | 26054 |
rs552578561 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634872 | TTCAATAGGTTTTCA[A/C]TTTTTTTAACCATTT | 26054 |
rs552584572 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648556 | ATCTTTTGTGCATGT[A/G]TTGAACATTTCTCTA | 26054 |
rs552607052 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717804 | AACTAATTAGATAGA[C/T]CTGTTGTATTGGTTT | 26054 |
rs552631595 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617022 | CTGGTACTACAGGCA[C/T]GCACCACCATGCCAG | 26054 |
rs552634390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613090 | CTGCACTCCAGCCTG[C/T]GTGACAGAGTGAGAT | 26054 |
rs552640766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698115 | GAACACCAGAAATAC[A/T]CTTGTAGTCGGAAAA | 26054 |
rs552651394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614619 | GAGATACTTTGAAAC[C/T]TGTAAATAACTTGTT | 26054 |
rs552670928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605234 | GTCCTTGAAAAACTA[A/G]ACTAGGTTTTCATTT | 26054 |
rs552744833 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75682719 | CTTCATCCATGTCCC[C/T]GCAAAGGACATGAAC | 26054 |
rs552756169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75646590 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 26054 |
rs552761460 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673079 | TGATCCGCCCATCTC[A/G]GCCTCCCAAAGTGCT | 26054 |
rs552766071 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710167 | CAAAAATATTATATT[G/T]TTTTCCCACTTTTCC | 26054 |
rs552782109 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75634271 | AAAATCAGAAATAGT[A/C]TTTAGGACTCCTGAT | 26054 |
rs552871787 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716849 | AAAGCCTAATCATCA[G/T]CAATTATTTTATTTT | 26054 |
rs552900613 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637051 | CACCAGGCTAACTTT[-/A]AAAAAAATTTTTTTT | 26054 |
rs552911957 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75693461 | ATAGTTTGGGCCAGC[A/G]AAAGTCTCATGGTTC | 26054 |
rs552956232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672286 | TTGCTGGTGATTTAG[A/C]CATTTAATTAGAAAG | 26054 |
rs552958056 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666372 | TTTTTTACACCTTAA[A/G]TTTTTTGGGACTCTG | 26054 |
rs552963030 | in-del | -/AC | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600161 | TAATTTAGCAATTTA[-/AC]ACAAATTTTTTTCTG | 26054 |
rs552992850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75712140 | AGACATGTTCCAACT[A/G]AGAACTCCAAATAAG | 26054 |
rs552996355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75623778 | AAAGACTGTGGTTTG[G/T]CCCTTTACAGAAAAA | 26054 |
rs553019566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665163 | TGGTGGTGGGTGCCT[A/G]TAGTCCCAGCTACTC | 26054 |
rs553022587 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75691163 | TTTTTTTTTTTCAAA[A/G]ACAGATTCTTACTTT | 26054 |
rs553033161 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75624368 | TTAATTTTTTTCTAA[A/C]ATAATCTGTAAATTA | 26054 |
rs553039610 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607435 | CCTATAAACTTTCTT[C/T]TGATATTCTACCTTT | 26054 |
rs553045034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644033 | TTGTGATAGGTAAGA[C/T]ACAGAATGAGTATGG | 26054 |
rs553077246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658704 | GTTTACCCAAACAAT[A/T]GTACTGTTTGAATTC | 26054 |
rs553113931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651709 | TTAATATATAACTCT[A/C]CAGATCTTTTCTATG | 26054 |
rs553115414 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663994 | AAAGATTAGAAATTA[C/T]TGGGGACTGGTTGAC | 26054 |
rs553121124 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601072 | CGGTTTTCTGCATCA[C/T]TTTAATTGCTGTTGA | 26054 |
rs553130867 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75714541 | TCATGGTTGTTTCCC[-/A]AAAAACATAAATCTA | 26054 |
rs553134975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671614 | GTAGTCCCAGCTGCT[C/T]GGGAGGCTGAGGCAG | 26054 |
rs553156885 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625943 | AAATAGTTTCACAAT[A/T]GTAATACCAACATAA | 26054 |
rs553158464 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667247 | AGTCATTTTGACAGA[G/T]ATATATTTTACTGTA | 26054 |
rs553169965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75711157 | TCAGTGTTGTAGCAT[C/T]GGATAATTGGAATTA | 26054 |
rs553226432 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656263 | TACAAAATCTAGTAG[A/G]GAGTATCCTAATCTT | 26054 |
rs553232801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628664 | CCAGTGCTGACAAAT[A/C]CTGGTTACATTCTAA | 26054 |
rs553242519 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75691795 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 26054 |
rs553249690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614208 | GGGGAAATTAACTTT[A/G]ATCACTTAGTTAAGG | 26054 |
rs553272467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629839 | CACATTTGAGGACTG[C/T]AACCTGGGAGCATAG | 26054 |
rs553301018 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660473 | ACTTTCATGATGTTT[C/G]ATGACTTACCTTGAT | 26054 |
rs553307654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685368 | TTTTGAAGGGTTTTT[C/T]TTGTCTCTATCTCCT | 26054 |
rs553322314 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621860 | GTACATGTAACCTTA[C/G]AATTAAAAATTGACT | 26054 |
rs553326255 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75637671 | AAGACTTATAAGAAC[C/G]TTATAAGAAATTCTT | 26054 |
rs553344000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626025 | CTAGCAGGTATATGT[A/G]TAGTTCCACTAGGAA | 26054 |
rs553344063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634616 | TTGGTAAAGGTTTTT[A/G]TGTGTTTGTTCAGAT | 26054 |
rs553368325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647282 | TGTAGTATTTAGATA[C/T]AGTACTTAGTTACTA | 26054 |
rs553443837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715133 | TGTTCCAATAAAACT[G/T]TATTACAGAAACAGG | 26054 |
rs553443844 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75641753 | GAGGGCAAAGCGGGA[C/G]TATCTCTTGAGCCCA | 26054 |
rs553499338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662985 | TTGATATTAAATCCC[A/G]ACTAACATTACTTAT | 26054 |
rs553515973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705778 | TGGAACTAATGAATC[G/T]TATTTGGATGAAAAA | 26054 |
rs553611055 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75685784 | GTGATTTCTATTCTT[C/T]TACATTTGCTGAGGA | 26054 |
rs553612534 | snp | A/G | 3.0782e-05 | 0.00392302 | intron-variant | SENP6 | GRCh38.p7 | 6:75670760 | TATACCAATTATAAC[A/G]TTAAAAATTCCGTTG | 26054 |
rs553614125 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714112 | TCTCTCCCATGATTC[A/G]CACTGCCTCTTTTAG | 26054 |
rs553684100 | in-del | -/TTTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615491 | TGCCTGCTAAGAGTT[-/TTTG]TTTGTTGTGAGTGGA | 26054 |
rs553684614 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679483 | GGAAAAATGCCTAGT[A/G]CAGTGTTAGAAGTTT | 26054 |
rs553708237 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698248 | TTCCTTGAGTGATAT[G/T]GGGGAGGGTCTAAAG | 26054 |
rs553725002 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650960 | TTCTTTATTTTGAAT[G/T]TGAGGCACTTAGTAT | 26054 |
rs553744038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672939 | TTCATGCCATTCTCC[C/T]GCCTCAGCCTCCCGA | 26054 |
rs553748948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649423 | TTTTTAAAGTTTATT[C/T]AACAGCATTCATTAA | 26054 |
rs553768347 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718276 | AGAACATATTTTAAT[A/G]TATAATATGACCAAG | 26054 |
rs553794777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75670204 | CGCCCATCTCGGCCT[A/C]CCAAAGTGCTGGGAG | 26054 |
rs553826487 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698076 | GTGTTTTATTCTTTC[A/G]CTTTTCTATGCCCTC | 26054 |
rs553888130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75694216 | AGCCGAGATCATGCC[A/G]TTGCACTCCAGCCTG | 26054 |
rs553891426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690187 | AAGTTCTGGGATTAC[A/G]GGCATAAGCCACTGC | 26054 |
rs553908859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647320 | TGTTTAAAATCCTTG[A/G]TATTGTGTGTATTTG | 26054 |
rs554027573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620198 | GCTGAGCATCTTTTC[A/G]TGGGAGGATATTTTA | 26054 |
rs554053419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648930 | ACTCTTAAACACTGT[A/G]CATTACTATATTCTT | 26054 |
rs554063556 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701459 | ATTTCTTTTTAATGT[A/G]TTAAATTTCAATATA | 26054 |
rs554084911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682499 | CCATGTTGGTTTGCT[A/G]TACCTATCAACTCAT | 26054 |
rs554090740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689592 | TCTCGTGCCACATAA[C/T]GTTTCAGTCAATTAT | 26054 |
rs554113842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613412 | TGTAAGATATTTACC[A/G]TCTGGCCTTTTACAG | 26054 |
rs554135403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642444 | GAATTGGCAGTGCCA[C/T]GATCATAAGAATGGC | 26054 |
rs554146288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75682910 | ATTTATAATCCTTTG[A/G]GTATATACCAGGTAA | 26054 |
rs554220936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686560 | TTCCATGTTTAGTGC[C/T]TCTTTCAGGAGCTCT | 26054 |
rs554242199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635438 | TATAACTAGTAACAT[C/T]TTAAGATTTGGCATA | 26054 |
rs554293389 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653283 | TGATCCCCCCGCCTC[A/G]GCCTCCCAAAGTGGC | 26054 |
rs554489500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605578 | TAATTAAGTAAACAC[C/T]TTAACTAAGAGACAC | 26054 |
rs554503295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699453 | ATCTGTTTTGTTTTT[A/G]TTTTTTCTGGTAGTA | 26054 |
rs554507253 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75707778 | GTCTCAACCTCCCAG[G/T]CTCAAGTGATCCTCC | 26054 |
rs554527949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653297 | CGGCCTCCCAAAGTG[A/G]CGGGATTACAGGCAT | 26054 |
rs554537197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715206 | TATAAGATCTATGAT[A/G]GAAACTGTGTCTTGT | 26054 |
rs554556418 | snp | A/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717827 | ATTGGTTTTCTTGTT[A/G]GATAGAATAACAGTT | 26054 |
rs554561457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75698935 | AGGATCGCCTGAACC[C/T]GGGAGGCAGAGGTTG | 26054 |
rs554566829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692980 | GGAGGAAGAGGTAAG[A/G]GGATGGCTTCAGCCC | 26054 |
rs554604747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75652460 | TTATATATTTGATCT[A/G]TTTCTTTGCATCAGA | 26054 |
rs554627564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75603336 | TGATTTTTTTGGCCT[A/G]TGAATATATAAGGAC | 26054 |
rs554635943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701162 | GATAACTTGTTTTTC[A/T]TCCAGCAAATATTTA | 26054 |
rs554669911 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75639031 | ACTCCAGCCTGGGTG[A/G]CAGAGCCAGACCCTG | 26054 |
rs554691970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700572 | GCTCACTGCAATCTC[C/T]GCCTCCCAGGCTCAA | 26054 |
rs554699702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75623478 | CTTTTCATTAGCTAA[A/G]GCTTTCTTTCCTTTC | 26054 |
rs554772092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705317 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCAGTAGG | 26054 |
rs554772210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75714457 | ATTTACTTGTTTATC[A/G]TCGAGTGTCGCTATT | 26054 |
rs554775874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647028 | GAAAGCTATGATTTA[C/T]ATTACTAGATCACCA | 26054 |
rs554846193 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715990 | AATATTCAAATATCT[A/G]TGGTAATATTTTGAC | 26054 |
rs554909401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75710902 | CCAAAAACCCTTTAA[A/G]TATTTCTGATGTGAA | 26054 |
rs554928882 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75667840 | GGTATATCCATATGA[A/T]GCAGCCATTGAAAAT | 26054 |
rs554979625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617007 | CAGTCTCCTGAGTAG[C/T]TGGTACTACAGGCAC | 26054 |
rs554982417 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75614064 | AATTTGCGTTTATCT[G/T]ATGTTTCCTTATGAT | 26054 |
rs555014202 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621035 | GAGCACATTTAGTGT[G/T]CTGATCTAGAGTTTT | 26054 |
rs555019655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614460 | TTTAGTAGAGATGGG[A/G]AATTACCATATTGGC | 26054 |
rs555031608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606392 | ACCCCTTTTCCACTT[A/G]TGATAGACAGTTTTG | 26054 |
rs555050873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661693 | TTCCTAGACAAGGTT[A/G]GTGGTTTTTTCTTTC | 26054 |
rs555102478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75683589 | TAAGGTGTAAGGAGG[A/G]GATCCAGTTTCAGCT | 26054 |
rs555120272 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711965 | GGCGTGACCCATCGC[A/G]CCCGGCCACAAGTTT | 26054 |
rs555138830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655034 | TTATTAACTAGAGTT[C/G]AATATTTGTTTACAG | 26054 |
rs555167501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684159 | ATTCTCTTTGTAGCA[A/G]CTGTGAATGGGAGTT | 26054 |
rs555210609 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689418 | GCTACTATTAAAACA[A/T]AAACAAAAAAAAACA | 26054 |
rs555232678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632620 | TTCTAGTCATTTGAT[C/T]TCTTTTCGAACAAAT | 26054 |
rs555360474 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660190 | TTGTAAATGATGTGT[C/G]TAGTTTTCAAGAATG | 26054 |
rs555361709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678079 | TGGGAGACAGTGCCA[A/G]AGGAAGAAAAGAGCA | 26054 |
rs555362866 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625642 | GGGAGGCCAAAGCAG[A/G]CAGATCACTTGAGGT | 26054 |
rs555372931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703634 | AGATATGGTGGTGCC[C/T]ATCGGTGGTCCCAGC | 26054 |
rs555390318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627940 | GCCTCCCGAAGTGCT[A/G]AGATTACAGGCGTGA | 26054 |
rs555412540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664422 | TATATATACATCTAT[A/G]TATGTCAGGTACTGT | 26054 |
rs555432266 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696382 | GTTCATCCATAATAT[A/C/G]TAAGAAAGGAACCTG | 26054 |
rs555455355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657664 | ATGCTGGGAAAACAC[A/C]TGACTAAAACGTAAT | 26054 |
rs555473996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665068 | GAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCA | 26054 |
rs555544408 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650838 | AGATTTCAAACCACA[A/G]GATCACTAATTACTT | 26054 |
rs555562484 | snp | A/G | 0.00026898 | 0.0115939 | intron-variant | SENP6 | GRCh38.p7 | 6:75677307 | TTGTGGGTAGTTTTA[A/G]AGGGAAATATGTTTT | 26054 |
rs555566121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75672891 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 26054 |
rs555593013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75622537 | GCACTCCAGCCTGGG[C/T]GACAGAGTAAGACTC | 26054 |
rs555606340 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677981 | AGGACTCCCCAGAGA[A/G]GAGCTGTAAATATAG | 26054 |
rs555635712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697306 | TCCCCAGTTTGTCAA[A/G]CCATTTTATGCAACT | 26054 |
rs555641230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636634 | CTATACAAAATACGT[C/G]TAGTAAAAACTACAG | 26054 |
rs555650393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620494 | GGGCAAACAGGCTCC[A/G]TTGGGCCTCTTTGAT | 26054 |
rs555658298 | snp | C/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601387 | GGACTTTTTAAAAAA[C/G]AAAAAAACACTGCCA | 26054 |
rs555658337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650372 | AGAAGAGATATACTC[C/T]GAAACTGTGCAAATA | 26054 |
rs555684777 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681933 | CTCAAAATACAAAAC[C/T]GAAATAATGACTTCA | 26054 |
rs555744100 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670330 | CTGAATGCCATACTA[C/T]TACTCAAATTTAAAT | 26054 |
rs555758854 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75685301 | GTCTTGCTAGCAGTC[A/T]GTCAATTTTGTTGAT | 26054 |
rs555812689 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633489 | CCCAATAGCTGTATG[C/T]TTTTACTACTTTTAA | 26054 |
rs555849224 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75681710 | GAACATGATGACAAC[C/T]CTTGAAACAAATGAA | 26054 |
rs555875820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633121 | ATTATTATTTGCATC[G/T]ATTGAAGTATAAAGT | 26054 |
rs555887384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75669213 | AAAAATTAGCCAGGC[A/G]TGGTGGTGTGTGCCT | 26054 |
rs555903217 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599607 | GAAAAAATATGTATA[A/G]ATTCAAAAGATAATC | 26054 |
rs555937796 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620599 | CCATCTGTATCTTGG[A/G]GTTAGGATTTCATCA | 26054 |
rs555969890 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647006 | AGTAAAATGATTTTA[A/G]TGAAATGAAAGCTAT | 26054 |
rs556005795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694699 | TTTCAAGGATTTTCT[A/G]TGATCATGTATTATC | 26054 |
rs556029956 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75644555 | AATGGTGCAACCTTG[C/G]CTCACTGCAACCTCT | 26054 |
rs556044427 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75647204 | TTTTTGCTTTTTTTC[C/T]CCCCAAATTTTGCTT | 26054 |
rs556044561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75640500 | GTTTATTTTGTATAT[C/T]GACAGAAATCGAAAA | 26054 |
rs556047918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75602877 | ATTTAAAAAATTTTG[A/G]GGTGGTGGCCTAAGG | 26054 |
rs556092233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75691744 | GGACCACAGGCGCCT[A/G]CCACCAGGCCTGGCT | 26054 |
rs556109632 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75695035 | ACTCGCCACCACACC[C/T]GGCTAAATTTTTGTA | 26054 |
rs556157609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75687965 | TTTAAGTCTGCAGTT[A/G]TCTGCTGCCTATTTT | 26054 |
rs556173092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75688857 | TGGATCATCTGAGGT[C/T]AGGAGGTGAAACCAA | 26054 |
rs556209948 | snp | C/T | 3.51111e-05 | 0.00418979 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675438 | CTTTTTTTTTAGTTT[C/T]GTTTAGATTTTATCA | 26054 |
rs556269831 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644524 | CAGTCTGGCTCTGTC[A/G]CCTAGGCTAGAGGGC | 26054 |
rs556274518 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704276 | ATTACTATTTTCACT[A/G]TCTCAGCAAGAGGAA | 26054 |
rs556297914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75651755 | TTAAATTGATACATA[A/G]TATTCATACTGTATG | 26054 |
rs556300014 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717290 | TTTTTTAATGAACTA[C/T]ATTTTGTCAGAATCT | 26054 |
rs556315595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75695488 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 26054 |
rs556319951 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624418 | TTGCACACATACAAG[C/T]GTATCTGTAGAATGA | 26054 |
rs556350407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648732 | ATTTATTCTGTTATA[C/T]CTTAAATGTTTATTG | 26054 |
rs556354702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75661952 | AGCTACTTGGGAGGC[C/T]GAGGCGGGAGAATCT | 26054 |
rs556393895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75662839 | TGCCCTCTTTACCTT[C/T]ATTATAGATACTAAA | 26054 |
rs556406613 | snp | A/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621825 | CTCCATCTTTTGAAA[A/T]GTATAAATATATGCT | 26054 |
rs556412307 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599683 | GGAGCGAGAAAGAGA[A/G]ATGAGAGATTCCTAG | 26054 |
rs556441232 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75626571 | TTTCCCCCAGTCTTT[A/T]GCTATTACGTATAAG | 26054 |
rs556575089 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75698847 | GAAACCTCGTCTCTA[C/G]TGAAAATACAAAAAT | 26054 |
rs556598066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605365 | GTTCTGTGAAAGCAT[A/G]TCTCTGTAATAAACT | 26054 |
rs556637472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692367 | ACTCACACCTATAAT[C/G]CCAGTACTTTGGGAG | 26054 |
rs556655493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608263 | CCCAGGAGTTCAAGA[C/T]CAGCCTGGGCAACAT | 26054 |
rs556660938 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75703637 | TATGGTGGTGCCCAT[C/T]GGTGGTCCCAGCTAC | 26054 |
rs556663062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642021 | TGGCTCTGCATGGGC[A/G]TGGTGGCCAGTGCTT | 26054 |
rs556685897 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601162 | GAAAGACAAGAAAAA[C/T]GCTATCAGAGGACTA | 26054 |
rs556727664 | in-del | -/ACAACTTCAAATTACCTCATGATGCCTT | 0.00993419 | 0.0697739 | intron-variant | SENP6 | GRCh38.p7 | 6:75689830 | TACACTCGATGATGC[-/ACAACTTCAAATTACCTCATGATGCCTT]ACAACTTCAAATTAC | 26054 |
rs556745633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665411 | AATACTGGCTAGTGT[A/G]CCTGGAGGATAAAGA | 26054 |
rs556746615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618819 | GAGAAACCTTGTTTC[C/T]ATCATCTACTATTTA | 26054 |
rs556749517 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692035 | CTAGTTTTGTATTTT[C/T]AGTAGAGATGGGGTT | 26054 |
rs556777189 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718041 | TAGTAACTTGTGCTT[A/G]AACTTTTAGTCAATT | 26054 |
rs556823986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701859 | TGCCCAGGCTGTTCT[C/T]GAACTCCTGAACTCA | 26054 |
rs556834494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612190 | CTCTTCAGATGGCCT[C/T]TGCAGCAGGGTACTC | 26054 |
rs556844735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619536 | AAATTTGGGTTGTTT[C/G]CACCATTTAGCTTAC | 26054 |
rs556856824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75655899 | CCTTTTGTGCATACC[C/T]GGAAATAGTGTAGTG | 26054 |
rs556889355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75705564 | TAAATAAATAAATTA[A/G]TTAATTAATTAAAAA | 26054 |
rs556896868 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609854 | GCGCCATCTCAGCTC[A/G]CTGGCTGACTGCAAC | 26054 |
rs556919356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715178 | TGGTCCACTGGCAAA[A/C]CCTGATCTAGACTAT | 26054 |
rs556923901 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75662350 | ATGTTGCCCAGGCTG[G/T]TCTTGAACTCTTGGC | 26054 |
rs556925986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608950 | CACTGACTACCTTTT[C/T]CTAGATATTAGCTGA | 26054 |
rs556960140 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607714 | CTACTAGGTTGAAAA[A/G]AGTGATGCTAAACTG | 26054 |
rs556984204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705256 | GTAGAACCTGTTAAA[C/T]CTAGTTTTGGCCAGG | 26054 |
rs556985061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616957 | CAGCCTCAACCTCCC[A/G]GGCTCAATTGATCCT | 26054 |
rs556988036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75652349 | TATAATCTTTTTTTT[A/T]AAATAAATGTGCAGT | 26054 |
rs557010369 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601931 | GAGGCGGTGGCAGAG[C/G]AGACCCACCCCTGTC | 26054 |
rs557019762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617761 | CACCCTTTTCATATT[C/T]GAGAGTCCAATCCAG | 26054 |
rs557080592 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75629666 | AATCCTTCAGAAGAT[C/T]TTTGTGTGTCCCAGG | 26054 |
rs557089379 | in-del | -/ACTT | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75717103 | CTCTTTATAGTAATA[-/ACTT]AGAGCTGTTAGCTCA | 26054 |
rs557100081 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640079 | TATGTCCAGGTGAGG[A/G]AAGTACATACTATTT | 26054 |
rs557102786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75712369 | GCTCCAAACTTTATA[A/T]AATTTTAGCAGGAAG | 26054 |
rs557109048 | snp | A/G/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716084 | ACTAAGCATCTTTAT[A/G/T]TGCTTGTGTAACAGG | 26054 |
rs557143809 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629699 | TATATACATATATCT[A/G]CTTGGATTTTGAATA | 26054 |
rs557150890 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613659 | AATGAAAGCACTAGC[-/T]TTTTTTTTTTTCTTT | 26054 |
rs557152971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621932 | TTTTAAAAAGGCATT[C/T]TGTTCAGGCAGCAAT | 26054 |
rs557217118 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621112 | TGTTTTTCTTCTGTT[-/A]AAAAGGCAGGTATCG | 26054 |
rs557292106 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604242 | TTTATTCTAATCTAA[A/G]GGTCTTTGAATGTAT | 26054 |
rs557307233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630832 | TAGACCTCCTAATAG[A/T]CATAAAACCATCATT | 26054 |
rs557399888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667708 | ATGTGTACTATTTGA[C/T]CAAATAATTAATTCC | 26054 |
rs557425524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627232 | CTCCCAAAGTGCTGA[C/G]ATTACAGGCGTGAGC | 26054 |
rs557436292 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75707685 | TTGTTGTTGTGGTGG[G/T]GGATTTTTGTTCTTT | 26054 |
rs557461040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668359 | TCTAAACACAATTTG[A/T]TAGGTAGATGCAAAT | 26054 |
rs557506329 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608803 | TTACTTAAAGCAATT[C/G]CAGGCATATAATAAG | 26054 |
rs557577941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710801 | TTTTACATTCAAGAG[A/G]ATCTACAGAATAAGG | 26054 |
rs557585367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75638847 | AGGATAGCCTGAGCC[C/T]AGGAGTTCGAGACCA | 26054 |
rs557591208 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689422 | TATTAAAACAAAAAC[-/A]AAAAAAAAACAGAAA | 26054 |
rs557615281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680859 | CAATAATGAGGTAAC[A/T]CCCTACTACCCACTG | 26054 |
rs557617659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637915 | GCCCATGCTGGAGTG[A/C]AGTGGCGTGATCTCC | 26054 |
rs557621877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639686 | CTTTTTGGAGTTTTC[A/G]TGAACTATGGAGAAG | 26054 |
rs557671037 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75673479 | CAGGTGCCTGCCACC[A/C]TGCCTGGCTAATTTT | 26054 |
rs557676528 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664346 | TTTTTCATTAAAAAT[A/G]TAGTTCATGGGCCTT | 26054 |
rs557723843 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689493 | AAAATGGTGCTGCCA[C/T]TGTGGAAAACAGTGC | 26054 |
rs557724793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643871 | TATGTATTTGGCCAT[C/G]TTTTATAATAATGGA | 26054 |
rs557732620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674061 | CTTTATGTCATCATT[A/G]TTGACACTTTTTGCA | 26054 |
rs557752180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75683556 | AAGTCTTTAATCCAT[C/T]TTGAATTAGTTTTTG | 26054 |
rs557754474 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650319 | GGTTTTTTCACTGTA[A/C]AATTACCGTTTTTCC | 26054 |
rs557759958 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652498 | AAATAAAATTTGGGG[G/T]ACAAATGATATACAG | 26054 |
rs557782299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710022 | ACTGATTAACTCACC[C/G]TAACTCAGCTACCAC | 26054 |
rs557790656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663573 | CAGTATTTTTCAGAT[A/T]TATTTTTACAACCAC | 26054 |
rs557791441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635160 | AATTACAGTTAATAC[C/T]GTACTTTCTTTATAA | 26054 |
rs557791966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75670874 | AAGAGTATATAAATA[A/G]TAGCTCCTTGCCATT | 26054 |
rs557805746 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675546 | ATAAAAGATTAAATA[A/G]TATTCATAGAATTTA | 26054 |
rs557855157 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622588 | AAACAAAAAAACATT[C/G]TTTTTAGTTTTTTGA | 26054 |
rs557870062 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75683611 | GTTTCAGCTTTCTAC[A/G]TATGGCTAGCCAGTT | 26054 |
rs557878724 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75656634 | ATCCTAATGGAATTT[C/G]TTAACCCTGAGGCTA | 26054 |
rs557887463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684679 | TTTTGTCATTGGTTC[G/T]GTTTATACGATGGAT | 26054 |
rs557899005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636564 | TAGAGATTGATTAGG[G/T]TACAGAAAGACAAGT | 26054 |
rs557900789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614011 | TTGACCTTGACATAT[C/T]TTAAGAAAACAGGGT | 26054 |
rs557926654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641865 | AGACAGTAAACAAAC[A/T]GGAAAGTCCAGCTAT | 26054 |
rs557932412 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673892 | GGGGTGTGGTGGCGT[G/T]CACCCGTAACCCCAG | 26054 |
rs557952678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682972 | TCTAGATCCTTGAGG[A/G]ATCGCCACACTGTCT | 26054 |
rs557955625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678750 | TCTCTGTTTTATTAC[A/T]TTTCAGTTGTGTATA | 26054 |
rs557969144 | snp | A/G | 1.74309e-05 | 0.00295214 | intron-variant | SENP6 | GRCh38.p7 | 6:75634690 | TTCAAGTTATTTTTT[A/G]TTTCTTGAATCTGCA | 26054 |
rs558001153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649610 | GCAACCTCCGCCTCC[C/T]GGGTTCAAATAATTC | 26054 |
rs558010180 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656614 | TTCTTTCCCTAGAAA[A/C]TGGAATCCTAATGGA | 26054 |
rs558038021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643288 | ACATGCTGATTTGAT[C/T]AAACCCAGCTATACT | 26054 |
rs558050675 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75657508 | GTCACAAAGGTAATG[C/T]CATTTTCAGAGATGA | 26054 |
rs558056386 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704132 | CTCGTCAGGTGGGAC[A/G]AGAGACTGAGAAAGA | 26054 |
rs558067367 | in-del | -/CTAG | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75697797 | TATGGTGCTTATTGT[-/CTAG]CAAGTAACCTATAGA | 26054 |
rs558128145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646728 | GTAGTCCTAGCTACT[C/T]GGGAGGCTGAGGCAG | 26054 |
rs558144028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75690964 | CCCCATCAGCTTCCC[A/G]AAGTGCTGGGATTAC | 26054 |
rs558296665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605778 | AGGGGGTGTAATGAT[A/G]TGGTTTATCTTTTTT | 26054 |
rs558313893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75652507 | TTGGGGGACAAATGA[C/T]ATACAGATTTTTAAG | 26054 |
rs558334463 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75703657 | GTCCCAGCTACTTAG[G/T]AGGTTGAGGAGGGAG | 26054 |
rs558357285 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670105 | CACCTGCCACCACAC[C/T]CAGCTAATTTTTTGT | 26054 |
rs558363952 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75659173 | AGGATATAATTATTG[A/G]TTTAGTCTTATGTTC | 26054 |
rs558426945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696323 | GTTTTTTTAAAATTA[C/G]TTAGATACTTACTAA | 26054 |
rs558451868 | snp | C/G | | | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718409 | GATACAGATAACAAG[C/G]CTGCTCTTTAGATAA | 26054 |
rs558458497 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600117 | TGTTTCCCATTCCAT[C/G]TGTTGCTGTAACACA | 26054 |
rs558476915 | in-del | -/AGAG | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75606938 | CAGTGCTTTCTAGGT[-/AGAG]AGAGTAAAATAGGGG | 26054 |
rs558488366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690373 | CTTCCTTAAAAAGGA[A/G]GGAAATACTGTTACT | 26054 |
rs558490009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697092 | CCAGTTACCCTAAGT[C/T]GTGCTTGGCTACACC | 26054 |
rs558524643 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691902 | ACTCTCGTTGTCCAG[G/T]CTGGAGTGCAATGGC | 26054 |
rs558535387 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690010 | ATAGCCTCCTGGGCT[C/G]AAGTGATCGTCCTGC | 26054 |
rs558556417 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75603208 | GCTTATTGACACAAT[G/T]TGAGTTTTACTCACT | 26054 |
rs558563026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701784 | AGCTGGGACTACAGG[C/T]GCACACTACCACGCC | 26054 |
rs558732101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75675299 | TAGGTGTTCATTATA[A/C]TGTTATACCAACTTC | 26054 |
rs558753980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75655801 | TGAAGGATCTTTTTT[C/T]AACTTGATTTTTTAA | 26054 |
rs558758902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75699072 | CTTGACTGGGTACTA[A/G]TTTGTCTTGTAAAGT | 26054 |
rs558759061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75706499 | GAGATTTCTAGTGCC[C/T]TCACCTACAAATTAA | 26054 |
rs558776198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604736 | ACTAATGTTTTCTGC[G/T]TATTTCCCATGATTC | 26054 |
rs558778486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75688168 | CGCTGTGCTAGCAGT[A/G]AGCAAGGCTCCATGG | 26054 |
rs558792142 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602205 | GCAGCCTGGGTGGGC[C/G]GTGGATGGGGAGTCG | 26054 |
rs558799289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629259 | AAAAACTGAAATCTT[A/G]TTAATTTCTATATGC | 26054 |
rs558822582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699598 | GCTTAAGTGATCCTC[C/T]GACCTCAGCCTCCTG | 26054 |
rs558843102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633470 | AATGCTATCCACCAT[C/T]ATTCCCAATAGCTGT | 26054 |
rs558873463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75602738 | GCTGCGAGCGCACCT[C/G]GTTCGAGTCCGCCTA | 26054 |
rs558887440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696597 | ATCCTTCCACCTCAG[A/C]CTCCCAAGTAGCTGG | 26054 |
rs558890643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668517 | ATAGTAATCCAAGTA[C/G]TGAAAATGAAATTAA | 26054 |
rs558916743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604076 | ATCTTCAGTATGCAG[A/T]TGATTATACTTTTGT | 26054 |
rs558969707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611264 | CATTTTGGCATTCAG[C/T]CTTCTGTTTTCAGCC | 26054 |
rs558986145 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654786 | AAGCCTCTTCCTTAC[C/T]CTGCTTCTCCCACAA | 26054 |
rs559055987 | in-del | -/AAAG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698306 | CATTCACTCATTAAT[-/AAAG]AAGAAGAATGTTGGC | 26054 |
rs559063179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75647471 | TTTGTTCTGATTTTG[C/G]AATTGTCCTCAAGAC | 26054 |
rs559075051 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705136 | TTCCTCACTCTCCTT[-/C]CACTGTTTTCAGTGG | 26054 |
rs559113607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690706 | TGTTTTTTGTTTTTT[G/T]TTTTGAGATGAGAGT | 26054 |
rs559144887 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612826 | GTATCAGAAAACTAT[A/G]CCCCAGACCAGGCGC | 26054 |
rs559152381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75625151 | CGGAGTCTGGCTCTT[A/G]CCCAGAATAGAGTGC | 26054 |
rs559172315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669123 | CGGAGACTGAGGTGG[A/G]CAGATTGCCTGAGGT | 26054 |
rs559210055 | snp | A/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679455 | TAAATGAGATCGTAC[A/G]TATCAAGTAGTAGGA | 26054 |
rs559224475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703672 | GAGGTTGAGGAGGGA[A/G]GATCGCTTGAGCTCA | 26054 |
rs559239294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75625758 | CCTGTAGTCCCAGCT[A/G]CGTGGGAGGCTGAGG | 26054 |
rs559240451 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620526 | AGGGCACCAATCCCA[C/T]TCGTGAGAGCTGTGC | 26054 |
rs559241437 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617991 | TGCTGAAGTGCTATT[G/T]TCATCATACCATATT | 26054 |
rs559271128 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611598 | CTCTCACTTTAAAGC[A/C/G]TAAGGAACATTTGGA | 26054 |
rs559282276 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614390 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 26054 |
rs559372175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75712126 | AAGGCAGACGTAAGA[A/G]ACATGTTCCAACTGA | 26054 |
rs559373346 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682546 | TTCTCCTAATGCTAT[C/T]CCTCCCCCAGCCCTC | 26054 |
rs559434639 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707624 | CAGCCTCCCAGAGTG[-/T]TGGGATTACAGATGT | 26054 |
rs559447670 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75614845 | AGTTATTCCTGTTTC[A/T]GATTAAGGGAGTGCC | 26054 |
rs559457016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613086 | GCCACTGCACTCCAG[A/C]CTGCGTGACAGAGTG | 26054 |
rs559467670 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75652033 | AATATAAAAATTAGC[C/T]GGGTATAGTGGCGTG | 26054 |
rs559481239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684424 | CCCTAGCCAGAACTT[A/C]CAACACTATGTTGAA | 26054 |
rs559499945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634883 | TTCACTTTTTTTAAC[C/G]ATTTTTTTCCTTTGT | 26054 |
rs559533219 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657622 | TTAATCCAGGAAACA[G/T]TTATTAAGCCCTTGT | 26054 |
rs559553859 | snp | C/T | 3.31846e-05 | 0.00407323 | missense, utr-variant-5-prime, intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621591 | AATTGGAGCTTTGAT[C/T]ATGAAGAAGAAAGTG | 26054 |
rs559588799 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632721 | TAGGGCGGTGGATTT[-/A]AAAGTTTTAGGGACT | 26054 |
rs559644269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656854 | TTTAATGTCATTTTT[C/T]TCTACCTATTATCAA | 26054 |
rs559658669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627032 | TGCATGGTGCGATAT[C/T]GGCTCACTGCAACTT | 26054 |
rs559710471 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602731 | GGAGTGTGCTGCGAG[A/C]GCACCTGGTTCGAGT | 26054 |
rs559731187 | in-del | -/T | 0.154661 | 0.231107 | intron-variant | SENP6 | GRCh38.p7 | 6:75698495 | AAGCTAGCTTCTGAA[-/T]TTTTTTTTTTTTAAC | 26054 |
rs559732405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75657801 | AGAGGCAGCTTCTTA[A/G]CAAAGAAGAGTTTGA | 26054 |
rs559742252 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75615417 | ACTCCTGACCTCAAG[C/G/T]GATCCACCCACCTCG | 26054 |
rs559756924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75659142 | GAGTGAAAAATAAAT[A/T]AGAGAAGAGTAATCC | 26054 |
rs559776505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654718 | CTGTCGTCTGGGTAC[C/T]TATTTTTCAGCGTAT | 26054 |
rs559776825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75709155 | TTCTGTTATTGGACA[C/T]AGGTTATTTTCAGAC | 26054 |
rs559835495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697939 | TTATGCCATTTTTCA[A/G]TTAAAAACCATGTGG | 26054 |
rs559852995 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75684878 | TTTTGTTGTGTGTCT[C/G]CCAGGCTTTGGTATC | 26054 |
rs559856996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75687155 | TTAATTTGACCTTCA[A/G]TCACTGATACTCTTT | 26054 |
rs559864309 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600685 | TCCACCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 26054 |
rs559870744 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717401 | ATGTTTGATAAGATA[A/C]AAATATAATTTATCC | 26054 |
rs559909407 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75613603 | GGGGATGTATAAATA[A/C]GCGATTATATTTATA | 26054 |
rs559912828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632315 | ACAGAAAGCAAAACC[A/G]TCGATAAAGGGGGAC | 26054 |
rs559914408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672008 | GTACCCTGGAGATTC[A/G]AAGCAAATTATATAT | 26054 |
rs559940625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678363 | GAAAATTACTGTTAC[A/G]TAAGTTGGGAGAGTA | 26054 |
rs560056327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75641745 | TACTTTGGGAGGGCA[A/G]AGCGGGAGTATCTCT | 26054 |
rs560067229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640561 | ATTATATATATATAA[G/T]GTATTTAAAACAAGT | 26054 |
rs560070076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672559 | GATTTTTAGCAAAGG[G/T]CATTCTTCATTGAAG | 26054 |
rs560193398 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75677384 | CAGAATTACTTACTT[C/T]TATGTGTGATTTGTA | 26054 |
rs560228202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708603 | TGTCTCTTAAAAAAT[A/T]AATAAGTGAGGCCAG | 26054 |
rs560237458 | snp | A/G | 3.3274e-05 | 0.00407871 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709559 | AGACTAAACTATAGC[A/G]ATGAATCACCTGAAG | 26054 |
rs560343806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681297 | CTCCCCCTTTGCTCT[C/T]TGTTACTCCTGCTCT | 26054 |
rs560373090 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75674856 | CCGCTAAATTTTACT[A/G]TTAGCATTTTATTGT | 26054 |
rs560409932 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716564 | TAAATTATTTTTTAC[A/G]TGTAAAAGTACTGTA | 26054 |
rs560422004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671034 | AAGAATATATTAAAG[A/G]ACTGTAGTGAGTGAA | 26054 |
rs560436811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668830 | GCGGTTTTCAGACTG[A/G]CACACTGAATCATAA | 26054 |
rs560455009 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652761 | AACACAGTATTATTT[G/T]AGTTGGCCTATTTTC | 26054 |
rs560546684 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676573 | TAATTGCTGCTTCAG[C/G]TTAATTATGAAAAAA | 26054 |
rs560563902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679771 | ACATGTATATGAAAT[A/G]AAACAGAACTTAGCA | 26054 |
rs560606670 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616658 | GGCTGAGGCAGGAGA[A/G]TCACTTGAACCCGGG | 26054 |
rs560607039 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651417 | TGGAGTACAGTGACA[C/T]GATTATGGCTCACTG | 26054 |
rs560614389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75670469 | TATTTACATTTCTTA[C/T]ATTGGGTCTTTGCAT | 26054 |
rs560615513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689061 | ACAAGAGTGAAACTC[C/T]GTCTCAAGAAAAAAA | 26054 |
rs560633195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75642092 | AGCAATGTTTCTACA[A/G]TTGTTTGAAATGGTA | 26054 |
rs560655142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619854 | CCAGCACTTTGAGTG[C/G]CTGAGGCAGGGAGGA | 26054 |
rs560658526 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698786 | GAGGCTGAGGTGGGC[A/G]GATTACTTGAGGTCA | 26054 |
rs560663182 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75714128 | CACTGCCTCTTTTAG[C/G]CTCTTTTCTCCTCTT | 26054 |
rs560669539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663128 | TTTGTTCTTTTGGAA[C/G]TTAAAGTTTATGAAC | 26054 |
rs560767161 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75688474 | TCACCCATCTTCTGC[A/C]TCGGTCATGCTGAGA | 26054 |
rs560779130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75691506 | TCAATATTTAAATGA[C/T]GTATGCACTTAGAGA | 26054 |
rs560799774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673046 | GTTAGCCAGGATGGT[C/T]TCGATCTCTTGACCT | 26054 |
rs560840768 | in-del | -/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717228 | TAAAAAATTGAAGTT[-/G]TTTTTTTTAAAACCT | 26054 |
rs560902091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75610321 | AAAATGCCAGTTAAT[C/T]CACTAAGTCACAGAC | 26054 |
rs560905320 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602380 | ATAGGCCCGTCTGAA[C/T]GTGGGAGCGCAGCCC | 26054 |
rs560925039 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708133 | GGCGCAGTCTTGGCT[A/T]ACTGCAACCTCTGTT | 26054 |
rs560972814 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600608 | AATTTTGTATTTTTA[C/G]TACAGACGGGGTTTC | 26054 |
rs561024400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607560 | TCCTTTTTTTTTTAA[C/T]CAAGTGAATTCCTTC | 26054 |
rs561076541 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75673642 | TGTCTACTTATAATA[G/T]TAATGTGTGACTTAC | 26054 |
rs561089869 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75692789 | TCCTTCCCTTCCCCC[A/G]CCAAAAAAAAAAAAT | 26054 |
rs561122995 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75714809 | TACTTTTTTGTTGCT[G/T]CTATTATACCTTGTC | 26054 |
rs561127566 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619584 | TGAACATTGGCATAC[A/G]AGTGTCTGTTTGAAT | 26054 |
rs561138098 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684570 | ATTTTGAGATATTTT[C/G]CATCAATACCTAGTT | 26054 |
rs561150716 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601494 | CATTTACTAAACATA[C/T]GATTCCAGTACCTCA | 26054 |
rs561186308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705986 | TAATCACCCAGGCTG[G/T]AGTGCAGTGGCGTAA | 26054 |
rs561187001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651844 | TTAAAAGATGACAGA[C/T]ATGGAACCAGCATGG | 26054 |
rs561229281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691852 | GCCCGCCTCGGCCTC[C/T]CATTGTTTTTTGGTT | 26054 |
rs561249923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75706876 | CACTACTTTCACTTG[C/T]TGTTTTTTCACTTGA | 26054 |
rs561252811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653574 | TCAATGCGTTTGGGT[A/G]AATGTCAGGAATGCC | 26054 |
rs561264240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75609520 | GACAAATAATTTGCA[A/G]CTATCTTTAATCTAT | 26054 |
rs561276307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644931 | AACTTTTCTGCAAAT[C/G]TAAAATTATTTCAAA | 26054 |
rs561277920 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608292 | ATAACGAGGCCCCAT[C/T]TCTGCAAAAAATACA | 26054 |
rs561317978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615806 | GTTTGAAAGAAATTA[C/G]TGGCGAAGCCTTCTG | 26054 |
rs561360701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686809 | GGGTAATCAACCTTT[C/G]TCTCTGGCTGCCCTT | 26054 |
rs561394318 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75605915 | GCTTCAATTAGCATG[A/G]TGTCAGTGGAGACTG | 26054 |
rs561416792 | snp | A/G | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677134 | GGTATAAAGAATAAC[A/G]TCTCCAATTTTTTTG | 26054 |
rs561484365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642710 | AGGGAAGTATTGTTA[C/T]CTGATAAATATTTGA | 26054 |
rs561491514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703155 | TTAAGATCCTGTTTT[A/T]AAAAAAAATCAGGTT | 26054 |
rs561524585 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718600 | CATTTGTCATTTCCT[A/G]CTCAGGAAGAAGAAA | 26054 |
rs561525755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624057 | TATAAACCCCAGTTA[C/T]CCACTTTCTCCACTC | 26054 |
rs561543391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75656675 | GTTTTTTTCTTAACT[C/T]TCTATAGATCTAGTT | 26054 |
rs561545554 | in-del | -/GT/GTCACCCAGGCTCTGGAG | 0.193848 | 0.247555 | intron-variant | SENP6 | GRCh38.p7 | 6:75690729 | TGAGAGTCTCGCTCT[-/GT/GTCACCCAGGCTCTGGAG]GTCACCCAGGCTCTG | 26054 |
rs561559020 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75695718 | CTCCAGCCTGGGCAA[C/G]AGAGTGAGACTCTGT | 26054 |
rs561662114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613022 | GGGAGGCTGAGGCAC[A/G]AGAATCGCTTGAACC | 26054 |
rs561693470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75695336 | ATAGCAATTTTCATT[A/G]CCTGAAGATAATCGG | 26054 |
rs561750685 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616135 | ATATGGAGAAAACTT[G/T]AGGTGTTTAATTTGT | 26054 |
rs561758306 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689722 | TATGGTATTCAGTAC[A/C/G]GTAACATACTATACA | 26054 |
rs561827202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669838 | AATCTGCTAAACTGC[A/T]TTTTATGCATTAACT | 26054 |
rs561909044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619330 | TGGAATCATACAATA[G/T]TTGTCCTTTTGCATC | 26054 |
rs561952208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75663086 | ATTCCTTAATGATGC[A/G]GTAAAATGCCAAAAT | 26054 |
rs561988804 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75663797 | ATGGGTAGATTTCCT[A/G]CTGATAGTGGGTTTT | 26054 |
rs562026908 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657297 | GTCTGCCTTCTTTTT[A/G]TAGTGTCACATCATA | 26054 |
rs562060502 | snp | A/C | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618629 | CACTGCTTCTAGACC[A/C]TCTAAGAAAGCAGCT | 26054 |
rs562131422 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626404 | TACACACTGTTGACA[A/C]CTTGATTTTTTTACT | 26054 |
rs562179378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614785 | AATAGACTTGCTGAT[A/G]GCTTATTGCTGGGGA | 26054 |
rs562185227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606722 | CATTGAATCAATTCA[C/G]ATTTTTGGATTTGGG | 26054 |
rs562216008 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75683951 | AGTCACTGGTAGCTT[C/G]ATGGGGATGACATTG | 26054 |
rs562217986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690609 | AGATCTGTTTTTAAC[A/G]CTGTGCATATACTTT | 26054 |
rs562224794 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624292 | TGCATAGTATTCCAT[A/T]GTATTATATACCATT | 26054 |
rs562229871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668672 | GGCAGTAATTCTAAA[C/T]GTGTACCACAACTGG | 26054 |
rs562233921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660790 | GCATCTGCCACCATA[C/T]CCGGCTTATTTTTGT | 26054 |
rs562247879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628348 | AGAACTCCTGCTACT[A/G]AAGTTTATTTTTTTA | 26054 |
rs562258485 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75648537 | TTTTCTACTTTGGGT[A/G]AAAATCTTTTGTGCA | 26054 |
rs562269768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661078 | GGTATTATTGTTTCT[C/T]GGCCTTCTCAGTGGA | 26054 |
rs562367128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674819 | GTTGAAAGACTTTTG[C/T]AGTGAACATTTATAT | 26054 |
rs562371386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75625216 | TCCCGGGTTCAAACA[A/T]TTCTCATGCCTCAGC | 26054 |
rs562388004 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707139 | TTTCTGGTTTAGTTT[C/G]TGTAAGGTAGATAGA | 26054 |
rs562409356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639992 | GATTTAACCATTCCC[A/T]TATTAGTAGATACTG | 26054 |
rs562447479 | snp | A/G | 0.000315204 | 0.01255 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715562 | CCTTTAGGCGAAGGA[A/G]CAGAACAATATGTCA | 26054 |
rs562488367 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610868 | GTTTTTGAAGATGCG[-/T]TTTTTTCCCCCTCCC | 26054 |
rs562493204 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624814 | CATCTTATTAAGATA[C/G]CATGATATGCTTTAA | 26054 |
rs562493798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75617375 | GTCTCCTGGGTTCAA[C/G]TGATTCTCCTGCTTC | 26054 |
rs562495165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75688382 | CGCCCTGCTTCAGCT[C/T]ACCCTCCATGGGCTG | 26054 |
rs562575910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680555 | AGCTGTTGAAGAAGT[A/T]AGAAGAGAAATTGAA | 26054 |
rs562585242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75610594 | CAGAATCTTCTGCAT[C/T]CATTGGCAAAAATTA | 26054 |
rs562605650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631274 | CTTAAATTACATGAT[A/G]TGATAATTTTGGGTG | 26054 |
rs562608500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707962 | TGCTAGAGGATTACA[C/G]GTGCTAGGCCACTGT | 26054 |
rs562644804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686318 | TGGGTTTCCTGAATA[C/G]AGCACACTGATGGGT | 26054 |
rs562708188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686756 | TTGTAGGGTTTCTGC[C/T]GAGAGATCCACTGTT | 26054 |
rs562770966 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639415 | ATTTTTAATGTGTTC[A/G]TGTAAAAACAAGTTA | 26054 |
rs562832264 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665246 | AGCCAAGATCGCGCC[A/G]CTGCGCTCCAGCCTG | 26054 |
rs562833032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75687634 | CCTTTCTGTTTGTTG[A/G]TGCTATTCCTTTCTG | 26054 |
rs562839087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75683065 | CATCCTCTCCAGCAT[A/C]TGTTGTTTCCTGACT | 26054 |
rs562939003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634058 | CTCCTTTAGGAAATA[C/G]TAATCAGGATTGTCT | 26054 |
rs562997521 | snp | G/T | 0.00022773 | 0.0106683 | intron-variant | SENP6 | GRCh38.p7 | 6:75675760 | GAGCATAATAAATAT[G/T]TGCTTACATTTACTT | 26054 |
rs563014254 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673956 | AACCCGGGAGGTGGA[A/G]GTTGCAGTGAGCCAA | 26054 |
rs563023615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611418 | GTCTCTTTTGCTTTC[A/G]CCATTTACAGGCTTC | 26054 |
rs563040832 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618693 | CCTGTACATCTGTGT[A/G]TGTATTAAATAAATG | 26054 |
rs563076708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647600 | GTTTTGTTATTTTAT[A/C]GTATCACTTTTTATA | 26054 |
rs563112344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654661 | AAATAATGTAAAAGC[A/C]AATACATAATCATTA | 26054 |
rs563137066 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628089 | GATTTATTTAGTGAA[C/T]TGTAAAGATTATTCT | 26054 |
rs563172229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75684945 | ATTTCCTCTTTTTCT[A/G]TTGATTGAAATAGTT | 26054 |
rs563188999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696648 | CACCCAGCTAATTTT[C/T]GTATTTTTTGTGGAG | 26054 |
rs563203798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75636866 | ATTTTCTTATTTTCT[A/G]AAGTCTTAATTTTTT | 26054 |
rs563247890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697677 | ACAAGAATTAATGCA[G/T]TTTCACAGTGAAGCA | 26054 |
rs563249803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75690794 | TCCGCCTCACGGGTT[C/G]ATGCCATTCTCCTGC | 26054 |
rs563253158 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75644153 | CATGGATGACACACG[A/C]ATTAGTAAAGCATTT | 26054 |
rs563260114 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600491 | GGGGTGCAATGGCAC[G/T]ATCTCCGTTCATCGC | 26054 |
rs563268243 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75658053 | AAGGGGAGCAAAATT[A/G]GGATAGAGGACATCA | 26054 |
rs563268985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684495 | TTCAAATGGAATGCT[G/T]CCAGTTTTTGCCCAT | 26054 |
rs563320224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703730 | TCGCACCACTGCAGT[C/T]CAGCCTGGGTGACAG | 26054 |
rs563354840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657902 | AAGAAATGAACCTTT[C/T]TGAGGTAAAGTTTAA | 26054 |
rs563376265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637700 | TTGTAATTCTTATAA[A/G]GTTCTTAGAAGTCTT | 26054 |
rs563400983 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75684262 | TGTATCCTGAGACTT[A/T]GCTGAAGTTGCTTAT | 26054 |
rs563434278 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75614268 | TTACTATCTTTTTTT[G/T]TTTTTTTTTTTGTTT | 26054 |
rs563484779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608691 | GATTACTTAACTTCT[C/T]TGTTTTCTCAGCTAT | 26054 |
rs563498294 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671418 | TCCTTTTTACATAAA[A/G]CACTTGTCTTTAAGA | 26054 |
rs563528228 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707745 | AAGAGTACAGCAATA[C/G]AATCACAGTTCACCG | 26054 |
rs563553394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658267 | TGAAACTTTGTGATT[A/G]CACTAAGCAAGAATA | 26054 |
rs563575762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607466 | TCTTTTTTTCACTCT[G/T]GGGGCTCTAACAAGC | 26054 |
rs563611830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75609207 | TCTCCCTTTCTCCCC[A/G]CTTCCTCATCACTTT | 26054 |
rs563652396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75615560 | CTTTTGCTTTTTAGA[A/G]TAAACCCTGCTTAAT | 26054 |
rs563669494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707940 | CTCCTGCCTCAGCCT[C/T]CCAAAGTGCTAGAGG | 26054 |
rs563685008 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602945 | ATGAAAAGTTTCAAA[C/T]TGCTAAGGTTGGGTG | 26054 |
rs563716462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75659769 | TTTATTGTCCTCACT[C/T]TCTATGCCTTTTTCC | 26054 |
rs563724314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75671565 | CATCTCTACTAAAAA[C/T]AGAAAAATTAGCCGG | 26054 |
rs563727836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643937 | AAACAACAATAACAA[A/G]AAGAGAAATGGTGTC | 26054 |
rs563777715 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602348 | GACAGGCCCGGGCGC[A/G]CCTGGCCTGCCTTTG | 26054 |
rs563832293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705480 | AACCTGGGGGCGGAG[C/G]TTGCAGTGAGCTGGG | 26054 |
rs563832595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672609 | TCTTCTTCAGATGGC[A/G]TAAATAAAAAGATGA | 26054 |
rs563854733 | snp | A/G | 0.000118547 | 0.007698 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659265 | TCCTTCCTTTAGAAC[A/G]TATAATGAAGAAAAC | 26054 |
rs563873136 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635488 | CATTTTTTAAAAATG[C/T]AATATCTAGACTGCT | 26054 |
rs563880732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648407 | ATCTTGTTTTTCTGA[A/G]GCCTTTGTTTGTTTA | 26054 |
rs563887880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75712939 | GAAAAACCCATCTCT[A/G]CAAAAAAAAATACAA | 26054 |
rs563914600 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630780 | AAACATTTTAGTCAT[A/T]ATCTCTGTGGATTTT | 26054 |
rs563944132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663024 | TCATGGTAGCCATGA[C/T]GGTAATGATGGGGAA | 26054 |
rs563956066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75666308 | CTACATGGAGTTTCA[C/T]ACATATTTACAATGC | 26054 |
rs563972768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75612971 | ATACAAAAATCAGCC[A/G]GGCATCGTGGCATAT | 26054 |
rs563980987 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75656124 | GGAGGCAGAGGCAGG[A/C]GAATTGCTTGAACCT | 26054 |
rs564003526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604971 | CCAACTACTCGGGAG[A/G]CTGAGGCAGGAGAAT | 26054 |
rs564053806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701369 | TGAATTCAGCTGTAT[C/G]ATAAGCACCTACTTG | 26054 |
rs564061853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619276 | TTGATTCTACTTTCT[A/G]TCTCTATGAATTTAC | 26054 |
rs564074477 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604398 | GCATTTTGGAGGGCC[A/G]AGGCAGGCGGATCAC | 26054 |
rs564085190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682595 | GGTGTGTGATGTTCC[C/T]CGCCCTGTATCCAAG | 26054 |
rs564115378 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75694704 | AGGATTTTCTATGAT[C/G]ATGTATTATCACTTC | 26054 |
rs564127938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75655523 | ATAGATTAATTTTAC[C/T]TGTTCTAGGACTTCA | 26054 |
rs564136727 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645917 | TTACAATACTTGGTA[A/G]GATTGTAGCTATCAT | 26054 |
rs564232123 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680582 | TGAAGGGAAGTGAGA[C/G]CTTTAAAGGAGATTA | 26054 |
rs564233177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75675132 | GACCCCCATGACATG[C/T]AATTTACCTGTATAA | 26054 |
rs564274749 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639566 | AGTTAGTTCCAAATA[C/T]TTCATTCCTTTTATA | 26054 |
rs564294551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668962 | CTTTCCTGTTTTATT[A/C]GTGAGCTAAATAACC | 26054 |
rs564320939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627697 | ATTGCTTTTTTTTTG[A/T]GACAGTCTTGCTCTG | 26054 |
rs564323712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649031 | TGCATTTCTGGCCTG[G/T]TATGGTGGCTCACAC | 26054 |
rs564355950 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75669570 | TCTTGTGATGATAAT[A/G]AAGATACTAATATAA | 26054 |
rs564364981 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717548 | ATTTTATTTTTGGAA[A/G]TTATGCTAGTGACAT | 26054 |
rs564410810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642568 | GCTTAGAGAGGAAAG[A/G]AGACAATGTTATGAG | 26054 |
rs564417643 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75670243 | TGAGCCACTGCTCCC[A/G]GCCAAGATCACATCT | 26054 |
rs564436121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662240 | TTAATTTTGTAAAAC[A/G]CCTTCCACTTCTACT | 26054 |
rs564443337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75711266 | CCAGTGTGCTATTTT[A/G]TTAGGTTATTAGTTA | 26054 |
rs564466852 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691509 | ATATTTAAATGATGT[A/G]TGCACTTAGAGAAAT | 26054 |
rs564468116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664719 | AGAAATACTGAGATG[A/G]TACTTCTCTGGGACA | 26054 |
rs564509764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620607 | ATCTTGGGGTTAGGA[G/T]TTCATCATATAAATT | 26054 |
rs564539839 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628269 | AATCTTTTTATTATC[C/G]TATCACACTTTAATA | 26054 |
rs564560553 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75710563 | TCTCTTGGTTTACAA[C/T]GTATGGCAACTAAAT | 26054 |
rs564561152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689642 | GCCCATAAGATTATA[A/G]TAACGTATTTTTACT | 26054 |
rs564595404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663933 | CTGTCTTTTTACTCT[G/T]ATGTGTATGTGTATG | 26054 |
rs564596532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621155 | GAGAGTCTAGCAGTC[C/T]GGATATAGTTCTCAT | 26054 |
rs564596589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613844 | ATCTACAAACATTTT[C/T]CCACTTTCATTAGTT | 26054 |
rs564623876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703263 | GAGTTTGAGACCAGC[A/G]TGGGCAACATAGCGA | 26054 |
rs564633948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657076 | TGTTTGAGCAAAATA[A/C]TGTGCAAAGATACTG | 26054 |
rs564635388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75635536 | GTCCTGAACCTTGCT[A/G]TATTTTTCTGTTTAC | 26054 |
rs564644652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75695608 | TGGGCGTGGTGGTGT[A/G]TGCCTGTAATCCCAG | 26054 |
rs564655385 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676773 | AAATTAGTTACATAC[A/G]TGAATAGATTTGTTC | 26054 |
rs564677347 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75689094 | CAGCTGGGCATGGTG[G/T]TGCACACCTATAGTC | 26054 |
rs564726670 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664922 | AACAAGTGAACATCC[A/G]CAACAAGGAACAACA | 26054 |
rs564733612 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668627 | TGGAATGTTGAATGT[A/G]TAAGTTGGTGTAACT | 26054 |
rs564786992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714927 | GTACTCTATACTTCT[A/G]TCATAATACTTGCCA | 26054 |
rs564795366 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648841 | CCTATAAGCTAAAAA[A/G]CTTCCTCAAGGACAT | 26054 |
rs564804035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627030 | AGTGCATGGTGCGAT[A/G]TCGGCTCACTGCAAC | 26054 |
rs564808567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645901 | ACACATTAGTTTAAT[G/T]TTACAATACTTGGTA | 26054 |
rs564811099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667436 | CTTAAAAATTACAGG[A/T]TAAAAACAAAATGAA | 26054 |
rs564850090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75706088 | CTGGGATTACGGGTG[C/T]GCACCACCTCACCCG | 26054 |
rs564897022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631204 | ATGGTTTCTATTAGG[C/T]TCTCTTATTATCTGA | 26054 |
rs564909080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693758 | GTTTTAAGCATTTGC[G/T]CTTTCTGTGTAAGAT | 26054 |
rs564912614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645322 | TCAAATTAAGAAATT[A/G]ATGTAAATGCTGGCC | 26054 |
rs565011922 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642150 | TTAGGCATACGCTTT[C/T]ATTCATTCCAAGTAT | 26054 |
rs565022838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639205 | GAAATAAATACATAG[A/G]ATAGGACAGACTAGA | 26054 |
rs565041625 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601603 | TCTGTGGTGCCAGAG[A/G]AGCAAACCCATCGCA | 26054 |
rs565104414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687039 | CAGGTACACCAATCA[A/G]ATGTAGATTTGGTCT | 26054 |
rs565123305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75692625 | AGTGAGACTTTATCT[C/T]AAAGAAATAAATAAA | 26054 |
rs565151937 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663598 | AACCACTCTCCCCAA[-/C]CCCATATATATTTTT | 26054 |
rs565181948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75686201 | AAGTCTGTTTTATCC[A/G]AGACTAGGATTGCAA | 26054 |
rs565187117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699951 | AGTCTCATTCTGTTG[C/T]CCAAGCTGGAGTACA | 26054 |
rs565192036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639267 | TTCTTTAATAGGGAT[A/G]TGATTATATTCCCTT | 26054 |
rs565198693 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671209 | CCACCAATCCAAGTT[A/T]TTATTTTCTATTTGA | 26054 |
rs565262650 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75647086 | CTCTTTTATTTTTAT[A/G]TGGTTTATTTAGAGT | 26054 |
rs565271444 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693149 | TCACGCCTATAATCC[C/T]AGCATTTTGGGAGGC | 26054 |
rs565313608 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75687540 | TCTTTGTGGTTTTAT[A/C]TACCTTTGGTCTTTG | 26054 |
rs565406068 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695459 | AAGCGAACTGTGGCC[A/G]GGCGCCATGGCTCAC | 26054 |
rs565411495 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75627209 | TCAGATGATCTACCC[A/T]CCTTGGCCTCCCAAA | 26054 |
rs565411823 | snp | A/C | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621297 | TTATTATAGCTTTCT[A/C]ATCTGAGCTTCTTTG | 26054 |
rs565449126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627868 | TTTTTAGTAAGAGAC[A/G]GGGTTTCACCATGTG | 26054 |
rs565492079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604630 | ATTCTGTCTCCAAAA[A/G]AAAAAAGCATAAGGA | 26054 |
rs565497835 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711219 | CCTAAATAGAGAAAA[A/G]GTTTTGACAATCATT | 26054 |
rs565535864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653724 | CACTGATATCTTAAA[C/G]TTAGGTATGATTATT | 26054 |
rs565551250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75602997 | AGGGAGGGGACAGAC[A/G]GTTTCATTGAGGTGT | 26054 |
rs565582205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605168 | TACATAGGCTCCTAG[A/G]ATTTAATATTAAGAC | 26054 |
rs565622502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75646612 | GAGGCTGAGACAGGC[A/G]GATCACGAGGTCAGG | 26054 |
rs565658758 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677554 | TACCCTACTTCCAAC[A/G]TATATATGCACACAC | 26054 |
rs565707653 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75699030 | AAAAAAAAGGAAAAG[-/A]AAAAAAAAAGACAGA | 26054 |
rs565712435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684070 | TGTCCTCTTTTATTT[C/T]GTTGAGCAGTGGTTT | 26054 |
rs565717236 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706010 | GGCGTAATCTTGTCT[C/G]ACTGCAACCTCCCCC | 26054 |
rs565756215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650059 | GTGATCCCACATAGC[A/G]TTTGTCATGTTCTCT | 26054 |
rs565783975 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75695433 | AAAAGATTTACTGAG[G/T]TTTTAATACAAAGCG | 26054 |
rs565788048 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675295 | TGTTTAGGTGTTCAT[A/T]ATAATGTTATACCAA | 26054 |
rs565851061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708671 | AGGCCGAGGCAGGTG[A/G]ATCACTTGAGGACAG | 26054 |
rs565912080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75688751 | TATAATGAAGCCCTG[C/T]GTCTACAAAAAAGAA | 26054 |
rs565937584 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75648563 | GTGCATGTATTGAAC[A/G]TTTCTCTATTTCATA | 26054 |
rs565944857 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624647 | AACATCATTTCATAT[A/G]TATAGTCTCATTCTT | 26054 |
rs565989245 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75690865 | CACACCTGGCTAATT[G/T]TTTTGTATTTTTATT | 26054 |
rs566055258 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681101 | ACAAAGATTTTAAAG[C/T]ATCTGATACAGTTGA | 26054 |
rs566063681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657991 | TATTAGAATGACAAA[A/G]TCATGATTTTTAACT | 26054 |
rs566065581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649454 | GTAAATAAGCATATT[C/T]AAGTTAAGAGAAAAA | 26054 |
rs566098036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75671400 | TCTTTCAAACTGATA[C/T]TGTCCTTTTTACATA | 26054 |
rs566151239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654042 | CAGACTGGCCAGCAT[A/G]GTGAGACCCTGTCTC | 26054 |
rs566176434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613984 | GAAATAGCTTTTCAG[A/G]CTTTGTCTTTCTTGA | 26054 |
rs566238938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687204 | GGCTATTGAAGCTTG[C/T]GCATGTGTCGTGAAG | 26054 |
rs566259079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606272 | ACAAAAGCACACTAA[A/G]ATTGTATGGATTTCA | 26054 |
rs566275676 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75674620 | CTGCCAGTACCCATG[C/G/T]TTAATGTCCCCAAAT | 26054 |
rs566281457 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651571 | TGCCCAGTTTGCTGT[C/G]AGGCTTCTGGGCTCC | 26054 |
rs566322466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75711693 | GTGTATATTTTTTGA[A/G]ACAGAGTCTTGCTCT | 26054 |
rs566331648 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639500 | CCACATGATAGGAGT[A/G]TAAGAATTGATATAG | 26054 |
rs566385491 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75614349 | CAGCTCACTGCAACC[G/T]CTGCCTCCCAGGTTT | 26054 |
rs566425083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660340 | TTAATAGGTATTTGA[A/C]TAATTCATTAATAAG | 26054 |
rs566430283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75602612 | GACGGGGAGAAGGGA[A/G]GGTATACTGGAAAAC | 26054 |
rs566432148 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75610636 | CTTCAGAGTATATGG[A/G]GCTTTCAGTGCTAAA | 26054 |
rs566461035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700099 | AAATTTTTTTGGAGA[C/T]GGGGTCTAGCTGTGT | 26054 |
rs566463814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653318 | TTACAGGCATGAGCC[A/G]CTGTGCCTGGCCTTA | 26054 |
rs566485663 | snp | A/T | 5.13422e-05 | 0.0050664 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675872 | CAGAACCAGACCATG[A/T]TCCTGTAGAGATTAT | 26054 |
rs566496659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75647165 | CCCCTTCTGTGATGC[A/G]CTTTTATACAATTAG | 26054 |
rs566508944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75693426 | AAAAAAAAAAAAAAA[A/G]AAACACCAAAGTAGC | 26054 |
rs566525181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708340 | TTATATTAATATCTT[A/C]ACACCTTTTTATTAA | 26054 |
rs566587352 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75708982 | TGATTAGCTTCTTTC[A/T]GCAAAATAGTTGCTT | 26054 |
rs566605610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640404 | AGCAGGGAATATTGT[A/G]TTCTAACATATCTTC | 26054 |
rs566615550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75673898 | TGGTGGCGTGCACCC[A/G]TAACCCCAGCTACTA | 26054 |
rs566655941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624244 | AGACCATCTGTAAGA[A/G]TTCATAAAAAGCACC | 26054 |
rs566660011 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606854 | AAGGGACACTTAACC[C/T]GAAATCATGAGAATT | 26054 |
rs566672214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715095 | GCATCTGCAGACCAT[A/T]TGTAAATGAGTTAGT | 26054 |
rs566675506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699506 | TCTTTCTTTTTTCTC[A/G]AGATAGGGTCTCTGT | 26054 |
rs566690354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616678 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGT | 26054 |
rs566695394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681642 | TTTCAGGTAGTTCTT[C/T]AGAGCAGTGAGAGAA | 26054 |
rs566736022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75706388 | GTCTCCTTTTGACCA[A/G]TAATGTTACATACTT | 26054 |
rs566750972 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717738 | GTAAAACAGAACTTA[C/T]AGAGGTTTGTTACTA | 26054 |
rs566753306 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614308 | TCTGGCTCTGTCACC[C/T]AGGCTGGAGTGCTGT | 26054 |
rs566769594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669911 | GGAACCAAAACTTAC[C/G]TAAGTTATTAAGTTT | 26054 |
rs566786541 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619414 | ATCCAATTCGTATCC[C/G]TTTAAGGCTGAATAA | 26054 |
rs566797379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707284 | GTGTTTTAGCTTTAA[A/G]CAGACTTAAAAATAC | 26054 |
rs566814376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669098 | CTCACACCTGTAATC[C/T]CAGCACTTTCGGAGA | 26054 |
rs566890770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612013 | GAAGTAGTAGTGATC[C/T]ATTAGTTTGTCTTCT | 26054 |
rs566901795 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604122 | CAGCTTCTATAGGCC[C/T]GATTGAGTTAAAATT | 26054 |
rs566923157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75712032 | TTTGGAGCAGAAATC[A/C]CTATATATCAAAACA | 26054 |
rs566939251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640900 | CAGGTATACAATGTG[G/T]ATGATCAGATCAGGG | 26054 |
rs567052501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75632628 | ATTTGATCTCTTTTC[A/G]AACAAATGGATTCAT | 26054 |
rs567087151 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SENP6 | GRCh38.p7 | 6:75690845 | GGACTACAGGCGCTC[A/G]CCACCACACCTGGCT | 26054 |
rs567105699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672197 | AAAAATGTTCAGGAG[C/T]GCCCTGTAACTTTTA | 26054 |
rs567129122 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693237 | AACCTGGCCTCTACT[-/A]AAAAAAAAAATACAG | 26054 |
rs567204827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679048 | GCCACTTACTGTGTG[A/G]CATTTGGGGAGTTAT | 26054 |
rs567208448 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672571 | AGGGCATTCTTCATT[A/G]AAGAATAATTAGTGG | 26054 |
rs567229806 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603221 | ATTTGAGTTTTACTC[A/G]CTCGTGAGGGAAAGT | 26054 |
rs567249367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629360 | CAGGAGTGCAGTGGC[G/T]CAATCTTGGCTCACT | 26054 |
rs567256142 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627951 | TGCTGAGATTACAGG[C/T]GTGAGCCACCACGCC | 26054 |
rs567266325 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75693114 | TTATAAAACAGCCAT[C/T]GTAGGCCAGGCACAG | 26054 |
rs567312582 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696959 | TATATTCTCTTATTT[C/T]AGCAATTCCTAATGT | 26054 |
rs567321759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622394 | GAGACCTCATCTCTA[C/T]TAAAAATACAAAAGA | 26054 |
rs567322166 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661881 | ATATGGTGAAATCCC[A/G]TCTCTACTAAAAAAA | 26054 |
rs567360479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75615141 | AGTGATTCACCCACC[C/T]TGGCCTCCCAAAGTG | 26054 |
rs567386145 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636819 | AGACTTCAGGTGAGG[G/T]TAAACACATTGGCTT | 26054 |
rs567392257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75630510 | CCTGATAAATTTTGC[A/G]TATCTCACAGAGCTC | 26054 |
rs567393599 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600007 | AGGCGGAGGTTGCCG[C/T]GAACCGAGATCATGC | 26054 |
rs567394548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639409 | TTGTATATTTTTAAT[A/G]TGTTCATGTAAAAAC | 26054 |
rs567429185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75631476 | TAATGTTATAAACAG[A/G]AGTTGTCACATTAAG | 26054 |
rs567457609 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663865 | AGTATGCATAGCCCA[A/G]TAAAATATTTGACAT | 26054 |
rs567496156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75705499 | CAGTGAGCTGGGATC[A/G]CGCAACTGCACTTCA | 26054 |
rs567512706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607927 | CAGCTTCTCCCAAAC[A/G]ATTGGCATTCCATGG | 26054 |
rs567539549 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658197 | TATTTAAATTTCTAG[C/T]TTTGGTGTCTAGGAA | 26054 |
rs567549488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608783 | GAGGATTGAGGAAAT[A/G]TATATTACTTAAAGC | 26054 |
rs567551305 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601059 | CACTTAATCATGTCG[A/G]TTTTCTGCATCATTT | 26054 |
rs567552401 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688546 | GCCACCCCACCCCCC[A/C]GTCCAGGATTATATT | 26054 |
rs567559859 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665982 | AGTGAGACAAGATCG[C/T]GCACTGTACTCCAGC | 26054 |
rs567570468 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75685178 | TAGATTTTCTAGATT[-/A]TTTGCATAGAGGTGT | 26054 |
rs567601854 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682998 | TGTCTTCCACAATGG[C/T]TAAACTAATTTACAC | 26054 |
rs567631035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685689 | AGTTGTTCAGTTTCC[A/T]TGTAGTTGTGCAGTT | 26054 |
rs567714453 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699594 | CCAGGCTTAAGTGAT[A/C]CTCCGACCTCAGCCT | 26054 |
rs567733300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641694 | ATCCATAAGAGTAGC[G/T]GGACTGGGCAAGGTG | 26054 |
rs567768425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642225 | ATACAGTGATGAACA[A/G]AGCAGACAAGATCCC | 26054 |
rs567770458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634522 | TCTTTAATTGGATTG[C/G]AAACATTTGAAAGAC | 26054 |
rs567785874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651666 | ACATATTAACTTTCA[A/G]CCAGTCATGGTAGCT | 26054 |
rs567804023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75691784 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 26054 |
rs567811798 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75604245 | ATTCTAATCTAAGGG[-/T]CTTTGAATGTATAGG | 26054 |
rs567824584 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75644559 | GTGCAACCTTGGCTC[A/C]CTGCAACCTCTGCCT | 26054 |
rs567848331 | snp | A/G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674843 | TTTATATAACTCCCC[A/G/T]CTAAATTTTACTATT | 26054 |
rs567856465 | snp | C/T | 0.000136435 | 0.00825826 | intron-variant | SENP6 | GRCh38.p7 | 6:75634984 | ATTTTATATCTGCTT[C/T]TGAGTAATCAGATTC | 26054 |
rs567904920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75611738 | GTAGCGCCAACTGCA[C/T]TGCTTTGGAATAGGT | 26054 |
rs567910049 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685948 | CAATTCCTGGGTATC[C/G]TTCTTCACTTTCTGT | 26054 |
rs567911789 | in-del | -/GTTTTAA | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75617185 | CACCCAGCCTTTGGT[-/GTTTTAA]AACTTTTTCTTTTGG | 26054 |
rs567950448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75692136 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 26054 |
rs567972670 | in-del | -/AT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75713396 | CAGTAGTACTGAGTC[-/AT]ACAAAGGGGATTTTG | 26054 |
rs567974495 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697713 | GATATTGAATTTTAG[A/G]GACAATAGACCAGAT | 26054 |
rs567999282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645491 | GCATGGTGGCGCACA[C/T]GTGTAATCCCAGCTA | 26054 |
rs568136934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676288 | TCATTTACAAAGTTT[A/C]TAAGTGGATTAAAAC | 26054 |
rs568140524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75657211 | TTAAGACTGCTTTAC[C/T]GTAAATTAAGTTTTT | 26054 |
rs568149697 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SENP6 | GRCh38.p7 | 6:75683252 | CCATTTTTTGATGGG[G/T]TTTTTTTTTCTTGTA | 26054 |
rs568207247 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701582 | TATATGCAATTCTTA[C/G]AATGTTGAAAAAATC | 26054 |
rs568269452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694845 | TATGCTCTACTCTAG[A/T]TTTAGAGTGTGCCCT | 26054 |
rs568291529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647911 | GTATAATAGATATAT[A/G]TGTAGAAAACCATTT | 26054 |
rs568305157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647271 | CAGTATTTGGATGTA[A/G]TATTTAGATATAGTA | 26054 |
rs568328093 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75638493 | TTAATCAGATACATT[-/ATA]ATGAATGCATTTTTT | 26054 |
rs568340475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703299 | AATCTCCAACAAAAA[A/T]AAATAAATAGAAAAT | 26054 |
rs568456452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613942 | TATTGCATTGATTGT[C/T]ATGTCCCATTTGTCT | 26054 |
rs568460337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75605520 | GGGAAGCCATTTTAC[A/G]TAGCATTGAAGTCAA | 26054 |
rs568501060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606108 | ATGAGAAGGAAATTA[A/G]CAACACTGGTCATAC | 26054 |
rs568507328 | snp | A/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679130 | AGTTGTGAAAATTGG[A/G]CCAGGGAGATATCTG | 26054 |
rs568514024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676927 | GACCTTTATACTGGG[A/G]TTTCTGATTATCCTC | 26054 |
rs568538779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627131 | AACAAACCAGCTAAC[C/T]TTTGTATTTTAGTAG | 26054 |
rs568541754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696743 | CTGCCTCCCCAAAGT[A/C]CTGGGATTTCAGGTG | 26054 |
rs568544010 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715638 | TCAGAAACTAAATGA[C/T]TTTCAAATTTGGGTA | 26054 |
rs568564752 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617635 | ATGTTGCCACCAAAT[A/G]TAGCCAGTGTATGTT | 26054 |
rs568615741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692918 | CCACCAAAAAAAAAC[A/T]AAGTTAGCCAGGTAT | 26054 |
rs568663024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75672888 | GCTGGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 26054 |
rs568721905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709879 | CTTCAACTAGTAATT[A/T]ATCATGGCTTCTGAA | 26054 |
rs568740191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620645 | ATTCAGACCATAGCA[C/G]TGACCATGGGGTGGA | 26054 |
rs568740795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75698925 | CTGAGGCAGGAGGAT[C/T]GCCTGAACCCGGGAG | 26054 |
rs568748626 | snp | A/G | 3.31538e-05 | 0.00407134 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702856 | AACAAAAAACATTGC[A/G]TAGCTGTAATTGATT | 26054 |
rs568836470 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75660193 | TAAATGATGTGTGTA[C/G]TTTTCAAGAATGCTT | 26054 |
rs568860143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608951 | ACTGACTACCTTTTT[C/G]TAGATATTAGCTGAT | 26054 |
rs568860187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616570 | TGACCAACATGGTGA[A/G]ACCCTGTCTTTACTA | 26054 |
rs568863448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699999 | CACTGAAGCTTCAAA[C/T]TCCTAGGCTTAAGCA | 26054 |
rs568877457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699427 | GTTAGATTGGCTGCC[A/G]TATATTTGTCATCTG | 26054 |
rs568900914 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715896 | AATAAAAAGAAAATA[C/T]TTATAGGAGGAAATG | 26054 |
rs568921503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653277 | CTGAGGTGATCCCCC[C/T]GCCTCGGCCTCCCAA | 26054 |
rs568956266 | snp | C/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602551 | CAAGAGCGGCGGTAG[C/G]GCAGGGGAGATTACT | 26054 |
rs568963551 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716748 | CTTTCAAATGAACTT[C/T]GAGACTTGAAACATA | 26054 |
rs568964581 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663749 | CCAGCATTCTGACTT[C/T]GGCCAGGTTAATTTA | 26054 |
rs569024857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75708272 | TCACCATGTTAGCCA[C/G]TCTGGATTATATATC | 26054 |
rs569025135 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653427 | TAAAGCTTTTCCAAC[C/T]CTGGGATTTTAAAAA | 26054 |
rs569039806 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633038 | AGGAATCTTTACAAA[C/T]TTATTTTGCTCCTTT | 26054 |
rs569057249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75673839 | CAGCCTGGTCAACAT[A/G]GTAAAACCCCATCTC | 26054 |
rs569073506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686511 | GTCTTTACAATTTGG[C/T]CTGTTTTTGCAGTGG | 26054 |
rs569097166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75623347 | AACCTGTTAATAGAT[A/G]CATTAGTTTAATCTT | 26054 |
rs569109655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682015 | CTGTCTACAAGGAAT[C/G]TCAAAGTAATGATAT | 26054 |
rs569114699 | in-del | -/ATTAG | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75637386 | TTGTTAAAATACCAC[-/ATTAG]ATTAGGTAGTCTTTG | 26054 |
rs569127203 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714404 | ATACAGTAGATGACC[A/G/T]CTAGGTTCTGTGAAT | 26054 |
rs569143558 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606618 | GTACAGCAATCAGTG[A/G]TGGATTGTTTATACA | 26054 |
rs569162999 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642765 | TGTGATTTATAATTT[A/G]GCATAAATAGAAGTT | 26054 |
rs569171304 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75675195 | AAAAGTTAAAAAAAG[A/G]AAAAAAAAAGAGGAA | 26054 |
rs569182659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674512 | ACTTTTAGTAGAGAT[G/T]GGGTTTCACCATGTT | 26054 |
rs569215717 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75625048 | TTGATGAAATAAGGT[A/T]TTTTGGAGAAATTGG | 26054 |
rs569257053 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618419 | TAACCTTTTGACATG[C/T]CCCTGTCTTTAAAAA | 26054 |
rs569288546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668367 | CAATTTGATAGGTAG[A/G]TGCAAATGGAAAAAT | 26054 |
rs569348646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669030 | ACAAAACACTTTTAA[A/G]CCTCTCTAACAGGTT | 26054 |
rs569354702 | in-del | -/A | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717687 | GTTTAAAGTGGGATC[-/A]AGCCTTTTAAAATGT | 26054 |
rs569364376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646659 | GGCTAACACAGTGAA[A/T]GCCCATCTCTACTAA | 26054 |
rs569376247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621026 | ATTCATAATGAGCAC[A/C]TTTAGTGTTCTGATC | 26054 |
rs569411536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621692 | AGAAAAACAATTTCT[A/G]TTGTATGGAAATATT | 26054 |
rs569500023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696098 | TTTTCATTCTTCATG[C/G]GTTCATATTCACCTT | 26054 |
rs569500132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689464 | TGAGGATGTGGAGAA[A/G]TTGAAACTGTTATAA | 26054 |
rs569500596 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640273 | CAGAAAGTGTGGTTG[A/G]CACCCATTTTATTTA | 26054 |
rs569523387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75681419 | TGGATCTGTGAGTCA[A/G]TTAAACCTCTTTTCT | 26054 |
rs569524034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640326 | CATTTTGGTATATTG[A/G]ATTCGGTACTATCAT | 26054 |
rs569561403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689994 | ACAGTCACAGCTCAC[A/G]ATAGCCTCCTGGGCT | 26054 |
rs569619976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75627498 | AGCAGGCACGGTGTC[C/T]TTTGCCTGTAATCCC | 26054 |
rs569622223 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664355 | AAAAATATAGTTCAT[C/G]GGCCTTTTTAAAAAA | 26054 |
rs569626809 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SENP6 | GRCh38.p7 | 6:75655509 | TGATTTTTCCTAGCA[C/T]AGATTAATTTTACCT | 26054 |
rs569670148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678409 | TACAGATAATAAGAA[A/G]GTGGCCCCTAGTTTT | 26054 |
rs569688085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710879 | GTTTCTCAAGGAAAA[C/T]AGTGTTTCCAAAAAC | 26054 |
rs569698499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628483 | TTATCTTTTAAAATG[A/G]GTGAGGCTGATGGTT | 26054 |
rs569728290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644343 | TATGAAATACCTGAC[A/G]AGTTCTCTCTAAATA | 26054 |
rs569737421 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75698599 | CTCAGCCTCCCAAGT[-/A]GCTGGGATTATAGAC | 26054 |
rs569765806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672108 | TGTGTTTTGTTACAG[A/C]CCTCATACTGCAGAC | 26054 |
rs569858943 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SENP6 | GRCh38.p7 | 6:75638536 | AGAAAAATGAGCATT[A/G]ATGTGTCTTTGTGTG | 26054 |
rs569884791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649202 | TACCTATAATCCCAG[C/G]TACTCGGAAGGCTGA | 26054 |
rs569912429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642122 | AAATATATTTTTGAT[G/T]ACATGCTGCCTTTTA | 26054 |
rs569921161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75680080 | ATTTAAGAAGCCTAT[C/T]TAAGATATTTTAGTT | 26054 |
rs569924498 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599639 | GGAAGGAGATTTGAT[C/T]TAAAAAAGAGGGGAA | 26054 |
rs569942623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75614969 | GATCTCGGCTCACTG[C/T]AATTTCCAGCTCCTG | 26054 |
rs569981139 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620047 | GCAGTGAGCCATGAT[G/T]GCACCACTGCACTCC | 26054 |
rs569995688 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600911 | ATTCATTACACTACT[C/T]TTGCCAATCAGGAAA | 26054 |
rs570093784 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694082 | AGCAACATGGAGAAA[C/T]CCCGTCTCTACTAAA | 26054 |
rs570094352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75629684 | TGTGTGTCCCAGGGA[C/T]ATATACATATATCTA | 26054 |
rs570103888 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661343 | TTTGGCTCAGGCCAT[A/G]CTGATATCACCTACT | 26054 |
rs570144145 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SENP6 | GRCh38.p7 | 6:75685649 | TTCTGTCTTCATTTC[A/G]TTATTTACCCGTCAT | 26054 |
rs570156877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658042 | GGGAAGGATTTAAGG[A/G]GAGCAAAATTGGGAT | 26054 |
rs570231008 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697192 | CACTAGAACTTCCAC[C/T]CCTCAGATGGAGTAA | 26054 |
rs570255265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641624 | TGTTTAAGAAAACAC[A/C]CACATTTCTTTGAAC | 26054 |
rs570277524 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600148 | TGGTAATTACCACTA[A/C]TTTAGCAATTTAACA | 26054 |
rs570303979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697138 | CAGGACCAATTCTGC[A/G]GTAATAAAAATAGTA | 26054 |
rs570315380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75711486 | AACATAACAGGACAG[G/T]TTTTTTTTTAAATAA | 26054 |
rs570319540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658456 | TTTGGTTTACAGATT[A/C]TTCACTTATGTTTTA | 26054 |
rs570341459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607804 | AGTGTTTTCCATTTC[G/T]CCTTAGCCAGTCTTT | 26054 |
rs570354499 | snp | A/C/T | 0.00637247 | 0.0561273 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620007 | CTGAGGCGGGAAGAT[A/C/T]ATTTGGGCCCAAGAA | 26054 |
rs570354698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651391 | CAGGGTCTTGCTCTA[C/T]TACCCAGGCTTGGAG | 26054 |
rs570368355 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75691035 | TTTTTAATAGAGGCA[A/G]GATCTCCCTGTGTGC | 26054 |
rs570368412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697994 | AATGGAGGTGTTTAA[A/C]GATTTGTATTATTCT | 26054 |
rs570476700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687806 | GCCTATGTGAGGTGT[C/G]TGTCGGCCCCTACTG | 26054 |
rs570482657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640994 | CTTTTTCTGGCTTTT[C/T]GAAAACATAAAATAA | 26054 |
rs570533110 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617335 | CTGGAGTGCAATGGC[A/G]TGATCTTGGCTCACT | 26054 |
rs570555919 | snp | C/T | 5.02088e-05 | 0.00501018 | intron-variant | SENP6 | GRCh38.p7 | 6:75715364 | TACAGTTTTCTAATA[C/T]GCATTTAATTGTATT | 26054 |
rs570562796 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716085 | CTAAGCATCTTTATA[C/T]GCTTGTGTAACAGGA | 26054 |
rs570566198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633522 | GGTTTTCAAATAGTT[G/T]TTGATAGATTGTCAC | 26054 |
rs570633115 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75695461 | GCGAACTGTGGCCGG[G/T]CGCCATGGCTCACGC | 26054 |
rs570683358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75675338 | ATTTTAAGAGATAAA[C/T]GAGTAATATAAGAAA | 26054 |
rs570684999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654768 | ATCTCAAATAAGAAA[G/T]TTAAGCCTCTTCCTT | 26054 |
rs570718387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700397 | TTTGTAGCTTAGCCA[C/T]ATTGGCATAGCTAAG | 26054 |
rs570752184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709825 | AAAAATGAAAAAAGG[A/G]AAAAGAAAAAGACTT | 26054 |
rs570778000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700928 | TAGCCTGATCTAAAT[C/T]CATAGGGTACTAAGG | 26054 |
rs570789726 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662756 | AGTAGGAATGTGTTT[G/T]TTCTGTTTTAGTATC | 26054 |
rs570803973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701785 | GCTGGGACTACAGGC[A/G]CACACTACCACGCCC | 26054 |
rs570807330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669973 | AATTTCGATCTTGTT[A/G]CCCAGGCTGGAGTGC | 26054 |
rs570812187 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75612607 | AACGCTAGGATTATA[A/G]GTGTGAGCTGTCTGA | 26054 |
rs570818882 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646232 | TATAAGACTGTTACT[A/G]CTACATCTCAGGCAA | 26054 |
rs570867489 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75673122 | GTGAGCCACTGCACC[C/T]GGCCAATTGGCATTA | 26054 |
rs570870057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605294 | ACAGTCAGTGTACCA[C/T]GGTGAAGTGCATAAG | 26054 |
rs570895747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75613164 | CCAAATTTGTCCAGC[C/T]GCCTGTTTTTAAGAG | 26054 |
rs570906695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75705168 | AAGAGGAGCACTGGT[C/T]CAATCTTTGTTTGTT | 26054 |
rs570916100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75700680 | TGTTTTTGGTAGAGA[C/T]GGGGTTTTGCCACGT | 26054 |
rs570931321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682776 | TTCCATGGTGTATAT[A/G]TGCCACATTTCCTTA | 26054 |
rs570933867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75634284 | GTATTTAGGACTCCT[A/G]ATTTTTATTTTAGTA | 26054 |
rs571017704 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674425 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 26054 |
rs571021484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626556 | ATGAATAGAGATTTT[C/T]TTCCCCCAGTCTTTT | 26054 |
rs571034802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75625825 | AGTGAGCTGAGATTG[C/T]GCCACTGCACTCCAG | 26054 |
rs571114515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665922 | ATCCCAGGTGCTGGG[G/T]AGGCTGAGGCAGGAG | 26054 |
rs571140865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679205 | GATCGCTTGAGCCCA[A/G]GAGTTCACGACCAGC | 26054 |
rs571141574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709080 | AATTTTCCACGTTTT[C/T]GAAATTTTAATTATA | 26054 |
rs571192129 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650199 | CTTCCACAGAAATGA[A/T]GTTGTGGCATTCTCA | 26054 |
rs571195853 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614920 | ACAGAGTCTCACACA[C/G]TTTTTTACCCAGGCT | 26054 |
rs571217760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714253 | TATGTTAAAATTGCT[C/T]TTGACTTTCCAGCAC | 26054 |
rs571270209 | in-del | -/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599909 | TCTCCACTAAAAATA[-/C]AAAAATTAGCCGGGC | 26054 |
rs571342688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608877 | GAAAAGAAAAAGAGC[A/T]TCCTTTACTTGCTTG | 26054 |
rs571380328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609786 | TTTTGTTTTTGTTTT[C/T]TGAGATGGAGTAGAT | 26054 |
rs571380353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624383 | AATAATCTGTAAATT[A/C]GCCTTCTATATGGGT | 26054 |
rs571396523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75652306 | ATGAGCCACCACGCC[C/G]AGCTGCAAATTTTTA | 26054 |
rs571403201 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75637184 | CTGTCTCAAGTCTTA[C/T]AATAATTTGAAATGA | 26054 |
rs571409576 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658448 | CAGGTTATTTTGGTT[C/T]ACAGATTCTTCACTT | 26054 |
rs571415929 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659795 | TTTCCCTCCTTCCTC[A/C]TGCCTACCCATAAAC | 26054 |
rs571418357 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75624972 | CTCCATCTCTAAAAA[A/C]TAAAAAATTTTGCAC | 26054 |
rs571451404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628709 | AAATAGTTTTGCTAT[A/G]GTATTATCATACAAT | 26054 |
rs571484833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75713206 | CAGAATTGTTTTGAC[A/T]TTTTACTAATTTTGA | 26054 |
rs571490259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699285 | TAGAAAATGAACTCT[A/G]TAAGAGAGCTCTACC | 26054 |
rs571538698 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600568 | GAGTAGCTGAGATTA[C/T]AGGCACGTGCCACGA | 26054 |
rs571538753 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75629543 | GACCTCAGGTGATCC[A/G]CCCACCTTGGCTTCC | 26054 |
rs571538828 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631789 | CTTGGCAGAAAAAGT[G/T]TGCTGATCCCTGTAT | 26054 |
rs571583821 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | SENP6 | GRCh38.p7 | 6:75681372 | TTCCAAGTTTCCTGA[A/C/G]GCCTCCACAGCTACG | 26054 |
rs571604038 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75628980 | TCCACCCACCTTGGC[C/T]TCCCAAAGTGCTGGA | 26054 |
rs571623274 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75632389 | AATAGCAAACTCTAG[C/G]CTTGCCAATAACTGT | 26054 |
rs571624655 | in-del | -/GTAAA | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75699081 | GTACTAATTTGTCTT[-/GTAAA]GTAACATGTGAACAG | 26054 |
rs571639178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680825 | CTAGTAGAGAACATG[C/T]ACTTTTAGTCCCACC | 26054 |
rs571702949 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75673952 | CTTGAACCCGGGAGG[G/T]GGAGGTTGCAGTGAG | 26054 |
rs571718661 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75703338 | AATTTACTTATAACA[A/G]TATAGTAACACAACT | 26054 |
rs571730267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692149 | GCGTGAGCCACCGCG[C/T]CTGGCCTCCCATAAG | 26054 |
rs571745890 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715805 | CCAGCATTTATAATT[A/T]TTTTTTTCACTTGTT | 26054 |
rs571765448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674441 | ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGCTGG | 26054 |
rs571797804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75685811 | AGGAGTGCTTTACTT[A/C]CAATTATGTGGTCAA | 26054 |
rs571801815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75638812 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGGCAAAA | 26054 |
rs571817758 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700907 | GAAATGAGGAGGTTG[G/T]TGTGTTAGCCTGATC | 26054 |
rs571826857 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678131 | CTCAAACTTCAGAGG[A/G]AGGTTCTTTCCTCCA | 26054 |
rs571846551 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617959 | TGGGATTATGAGTTT[C/T]AGGGAAAGGATCACA | 26054 |
rs571854076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75692848 | GCAAGCAGACCACCT[C/G]AGCCCAGAAGTTCGA | 26054 |
rs571885823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645517 | AGCTACTCAGGAGGC[C/T]GAGGCATGGGAATCA | 26054 |
rs571912401 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714145 | TCTTTTCTCCTCTTC[A/G]TAGATACATTTCTTA | 26054 |
rs571915267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686484 | TGATGCAGTTTCTTC[A/C]TAGCATCGATGGTCT | 26054 |
rs571923650 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688957 | TGTAATCCCAGCTAC[G/T]TGGGAGGCTGAGGCA | 26054 |
rs571924306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646094 | GTTTTTACTAAATCT[A/G]GGTAAACCTGGATTT | 26054 |
rs571967865 | in-del | -/GT | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75666152 | TGATATATATAAAAC[-/GT]ATATATGATATATAT | 26054 |
rs571969914 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647482 | TTTGGAATTGTCCTC[-/A]AGACAATCTCATTCA | 26054 |
rs571969917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633798 | AAAAACTTAGAAGCT[A/G]ATAGGCCCAACCTGT | 26054 |
rs571978591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669337 | CTCCAGCCTGTGCGA[C/G]AGAGCGAGACTCCAT | 26054 |
rs571979009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75670219 | CCCAAAGTGCTGGGA[A/G]TACAGGTGTGAGCCA | 26054 |
rs571994941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619062 | TTTTATTGTGGTATA[A/G]TATACATAACATATA | 26054 |
rs572026193 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75663000 | GACTAACATTACTTA[C/T]TTAGGCTCTCATGGT | 26054 |
rs572040733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676534 | CATGGCTTGACTGCT[C/T]AGAAGATATACACAT | 26054 |
rs572055902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626032 | GTATATGTATAGTTC[C/T]ACTAGGAATGTGTAT | 26054 |
rs572056733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75612766 | TTGAAAATGCACATC[C/T]CCAAGGACCAAATCA | 26054 |
rs572125606 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670969 | CTTTCAATGAGTTAG[A/G]AAACCTTCCAATATG | 26054 |
rs572129883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75688087 | CTTTGTTTACCTACT[C/T]AAGCCTCAGCAATGG | 26054 |
rs572139664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710012 | TTAATGTAATACTGA[C/T]TAACTCACCCTAACT | 26054 |
rs572147704 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601683 | CGTGTCTAGGCCGAG[C/G]CCGCGCCGTGAAAGG | 26054 |
rs572274011 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75656104 | CCTGTAATCCCAGCT[A/T]CTCAGGAGGCAGAGG | 26054 |
rs572310688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75656558 | ATTTTAGACTAGTTC[A/G]TTTTTACTTGAGTTA | 26054 |
rs572318610 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673784 | CCAGCACTTTGGGAG[G/T]CTGAGGCAGGTGGAT | 26054 |
rs572379282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75682913 | TATAATCCTTTGGGT[A/G]TATACCAGGTAATGG | 26054 |
rs572384006 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678413 | GATAATAAGAAAGTG[A/G]CCCCTAGTTTTGCCT | 26054 |
rs572390546 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676610 | CTACCACTAAATTTG[C/T]AAGAGTTGGCACATT | 26054 |
rs572397975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648943 | GTACATTACTATATT[C/G]TTGCTCTGTCACAAA | 26054 |
rs572426192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75643231 | ATGAAAACAAGTCCT[A/G]TCAGTAGTTATAATA | 26054 |
rs572445325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75704092 | CCTGAAGGGGTGGCC[C/T]GCCCTTCCACACCTG | 26054 |
rs572447250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684240 | TGTGATTTTTGCACA[C/T]TGATTTTGTATCCTG | 26054 |
rs572463394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636068 | AAACAACCCGTTAAT[A/G]GTCTGGAAATTGGGT | 26054 |
rs572501341 | snp | G/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621269 | TTCATACATATTCAT[G/T]TGCCCTCCGTTTTTA | 26054 |
rs572531150 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623728 | CTGTTTTCATACAAC[A/G]TATGAGTAGCTGCTA | 26054 |
rs572549999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686624 | AGCATTTGCTTTGTC[C/T]GTAAAGTATTTTATT | 26054 |
rs572569087 | snp | A/T | 1.72859e-05 | 0.00293984 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663517 | AGACCTAAATGATCC[A/T]AGTAAGTATTTTACT | 26054 |
rs572595712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75695102 | GCTGGTCTTGAGCTC[C/T]CAACCTCAGGTGATC | 26054 |
rs572653567 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701744 | TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 26054 |
rs572671174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658947 | ACTGAACTCCGGCCT[A/G]GGTGACAGAATGAGA | 26054 |
rs572706104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605590 | CACCTTAACTAAGAG[A/T]CACTTCAGAATATGG | 26054 |
rs572707430 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75651959 | GGCAGGAGGATCGCT[G/T]GAGCCCAGGAGTTTG | 26054 |
rs572716738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75676523 | AACACTTAAAGCATG[G/T]CTTGACTGCTTAGAA | 26054 |
rs572726545 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689760 | AGTGTAGAAGCAGTA[G/T]GTTATACCATATAGC | 26054 |
rs572734950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75692990 | GTAAGAGGATGGCTT[C/T]AGCCCAGGAGGCGGA | 26054 |
rs572769779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646267 | TCATTTTCATAATGC[A/G]TATCTTCACAAATTT | 26054 |
rs572785338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75667361 | TAGACAGTGTATCTA[A/G]GACAACTATTTGTAA | 26054 |
rs572816595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75639134 | GTGGCTACATTAGGT[A/G]TTAATGCCTAACTGT | 26054 |
rs572846828 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75695270 | GCTAACTGCATAGAA[A/T]GTGTCCTTGTTTTAA | 26054 |
rs572900035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700589 | CCTCCCAGGCTCAAG[C/T]TATCCTCCCACCTCA | 26054 |
rs572906472 | snp | A/G | 1.66294e-05 | 0.00288347 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666927 | TTGCCAAGAAAAGCA[A/G]GAATGAAAGACCAGG | 26054 |
rs572927289 | in-del | -/AGAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667347 | ATGAACGATGTCAAT[-/AGAC]AGTGTATCTAGGACA | 26054 |
rs572933604 | in-del | -/CATTTTTGGTTCCTCCA | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75677464 | TACAGGTCTCAGAAG[-/CATTTTTGGTTCCTCCA]CATTCTATCCTTATC | 26054 |
rs572937534 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639107 | TTTGGGCACAGCAGT[A/G]TAGAATTGGAAGTGG | 26054 |
rs572946542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616032 | CTTTTGTTAATCTCT[C/G]TTCTACTATTATCTC | 26054 |
rs572963429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701165 | AACTTGTTTTTCATC[C/T]AGCAAATATTTATTG | 26054 |
rs573024952 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75631942 | GAAACCATTCCATAA[A/G]CAAGTGACTGTCACC | 26054 |
rs573036466 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75638744 | TACCTATTTCCTTTC[C/T]TCTGTACAGGTGAGT | 26054 |
rs573052790 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75698946 | AACCCGGGAGGCAGA[G/T]GTTGCAGTGAGCCAA | 26054 |
rs573057877 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75634640 | TCAGATTTTAAAAGA[-/T]TTTTTTTTATAAATG | 26054 |
rs573070264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75608491 | GGAGAAAGAAAGAAG[A/G]GGAAAAAGAGGAAAG | 26054 |
rs573093521 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75715248 | CTAACACAGTACTTG[C/G]CATGTGATAGATAAT | 26054 |
rs573106895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609110 | TAGAAGGGTTGTTTG[G/T]CACAGCTTAAGTTAT | 26054 |
rs573171609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75706938 | CATGAAAAATGTGTA[C/T]GCTTAAACTCTAGAA | 26054 |
rs573193547 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602089 | GCCGCTCCGGCGCGG[C/G]GGGTGCGGCCATTTT | 26054 |
rs573236974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75707829 | CTGGGACCACAGGTG[C/T]CCACCACTACACCTG | 26054 |
rs573243019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75661049 | TTTGGGCACTAGTTA[C/T]GTTCATTCACATGGG | 26054 |
rs573250458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75693720 | TAACAGATCTCAAGA[A/G]TGTGCCCTCTAGGGG | 26054 |
rs573280099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75694289 | AACCAATGTAAGATC[A/C]CTTTACAGAGTCATT | 26054 |
rs573281635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654345 | ATGGAATGCAAAGGC[A/C]CAACAGGTGAAAGAG | 26054 |
rs573290324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647430 | AAATACTTGTTCCAC[A/G]ATTGCTGATCTTGTA | 26054 |
rs573305918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687437 | GTCCAGCTTTGTTCC[G/T]TTGCTGGCAAGAAGC | 26054 |
rs573331887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75606425 | AGGTTGCTCCCCTGT[A/G]TTTATTCAGTCAACA | 26054 |
rs573362527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75704101 | GTGGCCTGCCCTTCC[A/G]CACCTGTAGGTATGT | 26054 |
rs573391122 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599807 | CGGTCGCTCACGCCT[A/G]TAATCCAGCACTTTG | 26054 |
rs573393608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715208 | TAAGATCTATGATAG[A/G]AACTGTGTCTTGTAT | 26054 |
rs573416111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667848 | CATATGATGCAGCCA[C/T]TGAAAATAAAAATTA | 26054 |
rs573451387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75668453 | AAATAAAGAAATAGA[A/G]GCAAACCATAGGGAA | 26054 |
rs573467424 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75617972 | TTTAGGGAAAGGATC[A/G]CAGTGCTGAAGTGCT | 26054 |
rs573491096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75610326 | GCCAGTTAATCCACT[A/C]AGTCACAGACTGTTA | 26054 |
rs573508225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75664023 | ACTAGAGTATACAGC[A/G]TGTATACTCTAAAGG | 26054 |
rs573573364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75710199 | GTTATTTTTTTTTCT[C/T]CTGCCTGATTCGATT | 26054 |
rs573616159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75696468 | AATACTATTGTACAT[A/T]GTAGGCCTGATTTGT | 26054 |
rs573620761 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605736 | TTATATCTTTCTCAG[C/T]GGGAAGCCATTGACG | 26054 |
rs573633760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664563 | CAAAACCCCACCTCT[A/C]AAATGCTATATATGT | 26054 |
rs573648752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649750 | TCAAACTCCTGACCT[C/T]GTGATCCACCCACCT | 26054 |
rs573685555 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75643373 | ACAAGAGATGCAAAC[A/G]AAAAGAAAGCATGAG | 26054 |
rs573686996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75657708 | AGAGCTGGCAATACA[A/G]TGGGGGAACAGAAGT | 26054 |
rs573694725 | snp | G/T | 3.67411e-05 | 0.00428593 | intron-variant | SENP6 | GRCh38.p7 | 6:75697375 | TCACTACATATAAGC[G/T]GGAGCACTAGAAATA | 26054 |
rs573757678 | in-del | -/CTTA | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75608051 | ATTCCTTATTTACTC[-/CTTA]CTTAAGTATGTTTAT | 26054 |
rs573810857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75678091 | CCAGAGGAAGAAAAG[A/G]GCAGCATAATGCCAC | 26054 |
rs573821975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620499 | AACAGGCTCCATTGG[A/G]CCTCTTTGATAAGGG | 26054 |
rs573881076 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619698 | CTGCCAAATTATTTT[-/C]TACAGTGCCTGAACT | 26054 |
rs573885391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621084 | ACCACATTGCCAAAA[A/C]CGAAAACGTTGTTTG | 26054 |
rs573889964 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600249 | TCAGTTTTCCTTTCT[A/G]GAGACTCTTGAGGAG | 26054 |
rs573890257 | in-del | -/T | 0.0013633 | 0.0260728 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621633 | GATAAAGAGTAAGGA[-/T]TTTTTTTTCCCTCAG | 26054 |
rs573917869 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75628544 | ATTAATCTGTATTAC[C/T]TGAATGAAACTTTCA | 26054 |
rs573934131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622189 | TCTACTTGGAATGAC[A/T]GTTGTGTAAAAATTT | 26054 |
rs573955705 | in-del | -/AT | 0.0283406 | 0.115616 | intron-variant | SENP6 | GRCh38.p7 | 6:75666074 | TAAAACGTATATATG[-/AT]ATATATAAAACGTAT | 26054 |
rs573957391 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660222 | TTCAGAAATGATGCT[A/G]TAATCTTACTGCATT | 26054 |
rs573957393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75636731 | AACTGCATGCAGTAG[A/G]AATCACGTCTTCAAA | 26054 |
rs574039055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628942 | GCCACCAGGCTGGTC[A/T]TGGAACTCCTGACCT | 26054 |
rs574048343 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75622658 | AATTCAGAGATCCAC[A/G]AATATACACACAAAG | 26054 |
rs574060517 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708150 | CTGCAACCTCTGTTG[C/T]CTGGGTTCAAGCAAT | 26054 |
rs574128886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621218 | ATTTCTAGAATCAGT[A/G]ATCAAAGATGAGATT | 26054 |
rs574155542 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | SENP6 | GRCh38.p7 | 6:75691145 | ATTCCCAGCTAAAAT[A/T]TTTTTTTTTTTTTCA | 26054 |
rs574185170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75669222 | CCAGGCGTGGTGGTG[C/T]GTGCCTATAATCCCA | 26054 |
rs574215256 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707390 | TTTTTTTGAGACAGG[A/G]TCTCACTCTGTTGCC | 26054 |
rs574220018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75705360 | GACCAGCCTGACCAA[C/T]GTGGTAAAACCCCAT | 26054 |
rs574221692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714459 | TTACTTGTTTATCGT[C/T]GAGTGTCGCTATTCT | 26054 |
rs574279764 | in-del | -/A | 0.448452 | 0.152042 | intron-variant | SENP6 | GRCh38.p7 | 6:75692467 | TCTACAAAAACATAC[-/A]AAAAAAAAAATTAGT | 26054 |
rs574332620 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75640934 | TTAGTATATCCATCA[-/C]CTCAAACATTTTTTG | 26054 |
rs574341511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75674820 | TTGAAAGACTTTTGC[A/G]GTGAACATTTATATA | 26054 |
rs574352089 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670863 | CACATTGCTTTAAGA[A/G]TATATAAATAGTAGC | 26054 |
rs574357001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75625304 | ATTTTTATTAGAGAC[C/T]GGGTTTCACCATTTT | 26054 |
rs574389976 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75685302 | TCTTGCTAGCAGTCA[A/G]TCAATTTTGTTGATC | 26054 |
rs574420942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75625997 | TTATTTTGTTTCCTT[C/G]TTTTTGATGACACTA | 26054 |
rs574439389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633141 | AAGTATAAAGTATCA[A/G]TTTCTGCCTGTACAG | 26054 |
rs574439642 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75641094 | ATTTTGTATTTGTGA[A/T]CCCACCTCCCTCCAT | 26054 |
rs574475873 | in-del | -/A | 0.431325 | 0.172108 | intron-variant | SENP6 | GRCh38.p7 | 6:75613114 | TGAGATTCTGTCTTT[-/A]AAAAAAAAAAAAAGA | 26054 |
rs574490262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618843 | CTATTTATTTACTTA[C/T]GTTTTCAATCCCAGT | 26054 |
rs574535415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689580 | CTGGGTATACAGTCT[C/T]GTGCCACATAACGTT | 26054 |
rs574568045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646984 | ATTTCTTTGGAACTT[G/T]TGTTTGAGTAAAATG | 26054 |
rs574598839 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SENP6 | GRCh38.p7 | 6:75683665 | GGGAATCCTTTCCCC[A/G]TTTCTTGTTTTTGTC | 26054 |
rs574638769 | in-del | -/TCC | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75690151 | CCTGCCCTCAAGCAG[-/TCC]TCCTACCTTGGCTTC | 26054 |
rs574664427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662006 | GCAGTGAGCCAAGAT[G/T]GCGCCATTGCACTCC | 26054 |
rs574703075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75662864 | ACTAAAGTAATGGAG[C/T]CAGTCAGTACTCAGC | 26054 |
rs574727996 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SENP6 | GRCh38.p7 | 6:75687372 | CGGAGAAGTTTGTTA[C/T]TACTGACCTCCTGAA | 26054 |
rs574790613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75687976 | AGTTGTCTGCTGCCT[A/G]TTTTTCAGCTATGCC | 26054 |
rs574802194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648776 | CTATATGCTTAGTCC[A/G]GTGCTTTGCATTCAT | 26054 |
rs574838052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642372 | TGATTTCTTTAAATC[A/G]CATATTCAGGGAAAC | 26054 |
rs574866310 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639249 | GTTTATATTTTGCTT[C/T]GCTTCTTTAATAGGG | 26054 |
rs574868309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684913 | TGATTCTGGCCTCAT[A/G]AAATGAGTTAGGGAG | 26054 |
rs574868511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75691840 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAT | 26054 |
rs574929623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75670107 | CCTGCCACCACACCC[A/C]GCTAATTTTTTGTAC | 26054 |
rs574943056 | snp | A/G | 1.66355e-05 | 0.002884 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634733 | AAAATACGTCATTAT[A/G]TTCTGGAACTGTAGT | 26054 |
rs574948878 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678217 | CCCTGAGCCTCTGCC[C/G]CTACATCTTATAGAT | 26054 |
rs574956310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619573 | TAATGCTGCTATGAA[C/T]ATTGGCATACAAGTG | 26054 |
rs574966264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701245 | TGACATCTATAGCCT[A/G]TTCCTTGTATCCCAG | 26054 |
rs574986197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75701886 | CTCAGGCAATCCACC[C/T]GCCTCGGCCTCCCAA | 26054 |
rs574994251 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75685951 | TTCCTGGGTATCCTT[C/G]TTCACTTTCTGTCTC | 26054 |
rs575011801 | snp | C/T | 1.66579e-05 | 0.00288595 | intron-variant | SENP6 | GRCh38.p7 | 6:75675764 | ATAATAAATATGTGC[C/T]TACATTTACTTAAAC | 26054 |
rs575045229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75695048 | CCCGGCTAAATTTTT[G/T]TATTTTTAGTAGAGA | 26054 |
rs575069137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75703689 | ATCGCTTGAGCTCAG[C/G]GTGCTGAAGTTGCAG | 26054 |
rs575074912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75709157 | CTGTTATTGGACATA[A/G]GTTATTTTCAGACTG | 26054 |
rs575109238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75665955 | TCACTTGAACCCAGG[A/T]GGCGGAGTTGCAGTG | 26054 |
rs575117640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75715084 | GTCCAGTGAAAGCAT[C/T]TGCAGACCATATGTA | 26054 |
rs575155751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604282 | AAATTCGAGTTTCAC[A/C]ATGTCTTAAGCATTT | 26054 |
rs575217514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604864 | GATCACCTGAGGTCA[A/G]GAGTTTGAGACCAGC | 26054 |
rs575247504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679733 | CAATTTGTATGTTTT[C/T]ACTGGTTTGTGATAT | 26054 |
rs575257905 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75607312 | ACCCAAAAAAAAAAA[-/G]GGTCATCAGCTGCTA | 26054 |
rs575272198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75629934 | AAGAAGAGACTATTC[C/T]TAAGTTGTTTACCAA | 26054 |
rs575296649 | snp | C/G | | | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718761 | AAGGAATAGTGCTAG[C/G]GTTTCCTAAAATACC | 26054 |
rs575298007 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604605 | ACTCCAGCCAGGGCA[A/G]CTGAGCGAGATTCTG | 26054 |
rs575326082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75622500 | GGAGGTAGAGGTTGC[A/G]GTGAACCCAGATCAT | 26054 |
rs575334015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75644877 | TTAAGGTGTTGACAT[C/T]AGGGTAAGAGATATA | 26054 |
rs575359626 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711273 | GCTATTTTGTTAGGT[G/T]ATTAGTTATTTAGAT | 26054 |
rs575371402 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | SENP6 | GRCh38.p7 | 6:75634872 | TCAATAGGTTTTCAC[-/T]TTTTTTTAACCATTT | 26054 |
rs575401120 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697698 | CAGTGAAGCATGTAA[A/G/T]ATATTGAATTTTAGA | 26054 |
rs575419766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75607492 | CAAGCCTACCTACTC[C/T]CTTATACATTTCTTC | 26054 |
rs575448363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75650841 | TTTCAAACCACAAGA[C/T]CACTAATTACTTGCA | 26054 |
rs575458267 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600544 | GCGATTCTCCTGCCT[C/T]AGCCTCCTGAGTAGC | 26054 |
rs575493000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75658889 | AGGTGAGAAGATCAC[G/T]TGAGCTAAGGTGTTT | 26054 |
rs575497258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75714796 | TCCTAACCTGGAATA[A/C]TTTTTTGTTGCTTCT | 26054 |
rs575500473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75713437 | AATTTGATTGTTTAT[A/C]ATATGCCACTTTTAA | 26054 |
rs575531877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651819 | ATGATATCTAGTTTT[C/T]ACACTCTCATTAAAA | 26054 |
rs575558377 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75715184 | ACTGGCAAACCCTGA[C/T]CTAGACTATAAGATC | 26054 |
rs575576434 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75616452 | TGATTGAGTTTGTTA[A/G]AATTATGTGTACACA | 26054 |
rs575644509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75699667 | TAATTTTTGTATTTT[C/T]TTTTAGAGGATGGGG | 26054 |
rs575661490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667766 | GGCTTTATATGCAAA[C/T]ATGATTATTGGCAAA | 26054 |
rs575693047 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75653549 | TTTTATTAATTAACC[G/T]TGTTTTCCCTCAATG | 26054 |
rs575720482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660671 | GGAGTCTTGCTCTGT[C/T]ACCCAGGCTGGAGTT | 26054 |
rs575783727 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635600 | GTTAAGTAACCTCAT[A/T]CTTTATGATAAACCA | 26054 |
rs575814386 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607841 | ATATATAAACTCATT[A/G]CAGAACCCAATCAGT | 26054 |
rs575849203 | snp | G/T | 1.68009e-05 | 0.00289831 | intron-variant | SENP6 | GRCh38.p7 | 6:75623966 | AGGAAAAAAGGCAAG[G/T]GTTGCTTAAAATATT | 26054 |
rs575877342 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637976 | AGCAATTCTCAGCCT[C/T]CTGAGTGGCTGAAAT | 26054 |
rs575898676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75618336 | TTATAACCCAATGCC[A/G]ATGTTATTTATTTTT | 26054 |
rs575905149 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75664364 | TTCATGGGCCTTTTT[-/A]AAAAAATCTATATAC | 26054 |
rs575939657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75710060 | ACCCACCTTCCTCTT[G/T]CAAAGCATTTATGGG | 26054 |
rs575967078 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75663037 | GATGGTAATGATGGG[G/T]AAGAGAGGGACTTAA | 26054 |
rs575992926 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75663582 | TCAGATATATTTTTA[A/C]AACCACTCTCCCCAA | 26054 |
rs575997810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75667321 | AAAAAGTTCACATGG[A/T]AAAAGGTAATATGAA | 26054 |
rs576009193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75703108 | AAAGAATGAAAAAAT[C/T]CAGAATAATCTGGAT | 26054 |
rs576032826 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75656663 | TAACATTTTTGTGTT[A/T]TTTTCTTAACTCTCT | 26054 |
rs576042390 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75636586 | AAGACAAGTAAACAA[A/G]TGATTACATGCATGG | 26054 |
rs576054640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75671813 | ATAACTGTTTCTTTT[C/T]TGGTAAAGGTTCATG | 26054 |
rs576065743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75605794 | TGGTTTATCTTTTTT[A/T]AAAAAAAAGTTTGGC | 26054 |
rs576175671 | snp | G/T | 1.68701e-05 | 0.00290427 | intron-variant | SENP6 | GRCh38.p7 | 6:75634703 | TTGTTTCTTGAATCT[G/T]CAGTGAAAATACGCA | 26054 |
rs576180057 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75675598 | TATATCTTCTTATCA[A/G/T]AGGGCATATATCTTG | 26054 |
rs576195244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75649033 | CATTTCTGGCCTGGT[A/G]TGGTGGCTCACACCT | 26054 |
rs576211842 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704306 | ATGCCGTAGGAGAGC[A/G]AGGTGATAATAGGGA | 26054 |
rs576212385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75626747 | TGTTAACATTAGCCA[C/T]TCCCACTAGCAGTGT | 26054 |
rs576231477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75642601 | GGGTTTGGAGAGACT[A/G]GCTGGGACCTACGTC | 26054 |
rs576278786 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624499 | GCATACCAGATTTAC[A/G]CTTGTTCCATCGATA | 26054 |
rs576288650 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681521 | TACAGTGCAGTGGCG[C/T]GATCTTGGCCCACGG | 26054 |
rs576297905 | snp | C/T | 1.69095e-05 | 0.00290765 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677203 | GCCTGTACAAGAACC[C/T]ATGAAGAGAGCATCA | 26054 |
rs576332084 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75676621 | TTTGCAAGAGTTGGC[A/C]CATTAGTGAAAAGCT | 26054 |
rs576374973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75628326 | TCACTGAAGCTTAAC[A/G]TTAAGTAGAACTCCT | 26054 |
rs576456219 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701984 | TCCATCTTTTTACAT[A/G]AAGAGAAGGCAAAGG | 26054 |
rs576473120 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691905 | CTCGTTGTCCAGGCT[A/G]GAGTGCAATGGCACA | 26054 |
rs576542720 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75674708 | AAAGTATGTTTAGTG[A/T]CATTCTAGACTTTGC | 26054 |
rs576559502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621166 | AGTCTGGATATAGTT[C/T]TCATGAAGAAGGCAA | 26054 |
rs576576496 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599782 | AAAAAACCAGGAAAG[A/G]GGCCGGGCGCGGTCG | 26054 |
rs576577150 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75606316 | TGTGTTAAAATTTTC[A/T]ACTCTCCTCTCCCCT | 26054 |
rs576581435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SENP6 | GRCh38.p7 | 6:75649674 | GGCGCCTGCCACCAA[A/G]CCCAGCTAATTTTTG | 26054 |
rs576592478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75652531 | TTTTAAGACTTGATA[C/T]GTTAATGCCAAAATG | 26054 |
rs576611630 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599544 | GCTATTATTGTAGTA[C/T]AGTGAAAGATTATAG | 26054 |
rs576628801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75645928 | GGTAAGATTGTAGCT[A/G]TCATATGATGTATTC | 26054 |
rs576632083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75653379 | GTAGTTGAATCTGTT[A/G]TTAAAGTTGGGTTTC | 26054 |
rs576637734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75712457 | CAAAGCAGGAGGACC[A/G]CATGAGGCCAGGAGT | 26054 |
rs576665322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75684349 | CATCTGCAAACAGGG[A/T]CAGTTTGACTTCCCC | 26054 |
rs576690577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75689647 | TAAGATTATAATAAC[A/G]TATTTTTACTGTACC | 26054 |
rs576718255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75646458 | AGTATTAATATGTTA[C/T]ATAAGTTTATTGTGA | 26054 |
rs576747367 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690019 | TGGGCTCAAGTGATC[A/G]TCCTGCCTCAGCTTC | 26054 |
rs576781856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75640440 | TTTGATAGTTAAAGC[C/T]CTTTTAAGATTTTTT | 26054 |
rs576785221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75632081 | GCCTGACAGCATTGC[G/T]GCATAGTACCAGAGT | 26054 |
rs576928271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75660511 | TTGTCCCAGATTCCA[C/T]GTGAGTCCCTTCAAG | 26054 |
rs576964273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75624705 | TTTGCCCATTTTTCT[A/G]TCTGGTCTTTAGAAT | 26054 |
rs576965251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75609962 | CTGACTAATTTTTGT[A/G]TTTTTAGTAGAGATG | 26054 |
rs576966994 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602250 | CCGGGCCCGGGAAGC[A/G]CCGTCGTCGTCGTCG | 26054 |
rs576970551 | in-del | -/TA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610615 | GCAAAAATTATTAAC[-/TA]TTATCTTCAGAGTAT | 26054 |
rs576975370 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675117 | ATTGAGTGAAAGTCA[C/G]ACCCCCATGACATGC | 26054 |
rs576989370 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75602748 | CACCTGGTTCGAGTC[C/T]GCCTAGGCGAGGGGC | 26054 |
rs577050652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75625173 | ATAGAGTGCAGTGGC[A/G]CAATCTCAGCTTACT | 26054 |
rs577078909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75700642 | ACCACAGGCACGTGC[C/T]ATCACACCCAGCTAA | 26054 |
rs577090127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75686706 | AAATTCTTTCCTTTA[A/G]GAATGTTGAATATTG | 26054 |
rs577099275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75639970 | GTCTCCTCCTTATTT[G/T]TGGTTTGATTTAACC | 26054 |
rs577107960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75699599 | CTTAAGTGATCCTCC[C/G]ACCTCAGCCTCCTGA | 26054 |
rs577129176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75655196 | GGGATGCGCATGGAG[C/T]GATGAGGGAGGAAGT | 26054 |
rs577136129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75701217 | TATTATTGTGCTTGA[C/T]CAATAAGCTCCCTGA | 26054 |
rs577168133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75604203 | GATGTAGAGTTAATG[C/T]GAGTTTCAAACTACT | 26054 |
rs577207409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75688206 | AGCCGCCGAGCCAGG[C/T]ACGGGAGAGAATCAC | 26054 |
rs577215285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75697614 | AATTCATTTTAAAAC[A/G]TCTTTCTGAAATCTC | 26054 |
rs577224743 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673894 | GGTGTGGTGGCGTGC[A/T]CCCGTAACCCCAGCT | 26054 |
rs577269886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75688833 | AGCACTTTGGGAAGC[C/T]GAGGCAGGTGGATCA | 26054 |
rs577270581 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75682596 | GTGTGTGATGTTCCC[C/T]GCCCTGTATCCAAGT | 26054 |
rs577297252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75633937 | CTGAATAAAACATTG[C/T]AAGAAATACTTTGTT | 26054 |
rs577310460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75647500 | ACAATCTCATTCAAC[A/G]TTTATTCCTTTATTT | 26054 |
rs577358836 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75717205 | TTCAATCTATAATAA[A/T]ACTGGGATAAAAAAT | 26054 |
rs577387600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SENP6 | GRCh38.p7 | 6:75671671 | AGGTTGCAGTGAGCC[A/G]AGACGGCGCCACTGC | 26054 |
rs577405448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75641268 | TGGTTATATATATTT[A/G]TGCTAATAAGTGACT | 26054 |
rs577405461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75648086 | GCTATAGCTTTGAAA[C/T]TGAGTTTTATTGAAC | 26054 |
rs577422223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75708423 | TCAAATTTTTGAGAG[A/G]AAAATAAATAAATAA | 26054 |
rs577441721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75654578 | ATTTTACACTGAAAA[C/T]CAGTAGCAGCTACAT | 26054 |
rs577449388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672325 | TTAGTCTTAAAGCTG[C/T]TTATGAAGAACTACA | 26054 |
rs577508002 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612849 | CCAGGCGCAGTGGCT[C/T]ACGTCTGTAATCCTA | 26054 |
rs577624460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75691203 | GTTGGAGAGCAGTGA[C/T]GCAATCACGACTCAC | 26054 |
rs577662113 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SENP6 | GRCh38.p7 | 6:75685490 | TAGGGTGTCAATTTT[A/G]GATCTTTCCTGCTTT | 26054 |
rs577678835 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707636 | GTGTTGGGATTACAG[A/T]TGTGAGCCACTGCGC | 26054 |
rs577679694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75616262 | CAAAGGTCAACCATA[A/T]CAAGTTATTGAAATG | 26054 |
rs577687001 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SENP6 | GRCh38.p7 | 6:75605950 | AGAGAAGTTGATAGG[C/T]TGAGGATATGTTTGG | 26054 |
rs577749633 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607469 | TTTTTTCACTCTGGG[G/T]GCTCTAACAAGCCTA | 26054 |
rs577795386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75664593 | TAAATCTGTTTAGAT[C/T]GTCTAATCTGGCCTG | 26054 |
rs577800282 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623823 | TGAATTAGGTGAACA[C/T]AGAGGATAAAACCTC | 26054 |
rs577806406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75644061 | TGGTATCAGAAACCT[A/G]GAAAATGTTCAAAAA | 26054 |
rs577806452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75651749 | TCATTTTTAAATTGA[C/T]ACATAATATTCATAC | 26054 |
rs577816765 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710188 | CCACTTTTCCAGTTA[-/T]TTTTTTTTCTCCTGC | 26054 |
rs577838878 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SENP6 | GRCh38.p7 | 6:75712290 | ACAGAAACTCTATTA[A/G]GAGACTTTGAAAATG | 26054 |
rs577860243 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75606561 | TGAGGAAAGTAAAAA[A/C]TAATAAAATAATACT | 26054 |
rs577898605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621125 | GTTAAAAGGCAGGTA[C/T]CGTTGAGTTTAAGGG | 26054 |
rs577910561 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626026 | TAGCAGGTATATGTA[C/T]AGTTCCACTAGGAAT | 26054 |
rs577936832 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SENP6 | GRCh38.p7 | 6:75630382 | CATTTTAGGTAATTT[A/T]TCTGCTAGTCAGGAA | 26054 |
rs578012385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75705820 | GACATAGAATAAATT[A/G]TGTGAATTCAGAAAG | 26054 |
rs578032117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75659685 | ATTTTAAGAAGCCAA[A/G]AAGTTACAAAAAATA | 26054 |
rs578051319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75673424 | CACCTCACGGGTTCC[A/G]GCAATTCTCCTACCT | 26054 |
rs578136489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75637675 | CTTATAAGAACCTTA[G/T]AAGAAATTCTTGTAA | 26054 |
rs578196233 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614546 | GCTAGGATTACAGGC[A/G]TGAGCCACTGCACCC | 26054 |
rs578200238 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662527 | CTAAAACAGAGCAGT[A/T]TTGAGATTCTAGTTT | 26054 |
rs578229418 | in-del | -/A | 0.251859 | 0.249993 | intron-variant | SENP6 | GRCh38.p7 | 6:75665286 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 26054 |
rs578252443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75672954 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 26054 |
rs578252975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SENP6 | GRCh38.p7 | 6:75680191 | AAGGAGGAGAGGAAA[A/G]GGTACCAGGTAGCTC | 26054 |
rs745358779 | snp | A/G | 0.00026742 | 0.0115602 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663229 | TTCTAAGGATTTGCA[A/G]AGAAATTGCAGACAA | 26054 |
rs745411134 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685542 | ATTAATTTCCCTCTA[C/T]GCACTGCTTTAAATT | 26054 |
rs745434932 | snp | C/T | 1.76154e-05 | 0.00296772 | intron-variant | SENP6 | GRCh38.p7 | 6:75678803 | CTTGCCTTCTAATTT[C/T]GTTACAGGTTGATAG | 26054 |
rs745462726 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696161 | TTTTTTAACAACTTA[C/T]TTATATTGAGGCAAT | 26054 |
rs745476187 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691245 | CCTCCCTGGCTCAAG[C/T]GATCCTCCTGCCTCA | 26054 |
rs745483344 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639601 | GGATAAATAATATTA[C/G]ACATGAATCTCATTT | 26054 |
rs745487389 | snp | C/T | 1.7617e-05 | 0.00296786 | intron-variant | SENP6 | GRCh38.p7 | 6:75709656 | ATGCTTGGCAAAAAG[C/T]TCTAATGTTTTATCT | 26054 |
rs745501644 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619686 | CTTTTTGAGGAACTG[C/T]CAAATTATTTTCTAC | 26054 |
rs745508415 | snp | C/T | 1.86527e-05 | 0.00305385 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621676 | AATAAAACTTCTCAT[C/T]AGAAAAACAATTTCT | 26054 |
rs745508903 | snp | C/G/T | 0.000298426 | 0.0122118 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678674 | AAAACCACACCATCT[C/G/T]CATTGGCCCAGTAGA | 26054 |
rs745515056 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606623 | GCAATCAGTGGTGGA[A/T]TGTTTATACAAGTTG | 26054 |
rs745537228 | snp | A/C/G | 0.000100204 | 0.00707766 | synonymous-codon, missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663239 | TTGCAAAGAAATTGC[A/C/G]GACAAGCTATTACTT | 26054 |
rs745537366 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75703498 | GGGCACAGTGGCTCA[C/T]GACTGTAATCCTAGC | 26054 |
rs745539809 | snp | A/G | 1.68394e-05 | 0.00290162 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711361 | GGATTCCTCGCTGAT[A/G]ACAACTGCAGTTCAG | 26054 |
rs745559488 | in-del | -/ACCAACC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688868 | AGGTCAGGAGGTGAA[-/ACCAACC]TGACCAACATGGAGA | 26054 |
rs745566474 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655631 | CTGGTGCTTGCATCA[A/G]TAGTTTGTTTCTTTT | 26054 |
rs745602055 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627491 | AGATGTGAGCAGGCA[C/T]GGTGTCTTTTGCCTG | 26054 |
rs745635292 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644621 | TCCTGAGTAGCTGGG[A/C]TTACAGGCATGTACC | 26054 |
rs745645620 | in-del | -/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601315 | TTAAAAAAAAAAAAG[-/G]CCTCACTTGTAAGGT | 26054 |
rs745654803 | snp | G/T | 3.2189e-05 | 0.00401167 | intron-variant | SENP6 | GRCh38.p7 | 6:75602585 | CTGGAAGGTACGTCT[G/T]TTTCTGCCCTTGACG | 26054 |
rs745663403 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643496 | ACATAACAAATAAAT[A/G]TAAAGCCTCCCCTAA | 26054 |
rs745665302 | in-del | -/AG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615080 | ATTTTTAGTAGAAAC[-/AG]GGTTTCACCATGTTG | 26054 |
rs745708178 | snp | A/G | 4.9938e-05 | 0.00499665 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647733 | ATTTCTTTTTTAGGA[A/G]AGAATACCCACCTCA | 26054 |
rs745743296 | in-del | -/TTC | 1.7095e-05 | 0.00292356 | intron-variant | SENP6 | GRCh38.p7 | 6:75659424 | TAAGTAGAGAAATTA[-/TTC]TTTGTTGCTAATCAG | 26054 |
rs745743761 | in-del | -/GATG | 1.73307e-05 | 0.00294365 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621648 | TTTTTTTTTCCCTCA[-/GATG]TTTTATAAGAATAAA | 26054 |
rs745752096 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664017 | TGGTTGACTAGAGTA[C/T]ACAGCGTGTATACTC | 26054 |
rs745760574 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714744 | CTGAATGCCATTGTT[G/T]CATGTTCTTTCTTGC | 26054 |
rs745761342 | snp | G/T | 3.09e-05 | 0.00393052 | intron-variant | SENP6 | GRCh38.p7 | 6:75640652 | CAATGAGGTCTTGCC[G/T]CTTATATTTTTTTTC | 26054 |
rs745788710 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628810 | CTGCAGCCTCTTCCT[A/C]CTAGGCTCAAGCGAT | 26054 |
rs745806590 | snp | C/G | 1.66402e-05 | 0.00288441 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670637 | TTAGCTTTAAGCTGC[C/G]AAAGTTCCTTTGACA | 26054 |
rs745811724 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712502 | TGCAACACAGTGAGA[C/T]GCCATCTCTGGAAAA | 26054 |
rs745906515 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689208 | CACTGTACTCCAACC[A/T]GGGTGACAGAGCAAG | 26054 |
rs745919883 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699644 | AGGTGCATGCTACCA[C/T]GCCCAGCTAATTTTT | 26054 |
rs745952278 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627400 | TCTGGATTTCCTGAA[A/G]TGCTATTTTTTAGGT | 26054 |
rs746017388 | snp | A/G | 1.66388e-05 | 0.00288429 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695905 | GAGAGAGGAGAAATC[A/G]TGAAACAACTAATCT | 26054 |
rs746027306 | snp | A/G | 3.36315e-05 | 0.00410057 | intron-variant | SENP6 | GRCh38.p7 | 6:75715336 | TCTGTGATTGAAATG[A/G]AAGGTTATTTATTAC | 26054 |
rs746047788 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688982 | GAGGCAGGAGAATCA[C/T]TTGAACCCAGGAGGT | 26054 |
rs746048827 | snp | A/C | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666840 | GTAGAAGCAGCGCTA[A/C]ATGAAAATACTTGCA | 26054 |
rs746076568 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624569 | CTTCAACCTTTGATC[-/T]TTGCAAATGAAAACT | 26054 |
rs746092106 | snp | A/G | 2.1873e-05 | 0.00330696 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677254 | GAAAACAAAATTAAA[A/G]CTGTAATTATGTTTT | 26054 |
rs746092306 | snp | A/C | 1.65732e-05 | 0.00287859 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713766 | CCAAAAGTACCACAG[A/C]AAAACAACTTCAGTG | 26054 |
rs746141259 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637638 | ACATTTTTTGACTTT[C/T]TATTAAGTATAGATA | 26054 |
rs746144089 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687904 | CAGAGCTCAGATGCC[A/G]TGCTGGGAGAACCAC | 26054 |
rs746157436 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700822 | ACACATTTTTTTCAC[A/G]TTGCAACATGTCTAA | 26054 |
rs746197103 | snp | C/G | | | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623931 | AGTGTGGATGAAGAT[C/G]AGGATTCTGAAACCT | 26054 |
rs746237959 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642424 | TTAACTAAAGACTAA[A/T]TGGGGAATTGGCAGT | 26054 |
rs746247685 | in-del | -/TCAAAAAAAAA | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620081 | TTGGGCTACCTTGCC[-/TCAAAAAAAAA]AAAAAAAAAAAAGAG | 26054 |
rs746274355 | snp | C/T | 1.68207e-05 | 0.00290001 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659401 | AAAATGTTTAACCCA[C/T]TTAGAGGTAAGTAGA | 26054 |
rs746279334 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674464 | GTAGCTGGGATTACA[A/G]GCATGCATTACCACG | 26054 |
rs746288117 | snp | A/G | 1.67223e-05 | 0.00289151 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675996 | GCTGAGCATCCAACT[A/G]CAAATGAATAAGGAG | 26054 |
rs746312954 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694597 | CAGTCTTTTCTCTAT[A/C]TCTGGCTTTTTGTAT | 26054 |
rs746332828 | in-del | -/A | 1.83249e-05 | 0.0030269 | intron-variant | SENP6 | GRCh38.p7 | 6:75709487 | CTATGAGTGATAGAC[-/A]ATGGCCTTTTTTATT | 26054 |
rs746341676 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611250 | AGTGGGATTCCAAAC[A/T]TTTTGGCATTCAGTC | 26054 |
rs746391525 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693828 | AATATGGCCATAAGC[C/T]TGAACTTGCATAAGT | 26054 |
rs746423018 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659991 | TCCCATTCAAATTTC[A/T]GCTAAATAATGTCCT | 26054 |
rs746447586 | in-del | -/CTTTTTTTTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705925 | AAGCTATTTTTGAGC[-/CTTTTTTTTT]TTTTTTTTTTTTTTT | 26054 |
rs746487192 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682150 | GGATCAAGAAGGATG[C/T]TATGTAATGATAAAG | 26054 |
rs746495752 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695762 | AAATAAATAAAGTGA[A/G]CTGTTACATTAATTA | 26054 |
rs746507965 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658070 | GATAGAGGACATCAG[C/T]TTAGGCAAGAGTTAA | 26054 |
rs746537175 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647914 | TAATAGATATATATG[C/T]AGAAAACCATTTTTT | 26054 |
rs746542977 | snp | A/C/G | 8.29461e-05 | 0.00643949 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621556 | GATCAGAGTCTAAGA[A/C/G]AGATGGAGGTTTTAA | 26054 |
rs746557510 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649740 | CAGACTGGTCTCAAA[-/C]TCCTGACCTCGTGAT | 26054 |
rs746560442 | snp | C/G | 1.97085e-05 | 0.00313909 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670713 | GGCTGTTAATAGAGC[C/G]TGTAATTGTAAGTAC | 26054 |
rs746590048 | snp | A/G | 2.53489e-05 | 0.00356003 | intron-variant, missense, splice-acceptor-variant, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75640685 | TTTCATGTTTTAAGC[A/G]GTCTGGACCGAAAAG | 26054 |
rs746616938 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702381 | CACCACTGCGCCTGG[C/T]TAATTTTTGTATTTT | 26054 |
rs746630801 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634562 | AAATGGAAAACTCCC[A/C]AAAGACAATTGGGTT | 26054 |
rs746651248 | snp | C/T | 1.65679e-05 | 0.00287814 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713538 | CTACTTATGGACTCA[C/T]TCCGAGGCCCTTCTC | 26054 |
rs746736823 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606593 | TTAAATGTAAAATTA[C/T]AACTGACAAGTACAG | 26054 |
rs746752376 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670923 | TTCCAATATGTTATT[-/G]TTTATTATCATGCCA | 26054 |
rs746835490 | in-del | -/CA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656213 | AGCAAGACTCCGTCT[-/CA]AAAAAAAAAAAAAAA | 26054 |
rs746855273 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605575 | ACTTAATTAAGTAAA[C/T]ACCTTAACTAAGAGA | 26054 |
rs746888218 | snp | C/G | 5.06171e-05 | 0.00503051 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677192 | GCAGACTTGTTGCCT[C/G]TACAAGAACCTATGA | 26054 |
rs746891323 | snp | A/G | 8.29222e-05 | 0.00643849 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702918 | TTATAAGAGAAACAT[A/G]TGCAGTGTAAAATAC | 26054 |
rs746920839 | snp | C/G | 2.24248e-05 | 0.00334842 | intron-variant | SENP6 | GRCh38.p7 | 6:75659256 | ATTTTTTTCTCCTTC[C/G]TTTAGAACGTATAAT | 26054 |
rs746955585 | in-del | -/T | 0.0013633 | 0.0260728 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621632 | GATAAAGAGTAAGGA[-/T]TTTTTTTTTCCCTCA | 26054 |
rs747016896 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690908 | TCACCTTGTTGGCCA[C/T]GCTGGTCTTGAACTT | 26054 |
rs747049931 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613552 | CAATGTATGTAATAG[C/T]AAAAAGGTGGATATA | 26054 |
rs747098834 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649072 | AGCACTTTACGATGT[C/T]GATGCAGGCAATCAC | 26054 |
rs747124641 | in-del | -/A | 1.65883e-05 | 0.00287991 | frameshift-variant, intron-variant | SENP6 | GRCh38.p7 | 6:75702939 | GTAAAATACAGTGTG[-/A]AAAAAAATAAATCAT | 26054 |
rs747146607 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662634 | TATCTGCATTTTGTT[C/T]GTAATTCTCACAGAG | 26054 |
rs747175316 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599710 | CTAGTTTTCTGGCTT[A/G]TGAAACCAGAAATGC | 26054 |
rs747193912 | in-del | -/CC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656814 | GAGCCTTATAAATAA[-/CC]TTGATTTAGGTAGGG | 26054 |
rs747197296 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699466 | TTATTTTTTCTGGTA[A/G]TACCAGTTTTGTTTT | 26054 |
rs747202417 | snp | C/G | 1.67711e-05 | 0.00289573 | intron-variant | SENP6 | GRCh38.p7 | 6:75715358 | ATTTATTACAGTTTT[C/G]TAATACGCATTTAAT | 26054 |
rs747204351 | snp | A/T | 1.75366e-05 | 0.00296108 | intron-variant | SENP6 | GRCh38.p7 | 6:75666973 | TTGACATTTGTTCAG[A/T]TTAATGCCTCCATTT | 26054 |
rs747218276 | snp | A/G | 3.34521e-05 | 0.00408961 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697446 | GCAAAAACGGCATGG[A/G]AGAGTAAAAACATGG | 26054 |
rs747257607 | snp | A/C | 1.65822e-05 | 0.00287938 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715527 | AAAGAAAGCATAAGG[A/C]CACTTACTCAACAGA | 26054 |
rs747260741 | snp | A/G | 1.6641e-05 | 0.00288448 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634725 | AAATACGCAAAATAC[A/G]TCATTATGTTCTGGA | 26054 |
rs747269462 | in-del | -/TA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626340 | TGTGGCTTAGCTTTT[-/TA]TATATATATATATAT | 26054 |
rs747270439 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626900 | ATTTACTTTTTTTTC[C/T]GTCTTTCTGGGTTTT | 26054 |
rs747303011 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714489 | TGAACTGCTATACCA[A/G]TCTCTAACAGATTCC | 26054 |
rs747315961 | in-del | -/TGT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659045 | CACAGGAAGGGCTTC[-/TGT]TACCTTAGTAGAACA | 26054 |
rs747344200 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687712 | TGCTGGAGTTCCACT[C/T]CAGACCAGCAGAGGC | 26054 |
rs747346677 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620650 | GACCATAGCACTGAC[C/T]ATGGGGTGGATGTAC | 26054 |
rs747358143 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664877 | GTCCCTGTTCTCTTA[C/T]AGTTTATGTGTAGCA | 26054 |
rs747380434 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637347 | AGTGCTTTACACCTT[A/T]TTATCTAAACAGAAT | 26054 |
rs747406557 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698609 | CAAGTAGCTGGGATT[A/G]TAGACATGAGCCACT | 26054 |
rs747426204 | snp | A/G | 1.67351e-05 | 0.00289263 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663440 | ACTAATGGAAAAGTC[A/G]TTTTACCTGGGGCAA | 26054 |
rs747441414 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622241 | CTTTTTGTTTGTCAT[A/G]AGATTTGTTTTTAAA | 26054 |
rs747445878 | snp | C/G | 1.71661e-05 | 0.00292963 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711390 | AGAAATAGGACAGTG[C/G]CATTTAAAGCCTACT | 26054 |
rs747449733 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663795 | AAATGGGTAGATTTC[A/C]TGCTGATAGTGGGTT | 26054 |
rs747464522 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614975 | GGCTCACTGCAATTT[-/C]CAGCTCCTGGGTTCA | 26054 |
rs747519829 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608259 | TGAGCCCAGGAGTTC[A/C]AGACCAGCCTGGGCA | 26054 |
rs747525786 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704515 | GGGCGGTTTTTCTCC[C/T]ATCTCAGAATTGAAC | 26054 |
rs747531906 | snp | G/T | 1.89066e-05 | 0.00307457 | intron-variant | SENP6 | GRCh38.p7 | 6:75709675 | AATGTTTTATCTAAT[G/T]AAAAGTTTTTCTTGC | 26054 |
rs747565183 | in-del | -/TCC | 0.00012132 | 0.00778752 | intron-variant | SENP6 | GRCh38.p7 | 6:75675852 | CCATTTCATTTGTTT[-/TCC]TCCAGAACCAGACCA | 26054 |
rs747566891 | snp | A/T | 1.69905e-05 | 0.00291461 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676017 | GAATAAGGAGGATAA[A/T]GTTTGGAATGATTGT | 26054 |
rs747629596 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693652 | GAAATCTTAAATTAT[A/G]TCATTTTCATTGAAA | 26054 |
rs747637636 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645261 | TAGGCTTGATTTTCA[A/G]TGAGTTTGGAATTTG | 26054 |
rs747659630 | in-del | -/AGG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640106 | TTTATAAAAGTACAA[-/AGG]AGGAGGTACCATGGC | 26054 |
rs747687929 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682009 | AGTGAACTGTCTACA[A/G]GGAATGTCAAAGTAA | 26054 |
rs747689011 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618189 | AATTCATTTTTATCT[C/T]TGGAGAAGGGAGTAT | 26054 |
rs747711104 | snp | A/G | 5.80119e-05 | 0.00538541 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659267 | CTTCCTTTAGAACGT[A/G]TAATGAAGAAAACAG | 26054 |
rs747712291 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700747 | TATGCCTGCCTCAAC[C/G]TCCCAAAGTGTTGGG | 26054 |
rs747722444 | snp | A/G | 1.68445e-05 | 0.00290206 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703043 | AGAATGGCCTACAGA[A/G]TGAAAGTTTAAGTTC | 26054 |
rs747758103 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655710 | TAATCGATAATATAA[A/G]TAATCGATAAACAAC | 26054 |
rs747764103 | snp | C/G | 1.65853e-05 | 0.00287964 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647779 | AATTAATCCTGTAAG[C/G]TTAAGTCGGCTCCAA | 26054 |
rs747766034 | snp | A/G | 8.69845e-05 | 0.00659429 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675458 | AGATTTTATCAAGAT[A/G]CAGCTAGACGGTAAG | 26054 |
rs747787661 | in-del | -/TA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644328 | GACCGAGGGACACTC[-/TA]TGAAATACCTGACGA | 26054 |
rs747819566 | snp | A/G | 0.000109653 | 0.00740367 | intron-variant | SENP6 | GRCh38.p7 | 6:75670729 | TGTAATTGTAAGTAC[A/G]TCTTAAGCTCTTTAC | 26054 |
rs747854484 | snp | C/G | 1.66101e-05 | 0.0028818 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695844 | AAGGAAGACGCTGAC[C/G]GAATTCATATATTCA | 26054 |
rs747866502 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694430 | AAACAATACATAATG[A/T]TAACAGCTTTACTTA | 26054 |
rs747876272 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701302 | AATATTAGCCAGGAC[C/T]GTACAGCTTCTTGCT | 26054 |
rs747911492 | snp | A/C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616964 | AACCTCCCAGGCTCA[A/C/G]TTGATCCTCCGTCCA | 26054 |
rs747938688 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634460 | AGCATGTTGGCTGGG[C/T]TGGTCTCGATCTCCT | 26054 |
rs747966929 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615529 | GTAAATTACATTTAT[A/G]ATTTTCAAATGTTTA | 26054 |
rs748033265 | snp | C/G | 3.31285e-05 | 0.00406978 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666861 | AATACTTGCAGAGCA[C/G]AGCGTGAACTACGAA | 26054 |
rs748054072 | snp | A/G | 1.67153e-05 | 0.00289091 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709540 | AGATGGCTTAAGCAA[A/G]ATCAGACTAAACTAT | 26054 |
rs748059417 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689880 | AACATAACCCCATTC[G/T]TAAGCACTGCATGAC | 26054 |
rs748067954 | snp | A/G | 1.65814e-05 | 0.00287931 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621665 | TGTTTTATAAGAATA[A/G]AACTTCTCATTAGAA | 26054 |
rs748076694 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655010 | CTTCTAAACACTTCA[G/T]TGGGCATATTATTAA | 26054 |
rs748092453 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605217 | CTTTACTTTCCAGTC[A/G]AGTCCTTGAAAAACT | 26054 |
rs748110585 | in-del | -/AGTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675257 | TGTTAACAGTTTAAC[-/AGTT]AGTGGGTTTAGATAA | 26054 |
rs748125856 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625666 | TTGAGGTCAGTAGTT[C/T]GAGACCAGCCTGGCC | 26054 |
rs748134515 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610463 | CATCAGGTAATAAAA[C/T]AATGGCTACAGTTAC | 26054 |
rs748147584 | snp | A/G | | | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718635 | GTTATGAACACTGCT[A/G]TTCCAAAACTTATTA | 26054 |
rs748257325 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612349 | TCTTTTGCTGCATTT[A/G]TATTTCTAAGTTACG | 26054 |
rs748275561 | in-del | -/GAG | 1.67632e-05 | 0.00289505 | cds-indel, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666725 | GTCATTTTGTCCAGT[-/GAG]GATGATGATGATGAC | 26054 |
rs748285591 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612636 | GATAACCCCATGAGA[C/T]GTAGAAATTAAAACA | 26054 |
rs748289605 | snp | A/G | 1.73884e-05 | 0.00294854 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676033 | GTTTGGAATGATTGT[A/G]AAGGAGTAAATAAAT | 26054 |
rs748355400 | snp | A/G | 0.000100828 | 0.00709958 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702698 | TGGAAAAACCAAAGT[A/G]TGAACCTAATCCTCA | 26054 |
rs748356115 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711642 | CTGCATGCACATGTC[C/T]ACACACAAATGTTTT | 26054 |
rs748428841 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677791 | AAAGGCCACAATACT[A/G]CTAAACACATAGTAT | 26054 |
rs748530660 | snp | C/T | 2.65784e-05 | 0.00364534 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75678962 | ATCTTTTATTAAATC[C/T]TTAACATTCCGTCAT | 26054 |
rs748556149 | in-del | -/TCTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624701 | TCCTTTGCCCATTTT[-/TCTA]TCTATCTGGTCTTTA | 26054 |
rs748558944 | snp | A/G | 3.34102e-05 | 0.00408705 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633649 | GACATATGTAAGACG[A/G]AACAAGTCTGAAAGT | 26054 |
rs748585848 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603032 | ATACCCTCTGGTCTG[-/T]TTTCTCAGAGTTTCA | 26054 |
rs748622590 | snp | A/G | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713554 | TCCGAGGCCCTTCTC[A/G]GTCAAATGTTGTCAA | 26054 |
rs748626077 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618376 | GTTCCAACTTTGGCC[A/G]TTGGGAATTCTTTCA | 26054 |
rs748643857 | in-del | -/GTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663808 | TCCTGCTGATAGTGG[-/GTT]TTTTTTTTTGTGGGG | 26054 |
rs748754900 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608129 | GTGAGTTCATGTACT[C/T]GAAACAGTAAAGTAG | 26054 |
rs748769927 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656976 | GTATGGTGAAGAGAA[G/T]AGTGTGATTACATAA | 26054 |
rs748788848 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704491 | CAACATGTCTCGCCT[C/T]CTGCCATAGGGCGGT | 26054 |
rs748831223 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693478 | AAGTCTCATGGTTCA[C/T]TCATTACAGTATAGT | 26054 |
rs748833455 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700623 | TCCAACCCCAGTAGC[C/T]TGGACCACAGGCACG | 26054 |
rs748867465 | snp | A/G | 0.000122137 | 0.00781369 | intron-variant | SENP6 | GRCh38.p7 | 6:75677300 | TCTTAAATTGTGGGT[A/G]GTTTTAAAGGGAAAT | 26054 |
rs748884571 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692772 | GGCCCTGTGGCTCTT[-/C]CTCCTTCCCTTCCCC | 26054 |
rs748909335 | snp | A/G | 4.97971e-05 | 0.0049896 | synonymous-codon, utr-variant-5-prime, intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621599 | CTTTGATCATGAAGA[A/G]GAAAGTGAAGGAGAT | 26054 |
rs748909939 | snp | A/C | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679406 | GCAAAACTCTACCCC[A/C]ACACCCACCCCCGAA | 26054 |
rs748916510 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609287 | GAAGGGGCGACTGAA[C/G]AAGAGAAGGAAAAAT | 26054 |
rs748932060 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645016 | TGAACAGAGCATTCT[C/G]ATGTTATTTAAACAA | 26054 |
rs748960634 | snp | G/T | 1.88685e-05 | 0.00307146 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659271 | CTTTAGAACGTATAA[G/T]GAAGAAAACAGAAGA | 26054 |
rs748981303 | snp | A/G | 1.7251e-05 | 0.00293687 | splice-acceptor-variant | SENP6 | GRCh38.p7 | 6:75675858 | CATTTGTTTTCCTCC[A/G]GAACCAGACCATGAT | 26054 |
rs748986950 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643601 | ATGGCATGCGCCTGT[A/G]ATCCCAGCTACTCGG | 26054 |
rs749000686 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614748 | TTACTGCACCAACAA[C/T]AGGACCTTCACTATG | 26054 |
rs749015370 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627807 | CAGTCTCCTGAGTGA[C/T]TGGGATTACAGGCAT | 26054 |
rs749019226 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75715013 | TTGTTAATAAAGTAG[A/T]AAATACATTAGGCTT | 26054 |
rs749032426 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692599 | CCACTGCACTCCAGC[C/T]TGGGCGAGAGAGTGA | 26054 |
rs749064216 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680984 | CAGATTTCAAAATGA[A/G]AATCATTTGCCTTAC | 26054 |
rs749066882 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655353 | AATCTTAAGTATATA[A/C]AATTTGAAAACTACA | 26054 |
rs749154810 | snp | A/G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689292 | TCTCTTTTTTAAGTG[A/G/T]TCCATACAAGTGGCC | 26054 |
rs749157928 | snp | C/T | 1.65847e-05 | 0.0028796 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715530 | GAAAGCATAAGGACA[C/T]TTACTCAACAGAAGC | 26054 |
rs749164228 | snp | C/T | 1.68789e-05 | 0.00290503 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634802 | CAGTAGTAAAAACAG[C/T]AGCCCAAAGGTAAGA | 26054 |
rs749217842 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652806 | AACATTAGATTATTA[C/T]CATTCTTTTAGTTTT | 26054 |
rs749229224 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615406 | GCTAGTCTCAAACTC[C/G]TGACCTCAAGTGATC | 26054 |
rs749242666 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712262 | CTTTGACTTTTTTTT[A/G]TAGAAAATGTTGACA | 26054 |
rs749251019 | snp | A/G/T | 5.01738e-05 | 0.00500847 | intron-variant | SENP6 | GRCh38.p7 | 6:75715365 | ACAGTTTTCTAATAC[A/G/T]CATTTAATTGTATTT | 26054 |
rs749271384 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665391 | TGTGGTGTTTCAGGG[A/G]CAGAAATACTGGCTA | 26054 |
rs749279098 | in-del | -/A | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618429 | CATGCCCCTGTCTTT[-/A]AAAAAAAAATAATGA | 26054 |
rs749351858 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689018 | TTGCGGGGAGCCGAG[A/T]TCATGCCATTGAACT | 26054 |
rs749380947 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653740 | TTAGGTATGATTATT[A/T]ATTCAAGCTGGCCTT | 26054 |
rs749391869 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638960 | CTGCTCAAGGTGGGA[A/G]AATCACCTGAGCCTA | 26054 |
rs749402500 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660175 | GGGTTTGTCTGATGT[C/T]TGTAAATGATGTGTG | 26054 |
rs749423075 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644338 | CACTCTATGAAATAC[C/G]TGACGAGTTCTCTCT | 26054 |
rs749424101 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691425 | CTTCATCTTATAGTT[A/G]AAGGAGTTCTGATGA | 26054 |
rs749433980 | snp | C/G | 4.97195e-05 | 0.00498571 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713580 | GTCAAAATTTTAAGA[C/G]AGTAAGTTCACACTT | 26054 |
rs749435949 | snp | A/T | 6.92833e-05 | 0.00588531 | intron-variant | SENP6 | GRCh38.p7 | 6:75666696 | TATAAATTATAAATT[A/T]TTAAAATACTTTTAG | 26054 |
rs749443484 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624082 | CCACTCCAGAGGCAA[A/G]TGGTGTTCCCAGTTT | 26054 |
rs749451608 | snp | G/T | 1.6638e-05 | 0.00288422 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703017 | GAAAGTTGCTGATAG[G/T]ACTAAAAGTGAGAAT | 26054 |
rs749451982 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676064 | TAACAAGTAAGTTGT[A/G]TAAAACAGATTATAA | 26054 |
rs749467438 | in-del | -/TTTCTTTTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653025 | TTTTTCTGTTACTTT[-/TTTCTTTTC]TTTCTTTTCTTTTTT | 26054 |
rs749469032 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707881 | GTTTGTAGAGACAGG[A/G]TCTCACTATGTTGCC | 26054 |
rs749486990 | snp | G/T | 1.68975e-05 | 0.00290662 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677177 | TTGAAGAAGCTAATG[G/T]CAGACTTGTTGCCTG | 26054 |
rs749502411 | in-del | -/AGG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605829 | TTTGTGGAATTAATT[-/AGG]AGGGGGCAAGATTAA | 26054 |
rs749531742 | in-del | -/TATAAAT | 0.00115808 | 0.0240353 | intron-variant | SENP6 | GRCh38.p7 | 6:75666681 | TAACTATAGTTTTAA[-/TATAAAT]TATAAATTATTAAAA | 26054 |
rs749541754 | snp | C/T | 1.85641e-05 | 0.00304659 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677081 | ATGGCCTTGATCCTC[C/T]GGCAAATATGGTATT | 26054 |
rs749574889 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689764 | TAGAAGCAGTAGGTT[A/T]TACCATATAGCCTAG | 26054 |
rs749599190 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612595 | TTAGCCACCCAAAAC[A/G]CTAGGATTATAGGTG | 26054 |
rs749625005 | in-del | -/AA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704143 | GGACGAGAGACTGAG[-/AA]AGAAATAAGACACAG | 26054 |
rs749628320 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709736 | GTGACTTGGGAGGCT[A/G]AGGCAGAAAGATCTC | 26054 |
rs749645586 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694831 | ATAATGTGGGGACAT[A/G]TGCTCTACTCTAGAT | 26054 |
rs749675732 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619174 | CCAATATTTATTTTT[A/G]GATCTTTTAAATCAT | 26054 |
rs749680059 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707263 | CAAATGTTATTCAAA[-/T]TATAGGTGTTTTAGC | 26054 |
rs749680245 | snp | C/T | 1.73827e-05 | 0.00294806 | intron-variant | SENP6 | GRCh38.p7 | 6:75675474 | CAGCTAGACGGTAAG[C/T]TATTTTATGTCTTTT | 26054 |
rs749683289 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660880 | ACGTGGTCCACCCAC[C/T]TCAGCCTTCCAAAGT | 26054 |
rs749721925 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625579 | TGTTAATTTAATAAC[C/T]TATTTGGGGCTGGGC | 26054 |
rs749731715 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702218 | AAAAAAAAAATAGGC[-/T]TTTTTTTTTTTTTTT | 26054 |
rs749733419 | snp | C/T | 1.66087e-05 | 0.00288168 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695873 | CAGTTCTTTTTTCTA[C/T]AAACGCCTTAATCAG | 26054 |
rs749767198 | snp | A/T | 3.31422e-05 | 0.00407063 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713740 | CCAAAGATGTTATGA[A/T]GGGCTCTAATCCAAA | 26054 |
rs749793803 | snp | A/C/G | 1.83562e-05 | 0.00302948 | intron-variant | SENP6 | GRCh38.p7 | 6:75633770 | AGAAAAGATAAAGGA[A/C/G]GAGTTTGACACCAAA | 26054 |
rs749803450 | snp | A/G | 1.67195e-05 | 0.00289127 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633659 | AGACGAAACAAGTCT[A/G]AAAGTTTTAAAACTT | 26054 |
rs749846736 | in-del | -/AAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656214 | GCAAGACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 26054 |
rs749849339 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652144 | ATCGCGCCACTGTCC[C/T]CCAACCTGGGCAACA | 26054 |
rs749888611 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604334 | ACTTCTTTAGAGCAT[A/G]AGCATAAGGGTTCTG | 26054 |
rs749897897 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636961 | TCATAGCTCACTGCA[A/G]CCTCAAACTTCTGGT | 26054 |
rs749902412 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664513 | GTCCCTAATTCTACA[A/G]AGAAGAGAAATTGAG | 26054 |
rs749939916 | snp | A/T | 1.67105e-05 | 0.0028905 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633624 | ATAGCTCTGGTGAAT[A/T]CATCTTGAAGACATA | 26054 |
rs749950411 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650535 | GAAATCGTCTGTAGG[C/G]AAGATCTGTACCTTC | 26054 |
rs749955534 | in-del | -/TG | 1.65666e-05 | 0.00287802 | intron-variant | SENP6 | GRCh38.p7 | 6:75678552 | CTTTTCCTAATTGAC[-/TG]TAAATTGCTAATTTA | 26054 |
rs749965411 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710580 | TATGGCAACTAAATA[C/T]AGCTTTTCAATCCAA | 26054 |
rs749978579 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626466 | AAAGTATTTACAAAT[A/C]TTTATCATCCTTTTT | 26054 |
rs749985978 | in-del | -/AGAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608478 | AAAAGAGAGGGAGGG[-/AGAA]AGAAAGAAGAGGAAA | 26054 |
rs749991060 | snp | A/G | 5.44035e-05 | 0.00521525 | intron-variant | SENP6 | GRCh38.p7 | 6:75663545 | ACTCCCTTTAATATT[A/G]CTTATATCAATCCAG | 26054 |
rs750035349 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672482 | ATGCTAAATGAAATA[G/T]TCCAGCCAAAAAATA | 26054 |
rs750059026 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637926 | AGTGCAGTGGCGTGA[G/T]CTCCACTCACTGCAG | 26054 |
rs750080274 | snp | G/T | 0.000389788 | 0.013955 | intron-variant | SENP6 | GRCh38.p7 | 6:75676998 | TTACTTCTTTTGTGT[G/T]TTTTTTTGGACTTAT | 26054 |
rs750087794 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687411 | CTGTCAACTCGTCAA[A/G]GTCATTCTCCGTCCA | 26054 |
rs750154456 | in-del | -/CC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612826 | TATCAGAAAACTATG[-/CC]CCCCAGACCAGGCGC | 26054 |
rs750156149 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606140 | AAATTTGAGATGCCT[A/G]TTTGACATTTTTGCT | 26054 |
rs750175350 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609017 | GAAATTACATACTTT[C/G]TATGTCTAGACTTTC | 26054 |
rs750197605 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705475 | ACTTGAACCTGGGGG[C/T]GGAGGTTGCAGTGAG | 26054 |
rs750217071 | snp | A/C | 3.31022e-05 | 0.00406817 | intron-variant | SENP6 | GRCh38.p7 | 6:75659236 | TTAACTAAAACTTAA[A/C]GTTTATTTTTTTCTC | 26054 |
rs750218845 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643327 | TACAAGCATCATACT[-/A]AAATAACAATGTGAA | 26054 |
rs750229452 | snp | C/T | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666931 | CAAGAAAAGCAAGAA[C/T]GAAAGACCAGGTACT | 26054 |
rs750235076 | snp | A/G | 1.827e-05 | 0.00302236 | intron-variant | SENP6 | GRCh38.p7 | 6:75675405 | TTTCTTTGTAAGTCT[A/G]GAGCAATACTAATTC | 26054 |
rs750242444 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673889 | AGTGGGGTGTGGTGG[C/T]GTGCACCCGTAACCC | 26054 |
rs750256491 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657938 | AGTAAGATTGAAACA[A/G]GAACTTCTGCTTGCC | 26054 |
rs750275958 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702608 | TATAATAAACTTTTC[A/T]AATAACATATTTAGT | 26054 |
rs750287996 | snp | C/T | 1.6686e-05 | 0.00288838 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695809 | TATCAAATAGATACT[C/T]GGTGCTTGAAAAACT | 26054 |
rs750332702 | snp | A/G | 5.53797e-05 | 0.00526182 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670698 | TAGGAACACTCTTCC[A/G]GCTGTTAATAGAGCC | 26054 |
rs750333987 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701991 | TTTTACATAAAGAGA[A/T]GGCAAAGGGGAATGA | 26054 |
rs750373138 | snp | G/T | 1.66441e-05 | 0.00288474 | intron-variant | SENP6 | GRCh38.p7 | 6:75713631 | ATGAAGAACTATGTA[G/T]ATTTATATATGTGTG | 26054 |
rs750377724 | in-del | -/T | 1.73842e-05 | 0.00294819 | frameshift-variant, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675463 | TTATCAAGATACAGC[-/T]AGACGGTAAGCTATT | 26054 |
rs750379855 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617878 | AGTTGTACAAAATAC[C/T]GTATACAGGTATTTT | 26054 |
rs750387525 | snp | C/T | 2.33702e-05 | 0.00341827 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678916 | TGATGTTATTATAGA[C/T]TTTTATTTGAAGTAA | 26054 |
rs750388456 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706482 | CATATACACAAACTC[C/G]AGAGATTTCTAGTGC | 26054 |
rs750423237 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693259 | AAAATACAGAAATTA[G/T]CTGGGTGTGGTGGAG | 26054 |
rs750453175 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631846 | TCATAGATTGATATC[C/T]GGAGGCCCCCTTAAA | 26054 |
rs750465916 | snp | A/G | 1.66043e-05 | 0.00288129 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670587 | ACACACCTCTGAAAC[A/G]TCGTAAAGTGTTTTC | 26054 |
rs750473459 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654232 | TACAGAGTGAGACCC[C/T]ATCTCAAAAACAAAG | 26054 |
rs750488979 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714443 | TTAATGTCAGATAGA[C/T]TTACTTGTTTATCGT | 26054 |
rs750520357 | snp | C/G | 1.65935e-05 | 0.00288036 | intron-variant | SENP6 | GRCh38.p7 | 6:75678738 | CTTAAATGTCTTTCT[C/G]TGTTTTATTACATTT | 26054 |
rs750521178 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681624 | CCACCACACCCAGCT[A/G]ATTTTCAGGTAGTTC | 26054 |
rs750525530 | in-del | -/TT/TTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699360 | TGTTTTTGCTTTTTT[-/TT/TTT]TTTTTTTTTTTTTTG | 26054 |
rs750528937 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630403 | TAGTCAGGAAACTAC[C/T]GGCAAGAAAAAGCAC | 26054 |
rs750579575 | snp | C/T | 1.72222e-05 | 0.00293442 | intron-variant | SENP6 | GRCh38.p7 | 6:75666954 | CAGGTACTTTTCACT[C/T]TTGTTGACATTTGTT | 26054 |
rs750593342 | snp | A/T | 1.6717e-05 | 0.00289106 | intron-variant | SENP6 | GRCh38.p7 | 6:75623850 | CCTCAGAATTTAATA[A/T]AAGGATTGTGATTGC | 26054 |
rs750603626 | in-del | -/T/TT | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600425 | TCAAGCTGCTGAAAG[-/T/TT]TTTTTTTTTTTTTTT | 26054 |
rs750619828 | snp | A/C | 1.66377e-05 | 0.00288419 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678604 | TTTGAATCTAAAATA[A/C]AACTTAGAAGCAAAC | 26054 |
rs750643862 | snp | C/T | 4.99297e-05 | 0.00499623 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709598 | ATGCTTGAAGATGAA[C/T]TCGTCGACTTCTCAG | 26054 |
rs750684506 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616364 | AAAATCTCTTTTCTT[C/T]TTATAATTTATTTTT | 26054 |
rs750696769 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667025 | AAGGCAGTTTGGTAG[C/T]GCCAAGAAAAAATGA | 26054 |
rs750723173 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611706 | TATTTTTAAGAGATT[G/T]TGTATTCTGTGTAAA | 26054 |
rs750736875 | snp | A/T | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717887 | TGCCATAAAATTTGT[A/T]TGTCTCAGCTCTTGT | 26054 |
rs750756541 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654530 | TTTTTAAAGAAGATA[A/T]TGAGAATGTGATAGA | 26054 |
rs750774535 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694557 | CTGTTTTCTTCCAAT[C/T]CCTCCTCCAGGCCTA | 26054 |
rs750779021 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635553 | ATTTTTCTGTTTACA[C/T]AGATGGGCTATCAGA | 26054 |
rs750779444 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641542 | ATTTGTTCTCTTTGT[A/G]AGAACACTGGCAGAC | 26054 |
rs750797834 | snp | A/G | 2.59784e-05 | 0.00360396 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602535 | GGAAGATGGCGGCCG[A/G]CAAGAGCGGCGGTAG | 26054 |
rs750808921 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610071 | GGGATTAGAAGTGTG[A/C]GTCACCGCACCTGGC | 26054 |
rs750817805 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692940 | GCCAGGTATGGTGGC[A/G]TATGCCTGTAGTTCC | 26054 |
rs750829137 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604943 | TCTGGCGTGGTGGCG[C/T]GCGCCTGTAATCCCA | 26054 |
rs750845120 | snp | C/G | | | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702899 | AGGAAGAAAGTGACC[C/G]TCGTTATAAGAGAAA | 26054 |
rs750860852 | in-del | -/A | 0.000113682 | 0.00753843 | intron-variant | SENP6 | GRCh38.p7 | 6:75624003 | TTTTACATTATATAC[-/A]AAAAAATTGTTACCT | 26054 |
rs750874910 | in-del | -/ACTTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608679 | GATCTTGGATAGATT[-/ACTTA]ACTTAACTTCTCTGT | 26054 |
rs750902421 | snp | A/G | 0.000428403 | 0.0146294 | intron-variant | SENP6 | GRCh38.p7 | 6:75634944 | AGATATATCTCTGAA[A/G]TAATTCATGACATGA | 26054 |
rs750909230 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642551 | GGGCCACTAAGGCTG[A/G]AGCTTAGAGAGGAAA | 26054 |
rs750944659 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625288 | GGCTAATTTTTTTTT[A/T]ATTTTTATTAGAGAC | 26054 |
rs750960106 | snp | A/G | 2.08592e-05 | 0.00322942 | intron-variant | SENP6 | GRCh38.p7 | 6:75702615 | AACTTTTCTAATAAC[A/G]TATTTAGTCATTTCA | 26054 |
rs750970571 | snp | A/G | 1.66479e-05 | 0.00288508 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715588 | TGTCAATAGTATCTC[A/G]GATTGACCATTTCTG | 26054 |
rs750992626 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690349 | TATAATGCAATATGT[A/G]TACATTTCCTTCCTT | 26054 |
rs751021139 | snp | A/G | 5.14425e-05 | 0.00507135 | intron-variant | SENP6 | GRCh38.p7 | 6:75713852 | TTTGTTGGATCTGCT[A/G]TAATAAATAATAAAA | 26054 |
rs751028217 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648948 | TTACTATATTCTTGC[G/T]CTGTCACAAAGAAGG | 26054 |
rs751048459 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75683329 | GATGGGTAGATTGCA[A/G]AAATTTTGTCCCATT | 26054 |
rs751087504 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691143 | CATTCCCAGCTAAAA[-/TT]TTTTTTTTTTTTTTT | 26054 |
rs751128112 | in-del | -/T | 0.000766161 | 0.0195574 | intron-variant | SENP6 | GRCh38.p7 | 6:75640658 | GTCTTGCCTCTTATA[-/T]TTTTTTTTCTTTTTC | 26054 |
rs751152953 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612471 | TTAGTAGCTGGGACT[A/T]CAGGCTTGTGCCACC | 26054 |
rs751153174 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698871 | CAAAAATTAGCTGGG[C/T]GTGGTGGTGCGTGCC | 26054 |
rs751156786 | snp | C/T | 1.66977e-05 | 0.00288939 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633640 | CATCTTGAAGACATA[C/T]GTAAGACGAAACAAG | 26054 |
rs751156935 | snp | C/T | 1.65806e-05 | 0.00287924 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666774 | AGAGAAAGCATATCT[C/T]CTCAGCCTGCTGATT | 26054 |
rs751183259 | in-del | -/T | 0.00247862 | 0.0351165 | intron-variant | SENP6 | GRCh38.p7 | 6:75675424 | CAATACTAATTCATC[-/T]TTTTTTTTAGTTTTG | 26054 |
rs751189682 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650034 | CTTTTTCTGTTCCAC[A/G]ATTCATTCTGTGATC | 26054 |
rs751193005 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685408 | CTTTGATCTTAGTTA[C/T]TTCTTGCCTTCTGCT | 26054 |
rs751200681 | snp | C/T | 3.33084e-05 | 0.00408082 | intron-variant | SENP6 | GRCh38.p7 | 6:75713651 | ATATATGTGTGTATT[C/T]TTAATATATATGAAT | 26054 |
rs751220979 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602341 | GCCCGCGGACAGGCC[C/T]GGGCGCGCCTGGCCT | 26054 |
rs751245641 | snp | C/T | 1.80166e-05 | 0.00300133 | intron-variant | SENP6 | GRCh38.p7 | 6:75709499 | AGACATGGCCTTTTT[C/T]ATTATGTAATGTTTC | 26054 |
rs751248773 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691007 | CTGTGCTCAGCCTAA[-/T]TTTTTTTTTTTTTTT | 26054 |
rs751281343 | in-del | -/GG | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601314 | GTTAAAAAAAAAAAA[-/GG]CCTCACTTGTAAGGT | 26054 |
rs751298967 | snp | G/T | 1.7357e-05 | 0.00294588 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621650 | TTTTTTTCCCTCAGA[G/T]GTTTTATAAGAATAA | 26054 |
rs751302391 | snp | G/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619526 | CTGTTGATAGAAATT[G/T]GGGTTGTTTCCACCA | 26054 |
rs751354253 | snp | A/G | 1.68289e-05 | 0.00290072 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659337 | AAGTACAACAGAAAC[A/G]ACACTGTAGTACCTA | 26054 |
rs751384141 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662991 | TTAAATCCCGACTAA[C/T]ATTACTTATTTAGGC | 26054 |
rs751406525 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603932 | GGTTCGTTTCGTATT[A/G]CCTCCATTCCAGTTT | 26054 |
rs751407353 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697700 | GTGAAGCATGTAAGA[C/T]ATTGAATTTTAGAGA | 26054 |
rs751421068 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600894 | CAACAAAAATAAATT[A/G]CATTCATTACACTAC | 26054 |
rs751438960 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705003 | TCTCAGGGCAAAGCA[A/G]TTGTTCAGGGTACAG | 26054 |
rs751439924 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657699 | GCTCTTCCCAGAGCT[G/T]GCAATACAATGGGGG | 26054 |
rs751442669 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692213 | CTAAAATGAGAGATA[C/T]GATTATTATTTTAAA | 26054 |
rs751474686 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621091 | TGCCAAAACCGAAAA[C/T]GTTGTTTGTTTTTCT | 26054 |
rs751536314 | snp | A/G | 5.081e-05 | 0.00504008 | intron-variant | SENP6 | GRCh38.p7 | 6:75695957 | ATATTTAACAGATGT[A/G]AGTCACTCACATTTA | 26054 |
rs751585405 | snp | A/G | 1.71979e-05 | 0.00293235 | intron-variant | SENP6 | GRCh38.p7 | 6:75647702 | CTGTATTTCCTGTTA[A/G]AATAAAACTACATAA | 26054 |
rs751588268 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614865 | AAGGGAGTGCCTTTC[C/T]ATTCCTGGTTTGCAA | 26054 |
rs751590234 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672253 | TATTTATAACTCTTC[A/T]GTGTGATGAGTAAGG | 26054 |
rs751622590 | snp | C/T | 1.73972e-05 | 0.00294929 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715639 | CAGAAACTAAATGAC[C/T]TTCAAATTTGGGTAT | 26054 |
rs751636570 | snp | A/G | 1.73549e-05 | 0.0029457 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670680 | ACTGTCGAAGTATAC[A/G]AGTAGGAACACTCTT | 26054 |
rs751648179 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678401 | CTAGAAGCTACAGAT[-/A]ATAAGAAAGTGGCCC | 26054 |
rs751666810 | in-del | -/AGTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699261 | GCTTCCAGTCATCTT[-/AGTG]AGAGGTAGAAAATGA | 26054 |
rs751691157 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644328 | GACCGAGGGACACTC[A/T]ATGAAATACCTGACG | 26054 |
rs751714524 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616174 | CTGGGATCTCTCCTT[-/A]AACCTTTTTCTTTCC | 26054 |
rs751733199 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608885 | AAAGAGCTTCCTTTA[C/T]TTGCTTGTCTTCTCT | 26054 |
rs751735900 | snp | A/G | 1.91771e-05 | 0.00309648 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678860 | GGCATCTCTGTTACC[A/G]ATGAGGACCTGCACT | 26054 |
rs751767842 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640884 | AGTAATATATCAATA[-/C]CAGGTATACAATGTG | 26054 |
rs751780296 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716195 | CACAAATATTTAAGA[C/G]GAAAGAGTATTAAGA | 26054 |
rs751785240 | in-del | -/T | 1.68136e-05 | 0.0028994 | intron-variant | SENP6 | GRCh38.p7 | 6:75715343 | TGAAATGAAAGGTTA[-/T]TTTATTACAGTTTTC | 26054 |
rs751816278 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603736 | GGAACACAGTAGGTA[C/T]TCAGTGTTAGTCTAG | 26054 |
rs751864623 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616022 | TCTTTTTTCACTTTT[A/G]TTAATCTCTCTTCTA | 26054 |
rs751917699 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632328 | CCATCGATAAAGGGG[C/G]ACTACTATGTAGTAT | 26054 |
rs751941203 | snp | C/T | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717764 | TACTAGACACTGAAA[C/T]TGCATGACAAGTATC | 26054 |
rs751944021 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629549 | AGGTGATCCGCCCAC[C/T]TTGGCTTCCCAAAGT | 26054 |
rs751974173 | snp | A/C/T | 7.97361e-05 | 0.0063137 | intron-variant | SENP6 | GRCh38.p7 | 6:75677013 | TTTTTTTTGGACTTA[A/C/T]ATTTATTTCTTTTCA | 26054 |
rs751994657 | snp | A/C | 1.65748e-05 | 0.00287874 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702829 | GCCAAGCCTGTAATT[A/C]AGAAGATGCTAAACA | 26054 |
rs752007860 | snp | A/G | 3.4825e-05 | 0.00417268 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677124 | TAATGAAATTGGTAT[A/G]AAGAATAACATCTCC | 26054 |
rs752076165 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692787 | CCTCCTTCCCTTCCC[C/T]CGCCAAAAAAAAAAA | 26054 |
rs752142719 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604863 | GGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG | 26054 |
rs752144689 | snp | A/G | 1.65952e-05 | 0.00288051 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702979 | GAAAATGAAGAATTC[A/G]ATAAAGGAGAATCTA | 26054 |
rs752145923 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646167 | TGGAATTTGAAAATA[-/T]GCATTTTATTTTAAT | 26054 |
rs752165038 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701756 | GCAATTCTCCTGCCT[C/T]AGCCTCCCAAGTAGC | 26054 |
rs752226760 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675310 | TATAATGTTATACCA[A/C]CTTCTCTGTGGGATT | 26054 |
rs752233567 | in-del | -/C | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620642 | ACATTCAGACCATAG[-/C]CACTGACCATGGGGT | 26054 |
rs752263135 | in-del | -/TA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643875 | TATTTGGCCATCTTT[-/TA]TAATAATGGAAAAAT | 26054 |
rs752268330 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669117 | CACTTTCGGAGACTG[A/G]GGTGGGCAGATTGCC | 26054 |
rs752274690 | in-del | -/AT | 1.65869e-05 | 0.00287979 | frameshift-variant, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621574 | ATGGAGGTTTTAAAA[-/AT]AATTGGAGCTTTGAT | 26054 |
rs752298182 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704652 | CCTTCTCAGCACAGA[A/C]CCTTCACGGGTGTTG | 26054 |
rs752307223 | snp | A/G | 5.79761e-05 | 0.00538374 | intron-variant | SENP6 | GRCh38.p7 | 6:75675768 | TAAATATGTGCTTAC[A/G]TTTACTTAAACTTGT | 26054 |
rs752308020 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623546 | TTTTCAATCTAAGAC[A/G]AAAAGGAAAAATGAA | 26054 |
rs752313202 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641407 | GCTTTAATAGACTGG[C/G]GGAGGGAGAGGGAAA | 26054 |
rs752333117 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661801 | TGCCTGTAATCCCAG[C/T]ACTTTGGCAGGCCGA | 26054 |
rs752388376 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711646 | ATGCACATGTCCACA[-/C]ACAAATGTTTTGTTT | 26054 |
rs752427148 | snp | A/G | 1.83323e-05 | 0.00302751 | intron-variant | SENP6 | GRCh38.p7 | 6:75711306 | TATATTTTCAGTATT[A/G]ACAGTAGGCTGTCTT | 26054 |
rs752473079 | snp | A/G | 1.66161e-05 | 0.00288232 | intron-variant | SENP6 | GRCh38.p7 | 6:75623887 | TGTTTTTTTCCCCTT[A/G]TTTTCTGTGTAGTGG | 26054 |
rs752512722 | in-del | -/AAAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655719 | ATATAAATAATCGAT[-/AAAC]AACACCTGGGTTGTT | 26054 |
rs752519223 | in-del | -/TTAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672237 | CCCACATTAATGCTG[-/TTAT]TTATAACTCTTCAGT | 26054 |
rs752520348 | snp | G/T | | | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703034 | CTAAAAGTGAGAATG[G/T]CCTACAGAATGAAAG | 26054 |
rs752522752 | snp | A/G | 1.6777e-05 | 0.00289624 | intron-variant | SENP6 | GRCh38.p7 | 6:75623964 | AAAGGAAAAAAGGCA[A/G]GTGTTGCTTAAAATA | 26054 |
rs752549677 | snp | A/G | 1.66032e-05 | 0.0028812 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678618 | ACAACTTAGAAGCAA[A/G]CAAGAATTTCAGTTT | 26054 |
rs752618208 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662484 | TTAACATAAAATTTT[A/T]ATGAAAATTTATTTA | 26054 |
rs752629922 | snp | C/T | 3.34846e-05 | 0.0040916 | intron-variant | SENP6 | GRCh38.p7 | 6:75663214 | TTGTGGTGTTCTTTT[C/T]TCTAAGGATTTGCAA | 26054 |
rs752703974 | snp | C/T | 1.66407e-05 | 0.00288446 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621518 | ATACTTACTGCAGTT[C/T]GTTTTTATTTCAGCT | 26054 |
rs752737601 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643142 | TGCAAACAGTGTTGT[A/G]TAAAAATAGGAGAAA | 26054 |
rs752758532 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614468 | AGATGGGGAATTACC[A/G]TATTGGCCAGACTGG | 26054 |
rs752762685 | snp | A/G | 1.66106e-05 | 0.00288184 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703006 | TCTACATCCCAGAAA[A/G]TTGCTGATAGGACTA | 26054 |
rs752782501 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657551 | GTCTCTTCCTCCGAC[C/T]CCTGTAATTTCATTT | 26054 |
rs752796000 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692939 | AGCCAGGTATGGTGG[C/T]GTATGCCTGTAGTTC | 26054 |
rs752800757 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697604 | TGAGGTGAAGAATTC[A/G]TTTTAAAACATCTTT | 26054 |
rs752811221 | snp | C/T | 0.00010804 | 0.00734903 | intron-variant | SENP6 | GRCh38.p7 | 6:75659225 | ACTAGCTTATTTTAA[C/T]TAAAACTTAAAGTTT | 26054 |
rs752853868 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704232 | GACCTGCCCCGTCAC[C/T]GGTCTTTGAGTTCTC | 26054 |
rs752860145 | snp | A/G | 0.000202593 | 0.0100626 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602576 | ATTACTTTTCTGGAA[A/G]GTACGTCTGTTTCTG | 26054 |
rs752866706 | snp | C/G | 1.84218e-05 | 0.00303489 | intron-variant | SENP6 | GRCh38.p7 | 6:75675384 | AATAAAAAAGTGAAG[C/G]CTGCCTTTCTTTGTA | 26054 |
rs752866790 | snp | C/T | 1.68286e-05 | 0.0029007 | intron-variant | SENP6 | GRCh38.p7 | 6:75647713 | GTTAGAATAAAACTA[C/T]ATAAATTTCTTTTTT | 26054 |
rs752878878 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675122 | GTGAAAGTCAGACCC[C/T]CATGACATGCAATTT | 26054 |
rs752917627 | snp | A/T | 5.38121e-05 | 0.00518683 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670690 | TATACGAGTAGGAAC[A/T]CTCTTCCGGCTGTTA | 26054 |
rs752937171 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614229 | TTAGTTAAGGTGGTG[G/T]TCACCAGATTTTTCC | 26054 |
rs752973945 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714370 | TTTACTCTGATCTTG[C/G]CTCCTATCTTCATCC | 26054 |
rs752977312 | in-del | -/GAA | 1.66371e-05 | 0.00288414 | cds-indel, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695825 | GGTGCTTGAAAAACT[-/GAA]GAAGGAAGACGCTGA | 26054 |
rs752998536 | snp | C/T | 1.65685e-05 | 0.00287819 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666890 | AAGCATTCCAGAAGA[C/T]TCAGAGTTAAATACA | 26054 |
rs753013090 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691908 | GTTGTCCAGGCTGGA[A/G]TGCAATGGCACAATC | 26054 |
rs753035942 | snp | C/G | 1.65743e-05 | 0.00287869 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713711 | AGTTAAAAAAGGAAG[C/G]AAAAGAAGTTTTTCC | 26054 |
rs753058617 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653566 | GTTTTCCCTCAATGC[A/G]TTTGGGTGAATGTCA | 26054 |
rs753079439 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710646 | CACTTAGGTACTTTT[G/T]GTTATAGCAGTTACC | 26054 |
rs753102413 | snp | C/T | 4.30506e-05 | 0.00463933 | intron-variant | SENP6 | GRCh38.p7 | 6:75666681 | TAACTATAGTTTTAA[C/T]ATAAATTATAAATTA | 26054 |
rs753117762 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627972 | CCACCACGCCTGGCC[A/T]GCTTTCAGATTTCTT | 26054 |
rs753136448 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700591 | TCCCAGGCTCAAGCT[A/G]TCCTCCCACCTCAGC | 26054 |
rs753136813 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680277 | GCAGAAGGAGAACAG[C/G]CTTGGGTGAGGAGGG | 26054 |
rs753150398 | snp | A/G | 1.65715e-05 | 0.00287845 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666792 | CAGCCTGCTGATTCA[A/G]CATGTTCTTCCCCTG | 26054 |
rs753155552 | snp | A/T | 1.72642e-05 | 0.00293799 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677142 | GAATAACATCTCCAA[A/T]TTTTTTGCGAAAATT | 26054 |
rs753197087 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688727 | GAGTTGGAGACCCAG[C/T]CTGTGCAATATAATG | 26054 |
rs753205406 | snp | A/G | 1.71267e-05 | 0.00292627 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677219 | ATGAAGAGAGCATCA[A/G]AGGAAGTTGTGGGCA | 26054 |
rs753208360 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75713445 | TGTTTATAATATGCC[A/G]CTTTTAATCCTTTTA | 26054 |
rs753229233 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609435 | TCCACATTGTATTGG[A/C]CAAAAGAATACAGAG | 26054 |
rs753268684 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615151 | CCACCTTGGCCTCCC[A/G]AAGTGCTGGGATTAT | 26054 |
rs753275711 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601370 | GGCACGTAAATGACA[A/G]GGGACTTTTTAAAAA | 26054 |
rs753293289 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629102 | AAAATAATTTGTAAT[A/C]CAGTCATTAGGTACT | 26054 |
rs753300298 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664759 | CTCAGTAAAAATTAA[A/G]CATTTATGTTTGAAA | 26054 |
rs753324185 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630896 | TAAAAGCAAAAAAGG[-/A]AAAAAAAATGGCTAA | 26054 |
rs753337645 | snp | A/T | 1.67245e-05 | 0.00289171 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663224 | CTTTTTTCTAAGGAT[A/T]TGCAAAGAAATTGCA | 26054 |
rs753367993 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688615 | ATTTTTCCTTTTGGT[A/G]TGTTTCAAAGTTCTT | 26054 |
rs753383092 | snp | A/T | 1.66197e-05 | 0.00288263 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663359 | AAGTTTTATGGCAAC[A/T]ATGTGGAAAAGGTTC | 26054 |
rs753389382 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664701 | ATTAAAAAGACAGGT[-/A]AGAGAAATACTGAGA | 26054 |
rs753390040 | snp | A/G | 4.97756e-05 | 0.00498852 | missense, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623907 | CTGTGTAGTGGGACA[A/G]ATCTGCTCAGTGTGG | 26054 |
rs753390870 | snp | C/T | 4.99355e-05 | 0.00499652 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675973 | GCAATTCCAGCAGTT[C/T]ATCAAAAGCTGAGCA | 26054 |
rs753419810 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606708 | CCCTAAGAAATGCTC[A/G]TTGAATCAATTCAGA | 26054 |
rs753422633 | in-del | -/CTTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672755 | TTATAAAATTCTACA[-/CTTG]CTTATTATTAGATAA | 26054 |
rs753426185 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603299 | TGTTTTTGTTGGGGA[A/G]GGTGGTAATGGGGAA | 26054 |
rs753486069 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706708 | CCATATCAACTATCT[C/T]TTCCTCTGAAACAAA | 26054 |
rs753525292 | in-del | -/AAATG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643492 | GGGAACATAACAAAT[-/AAATG]TAAAGCCTCCCCTAA | 26054 |
rs753526234 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675128 | GTCAGACCCCCATGA[C/T]ATGCAATTTACCTGT | 26054 |
rs753568603 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612291 | CCTGCAGAGCCACAT[A/G]AAATTGCTTTTCGAA | 26054 |
rs753630723 | snp | A/G | 2.01169e-05 | 0.00317144 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678873 | CCAATGAGGACCTGC[A/G]CTGTCTAAATGAAGG | 26054 |
rs753653439 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618030 | CATGCCATGAATAAG[A/G]CATATCACTATGAAT | 26054 |
rs753658206 | in-del | -/ATTTATTCCTTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647500 | ACAATCTCATTCAAC[-/ATTTATTCCTTT]ATTTATTAATTTGTT | 26054 |
rs753660717 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680884 | CCACTGGAGTGTGGT[A/G]CTAGAGGAAGTCTGC | 26054 |
rs753672264 | snp | A/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718165 | AAAAATGATCTCTGA[A/G]AACTGTGAGACAATG | 26054 |
rs753717917 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708646 | ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 26054 |
rs753732494 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702091 | CAGGGATTGTTTGCA[A/C]AAGTAAATACAGGCT | 26054 |
rs753741154 | snp | G/T | 1.7357e-05 | 0.00294588 | intron-variant | SENP6 | GRCh38.p7 | 6:75678789 | GATTTGTTTATTTGC[G/T]TGCCTTCTAATTTTG | 26054 |
rs753754011 | snp | A/G | 1.65919e-05 | 0.00288022 | intron-variant | SENP6 | GRCh38.p7 | 6:75713481 | TTGTAATATTATGAA[A/G]TATTCGACTTTTGGT | 26054 |
rs753768852 | snp | A/G | 1.71026e-05 | 0.00292421 | intron-variant | SENP6 | GRCh38.p7 | 6:75623976 | GCAAGTGTTGCTTAA[A/G]ATATTTTCTTCTTTT | 26054 |
rs753770425 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695362 | ATCGGATAGTTATCA[A/C]ACTTTGCTAATAACT | 26054 |
rs753791555 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605108 | ACCATAATTTGCTGC[A/G]TATTTTGTATTACCA | 26054 |
rs753792091 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632109 | AGTTAAGCTGTCCTT[C/T]CATGTTTTATGCCCT | 26054 |
rs753796914 | snp | A/G | 3.37701e-05 | 0.004109 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711343 | GATGATAGCAGTGAC[A/G]ATGGATTCCTCGCTG | 26054 |
rs753802036 | in-del | -/AGTTGT | 3.49858e-05 | 0.00418231 | intron-variant | SENP6 | GRCh38.p7 | 6:75678798 | TTTGCTTGCCTTCTA[-/AGTTGT]ATTTTGTTACAGGTT | 26054 |
rs753803580 | snp | A/G | 1.66194e-05 | 0.00288261 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709577 | GAATCACCTGAAGCT[A/G]GTAAAATGCTTGAAG | 26054 |
rs753814567 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626559 | AATAGAGATTTTTTT[-/C]CCCCAGTCTTTTGCT | 26054 |
rs753836195 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702025 | GTTGCAAAGTGACAT[C/T]ACTTGCCAGAAAAAG | 26054 |
rs753854282 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694863 | AGAGTGTGCCCTTGG[-/T]TTTTTTTTAATTTAT | 26054 |
rs753861348 | in-del | -/CACAC/CACACAT/CACACATAT/T | 0.000137736 | 0.00829777 | intron-variant | SENP6 | GRCh38.p7 | 6:75713861 | CTGCTATAATAAATA[-/CACAC/CACACAT/CACACATAT/T]ATAAAATAGTGCATT | 26054 |
rs753872294 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654730 | TACTTATTTTTCAGC[A/G]TATTAGTAGTATCAC | 26054 |
rs753872451 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669984 | TGTTGCCCAGGCTGG[A/C]GTGCGGTGGTGCGTT | 26054 |
rs753925218 | snp | A/G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668502 | TAGAATTCAAAAAAA[A/G/T]TAGTAATCCAAGTAG | 26054 |
rs753932099 | in-del | -/TTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626127 | TAGAGAGTTAGGTTT[-/TTT]GTTGTTGTTGTTGTT | 26054 |
rs753952445 | snp | C/T | 1.71879e-05 | 0.00293149 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621642 | TAAGGATTTTTTTTT[C/T]CCTCAGATGTTTTAT | 26054 |
rs754028050 | snp | A/G | 1.83363e-05 | 0.00302784 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677235 | AGGAAGTTGTGGGCA[A/G]AAGGAAAACAAAATT | 26054 |
rs754045028 | in-del | -/ATC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75679973 | GATCAGAGAAATGAT[-/ATC]ATAATTGAATTTCTG | 26054 |
rs754076474 | in-del | -/AT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666155 | ATATATATAAAACAT[-/AT]ATGATATATATATAA | 26054 |
rs754088629 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626706 | ATGTAGTTTTGCTAG[A/G]TACTGCCAAATTCCC | 26054 |
rs754123199 | snp | A/G | 1.82723e-05 | 0.00302256 | intron-variant | SENP6 | GRCh38.p7 | 6:75709490 | ATGAGTGATAGACAT[A/G]GCCTTTTTTATTATG | 26054 |
rs754135870 | in-del | -/GTGA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648241 | TACTGGAAAATCATG[-/GTGA]GTAAGTATTTATATT | 26054 |
rs754136700 | snp | C/G | 1.65833e-05 | 0.00287948 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715468 | AAAAAGAGAAGAAAT[C/G]CGAAACATAATTCTG | 26054 |
rs754137156 | snp | A/C | 1.79332e-05 | 0.00299437 | intron-variant | SENP6 | GRCh38.p7 | 6:75697398 | TAGAAATATTTCAGA[A/C]GCTTATAATTTATCT | 26054 |
rs754154175 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672666 | TTCCTTATATTTTGT[A/G]GTGAAATGATTTATC | 26054 |
rs754190970 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607019 | ATAGGAGAGCGGTGC[A/C]AGATGATACTGGAGG | 26054 |
rs754275417 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691768 | CCTGGCTAATTTTTT[C/G]TATTTTTAGTAGAGA | 26054 |
rs754309107 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707206 | GCTGCTGGAAGTAAC[C/T]TGATTATAACTGACT | 26054 |
rs754317341 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697966 | GTGGACTACTTGAAG[C/T]AGTTTCTGAGTAAAT | 26054 |
rs754343928 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627756 | TCTCAGCTCACTGCA[A/G]CCTCCACCTCCTGGG | 26054 |
rs754346919 | snp | C/G | 1.65839e-05 | 0.00287953 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666915 | AATACAGTTACATTG[C/G]CAAGAAAAGCAAGAA | 26054 |
rs754352104 | snp | C/G | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663296 | AGAACGTCAATTCAT[C/G]AGAATTCTGGAGGAC | 26054 |
rs754369750 | snp | A/G | 1.74105e-05 | 0.00295042 | intron-variant | SENP6 | GRCh38.p7 | 6:75713870 | ATAAATAATAAAATA[A/G]TGCATTTGACTTTAC | 26054 |
rs754400144 | snp | C/T | 1.65677e-05 | 0.00287812 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666818 | CCCTGCACCATCCAC[C/T]GGAAAAGTAGAAGCA | 26054 |
rs754400299 | snp | A/G | 1.71343e-05 | 0.00292692 | intron-variant | SENP6 | GRCh38.p7 | 6:75678564 | GACTGTAAATTGCTA[A/G]TTTAATTTCCTTTAC | 26054 |
rs754406686 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711114 | ACAATTTGTTATAAA[C/T]CTCTGGTAGTTTATT | 26054 |
rs754420654 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613277 | ATTACATGAAATTCA[A/G]ATGTCACTGCCCTTA | 26054 |
rs754435049 | snp | C/T | 3.7255e-05 | 0.0043158 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678850 | AGCTAAGGGAGGCAT[C/T]TCTGTTACCAATGAG | 26054 |
rs754443071 | in-del | -/TGCAGTAATTTTTC | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718131 | AGCCACCAAAATGAA[-/TGCAGTAATTTTTC]TTTAAAAAAATGATC | 26054 |
rs754460088 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674037 | AATAAATAAATGAAT[A/G]AGTGAATGCTTTATG | 26054 |
rs754483779 | snp | G/T | 1.74619e-05 | 0.00295477 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675448 | AGTTTTGTTTAGATT[G/T]TATCAAGATACAGCT | 26054 |
rs754568103 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667364 | ACAGTGTATCTAGGA[C/T]AACTATTTGTAATGC | 26054 |
rs754599032 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605096 | ATAAAATATTCCACC[A/G]TAATTTGCTGCATAT | 26054 |
rs754601446 | snp | C/T | 1.95314e-05 | 0.00312495 | intron-variant | SENP6 | GRCh38.p7 | 6:75634667 | AATGTGTATATAATT[C/T]TTCCGTGTTCAAGTT | 26054 |
rs754607612 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611078 | TTCAAAAATCTACAA[C/T]TTTCTACCTTCATAA | 26054 |
rs754626669 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612165 | AGTTCCATGTCTGCA[-/G]TCTAAAGACCTCTTC | 26054 |
rs754661208 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643834 | TAAAATAAATAAGAC[-/TT]GATTCATTTTCATAG | 26054 |
rs754675955 | snp | C/T | 0.000132919 | 0.00815119 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695837 | ACTGAAGAAGGAAGA[C/T]GCTGACCGAATTCAT | 26054 |
rs754686915 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643538 | TTCAAGAAATTCAAC[A/G]TGGTAAAACCCCGCC | 26054 |
rs754698926 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623348 | ACCTGTTAATAGATA[A/C]ATTAGTTTAATCTTC | 26054 |
rs754700789 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706779 | CAACAAGTGTTGACT[A/G]CTTATGTCAGATAAC | 26054 |
rs754716149 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681870 | CCTCATCTCTACAAA[A/C]AAACAAAAATATAAA | 26054 |
rs754723593 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659471 | AATATTAGTTTCAGT[A/G]CTTATTAAATTCTAG | 26054 |
rs754754279 | snp | C/T | 4.47738e-05 | 0.00473127 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677255 | AAAACAAAATTAAAA[C/T]TGTAATTATGTTTTT | 26054 |
rs754763006 | snp | A/G | 1.70467e-05 | 0.00291943 | intron-variant | SENP6 | GRCh38.p7 | 6:75709520 | GTAATGTTTCTTATT[A/G]ATACAGATGGCTTAA | 26054 |
rs754767639 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694204 | GAAGTTGTGGTGAGC[C/T]GAGATCATGCCATTG | 26054 |
rs754786414 | in-del | -/T | 0.000315557 | 0.012557 | intron-variant | SENP6 | GRCh38.p7 | 6:75675688 | GAAAAAATAAAAAAG[-/T]TTCTTTAAGGCAGTT | 26054 |
rs754789198 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695455 | TACAAAGCGAACTGT[A/G]GCCGGGCGCCATGGC | 26054 |
rs754845724 | in-del | -/TAGATTCAAA | 3.51259e-05 | 0.00419067 | intron-variant | SENP6 | GRCh38.p7 | 6:75678802 | CTTGCCTTCTAATTT[-/TAGATTCAAA]TGTTACAGGTTGATA | 26054 |
rs754851133 | snp | A/T | 1.65875e-05 | 0.00287984 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621559 | CAGAGTCTAAGAGAG[A/T]TGGAGGTTTTAAAAA | 26054 |
rs754870821 | snp | A/G | 1.75946e-05 | 0.00296598 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621656 | TCCCTCAGATGTTTT[A/G]TAAGAATAAAACTTC | 26054 |
rs754900765 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634255 | TTTCAAGTCAGTGGC[-/A]AAAATCAGAAATAGT | 26054 |
rs754902774 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616617 | CGGGCGTGGTAGCAT[C/G]CGCCTGTAATCCCAG | 26054 |
rs754904221 | snp | C/T | 6.00066e-05 | 0.0054772 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659264 | CTCCTTCCTTTAGAA[C/T]GTATAATGAAGAAAA | 26054 |
rs754915767 | in-del | -/ATTTTTGCTC | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601111 | TGACATTTAGCATAG[-/ATTTTTGCTC]ATTTTTGTTTTTTAA | 26054 |
rs754921182 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705924 | AAAGCTATTTTTGAG[-/C]CTTTTTTTTTTTTTT | 26054 |
rs754968970 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647855 | AATTGCTGTATGAAA[A/G]GTACAATGGAGATAC | 26054 |
rs754977831 | snp | A/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718273 | TAAAGAACATATTTT[A/G]ATATATAATATGACC | 26054 |
rs754979153 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612303 | CATAAAATTGCTTTT[C/T]GAACATACACATTTA | 26054 |
rs754999810 | snp | A/G | 0.000140964 | 0.00839418 | intron-variant | SENP6 | GRCh38.p7 | 6:75675762 | GCATAATAAATATGT[A/G]CTTACATTTACTTAA | 26054 |
rs755015453 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654938 | AGTCATCCCTTACTA[C/T]GTTAATTCATCTTAT | 26054 |
rs755017013 | snp | A/G | 1.71e-05 | 0.00292399 | intron-variant | SENP6 | GRCh38.p7 | 6:75647706 | ATTTCCTGTTAGAAT[A/G]AAACTACATAAATTT | 26054 |
rs755028692 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632238 | CCTTAGTAGCTACTA[A/G]TAGAGGAGTGGTTAA | 26054 |
rs755100397 | snp | A/G | 1.76502e-05 | 0.00297066 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715644 | ACTAAATGACTTTCA[A/G]ATTTGGGTATAGACA | 26054 |
rs755131371 | snp | A/G | 1.65756e-05 | 0.00287881 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702842 | TTAAGAAGATGCTAA[A/G]CAAAAAACATTGCAT | 26054 |
rs755135132 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618014 | ACCATATTAAAGGGT[A/G]CATGCCATGAATAAG | 26054 |
rs755140468 | snp | A/G | 3.43236e-05 | 0.00414254 | intron-variant | SENP6 | GRCh38.p7 | 6:75635039 | GACCTGTTGTATTGC[A/G]TTATAATCCAGAGAA | 26054 |
rs755163486 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635797 | ATAAAAGGAGAGTAA[-/T]TAGGGGAGAGAAAAA | 26054 |
rs755166746 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621736 | TATTCTTAAGAAAAC[-/AT]ATAACTCTTTCACAG | 26054 |
rs755186868 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672774 | CTTATTATTAGATAA[C/T]TTAATCATTTTAATT | 26054 |
rs755189527 | snp | A/T | 3.31917e-05 | 0.00407367 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670617 | CTCAAGAACCTCCAG[A/T]TGCTTTAGCTTTAAG | 26054 |
rs755192315 | snp | A/G/T | 3.3166e-05 | 0.00407211 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715529 | AGAAAGCATAAGGAC[A/G/T]CTTACTCAACAGAAG | 26054 |
rs755203775 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606274 | AAAAGCACACTAAAA[G/T]TGTATGGATTTCATT | 26054 |
rs755204666 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687372 | CGGAGAAGTTTGTTA[-/TT]ACTGACCTCCTGAAG | 26054 |
rs755262814 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656103 | GCCTGTAATCCCAGC[G/T]ACTCAGGAGGCAGAG | 26054 |
rs755343856 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662422 | TTACAGACCTGAGCC[A/T]CCATGTCCAGGTTTA | 26054 |
rs755371941 | snp | C/T | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678872 | ACCAATGAGGACCTG[C/T]ACTGTCTAAATGAAG | 26054 |
rs755379434 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626523 | GATATACTGTAGATA[C/T]TCAGTTTGTCCCTAC | 26054 |
rs755379754 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650885 | AATTTTCTCCTAAAC[A/G]ATATCATGGTCTTTC | 26054 |
rs755430958 | snp | A/G | 1.72502e-05 | 0.0029368 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677140 | AAGAATAACATCTCC[A/G]ATTTTTTTGCGAAAA | 26054 |
rs755467278 | snp | C/G | 1.67503e-05 | 0.00289393 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663446 | GGAAAAGTCATTTTA[C/G]CTGGGGCAAAAATAC | 26054 |
rs755474108 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651366 | TTTTGCTTTTTGTTC[A/G]TTTTTGAGACAGGGT | 26054 |
rs755488357 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602710 | GGGATGAGCGATGAC[C/G]GGGAGGGAGTGTGCT | 26054 |
rs755499866 | snp | C/T | 6.64662e-05 | 0.00576443 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663352 | AACCAAGAAGTTTTA[C/T]GGCAACAATGTGGAA | 26054 |
rs755519155 | snp | C/T | 1.66358e-05 | 0.00288402 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675942 | TGTCCGAAAATTACC[C/T]GTAGTGTTTCTTCAA | 26054 |
rs755531015 | snp | G/T | 0.000401848 | 0.0141691 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602557 | CGGCGGTAGCGCAGG[G/T]GAGATTACTTTTCTG | 26054 |
rs755572041 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649100 | CACCTGAGGTCAGGA[A/G]TTCGAGACCAGCCTG | 26054 |
rs755577406 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624355 | AGTTGTCAACTTTTT[A/G]ATTTTTTTCTAAAAT | 26054 |
rs755579481 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613392 | GGACTGTATGGACTA[C/T]ACAGTGTAAGATATT | 26054 |
rs755615414 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685592 | CAAGAGATTCTGGTA[C/T]GTTGTGCCTTTGTTC | 26054 |
rs755625296 | snp | C/T | 1.66538e-05 | 0.00288559 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659357 | TGTAGTACCTATCAG[C/T]CTACTCCTCCTCTAT | 26054 |
rs755634599 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687422 | TCAAAGTCATTCTCC[A/G]TCCAGCTTTGTTCCG | 26054 |
rs755664738 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698888 | TGGTGGTGCGTGCCT[A/G]TAATCCCAGCTACTC | 26054 |
rs755673884 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673911 | CCGTAACCCCAGCTA[A/C]TAGGGAGGCTGAGGC | 26054 |
rs755689036 | snp | A/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601249 | TCCATATTTCCTTGA[A/T]TGAGAATGTATTATT | 26054 |
rs755778664 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657945 | TTGAAACAGGAACTT[C/T]TGCTTGCCAAAAGAT | 26054 |
rs755779767 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607969 | GGTTTCTAGTTTCTG[C/G]CTACTTAGGGGAATA | 26054 |
rs755783668 | snp | C/G | 1.7556e-05 | 0.00296272 | intron-variant | SENP6 | GRCh38.p7 | 6:75675818 | CATTCATGATATTAC[C/G]CTCTTAAGAATTATT | 26054 |
rs755787687 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639697 | TTTCATGAACTATGG[A/G]GAAGGGTGGAACTTT | 26054 |
rs755806014 | snp | A/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619743 | CTAGCAATGCACAAG[A/T]GTTCCAGTTTCTCCC | 26054 |
rs755807950 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637945 | CACTCACTGCAGCCT[C/G]CACCTCCTAGGTTTA | 26054 |
rs755849330 | snp | A/G | 1.72044e-05 | 0.0029329 | intron-variant | SENP6 | GRCh38.p7 | 6:75678779 | TATATATATAGATTT[A/G]TTTATTTGCTTGCCT | 26054 |
rs755883068 | snp | A/G | 1.89737e-05 | 0.00308002 | intron-variant | SENP6 | GRCh38.p7 | 6:75666992 | ATGCCTCCATTTTGG[A/G]GTGTAAATTTTTTTT | 26054 |
rs755890752 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609154 | CTGTAGCCTGGGACC[C/T]GACTTAATAGCTTCA | 26054 |
rs755909236 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617935 | TCTGATGTTTTCTTA[C/T]GATTAAACTGGGATT | 26054 |
rs755940663 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644702 | GTTGGCCAGTCTGGC[C/T]GCGAACTCCTGGCCT | 26054 |
rs755946341 | in-del | -/T | 3.47929e-05 | 0.00417076 | intron-variant | SENP6 | GRCh38.p7 | 6:75675482 | CGGTAAGCTATTTTA[-/T]GTCTTTTTACTTACC | 26054 |
rs755966345 | in-del | -/TC | 1.71141e-05 | 0.00292519 | intron-variant | SENP6 | GRCh38.p7 | 6:75659425 | AAGTAGAGAAATTAT[-/TC]TTTGTTGCTAATCAG | 26054 |
rs755970518 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616613 | AGCCGGGCGTGGTAG[-/C]CATGCGCCTGTAATC | 26054 |
rs755986588 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707027 | ATTGAGAGAACCACT[-/G]GATCAAGTCATCACC | 26054 |
rs755992472 | snp | A/G | 4.99904e-05 | 0.00499927 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709604 | GAAGATGAACTCGTC[A/G]ACTTCTCAGAAGATC | 26054 |
rs756023605 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630410 | GAAACTACCGGCAAG[A/G]AAAAGCACAAAACAC | 26054 |
rs756045339 | snp | A/C/G | 6.63596e-05 | 0.00575986 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678638 | AATTTCAGTTTTTTG[A/C/G]TGAAGAAGAAGAAAC | 26054 |
rs756072743 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654607 | ATGATGGAGAAAACC[A/G]TTTTTCTAGTTTGTC | 26054 |
rs756078376 | snp | A/G | 1.7989e-05 | 0.00299903 | intron-variant | SENP6 | GRCh38.p7 | 6:75711310 | TTTTCAGTATTAACA[A/G]TAGGCTGTCTTTTAT | 26054 |
rs756078649 | snp | A/T | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717999 | TTATTTCAAGTTCAC[A/T]TAACCCTAAAAAAGG | 26054 |
rs756097349 | snp | A/G | 1.65993e-05 | 0.00288086 | intron-variant | SENP6 | GRCh38.p7 | 6:75623896 | CCCCTTATTTTCTGT[A/G]TAGTGGGACAAATCT | 26054 |
rs756150201 | snp | A/G | 1.65853e-05 | 0.00287964 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621667 | TTTTATAAGAATAAA[A/G]CTTCTCATTAGAAAA | 26054 |
rs756183940 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631867 | CCCCCTTAAAGACTC[C/G]CAGTGAATGACTGAG | 26054 |
rs756193221 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700856 | TGAGATGTGACTTTA[C/T]AAATAAAATAAAATT | 26054 |
rs756194195 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656757 | AAAGTCTCAGCTTAA[C/T]TTTCTTAATTATGTC | 26054 |
rs756224987 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640056 | TGAATTTTTCAGATA[C/T]TGAGAATTATGTCCA | 26054 |
rs756265587 | snp | C/G/T | 0.000101611 | 0.00712706 | intron-variant | SENP6 | GRCh38.p7 | 6:75602583 | TTCTGGAAGGTACGT[C/G/T]TGTTTCTGCCCTTGA | 26054 |
rs756267425 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630048 | AATGAATGAGGGCCA[C/G]AATGTGCAACTTGTG | 26054 |
rs756271354 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716314 | CAGGTTAAAACTATT[G/T]TGGTAAGTGCAGCTT | 26054 |
rs756279620 | snp | A/T | 1.66322e-05 | 0.00288371 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621520 | ACTTACTGCAGTTTG[A/T]TTTTATTTCAGCTTT | 26054 |
rs756292383 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691093 | AGCGATCCTCCCACC[-/T]TTGGCCTCCAAAGTG | 26054 |
rs756300169 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654549 | GAATGTGATAGATAC[A/G]TGACTTTAGTTTTAT | 26054 |
rs756325031 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633413 | TGCATTGTCTTTAGG[-/A]AAAAAAAAAGTAGGC | 26054 |
rs756356154 | snp | C/T | 1.67349e-05 | 0.0028926 | intron-variant | SENP6 | GRCh38.p7 | 6:75647722 | AAACTACATAAATTT[C/T]TTTTTTAGGAAAGAA | 26054 |
rs756366043 | snp | A/G | 7.67283e-05 | 0.00619341 | intron-variant | SENP6 | GRCh38.p7 | 6:75634672 | GTATATAATTTTTCC[A/G]TGTTCAAGTTATTTT | 26054 |
rs756388572 | snp | A/G | 6.6433e-05 | 0.00576299 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695845 | AGGAAGACGCTGACC[A/G]AATTCATATATTCAG | 26054 |
rs756422272 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701966 | CTTTAAGATGGATAG[C/T]TTTCCATCTTTTTAC | 26054 |
rs756427016 | in-del | -/A | 0.000207147 | 0.010175 | intron-variant | SENP6 | GRCh38.p7 | 6:75602623 | GGGAGGGTATACTGG[-/A]AAACGTGGCCCCCAG | 26054 |
rs756462502 | snp | A/C | 3.31461e-05 | 0.00407086 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713713 | TTAAAAAAGGAAGCA[A/C]AAGAAGTTTTTCCAA | 26054 |
rs756490167 | snp | A/G | 9.99034e-05 | 0.00706695 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675932 | AATGGTGTAATGTCC[A/G]AAAATTACCTGTAGT | 26054 |
rs756492692 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621188 | AGAAGGCAAGCAAAC[-/TA]TTTATAGGTACTTAT | 26054 |
rs756513691 | snp | A/T | 6.94288e-05 | 0.00589148 | intron-variant | SENP6 | GRCh38.p7 | 6:75713862 | CTGCTATAATAAATA[A/T]TAAAATAGTGCATTT | 26054 |
rs756526656 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641582 | TCTTTTAGAGGATAT[A/T]TGAATGGTATAAATG | 26054 |
rs756530246 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690356 | CAATATGTATACATT[C/T]CCTTCCTTAAAAAGG | 26054 |
rs756539335 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669617 | TTACATACCTATATG[A/C]AGTGTTTATGATAAA | 26054 |
rs756561999 | snp | C/T | 1.65721e-05 | 0.0028785 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666793 | AGCCTGCTGATTCAG[C/T]ATGTTCTTCCCCTGC | 26054 |
rs756569468 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624059 | TAAACCCCAGTTACC[C/T]ACTTTCTCCACTCCA | 26054 |
rs756580478 | snp | G/T | 0.000613685 | 0.0175062 | intron-variant | SENP6 | GRCh38.p7 | 6:75676997 | TTTACTTCTTTTGTG[G/T]TTTTTTTTGGACTTA | 26054 |
rs756607043 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709424 | AGATTTTGTGTTCTT[C/G]ACTACTGTATCATTA | 26054 |
rs756653593 | snp | A/G | 3.32757e-05 | 0.00407881 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663377 | GTGGAAAAGGTTCCA[A/G]TTGATATTATTGTGA | 26054 |
rs756723141 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712449 | CTGAAGACCAAAGCA[-/G]GAGGACCGCATGAGG | 26054 |
rs756724519 | snp | A/G | 3.44905e-05 | 0.0041526 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677221 | GAAGAGAGCATCAAA[A/G]GAAGTTGTGGGCAAA | 26054 |
rs756728705 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625501 | AAATATATTTCCTTA[C/T]GTCATCAGATGTATC | 26054 |
rs756748511 | in-del | -/TGAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707011 | CTCAGGAACTGACAC[-/TGAT]TGAGAGAACCACTGA | 26054 |
rs756756276 | in-del | -/TG | 5.21735e-05 | 0.00510725 | intron-variant | SENP6 | GRCh38.p7 | 6:75647688 | TTTCATTTTGAAAAC[-/TG]TATTTCCTGTTAGAA | 26054 |
rs756763975 | snp | A/C | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695913 | AGAAATCATGAAACA[A/C]CTAATCTGTCGTAAG | 26054 |
rs756814992 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604236 | TTTTACTTTATTCTA[A/G]TCTAAGGGTCTTTGA | 26054 |
rs756823297 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687396 | TCCTGAAGCCTGCTT[C/T]TGTCAACTCGTCAAA | 26054 |
rs756852752 | in-del | -/CAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656213 | AGCAAGACTCCGTCT[-/CAA]AAAAAAAAAAAAAAA | 26054 |
rs756933200 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670337 | CCATACTATTACTCA[A/G]ATTTAAATAACAACC | 26054 |
rs756971049 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635019 | AATAGAGAATTTTTC[A/G]CTAAGACCTGTTGTA | 26054 |
rs756971637 | snp | C/T | 1.66788e-05 | 0.00288775 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675987 | TTATCAAAAGCTGAG[C/T]ATCCAACTGCAAATG | 26054 |
rs756987394 | snp | C/G/T | 3.67689e-05 | 0.00428758 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670697 | GTAGGAACACTCTTC[C/G/T]GGCTGTTAATAGAGC | 26054 |
rs756988193 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685435 | TGCTAGCTTTTGAAT[A/T]TGTTTGCTCTTGCTT | 26054 |
rs757035575 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619578 | CTGCTATGAACATTG[A/G]CATACAAGTGTCTGT | 26054 |
rs757098248 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672282 | GGTTTTGCTGGTGAT[C/T]TAGACATTTAATTAG | 26054 |
rs757161819 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616177 | GGGATCTCTCCTTAA[C/G]CTTTTTCTTTCCATC | 26054 |
rs757172033 | snp | A/G | 1.65897e-05 | 0.00288003 | intron-variant | SENP6 | GRCh38.p7 | 6:75713483 | GTAATATTATGAAGT[A/G]TTCGACTTTTGGTCA | 26054 |
rs757179270 | snp | A/G | 1.66225e-05 | 0.00288287 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670632 | ATGCTTTAGCTTTAA[A/G]CTGCCAAAGTTCCTT | 26054 |
rs757187259 | snp | G/T | 1.7409e-05 | 0.00295029 | intron-variant | SENP6 | GRCh38.p7 | 6:75678791 | TTTGTTTATTTGCTT[G/T]CCTTCTAATTTTGTT | 26054 |
rs757189951 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688361 | TCCTGGGTGAGGTGA[-/T]TGCCCCGCCCTGCTT | 26054 |
rs757195206 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607383 | TAGGAGATGATTGGA[A/G]TAGAGGACAAAGGTG | 26054 |
rs757205922 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705257 | TAGAACCTGTTAAAT[A/C]TAGTTTTGGCCAGGT | 26054 |
rs757210118 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692218 | ATGAGAGATATGATT[A/G]TTATTTTAAAGTTAA | 26054 |
rs757212981 | snp | C/T | 2.30694e-05 | 0.0033962 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678909 | TTTTAAATGATGTTA[C/T]TATAGACTTTTATTT | 26054 |
rs757215062 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608909 | CTTCTCTTCTATTTG[A/C]ATTTTAGTTTGCATT | 26054 |
rs757216987 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676141 | ATGTGAGTGCACTTT[C/G]ACAGATGCCTTAGGT | 26054 |
rs757239249 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630455 | CTTTGGGCATGGATC[-/A]GGGGCTATGACTGAA | 26054 |
rs757280072 | snp | C/G | 1.76805e-05 | 0.0029732 | intron-variant | SENP6 | GRCh38.p7 | 6:75623987 | TTAAAATATTTTCTT[C/G]TTTTACATTATATAC | 26054 |
rs757328850 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657718 | ATACAATGGGGGAAC[A/G]GAAGTACAAATAACA | 26054 |
rs757351069 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628474 | ATTGGAAATTTATCT[C/T]TTAAAATGGGTGAGG | 26054 |
rs757353595 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644638 | TACAGGCATGTACCA[A/C]CATGCCTGGCTGATT | 26054 |
rs757356969 | in-del | -/A | 3.31636e-05 | 0.00407194 | frameshift-variant, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715511 | GATCAGAGCAAAGAG[-/A]AAAGAAAGCATAAGG | 26054 |
rs757372246 | snp | C/T | 1.82314e-05 | 0.00301916 | intron-variant | SENP6 | GRCh38.p7 | 6:75709492 | GAGTGATAGACATGG[C/T]CTTTTTTATTATGTA | 26054 |
rs757442596 | snp | C/T | 1.72612e-05 | 0.00293774 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621644 | AGGATTTTTTTTTCC[C/T]TCAGATGTTTTATAA | 26054 |
rs757451752 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699556 | GTAGTAGCATGATGT[C/T]GGCTTACTGCAGCCT | 26054 |
rs757497618 | snp | C/T | 1.65897e-05 | 0.00288003 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621551 | GGCTAGATCAGAGTC[C/T]AAGAGAGATGGAGGT | 26054 |
rs757508292 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652540 | TTGATACGTTAATGC[A/C]AAAATGCCTTGTGTG | 26054 |
rs757512201 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614358 | GCAACCTCTGCCTCC[C/G]AGGTTTAAGCCATTC | 26054 |
rs757515346 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715872 | CTAAAATTGCAACTT[A/C]TAAACACAAATAAAA | 26054 |
rs757547841 | snp | A/G | 3.70137e-05 | 0.0043018 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677239 | AGTTGTGGGCAAAAG[A/G]AAAACAAAATTAAAA | 26054 |
rs757584458 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716259 | AAAAAAATTCTTGCA[C/T]ATATTATCATCAAAT | 26054 |
rs757601021 | snp | C/T | 1.68721e-05 | 0.00290444 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677186 | CTAATGGCAGACTTG[C/T]TGCCTGTACAAGAAC | 26054 |
rs757636396 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643970 | GATCCTGGTTTCTAA[A/G]TACCACTCTCCACTA | 26054 |
rs757646436 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623643 | AACTATGATCCATGG[G/T]CTAATCTTGCGTGCC | 26054 |
rs757669811 | snp | A/G | 1.81529e-05 | 0.00301266 | intron-variant | SENP6 | GRCh38.p7 | 6:75697568 | ATCATGTAAATGATG[A/G]CAATTTTTAAATAAT | 26054 |
rs757675067 | in-del | -/GC | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620078 | AGCTTGGGCTACCTT[-/GC]CTCAAAAAAAAAAAA | 26054 |
rs757685340 | snp | A/G | 3.33522e-05 | 0.0040835 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634775 | GTTTTCATCATGCTC[A/G]TGCACAGATACCAGT | 26054 |
rs757706873 | snp | C/G | 1.76325e-05 | 0.00296916 | intron-variant | SENP6 | GRCh38.p7 | 6:75713873 | AATAATAAAATAGTG[C/G]ATTTGACTTTACCTT | 26054 |
rs757721876 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689554 | TACAATATGATCCAG[C/T]AATCCCACTTCTGGG | 26054 |
rs757776173 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674351 | TTTGAGATGATGTCT[C/T]ACTATTTTTGCCCAG | 26054 |
rs757812298 | snp | C/T | 6.87474e-05 | 0.00586251 | intron-variant | SENP6 | GRCh38.p7 | 6:75634694 | AGTTATTTTTTGTTT[C/T]TTGAATCTGCAGTGA | 26054 |
rs757845815 | in-del | -/A | | | frameshift-variant, intron-variant | SENP6 | GRCh38.p7 | 6:75702911 | CCCTCGTTATAAGAG[-/A]AAACATATGCAGTGT | 26054 |
rs757862783 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667528 | ATTAAGGAAAATGAA[A/G]TATAACTGTATTCAA | 26054 |
rs757864232 | snp | C/T | 4.9831e-05 | 0.00499129 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703007 | CTACATCCCAGAAAG[C/T]TGCTGATAGGACTAA | 26054 |
rs757872641 | snp | C/G | 3.32276e-05 | 0.00407586 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666925 | CATTGCCAAGAAAAG[C/G]AAGAATGAAAGACCA | 26054 |
rs757875388 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611139 | TGGAGACAAGATGAA[C/G]GTACTACTTAACTAC | 26054 |
rs757895932 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706949 | TGTACGCTTAAACTC[C/T]AGAATCACACTCAAC | 26054 |
rs757929357 | in-del | -/AGATAC | 6.64794e-05 | 0.00576501 | cds-indel, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621611 | AGAAGAAAGTGAAGG[-/AGATAC]AGATAAAGAGTAAGG | 26054 |
rs757930644 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648658 | TATACTTTACATACT[A/G]AGCATAGTTAAGCTT | 26054 |
rs757932183 | snp | C/T | 2.3583e-05 | 0.00343379 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678919 | TGTTATTATAGACTT[C/T]TATTTGAAGTAAGTT | 26054 |
rs757959567 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625203 | TGCCACCTCTGTCTC[C/T]CGGGTTCAAACAATT | 26054 |
rs757977200 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694441 | AATGATAACAGCTTT[A/C]CTTAGATATAATACA | 26054 |
rs757978880 | snp | A/C | 3.31549e-05 | 0.0040714 | intron-variant | SENP6 | GRCh38.p7 | 6:75713497 | TATTCGACTTTTGGT[A/C]ATTTTTACCCTGCAG | 26054 |
rs757980611 | in-del | -/A | 1.92706e-05 | 0.00310402 | intron-variant | SENP6 | GRCh38.p7 | 6:75634933 | TGTCTGTAGAGAGAT[-/A]TATCTCTGAAATAAT | 26054 |
rs758000719 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633245 | TGTAGTGTTCTCCAG[A/T]TAGCAGCAAGGCCTG | 26054 |
rs758023710 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649158 | GGAAAAAAAAAAAAT[-/A]ACAAAAATTAGCTGG | 26054 |
rs758023797 | snp | C/T | 3.63696e-05 | 0.00426421 | intron-variant | SENP6 | GRCh38.p7 | 6:75663546 | CTCCCTTTAATATTG[C/T]TTATATCAATCCAGT | 26054 |
rs758060457 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704809 | TGCCCCTGGTTTATC[A/G]AGACTAGAGAATGGT | 26054 |
rs758068917 | snp | G/T | 1.68806e-05 | 0.00290517 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711371 | CTGATGACAACTGCA[G/T]TTCAGAAATAGGACA | 26054 |
rs758078754 | snp | C/T | 5.0078e-05 | 0.00500365 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663418 | CAGTAAACACACTTA[C/T]TTACAGACTAATGGA | 26054 |
rs758115485 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661869 | CCAGTCTGGCCAATA[C/T]GGTGAAATCCCGTCT | 26054 |
rs758147961 | snp | A/T | 1.65679e-05 | 0.00287814 | intron-variant | SENP6 | GRCh38.p7 | 6:75659241 | TAAAACTTAAAGTTT[A/T]TTTTTTTCTCCTTCC | 26054 |
rs758208957 | in-del | -/CATT | 1.75863e-05 | 0.00296527 | intron-variant | SENP6 | GRCh38.p7 | 6:75713872 | AATAATAAAATAGTG[-/CATT]CATTTGACTTTACCT | 26054 |
rs758255314 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685111 | GAGATTCAACTTCTT[C/T]CTGGTTTAGTCTTGG | 26054 |
rs758256014 | snp | A/G | 0.000149799 | 0.00865315 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703021 | GTTGCTGATAGGACT[A/G]AAAGTGAGAATGGCC | 26054 |
rs758277840 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655297 | CAGATCACCCTCACA[C/T]TCTTTCTTTTGAAAT | 26054 |
rs758306714 | snp | A/G | 5.71706e-05 | 0.00534622 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670706 | CTCTTCCGGCTGTTA[A/G]TAGAGCCTGTAATTG | 26054 |
rs758311047 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656360 | TCAGCATAATGTCAC[A/G]TGGTTTTTGTCTTAA | 26054 |
rs758318806 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75683108 | CCATTCTAACTGGCA[C/T]GAGATGGTTATCTCA | 26054 |
rs758344169 | snp | A/G | 1.79519e-05 | 0.00299593 | intron-variant | SENP6 | GRCh38.p7 | 6:75675421 | GAGCAATACTAATTC[A/G]TCTTTTTTTTTAGTT | 26054 |
rs758348365 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638244 | TCCCTTTTCTTTTGT[-/TT]TTTTTTTTTTTAATT | 26054 |
rs758385162 | in-del | -/TTATAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682420 | CTTTTTTTTTTTTAA[-/TTATAC]TTTAAGATCTATGGT | 26054 |
rs758393627 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662697 | GCATATGGTAATAGC[C/T]CAGAACATACTTCTG | 26054 |
rs758394560 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606572 | AAAAATAATAAAATA[A/T]TACTTTTAAATGTAA | 26054 |
rs758396914 | in-del | -/GTTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675570 | GAATTTATTAAGATG[-/GTTA]GTTGTTACATATATC | 26054 |
rs758398634 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619314 | GGGTACTTCATATAT[A/G]TGGAATCATACAATA | 26054 |
rs758405065 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691928 | ATGGCACAATCTCGG[C/T]TTACTGCAACATCCG | 26054 |
rs758448377 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697632 | TTTCTGAAATCTCTT[G/T]TGTATATTCATATTT | 26054 |
rs758449501 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618116 | TTGTTTTTCCTCCCT[C/T]TTATGTCTGTGTTTT | 26054 |
rs758491283 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613512 | CTTAATAGCAATATG[A/C]GACATACTAAAATGT | 26054 |
rs758495211 | in-del | -/A | 1.69605e-05 | 0.00291204 | intron-variant | SENP6 | GRCh38.p7 | 6:75697420 | ATTTATCTCTTTCTT[-/A]ACAGAATACAGCAAA | 26054 |
rs758520985 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704249 | GTCTTTGAGTTCTCT[C/T]TGTTTTGGTTGATTA | 26054 |
rs758536273 | snp | A/G/T | 3.48161e-05 | 0.00417218 | intron-variant | SENP6 | GRCh38.p7 | 6:75666967 | CTTTTGTTGACATTT[A/G/T]TTCAGATTAATGCCT | 26054 |
rs758544748 | snp | A/G | 1.65847e-05 | 0.0028796 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715493 | ATTCTGAAGCTACAG[A/G]AAGATCAGAGCAAAG | 26054 |
rs758555772 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627989 | CTTTCAGATTTCTTA[C/T]GATTTTTTGTAAAAG | 26054 |
rs758559915 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607115 | CATTTTGGGAGGCCA[A/G]GTTGAGAGGATTGCT | 26054 |
rs758564488 | snp | C/T | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679168 | TCTATAATCCTGACA[C/T]TTTGGGAGGTCAAGG | 26054 |
rs758606694 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680326 | GGTCTGTGATATAAC[A/G]AAAGGACAGTGCCAA | 26054 |
rs758615024 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632619 | TTTCTAGTCATTTGA[-/T]CTCTTTTCGAACAAA | 26054 |
rs758616255 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614616 | GGAGAGATACTTTGA[A/C]ACCTGTAAATAACTT | 26054 |
rs758644599 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648871 | TAGGGCTAGTAAATG[A/G]CAGAGCTGGTATTGG | 26054 |
rs758705918 | snp | A/G/T | 0.000241077 | 0.0109768 | intron-variant | SENP6 | GRCh38.p7 | 6:75677012 | TTTTTTTTTGGACTT[A/G/T]TATTTATTTCTTTTC | 26054 |
rs758762299 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638082 | GGTCAGGCTGGTCTC[A/G]AACTCTTTACCTCAA | 26054 |
rs758796405 | in-del | -/AAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710757 | GAAGCTTTCTCAAAG[-/AAC]AACAATGACCAAAAA | 26054 |
rs758818588 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650992 | TTTTTTTATAAGTTA[C/T]AGCCACATATCAGTA | 26054 |
rs758823915 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603588 | CTTTTAGTATGTTTC[A/G]GAAAGATTACTGAAT | 26054 |
rs758832200 | snp | C/G | 1.65751e-05 | 0.00287876 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702820 | AACTCTTCTGCCAAG[C/G]CTGTAATTAAGAAGA | 26054 |
rs758889829 | snp | C/T | 1.80856e-05 | 0.00300707 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75702645 | ATTTGTTTTTTACAG[C/T]GCACACTGGTTTTTG | 26054 |
rs758902206 | snp | G/T | 1.6804e-05 | 0.00289858 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676002 | CATCCAACTGCAAAT[G/T]AATAAGGAGGATAAA | 26054 |
rs758933544 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605809 | TAAAAAAAAGTTTGG[C/T]TGCTTTTTGTGGAAT | 26054 |
rs758939639 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602538 | AGATGGCGGCCGGCA[A/G]GAGCGGCGGTAGCGC | 26054 |
rs758954089 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702510 | GGCGTGAGCTACTGC[A/G]CCCGGCCAGAATTAG | 26054 |
rs758954375 | in-del | -/ATAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666153 | TGATATATATAAAAC[-/ATAT]ATGATATATATATAA | 26054 |
rs758972976 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690581 | GTTCAGTTTTGCAAA[A/G]CAAAGTTACTGGAGA | 26054 |
rs758989460 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688805 | AGGCGTGGTGGCTCA[C/T]GCCTATAATCCCAGC | 26054 |
rs758997510 | snp | A/G | 5.37953e-05 | 0.00518601 | intron-variant | SENP6 | GRCh38.p7 | 6:75634976 | ATTATACTATTTTAT[A/G]TCTGCTTTTGAGTAA | 26054 |
rs759023879 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643688 | GATAGTGCCACTGCA[C/T]TCCAGCCTGGGTGAC | 26054 |
rs759084895 | snp | A/T | 1.65663e-05 | 0.002878 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666881 | TGAACTACGAAGCAT[A/T]CCAGAAGACTCAGAG | 26054 |
rs759097240 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624931 | TTAGGCCAGGAGTTT[C/G]AGACTACCTGGACAA | 26054 |
rs759102812 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604791 | ATAATAAAATATTCC[G/T]GCCAGGCGTGGTGGC | 26054 |
rs759111452 | snp | A/T | 0.000103914 | 0.00720737 | intron-variant | SENP6 | GRCh38.p7 | 6:75713857 | TGGATCTGCTATAAT[A/T]AATAATAAAATAGTG | 26054 |
rs759112613 | snp | G/T | 1.66424e-05 | 0.0028846 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634753 | GGAACTGTAGTTCAT[G/T]GTAGACGTTTTCATC | 26054 |
rs759150732 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654192 | TTGAGGCACTGTGAT[C/T]ACGCCTCTGCACTCC | 26054 |
rs759171407 | snp | C/T | 1.69989e-05 | 0.00291533 | intron-variant | SENP6 | GRCh38.p7 | 6:75695961 | TTAACAGATGTAAGT[C/T]ACTCACATTTAACTA | 26054 |
rs759302673 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623349 | CCTGTTAATAGATAC[A/G]TTAGTTTAATCTTCT | 26054 |
rs759311553 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624179 | CACAATTGGTAATAT[-/A]ACTGTGCATGGTTTT | 26054 |
rs759318442 | snp | A/G | 1.6759e-05 | 0.00289469 | intron-variant | SENP6 | GRCh38.p7 | 6:75663206 | TGCCAAAGTTGTGGT[A/G]TTCTTTTTTCTAAGG | 26054 |
rs759326562 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649476 | AGAGAAAAAAGAGCA[G/T]GCTTATTTACTGTTC | 26054 |
rs759328709 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684678 | TTTTTGTCATTGGTT[C/G]TGTTTATACGATGGA | 26054 |
rs759333913 | snp | A/G | 1.82573e-05 | 0.00302131 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676054 | GTAAATAAATTAACA[A/G]GTAAGTTGTGTAAAA | 26054 |
rs759353083 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684918 | CTGGCCTCATAAAAT[G/T]AGTTAGGGAGGATTT | 26054 |
rs759361535 | in-del | -/GTATGA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655659 | TTTTAACATTGCATT[-/GTATGA]GTATAACAAGTTATT | 26054 |
rs759379066 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625907 | ACCCACTTTTATTTG[C/T]TTTGTCTTATTAGAT | 26054 |
rs759393039 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710104 | TTAACCTGACTTGAC[A/G]TTCAAGAAGCAAATG | 26054 |
rs759427542 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601238 | TTTCTGTGCTTTCCA[C/T]ATTTCCTTGAATGAG | 26054 |
rs759449477 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662852 | TTTATTATAGATACT[A/G]AAGTAATGGAGCCAG | 26054 |
rs759482603 | snp | C/T | 1.72427e-05 | 0.00293616 | intron-variant | SENP6 | GRCh38.p7 | 6:75634819 | GCCCAAAGGTAAGAA[C/T]TCTAATTGTCTTTGG | 26054 |
rs759485188 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634618 | GGTAAAGGTTTTTGT[A/G]TGTTTGTTCAGATTT | 26054 |
rs759505637 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698640 | GCTCCTAGCAAAGCT[A/G]TATATTTTTAAATTC | 26054 |
rs759511551 | snp | C/T | 1.67139e-05 | 0.00289079 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697491 | TATTTTTGAGAAGGA[C/T]TTTATTTTTGTACCC | 26054 |
rs759527952 | snp | A/C | 1.67005e-05 | 0.00288963 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675918 | TCTAACTAAATGTGA[A/C]TGGTGTAATGTCCGA | 26054 |
rs759541793 | snp | C/T | 8.94614e-05 | 0.0066875 | intron-variant | SENP6 | GRCh38.p7 | 6:75670771 | TAACATTAAAAATTC[C/T]GTTGCTAAAGCTAAT | 26054 |
rs759542793 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682737 | AAAGGACATGAACTC[A/C]TCCTTTTTTATGGCT | 26054 |
rs759564502 | snp | C/T | 1.65817e-05 | 0.00287933 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702749 | TACAGAAATGTTCAA[C/T]TGTAGAGGACAGTTG | 26054 |
rs759623597 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603657 | TAAACAGGTTCTATA[A/G]GAGGGTGTTGAGGAA | 26054 |
rs759672639 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600116 | TTGTTTCCCATTCCA[C/T]GTGTTGCTGTAACAC | 26054 |
rs759724006 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687568 | TTGATGTTGGTGACC[A/G]ACAGATGGGGTTTTG | 26054 |
rs759738134 | snp | A/G | 1.83249e-05 | 0.0030269 | intron-variant | SENP6 | GRCh38.p7 | 6:75695760 | AGAAATAAATAAAGT[A/G]AACTGTTACATTAAT | 26054 |
rs759749809 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662233 | GAATTATTTAATTTT[A/G]TAAAACGCCTTCCAC | 26054 |
rs759766969 | snp | C/T | 8.29249e-05 | 0.0064386 | intron-variant | SENP6 | GRCh38.p7 | 6:75713601 | GTTCACACTTTATTT[C/T]GTATTCTGATGGGGA | 26054 |
rs759790963 | snp | A/G | 3.85067e-05 | 0.0043877 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678861 | GCATCTCTGTTACCA[A/G]TGAGGACCTGCACTG | 26054 |
rs759795902 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607085 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 26054 |
rs759820135 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704188 | AGAAAGAACAGTGGG[C/T]CCAGGAGAACGGCAC | 26054 |
rs759828568 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608423 | CAATTCATGACACTG[C/T]ACTTCAGCCTGGGTG | 26054 |
rs759883077 | in-del | -/AGG | 2.68583e-05 | 0.00366448 | intron-variant | SENP6 | GRCh38.p7 | 6:75670748 | AAGCTCTTTACTATA[-/AGG]CCAATTATAACATTA | 26054 |
rs759886284 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618917 | AAGACTTATTTCCTC[C/T]TGTTCATGATATTTC | 26054 |
rs759900985 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663807 | TTCCTGCTGATAGTG[-/G]GTTTTTTTTTTTGTG | 26054 |
rs759924928 | in-del | -/TTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75683666 | GAATCCTTTCCCCGT[-/TTC]TTCTTGTTTTTGTCA | 26054 |
rs759927677 | snp | C/T | 9.99817e-05 | 0.00706971 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621513 | AATGAATACTTACTG[C/T]AGTTTGTTTTTATTT | 26054 |
rs759928194 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658213 | TTTGGTGTCTAGGAA[A/C]ATAGACGTGCAAACA | 26054 |
rs759930379 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617242 | GAAGTTTCAATGATG[A/G]TTTGGAGAATTTCTT | 26054 |
rs759936157 | in-del | -/G | 0.000127673 | 0.00798876 | intron-variant | SENP6 | GRCh38.p7 | 6:75676995 | ATTTACTTCTTTTGT[-/G]GTTTTTTTTTGGACT | 26054 |
rs759976301 | in-del | -/AAAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662053 | TGAATCTCCTTCTCA[-/AAAT]AAATAAATAAATAAA | 26054 |
rs759982791 | snp | A/G | 3.31824e-05 | 0.00407309 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647794 | GTTAAGTCGGCTCCA[A/G]GGTGTTGGTAAGTGT | 26054 |
rs759994329 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626552 | ACTGATGAATAGAGA[-/T]TTTTTTCCCCCAGTC | 26054 |
rs760039636 | snp | C/T | 3.32984e-05 | 0.00408021 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709555 | AATCAGACTAAACTA[C/T]AGCGATGAATCACCT | 26054 |
rs760069233 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677999 | GCTGTAAATATAGTT[A/C]AGTGGGTTGAGAAAA | 26054 |
rs760071691 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629885 | CATGTATGCTTTGAT[A/T]AGCAGCAGATATGAG | 26054 |
rs760129247 | snp | G/T | 5.24462e-05 | 0.00512058 | intron-variant | SENP6 | GRCh38.p7 | 6:75703082 | ATACAGGTATGTATC[G/T]AAATGTTTTGAAAGA | 26054 |
rs760150155 | in-del | -/TC | 6.8646e-05 | 0.00585818 | intron-variant | SENP6 | GRCh38.p7 | 6:75713856 | TGGATCTGCTATAAT[-/TC]AAATAATAAAATAGT | 26054 |
rs760165220 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717562 | AGTTATGCTAGTGAC[A/G]TTGCAATATATATTG | 26054 |
rs760172665 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656013 | TGAAGCCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 26054 |
rs760174854 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667295 | GTTTTATATTTTACT[A/G]TAAAAATTTCAAAAA | 26054 |
rs760211511 | snp | C/G | 1.75554e-05 | 0.00296267 | intron-variant | SENP6 | GRCh38.p7 | 6:75634829 | AAGAATTCTAATTGT[C/G]TTTGGTTAGTATATA | 26054 |
rs760248313 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688497 | TGCTGAGAGCTGCAG[A/C]CCGGAGCTATTCCTA | 26054 |
rs760252586 | snp | A/G | 1.7412e-05 | 0.00295055 | intron-variant | SENP6 | GRCh38.p7 | 6:75697544 | TTTCCTTTAAAGGAA[A/G]ATCTTTAAATCATGT | 26054 |
rs760264982 | snp | A/T | 6.72359e-05 | 0.00579771 | splice-acceptor-variant | SENP6 | GRCh38.p7 | 6:75670551 | TTTCTTTTCCTTTTT[A/T]GTTTGGCAATTCTAT | 26054 |
rs760275710 | snp | C/T | 1.6588e-05 | 0.00287988 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715434 | TGGCAAACTGGTTTC[C/T]TCCACCAAGAATGAG | 26054 |
rs760292605 | snp | A/G | 1.6577e-05 | 0.00287893 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702760 | TCAACTGTAGAGGAC[A/G]GTTGTATTTCTTCTT | 26054 |
rs760307496 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653091 | GCTGGTGTGCAATGG[C/T]GCAATCTCAGCTCAC | 26054 |
rs760310889 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654081 | AAAAAAAAATTAGCC[A/T]GGTGTGGTTATGAGC | 26054 |
rs760326621 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701567 | AAAAGAACAAAACTA[C/T]ATATGCAATTCTTAG | 26054 |
rs760368609 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604557 | GAATCGCTTGGAAAC[C/G]GGAGGCAGAGGTTGC | 26054 |
rs760370732 | in-del | -/TAATG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671784 | AGGTATTTTATTATT[-/TAATG]TAATGAATAATAACT | 26054 |
rs760394532 | snp | C/G | 1.66601e-05 | 0.00288614 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634765 | CATGGTAGACGTTTT[C/G]ATCATGCTCATGCAC | 26054 |
rs760435193 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645663 | TCATTTTAGATCATC[A/T]AGCAAAAAGGTTTTA | 26054 |
rs760440543 | snp | C/T | 7.1101e-05 | 0.005962 | intron-variant | SENP6 | GRCh38.p7 | 6:75711466 | ATTTTTAAGTATGCT[C/T]ATAAAACATAACAGG | 26054 |
rs760486436 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675045 | TAGTTAGAAAATACC[A/G]TGTTGTAACCACCAG | 26054 |
rs760491865 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695215 | TGTGTGACAGAGTCT[C/T]ACTCTGTTTCTCAGG | 26054 |
rs760506105 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706429 | TCAAATGAATTAAGG[-/T]ACTTGACTTAAAGCA | 26054 |
rs760553562 | snp | C/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620542 | TCGTGAGAGCTGTGC[C/G]CTCGTGATCTAATCA | 26054 |
rs760585808 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676477 | TTATAATACATAGAT[A/G]TGGTTCTCCAGGTTT | 26054 |
rs760620006 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661212 | ATTTTTCCCACGTTG[A/C]ATGTTTGTAACTCCC | 26054 |
rs760621594 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709956 | TGCCAGGATAAATGT[A/G]TACATGCTGTTGTTG | 26054 |
rs760695416 | snp | C/T | 1.67804e-05 | 0.00289653 | intron-variant | SENP6 | GRCh38.p7 | 6:75676087 | GATTATAATAGATAA[C/T]AATAGATACTGTATT | 26054 |
rs760750701 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660500 | TGATGCTTCAATTGT[C/T]CCAGATTCCATGTGA | 26054 |
rs760753742 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612754 | TACCTATTGAACTTG[A/C]AAATGCACATCCCCA | 26054 |
rs760767756 | in-del | -/TA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709382 | TAAAATAACTTACTT[-/TA]TGTTTGTGATATTAC | 26054 |
rs760788149 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696774 | TGAGCCACCATGCCC[C/T]ACCTTTTTCTTTATA | 26054 |
rs760792123 | snp | C/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599991 | ATCGCTTGAACCTGG[C/G]AGGCGGAGGTTGCCG | 26054 |
rs760809028 | snp | C/T | 1.73066e-05 | 0.0029416 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659301 | AGTCCGAATCACAAG[C/T]GGAGCCTGAAATTAA | 26054 |
rs760829236 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669796 | TCACTGCCACTATAA[C/T]TAGCAGCATTTTACT | 26054 |
rs760864097 | snp | A/G | 0.000146316 | 0.00855201 | intron-variant | SENP6 | GRCh38.p7 | 6:75675698 | AAAAGTTTCTTTAAG[A/G]CAGTTATAAAGATTT | 26054 |
rs760883423 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682604 | TGTTCCCCGCCCTGT[A/G]TCCAAGTGATCTCAT | 26054 |
rs760889795 | snp | A/C | 1.81754e-05 | 0.00301452 | intron-variant | SENP6 | GRCh38.p7 | 6:75703118 | AAAATTCAGAATAAT[A/C]TGGATTTTTTAATAA | 26054 |
rs760898252 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635665 | CAAATAGTGTTCACC[C/T]GAGATGCTTGAGAAA | 26054 |
rs760915502 | snp | A/C | 1.84062e-05 | 0.00303361 | intron-variant | SENP6 | GRCh38.p7 | 6:75675385 | ATAAAAAAGTGAAGC[A/C]TGCCTTTCTTTGTAA | 26054 |
rs760918506 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661908 | AAAACAAAAATTAGC[C/T]GAGCATGGTGGTGGG | 26054 |
rs760920815 | snp | C/G/T | 6.74677e-05 | 0.00580775 | intron-variant | SENP6 | GRCh38.p7 | 6:75695945 | CAAACTCTGAAAATA[C/G/T]TTAACAGATGTAAGT | 26054 |
rs760935384 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617936 | CTGATGTTTTCTTAT[A/G]ATTAAACTGGGATTA | 26054 |
rs760940873 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620092 | TGCCTCAAAAAAAAA[-/AA]AAAAAAAAAAGAGGA | 26054 |
rs760952275 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684688 | TGGTTCTGTTTATAC[A/G]ATGGATTATGTTTAT | 26054 |
rs760981730 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694758 | GTATAAATGTAACAC[-/TT]TATTTTTCCATTTGT | 26054 |
rs760985448 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660031 | TAGAATTGAATTCAG[G/T]GTCATGTGCTGCATT | 26054 |
rs760993533 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634363 | GTGATTCTCCTGCTT[C/T]ATCCTCCCGAGTAGC | 26054 |
rs761006852 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684609 | GTTTTTAGCATGAAG[C/G]GATGTTGAATTTTGT | 26054 |
rs761034211 | snp | A/C | 1.65696e-05 | 0.00287828 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666893 | CATTCCAGAAGACTC[A/C]GAGTTAAATACAGTT | 26054 |
rs761049259 | in-del | -/TTT | 3.3184e-05 | 0.00407319 | cds-indel, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670598 | AAACGTCGTAAAGTG[-/TTT]TCTCAAGAACCTCCA | 26054 |
rs761102583 | snp | A/C | 1.66785e-05 | 0.00288773 | missense, utr-variant-5-prime, intron-variant, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621621 | GAAGGAGATACAGAT[A/C]AAGAGTAAGGATTTT | 26054 |
rs761132824 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642605 | TTGGAGAGACTGGCT[A/G]GGACCTACGTCATAA | 26054 |
rs761154773 | in-del | -/T | 1.81279e-05 | 0.00301059 | intron-variant | SENP6 | GRCh38.p7 | 6:75633547 | TGTCACATTATAGCA[-/T]TTTTGACTCATATTT | 26054 |
rs761165996 | snp | C/G | | | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702935 | GCAGTGTAAAATACA[C/G]TGTGAAAAAAATAAA | 26054 |
rs761185194 | snp | A/T | 1.70977e-05 | 0.00292379 | intron-variant | SENP6 | GRCh38.p7 | 6:75659422 | GGTAAGTAGAGAAAT[A/T]ATTCTTTGTTGCTAA | 26054 |
rs761206332 | snp | C/G | 0.000185925 | 0.00963993 | intron-variant, splice-acceptor-variant | SENP6 | GRCh38.p7 | 6:75622750 | TGGCTAAATATTGTA[C/G]GTGCTTCACTTCTGT | 26054 |
rs761225429 | snp | A/G | 4.99014e-05 | 0.00499482 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709560 | GACTAAACTATAGCG[A/G]TGAATCACCTGAAGC | 26054 |
rs761247493 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619448 | TCCGTTGTGTCTATG[-/TG]TGTGTGTGTGTGTGT | 26054 |
rs761248110 | snp | A/G | 1.73171e-05 | 0.00294249 | intron-variant | SENP6 | GRCh38.p7 | 6:75678557 | CCTAATTGACTGTAA[A/G]TTGCTAATTTAATTT | 26054 |
rs761252292 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626579 | AGTCTTTTGCTATTA[C/T]GTATAAGACTTCACT | 26054 |
rs761266285 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691623 | TTTTTTTTTTGAGAC[A/G]GAGCCTCGCTCTGTT | 26054 |
rs761291722 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657123 | TAATGAAGTATGTTT[A/T]TAAGGAAAAAGCTTT | 26054 |
rs761304881 | in-del | -/TT | 0.000431748 | 0.0146863 | intron-variant | SENP6 | GRCh38.p7 | 6:75676997 | TTTACTTCTTTTGTG[-/TT]TTTTTTTGGACTTAT | 26054 |
rs761305557 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75713999 | TCAAGGCATAAAAAT[A/C]GTATATTTACAGTTC | 26054 |
rs761335272 | snp | G/T | 0.000100195 | 0.00707726 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602503 | CCATGGATTAAGAAG[G/T]AGGCGGCGTGGGAGG | 26054 |
rs761341679 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600912 | TTCATTACACTACTC[C/T]TGCCAATCAGGAAAG | 26054 |
rs761357838 | snp | A/T | 2.62395e-05 | 0.00362202 | intron-variant | SENP6 | GRCh38.p7 | 6:75676988 | AAGTATCTATTTACT[A/T]CTTTTGTGTTTTTTT | 26054 |
rs761360534 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614062 | CCAATTTGCGTTTAT[C/G]TGATGTTTCCTTATG | 26054 |
rs761372661 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652653 | ACCAGTCTGGCCAAC[A/G]TGGTGAAATCCCATC | 26054 |
rs761380539 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698872 | AAAAATTAGCTGGGC[G/T]TGGTGGTGCGTGCCT | 26054 |
rs761415688 | snp | A/G | 1.65762e-05 | 0.00287886 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702782 | TTTCTTCTTCAGCCA[A/G]TGAAATGGAGAGTTG | 26054 |
rs761416224 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627732 | CCAGGCCAGAGGGCA[A/G]TGGTGTGATCTCAGC | 26054 |
rs761437077 | snp | C/T | 0.000117609 | 0.00766749 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621483 | CATATTTGTTTTATA[C/T]TGAATAGCTCTATTA | 26054 |
rs761450201 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688197 | GGGCGTGGGAGCCGC[C/T]GAGCCAGGCACGGGA | 26054 |
rs761456095 | snp | G/T | 3.54648e-05 | 0.00421083 | intron-variant | SENP6 | GRCh38.p7 | 6:75695776 | AACTGTTACATTAAT[G/T]ATATTTGAATTATTT | 26054 |
rs761468531 | snp | A/T | 1.65875e-05 | 0.00287984 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702951 | TGTGAAAAAAATAAA[A/T]CATACTGCGAGTGAA | 26054 |
rs761490198 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700425 | AAGAAATATTAAGAA[C/T]TGTGATAGGCTTTAT | 26054 |
rs761496973 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608880 | AAGAAAAAGAGCTTC[C/G]TTTACTTGCTTGTCT | 26054 |
rs761574753 | snp | A/G | 1.71023e-05 | 0.00292419 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633711 | TTAACATGTTGAGCA[A/G]CAATAAGAAATTGAG | 26054 |
rs761575033 | snp | A/G | 2.40764e-05 | 0.00346953 | intron-variant | SENP6 | GRCh38.p7 | 6:75640708 | CCGAAAAGAAAGGTA[A/G]GCTTAATATTGAAGA | 26054 |
rs761600888 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643237 | ACAAGTCCTATCAGT[A/C]GTTATAATAACTGTA | 26054 |
rs761603571 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629157 | TACTAAAAAAGCTTT[A/G]CCAAGATTTGAATAG | 26054 |
rs761610222 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612087 | GCTTAGCTAGGTGAC[-/T]TTTCTTCTTCATGTA | 26054 |
rs761616369 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652902 | GATTAATGGCCATTT[G/T]AATTTATTTTATTTA | 26054 |
rs761625649 | snp | C/G | 1.6593e-05 | 0.00288031 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666762 | AGAACTAACAGAAGA[C/G]AAAGCATATCTCCTC | 26054 |
rs761630505 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637889 | TTGAGACTGAGTCTC[A/G]CTCTTCTACTGCCCA | 26054 |
rs761641702 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688419 | CTGTCCAACCAGTCC[A/C]AATGAGATGAACTAG | 26054 |
rs761645067 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689509 | TGTGGAAAACAGTGC[A/G]TAGGCTCCTCAAAAA | 26054 |
rs761654210 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622484 | GAATCACTTGAACCC[A/G]GGAGGTAGAGGTTGC | 26054 |
rs761662453 | snp | A/T | 1.65971e-05 | 0.00288067 | intron-variant | SENP6 | GRCh38.p7 | 6:75713610 | TTATTTCGTATTCTG[A/T]TGGGGATGAAGAACT | 26054 |
rs761665170 | snp | A/C | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695916 | AATCATGAAACAACT[A/C]ATCTGTCGTAAGTCA | 26054 |
rs761721536 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689104 | TGGTGGTGCACACCT[A/G]TAGTCCTAGCTATTG | 26054 |
rs761727297 | snp | G/T | 1.66726e-05 | 0.00288722 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713817 | CAGTATGTAGAGAGC[G/T]TTTTTGAGGTGGGTT | 26054 |
rs761792052 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639209 | TAAATACATAGGATA[A/G]GACAGACTAGATTTA | 26054 |
rs761834273 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706420 | AATGTGAATTCAAAT[G/T]AATTAAGGTACTTGA | 26054 |
rs761835430 | snp | C/G | 1.77178e-05 | 0.00297634 | intron-variant | SENP6 | GRCh38.p7 | 6:75663533 | AGTAAGTATTTTACT[C/G]CCTTTAATATTGCTT | 26054 |
rs761856628 | snp | A/T | 1.65737e-05 | 0.00287864 | intron-variant | SENP6 | GRCh38.p7 | 6:75711279 | TTGTTAGGTTATTAG[A/T]TATTTAGATTATATA | 26054 |
rs761871887 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694005 | CTCACGCCTGTAATC[C/T]CAGCACCTTAGGAGG | 26054 |
rs761873091 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682238 | TGTGTGAAGCAAAAA[C/T]TGATAGACCTGAAAG | 26054 |
rs761902966 | in-del | -/AAAATCT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606791 | CCAAAATCCAAAAAA[-/AAAATCT]AAAATCTGAAATCTG | 26054 |
rs761915246 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611656 | GGTTTAATTTCTGGC[C/T]TTAGAAGTTTGTGTG | 26054 |
rs761935996 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708051 | CACAAGAGTTAGATT[A/T]ATGTATCTTTTCTCT | 26054 |
rs761939448 | snp | A/G | 0.000186064 | 0.00964351 | intron-variant, utr-variant-5-prime | SENP6 | GRCh38.p7 | 6:75622820 | CTTCACCGATGAGAT[A/G]TTGATTTGAAGTTTT | 26054 |
rs761943850 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699353 | TTGTTTTTGTTTTTG[-/TT]CTTTTTTTTTTTTTT | 26054 |
rs761969332 | in-del | -/TTTT | 1.71469e-05 | 0.002928 | intron-variant | SENP6 | GRCh38.p7 | 6:75623977 | AAGTGTTGCTTAAAA[-/TTTT]TATTTTCTTCTTTTA | 26054 |
rs762034485 | in-del | -/AAAC | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600390 | TATTTTTAATTAAAA[-/AAAC]AATTTTTCCAAATGG | 26054 |
rs762068654 | snp | A/G | 1.7389e-05 | 0.0029486 | intron-variant | SENP6 | GRCh38.p7 | 6:75659445 | GTTGCTAATCAGATT[A/G]TGTTTTGATTAATAT | 26054 |
rs762083083 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631689 | ACTTTTGTGCTACAA[C/G]AACAGATTTGAATAT | 26054 |
rs762091525 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634091 | ATAGGGGACTTAAAA[A/G]TTTCTTATTCCTCCT | 26054 |
rs762100696 | snp | C/T | 0.000299098 | 0.0122254 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709579 | ATCACCTGAAGCTGG[C/T]AAAATGCTTGAAGAT | 26054 |
rs762102736 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681534 | CGCGATCTTGGCCCA[C/T]GGCAGCCTTTGCCTT | 26054 |
rs762116953 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680316 | CCCTTTTAGAGGTCT[A/G]TGATATAACAAAAGG | 26054 |
rs762119858 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617757 | TTAACACCCTTTTCA[C/T]ATTCGAGAGTCCAAT | 26054 |
rs762121114 | snp | C/G | 8.4122e-05 | 0.0064849 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675901 | ATATTAAATACCTCT[C/G]ATCTAACTAAATGTG | 26054 |
rs762128610 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716812 | AAATACACATATATC[-/A]AAAATAGTTGAGAAT | 26054 |
rs762136182 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635401 | AATAAATAATTTGTT[A/T]ATTGCATTATAAACA | 26054 |
rs762181805 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75703780 | ATTAAAAAACAAAAA[A/C]ATTGAGAACTTTCCA | 26054 |
rs762215044 | in-del | -/AGAG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651236 | TTTTGTATCCTTGTT[-/AGAG]AGAACAGACATATAT | 26054 |
rs762248073 | in-del | CGGATTACTTGA/GG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695511 | GGAGGCTGAGGCGGG[CGGATTACTTGA/GG]GGTCAGGAGTTCGAG | 26054 |
rs762259176 | snp | A/T | 1.65875e-05 | 0.00287984 | intron-variant | SENP6 | GRCh38.p7 | 6:75678728 | TTGCAATGATCTTAA[A/T]TGTCTTTCTCTGTTT | 26054 |
rs762260971 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637136 | CTGCCTCAGCACCGT[A/G]AAGTGCTGGAATTAC | 26054 |
rs762283861 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654494 | CTGTATGCCAAAAGT[A/G]TAGTATTTAGCCAGA | 26054 |
rs762314049 | snp | G/T | 0.000149414 | 0.00864202 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623939 | TGAAGATGAGGATTC[G/T]GAAACCTCAAAAGGA | 26054 |
rs762316948 | snp | C/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717775 | GAAACTGCATGACAA[C/G]TATCTGGTGTCTTAA | 26054 |
rs762317325 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694217 | GCCGAGATCATGCCA[G/T]TGCACTCCAGCCTGC | 26054 |
rs762326831 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684938 | AGGGAGGATTTCCTC[-/TT]TTTCTGTTGATTGAA | 26054 |
rs762337536 | snp | A/G | 1.79422e-05 | 0.00299513 | intron-variant | SENP6 | GRCh38.p7 | 6:75634846 | TTGGTTAGTATATAC[A/G]TGGCATCTTCTTCAA | 26054 |
rs762351425 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691468 | CATTTTATGGAATAG[C/G]AACTAAACAGCTTCA | 26054 |
rs762360664 | snp | C/T | 1.79474e-05 | 0.00299556 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678828 | TGATAGTATATCCAC[C/T]ACCTCCAGCTAAGGG | 26054 |
rs762390347 | snp | C/T | 1.6623e-05 | 0.00288292 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670578 | CTATTATCAACACAC[C/T]TCTGAAACGTCGTAA | 26054 |
rs762393122 | snp | A/G | 0.000171703 | 0.00926402 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702679 | GTTGTTTGTTTCCCC[A/G]GTTTGGAAAAACCAA | 26054 |
rs762432379 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676752 | TTTAGATTTATTAGA[C/T]GAAGTAAATTAGTTA | 26054 |
rs762478173 | snp | C/T | 1.69453e-05 | 0.00291073 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703052 | TACAGAATGAAAGTT[C/T]AAGTTCCACACATCA | 26054 |
rs762510106 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606751 | GGATGCTCAGTTGGG[A/C]TAATATAATAAAATT | 26054 |
rs762520448 | snp | A/G | 1.65864e-05 | 0.00287974 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666768 | AACAGAAGAGAAAGC[A/G]TATCTCCTCAGCCTG | 26054 |
rs762535177 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710410 | TATAAGAATCCTACA[G/T]CATACCATTTTGTTA | 26054 |
rs762536744 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663115 | ATCTTTTATTTCTTT[G/T]GTTCTTTTGGAACTT | 26054 |
rs762573842 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642459 | CGATCATAAGAATGG[C/G]TTTTCCAGATAGGGA | 26054 |
rs762574501 | snp | A/C/G | 0.000135905 | 0.00824231 | synonymous-codon, missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677211 | AAGAACCTATGAAGA[A/C/G]AGCATCAAAGGAAGT | 26054 |
rs762589987 | snp | C/T | 0.000242395 | 0.0110063 | intron-variant | SENP6 | GRCh38.p7 | 6:75675727 | TTTTTTTATTACCCA[C/T]AAGAGTAATGATTTA | 26054 |
rs762593133 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706836 | GGTTTTTACAGAAAA[-/C]TAGGGAAATAACAAT | 26054 |
rs762600378 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671466 | CGGTGTCTCACGCCT[C/G]TAATCCCAGCACTTT | 26054 |
rs762706720 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623906 | TCTGTGTAGTGGGAC[A/G]AATCTGCTCAGTGTG | 26054 |
rs762725440 | in-del | -/CA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647982 | TACCTGGAACAGTTG[-/CA]CAGTTAGGTGATTAC | 26054 |
rs762752599 | in-del | -/AA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659936 | ATCTGTCAAAATCTC[-/AA]AGTTAACATTGATCT | 26054 |
rs762755212 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671985 | ATTTAAAAACTAAAG[A/T]TTCAGAAGTACCCTG | 26054 |
rs762769404 | snp | A/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600777 | CTGTACAAATGGCCA[A/G]TTACCCACATTTGCC | 26054 |
rs762787965 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637731 | TTTATCATCTTTATC[G/T]TTTAAGTCTTCCCCC | 26054 |
rs762826377 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698818 | GGGTTCAAGACCAAC[C/T]TGGCGAACATGGCGA | 26054 |
rs762839109 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649795 | GCTGGGATTACACGC[A/G]TCAGCCACCGCGCCT | 26054 |
rs762874207 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625694 | GCCAACATGTTGAAA[C/G]CTCGTCTCTACTAAA | 26054 |
rs762879310 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697718 | TGAATTTTAGAGACA[A/G]TAGACCAGATACCTT | 26054 |
rs762893885 | snp | A/G | 1.65647e-05 | 0.00287786 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666869 | CAGAGCAGAGCGTGA[A/G]CTACGAAGCATTCCA | 26054 |
rs762938558 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688208 | CCGCCGAGCCAGGCA[C/T]GGGAGAGAATCACCT | 26054 |
rs762961834 | snp | C/T | 7.05928e-05 | 0.00594066 | intron-variant | SENP6 | GRCh38.p7 | 6:75633742 | GTATAGGCACTTCAC[C/T]ACACATTCCTACAGA | 26054 |
rs762988229 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636414 | TTTGATGTTCAAAGA[C/G]AAGTCATTGAGAGTT | 26054 |
rs762991177 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687301 | TAGCTATTCATCTAA[C/T]CTTTTTTCATGGTGT | 26054 |
rs762996910 | snp | A/G/T | 5.07862e-05 | 0.00503894 | intron-variant | SENP6 | GRCh38.p7 | 6:75695955 | AAATATTTAACAGAT[A/G/T]TAAGTCACTCACATT | 26054 |
rs763057992 | in-del | -/CT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642817 | AGGCTGGGCAAGTTC[-/CT]CTCTAAATGGAGGTG | 26054 |
rs763094995 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645476 | ACAAAAATTAGCACA[A/G]CATGGTGGCGCACAC | 26054 |
rs763099628 | snp | A/G | 1.67103e-05 | 0.00289048 | intron-variant | SENP6 | GRCh38.p7 | 6:75623853 | CAGAATTTAATATAA[A/G]GATTGTGATTGCTAC | 26054 |
rs763101485 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616004 | TCATCCACCGAATGT[G/T]TATCTTTTTTCACTT | 26054 |
rs763149666 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665983 | GTGAGACAAGATCGC[A/G]CACTGTACTCCAGCC | 26054 |
rs763166731 | in-del | -/ATG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666233 | TGATATATATAAAAT[-/ATG]ATGATATATAAAATA | 26054 |
rs763172212 | snp | A/G | 1.91133e-05 | 0.00309133 | intron-variant | SENP6 | GRCh38.p7 | 6:75711430 | CAGTAAGCATTAACT[A/G]TGTATCTTGAAAACT | 26054 |
rs763174416 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706128 | GCTCTTGTAAGAAAT[C/G]TCCTGAGCAGGAAAA | 26054 |
rs763202374 | snp | A/T | 1.66696e-05 | 0.00288696 | missense, stop-gained, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623959 | CCTCAAAAGGAAAAA[A/T]GGCAAGTGTTGCTTA | 26054 |
rs763206206 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681436 | TAAACCTCTTTTCTT[C/T]ATAAATTACCCAGTC | 26054 |
rs763220740 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617362 | CACTGCGACCTCCGT[C/T]TCCTGGGTTCAAGTG | 26054 |
rs763225165 | in-del | -/G | 1.66492e-05 | 0.00288519 | intron-variant | SENP6 | GRCh38.p7 | 6:75623873 | GTGATTGCTACTTAT[-/G]TTTTTTTCCCCTTAT | 26054 |
rs763225657 | snp | A/G | 6.80747e-05 | 0.00583376 | intron-variant | SENP6 | GRCh38.p7 | 6:75678763 | ACATTTCAGTTGTGT[A/G]TATATATATAGATTT | 26054 |
rs763250280 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692956 | TATGCCTGTAGTTCC[A/G]GCTACTCTGGAGGAA | 26054 |
rs763256126 | snp | C/T | 0.000216157 | 0.0103938 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663303 | CAATTCATCAGAATT[C/T]TGGAGGACAGAAGTC | 26054 |
rs763330156 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646574 | GGGCGCGGTGGCTCA[A/C]GCCTGTAATCCCAGC | 26054 |
rs763361697 | in-del | -/T | 1.65864e-05 | 0.00287974 | intron-variant | SENP6 | GRCh38.p7 | 6:75713490 | TATGAAGTATTCGAC[-/T]TTTGGTCATTTTTAC | 26054 |
rs763367284 | snp | A/C/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679837 | TCTTATACTGTGTTT[A/C/G]ATTAAACAAAACAAA | 26054 |
rs763383871 | in-del | -/CT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644573 | CACTGCAACCTCTGC[-/CT]CTCAGGTTCAAGCAA | 26054 |
rs763394690 | snp | A/C | 1.72039e-05 | 0.00293285 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670673 | ATTTTAAACTGTCGA[A/C]GTATACGAGTAGGAA | 26054 |
rs763415254 | snp | C/T | 3.31994e-05 | 0.00407414 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670589 | ACACCTCTGAAACGT[C/T]GTAAAGTGTTTTCTC | 26054 |
rs763417216 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615152 | CACCTTGGCCTCCCA[A/G]AGTGCTGGGATTATC | 26054 |
rs763431068 | snp | A/G | 4.97739e-05 | 0.00498844 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75702960 | AATAAATCATACTGC[A/G]AGTGAAAATGAAGAA | 26054 |
rs763467855 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631425 | TGTGGAACTTAAATT[C/G]TAATAACTTGCTATG | 26054 |
rs763478677 | snp | A/G | 2.69132e-05 | 0.00366822 | intron-variant | SENP6 | GRCh38.p7 | 6:75676088 | ATTATAATAGATAAT[A/G]ATAGATACTGTATTT | 26054 |
rs763492598 | snp | A/G | 1.65778e-05 | 0.002879 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702761 | CAACTGTAGAGGACA[A/G]TTGTATTTCTTCTTC | 26054 |
rs763497714 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668084 | AAGATGGGAACCTTA[A/T]AAAATGAAAAACAAC | 26054 |
rs763501379 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631316 | TGATAATTTTCACAT[A/G]TTTAGTATTCTCAAT | 26054 |
rs763504644 | in-del | -/GGAGC | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599667 | AAAGAGGAGAGAGAA[-/GGAGC]GGAGCGAGAAAGAGA | 26054 |
rs763524550 | snp | A/G | 3.47675e-05 | 0.00416924 | intron-variant | SENP6 | GRCh38.p7 | 6:75647689 | TTCATTTTGAAAACT[A/G]TATTTCCTGTTAGAA | 26054 |
rs763531978 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705292 | TGGCTCACGCCTGTA[A/C]TCCCAGCACTTTGGG | 26054 |
rs763537260 | snp | A/G | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717725 | GTACTTAGAAGTTGT[A/G]AAACAGAACTTATAG | 26054 |
rs763551198 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716273 | ATATATTATCATCAA[A/T]TGCATTTTTGAAGAC | 26054 |
rs763588310 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682175 | ATAAAGGAATGATCC[A/G]CCAAGAAAACATACT | 26054 |
rs763590342 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678454 | TTTAATTGTTAAGTA[C/T]CATGCATACTTTTTA | 26054 |
rs763609338 | in-del | -/T | 0.000766161 | 0.0195574 | intron-variant | SENP6 | GRCh38.p7 | 6:75640659 | GTCTTGCCTCTTATA[-/T]TTTTTTTCTTTTTCA | 26054 |
rs763619066 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710443 | TCTCTGACCTTTCAT[G/T]AGTTGTTAGGACATA | 26054 |
rs763628572 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75713039 | CTGCGCTCAGGACAT[A/T]GAAGCTGCAGTGAGC | 26054 |
rs763705608 | in-del | -/CAGT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685296 | TATTAGTCTTGCTAG[-/CAGT]CAGTCAATTTTGTTG | 26054 |
rs763707669 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710000 | GTGGACTGAACTTTA[A/T]TGTAATACTGATTAA | 26054 |
rs763747402 | in-del | -/CTTTAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662830 | ATTTAGATTTGCCCT[-/CTTTAC]CTTTATTATAGATAC | 26054 |
rs763760330 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648812 | ACTTTTATCCTAGCT[C/T]TCTGTTGAAGATCCC | 26054 |
rs763790632 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602316 | GGGCCGCGGGCCTCG[A/C]TGCCCGCCAGCCCGC | 26054 |
rs763797149 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706878 | TACTTTCACTTGCTG[-/T]TTTTTTCACTTGACA | 26054 |
rs763803458 | in-del | -/TCA | 1.80166e-05 | 0.00300133 | intron-variant | SENP6 | GRCh38.p7 | 6:75675419 | TAGAGCAATACTAAT[-/TCA]TCTTTTTTTTTAGTT | 26054 |
rs763803618 | snp | C/T | 1.66222e-05 | 0.00288285 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715576 | AACAGAACAATATGT[C/T]AATAGTATCTCAGAT | 26054 |
rs763817460 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600872 | AGGATCATGCAATAA[C/T]CTCAGGCAACAAAAA | 26054 |
rs763817589 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688031 | GGCAGTAGGCCTTGT[C/T]GAGCTGCAGTGGGCT | 26054 |
rs763841386 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650198 | ACTTCCACAGAAATG[A/G]TGTTGTGGCATTCTC | 26054 |
rs763850753 | snp | A/G | 1.95276e-05 | 0.00312465 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678865 | CTCTGTTACCAATGA[A/G]GACCTGCACTGTCTA | 26054 |
rs763853306 | snp | A/G | 0.000123875 | 0.00786907 | intron-variant | SENP6 | GRCh38.p7 | 6:75634837 | TAATTGTCTTTGGTT[A/G]GTATATACATGGCAT | 26054 |
rs763858351 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698838 | GAACATGGCGAAACC[C/T]CGTCTCTACTGAAAA | 26054 |
rs763862542 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652014 | AACCCTAACTCTCCA[A/G]AAAAATATAAAAATT | 26054 |
rs763869422 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613063 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 26054 |
rs763875760 | snp | C/T | 1.76039e-05 | 0.00296676 | intron-variant | SENP6 | GRCh38.p7 | 6:75697550 | TTAAAGGAAAATCTT[C/T]AAATCATGTAAATGA | 26054 |
rs763913045 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633545 | ATTGTCACATTATAG[C/T]ATTTTTGACTCATAT | 26054 |
rs763931032 | snp | A/G | 6.75927e-05 | 0.00581307 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633597 | TAAATCGTCGATCTG[A/G]AATTGTTGCTAATAG | 26054 |
rs763982190 | snp | A/C | 3.38547e-05 | 0.00411415 | intron-variant | SENP6 | GRCh38.p7 | 6:75623971 | AAAAGGCAAGTGTTG[A/C]TTAAAATATTTTCTT | 26054 |
rs763984414 | snp | C/T | 1.75974e-05 | 0.00296621 | intron-variant | SENP6 | GRCh38.p7 | 6:75663526 | TGATCCAAGTAAGTA[C/T]TTTACTCCCTTTAAT | 26054 |
rs763999251 | snp | C/T | 1.70746e-05 | 0.00292182 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711330 | CTGTCTTTTATAGGA[C/T]GATAGCAGTGACGAT | 26054 |
rs764005868 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704296 | AGCAAGAGGAATGCC[A/G]TAGGAGAGCAAGGTG | 26054 |
rs764033830 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693003 | TTCAGCCCAGGAGGC[G/T]GAGGCTGCAGTGAGC | 26054 |
rs764053270 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621043 | TTAGTGTTCTGATCT[A/G]GAGTTTTTCAGGTTG | 26054 |
rs764078781 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658641 | GAAAAATTCTCTTGC[A/G]TGTTCCAAAGTTAGA | 26054 |
rs764108230 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706253 | GTTTCTTTTTGAGAT[A/G]ATGAAAAGGTTTAAA | 26054 |
rs764108390 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637733 | TATCATCTTTATCTT[G/T]TAAGTCTTCCCCCGC | 26054 |
rs764162159 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672005 | GAAGTACCCTGGAGA[G/T]TCGAAGCAAATTATA | 26054 |
rs764165963 | snp | A/C | 3.41064e-05 | 0.00412941 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659312 | CAAGTGGAGCCTGAA[A/C]TTAAGAGGAAAGTAC | 26054 |
rs764184627 | snp | A/T | 8.30958e-05 | 0.00644523 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663357 | AGAAGTTTTATGGCA[A/T]CAATGTGGAAAAGGT | 26054 |
rs764236712 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645492 | CATGGTGGCGCACAC[A/G]TGTAATCCCAGCTAC | 26054 |
rs764239875 | snp | C/T | 1.83374e-05 | 0.00302793 | intron-variant | SENP6 | GRCh38.p7 | 6:75709483 | ATATACTATGAGTGA[C/T]AGACATGGCCTTTTT | 26054 |
rs764245989 | snp | A/G | 1.77979e-05 | 0.00298306 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677232 | CAAAGGAAGTTGTGG[A/G]CAAAAGGAAAACAAA | 26054 |
rs764258687 | snp | C/T | 3.32463e-05 | 0.00407702 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709569 | ATAGCGATGAATCAC[C/T]TGAAGCTGGTAAAAT | 26054 |
rs764266753 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697633 | TTCTGAAATCTCTTG[C/T]GTATATTCATATTTG | 26054 |
rs764281784 | snp | C/T | 0.00126716 | 0.0251391 | intron-variant | SENP6 | GRCh38.p7 | 6:75675705 | TCTTTAAGGCAGTTA[C/T]AAAGATTTTTTTTAT | 26054 |
rs764285432 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657636 | ATTTATTAAGCCCTT[A/G]TGTAGTTTCTAGATG | 26054 |
rs764321466 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673401 | CAATCTTGGCTCACT[G/T]CAGCCTCCACCTCAC | 26054 |
rs764322771 | snp | C/T | 1.66649e-05 | 0.00288655 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634768 | GGTAGACGTTTTCAT[C/T]ATGCTCATGCACAGA | 26054 |
rs764355768 | snp | A/G | 3.34454e-05 | 0.0040892 | intron-variant | SENP6 | GRCh38.p7 | 6:75659235 | TTTAACTAAAACTTA[A/G]AGTTTATTTTTTTCT | 26054 |
rs764377961 | snp | A/G | 1.6577e-05 | 0.00287893 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666911 | GTTAAATACAGTTAC[A/G]TTGCCAAGAAAAGCA | 26054 |
rs764400734 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629522 | CCAGGCTGGTCTCGA[A/G]CTCCAGACCTCAGGT | 26054 |
rs764411213 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631378 | GAGCACAGTGTTCTA[A/C]GTGTTGGAGCAAAAC | 26054 |
rs764424091 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617419 | GGTGGGGTTACAGGC[A/G]TGCACCACCACACCG | 26054 |
rs764460022 | snp | C/T | 0.000132683 | 0.00814395 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715440 | ACTGGTTTCCTCCAC[C/T]AAGAATGAGAACAAA | 26054 |
rs764479398 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700629 | CCCAGTAGCTTGGAC[C/T]ACAGGCACGTGCCAT | 26054 |
rs764511805 | snp | C/G | 1.66513e-05 | 0.00288537 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670570 | TGGCAATTCTATTAT[C/G]AACACACCTCTGAAA | 26054 |
rs764514667 | in-del | -/TTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672760 | AAATTCTACACTTGC[-/TTA]TTATTAGATAATTTA | 26054 |
rs764581707 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681439 | ACCTCTTTTCTTTAT[A/C]AATTACCCAGTCTCA | 26054 |
rs764597158 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75632245 | AGCTACTAATAGAGG[A/G]GTGGTTAAATTAAAA | 26054 |
rs764614730 | snp | C/G | 1.7789e-05 | 0.00298231 | intron-variant | SENP6 | GRCh38.p7 | 6:75663535 | TAAGTATTTTACTCC[C/G]TTTAATATTGCTTAT | 26054 |
rs764615770 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664790 | TACTAATAAAGTCAA[C/G]GCATGACTTTTGAAT | 26054 |
rs764629794 | snp | A/G | 0.000371747 | 0.0136285 | intron-variant, utr-variant-5-prime | SENP6 | GRCh38.p7 | 6:75622781 | CTGGGCAACAGCTCC[A/G]TTCATCATTACCACT | 26054 |
rs764723692 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603728 | CAGTGCCTGGAACAC[A/T]GTAGGTACTCAGTGT | 26054 |
rs764763119 | snp | A/G | 1.72549e-05 | 0.0029372 | intron-variant | SENP6 | GRCh38.p7 | 6:75678560 | AATTGACTGTAAATT[A/G]CTAATTTAATTTCCT | 26054 |
rs764779914 | in-del | -/ATAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696253 | GAATACCTGGAATTT[-/ATAA]ATAAATGTTCTGGGT | 26054 |
rs764784358 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647886 | GATGCTGGCTTTAGA[A/G]TATTCCCAGGTATAA | 26054 |
rs764791896 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669077 | AAAATAGGCCGGATG[C/T]GGTGGCTCACACCTG | 26054 |
rs764819324 | snp | C/G | 1.66604e-05 | 0.00288616 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663398 | ATTATTGTGAATTGT[C/G]ATGACAGTAAACACA | 26054 |
rs764826263 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612312 | GCTTTTCGAACATAC[A/G]CATTTAATTCTCTCT | 26054 |
rs764830706 | in-del | -/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619659 | TAGCTCGTAGGGTAA[-/T]TCTATGTTTAACTTT | 26054 |
rs764845685 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611172 | TGACCCCTGCTGACT[C/T]TGCTTCTGTGGAAAC | 26054 |
rs764879829 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654271 | AAGTAAAGCTGAGTT[C/T]TGAATCACTGGAATT | 26054 |
rs764927803 | snp | C/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620956 | CTGGGTTCCCACTTT[C/G]TAATTGTTAATGGCT | 26054 |
rs764939257 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648653 | ATTATTATACTTTAC[A/G]TACTAAGCATAGTTA | 26054 |
rs764948361 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646044 | TCTCTATACATGCAT[A/G]TATGATTTACTGTCT | 26054 |
rs764954334 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624934 | GGCCAGGAGTTTGAG[A/G]CTACCTGGACAACAT | 26054 |
rs764977031 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660626 | ATGGTCTTAACTTAT[C/T]TTGTATTTCTTTTTT | 26054 |
rs764980879 | in-del | -/TCTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623512 | TCATTTCTTTGTTTC[-/TCTA]TCTTTCTACCCTTAA | 26054 |
rs764981590 | snp | A/G | 0.000199661 | 0.00998952 | utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602517 | GGAGGCGGCGTGGGA[A/G]GAGGAAGATGGCGGC | 26054 |
rs765014853 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710197 | CAGTTATTTTTTTTT[-/C]TCCTGCCTGATTCGA | 26054 |
rs765015725 | snp | A/G | 2.30864e-05 | 0.00339745 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678911 | TTAAATGATGTTATT[A/G]TAGACTTTTATTTGA | 26054 |
rs765026134 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706607 | ACTTGTTTTATGTAG[G/T]TTGCCTTCTTAATAC | 26054 |
rs765048847 | snp | A/G | 1.83552e-05 | 0.0030294 | intron-variant | SENP6 | GRCh38.p7 | 6:75675397 | AGCCTGCCTTTCTTT[A/G]TAAGTCTAGAGCAAT | 26054 |
rs765075724 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697675 | TTACAAGAATTAATG[C/T]AGTTTCACAGTGAAG | 26054 |
rs765102061 | snp | C/T | 1.68989e-05 | 0.00290674 | intron-variant | SENP6 | GRCh38.p7 | 6:75695794 | ATTTGAATTATTTTC[C/T]ATCAAATAGATACTT | 26054 |
rs765126986 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710231 | ATATGTGTCATGGCA[C/G]AAGCAGATAATATTT | 26054 |
rs765136792 | in-del | -/CTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692741 | CCTCCCCGCATCCCA[-/CTC]CTCCCTCACACCTGG | 26054 |
rs765140381 | snp | A/G | 3.35548e-05 | 0.00409588 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633609 | CTGAAATTGTTGCTA[A/G]TAGCTCTGGTGAATT | 26054 |
rs765182991 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704199 | TGGGCCCAGGAGAAC[C/G]GCACTCAGCATATCA | 26054 |
rs765194776 | in-del | -/ATCG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659814 | TACCCATAAACGTGT[-/ATCG]GTATATGTATTTTTT | 26054 |
rs765236611 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649479 | GAAAAAAGAGCATGC[G/T]TATTTACTGTTCTTT | 26054 |
rs765247443 | in-del | -/AG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662457 | TTTTTGTTTTCCAAA[-/AG]AGAAACTACACTTAA | 26054 |
rs765256572 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant | SENP6 | GRCh38.p7 | 6:75678578 | AATTTAATTTCCTTT[A/G]CCAGGTATCATTTGA | 26054 |
rs765290024 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684798 | TGCTGGACTTCGTTT[G/T]CCAGTGTTTTATTGA | 26054 |
rs765330738 | snp | C/T | 1.65927e-05 | 0.00288029 | intron-variant | SENP6 | GRCh38.p7 | 6:75678732 | AATGATCTTAAATGT[C/T]TTTCTCTGTTTTATT | 26054 |
rs765333313 | snp | A/G | 1.66001e-05 | 0.00288094 | intron-variant | SENP6 | GRCh38.p7 | 6:75713613 | TTTCGTATTCTGATG[A/G]GGATGAAGAACTATG | 26054 |
rs765374559 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619044 | TTCCTTTTAAAAGCA[A/G]TTTTTTATTGTGGTA | 26054 |
rs765387634 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614426 | GTGCACCACCACGCC[A/T]GGCAAATTTTTTTGT | 26054 |
rs765418005 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670135 | TACTTTTAGTAGAGA[C/T]GAGGTTTCACTGTGT | 26054 |
rs765429723 | snp | C/G | 1.68337e-05 | 0.00290114 | intron-variant | SENP6 | GRCh38.p7 | 6:75663184 | GGAAAAAGAAAATCA[C/G]ACCAAATGCCAAAGT | 26054 |
rs765433385 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607090 | TGGTGGCTCACGCCT[A/G]TAATCCCAGCATTTT | 26054 |
rs765442064 | snp | A/G | 1.67108e-05 | 0.00289052 | intron-variant | SENP6 | GRCh38.p7 | 6:75623849 | ACCTCAGAATTTAAT[A/G]TAAGGATTGTGATTG | 26054 |
rs765443762 | snp | G/T | 1.66252e-05 | 0.00288311 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709584 | CTGAAGCTGGTAAAA[G/T]GCTTGAAGATGAACT | 26054 |
rs765468317 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704693 | CGGTCAGGTCCTTCC[C/T]GTCCCACGAGGCCAT | 26054 |
rs765488970 | snp | C/G | 3.32995e-05 | 0.00408027 | stop-gained, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715587 | ATGTCAATAGTATCT[C/G]AGATTGACCATTTCT | 26054 |
rs765493796 | snp | A/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621647 | ATTTTTTTTTCCCTC[A/T]GATGTTTTATAAGAA | 26054 |
rs765503941 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697328 | TATGCAACTGTTTGA[A/G]CTATTACATCTGAAT | 26054 |
rs765540963 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678035 | AAAGAAGAAAGGGAA[A/G]TGGTTCTTTTTCTTT | 26054 |
rs765568872 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640371 | CATTGGGGGTCTTGG[-/A]AAGGATCGTTAGAGA | 26054 |
rs765575430 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645413 | TTGAGGCCAGGAGTT[C/T]GAGGCCAGCCTGGCT | 26054 |
rs765592310 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651379 | TCGTTTTTGAGACAG[G/T]GTCTTGCTCTATTAC | 26054 |
rs765600665 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714152 | TCCTCTTCATAGATA[C/G]ATTTCTTAAGAAGTG | 26054 |
rs765612530 | snp | C/T | 3.31499e-05 | 0.0040711 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702808 | AGTTGTTCACAAAAC[C/T]CTTCTGCCAAGCCTG | 26054 |
rs765623465 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631240 | TTCGGTGCTAAACTT[-/C]CTGAATATCAGTACT | 26054 |
rs765646662 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629098 | ATTAAAAATAATTTG[C/T]AATCCAGTCATTAGG | 26054 |
rs765649537 | snp | A/G | 9.80993e-05 | 0.00700286 | intron-variant | SENP6 | GRCh38.p7 | 6:75640733 | TGAAGAAATTAGAGC[A/G]TGGATATAGTGGTAA | 26054 |
rs765704866 | snp | A/G | 1.69913e-05 | 0.00291468 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670668 | GTGTCATTTTAAACT[A/G]TCGAAGTATACGAGT | 26054 |
rs765759270 | snp | A/G | 1.81496e-05 | 0.00301239 | intron-variant | SENP6 | GRCh38.p7 | 6:75633765 | CCTACAGAAAAGATA[A/G]AGGAAGAGTTTGACA | 26054 |
rs765834773 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688641 | TTCTTCATAGCTGAC[C/G]AGACACAGTGGCTCA | 26054 |
rs765854646 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690107 | ATACAGATGGTGTCT[C/T]ACTTTGTTGGCCAGG | 26054 |
rs765878382 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664577 | TCAAATGCTATATAT[A/G]TAAATCTGTTTAGAT | 26054 |
rs765892361 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710623 | TTACATTCATGATTT[A/T]TAATGAGCACTTAGG | 26054 |
rs765902820 | snp | C/T | 1.66043e-05 | 0.00288129 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670586 | AACACACCTCTGAAA[C/T]GTCGTAAAGTGTTTT | 26054 |
rs765903085 | in-del | -/AAG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702064 | TTTCATTCCAAAAAC[-/AAG]AAGAAAGCGTTCAGG | 26054 |
rs765918500 | snp | A/C | 1.66991e-05 | 0.00288951 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633639 | TCATCTTGAAGACAT[A/C]TGTAAGACGAAACAA | 26054 |
rs765928232 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668740 | ATCGCAAGAGATTGG[A/G]AAGAACTTAGATGTC | 26054 |
rs765935465 | in-del | -/TATATATTAAG | 6.92785e-05 | 0.0058851 | intron-variant | SENP6 | GRCh38.p7 | 6:75713857 | GGATCTGCTATAATA[-/TATATATTAAG]AATAATAAAATAGTG | 26054 |
rs765962590 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623203 | TGGCAGATTTACTGT[A/G]GTTATACATTTTTTA | 26054 |
rs765966151 | snp | C/T | 0.000116607 | 0.0076348 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695816 | TAGATACTTGGTGCT[C/T]GAAAAACTGAAGAAG | 26054 |
rs765982265 | in-del | -/GTAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666087 | TGATATATATAAAAC[-/GTAT]ATATGATATATATAA | 26054 |
rs766009027 | snp | C/T | 1.71056e-05 | 0.00292446 | intron-variant | SENP6 | GRCh38.p7 | 6:75713851 | ATTTGTTGGATCTGC[C/T]ATAATAAATAATAAA | 26054 |
rs766022376 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606299 | TTCATTAAGCCACAG[C/T]TTGTGTTAAAATTTT | 26054 |
rs766036935 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694173 | AGGCAAGAGAATCGC[C/T]TGAACCCGGGAGGTG | 26054 |
rs766050554 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689301 | TAAGTGATCCATACA[A/G]GTGGCCAAAAAGCAT | 26054 |
rs766051285 | snp | G/T | 1.68057e-05 | 0.00289872 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675903 | ATTAAATACCTCTGA[G/T]CTAACTAAATGTGAA | 26054 |
rs766119714 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617961 | GGATTATGAGTTTTA[A/G]GGAAAGGATCACAGT | 26054 |
rs766130219 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610999 | AAGAGTGGACGACGA[C/G]GAACTAGAAATTCTC | 26054 |
rs766151227 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609294 | CGACTGAACAAGAGA[A/C]GGAAAAATAATAAGT | 26054 |
rs766158115 | snp | C/T | 6.73378e-05 | 0.0058021 | stop-gained, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659336 | AAAGTACAACAGAAA[C/T]GACACTGTAGTACCT | 26054 |
rs766199058 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604710 | ATCTTTCCAAATAAA[C/T]GATATTTAATACTAA | 26054 |
rs766211666 | snp | C/T | 0.000100447 | 0.00708614 | intron-variant | SENP6 | GRCh38.p7 | 6:75675743 | AAGAGTAATGATTTA[C/T]AGAGCATAATAAATA | 26054 |
rs766233447 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610777 | CTATGTTCTGATCTT[A/G]CCTTTGGAGGTTGTT | 26054 |
rs766374683 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631914 | GATATATATCCTCGG[A/G]TGAAGCATTGATGAA | 26054 |
rs766375742 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668483 | AATAAGGAAAGGAAA[A/T]GAATAGAATTCAAAA | 26054 |
rs766386722 | snp | A/G | 3.31978e-05 | 0.00407404 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670590 | CACCTCTGAAACGTC[A/G]TAAAGTGTTTTCTCA | 26054 |
rs766439427 | snp | C/T | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75717800 | TCTTAACTAATTAGA[C/T]AGATCTGTTGTATTG | 26054 |
rs766444990 | snp | A/G | 1.72047e-05 | 0.00293293 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670674 | TTTTAAACTGTCGAA[A/G]TATACGAGTAGGAAC | 26054 |
rs766456737 | in-del | -/TA | 0.000341504 | 0.0130627 | intron-variant | SENP6 | GRCh38.p7 | 6:75678762 | TACATTTCAGTTGTG[-/TA]TATATATATAGATTT | 26054 |
rs766470383 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606035 | ATCAAAAGGTTTTGT[G/T]TAGCCTGAGGTATTA | 26054 |
rs766493892 | snp | C/T | 1.72543e-05 | 0.00293715 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715635 | CTTTCAGAAACTAAA[C/T]GACTTTCAAATTTGG | 26054 |
rs766499680 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611854 | CTGAACTGACTATGC[C/T]ATCATCTTGCTGAAA | 26054 |
rs766517547 | snp | A/G | 1.92747e-05 | 0.00310435 | intron-variant | SENP6 | GRCh38.p7 | 6:75711432 | GTAAGCATTAACTGT[A/G]TATCTTGAAAACTAC | 26054 |
rs766520119 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617938 | GATGTTTTCTTATGA[C/T]TAAACTGGGATTATG | 26054 |
rs766557923 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634454 | GGTTACAGCATGTTG[A/G]CTGGGCTGGTCTCGA | 26054 |
rs766558840 | snp | A/G | 1.67052e-05 | 0.00289004 | synonymous-codon, splice-donor-variant, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623960 | CTCAAAAGGAAAAAA[A/G]GCAAGTGTTGCTTAA | 26054 |
rs766605964 | in-del | -/AT | 9.00698e-05 | 0.0067102 | intron-variant | SENP6 | GRCh38.p7 | 6:75633557 | TAGCATTTTTGACTC[-/AT]ATTTCTGGATCTTTT | 26054 |
rs766609420 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669963 | TTTAAGAAGGAATTT[C/T]GATCTTGTTGCCCAG | 26054 |
rs766628287 | snp | A/G | 1.65916e-05 | 0.00288019 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702962 | TAAATCATACTGCGA[A/G]TGAAAATGAAGAATT | 26054 |
rs766656702 | snp | C/T | 1.65891e-05 | 0.00287998 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647791 | AAGGTTAAGTCGGCT[C/T]CAAGGTGTTGGTAAG | 26054 |
rs766658206 | snp | A/C/T | 5.11621e-05 | 0.00505756 | intron-variant | SENP6 | GRCh38.p7 | 6:75678771 | GTTGTGTATATATAT[A/C/T]TAGATTTGTTTATTT | 26054 |
rs766672526 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696625 | TGGGACTAAGGCACA[C/T]GCCACTCCACCCAGC | 26054 |
rs766690644 | snp | C/T | | | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702959 | AAATAAATCATACTG[C/T]GAGTGAAAATGAAGA | 26054 |
rs766701592 | snp | A/G | 1.74388e-05 | 0.00295281 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677122 | ATTAATGAAATTGGT[A/G]TAAAGAATAACATCT | 26054 |
rs766704617 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672593 | AATTAGTGGATCTGT[A/T]TCTTCTTCAGATGGC | 26054 |
rs766716997 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661946 | AGTCCCAGCTACTTG[A/G]GAGGCCGAGGCGGGA | 26054 |
rs766725762 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687110 | TTTTTACTTTTTTTT[-/C]CTCTAACCTTGTCTT | 26054 |
rs766743372 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606997 | GGGAGGACAATAATG[A/G]TGTCAGATAGGAGAG | 26054 |
rs766749296 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642616 | GGCTGGGACCTACGT[C/T]ATAAAAGGTTTTTGT | 26054 |
rs766760738 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694757 | TGTATAAATGTAACA[C/G]TTTATTTTTCCATTT | 26054 |
rs766767025 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656068 | AAAAATACAAAAACT[A/G]GCCAGGCATGGTGAC | 26054 |
rs766771167 | in-del | -/TGT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650695 | TTTCAGCTTCTTTTG[-/TGT]TAGGTAGGTACATGT | 26054 |
rs766774008 | in-del | -/TACTA | 2.43846e-05 | 0.00349166 | intron-variant | SENP6 | GRCh38.p7 | 6:75670742 | ACATCTTAAGCTCTT[-/TACTA]TACCAATTATAACAT | 26054 |
rs766800834 | snp | C/G | 5.03411e-05 | 0.00501677 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621493 | TTATATTGAATAGCT[C/G]TATTAATGAATACTT | 26054 |
rs766813203 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644086 | CAAAAAATTAAGAGT[C/G]CCCACTTCAAAAGCA | 26054 |
rs766854901 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710757 | GAAGCTTTCTCAAAG[A/C]ACAACAATGACCAAA | 26054 |
rs766858304 | in-del | -/TAG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674313 | GGTACATGCCATCTA[-/TAG]TACCTAGGTAAGTTT | 26054 |
rs766897144 | in-del | -/A | 1.76449e-05 | 0.00297021 | splice-acceptor-variant | SENP6 | GRCh38.p7 | 6:75675432 | TTCATCTTTTTTTTT[-/A]AGTTTTGTTTAGATT | 26054 |
rs766914238 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690426 | GAGGTCATTGTGCCA[A/G]GCACAGTAAGTCAGT | 26054 |
rs766955425 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613204 | CTCAGAATGGCTTTT[A/G]TATTTTTAATGACTG | 26054 |
rs766962536 | snp | G/T | 1.67464e-05 | 0.0028936 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697499 | AGAAGGATTTTATTT[G/T]TGTACCCCTTAATGA | 26054 |
rs766974367 | snp | G/T | 1.65748e-05 | 0.00287874 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702828 | TGCCAAGCCTGTAAT[G/T]AAGAAGATGCTAAAC | 26054 |
rs766990056 | snp | G/T | 0.00010071 | 0.00709541 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602548 | CGGCAAGAGCGGCGG[G/T]AGCGCAGGGGAGATT | 26054 |
rs767008115 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650517 | TTTTACATTTATTGA[C/T]TGGAAATCGTCTGTA | 26054 |
rs767008820 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698881 | CTGGGCGTGGTGGTG[C/G]GTGCCTGTAATCCCA | 26054 |
rs767018357 | snp | C/T | 4.99455e-05 | 0.00499702 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634759 | GTAGTTCATGGTAGA[C/T]GTTTTCATCATGCTC | 26054 |
rs767022157 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714056 | TTCTATCACTGAACA[A/G]TCAACCTGCCCTCTC | 26054 |
rs767045883 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664426 | TATACATCTATATAT[A/G]TCAGGTACTGTGCTA | 26054 |
rs767048557 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700486 | TACTATATTTCATCA[A/C]TTTTATTTTATTTAT | 26054 |
rs767066429 | in-del | -/AGA | 3.32176e-05 | 0.00407526 | cds-indel, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677034 | TTTCTTTTCAGATTT[-/AGA]AGAACAATATATAAT | 26054 |
rs767102514 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614082 | GTTTCCTTATGATTC[A/G]AGTCAGGTTATGCAT | 26054 |
rs767103143 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680018 | TGATAGGCATGACAT[C/T]GTGGAAGTCTAGATG | 26054 |
rs767124328 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664413 | GTATGTATATATATA[C/T]ACATCTATATATGTC | 26054 |
rs767164104 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687406 | TGCTTCTGTCAACTC[C/G]TCAAAGTCATTCTCC | 26054 |
rs767170749 | in-del | -/AT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640838 | AAAGTTTTAGTTGAC[-/AT]GTAATAATTGTACAT | 26054 |
rs767174945 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705414 | GCTGGGTGTGGTGGT[G/T]CCCGCCTGTAATCCT | 26054 |
rs767189487 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621206 | TTATAGGTACTTATT[C/T]CTAGAATCAGTGATC | 26054 |
rs767212632 | snp | C/T | 3.88674e-05 | 0.0044082 | intron-variant | SENP6 | GRCh38.p7 | 6:75634670 | GTGTATATAATTTTT[C/T]CGTGTTCAAGTTATT | 26054 |
rs767214541 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688339 | GAAATCCCCCAACCT[C/G]TTGCACTTCCTGGGT | 26054 |
rs767232606 | in-del | -/CTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705924 | AAGCTATTTTTGAGC[-/CTT]CTTTTTTTTTTTTTT | 26054 |
rs767248986 | snp | C/T | | | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666910 | AGTTAAATACAGTTA[C/T]ATTGCCAAGAAAAGC | 26054 |
rs767254420 | snp | A/G | 3.31334e-05 | 0.00407009 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666884 | ACTACGAAGCATTCC[A/G]GAAGACTCAGAGTTA | 26054 |
rs767264592 | snp | A/C/T | 0.000190806 | 0.00976593 | intron-variant | SENP6 | GRCh38.p7 | 6:75713858 | GGATCTGCTATAATA[A/C/T]ATAATAAAATAGTGC | 26054 |
rs767273603 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639250 | TTTATATTTTGCTTC[A/G]CTTCTTTAATAGGGA | 26054 |
rs767294826 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628818 | TCTTCCTCCTAGGCT[C/G]AAGCGATCCTACCGC | 26054 |
rs767301399 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623872 | TGTGATTGCTACTTA[C/T]GTTTTTTTCCCCTTA | 26054 |
rs767318922 | snp | A/G | 1.86152e-05 | 0.00305078 | intron-variant | SENP6 | GRCh38.p7 | 6:75711303 | TTATATATTTTCAGT[A/G]TTAACAGTAGGCTGT | 26054 |
rs767335480 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601057 | TGCACTTAATCATGT[C/T]GGTTTTCTGCATCAT | 26054 |
rs767351659 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673637 | CCCAGTGTCTACTTA[C/T]AATATTAATGTGTGA | 26054 |
rs767431453 | snp | C/T | 3.35093e-05 | 0.0040931 | intron-variant | SENP6 | GRCh38.p7 | 6:75663208 | CCAAAGTTGTGGTGT[C/T]CTTTTTTCTAAGGAT | 26054 |
rs767531142 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681589 | TCAGCCTCCCAGGTA[C/G]CTTGGATTACAGGTA | 26054 |
rs767536857 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619407 | ATCCTGTATCCAATT[C/T]GTATCCCTTTAAGGC | 26054 |
rs767584876 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658944 | GCCACTGAACTCCGG[A/C]CTAGGTGACAGAATG | 26054 |
rs767596719 | snp | A/G | 9.44287e-05 | 0.00687062 | intron-variant | SENP6 | GRCh38.p7 | 6:75670772 | AACATTAAAAATTCC[A/G]TTGCTAAAGCTAATA | 26054 |
rs767625903 | snp | C/T | 1.66535e-05 | 0.00288556 | stop-gained, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675931 | GAATGGTGTAATGTC[C/T]GAAAATTACCTGTAG | 26054 |
rs767655716 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694022 | AGCACCTTAGGAGGC[C/T]GAGGCAGGTGGATCA | 26054 |
rs767665225 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678759 | TATTACATTTCAGTT[A/G]TGTATATATATATAG | 26054 |
rs767697495 | in-del | -/CGCTTTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642144 | TGCCTTTTAGGCATA[-/CGCTTTT]ATTCATTCCAAGTAT | 26054 |
rs767698153 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656709 | TATAACACTATCAAT[C/G]ATTTACCATTTCTCC | 26054 |
rs767723788 | snp | C/T | 1.6601e-05 | 0.00288101 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702998 | AAGGAGAATCTACAT[C/T]CCAGAAAGTTGCTGA | 26054 |
rs767734143 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701969 | TAAGATGGATAGCTT[C/T]CCATCTTTTTACATA | 26054 |
rs767739263 | snp | C/G | 1.65743e-05 | 0.00287869 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666781 | GCATATCTCCTCAGC[C/G]TGCTGATTCAGCATG | 26054 |
rs767742160 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660469 | TGTAACTTTCATGAT[A/G]TTTCATGACTTACCT | 26054 |
rs767790534 | snp | A/G | 3.40559e-05 | 0.00412635 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677215 | ACCTATGAAGAGAGC[A/G]TCAAAGGAAGTTGTG | 26054 |
rs767792628 | snp | C/G | 1.81385e-05 | 0.00301146 | intron-variant | SENP6 | GRCh38.p7 | 6:75695769 | TAAAGTGAACTGTTA[C/G]ATTAATTATATTTGA | 26054 |
rs767860135 | in-del | -/A | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679482 | GGAAAAATGCCTAGT[-/A]ACAGTGTTAGAAGTT | 26054 |
rs767867966 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692893 | ACATGGCGAAACCCC[A/G]TGTTTACCCCCACCA | 26054 |
rs767876345 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689638 | GTGAGCCCATAAGAT[G/T]ATAATAACGTATTTT | 26054 |
rs767882962 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690277 | TCATAATAGCTGAGT[A/G]GTGGAAACAATCCTG | 26054 |
rs767888669 | snp | C/T | 1.75302e-05 | 0.00296054 | intron-variant | SENP6 | GRCh38.p7 | 6:75678547 | TGAAACTTTTCCTAA[C/T]TGACTGTAAATTGCT | 26054 |
rs767919214 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654510 | TAGTATTTAGCCAGA[A/G]GTGATTTTTAAAGAA | 26054 |
rs767921840 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655922 | GTGTAGTGTATTTAA[A/G]AAGACATTGAGCTAG | 26054 |
rs768027734 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658011 | GATTTTTAACTAGAT[C/T]ACTTTTTCAGTAGTG | 26054 |
rs768081542 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605946 | GGGAAGAGAAGTTGA[G/T]AGGTTGAGGATATGT | 26054 |
rs768087223 | in-del | -/AAAAGCAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630883 | CTATATTTTATGTTT[-/AAAAGCAA]AAAAGGAAAAAAAAT | 26054 |
rs768096248 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642468 | GAATGGCTTTTCCAG[A/G]TAGGGAAGAGGTTGT | 26054 |
rs768104639 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671558 | AAAACCCCATCTCTA[C/T]TAAAAATAGAAAAAT | 26054 |
rs768115355 | snp | A/G | 1.6654e-05 | 0.00288561 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621514 | ATGAATACTTACTGC[A/G]GTTTGTTTTTATTTC | 26054 |
rs768131899 | in-del | -/A | 0.000113682 | 0.00753843 | intron-variant | SENP6 | GRCh38.p7 | 6:75624002 | TTTTACATTATATAC[-/A]AAAAAAATTGTTACC | 26054 |
rs768138663 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690317 | ATGAACGGATAAACC[-/A]AAATGTGGTGTATAC | 26054 |
rs768158333 | snp | C/T | 3.3173e-05 | 0.00407252 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647771 | AAAGTTGAAATTAAT[C/T]CTGTAAGGTTAAGTC | 26054 |
rs768175656 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608168 | TTGGAATGAAAGTGA[G/T]TTTCAGGCAAAGTTT | 26054 |
rs768186035 | snp | A/G | 1.65853e-05 | 0.00287964 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702923 | AGAGAAACATATGCA[A/G]TGTAAAATACAGTGT | 26054 |
rs768193316 | snp | A/G | 9.79696e-05 | 0.00699823 | intron-variant, missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75640695 | TAAGCAGTCTGGACC[A/G]AAAAGAAAGGTAAGC | 26054 |
rs768208892 | snp | C/T | 1.78395e-05 | 0.00298654 | intron-variant | SENP6 | GRCh38.p7 | 6:75703099 | AATGTTTTGAAAGAA[C/T]GAAAAAATTCAGAAT | 26054 |
rs768213719 | snp | C/T | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679686 | AACATAACACATGTA[C/T]ACACCTATGTGCAAT | 26054 |
rs768255976 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643789 | ATTAAACTGGTTTAT[C/T]AGTTAAATAGGAATA | 26054 |
rs768340836 | snp | G/T | 1.68932e-05 | 0.00290625 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677198 | TTGTTGCCTGTACAA[G/T]AACCTATGAAGAGAG | 26054 |
rs768360273 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629123 | ATTAGGTACTGGCCT[C/T]CCAGATTTTGGATAA | 26054 |
rs768361216 | snp | A/G | 8.29428e-05 | 0.0064393 | intron-variant | SENP6 | GRCh38.p7 | 6:75713602 | TTCACACTTTATTTC[A/G]TATTCTGATGGGGAT | 26054 |
rs768374855 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693507 | GTCCCTGGACTGATA[A/G]CTATTTATCTACATA | 26054 |
rs768379969 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712419 | CACAGTGGGTCACAC[A/T]TTGTGCTAGCACTTC | 26054 |
rs768436168 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700262 | TAACGTAGCTGTTAT[C/T]AAAAGGAATCATAAA | 26054 |
rs768440822 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75639100 | CTTATTTTTTGGGCA[C/T]AGCAGTATAGAATTG | 26054 |
rs768474460 | snp | C/G | 1.672e-05 | 0.00289132 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670651 | CCAAAGTTCCTTTGA[C/G]AGTGTCATTTTAAAC | 26054 |
rs768478373 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664353 | TTAAAAATATAGTTC[A/G]TGGGCCTTTTTAAAA | 26054 |
rs768510574 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701211 | GACAAATATTATTGT[A/G]CTTGACCAATAAGCT | 26054 |
rs768521893 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614758 | AACAATAGGACCTTC[A/G]CTATGTACTTGAATA | 26054 |
rs768532343 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680993 | AAATGAAAATCATTT[A/G]CCTTACCCAGAATCA | 26054 |
rs768584708 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652861 | CTTATATTTTCTTCA[C/T]AACTGGTGAGATATC | 26054 |
rs768600163 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622478 | GCAGGAGAATCACTT[C/G]AACCCGGGAGGTAGA | 26054 |
rs768610264 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615097 | GGTTTCACCATGTTG[A/G]CCAAGCTGGTCTTGA | 26054 |
rs768612382 | snp | A/G | 0.000118508 | 0.00769677 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75702690 | CCCCGGTTTGGAAAA[A/G]CCAAAGTATGAACCT | 26054 |
rs768646204 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689333 | TGAAAGATGCTCAAC[-/A]TCAGTAATCATTAGA | 26054 |
rs768673316 | snp | G/T | 0.000102338 | 0.00715253 | intron-variant | SENP6 | GRCh38.p7 | 6:75602600 | GTTTCTGCCCTTGAC[G/T]GGGAGAAGGGAGGGT | 26054 |
rs768674811 | snp | G/T | 1.72202e-05 | 0.00293424 | intron-variant | SENP6 | GRCh38.p7 | 6:75659433 | AAATTATTCTTTGTT[G/T]CTAATCAGATTGTGT | 26054 |
rs768697614 | snp | C/T | 1.79319e-05 | 0.00299427 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677095 | CCGGCAAATATGGTA[C/T]TTGAAAGTATCATTA | 26054 |
rs768720330 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674920 | TATTCATTTATCTTG[-/T]TTTTTTAATACATTT | 26054 |
rs768720750 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660894 | CCTCAGCCTTCCAAA[A/G]TGCTGGGATTACAGG | 26054 |
rs768748172 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688250 | TGCTAAGACCTTGGG[A/C]AAAGCACAGTATTTG | 26054 |
rs768787916 | snp | G/T | 1.69971e-05 | 0.00291518 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675885 | TGATCCTGTAGAGAT[G/T]ATATTAAATACCTCT | 26054 |
rs768822353 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698561 | GCTGGTCTTGAACTC[-/T]TGGCCTCAAGCCATC | 26054 |
rs768839222 | snp | A/C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682189 | CACCAAGAAAACATA[A/C/G]TAATCCTATGTACTA | 26054 |
rs768860262 | in-del | -/T | 3.31137e-05 | 0.00406887 | intron-variant | SENP6 | GRCh38.p7 | 6:75623873 | TGATTGCTACTTATG[-/T]TTTTTTTCCCCTTAT | 26054 |
rs768863593 | snp | A/G | 1.66935e-05 | 0.00288903 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697466 | TAAAAACATGGACCC[A/G]GCACGTAGATATTTT | 26054 |
rs768938909 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645196 | GTAGAGCTTCTCTGC[C/G]TCTGGTTGGTTAGGG | 26054 |
rs768942720 | snp | A/G | 4.0036e-05 | 0.00447397 | intron-variant | SENP6 | GRCh38.p7 | 6:75624012 | ATATACAAAAAAATT[A/G]TTACCTCAAAAGATT | 26054 |
rs768978508 | snp | A/C | 1.93194e-05 | 0.00310794 | intron-variant | SENP6 | GRCh38.p7 | 6:75709679 | TTTTATCTAATTAAA[A/C]GTTTTTCTTGCTGAA | 26054 |
rs769009560 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676107 | GATACTGTATTTACA[A/G]TATCTGTTAAATAGC | 26054 |
rs769051392 | snp | A/T | 1.72353e-05 | 0.00293553 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711394 | ATAGGACAGTGGCAT[A/T]TAAAGCCTACTATCT | 26054 |
rs769054714 | in-del | -/TGA | 3.35765e-05 | 0.00409721 | cds-indel, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666725 | AGTCATTTTGTCCAG[-/TGA]TGATGATGATGACAA | 26054 |
rs769085521 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617529 | CGCCCGCCTCCGCCT[C/T]CACCTCCCAAAGTGC | 26054 |
rs769087630 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635599 | TGTTAAGTAACCTCA[C/T]ACTTTATGATAAACC | 26054 |
rs769102372 | in-del | -/TTAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650577 | ATTGATGATTATTAA[-/TTAT]TTATAGCTGTGGACT | 26054 |
rs769103508 | snp | C/T | 5.29684e-05 | 0.00514601 | intron-variant | SENP6 | GRCh38.p7 | 6:75678808 | CTTCTAATTTTGTTA[C/T]AGGTTGATAGTATAT | 26054 |
rs769117517 | in-del | -/TGGGG | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601635 | ACGCCAGGTCTGCCA[-/TGGGG]CCCTGGGCGGTGGGG | 26054 |
rs769139029 | snp | G/T | 1.65919e-05 | 0.00288022 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623928 | CTCAGTGTGGATGAA[G/T]ATGAGGATTCTGAAA | 26054 |
rs769170510 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670785 | CCGTTGCTAAAGCTA[A/G]TATATAATATTTAAA | 26054 |
rs769195466 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622198 | AATGACTGTTGTGTA[A/C]AAATTTTAAATGATA | 26054 |
rs769210471 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633815 | TAGGCCCAACCTGTA[A/C]CTTTTCTTCTGAATT | 26054 |
rs769229970 | in-del | -/TTTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684047 | TGGAATATTCTTCCA[-/TTTG]TTTGTGTCCTCTTTT | 26054 |
rs769255313 | snp | A/G | 6.7706e-05 | 0.00581794 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677206 | TGTACAAGAACCTAT[A/G]AAGAGAGCATCAAAG | 26054 |
rs769317843 | snp | A/G | 1.6797e-05 | 0.00289797 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621487 | TTTGTTTTATATTGA[A/G]TAGCTCTATTAATGA | 26054 |
rs769322158 | snp | G/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599521 | GATTAAGGAATAACC[G/T]GTTTGAAGCTATTAT | 26054 |
rs769330969 | snp | C/G/T | 3.3393e-05 | 0.00408603 | missense, synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709543 | TGGCTTAAGCAAAAT[C/G/T]AGACTAAACTATAGC | 26054 |
rs769335116 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636823 | TTCAGGTGAGGGTAA[A/G]CACATTGGCTTTTAC | 26054 |
rs769354411 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613060 | CAGAGGTTGCAGTGA[A/G]CCGAGATTGTGCCAC | 26054 |
rs769366591 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691302 | TGCGAGCTACCACAC[A/T]CTGCTAATTTTTAAA | 26054 |
rs769372959 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606691 | TTGAAGCAACATGAC[C/T]CCCCTAAGAAATGCT | 26054 |
rs769383598 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694123 | TAGCCTGGCATGGTG[A/G]TCCATGCCTATAATC | 26054 |
rs769388723 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669442 | ATATGATCATATTTT[A/G]TTTAAAATACATTTT | 26054 |
rs769414275 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655726 | TAATCGATAAACAAC[A/T]CCTGGGTTGTTTCCA | 26054 |
rs769452793 | in-del | -/TTATAAG | 1.7524e-05 | 0.00296002 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621654 | TTTCCCTCAGATGTT[-/TTATAAG]AATAAAACTTCTCAT | 26054 |
rs769499332 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710197 | AGTTATTTTTTTTTC[-/C]TCCTGCCTGATTCGA | 26054 |
rs769557928 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673645 | CTACTTATAATATTA[A/G]TGTGTGACTTACTTA | 26054 |
rs769558115 | snp | A/G | 3.81745e-05 | 0.00436873 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659269 | TCCTTTAGAACGTAT[A/G]ATGAAGAAAACAGAA | 26054 |
rs769572345 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656707 | CCTATAACACTATCA[A/G]TCATTTACCATTTCT | 26054 |
rs769575215 | snp | A/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679363 | CTGAGCCATGATGGC[A/G]CCACTGCACTCCAGC | 26054 |
rs769576457 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696202 | TCTCTTATCAGTTTA[C/T]AAAATTAATATAATT | 26054 |
rs769611177 | snp | G/T | 1.65864e-05 | 0.00287974 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647785 | TCCTGTAAGGTTAAG[G/T]CGGCTCCAAGGTGTT | 26054 |
rs769611514 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627492 | GATGTGAGCAGGCAC[A/G]GTGTCTTTTGCCTGT | 26054 |
rs769613186 | snp | G/T | 1.73848e-05 | 0.00294824 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675461 | TTTTATCAAGATACA[G/T]CTAGACGGTAAGCTA | 26054 |
rs769614667 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627547 | AGCGGGAGGATCGTT[C/T]GAAGCCAGGAGTTTG | 26054 |
rs769665304 | snp | A/C | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600142 | AACACATGGTAATTA[A/C]CACTAATTTAGCAAT | 26054 |
rs769670853 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649269 | GCAGTGAGCCGAGAT[C/T]GCATCACTACGCTCC | 26054 |
rs769683005 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692584 | TGAGCTGTGACCATG[C/T]CACTGCACTCCAGCC | 26054 |
rs769699863 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711916 | GGCCTCAAGTGATCC[A/G]CCCCTCTGAGCCTTC | 26054 |
rs769712463 | snp | C/G | 1.67897e-05 | 0.00289733 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663461 | CCTGGGGCAAAAATA[C/G]CCAAAATCACAAACT | 26054 |
rs769723544 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663987 | AATAGCAAAAGATTA[A/G]AAATTATTGGGGACT | 26054 |
rs769731428 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637641 | TTTTTTGACTTTTTA[G/T]TAAGTATAGATAAAA | 26054 |
rs769740791 | snp | A/C | 5.02803e-05 | 0.00501374 | intron-variant | SENP6 | GRCh38.p7 | 6:75715360 | TTATTACAGTTTTCT[A/C]ATACGCATTTAATTG | 26054 |
rs769744416 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644677 | TTAGTAGAGACGGTG[-/T]TTTCGCCATGTTGGC | 26054 |
rs769774947 | snp | G/T | 0.000428276 | 0.0146272 | intron-variant | SENP6 | GRCh38.p7 | 6:75677284 | TTTAATTTAAAAATA[G/T]TCTTAAATTGTGGGT | 26054 |
rs769794790 | snp | A/G | 5.27737e-05 | 0.00513654 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711406 | CATTTAAAGCCTACT[A/G]TCTGTAAACAGTAAG | 26054 |
rs769809559 | snp | A/G | 1.6631e-05 | 0.00288362 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623949 | GATTCTGAAACCTCA[A/G]AAGGAAAAAAGGCAA | 26054 |
rs769819135 | snp | A/G | 1.65899e-05 | 0.00288005 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666765 | ACTAACAGAAGAGAA[A/G]GCATATCTCCTCAGC | 26054 |
rs769822521 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698762 | ACGCCTGTAATCCCA[A/G]CACTTTGAGAGGCTG | 26054 |
rs769837514 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613706 | ATTTCAGACATGCTG[C/T]TCATTTAACCGTAAT | 26054 |
rs769847836 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688000 | CTATGCCCTGCCCAC[A/C]GTGGTGGAGTCTAGA | 26054 |
rs769894636 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652617 | CGAGGCAGGTGGATC[A/G]CTTGAGGTCAGGAGT | 26054 |
rs769897443 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602713 | ATGAGCGATGACGGG[C/G]AGGGAGTGTGCTGCG | 26054 |
rs769897732 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624387 | ATCTGTAAATTAGCC[-/T]TCTATATGGGTTATT | 26054 |
rs769931729 | in-del | -/AAAG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668442 | TAATTTTTAAAAAAT[-/AAAG]AAATAGAGGCAAACC | 26054 |
rs769934392 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689006 | AGGAGGTGGAGGTTG[C/T]GGGGAGCCGAGATCA | 26054 |
rs769984381 | in-del | -/GATA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610486 | ACAGTTACAGAAAGT[-/GATA]GATAATCTGTGCCAT | 26054 |
rs769994479 | snp | A/G | 2.42504e-05 | 0.00348204 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677055 | ACAATATATAATTTT[A/G]ATTTTTCAAAATGGC | 26054 |
rs770034261 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607932 | TCTCCCAAACGATTG[G/T]CATTCCATGGAATAT | 26054 |
rs770042949 | in-del | -/CTTTTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699354 | TTGTTTTTGTTTTTG[-/CTTTTT]TTTTTTTTTTTTTTT | 26054 |
rs770068485 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665774 | GCTCACGCCTGTAAT[A/C]CCAACATTTTGGGAG | 26054 |
rs770076976 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622355 | TTGAGGTCAGGAGTT[C/T]AAGATCAGCTTGGCC | 26054 |
rs770078660 | snp | G/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600397 | AATTAAAAAAACAAT[G/T]TTTCCAAATGGAATC | 26054 |
rs770095951 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701500 | AAACATTACTTATAT[A/G]CATATTTTTGATATT | 26054 |
rs770123036 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706046 | GGTTCAAGAGATTGT[A/C]TTCTCTTGCCTCAGC | 26054 |
rs770135971 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707759 | ACAATCACAGTTCAC[C/T]GCAGTCTCAACCTCC | 26054 |
rs770146880 | in-del | -/CTCATAAAAC | 2.25583e-05 | 0.00335837 | intron-variant | SENP6 | GRCh38.p7 | 6:75711464 | TAATTTTTAAGTATG[-/CTCATAAAAC]ATAACAGGACAGTTT | 26054 |
rs770197606 | snp | A/C | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620992 | GGGTTTCAGCCATGC[A/C]CTTATAAAATTTTTT | 26054 |
rs770237156 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647932 | AAAACCATTTTTTTG[C/T]AACTGATTTGAGAAT | 26054 |
rs770264240 | snp | C/G/T | 0.000181742 | 0.00953109 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678838 | TCCACCACCTCCAGC[C/G/T]AAGGGAGGCATCTCT | 26054 |
rs770273640 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681658 | AGAGCAGTGAGAGAA[C/T]GGACTGATACAGCAT | 26054 |
rs770274947 | snp | A/C | 1.65704e-05 | 0.00287836 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713569 | GGTCAAATGTTGTCA[A/C]AATTTTAAGAGAGTA | 26054 |
rs770290311 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646549 | TATTATAAGTACACT[A/G]CTGTCAGCCGGGCGC | 26054 |
rs770294118 | in-del | -/AG | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679776 | TATATGAAATAAAAC[-/AG]AACTTAGCATCAGTA | 26054 |
rs770325230 | snp | C/T | 3.57462e-05 | 0.00422751 | intron-variant | SENP6 | GRCh38.p7 | 6:75633563 | TTTTGACTCATATTT[C/T]TGGATCTTTTTTTAC | 26054 |
rs770330411 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617310 | CGGAGTTTCGCTCTT[-/G]TTGCCCAGGCTGGAG | 26054 |
rs770350544 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674147 | TTCGCAAGCTACTCC[-/T]TTTTTTTTTTTTTTT | 26054 |
rs770366672 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694646 | ATAGAACCATAAAAT[A/G]TGTGGTTTTTATGAG | 26054 |
rs770382103 | snp | C/T | 1.65649e-05 | 0.00287788 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666870 | AGAGCAGAGCGTGAA[C/T]TACGAAGCATTCCAG | 26054 |
rs770429410 | snp | A/G | 1.66643e-05 | 0.0028865 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709550 | AGCAAAATCAGACTA[A/G]ACTATAGCGATGAAT | 26054 |
rs770439666 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641112 | CACCTCCCTCCATCC[A/T]CTCCTCCCCTACCCT | 26054 |
rs770457265 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681375 | CAAGTTTCCTGAGGC[C/G]TCCACAGCTACGCTT | 26054 |
rs770465095 | snp | C/G | 0.000119057 | 0.00771454 | intron-variant | SENP6 | GRCh38.p7 | 6:75709637 | GATAACCAGGTAAAA[C/G]TTAATGCTTGGCAAA | 26054 |
rs770467481 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611313 | TTAACCACAGGAGAT[A/G]TAAAAGAATGATTTA | 26054 |
rs770518228 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712024 | TACAATGTTTTGGAG[C/T]AGAAATCACTATATA | 26054 |
rs770539437 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702430 | GCCATGTTGGCTAGG[C/T]TGGTCTCGAACTGCT | 26054 |
rs770542765 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717685 | TAGTTTAAAGTGGGA[C/T]CAAGCCTTTTAAAAT | 26054 |
rs770565424 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667879 | GAACTTATATCAGTG[A/G]CTTTTAGGAGTTCTG | 26054 |
rs770597046 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696049 | TTTTAAATTCTCCAG[C/T]CAGGAAGAGAACACA | 26054 |
rs770601275 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624936 | CCAGGAGTTTGAGAC[C/T]ACCTGGACAACATAG | 26054 |
rs770617459 | snp | C/T | 1.65836e-05 | 0.0028795 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715531 | AAAGCATAAGGACAC[C/T]TACTCAACAGAAGCA | 26054 |
rs770653302 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605612 | AGAATATGGCAGAGG[A/G]GATGCGTGTAAAGAT | 26054 |
rs770693907 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676519 | CTTTAACACTTAAAG[C/T]ATGGCTTGACTGCTT | 26054 |
rs770722675 | in-del | -/ATC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670930 | ATGTTATTGTTTATT[-/ATC]ATGCCAGCTTCGTGC | 26054 |
rs770726650 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642258 | CAGTCCTGTAGTTTA[C/T]ATTCTTATGGGACAA | 26054 |
rs770745509 | snp | A/G | 4.98053e-05 | 0.00499001 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621601 | TTGATCATGAAGAAG[A/G]AAGTGAAGGAGATAC | 26054 |
rs770770655 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690012 | AGCCTCCTGGGCTCA[A/G]GTGATCGTCCTGCCT | 26054 |
rs770784771 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612794 | TCATTCCATTGCTAA[A/G]GGATACCCTAGGTCA | 26054 |
rs770793883 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606611 | CTGACAAGTACAGCA[A/G]TCAGTGGTGGATTGT | 26054 |
rs770797371 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678041 | GAAAGGGAAATGGTT[A/C]TTTTTCTTTTGCATA | 26054 |
rs770799162 | in-del | -/TTTTTTTTCCC | 1.73978e-05 | 0.00294934 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621634 | ATAAAGAGTAAGGAT[-/TTTTTTTTCCC]TCAGATGTTTTATAA | 26054 |
rs770816319 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612959 | TCACTACTAAAAATA[-/C]AAAAATCAGCCGGGC | 26054 |
rs770833341 | snp | A/G | 1.66966e-05 | 0.00288929 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697473 | ATGGACCCGGCACGT[A/G]GATATTTTTGAGAAG | 26054 |
rs770848092 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623022 | GAAAATATACCACTT[C/T]TTAAACATGTTTATA | 26054 |
rs770850005 | snp | G/T | 1.69246e-05 | 0.00290896 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634804 | GTAGTAAAAACAGCA[G/T]CCCAAAGGTAAGAAT | 26054 |
rs770854659 | snp | C/T | 1.67506e-05 | 0.00289396 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633675 | AAAGTTTTAAAACTT[C/T]GAAAGGCAACCCAAT | 26054 |
rs770901366 | snp | A/G | 1.73198e-05 | 0.00294272 | intron-variant | SENP6 | GRCh38.p7 | 6:75670532 | TAAATTATTAAGTGA[A/G]CATTTTCTTTTCCTT | 26054 |
rs770903144 | snp | C/T | 1.6636e-05 | 0.00288405 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634736 | ATACGTCATTATGTT[C/T]TGGAACTGTAGTTCA | 26054 |
rs770913419 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625840 | CGCCACTGCACTCCA[A/G]CCTGGGTGACAGAGC | 26054 |
rs770921173 | in-del | -/AT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622660 | TTCAGAGATCCACAA[-/AT]ATACACACAAAGTTC | 26054 |
rs770962764 | snp | C/T | 1.83748e-05 | 0.00303101 | intron-variant | SENP6 | GRCh38.p7 | 6:75695754 | AAAAATAGAAATAAA[C/T]AAAGTGAACTGTTAC | 26054 |
rs770975405 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696881 | TACTTTTAAAATTTA[A/T]AACTAGTGTTAGATG | 26054 |
rs770980755 | snp | C/T | 1.65806e-05 | 0.00287924 | intron-variant | SENP6 | GRCh38.p7 | 6:75713593 | GAGAGTAAGTTCACA[C/T]TTTATTTCGTATTCT | 26054 |
rs770999908 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605189 | ATATTAAGACATCTA[C/T]ATATTACACTTTCTT | 26054 |
rs771019694 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613553 | AATGTATGTAATAGT[A/G]AAAAGGTGGATATAA | 26054 |
rs771031058 | in-del | -/AAAG | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716830 | AATAGTTGAGAATAA[-/AAAG]AAAGCCTAATCATCA | 26054 |
rs771034288 | snp | C/G | 0.000414206 | 0.0143851 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713746 | ATGTTATGAAGGGCT[C/G]TAATCCAAAAGTACC | 26054 |
rs771040336 | in-del | -/TT | | | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718645 | CTGCTATTCCAAAAC[-/TT]ATTACCTGTAGAGGG | 26054 |
rs771088788 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75684655 | CATCTATTGAGATAA[A/T]CATGTGGTTTTTGTC | 26054 |
rs771123649 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649306 | GGTGACAGAGTGAGA[C/G]TTGGTCTCAAAAGTG | 26054 |
rs771144907 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704516 | GGCGGTTTTTCTCCT[A/G]TCTCAGAATTGAACA | 26054 |
rs771177622 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620686 | TTGTCTTTAGTTCAA[C/T]TCAGAAAGCCAGAGC | 26054 |
rs771180086 | snp | A/G | 1.71164e-05 | 0.00292539 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633588 | TTTTACAGTTAAATC[A/G]TCGATCTGAAATTGT | 26054 |
rs771206716 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75686956 | CTGCCTTGCTAGGCT[G/T]GGGAAGTTCTCCTGG | 26054 |
rs771206913 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636171 | GATTAGATTCAGTTC[A/G]TATGAACTAGTTTAT | 26054 |
rs771215154 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603323 | GGGGAACAATATTGA[-/T]TTTTTTTGGCCTATG | 26054 |
rs771221347 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599821 | TATAATCCAGCACTT[C/T]GGGATGCCGAGGCGG | 26054 |
rs771236132 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637386 | TTGTTAAAATACCAC[A/C]TTAGATTAGGTAGTC | 26054 |
rs771269163 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657157 | TTGGGTACATTATCA[A/C]ATTTAGTAAGGCCAA | 26054 |
rs771272870 | snp | C/T | 2.00302e-05 | 0.0031646 | intron-variant | SENP6 | GRCh38.p7 | 6:75666708 | ATTATTAAAATACTT[C/T]TAGTCATTTTGTCCA | 26054 |
rs771276594 | snp | A/G | 5.43237e-05 | 0.00521142 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659281 | TATAATGAAGAAAAC[A/G]GAAGAGTCCGAATCA | 26054 |
rs771284922 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651376 | TGTTCGTTTTTGAGA[C/T]AGGGTCTTGCTCTAT | 26054 |
rs771286868 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687260 | ATCAGGTCATTTAAG[G/T]TCTTCTCTACACTCT | 26054 |
rs771289045 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75636275 | TCTTAATGATTAGGG[A/G]CAGCAAAGAAAACTG | 26054 |
rs771323874 | snp | A/G | 1.68926e-05 | 0.0029062 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663487 | AAACTTGAAAGAAAG[A/G]AAAACAAGTTTGTCA | 26054 |
rs771359712 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615824 | GCGAAGCCTTCTGAG[A/C]CTGAGTTTTGATTTT | 26054 |
rs771396529 | snp | A/G | 3.34969e-05 | 0.00409235 | intron-variant | SENP6 | GRCh38.p7 | 6:75670764 | CCAATTATAACATTA[A/G]AAATTCCGTTGCTAA | 26054 |
rs771400441 | in-del | -/AAC | 1.7915e-05 | 0.00299286 | cds-indel, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676050 | AGGAGTAAATAAATT[-/AAC]AAGTAAGTTGTGTAA | 26054 |
rs771431885 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645298 | ATACCTGCAAGAGTA[A/G]TGGAATCCTCAAATT | 26054 |
rs771445748 | in-del | -/C | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679504 | TTAGAAGTTTATGGT[-/C]TTGTAGGAAGCACAA | 26054 |
rs771459534 | in-del | -/TAAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696928 | GCTATGCATAATAAA[-/TAAT]TAATAATAATAATAT | 26054 |
rs771463787 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646305 | TTCAGTGTGGAAATT[A/G]CCCAGTTTTACCAGA | 26054 |
rs771486318 | snp | C/T | 3.39524e-05 | 0.00412008 | intron-variant | SENP6 | GRCh38.p7 | 6:75670543 | GTGAACATTTTCTTT[C/T]CCTTTTTAGTTTGGC | 26054 |
rs771492161 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698749 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAACA | 26054 |
rs771518387 | snp | G/T | 1.745e-05 | 0.00295376 | intron-variant | SENP6 | GRCh38.p7 | 6:75634826 | GGTAAGAATTCTAAT[G/T]GTCTTTGGTTAGTAT | 26054 |
rs771533771 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622288 | TTTGGCCGGGCACAG[G/T]GGCTCATGCCTGTAA | 26054 |
rs771566705 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653043 | CTTTTCTTTTTTTTC[-/T]TTTTTTGACGGAGTT | 26054 |
rs771575017 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629508 | TTTCACCATGGTGGC[C/T]AGGCTGGTCTCGAAC | 26054 |
rs771615446 | snp | A/T | 1.76135e-05 | 0.00296757 | intron-variant | SENP6 | GRCh38.p7 | 6:75678805 | TGCCTTCTAATTTTG[A/T]TACAGGTTGATAGTA | 26054 |
rs771637962 | snp | A/G | 1.6591e-05 | 0.00288015 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715556 | GAAGCACCTTTAGGC[A/G]AAGGAACAGAACAAT | 26054 |
rs771656124 | snp | G/T | 1.65897e-05 | 0.00288003 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623914 | GTGGGACAAATCTGC[G/T]CAGTGTGGATGAAGA | 26054 |
rs771678669 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712728 | GAGTGTTCTGAAGTG[A/G]AATCTTGAAAAAAAA | 26054 |
rs771684823 | in-del | -/T | 1.66088e-05 | 0.00288169 | intron-variant | SENP6 | GRCh38.p7 | 6:75713617 | GTATTCTGATGGGGA[-/T]GAAGAACTATGTATA | 26054 |
rs771752341 | snp | A/G | 0.000132674 | 0.00814368 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702902 | AAGAAAGTGACCCTC[A/G]TTATAAGAGAAACAT | 26054 |
rs771790350 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702358 | GAGTAGCTGGGATTA[C/T]GGGTGCACACCACTG | 26054 |
rs771792257 | snp | A/C/T | 0.000203671 | 0.0100897 | intron-variant | SENP6 | GRCh38.p7 | 6:75602589 | AAGGTACGTCTGTTT[A/C/T]TGCCCTTGACGGGGA | 26054 |
rs771830390 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689116 | CCTATAGTCCTAGCT[A/G]TTGAGGAGGCTGAGA | 26054 |
rs771874241 | in-del | -/AAAAAAAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652683 | TCTACTAAAAATCTC[-/AAAAAAAA]AAAAAAAAAAAAAAA | 26054 |
rs771875539 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682026 | GAATGTCAAAGTAAT[G/T]ATATTAAATAGGTTG | 26054 |
rs771923969 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689911 | TGGATGTCCAAAAGA[A/G]CTGAAAGCAGCGTCT | 26054 |
rs771944733 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667767 | GCTTTATATGCAAAC[A/G]TGATTATTGGCAAAC | 26054 |
rs771949480 | snp | A/G | 7.39946e-05 | 0.00608209 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677082 | TGGCCTTGATCCTCC[A/G]GCAAATATGGTATTT | 26054 |
rs771974066 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694127 | CTGGCATGGTGGTCC[A/C]TGCCTATAATCCCAA | 26054 |
rs771980616 | snp | A/G | 1.72421e-05 | 0.00293611 | intron-variant | SENP6 | GRCh38.p7 | 6:75670534 | AATTATTAAGTGAAC[A/G]TTTTCTTTTCCTTTT | 26054 |
rs772026117 | in-del | -/TT | 1.69158e-05 | 0.00290819 | intron-variant | SENP6 | GRCh38.p7 | 6:75666946 | TGAAAGACCAGGTAC[-/TT]TTCACTTTTGTTGAC | 26054 |
rs772085179 | snp | A/G | 3.35143e-05 | 0.00409341 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697439 | GAATACAGCAAAAAC[A/G]GCATGGGAGAGTAAA | 26054 |
rs772127609 | snp | C/T | 1.66882e-05 | 0.00288857 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695914 | GAAATCATGAAACAA[C/T]TAATCTGTCGTAAGT | 26054 |
rs772177756 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677859 | GTTTATTTCCTATTA[C/T]AGCAACTTAGCTTTG | 26054 |
rs772217198 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704116 | ACACCTGTAGGTATG[C/T]CTCGTCAGGTGGGAC | 26054 |
rs772241200 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708621 | AAGTGAGGCCAGGCA[-/C]CGGTGGCTCATGCCT | 26054 |
rs772261987 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660923 | GGCGTGAGCCACCGC[A/G]CCTGGCCATTATTTT | 26054 |
rs772267706 | snp | C/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599815 | CACGCCTATAATCCA[C/G]CACTTTGGGATGCCG | 26054 |
rs772269977 | snp | A/G | 1.65866e-05 | 0.00287976 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713792 | CAGTGACTGTGGTGT[A/G]TATGTATTGCAGTAT | 26054 |
rs772306057 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75635803 | GGAGAGTAATTAGGG[C/G]AGAGAAAAAGAGTAG | 26054 |
rs772315570 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696576 | TCTACCTCCCACTCT[A/C]AAGTGATCCTTCCAC | 26054 |
rs772341095 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648340 | TTATAAAAAATATAT[A/C]ATCATAAAATCAGTT | 26054 |
rs772368297 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649229 | CTGAGACACAAGAAT[C/T]GCTTGAACCCAGGAG | 26054 |
rs772380466 | snp | C/T | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666850 | CGCTAAATGAAAATA[C/T]TTGCAGAGCAGAGCG | 26054 |
rs772419718 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685939 | AGCTGAGTTCAATTC[C/T]TGGGTATCCTTCTTC | 26054 |
rs772420900 | snp | A/G | 1.8675e-05 | 0.00305568 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621677 | ATAAAACTTCTCATT[A/G]GAAAAACAATTTCTA | 26054 |
rs772465691 | snp | G/T | 1.6884e-05 | 0.00290547 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633697 | CAACCCAATTGGACT[G/T]AACATGTTGAGCAAC | 26054 |
rs772498884 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606756 | CTCAGTTGGGATAAT[A/G]TAATAAAATTTGCAA | 26054 |
rs772501214 | snp | A/G | 0.000175966 | 0.00937829 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659291 | AAAACAGAAGAGTCC[A/G]AATCACAAGTGGAGC | 26054 |
rs772505814 | in-del | -/GTCCAATCT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656502 | GCCATCCTTGAACCA[-/GTCCAATCT]TAAGCTTTTTGCCAT | 26054 |
rs772561511 | snp | C/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620191 | TAGTGATGCTGAGCA[C/T]CTTTTCATGGGAGGA | 26054 |
rs772597781 | snp | A/C | 1.76418e-05 | 0.00296995 | intron-variant | SENP6 | GRCh38.p7 | 6:75709658 | GCTTGGCAAAAAGTT[A/C]TAATGTTTTATCTAA | 26054 |
rs772615345 | snp | A/G | 1.70484e-05 | 0.00291957 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675879 | AGACCATGATCCTGT[A/G]GAGATTATATTAAAT | 26054 |
rs772643145 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663679 | ATAGTTAAAAAAAAC[-/A]AAAAAAAAGAACCAC | 26054 |
rs772647185 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671202 | TATTCTGCCACCAAT[C/G]CAAGTTTTTATTTTC | 26054 |
rs772681744 | in-del | -/TTTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608928 | TTAGTTTGCATTGTT[-/TTTC]TTTCACTGACTACCT | 26054 |
rs772698969 | snp | A/G | 1.80651e-05 | 0.00300536 | intron-variant | SENP6 | GRCh38.p7 | 6:75677291 | TAAAAATATTCTTAA[A/G]TTGTGGGTAGTTTTA | 26054 |
rs772699241 | snp | C/T | 1.65886e-05 | 0.00287993 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666767 | TAACAGAAGAGAAAG[C/T]ATATCTCCTCAGCCT | 26054 |
rs772718942 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631014 | TGCTATTTAATCCAT[A/G]CATTGGATTTTTTTT | 26054 |
rs772720075 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667788 | ATTGGCAAACAAAAT[C/T]GTTGCCTGTTAATAT | 26054 |
rs772727017 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665721 | TTTAGTAGCTTCCTG[G/T]GTGAGATAAAATTAC | 26054 |
rs772752136 | snp | A/G | 1.69335e-05 | 0.00290972 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677207 | GTACAAGAACCTATG[A/G]AGAGAGCATCAAAGG | 26054 |
rs772786015 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615017 | TGCCTCAGCCTCCCA[A/G]TTAGCTGGGATTACA | 26054 |
rs772804556 | snp | A/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679644 | CCTGGAAGAGCTTAC[A/G]TTATGACCCAATATA | 26054 |
rs772857077 | in-del | -/TATG | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619444 | ACATTCCGTTGTGTC[-/TATG]TGTGTGTGTGTGTGT | 26054 |
rs772871460 | snp | A/G | 1.65965e-05 | 0.00288062 | synonymous-codon, utr-variant-5-prime, intron-variant, missense, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621596 | GAGCTTTGATCATGA[A/G]GAAGAAAGTGAAGGA | 26054 |
rs772886314 | in-del | -/ATTC | 6.86201e-05 | 0.00585707 | intron-variant | SENP6 | GRCh38.p7 | 6:75713854 | GTTGGATCTGCTATA[-/ATTC]ATAAATAATAAAATA | 26054 |
rs772886484 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653045 | TTTTCTTTTTTTTCT[G/T]TTTTGACGGAGTTTC | 26054 |
rs772895562 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689250 | AAGAAAAAAATAAAA[A/T]CTTTATAGATAAGTC | 26054 |
rs772901461 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717440 | AACTCAAGTCAATCA[G/T]ATTTTAACATGAAAA | 26054 |
rs772902866 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700513 | TTATTTTGAGATGGG[C/G]TCTCACTCTGTCGCC | 26054 |
rs772920861 | snp | A/G | 0.000193335 | 0.00983006 | intron-variant, missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75640700 | AGTCTGGACCGAAAA[A/G]AAAGGTAAGCTTAAT | 26054 |
rs772956704 | snp | A/G | 1.74066e-05 | 0.00295008 | intron-variant | SENP6 | GRCh38.p7 | 6:75633731 | AAGAAATTGAGGTAT[A/G]GGCACTTCACCACAC | 26054 |
rs772984093 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668575 | GAAAAATTTAAAACT[A/G]TGATATTGTCTCAAT | 26054 |
rs773010205 | snp | A/G | 3.37895e-05 | 0.00411018 | intron-variant | SENP6 | GRCh38.p7 | 6:75695951 | CTGAAAATATTTAAC[A/G]GATGTAAGTCACTCA | 26054 |
rs773018586 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689923 | AGAACTGAAAGCAGC[A/G]TCTTTTTGTTTTGAG | 26054 |
rs773029730 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615926 | CTTGTGTTCATTTGG[C/T]AACTTGTGCCCTCAT | 26054 |
rs773055273 | snp | A/C | 1.79432e-05 | 0.00299521 | intron-variant | SENP6 | GRCh38.p7 | 6:75675724 | GATTTTTTTTATTAC[A/C]CACAAGAGTAATGAT | 26054 |
rs773071793 | snp | A/G | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666865 | CTTGCAGAGCAGAGC[A/G]TGAACTACGAAGCAT | 26054 |
rs773103512 | in-del | -/ACTTAA | 1.6617e-05 | 0.00288239 | intron-variant | SENP6 | GRCh38.p7 | 6:75675772 | TATGTGCTTACATTT[-/ACTTAA]ACTTGTATTTCCTCA | 26054 |
rs773103747 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622501 | GAGGTAGAGGTTGCA[G/T]TGAACCCAGATCATG | 26054 |
rs773110436 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712736 | TGAAGTGGAATCTTG[-/A]AAAAAAAAAGTTCTA | 26054 |
rs773121379 | in-del | -/AA | 0.000488003 | 0.0156129 | intron-variant | SENP6 | GRCh38.p7 | 6:75675681 | TCATTTGGAAAAAAT[-/AA]AAAAGTTTCTTTAAG | 26054 |
rs773139139 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708176 | GCAATTCTCCTGTCT[C/T]TCAGCCTCTCAAGTA | 26054 |
rs773177839 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676220 | TTCTCCATTTTACAG[A/G]TGAGGAAAAACTCAC | 26054 |
rs773186282 | snp | C/G/T | 1.66815e-05 | 0.00288799 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670645 | AAGCTGCCAAAGTTC[C/G/T]TTTGACAGTGTCATT | 26054 |
rs773186966 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604525 | TAGTCCCAGCTACTG[C/T]GGAGGCTGAGGCAGG | 26054 |
rs773191480 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709922 | CTTAAAAAACAAATT[C/G]AGCTTTCAAGTCAGA | 26054 |
rs773225149 | snp | A/G | 1.80651e-05 | 0.00300536 | splice-donor-variant | SENP6 | GRCh38.p7 | 6:75711417 | TACTATCTGTAAACA[A/G]TAAGCATTAACTGTG | 26054 |
rs773316020 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625707 | AACCTCGTCTCTACT[A/G]AAAATAGAAAAATTA | 26054 |
rs773320521 | snp | C/T | 1.70179e-05 | 0.00291696 | intron-variant | SENP6 | GRCh38.p7 | 6:75713847 | TTCAATTTGTTGGAT[C/T]TGCTATAATAAATAA | 26054 |
rs773332934 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75634339 | TCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 26054 |
rs773343355 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659771 | TATTGTCCTCACTCT[C/T]TATGCCTTTTTCCCT | 26054 |
rs773365100 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648511 | TGCTTTTAAAAAACA[C/T]CCACATTTTTTTTTC | 26054 |
rs773370055 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599881 | CCAGGCTGGCCAAGG[C/T]GGTGAAACCCCGTCT | 26054 |
rs773376368 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619748 | AATGCACAAGAGTTC[-/CA]GTTTCTCCCACATCC | 26054 |
rs773428838 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704278 | TACTATTTTCACTAT[C/T]TCAGCAAGAGGAATG | 26054 |
rs773462728 | snp | A/T | 2.03246e-05 | 0.00318777 | intron-variant | SENP6 | GRCh38.p7 | 6:75711283 | TAGGTTATTAGTTAT[A/T]TAGATTATATATTTT | 26054 |
rs773482564 | snp | A/G | 2.92487e-05 | 0.00382407 | intron-variant | SENP6 | GRCh38.p7 | 6:75670755 | TTTACTATACCAATT[A/G]TAACATTAAAAATTC | 26054 |
rs773492423 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617910 | TACAGTGTCCCTCAG[G/T]TTGGGTTTGTCTGAT | 26054 |
rs773537630 | snp | C/T | 0.000334756 | 0.0129331 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75678972 | AAATCTTTAACATTC[C/T]GTCATATCTTATGTC | 26054 |
rs773540991 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649242 | ATCGCTTGAACCCAG[A/G]AGGCAGAGGTTGCAG | 26054 |
rs773557797 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657107 | TGTGGCTTAAAAAGA[A/T]TAATGAAGTATGTTT | 26054 |
rs773562551 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637477 | ATATTTAAAAGATAG[A/T]TTGTTTATACACTAA | 26054 |
rs773564660 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75618491 | CAGGTTCATATTGGT[A/G]TTTTTTCTGCCTCTG | 26054 |
rs773584488 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691588 | GTGTTTTGTTTTTTG[G/T]TTTTTGTTTTTGTTT | 26054 |
rs773644391 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661906 | AAAAAACAAAAATTA[A/G]CTGAGCATGGTGGTG | 26054 |
rs773647016 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75686734 | TTGGCCCCCACTCTC[-/TT]CTGGCTTGTAGGGTT | 26054 |
rs773692165 | snp | C/T | 1.65869e-05 | 0.00287979 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647786 | CCTGTAAGGTTAAGT[C/T]GGCTCCAAGGTGTTG | 26054 |
rs773715687 | snp | A/G | 1.71272e-05 | 0.00292632 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670671 | TCATTTTAAACTGTC[A/G]AAGTATACGAGTAGG | 26054 |
rs773743706 | snp | G/T | 1.74148e-05 | 0.00295078 | intron-variant | SENP6 | GRCh38.p7 | 6:75647681 | TTAACTTTTTCATTT[G/T]GAAAACTGTATTTCC | 26054 |
rs773745786 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678525 | GCCTTGTGCTTACCC[C/T]TTTTATTGAAACTTT | 26054 |
rs773769362 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613943 | ATTGCATTGATTGTT[A/G]TGTCCCATTTGTCTT | 26054 |
rs773795535 | in-del | -/A | 1.79374e-05 | 0.00299472 | intron-variant | SENP6 | GRCh38.p7 | 6:75670504 | TTATACTTAGCTTGC[-/A]GCCTTATTTTAGTAA | 26054 |
rs773833083 | snp | C/T | 3.45943e-05 | 0.00415884 | intron-variant | SENP6 | GRCh38.p7 | 6:75670533 | AAATTATTAAGTGAA[C/T]ATTTTCTTTTCCTTT | 26054 |
rs773836910 | snp | C/T | 1.66355e-05 | 0.002884 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634737 | TACGTCATTATGTTC[C/T]GGAACTGTAGTTCAT | 26054 |
rs773840540 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645212 | TCTGGTTGGTTAGGG[G/T]TAGAAAAGAAATAGC | 26054 |
rs773853912 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704511 | CATAGGGCGGTTTTT[C/G]TCCTATCTCAGAATT | 26054 |
rs773888324 | snp | A/G | 6.62603e-05 | 0.0057555 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666874 | CAGAGCGTGAACTAC[A/G]AAGCATTCCAGAAGA | 26054 |
rs773898510 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608219 | CTGAGATAACACTTC[A/G]GGAGGCCAAGGCAGG | 26054 |
rs773945704 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627722 | GCTCTGTCACCCAGG[C/T]CAGAGGGCAGTGGTG | 26054 |
rs773952477 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637741 | TTATCTTTTAAGTCT[C/T]CCCCCGCAACTTAGG | 26054 |
rs773969983 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664390 | TATACATGTACACAC[A/G]TACGTCTGTATGTAT | 26054 |
rs774001266 | snp | C/T | 1.75844e-05 | 0.00296511 | intron-variant | SENP6 | GRCh38.p7 | 6:75678539 | CTTTTTATTGAAACT[C/T]TTCCTAATTGACTGT | 26054 |
rs774017683 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712422 | AGTGGGTCACACTTT[C/G]TGCTAGCACTTCTGA | 26054 |
rs774022326 | in-del | -/T | 0.000226886 | 0.0106485 | intron-variant | SENP6 | GRCh38.p7 | 6:75676996 | TTTACTTCTTTTGTG[-/T]TTTTTTTTTGGACTT | 26054 |
rs774040434 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700377 | CTAGTTTTTAGGTGA[C/G]GATATTTGTAGCTTA | 26054 |
rs774052151 | snp | A/C | 1.66604e-05 | 0.00288616 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709551 | GCAAAATCAGACTAA[A/C]CTATAGCGATGAATC | 26054 |
rs774071558 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652867 | TTTTCTTCATAACTG[A/G]TGAGATATCTTACTT | 26054 |
rs774077082 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75665521 | GTTTGTATTTGACTC[A/G]AATACAATGTGAGTG | 26054 |
rs774146777 | snp | G/T | 1.67016e-05 | 0.00288973 | intron-variant | SENP6 | GRCh38.p7 | 6:75715368 | GTTTTCTAATACGCA[G/T]TTAATTGTATTTTCA | 26054 |
rs774192731 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652602 | GGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCG | 26054 |
rs774209210 | snp | A/T | 1.65897e-05 | 0.00288003 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621675 | GAATAAAACTTCTCA[A/T]TAGAAAAACAATTTC | 26054 |
rs774230652 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645345 | TGCTGGCCAGGTGTG[C/G]TGGTTTATGCCTGTA | 26054 |
rs774246708 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660380 | ATGAGCTAGAAGTAT[G/T]TCTTATTCCATATTT | 26054 |
rs774274512 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669951 | AGATTTTTTTTTTTT[-/A]AGAAGGAATTTCGAT | 26054 |
rs774285395 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701805 | CTACCACGCCCAGCT[A/C]ATTTTCTGTATTTTA | 26054 |
rs774310717 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666408 | GACCTACTGTTCTTC[C/T]TGTAACTTGCTGATA | 26054 |
rs774321882 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627905 | GTCTCGAACTCTGAC[C/T]TCGTGATCTGCCCGC | 26054 |
rs774332173 | snp | C/T | 5.0145e-05 | 0.00500699 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675915 | TGATCTAACTAAATG[C/T]GAATGGTGTAATGTC | 26054 |
rs774367284 | snp | C/T | 1.70953e-05 | 0.00292359 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633589 | TTTACAGTTAAATCG[C/T]CGATCTGAAATTGTT | 26054 |
rs774390804 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701290 | TAGCAAAAAATGAAT[A/C]TTAGCCAGGACTGTA | 26054 |
rs774392962 | snp | A/C | 3.31697e-05 | 0.00407231 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715547 | TACTCAACAGAAGCA[A/C]CTTTAGGCGAAGGAA | 26054 |
rs774406963 | snp | A/G | 1.66172e-05 | 0.00288242 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695888 | TAAACGCCTTAATCA[A/G]AGAGAGAGGAGAAAT | 26054 |
rs774460033 | snp | A/G | 5.50737e-05 | 0.00524727 | intron-variant | SENP6 | GRCh38.p7 | 6:75695755 | AAAATAGAAATAAAT[A/G]AAGTGAACTGTTACA | 26054 |
rs774466929 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688392 | CAGCTCACCCTCCAT[G/T]GGCTGCATCCCCTGT | 26054 |
rs774475367 | snp | A/G | 1.67089e-05 | 0.00289035 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697488 | AGATATTTTTGAGAA[A/G]GATTTTATTTTTGTA | 26054 |
rs774482928 | snp | C/G | 4.19489e-05 | 0.0045796 | intron-variant | SENP6 | GRCh38.p7 | 6:75670770 | ATAACATTAAAAATT[C/G]CGTTGCTAAAGCTAA | 26054 |
rs774499137 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619376 | AGTAACTGTTTTCAA[A/G]GTTCATCTGTCTTGT | 26054 |
rs774511964 | in-del | -/A | 1.65979e-05 | 0.00288074 | splice-acceptor-variant | SENP6 | GRCh38.p7 | 6:75623897 | CCTTATTTTCTGTGT[-/A]AGTGGGACAAATCTG | 26054 |
rs774525902 | snp | C/T | 1.7464e-05 | 0.00295495 | intron-variant | SENP6 | GRCh38.p7 | 6:75703081 | CATACAGGTATGTAT[C/T]TAAATGTTTTGAAAG | 26054 |
rs774547118 | snp | C/T | 6.80944e-05 | 0.0058346 | intron-variant | SENP6 | GRCh38.p7 | 6:75711464 | TAATTTTTAAGTATG[C/T]TCATAAAACATAACA | 26054 |
rs774578807 | snp | A/G/T | 3.40022e-05 | 0.00412312 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677213 | GAACCTATGAAGAGA[A/G/T]CATCAAAGGAAGTTG | 26054 |
rs774593529 | snp | C/T | 1.68029e-05 | 0.00289848 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633686 | ACTTTGAAAGGCAAC[C/T]CAATTGGACTTAACA | 26054 |
rs774650695 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702627 | AACATATTTAGTCAT[G/T]TCATTTGTTTTTTAC | 26054 |
rs774653296 | in-del | -/AAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705554 | ATCTCAAAAATAAAT[-/AAA]TAAATTAATTAATTA | 26054 |
rs774658892 | snp | C/T | 6.99496e-05 | 0.00591354 | intron-variant | SENP6 | GRCh38.p7 | 6:75675502 | TTTTACTTACCAAAG[C/T]TTTCTTTACACCAAA | 26054 |
rs774692588 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659124 | TGTGGAGATCCTGCT[A/G]AGGAGTGAAAAATAA | 26054 |
rs774695548 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669493 | GGTAGAAATACCTTT[A/G]GAAGGATAATGGGAA | 26054 |
rs774706239 | in-del | -/TGA | 3.35765e-05 | 0.00409721 | cds-indel, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666724 | AGTCATTTTGTCCAG[-/TGA]TGATGATGATGATGA | 26054 |
rs774739886 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668264 | GAATGCCTTTCCCAC[A/G]TGGTAGCACGAGCAA | 26054 |
rs774759058 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619449 | CGTTGTGTCTATGTG[-/TG]TGTGTGTGTGTGTGT | 26054 |
rs774766079 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631455 | GCTTATTAGTTACTT[A/G]ATGATTAATGTTATA | 26054 |
rs774768911 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661686 | ACTTTAATTCCTAGA[C/T]AAGGTTAGTGGTTTT | 26054 |
rs774777884 | in-del | -/CTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708068 | TGTATCTTTTCTCTT[-/CTC]CTTTTTTGAGACAGA | 26054 |
rs774777959 | in-del | -/TTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645750 | CTTGAAATGTTTATA[-/TTC]TTGTATTTAAGATAC | 26054 |
rs774789524 | in-del | -/AGAG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678327 | TTTCATGTAGATAGT[-/AGAG]AGAGAAGTAAGATAC | 26054 |
rs774790913 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682218 | TAAACAACAGAACTA[C/T]AAAATGTGTGAAGCA | 26054 |
rs774833035 | snp | C/G/T | 3.32111e-05 | 0.00407488 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621604 | ATCATGAAGAAGAAA[C/G/T]TGAAGGAGATACAGA | 26054 |
rs774838446 | snp | C/G | 5.82717e-05 | 0.00539745 | intron-variant | SENP6 | GRCh38.p7 | 6:75640667 | TCTTATATTTTTTTT[C/G]TTTTTCATGTTTTAA | 26054 |
rs774862592 | snp | A/C | 1.65905e-05 | 0.0028801 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647793 | GGTTAAGTCGGCTCC[A/C]AGGTGTTGGTAAGTG | 26054 |
rs774887596 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690204 | GCATAAGCCACTGCT[A/C]CCAACCAGAAAGCAG | 26054 |
rs774893974 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611501 | TCCTGAATTACGTGT[C/T]TGCACTTTCAAAGTT | 26054 |
rs774907737 | in-del | -/AAAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662062 | CTTCTCAAAATAAAT[-/AAAT]AAATAAATAAATAAA | 26054 |
rs774911032 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714127 | ACACTGCCTCTTTTA[C/G]CCTCTTTTCTCCTCT | 26054 |
rs774977953 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654391 | ACAAATAATGTATTT[A/G]ATTGGAGAATGGGTA | 26054 |
rs775013518 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637051 | GCACCAGGCTAACTT[C/T]AAAAAAATTTTTTTT | 26054 |
rs775061071 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606723 | ATTGAATCAATTCAG[A/G]TTTTTGGATTTGGGA | 26054 |
rs775068973 | snp | A/G | | | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675999 | GAGCATCCAACTGCA[A/G]ATGAATAAGGAGGAT | 26054 |
rs775082153 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642376 | TTCTTTAAATCGCAT[A/G]TTCAGGGAAACTCTT | 26054 |
rs775098338 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649794 | TGCTGGGATTACACG[C/T]GTCAGCCACCGCGCC | 26054 |
rs775148648 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710380 | TTAAAAGAGGATTTT[A/G]TATTGAGAAAAGTTT | 26054 |
rs775150574 | snp | C/T | 1.68812e-05 | 0.00290522 | intron-variant | SENP6 | GRCh38.p7 | 6:75670547 | ACATTTTCTTTTCCT[C/T]TTTAGTTTGGCAATT | 26054 |
rs775156098 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694180 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAAGTTG | 26054 |
rs775179671 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712878 | GGAAGGCTGAGGTGG[A/G]CAGATAGCTTGAGCC | 26054 |
rs775242565 | snp | C/T | 4.97665e-05 | 0.00498806 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715433 | TTGGCAAACTGGTTT[C/T]CTCCACCAAGAATGA | 26054 |
rs775252774 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691437 | GTTAAAGGAGTTCTG[A/G]TGATGTTAGATTTTC | 26054 |
rs775256534 | in-del | -/TATA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709840 | AAAAGAAAAAGACTT[-/TATA]TATAAAGTCTTGTAA | 26054 |
rs775271374 | snp | A/C | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679404 | AAGCAAAACTCTACC[A/C]CCACACCCACCCCCG | 26054 |
rs775288606 | snp | A/C | 1.65778e-05 | 0.002879 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702758 | GTTCAACTGTAGAGG[A/C]CAGTTGTATTTCTTC | 26054 |
rs775311795 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643551 | ACATGGTAAAACCCC[A/G]CCTCTATTAAAAATA | 26054 |
rs775374774 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638958 | AGCTGCTCAAGGTGG[A/G]AGAATCACCTGAGCC | 26054 |
rs775394355 | snp | C/G/T | 0.000125967 | 0.00793531 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677093 | CTCCGGCAAATATGG[C/G/T]ATTTGAAAGTATCAT | 26054 |
rs775395275 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75673231 | TATGCACAAATTCAT[C/T]TTTCAAATGAGAAGA | 26054 |
rs775414504 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600749 | AGATTTTTTTAAAAC[C/T]ACATGTTGAAGTCTG | 26054 |
rs775456391 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689267 | TTTATAGATAAGTCA[A/G]AAGATGTTATCTCTT | 26054 |
rs775465548 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603767 | TGAAAGAATAGTGAA[G/T]AATAGAGGTAATTTT | 26054 |
rs775466080 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651774 | TCATACTGTATGTAC[C/T]GTTCTGTATGTAACT | 26054 |
rs775474616 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75600820 | TTCTCAGTATTATAC[C/T]GTCATTGGCACAGAC | 26054 |
rs775516350 | snp | A/G | 2.62912e-05 | 0.00362559 | intron-variant | SENP6 | GRCh38.p7 | 6:75676083 | AACAGATTATAATAG[A/G]TAATAATAGATACTG | 26054 |
rs775531092 | snp | A/G | 1.74184e-05 | 0.00295109 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659296 | AGAAGAGTCCGAATC[A/G]CAAGTGGAGCCTGAA | 26054 |
rs775535147 | snp | C/G/T | 0.000170044 | 0.00921937 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675884 | ATGATCCTGTAGAGA[C/G/T]TATATTAAATACCTC | 26054 |
rs775543637 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714996 | AACTGGAGCTGGCAA[A/G]CTTGTTAATAAAGTA | 26054 |
rs775548052 | snp | C/T | 9.95025e-05 | 0.00705275 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75702915 | TCGTTATAAGAGAAA[C/T]ATATGCAGTGTAAAA | 26054 |
rs775552627 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658253 | TGATGATCACTTAGT[G/T]AAACTTTGTGATTGC | 26054 |
rs775558049 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627741 | AGGGCAGTGGTGTGA[C/T]CTCAGCTCACTGCAA | 26054 |
rs775572866 | snp | C/T | 1.65985e-05 | 0.00288079 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713797 | ACTGTGGTGTATATG[C/T]ATTGCAGTATGTAGA | 26054 |
rs775585922 | snp | C/T | 0.000163948 | 0.00905246 | intron-variant | SENP6 | GRCh38.p7 | 6:75675662 | ACTTTTTAGAAACCC[C/T]TTTTCATTTGGAAAA | 26054 |
rs775616170 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698813 | GTCAGGGGTTCAAGA[C/G]CAACCTGGCGAACAT | 26054 |
rs775620933 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706101 | TGCGCACCACCTCAC[C/G]CGACCTGTTGAGCTC | 26054 |
rs775653867 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671679 | GTGAGCCGAGACGGC[A/G]CCACTGCACTCCAGT | 26054 |
rs775654996 | snp | G/T | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621016 | ATTTTTTAAAATTCA[G/T]AATGAGCACATTTAG | 26054 |
rs775707020 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637663 | TAGATAAAAAGACTT[A/C]TAAGAACCTTATAAG | 26054 |
rs775742626 | snp | C/G | 0.000186619 | 0.00965789 | intron-variant | SENP6 | GRCh38.p7 | 6:75622725 | ATACAAGAAGTCATT[C/G]AGAATATATTGGCTA | 26054 |
rs775762412 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674479 | GGCATGCATTACCAC[A/G]CCTGGCTAATTTTTT | 26054 |
rs775774053 | in-del | -/T | 1.65957e-05 | 0.00288055 | intron-variant | SENP6 | GRCh38.p7 | 6:75713476 | GCATTTGTAATATTA[-/T]TGAAGTATTCGACTT | 26054 |
rs775783086 | snp | A/C | 1.79493e-05 | 0.00299572 | intron-variant | SENP6 | GRCh38.p7 | 6:75695773 | GTGAACTGTTACATT[A/C]ATTATATTTGAATTA | 26054 |
rs775795644 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717703 | AGCCTTTTAAAATGT[A/G]TTATTAGTACTTAGA | 26054 |
rs775803368 | in-del | -/TGT | 0.000186411 | 0.00965249 | intron-variant, utr-variant-5-prime | SENP6 | GRCh38.p7 | 6:75622856 | AGGAGAGCTTTGAAC[-/TGT]TGGTAAGTCTCTCAT | 26054 |
rs775827535 | snp | C/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679794 | ACTTAGCATCAGTAT[C/G]CATAGTTCTCTGTAA | 26054 |
rs775850944 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682163 | TGTTATGTAATGATA[A/G]AGGAATGATCCACCA | 26054 |
rs775888251 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608544 | AGAGAGGAAGGAAAG[A/C]AAGGAAGAAAGAAAG | 26054 |
rs775900965 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645471 | AAATAACAAAAATTA[A/G]CACAGCATGGTGGCG | 26054 |
rs775903970 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694796 | GTTAGCATTTTTCTT[A/T]TGCTTTTGGGCTATT | 26054 |
rs775924894 | snp | C/T | 1.66427e-05 | 0.00288462 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634724 | AAAATACGCAAAATA[C/T]GTCATTATGTTCTGG | 26054 |
rs775940473 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701705 | AGTGCAGTGGCACAA[C/T]CTCAGCTCACTGCAA | 26054 |
rs775946508 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693881 | AAATAAATTTAATAT[A/G]TCATAATTTCCCTTT | 26054 |
rs775951261 | snp | G/T | 3.68779e-05 | 0.0042939 | intron-variant | SENP6 | GRCh38.p7 | 6:75709671 | TTCTAATGTTTTATC[G/T]AATTAAAAGTTTTTC | 26054 |
rs775987963 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75604761 | TGATTCTTTTGGTGT[C/T]TTACACTTTTAATAA | 26054 |
rs775992223 | snp | A/C | 1.65814e-05 | 0.00287931 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678690 | CATTGGCCCAGTAGA[A/C]AAGTGAGAGAATTCC | 26054 |
rs775998856 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631273 | ACTTAAATTACATGA[A/T]GTGATAATTTTGGGT | 26054 |
rs775999966 | snp | A/G | 1.77612e-05 | 0.00297998 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677102 | ATATGGTATTTGAAA[A/G]TATCATTAATGAAAT | 26054 |
rs776027526 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656241 | AAAAAAAGAATACAC[A/G]TTGAGCTACAAAATC | 26054 |
rs776027550 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681800 | TTTGGAGGCCAAGGT[A/G]GGAGGATCACTTGAG | 26054 |
rs776029409 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617352 | GATCTTGGCTCACTG[C/T]GACCTCCGTCTCCTG | 26054 |
rs776030959 | snp | C/T | 1.65864e-05 | 0.00287974 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647772 | AAGTTGAAATTAATC[C/T]TGTAAGGTTAAGTCG | 26054 |
rs776043509 | snp | A/G | 0.000208435 | 0.0102066 | intron-variant | SENP6 | GRCh38.p7 | 6:75678555 | TTCCTAATTGACTGT[A/G]AATTGCTAATTTAAT | 26054 |
rs776070542 | snp | A/C | 1.65858e-05 | 0.00287969 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702929 | ACATATGCAGTGTAA[A/C]ATACAGTGTGAAAAA | 26054 |
rs776105764 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681402 | GCTTCCTGTATAGCC[A/T]GTGGATCTGTGAGTC | 26054 |
rs776193544 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617434 | ATGCACCACCACACC[A/G]GCTAATTTTGTATTT | 26054 |
rs776229477 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625881 | CTCCAAACAAAAAAC[A/G]AAACAAAAAAACCCA | 26054 |
rs776252127 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75661506 | TGTTACATAGGTAAA[C/T]GTGTGCCGTGGTGGT | 26054 |
rs776253373 | snp | A/C/G | 4.98959e-05 | 0.00499459 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715583 | CAATATGTCAATAGT[A/C/G]TCTCAGATTGACCAT | 26054 |
rs776261871 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690018 | CTGGGCTCAAGTGAT[C/T]GTCCTGCCTCAGCTT | 26054 |
rs776304675 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689378 | AAACAATATAACACA[A/G]TGTCATCTCACATCC | 26054 |
rs776373398 | snp | C/T | 3.53176e-05 | 0.00420209 | intron-variant | SENP6 | GRCh38.p7 | 6:75663531 | CAAGTAAGTATTTTA[C/T]TCCCTTTAATATTGC | 26054 |
rs776389609 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669004 | GATATAACTCTACAG[C/T]TAAAAACAAAACAAA | 26054 |
rs776394431 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655598 | TCATTCAGGATCTTA[C/T]TTTGAGACTCATCCA | 26054 |
rs776431607 | snp | A/G | 4.97822e-05 | 0.00498885 | intron-variant | SENP6 | GRCh38.p7 | 6:75713609 | TTTATTTCGTATTCT[A/G]ATGGGGATGAAGAAC | 26054 |
rs776517903 | snp | C/G | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601175 | AATGCTATCAGAGGA[C/G]TACAAACCTACAGGA | 26054 |
rs776518048 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651390 | ACAGGGTCTTGCTCT[A/G]TTACCCAGGCTTGGA | 26054 |
rs776522655 | snp | C/T | 3.32845e-05 | 0.00407936 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666743 | TGATGATGATGACAA[C/T]GACAGAACTAACAGA | 26054 |
rs776547797 | snp | A/G | 1.71038e-05 | 0.00292431 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633710 | CTTAACATGTTGAGC[A/G]ACAATAAGAAATTGA | 26054 |
rs776552696 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657417 | CTCGGGAGAAAAAAA[-/G]CACTTTTTAGTTACT | 26054 |
rs776555487 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624739 | ATTCATAGGAATTAT[G/T]TTTATATTTAGTCTA | 26054 |
rs776578850 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612846 | AGACCAGGCGCAGTG[G/T]CTCACGTCTGTAATC | 26054 |
rs776612871 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662721 | ACTTCTGTTCATATT[C/T]TAATATTGGGGATTT | 26054 |
rs776642274 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603573 | TTCAAAAAATAACTT[A/C]TTTTAGTATGTTTCG | 26054 |
rs776661308 | snp | C/T | 1.69752e-05 | 0.0029133 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675887 | ATCCTGTAGAGATTA[C/T]ATTAAATACCTCTGA | 26054 |
rs776673199 | snp | C/T | 0.000186029 | 0.00964261 | intron-variant, utr-variant-5-prime | SENP6 | GRCh38.p7 | 6:75622814 | ATGTGCCTTCACCGA[C/T]GAGATGTTGATTTGA | 26054 |
rs776681701 | in-del | -/TTTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605328 | GTCAAGGACTCTGCC[-/TTTA]TTTAGTCTTCTGTCT | 26054 |
rs776742660 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613598 | AATAGGGGGATGTAT[A/C]AATAAGCGATTATAT | 26054 |
rs776822267 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75671422 | TTTTACATAAAGCAC[C/T]TGTCTTTAAGAGAAC | 26054 |
rs776924819 | in-del | -/AAA | 2.61605e-05 | 0.00361657 | intron-variant | SENP6 | GRCh38.p7 | 6:75670745 | CTTAAGCTCTTTACT[-/AAA]ATACCAATTATAACA | 26054 |
rs776928716 | in-del | -/AT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609614 | TATTTTTCAACAGTC[-/AT]GTGGTATTTTAAATG | 26054 |
rs776937048 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658212 | CTTTGGTGTCTAGGA[A/G]AATAGACGTGCAAAC | 26054 |
rs776968080 | in-del | -/AT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699091 | GTCTTGTAAAGTAAC[-/AT]GTGAACAGCTTACTA | 26054 |
rs776976335 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645336 | TAATGTAAATGCTGG[C/T]CAGGTGTGGTGGTTT | 26054 |
rs776982419 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696804 | AATTCCTCTCCAATA[A/G]TGATGGCATCTAGCT | 26054 |
rs776988122 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657405 | CAGATTTTAGATCTC[A/G]GGAGAAAAAAAGCAC | 26054 |
rs776992086 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615830 | CCTTCTGAGCCTGAG[-/TT]TTGATTTTTTGGGAA | 26054 |
rs777007008 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75609840 | GCTGGAGTGTAGTGG[C/T]GCCATCTCAGCTCAC | 26054 |
rs777008465 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644091 | AATTAAGAGTGCCCA[C/T]TTCAAAAGCACCTGT | 26054 |
rs777013999 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637481 | TTAAAAGATAGATTG[C/T]TTATACACTAATAGT | 26054 |
rs777053821 | in-del | -/ATTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631056 | AAAGATTTCAATGAC[-/ATTT]ATCATTTATAGAACT | 26054 |
rs777054028 | snp | A/C | 1.73812e-05 | 0.00294793 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711400 | CAGTGGCATTTAAAG[A/C]CTACTATCTGTAAAC | 26054 |
rs777121072 | in-del | -/ATA | 1.67598e-05 | 0.00289476 | intron-variant | SENP6 | GRCh38.p7 | 6:75676083 | AACAGATTATAATAG[-/ATA]ATAATAGATACTGTA | 26054 |
rs777122359 | snp | A/G | 1.67239e-05 | 0.00289166 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670652 | CAAAGTTCCTTTGAC[A/G]GTGTCATTTTAAACT | 26054 |
rs777177323 | snp | C/T | 1.66308e-05 | 0.00288359 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670575 | ATTCTATTATCAACA[C/T]ACCTCTGAAACGTCG | 26054 |
rs777182358 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640450 | AAAGCCCTTTTAAGA[-/TT]TTTTTATATTTTTGT | 26054 |
rs777190222 | snp | G/T | 2.04627e-05 | 0.00319858 | intron-variant | SENP6 | GRCh38.p7 | 6:75711278 | TTTGTTAGGTTATTA[G/T]TTATTTAGATTATAT | 26054 |
rs777199023 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75647889 | GCTGGCTTTAGAATA[C/T]TCCCAGGTATAATAG | 26054 |
rs777202812 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75681496 | TGGAGTCTTGCTCTC[G/T]CACCCAGTCTACAGT | 26054 |
rs777219844 | snp | A/C | 1.72904e-05 | 0.00294022 | intron-variant | SENP6 | GRCh38.p7 | 6:75675856 | TTCATTTGTTTTCCT[A/C]CAGAACCAGACCATG | 26054 |
rs777263494 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693811 | CTCATTTTGATAATA[A/T]TAATATGGCCATAAG | 26054 |
rs777316472 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692861 | CTGAGCCCAGAAGTT[C/G]GAGATCAGCCTGGAC | 26054 |
rs777320065 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75633304 | TCTCTGGAGAAAGCT[A/G]TCCTAAGATCCTCTA | 26054 |
rs777323391 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660792 | ATCTGCCACCATACC[C/T]GGCTTATTTTTGTAT | 26054 |
rs777382347 | snp | A/G | 1.67267e-05 | 0.0028919 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663222 | TTCTTTTTTCTAAGG[A/G]TTTGCAAAGAAATTG | 26054 |
rs777386460 | snp | A/T | 1.65883e-05 | 0.00287991 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621670 | TATAAGAATAAAACT[A/T]CTCATTAGAAAAACA | 26054 |
rs777399757 | snp | C/T | | | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718648 | CTATTCCAAAACTTA[C/T]TACCTGTAGAGGGAG | 26054 |
rs777439105 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75694537 | CTAGTACCCATTAGC[A/G]ATCACTGTTTTCTTC | 26054 |
rs777444910 | snp | A/T | 1.66554e-05 | 0.00288573 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659360 | AGTACCTATCAGCCT[A/T]CTCCTCCTCTATCTC | 26054 |
rs777548553 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690855 | CGCTCACCACCACAC[C/T]TGGCTAATTGTTTTG | 26054 |
rs777569339 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75655401 | AATCCCCATGAAGAC[A/C]TAGTAGAAATGGTAT | 26054 |
rs777570340 | snp | C/T | 1.78908e-05 | 0.00299084 | intron-variant | SENP6 | GRCh38.p7 | 6:75670506 | ATACTTAGCTTGCAG[C/T]CTTATTTTAGTAAAT | 26054 |
rs777589037 | in-del | -/AAAC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622569 | GTCTCAACAAAACAA[-/AAAC]AAACAAAAAAACATT | 26054 |
rs777603592 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656445 | ATCACTTCTGTGATC[A/C]GTTAGCTAGTAAAAC | 26054 |
rs777618298 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75618130 | TTTTATGTCTGTGTT[G/T]TTGACGTAAGTTACC | 26054 |
rs777687608 | snp | A/G | 9.91031e-05 | 0.00703859 | intron-variant | SENP6 | GRCh38.p7 | 6:75666693 | TAATATAAATTATAA[A/G]TTATTAAAATACTTT | 26054 |
rs777702951 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605555 | GGCATCCCTGAGGAG[G/T]TTACACTTAATTAAG | 26054 |
rs777721877 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677883 | AGCTTTGCTGACCTA[A/G]TTTATTGGGAACAGA | 26054 |
rs777777918 | in-del | -/GAAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75675208 | AGAAAAAAAAAAGAG[-/GAAA]GAAAGACTGATGGAA | 26054 |
rs777807901 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614326 | GCTGGAGTGCTGTGG[C/T]GCATTCTCAGCTCAC | 26054 |
rs777815655 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626898 | ACATTTACTTTTTTT[C/T]CCGTCTTTCTGGGTT | 26054 |
rs777831729 | snp | G/T | 3.31411e-05 | 0.00407056 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713572 | CAAATGTTGTCAAAA[G/T]TTTAAGAGAGTAAGT | 26054 |
rs777831873 | snp | A/C/G | 3.31891e-05 | 0.00407353 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621546 | GCTTTGGCTAGATCA[A/C/G]AGTCTAAGAGAGATG | 26054 |
rs777839411 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614698 | CTGAATCCCCCAATT[A/G]TTAATATAATGGTTC | 26054 |
rs777861780 | snp | C/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679177 | CTGACACTTTGGGAG[C/G]TCAAGGTGGGAGGAT | 26054 |
rs777864034 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606582 | AAATAATACTTTTAA[A/G]TGTAAAATTACAACT | 26054 |
rs777868009 | in-del | -/AGT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687963 | GTTTAAGTCTGCAGT[-/AGT]TGTCTGCTGCCTATT | 26054 |
rs777881195 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643319 | ACATTGTTTACAAGC[A/G]TCATACTAAAATAAC | 26054 |
rs777898579 | in-del | -/TTAT | 1.6819e-05 | 0.00289987 | intron-variant | SENP6 | GRCh38.p7 | 6:75715341 | GATTGAAATGAAAGG[-/TTAT]TTATTACAGTTTTCT | 26054 |
rs777907837 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627208 | TCAGATGATCTACCC[-/A]ACCTTGGCCTCCCAA | 26054 |
rs777913957 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691997 | GAGTAGCTGGGATTA[C/T]AGGCATGTGCTACCA | 26054 |
rs777915090 | snp | A/C | 1.65927e-05 | 0.00288029 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623905 | TTCTGTGTAGTGGGA[A/C]AAATCTGCTCAGTGT | 26054 |
rs777939239 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637323 | TTCTTTAGTAATAAT[A/G]TGGGAACGAGTGCTT | 26054 |
rs777954021 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662615 | TATCTTATTCAGCAT[A/G]GTGTATCTGCATTTT | 26054 |
rs777959788 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605052 | GCACTCCAGCCTGGG[C/T]GAGGAGCGAAACTAC | 26054 |
rs777969998 | in-del | -/GG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75663806 | TTTCCTGCTGATAGT[-/GG]GTTTTTTTTTTTGTG | 26054 |
rs777975624 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628006 | ATTTTTTGTAAAAGT[A/G]TGTGCTTTATTACAT | 26054 |
rs777985215 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714832 | ACCTTGTCTGTCTAA[-/C]ATGTATTCATTCTTC | 26054 |
rs777999360 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599709 | CCTAGTTTTCTGGCT[C/T]GTGAAACCAGAAATG | 26054 |
rs778015537 | snp | A/G | 3.65077e-05 | 0.0042723 | intron-variant | SENP6 | GRCh38.p7 | 6:75697387 | AGCTGGAGCACTAGA[A/G]ATATTTCAGAAGCTT | 26054 |
rs778028627 | snp | A/T | 1.69103e-05 | 0.00290773 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677175 | CTTTGAAGAAGCTAA[A/T]GGCAGACTTGTTGCC | 26054 |
rs778037624 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651496 | GCTGGGACTGCAGGC[A/G]CATGCTGCCACATCC | 26054 |
rs778044340 | in-del | -/T | 2.05151e-05 | 0.00320268 | intron-variant | SENP6 | GRCh38.p7 | 6:75702618 | TTTTCTAATAACATA[-/T]TTAGTCATTTCATTT | 26054 |
rs778060762 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75613524 | ATGAGACATACTAAA[A/C]TGTTCATAGTAGCAA | 26054 |
rs778062102 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687667 | TTCCTTCTAACAGTC[A/G]GGTCCCTCAGCTGTA | 26054 |
rs778074142 | snp | A/G | 3.48462e-05 | 0.00417396 | intron-variant | SENP6 | GRCh38.p7 | 6:75713866 | TATAATAAATAATAA[A/G]ATAGTGCATTTGACT | 26054 |
rs778079643 | snp | A/T | 1.88827e-05 | 0.00307262 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677076 | TCAAAATGGCCTTGA[A/T]CCTCCGGCAAATATG | 26054 |
rs778179942 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75708138 | AGTCTTGGCTTACTG[C/T]AACCTCTGTTGCCTG | 26054 |
rs778183521 | snp | C/T | 6.94987e-05 | 0.00589445 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675467 | CAAGATACAGCTAGA[C/T]GGTAAGCTATTTTAT | 26054 |
rs778202339 | snp | C/G | 0.000116392 | 0.00762775 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703016 | AGAAAGTTGCTGATA[C/G]GACTAAAAGTGAGAA | 26054 |
rs778209589 | snp | A/G | 1.67108e-05 | 0.00289052 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633654 | ATGTAAGACGAAACA[A/G]GTCTGAAAGTTTTAA | 26054 |
rs778210028 | snp | C/G | 1.82018e-05 | 0.00301672 | intron-variant | SENP6 | GRCh38.p7 | 6:75634680 | TTTTTCCGTGTTCAA[C/G]TTATTTTTTGTTTCT | 26054 |
rs778219033 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652476 | TTTCTTTGCATCAGA[G/T]CCCTAGAAATAAAAT | 26054 |
rs778220611 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688926 | ACAAAATTAGCCAGG[G/T]GTGGTAGTGCATGCC | 26054 |
rs778231684 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75688794 | CTGGGCAAGCCAGGC[A/G]TGGTGGCTCACGCCT | 26054 |
rs778232014 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659490 | ATTAAATTCTAGGTG[A/T]TCTTTTATCATAGGA | 26054 |
rs778234276 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75643729 | CATCTCAAAAAAATG[A/G]AAACAATAGAATACA | 26054 |
rs778236497 | snp | C/T | 3.32094e-05 | 0.00407475 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695858 | CCGAATTCATATATT[C/T]AGTTCTTTTTTCTAT | 26054 |
rs778281126 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700682 | TTTTTGGTAGAGACG[A/G]GGTTTTGCCACGTTG | 26054 |
rs778281329 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623473 | ACTTTCTTTTCATTA[A/G]CTAAGGCTTTCTTTC | 26054 |
rs778305093 | snp | C/T | 1.65712e-05 | 0.00287843 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713732 | AAGTTTTTCCAAAGA[C/T]GTTATGAAGGGCTCT | 26054 |
rs778324052 | snp | C/T | 1.6582e-05 | 0.00287936 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678663 | AGAAACTGGAGAAAA[C/T]CACACCATCTTCATT | 26054 |
rs778343253 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651267 | TATTGTCCCTGAATG[C/T]ACATTTAATTATATT | 26054 |
rs778343809 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616974 | GCTCAATTGATCCTC[C/T]GTCCAATCCTCCTAT | 26054 |
rs778355367 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607012 | GTGTCAGATAGGAGA[A/G]CGGTGCAAGATGATA | 26054 |
rs778370580 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695798 | GAATTATTTTCTATC[-/A]AATAGATACTTGGTG | 26054 |
rs778406391 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664838 | CTGTTTCAGGCCTGG[A/G]GATATAGCAGTGAAT | 26054 |
rs778410559 | snp | C/T | 1.65701e-05 | 0.00287833 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666801 | GATTCAGCATGTTCT[C/T]CCCCTGCACCATCCA | 26054 |
rs778449364 | snp | C/T | 0.000286275 | 0.0119606 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711356 | ACGATGGATTCCTCG[C/T]TGATGACAACTGCAG | 26054 |
rs778449391 | snp | C/T | 1.8103e-05 | 0.00300852 | intron-variant | SENP6 | GRCh38.p7 | 6:75623993 | TATTTTCTTCTTTTA[C/T]ATTATATACAAAAAA | 26054 |
rs778465124 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646258 | GGCAAATTCTCATTT[A/T]CATAATGCATATCTT | 26054 |
rs778469864 | snp | C/G | 1.74705e-05 | 0.00295549 | intron-variant | SENP6 | GRCh38.p7 | 6:75678796 | TTATTTGCTTGCCTT[C/G]TAATTTTGTTACAGG | 26054 |
rs778497138 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75702590 | TTGATATGTATTGCC[-/A]AATATAATAAACTTT | 26054 |
rs778529260 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75706922 | TTGACTTGCCATGGT[C/G]CATGAAAAATGTGTA | 26054 |
rs778644491 | snp | C/T | 8.3469e-05 | 0.00645968 | intron-variant | SENP6 | GRCh38.p7 | 6:75647727 | ACATAAATTTCTTTT[C/T]TAGGAAAGAATACCC | 26054 |
rs778665551 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605197 | ACATCTACATATTAC[A/G]CTTTCTTTACTTTCC | 26054 |
rs778670246 | in-del | -/A | 1.66941e-05 | 0.00288908 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621508 | TATTAATGAATACTT[-/A]ACTGCAGTTTGTTTT | 26054 |
rs778691850 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75610385 | GTATACCTAAGTCAT[A/G]TTACTTAGAATGATG | 26054 |
rs778745068 | snp | A/G | | | | | GRCh38.p7 | 6:75668725 | GAAGAATAGTTTGCT[A/G]TCGCAAGAGATTGGA | 26054 |
rs778771241 | in-del | -/TTTTTC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705731 | AATAGATCTAATACA[-/TTTTTC]TTTTTCTTCTTTTTT | 26054 |
rs778792883 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75717141 | TCTTAATTAGCTCAT[A/G]TGAAAAACAAGTTTA | 26054 |
rs778797087 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657579 | TTTTTTTATGTGTCA[C/T]ATAGTTTTATGTTTC | 26054 |
rs778813611 | in-del | -/T | 2.85604e-05 | 0.00377881 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75678981 | ACATTCCGTCATATC[-/T]TATGTCTTTGTTTTC | 26054 |
rs778848890 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75653814 | GGCTAGATAGACTAC[A/G]AACTTGTAAACATAC | 26054 |
rs778858719 | snp | A/G | 1.65784e-05 | 0.00287905 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702875 | CTGTAATTGATTCCA[A/G]TCCTGGGCAGGAAGA | 26054 |
rs778859025 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638554 | TGTCTTTGTGTGTGT[-/A]AGTGTGTGTGTGTGT | 26054 |
rs778859769 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689858 | TACCTCATGATGCCT[G/T]TCTCAGAACATAACC | 26054 |
rs778863856 | snp | C/T | 1.68179e-05 | 0.00289977 | intron-variant | SENP6 | GRCh38.p7 | 6:75715334 | TTTCTGTGATTGAAA[C/T]GAAAGGTTATTTATT | 26054 |
rs778900747 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652732 | AATGCCTTGTGTAAA[A/G]ATGGTTAGCTCCCAA | 26054 |
rs778902065 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641821 | TGTCTCTACAAAAAA[A/G]TAAAATAATTGGCCT | 26054 |
rs778909154 | in-del | -/TA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626341 | TGGCTTAGCTTTTTA[-/TA]TATATATATATATAT | 26054 |
rs778918530 | snp | C/T | 3.31428e-05 | 0.00407066 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713752 | TGAAGGGCTCTAATC[C/T]AAAAGTACCACAGCA | 26054 |
rs778928780 | in-del | -/AGTTAGATCAAGAGGTCCAGATTC | | | intron-variant, upstream-variant-2KB, cds-indel | SENP6 | GRCh38.p7 | 6:75620389 | TTCTGGAAGCTGGGA[-/AGTTAGATCAAGAGGTCCAGATTC]AGTATCTGGTAAGGT | 26054 |
rs778985805 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75693520 | TAGCTATTTATCTAC[A/G]TAGTGTGTTTTGAAG | 26054 |
rs778999293 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75690840 | AGCTGGGACTACAGG[C/T]GCTCACCACCACACC | 26054 |
rs779007131 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75612344 | TATTTTCTTTTGCTG[C/T]ATTTATATTTCTAAG | 26054 |
rs779010321 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654961 | CATCTTATTTTTTGA[C/T]GCATTTTAAAGTCGA | 26054 |
rs779015690 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606463 | ATTGAACACCTACTA[C/T]GTTGTAGGCAATGAC | 26054 |
rs779056267 | snp | C/G | | | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75703033 | ACTAAAAGTGAGAAT[C/G]GCCTACAGAATGAAA | 26054 |
rs779083284 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75676110 | ACTGTATTTACAATA[C/T]CTGTTAAATAGCAAA | 26054 |
rs779102632 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75624486 | ATTTCTAATTTTGGC[A/G]TACCAGATTTACACT | 26054 |
rs779106368 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75709842 | AAAGAAAAAGACTTT[A/G]TAAAGTCTTGTAAAG | 26054 |
rs779114565 | in-del | -/TTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626125 | AAATAGAGAGTTAGG[-/TTT]GTTGTTGTTGTTGTT | 26054 |
rs779123970 | snp | C/T | 2.0311e-05 | 0.0031867 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677249 | AAAAGGAAAACAAAA[C/T]TAAAACTGTAATTAT | 26054 |
rs779191007 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75626756 | TAGCCATTCCCACTA[A/G]CAGTGTATGACTCTA | 26054 |
rs779208248 | snp | A/C/G | 3.4555e-05 | 0.0041565 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666714 | AAAATACTTTTAGTC[A/C/G]TTTTGTCCAGTGATG | 26054 |
rs779219248 | snp | C/T | 0.000242657 | 0.0110122 | intron-variant | SENP6 | GRCh38.p7 | 6:75702595 | ATGTATTGCCAAATA[C/T]AATAAACTTTTCTAA | 26054 |
rs779227296 | snp | A/C | 3.3365e-05 | 0.00408429 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675990 | TCAAAAGCTGAGCAT[A/C]CAACTGCAAATGAAT | 26054 |
rs779246716 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75677644 | GGTGTACATTTGTAT[A/G]TAATATAGGCATATA | 26054 |
rs779246764 | in-del | -/CTAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680641 | CAAGGCAGATAAGGG[-/CTAA]CTAAGTATAATTTTG | 26054 |
rs779249555 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646734 | CTAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT | 26054 |
rs779266151 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711620 | CATTTGCCAGTTTCC[C/T]CAGCCTCTGCATGCA | 26054 |
rs779324397 | in-del | -/A | 0.000138937 | 0.00833362 | intron-variant | SENP6 | GRCh38.p7 | 6:75675710 | AAGGCAGTTATAAAG[-/A]TTTTTTTTATTACCC | 26054 |
rs779351067 | snp | A/C/T | 5.04217e-05 | 0.00502083 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663468 | CAAAAATACCCAAAA[A/C/T]CACAAACTTGAAAGA | 26054 |
rs779369102 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664689 | ACTGGACAGTAAAAT[C/T]AAAAAGACAGGTAGA | 26054 |
rs779373263 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672778 | TTATTAGATAATTTA[A/G]TCATTTTAATTTGCT | 26054 |
rs779474837 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75662431 | TGAGCCACCATGTCC[A/G]GGTTTAGTCAGTTTT | 26054 |
rs779491922 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650894 | CTAAACGATATCATG[C/G]TCTTTCTATAGTTAA | 26054 |
rs779521784 | snp | G/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601277 | ATTTTTATAATAAGA[G/T]AAAATTTTTAAAGGA | 26054 |
rs779537857 | snp | A/G | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619884 | ATGGATTGAGGCTGG[A/G]AGTTCGAGACCAGCC | 26054 |
rs779563746 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692598 | GCCACTGCACTCCAG[A/C]CTGGGCGAGAGAGTG | 26054 |
rs779569069 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602924 | TTCACATCTTGTCTG[G/T]TGTTCATGAAAAGTT | 26054 |
rs779576875 | snp | C/T | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75599557 | TATAGTGAAAGATTA[C/T]AGTGGCTAAGATTGA | 26054 |
rs779595864 | snp | C/T | 1.96069e-05 | 0.00313098 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670712 | CGGCTGTTAATAGAG[C/T]CTGTAATTGTAAGTA | 26054 |
rs779603091 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75687429 | CATTCTCCGTCCAGC[C/T]TTGTTCCGTTGCTGG | 26054 |
rs779610540 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704489 | GCCAACATGTCTCGC[C/T]TCCTGCCATAGGGCG | 26054 |
rs779624217 | snp | A/C/G | 3.33668e-05 | 0.00408442 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634779 | TCATCATGCTCATGC[A/C/G]CAGATACCAGTAGTA | 26054 |
rs779633491 | snp | A/T | 3.72474e-05 | 0.00431536 | intron-variant | SENP6 | GRCh38.p7 | 6:75624000 | TTCTTTTACATTATA[A/T]ACAAAAAAATTGTTA | 26054 |
rs779645964 | in-del | -/A | 1.68519e-05 | 0.0029027 | intron-variant | SENP6 | GRCh38.p7 | 6:75663176 | GTGGAAAGGAAAAAG[-/A]AAAATCAGACCAAAT | 26054 |
rs779660941 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616534 | CGGGTGGATCACAAG[C/G]TCAGGGGTTCGAGAC | 26054 |
rs779668116 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75637116 | GTCTCCAGCTTCAAG[C/G]AGTCCTGCCTCAGCA | 26054 |
rs779668712 | in-del | -/TTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614886 | TGGTTTGCAAGTTTT[-/TTG]TTGTTGTTGTTTTGA | 26054 |
rs779674860 | snp | A/G | 1.66518e-05 | 0.00288542 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75703023 | TGCTGATAGGACTAA[A/G]AGTGAGAATGGCCTA | 26054 |
rs779683222 | snp | A/G | 1.67458e-05 | 0.00289355 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621501 | AATAGCTCTATTAAT[A/G]AATACTTACTGCAGT | 26054 |
rs779697420 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608059 | TTTACTCCTTACTTA[A/G]GTATGTTTATTTCCT | 26054 |
rs779699400 | snp | G/T | 1.68701e-05 | 0.00290427 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677191 | GGCAGACTTGTTGCC[G/T]GTACAAGAACCTATG | 26054 |
rs779729963 | snp | C/T | 2.5753e-05 | 0.00358829 | intron-variant | SENP6 | GRCh38.p7 | 6:75659250 | AAGTTTATTTTTTTC[C/T]CCTTCCTTTAGAACG | 26054 |
rs779743040 | snp | A/C/G | 5.00754e-05 | 0.00500357 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75678943 | GTAAGTTAATTTTCC[A/C/G]CTGATCTTTTATTAA | 26054 |
rs779747745 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75705500 | AGTGAGCTGGGATCG[C/T]GCAACTGCACTTCAG | 26054 |
rs779807266 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642389 | TATTCAGGGAAACTC[-/T]TTTACTATGAAGCTA | 26054 |
rs779827893 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630097 | TTTTTGAGATGGAGT[C/G]TCGCTCTTGCCACCC | 26054 |
rs779848584 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716493 | ATTTTTTCATTGCTC[A/G]TTTTGTTCTTATTAT | 26054 |
rs779910495 | snp | A/C | 1.65674e-05 | 0.00287809 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713523 | TGCAGACCTTGTATC[A/C]TACTTATGGACTCAC | 26054 |
rs779913295 | snp | C/T | 1.80696e-05 | 0.00300574 | intron-variant | SENP6 | GRCh38.p7 | 6:75709497 | ATAGACATGGCCTTT[C/T]TTATTATGTAATGTT | 26054 |
rs779922188 | snp | G/T | 1.76655e-05 | 0.00297194 | intron-variant | SENP6 | GRCh38.p7 | 6:75675428 | ACTAATTCATCTTTT[G/T]TTTTAGTTTTGTTTA | 26054 |
rs779988305 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75646114 | AACCTGGATTTGGAA[A/G]TAAGACTATATTATA | 26054 |
rs780023807 | in-del | -/TATATTACTCG | 1.75108e-05 | 0.0029589 | intron-variant | SENP6 | GRCh38.p7 | 6:75675507 | TTACCAAAGCTTTCT[-/TATATTACTCG]TTACACCAAAGCACT | 26054 |
rs780041541 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644730 | CCTCAAGTGATCTGA[C/T]GGCCTTGGCCTCCCA | 26054 |
rs780054973 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652792 | TCCTGCTTTTCAGCA[A/G]CATTAGATTATTATC | 26054 |
rs780108553 | snp | A/G/T | 3.31957e-05 | 0.00407394 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75647750 | GAATACCCACCTCAT[A/G/T]TCCAAAAAGTTGAAA | 26054 |
rs780141438 | snp | C/T | 1.67351e-05 | 0.00289263 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75697443 | ACAGCAAAAACGGCA[C/T]GGGAGAGTAAAAACA | 26054 |
rs780148460 | snp | A/G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630512 | TGATAAATTTTGCAT[A/G/T]TCTCACAGAGCTCAG | 26054 |
rs780165252 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667337 | AAAAGGTAATATGAA[C/T]GATGTCAATAGACAG | 26054 |
rs780192509 | snp | G/T | | | utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75718065 | GTCAATTAAATGTAG[G/T]AGGTTTTATTTGAAA | 26054 |
rs780279824 | in-del | -/TATAAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75703375 | TAATTTATACTGAGG[-/TATAAT]TATAATAGCATTCAC | 26054 |
rs780291313 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700966 | ATGAAGAACAGGAGA[A/G]AAGCAAGCTTTCATC | 26054 |
rs780295357 | snp | C/G/T | 3.345e-05 | 0.00408951 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75634787 | CTCATGCACAGATAC[C/G/T]AGTAGTAAAAACAGC | 26054 |
rs780312607 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669779 | CTGATTTAATTCAAG[G/T]ATCACTGCCACTATA | 26054 |
rs780334819 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641731 | ACCTATAATCTTAGT[A/G]CTTTGGGAGGGCAAA | 26054 |
rs780335377 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605059 | AGCCTGGGCGAGGAG[C/T]GAAACTACATCTCAA | 26054 |
rs780347129 | snp | C/T | 1.66324e-05 | 0.00288374 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75675963 | GTTTCTTCAAGCAAT[C/T]CCAGCAGTTTATCAA | 26054 |
rs780366344 | snp | G/T | 1.67153e-05 | 0.00289091 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75663432 | ATTTACAGACTAATG[G/T]AAAAGTCATTTTACC | 26054 |
rs780372171 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668101 | AAATGAAAAACAACA[A/G]AAGCAATCATAAGGA | 26054 |
rs780374073 | snp | C/T | 1.67857e-05 | 0.00289699 | intron-variant | SENP6 | GRCh38.p7 | 6:75715354 | GGTTATTTATTACAG[C/T]TTTCTAATACGCATT | 26054 |
rs780392974 | in-del | -/AATC | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621445 | AACAAAATCTAGAAT[-/AATC]AAAGAGCTTGGGAAA | 26054 |
rs780417699 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707820 | CCTGAGTAACTGGGA[C/G]CACAGGTGCCCACCA | 26054 |
rs780439657 | snp | A/C/G | 3.31775e-05 | 0.00407282 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75623923 | ATCTGCTCAGTGTGG[A/C/G]TGAAGATGAGGATTC | 26054 |
rs780440790 | in-del | -/TTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701633 | GAAGACAGTTTAATC[-/TTT]TTTTTTTTTTTTTTT | 26054 |
rs780472784 | snp | A/T | 3.36644e-05 | 0.00410257 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676005 | CCAACTGCAAATGAA[A/T]AAGGAGGATAAAGTT | 26054 |
rs780522978 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685527 | TGGGCATTTAGTGCT[A/G]TTAATTTCCCTCTAC | 26054 |
rs780532905 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602584 | TCTGGAAGGTACGTC[A/T]GTTTCTGCCCTTGAC | 26054 |
rs780567895 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697965 | TGTGGACTACTTGAA[G/T]CAGTTTCTGAGTAAA | 26054 |
rs780571297 | snp | C/G | 0.000153167 | 0.00874985 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75711383 | GCAGTTCAGAAATAG[C/G]ACAGTGGCATTTAAA | 26054 |
rs780574973 | snp | C/T | 9.98851e-05 | 0.0070663 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709600 | GCTTGAAGATGAACT[C/T]GTCGACTTCTCAGAA | 26054 |
rs780612052 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75685556 | ACGCACTGCTTTAAA[G/T]TAAGGTGATTTAAAT | 26054 |
rs780627483 | in-del | -/TTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649986 | ACTAAGCTGTAGAAC[-/TTA]TTTAGATTTCACTAG | 26054 |
rs780645548 | snp | A/G | 1.66139e-05 | 0.00288213 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75695838 | CTGAAGAAGGAAGAC[A/G]CTGACCGAATTCATA | 26054 |
rs780657805 | in-del | -/CACTAC | | | upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75601508 | ATGATTCCAGTACCT[-/CACTAC]CTTTTCTCTTCGGTT | 26054 |
rs780663987 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606614 | ACAAGTACAGCAATC[A/G]GTGGTGGATTGTTTA | 26054 |
rs780702635 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75703377 | ATTTATACTGAGGTA[C/T]AATTATAATAGCATT | 26054 |
rs780728211 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649066 | AATCCCAGCACTTTA[C/T]GATGTCGATGCAGGC | 26054 |
rs780752051 | in-del | -/AA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656215 | CAAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 26054 |
rs780775634 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622109 | AAAGCAGAACCATTA[C/T]AAATGATAAACACAG | 26054 |
rs780827507 | snp | C/G | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75666854 | AAATGAAAATACTTG[C/G]AGAGCAGAGCGTGAA | 26054 |
rs780891486 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701590 | TTCTTAGAATGTTGA[-/A]AAAAATCATATGACC | 26054 |
rs780926912 | snp | A/G | 2.15822e-05 | 0.00328491 | intron-variant | SENP6 | GRCh38.p7 | 6:75670727 | CCTGTAATTGTAAGT[A/G]CATCTTAAGCTCTTT | 26054 |
rs780963837 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75670539 | TTAAGTGAACATTTT[A/C]TTTTCCTTTTTAGTT | 26054 |
rs780978751 | in-del | -/CATTAATAGAGCTA | 1.70787e-05 | 0.00292217 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75621634 | TAAAGAGTAAGGATT[-/CATTAATAGAGCTA]TTTTTTTCCCTCAGA | 26054 |
rs780991619 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614989 | CCAGCTCCTGGGTTC[-/A]AAGCAATTCTCCTGC | 26054 |
rs780997194 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75616256 | TAATTACAAAGGTCA[A/G]CCATAACAAGTTATT | 26054 |
rs781009950 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607421 | GTGGCTAGCTTGTTC[C/T]TATAAACTTTCTTTT | 26054 |
rs781013506 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644390 | AGGAGACTAAGGAGA[A/C]ATGATGACTTAATGC | 26054 |
rs781050990 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75704425 | CAGATTTATGTTTCT[C/T]TCCACCCAAACATCT | 26054 |
rs781065985 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75657784 | TGTGCCTAGAGTGGG[G/T]CAGAGGCAGCTTCTT | 26054 |
rs781070323 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698170 | GAATGACACACACCA[C/T]GGGCCACTCTGGAGC | 26054 |
rs781088288 | snp | A/G | | | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679339 | TGAGCCCATGAGTTC[A/G]AAGTTGCACTGAGCC | 26054 |
rs781090940 | snp | A/G | 0.000101271 | 0.00711514 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75602574 | AGATTACTTTTCTGG[A/G]AGGTACGTCTGTTTC | 26054 |
rs781113746 | snp | A/T | 3.15025e-05 | 0.00396866 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677036 | TCTTTTCAGATTTAG[A/T]AGAACAATATATAAT | 26054 |
rs781159844 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75696104 | TTCTTCATGGGTTCA[C/T]ATTCACCTTCCTTAA | 26054 |
rs781162209 | snp | A/G | 1.68508e-05 | 0.0029026 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75709527 | TTCTTATTGATACAG[A/G]TGGCTTAAGCAAAAT | 26054 |
rs781177729 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75628734 | TACAATTCTTTTTTT[A/G]TTTGAGACAGAATCT | 26054 |
rs781193142 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656658 | GAGGCTAACATTTTT[C/G]TGTTTTTTTCTTAAC | 26054 |
rs781198943 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75627395 | TGACATCTGGATTTC[C/T]TGAAGTGCTATTTTT | 26054 |
rs781239090 | in-del | -/AAGTTT | 3.38061e-05 | 0.00411119 | intron-variant | SENP6 | GRCh38.p7 | 6:75659235 | TTTAACTAAAACTTA[-/AAGTTT]ATTTTTTTCTCCTTC | 26054 |
rs781245967 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75614567 | CACTGCACCCAGCCA[C/T]TATCTTTCTCTTTGA | 26054 |
rs781251360 | snp | A/G | 1.65875e-05 | 0.00287984 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75621571 | GAGATGGAGGTTTTA[A/G]AAATAATTGGAGCTT | 26054 |
rs781276225 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75664886 | CTCTTATAGTTTATG[A/T]GTAGCAGGGAGAAAC | 26054 |
rs781281421 | in-del | -/A | 0.000512464 | 0.015999 | intron-variant | SENP6 | GRCh38.p7 | 6:75633769 | CAGAAAAGATAAAGG[-/A]AGAGTTTGACACCAA | 26054 |
rs781288693 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75668044 | GTACAGATACAAATA[-/C]TGGGAACATATATAC | 26054 |
rs781318533 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75680821 | AGGTCTAGTAGAGAA[C/T]ATGTACTTTTAGTCC | 26054 |
rs781321034 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75714381 | CTTGGCTCCTATCTT[C/T]ATCCACCATACAGTA | 26054 |
rs781330533 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75711739 | GTGCAGTGGCACGAT[C/T]CCAGCTCACCACAAC | 26054 |
rs781355514 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603741 | ACAGTAGGTACTCAG[C/T]GTTAGTCTAGTGAAA | 26054 |
rs781367089 | snp | C/T | 1.73198e-05 | 0.00294272 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75676030 | AAAGTTTGGAATGAT[C/T]GTAAAGGAGTAAATA | 26054 |
rs781371648 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607522 | CATTTTTGTACTGCA[C/G]TTGTTCATATCTAGT | 26054 |
rs781386817 | snp | A/G | 3.31587e-05 | 0.00407164 | missense, intron-variant | SENP6 | GRCh38.p7 | 6:75702854 | TAAACAAAAAACATT[A/G]CATAGCTGTAATTGA | 26054 |
rs781396032 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605473 | GATGATAAACAGTAT[A/G]ATAAATACGGAAGAC | 26054 |
rs781406973 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75615360 | AATTTTTGTATTTTT[-/A]GTAGAGACGGGGTTT | 26054 |
rs781408516 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602622 | AGGGAGGGTATACTG[G/T]AAAACGTGGCCCCCA | 26054 |
rs781421172 | snp | A/G | 1.65919e-05 | 0.00288022 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713685 | TGCAGGTATTTAGAA[A/G]TGGAATGGGAAGTTA | 26054 |
rs781488098 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75674424 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 26054 |
rs781502666 | in-del | -/ATATATATAAAACGTATATATG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75666162 | TAAAACATATATGAT[-/ATATATATAAAACGTATATATG]ATATATATAAAACGT | 26054 |
rs781504434 | snp | C/T | 1.66999e-05 | 0.00288958 | missense, utr-variant-5-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75633642 | TCTTGAAGACATATG[C/T]AAGACGAAACAAGTC | 26054 |
rs781508261 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652587 | CACGCCTGTAATCCT[A/G]GCACTTTGGGAGGCC | 26054 |
rs781516280 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699586 | TCAACCTCCCAGGCT[G/T]AAGTGATCCTCCGAC | 26054 |
rs781526433 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75689206 | ACCACTGTACTCCAA[A/C]CTGGGTGACAGAGCA | 26054 |
rs781542874 | snp | A/G | 3.32674e-05 | 0.0040783 | intron-variant | SENP6 | GRCh38.p7 | 6:75640636 | TACAGTGATATATCA[A/G]CAATGAGGTCTTGCC | 26054 |
rs781550299 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700787 | GTGAGCCACCGTGCC[C/T]GGCATCATCAATTTT | 26054 |
rs781551725 | snp | A/G | 1.823e-05 | 0.00301905 | intron-variant | SENP6 | GRCh38.p7 | 6:75633533 | AGTTGTTGATAGATT[A/G]TCACATTATAGCATT | 26054 |
rs781579463 | snp | C/T | 1.65693e-05 | 0.00287826 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75713553 | CTCCGAGGCCCTTCT[C/T]GGTCAAATGTTGTCA | 26054 |
rs781619667 | snp | A/G | 1.68675e-05 | 0.00290405 | synonymous-codon, intron-variant | SENP6 | GRCh38.p7 | 6:75702693 | CGGTTTGGAAAAACC[A/G]AAGTATGAACCTAAT | 26054 |
rs781635304 | snp | A/T | 1.66891e-05 | 0.00288864 | intron-variant | SENP6 | GRCh38.p7 | 6:75663566 | ATCAATCCAGTATTT[A/T]TCAGATATATTTTTA | 26054 |
rs781644910 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659755 | TTGTTCACATTTGCT[G/T]TATTGTCCTCACTCT | 26054 |
rs781679218 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75622295 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAAC | 26054 |
rs781690606 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75611165 | ACTACCATGACCCCT[A/G]CTGACTCTGCTTCTG | 26054 |
rs781695441 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75700785 | GTGTGAGCCACCGTG[-/C]CCGGCATCATCAATT | 26054 |
rs781718384 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638869 | TCGAGACCAGCCTTA[C/T]CAACATGGCGAAATC | 26054 |
rs781719791 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75707202 | ATTTGCTGCTGGAAG[G/T]AACCTGATTATAACT | 26054 |
rs781752851 | in-del | -/AAT | 0.000116103 | 0.00761826 | cds-indel, intron-variant | SENP6 | GRCh38.p7 | 6:75702945 | ATACAGTGTGAAAAA[-/AAT]AAATCATACTGCGAG | 26054 |
rs781782168 | snp | A/G | 3.45764e-05 | 0.00415776 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75677141 | AGAATAACATCTCCA[A/G]TTTTTTTGCGAAAAT | 26054 |
rs796077960 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75698823 | CAAGACCAACCTGGC[A/G]AACATGGCGAAACCT | 26054 |
rs796091955 | in-del | AT/GAA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659004 | AAAAAAAAAAAGGGG[AT/GAA]TGTGAGTATGTGAGT | 26054 |
rs796111607 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75710931 | AAAACATTATTCATG[C/T]AAAATAACATGTTAT | 26054 |
rs796153446 | in-del | -/AA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75692791 | TTCCCTTCCCCCGCC[-/AA]AAAAAAAAAAAATCT | 26054 |
rs796153696 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75642704 | TGAGATAGGGAAGTA[G/T]TGTTACCTGATAAAT | 26054 |
rs796183718 | in-del | AGAAA/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75608550 | AAGGAAAGAAAGGAA[AGAAA/G]AAAGGAAGGAGAAAA | 26054 |
rs796218486 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75669072 | AAGGGAAAATAGGCC[G/T]GATGCGGTGGCTCAC | 26054 |
rs796219475 | in-del | -/AAAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75605073 | GCGAAACTACATCTC[-/AAAT]AATAATAAAATATTC | 26054 |
rs796238671 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625760 | TGTAGTCCCAGCTAC[A/G]TGGGAGGCTGAGGAA | 26054 |
rs796240379 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656618 | TTCCCTAGAAAATGG[A/C]ATCCTAATGGAATTT | 26054 |
rs796268150 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75602704 | GTACGAGGGATGAGC[C/G]ATGACGGGGAGGGAG | 26054 |
rs796284042 | in-del | -/AG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606909 | TGGGTATTAGAGAAC[-/AG]AAGGTAGAGAGGCAG | 26054 |
rs796304069 | in-del | -/AAAT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75682104 | AAAGCAGAGTCTGAC[-/AAAT]AAACTTCTGAGGAAA | 26054 |
rs796351763 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619444 | ACATTCCGTTGTGTC[-/TA]TGTGTGTGTGTGTGT | 26054 |
rs796366136 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75603115 | TTTCGGAATGTGTTT[C/T]TATAAAAATATTCTG | 26054 |
rs796366889 | in-del | -/TGTT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75640480 | GTGTATTCATCTTCC[-/TGTT]TGTTTATTTTGTATA | 26054 |
rs796396118 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699222 | TCTTAGTCACTATAC[A/C]TCTGCATGGAAGTTA | 26054 |
rs796399575 | in-del | -/AGTA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648244 | TGGAAAATCATGGTG[-/AGTA]AGTATTTATATTCAT | 26054 |
rs796401361 | snp | A/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638241 | TTTTCCCTTTTCTTT[A/T]GTTTTTTTTTTTTTT | 26054 |
rs796402462 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638596 | TGTGTGTGTGTATAT[A/G]TATATATATATATAT | 26054 |
rs796424960 | in-del | -/TT | | | intron-variant | SENP6 | GRCh38.p7 | 6:75638243 | TTCCCTTTTCTTTTG[-/TT]TTTTTTTTTTTTAAT | 26054 |
rs796426629 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617574 | GGAGCCACTGTGCCC[A/G]GCCGGTTTAGAGAAC | 26054 |
rs796431224 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75606776 | AAAATTTGCAAATAT[C/T]CCAAAATCCAAAAAA | 26054 |
rs796435249 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656035 | GCCTGGCCAACGTGG[C/T]GAAACCCTGTCTCTA | 26054 |
rs796505267 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697902 | TCTGTTTTTAGCCAG[-/A]AAGGAGAAACGATGG | 26054 |
rs796549538 | in-del | -/AAG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75652696 | TCAAAAAAAAAAAAA[-/AAG]AAAAAAAGAAAAAGA | 26054 |
rs796568701 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75617267 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 26054 |
rs796569805 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75651209 | TTAAACTCCCTTTTT[C/T]TTCAGCCTGTTTTTT | 26054 |
rs796578544 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75645977 | AGCAAAGATGGCTCA[-/G]TACACAAGTTCAAAT | 26054 |
rs796591074 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75691196 | CGTTCAGGTTGGAGA[G/T]CAGTGACGCAATCAC | 26054 |
rs796604963 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75672913 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAT | 26054 |
rs796607526 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75607576 | CAAGTGAATTCCTTC[G/T]CCTATATTTTCTCCC | 26054 |
rs796607900 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649785 | CTCCCAAAGTGCTGG[A/G]ATTACACGCGTCAGC | 26054 |
rs796608269 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656610 | TCTCTTCTTTCCCTA[A/G]AAAATGGAATCCTAA | 26054 |
rs796616672 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75625749 | TAGTGGGCTCCTGTA[A/G]TCCCAGCTACGTGGG | 26054 |
rs796632478 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75712522 | TCTCTGGAAAAAGTT[-/A]AAAAAAAAAAATAAT | 26054 |
rs796634718 | in-del | -/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75699354 | TTGTTTTTGTTTTTG[-/C]TTTTTTTTTTTTTTT | 26054 |
rs796674351 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75629526 | GCTGGTCTCGAACTC[C/T]AGACCTCAGGTGATC | 26054 |
rs796679868 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619445 | CATTCCGTTGTGTCT[-/AT]GTGTGTGTGTGTGTG | 26054 |
rs796692670 | snp | G/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75695119 | AACCTCAGGTGATCT[G/T]CCCACCTCAGCCTCC | 26054 |
rs796708176 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75631784 | TAGCCCTTGGCAGAA[A/G]AAGTTTGCTGATCCC | 26054 |
rs796710277 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75623225 | CATTTTTTAAAAACT[A/G]TCTTTACGGTGCTAG | 26054 |
rs796729720 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75697907 | TTTTAGCCAGAAAGG[A/G]GAAACGATGGTTGGA | 26054 |
rs796756897 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75630796 | ATCTCTGTGGATTTT[A/G]CCTTTCTACATTATT | 26054 |
rs796778760 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649473 | TTAAGAGAAAAAAGA[A/G]CATGCTTATTTACTG | 26054 |
rs796785030 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75701595 | TAGAATGTTGAAAAA[-/A]TCATATGACCTAATT | 26054 |
rs796805767 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75660635 | CTTATCTTGTATTTC[-/T]TTTTTTTTTTTCCCC | 26054 |
rs796833145 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75667070 | GGGCTTAAATACCAC[A/G]TGGGAGATTATTTGG | 26054 |
rs796840873 | snp | C/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75650201 | TCCACAGAAATGATG[C/T]TGTGGCATTCTCAGT | 26054 |
rs796848928 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75644476 | AAATTTCTTTCTTTC[-/T]TTTTTTTTTTTTTGT | 26054 |
rs796861625 | in-del | -/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659004 | AAAAAAAAAAAAGGG[-/G]AATTGTGAGTATGTG | 26054 |
rs796879147 | snp | C/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75656187 | CCACTGCACTCCAGC[C/G]TGGGCGACAGAGCAA | 26054 |
rs796880851 | in-del | GT/TTG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75649516 | GGTTTTGTTTGTTTG[GT/TTG]TGTTGTTGTTGTTTT | 26054 |
rs796947096 | in-del | -/CA | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658974 | GAGACCTTGTCTCCC[-/CA]AAAAAAAAAAAAAAA | 26054 |
rs796948338 | in-del | -/A | | | intron-variant | SENP6 | GRCh38.p7 | 6:75641912 | ACTGTTGAATCAATT[-/A]AAAAAAAAAAACGAG | 26054 |
rs796953151 | in-del | -/AG | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659000 | AAAAAAAAAAAAAAA[-/AG]GGGAATTGTGAGTAT | 26054 |
rs796966040 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75678111 | CATAATGCCACTGGG[A/G]TGGACTCAAACTTCA | 26054 |
rs796970204 | snp | A/G | | | intron-variant | SENP6 | GRCh38.p7 | 6:75654597 | TAGCAGCTACATGAT[A/G]GAGAAAACCATTTTT | 26054 |
rs796973523 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717694 | GTGGGATCAAGCCTT[C/T]TAAAATGTGTTATTA | 26054 |
rs796977330 | multinucleotide-polymorphism | ACT/GCC | | | intron-variant | SENP6 | GRCh38.p7 | 6:75648655 | ATTATACTTTACATA[ACT/GCC]AGCATAGTTAAGCTT | 26054 |
rs797002615 | multinucleotide-polymorphism | CCCCC/TGGGG | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75601635 | CGCCAGGTCTGCCAT[CCCCC/TGGGG]CCTGGGCGGTGGGGA | 26054 |
rs797010048 | in-del | -/T | | | intron-variant | SENP6 | GRCh38.p7 | 6:75659194 | CTTATGTTCTGATTA[-/T]TTTTTTTGCTGAAAC | 26054 |