chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204796010647960109GTC59GENIChomozygous130003112
204796024747960248GA57GENIChomozygous140566497
204796051247960513GA64GENIChomozygous130124558
204796173847961739TA58GENIChomozygous140566498
204796176947961770AC55GENIChomozygous140566499
204796178647961787TC56GENIChomozygous140566500
204796219247962193TG48GENIChomozygous140566501
204796300847963009TC59GENIChomozygous130124559
204796313247963133GT60GENICpossibly homozygous130124560
204796350247963503TC62GENIChomozygous130124561
204796360047963601TC68GENIChomozygous130124562
204796432447964325CG52GENIChomozygous130124563
204796493847964939TC56GENIChomozygous130124566
204796527547965276CT66GENIChomozygous130124567
204796578447965785CT66GENIChomozygous130124568
204796587447965875CT66GENIChomozygous140566502
204796684347966844CT61GENIChomozygous140566503
204796898547968986CT52GENIChomozygous140566504
204796926947969270TA47GENIChomozygous140566505
204796930047969300A38GENIChomozygous140496661
204796157747961577T45GENIChomozygous140496658
204796291147962911GGT18GENIChomozygous140496659
204796866247968664AG46GENIChomozygous140496660
204796963347969634GC67GENIChomozygous140566506
204796970247969703AC74GENICpossibly homozygous130124569
204796997447969975CT70GENIChomozygous130124571
204797004647970047AG60GENIChomozygous130124572
204797011647970117TC54GENIChomozygous130124573
204797122147971222CT46GENIChomozygous140566507
204797261847972618A63GENICpossibly homozygous130003114
204797320947973210T48GENICpossibly homozygous140496662
204797399647973997CA66GENIChomozygous140566508
204797546847975469GA66GENIChomozygous130124578
204797739747977398TA34GENIChomozygous130124579
204797819847978199T54GENICpossibly homozygous140496663
204798111047981111GA36GENIChomozygous130124581
204798114547981146G20GENICheterozygous403471332
204798114547981146GA20GENICheterozygous403471333
204798114447981145G20GENICheterozygous403471330
204798114447981145GA20GENICheterozygous403471331