chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266483552266483553CT51GENIChomozygous806126651
1266485652266485653TA58GENIChomozygous806126652
1266486512266486513CT40GENIChomozygous806126653
1266486751266486752GA42GENIChomozygous806126654
1266486995266486996CT32GENIChomozygous806126655
1266487275266487276CT36GENICpossibly homozygous806126656
1266487893266487894CT35GENIChomozygous806126657
1266488317266488318AG38GENIChomozygous806126658
1266488453266488454TG40GENICpossibly homozygous806126659
1266488457266488458CG41GENICpossibly homozygous806126660
1266488584266488585TC46GENIChomozygous806126661
1266490497266490498CT29GENICpossibly homozygous806126662
1266491321266491322CT38GENIChomozygous806126663
1266491378266491379GA44GENIChomozygous806126664
1266491881266491882GA47GENIChomozygous806126665
1266492131266492132TA57GENIChomozygous806126666
1266492532266492533GA2GENIChomozygous806126667
1266492739266492740CA32GENICpossibly homozygous806126668
1266492936266492937CT41GENIChomozygous806126669
1266492999266493000GA46GENIChomozygous806126670
1266493001266493002GT46GENICpossibly homozygous806126671
1266493020266493021CT42GENIChomozygous806126672
1266493113266493114CT41GENIChomozygous806126673
1266493239266493240GA52GENIChomozygous806126674
1266493336266493337CT40GENICpossibly homozygous806126675
1266493393266493394GA34GENICpossibly homozygous806126676
1266493415266493416GA28GENICheterozygous806126677
1266494063266494064GA49GENIChomozygous806126678
1266494693266494694AG45GENIChomozygous806126679
1266495284266495285AC30GENICheterozygous806126680
1266495790266495791GA68GENICheterozygous806126681
1266496035266496036GA62GENIChomozygous806126682
1266496133266496134TA35GENICpossibly homozygous806126683
1266496267266496268TC43GENIChomozygous806126684
1266497384266497385AG69GENIChomozygous806126685
1266497641266497642TG49GENIChomozygous806126686
1266497715266497716AG49GENIChomozygous806126687
1266497812266497813CT59GENIChomozygous806126688
1266500992266500993TG35GENICheterozygous806126689
1266501447266501448GA29GENICpossibly homozygous806126690
1266501461266501462AG8GENICheterozygous806126691
1266501463266501464AG4GENICheterozygous806126692
1266501466266501467TC4GENICheterozygous806126693
1266501507266501508GA43GENICpossibly homozygous806126694
1266501652266501653AT49GENICheterozygous806126695
1266503241266503242AG29GENIChomozygous806126696
1266506333266506334TC97GENICheterozygous806126697
1266506374266506375CT101GENICheterozygous806126698
1266506394266506395CT93GENICheterozygous806126699
1266506405266506406CT75GENIChomozygous806126700
1266507858266507859TC46GENICpossibly homozygous806126701
1266510619266510620TC48GENIChomozygous806126702
1266512200266512201GA48GENICheterozygous806126703