chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151328892151328893CT27GENIChomozygous114155891
5151328958151328959AT47GENICpossibly homozygous114155892
5151329133151329134GT20GENIChomozygous114056641
5151329185151329186TG32GENIChomozygous114056643
5151331423151331424CT53GENICheterozygous114155893
5151338358151338359CA23GENIChomozygous114056645
5151338416151338417GT39GENICpossibly homozygous114056646
5151338447151338448TC48GENICpossibly homozygous114056648
5151349809151349810TA130GENICheterozygous114056650
5151349826151349827CT128GENICheterozygous114056652
5151349883151349884GT119GENICheterozygous114056654
5151349887151349888AC121GENICheterozygous114056656
5151349895151349896AT113GENICheterozygous114155894
5151349902151349903GT106GENICheterozygous114155895
5151349905151349906CA105GENICheterozygous114155896
5151349914151349915CT113GENICheterozygous114155897
5151354052151354053GC38GENICheterozygous114155898
5151354087151354088CT55GENICheterozygous114155899
5151380024151380025GC38GENIChomozygous114056658
5151380048151380049TG25GENICpossibly homozygous114056660
5151380131151380132TC24GENIChomozygous114155900
5151380305151380306GA65GENIChomozygous114056662
5151380427151380428GA44GENIChomozygous114056664