chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266050963266050964AC63GENICpossibly homozygous108637474
1266051441266051442GT57GENIChomozygous108637475
1266052451266052452GA77GENIChomozygous108637476
1266055639266055640GA59GENIChomozygous108637478
1266056737266056738GC66GENIChomozygous108637479
1266056762266056763GT71GENIChomozygous108637480
1266057629266057630CT74GENIChomozygous108637481
1266057650266057651TC77GENIChomozygous108637482
1266057701266057702AG77GENIChomozygous108637483
1266058549266058550GA74GENIChomozygous108637484
1266059060266059061GA66GENIChomozygous108637485