chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256704774256704775TC22GENIChomozygous108622561
1256705571256705572TC23GENIChomozygous109023905
1256705931256705932CT28GENIChomozygous109023906
1256707537256707538CT36GENIChomozygous108622562
1256708065256708066AG12GENIChomozygous108622563
1256710009256710010AG11GENIChomozygous109023907
1256711096256711097TC34GENICpossibly homozygous108622564
1256711165256711166AG32GENIChomozygous109023908
1256711945256711946GT23GENICpossibly homozygous109023909
1256712234256712235AC17GENIChomozygous108622566
1256712284256712285TG24GENIChomozygous108622567
1256712440256712441AG38GENIChomozygous109023910
1256712627256712628AG35GENIChomozygous108622568
1256712817256712818AT18GENIChomozygous109023911
1256712905256712906CT26GENIChomozygous108622570
1256712915256712916AG24GENIChomozygous108622571
1256712917256712918GA25GENIChomozygous109023912