chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187656277176562772CT27GENIChomozygous119502325
187657029476570295CG53GENIChomozygous119502326
187657039576570396AG40GENIChomozygous119502327
187658289476582895AG23GENIChomozygous119502328
187661448176614482GT48GENIChomozygous110409540
187661827176618272TC22GENIChomozygous119502329
187661828376618284CT21GENIChomozygous119502330
187661971976619720AG42GENIChomozygous110409542
187662118576621186AT34GENIChomozygous110409544
187662130576621306AG58GENIChomozygous110601396
187662177276621773AG54GENICpossibly homozygous110409546
187662285076622851TC36GENIChomozygous110409548
187662295576622956TC37GENIChomozygous110409550
187662458876624589AC68GENICpossibly homozygous110409552
187662513076625131TA58GENIChomozygous110409554
187662674976626750TA46GENIChomozygous110409556
187662739376627394GA35GENICpossibly homozygous110409558
187662770776627708TG40GENIChomozygous110409560