chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123809583538095836AC12GENICpossibly homozygous790919233
123810097338100974GC18GENICpossibly homozygous790919234
123810111338101114GA21GENIChomozygous790919235
123810112338101124GT18GENIChomozygous790919236
123810441738104418AT21GENIChomozygous790919237
123811057838110579AG33GENIChomozygous790919238
123811271138112712GA18GENIChomozygous790919239
123811392338113924GC12GENIChomozygous790919240
123811394538113946TC10GENIChomozygous790919241
123811397738113978GA7GENIChomozygous790919242
123811400038114001TG8GENIChomozygous790919243
123811725638117257GA24GENIChomozygous790919244