chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89655176996551770CG43GENIChomozygous776129142
89655188596551886GA23GENICpossibly homozygous776129143
89655217896552179GA51GENICheterozygous776129144
89655220196552202TC47GENICheterozygous776129145
89655242196552422GC50GENIChomozygous776129146
89655296696552967TG47GENIChomozygous776129147
89655352896553529TC17GENIChomozygous776129148
89655356696553567GA21GENIChomozygous776129149
89655385296553853TC24GENIChomozygous776129150
89655454496554545AG20GENIChomozygous776129151
89655533696555337TG16GENIChomozygous776129152
89655576096555761CT24GENIChomozygous776129153
89655601896556019CT11GENIChomozygous776129154
89655667896556679TC20GENIChomozygous776129155
89655763596557636GA57GENIChomozygous776129156
89655813296558133TC27GENIChomozygous776129157
89655821896558219TC30GENICheterozygous776129158