chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X123774109123774110CT6GENIChomozygous108424388
X123774202123774203CG11GENIChomozygous108325290
X123777934123777935TC20GENIChomozygous108424390
X123778480123778481GA30GENIChomozygous108424392
X123780128123780129TC16GENIChomozygous108325306
X123781959123781960TC21GENIChomozygous120061044
X123782742123782743GA17GENIChomozygous108325312
X123785991123785992GA13GENIChomozygous108424394
X123786693123786694TG17GENICpossibly homozygous119951329
X123786697123786698TG18GENICpossibly homozygous119951330
X123786701123786702TG17GENICheterozygous120061046
X123786734123786735TC15GENICheterozygous119951333
X123786738123786739TC15GENICheterozygous119951334
X123788401123788402GA20GENIChomozygous108424396
X123788513123788514GA53GENICheterozygous120098162
X123788525123788526GA39GENICheterozygous120098163
X123788844123788845TC17GENIChomozygous108325318
X123785721123785722CT3GENIChomozygous108688547