chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X16192321619232A12GENIChomozygous140574091
X16214111621412CT16GENIChomozygous140602322
X16214901621491TC14GENIChomozygous140602323
X16215531621554T10GENIChomozygous403473562
X16215531621554TC10GENICheterozygous403473563
X16215491621550T10GENIChomozygous403473560
X16215491621550TC10GENICheterozygous403473561
X16215811621582T10GENIChomozygous403473564
X16215811621582TC10GENICheterozygous403473565
X16216011621602T10GENIChomozygous403473566
X16216011621602TC10GENICheterozygous403473567
X16223601622361A8GENIChomozygous140574092
X16243101624311CG6GENIChomozygous140602324
X16256781625678T11GENIChomozygous140574093
X16261561626157GA9GENIChomozygous140602325
X16270221627023GC7GENIChomozygous140602326
X16335741633575AG5GENIChomozygous140602330
X16342891634290GA7GENIChomozygous140602331
X16343841634385TG8GENIChomozygous140602332