chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X16192321619232A25GENICpossibly homozygous140574091
X16214111621412CT24GENIChomozygous140602322
X16214901621491TC15GENIChomozygous140602323
X16223601622361A20GENIChomozygous140574092
X16243101624311CG25GENIChomozygous140602324
X16256781625678T21GENIChomozygous140574093
X16261561626157GA25GENIChomozygous140602325
X16270221627023GC34GENIChomozygous140602326
X16335741633575AG31GENIChomozygous140602330
X16342891634290GA15GENIChomozygous140602331
X16343841634385TG16GENIChomozygous140602332