chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
49802854498028545CT76GENIChomozygous112792125
49803004898030049CA62GENICpossibly homozygous112792127
49803051298030513CT94GENIChomozygous112792129
49803206798032068GA69GENIChomozygous112792131
49803269598032696TC53GENIChomozygous112792133
49803337598033376CT62GENIChomozygous112792135
49803830698038307AT45GENIChomozygous112792137
49803939198039392CT58GENIChomozygous112792139
49804295398042954TC43GENIChomozygous112792141
49804388298043883AG62GENIChomozygous112792143