chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183076986330769864GT49GENICpossibly homozygous63854899
183077020430770205TC37GENIChomozygous63854900
183077725830777259GA33GENIChomozygous63854901
183077744730777448AT22GENIChomozygous63854902
183077757930777580CT28GENICheterozygous63854903
183077864230778643GA44GENICpossibly homozygous63854904