chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101454309114543092AG8GENIChomozygous51329664
101454391314543914GA16GENICpossibly homozygous51623302
101454400914544010CT28GENIChomozygous51623303
101454456614544567TC5GENIChomozygous51329666
101454472214544723AG13GENICpossibly homozygous51329667
101454633214546333GA18GENIChomozygous51623304
101454636114546362CT8GENIChomozygous51623305
101454657414546575AG13GENIChomozygous51623306