chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139209069492090695GA16GENICpossibly homozygous141042798
139209069492090695G16GENICheterozygous403346142
139209070692090707GA17GENICpossibly homozygous141042799
139209070692090707G17GENICheterozygous403346144
139211846092118461A9GENICpossibly homozygous141041769