chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109563320109563321AG28GENICpossibly homozygous993968407
6109563636109563637CT21GENICpossibly homozygous993968408
6109564792109564793CA19GENIChomozygous993968409
6109565576109565577AG19GENICpossibly homozygous993968410
6109565688109565689GA33GENIChomozygous993968411
6109566215109566216GA29GENIChomozygous993968412
6109571828109571829TC26GENIChomozygous993968413
6109580594109580595CT10GENIChomozygous993968414