chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71293764812937649TC26GENICpossibly homozygous53792218
71293803312938034AG21GENIChomozygous53792219
71293866912938670TC21GENIChomozygous53792220
71293897212938973TC23GENIChomozygous53792221
71293931612939317TC29GENIChomozygous53792222
71293954512939546GA34GENIChomozygous53792223
71293970512939706CT32GENIChomozygous53792224