chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106621006266210063G-9GENIChomozygous51907778
106621038566210386AAG13GENIChomozygous51907780
106621084766210848CT24GENICpossibly homozygous51479323
106621126766211268AG24GENIChomozygous51479324
106621168966211690AG31GENIChomozygous51907782
106621277566212776TC30GENIChomozygous51479325
106621297666212977GA31GENIChomozygous51907784
106621308266213083CCA25GENIChomozygous51479326
106621351666213517AG37GENIChomozygous51479327
106621453966214540AC38GENIChomozygous51907786
106621490766214908TC23GENICpossibly homozygous51479328
106621516366215164CT27GENIChomozygous51907788