chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12275832222758323CT9GENIChomozygous108053473
12275906422759065AT29GENIChomozygous108053474
12275914922759150AG28GENIChomozygous108053475
12275917022759171AG32GENIChomozygous108053476
12275921322759214TC27GENIChomozygous108053477
12275940522759406TC27GENICpossibly homozygous108053478
12275960822759609GC28GENIChomozygous120654133
12275992722759928GA24GENIChomozygous120654135
12275997322759974GA21GENIChomozygous108053479
12276003322760034AG19GENIChomozygous120654137
12276023222760233GA13GENICpossibly homozygous108053480