chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1270577151270577152T-10GENICpossibly homozygous61214162
1270578659270578660AG12GENIChomozygous61214166
1270578730270578731CT14GENIChomozygous61214168
1270578745270578746GGT7GENICpossibly homozygous61214170
1270579191270579192TA16GENIChomozygous61214172