chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12628876628877GT25GENIChomozygous976732531
12629151629152CT14GENIChomozygous976732532
12631942631943CA30GENICpossibly homozygous976732533
12634650634651AG20GENIChomozygous976732534
12635418635419AG4GENIChomozygous976732535
12639307639308CT17GENIChomozygous976732536
12641063641064AT9GENIChomozygous976732537
12648151648152CA5GENIChomozygous976732538
12648164648165TG4GENIChomozygous976732539