chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9100105799100105800TC22GENIChomozygous117618426
9100105805100105806AC21GENIChomozygous117618428
9100105921100105922AG18GENIChomozygous117618430
9100106389100106390GA20GENIChomozygous117618432
9100109302100109303TC25GENICpossibly homozygous117618434
9100109354100109355AG31GENICpossibly homozygous117618436
9100111243100111244AG15GENIChomozygous117618438