chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3150049372150049373TC16GENIChomozygous111773519
3150050796150050797CA16GENIChomozygous111773521
3150051136150051137GA11GENIChomozygous111773523
3150051412150051413AG15GENIChomozygous111773525
3150052254150052255CT7GENIChomozygous111773527
3150053996150053997CT14GENIChomozygous111773531
3150055198150055199CG18GENIChomozygous111773533
3150057072150057073CG26GENIChomozygous111773535
3150060089150060090TC23GENIChomozygous111773537
3150060519150060520CT13GENIChomozygous111773539
3150060776150060777AG5GENIChomozygous111773541
3150061537150061538GA19GENIChomozygous111773543
3150061262150061263TG3GENICheterozygous125965242