chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2173649134173649135CG28GENIChomozygous110132925
2173652195173652196GT25GENIChomozygous111143895
2173650315173650316GA20GENIChomozygous111143892
2173650778173650779AC26GENIChomozygous111143893
2173652060173652061TC21GENICpossibly homozygous111143894
2173655912173655913AG26GENIChomozygous110132952
2173658399173658400TC21GENIChomozygous111143896
2173660979173660980TG15GENIChomozygous110132965
2173662274173662275CT19GENIChomozygous110132970
2173668145173668146GA16GENIChomozygous111143899
2173668519173668520GA37GENICpossibly homozygous110132997