chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138001872480018725AT53GENIChomozygous66123648
138001884780018848CT68GENICpossibly homozygous66123650
138001903180019032AG59GENIChomozygous66123652
138001903680019037TC57GENIChomozygous66123654
138001941880019419GA39GENIChomozygous66123656
138002017380020174GA81GENICpossibly homozygous66123658
138002035680020357GA53GENIChomozygous66123660
138002078080020781CG51GENICheterozygous66123662
138002122480021225GA47GENIChomozygous66123664
138002270080022701GA70GENIChomozygous66123666
138002648780026488CT58GENIChomozygous66123668
138002922680029227TC29GENICheterozygous66123670