chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1223317926223317927GA47GENIChomozygous135816938
1223317977223317978GA51GENIChomozygous135816939
1223318191223318192AC67GENIChomozygous135816940
1223318796223318797CT48GENIChomozygous135816941
1223319871223319871T61GENIChomozygous135461987
1223319899223319900CG62GENIChomozygous135816942
1223319964223319965GA63GENIChomozygous135816943
1223320451223320452GA35GENIChomozygous135816944
1223321010223321011CT42GENIChomozygous135816945
1223321100223321101TG45GENIChomozygous135816946
1223321142223321143CG51GENIChomozygous135816947
1223321198223321199CT52GENIChomozygous135816948
1223322277223322277C41GENICpossibly homozygous135461988
1223322549223322550CT47GENICpossibly homozygous135816949
1223322601223322602AT50GENICpossibly homozygous135816950