chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47128472271284723CT18GENIChomozygous112704794
47128567771285678CT27GENIChomozygous112704798
47128569871285699CT26GENIChomozygous112704800
47128582071285821AC11GENIChomozygous112704802
47128582371285824TG11GENIChomozygous112704804
47128627571286276TC41GENIChomozygous112704806
47128635271286353GA43GENIChomozygous112704808
47128649871286499TC24GENIChomozygous112704810
47128677971286780TC9GENIChomozygous112704812
47128679471286795AG9GENIChomozygous113116551
47128700071287001AG34GENICheterozygous112704818
47128703771287038AG35GENICheterozygous112704820
47128706271287063AG35GENICheterozygous112704822
47128711071287111AG32GENICpossibly homozygous112704824
47128714071287141TC22GENICpossibly homozygous112704826
47128715471287155CG25GENICpossibly homozygous112704828
47128717671287177GC22GENICpossibly homozygous112704830
47128720571287206CG16GENICpossibly homozygous112704832
47128723171287232CT22GENIChomozygous112704834
47128723671287237AG23GENIChomozygous112704836