chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4118048312118048313GA19GENIChomozygous137191725
4118048914118048915TC19GENIChomozygous137191726
4118049417118049418AG13GENIChomozygous137191727
4118049735118049736CT19GENIChomozygous137191728
4118049842118049843CT19GENIChomozygous137191729
4118049996118049997GT20GENIChomozygous137191730
4118050187118050188TC10GENIChomozygous137191731