chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115029934050299341CCT13GENIChomozygous51004661
115029948050299481AG14GENIChomozygous51004662
115029973750299738GGCA14GENIChomozygous51357571
115030074450300745CT21GENIChomozygous51357573
115030106750301068AG24GENIChomozygous51004664
115030147250301473TTAAA16GENIChomozygous51357575
115030175650301757TTA28GENICheterozygous51004667
115030175650301757TTAA28GENICpossibly homozygous51201763
115030238350302386TTT---21GENIChomozygous51196007