chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122472057924720580TC17GENICpossibly homozygous50135970
122472059524720596TC10GENICpossibly homozygous50135972
122472062324720624GA5GENIChomozygous50135974
122472062724720628AC3GENIChomozygous50135976
122472064324720644TC1GENIChomozygous50135978
122472067024720671CT4GENIChomozygous50135980
122472067524720676AG5GENIChomozygous50135982
122472090524720906TC12GENICpossibly homozygous50135986
122472117224721176TGAT----11GENIChomozygous50135988
122472118224721183GA14GENIChomozygous50135990
122472152424721525AG16GENIChomozygous50135992