chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79158859091588591GA23GENICpossibly homozygous54021304
79158879091588791CT9GENIChomozygous54021307
79158885791588858T-6GENIChomozygous54021308
79158945991589460GA25GENICpossibly homozygous54021311
79159086591590866CA16GENIChomozygous54021312
79159110591591106AG25GENICpossibly homozygous54021313
79159160791591608TC16GENIChomozygous54021314
79159190191591902TC13GENIChomozygous54021315
79159192891591929T-13GENICheterozygous54021316
79159203491592035TC10GENICpossibly homozygous54021317
79159228991592290AG27GENICpossibly homozygous54208191
79159178791591788CT21GENIChomozygous54208187
79159220291592203TC30GENIChomozygous54208189
79159223991592240AC28GENICpossibly homozygous54208190
79159192591591926CT11GENICheterozygous54912029
79159276891592769TA5GENIChomozygous54021319