chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14693830146938302AG17GENIChomozygous74997138
14693925346939254AG27GENICpossibly homozygous74997139
14693937146939372CT20GENIChomozygous74997140
14694054246940543TG17GENIChomozygous74997141
14694253546942536GA13GENIChomozygous74997142
14694311546943116AG28GENIChomozygous74997143