chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173563891635638917AG60GENIChomozygous111243074
173563910735639108CA43GENICpossibly homozygous111034636
173563945035639451GT40GENIChomozygous111243076
173563968135639682GT34GENIChomozygous111243078
173563974035639741TC43GENIChomozygous111243080
173564034935640350TG45GENIChomozygous111345908
173564045435640455CT62GENIChomozygous111586894
173564055735640558CT46GENIChomozygous111345910
173564062435640625GA56GENIChomozygous111034638
173564094335640944TC70GENIChomozygous111034642
173564094835640949AG72GENIChomozygous111034644
173564102935641030CG51GENIChomozygous111243082
173564106835641069AG57GENIChomozygous111243084
173564132535641326CA61GENIChomozygous111034646
173564162935641630GA50GENIChomozygous111243086
173564167435641675GA45GENIChomozygous111034648
173564192235641923CT39GENIChomozygous111243088
173564210535642106TG48GENIChomozygous111034650