chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108828880088288801TC13GENIChomozygous68447371
108828957588289576AG20GENIChomozygous68447374
108829049188290492TC7GENICpossibly homozygous68447377
108829061188290612TC53GENIChomozygous68447381
108829072988290730GT23GENIChomozygous68447384
108829103488291035TG25GENIChomozygous68447387
108829106688291067AG28GENIChomozygous68447390
108829113288291133GA41GENIChomozygous68447393
108829145188291452CT28GENIChomozygous68447396
108829193688291937AG37GENICpossibly homozygous68447399
108829222988292230GA30GENIChomozygous68447402
108829227188292272AT28GENICheterozygous68447405