chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108907046689070467CA34GENIChomozygous116950452
108907177989071780AT19GENIChomozygous116950458
108907186189071862GA18GENIChomozygous116950460
108907204789072048AG28GENIChomozygous116950462
108907239089072391TG21GENIChomozygous116950464
108907239189072392TC21GENIChomozygous116950466
108907239289072393TA21GENIChomozygous116950468
108907543889075439CT19GENICpossibly homozygous116675032
108907545589075456TC19GENIChomozygous116675034