chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185702520257025203AG12GENICheterozygous63900868
185704317857043179TG46GENIChomozygous63900906
185704322557043226AG44GENICpossibly homozygous63900907
185704342057043421AG65GENIChomozygous63900908
185704542757045428CG54GENIChomozygous63900912
185704550557045506GA42GENIChomozygous63900913
185704552457045525TA36GENIChomozygous63900914
185704553857045539GT28GENIChomozygous63900915
185704554157045542AT29GENIChomozygous63900916
185704554757045548CT28GENIChomozygous63900917
185704555457045555AT24GENIChomozygous63900918
185704555857045559GT22GENIChomozygous63900919
185704556657045567CA21GENIChomozygous63900920
185704557357045574GA21GENIChomozygous63900921
185704610757046108AG37GENIChomozygous63900924
185704612757046128TA40GENICpossibly homozygous63900925