chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55742392257423923TC18GENIChomozygous113815253
55742426757424268TG49GENICpossibly homozygous114632428
55742445757424458TC42GENIChomozygous113815259
55742456557424566GT48GENICpossibly homozygous113815261
55742465157424652AG28GENIChomozygous113815267
55742537557425376TC58GENIChomozygous114205614
55742586557425866GA45GENIChomozygous114205615
55742616757426168CT47GENIChomozygous113815276
55742623557426236CT35GENICpossibly homozygous114205616
55742658457426585TC51GENIChomozygous113815278
55742666157426662GT53GENIChomozygous114205617
55742672257426723AG52GENIChomozygous113815280
55742680057426801CT53GENIChomozygous114205618
55742687257426873GA60GENIChomozygous114205619
55742716457427165CT57GENIChomozygous114205620
55742717457427175AC58GENIChomozygous113815284
55742747857427479GA44GENIChomozygous114205621
55742779457427795GA39GENIChomozygous114205622
55742785857427859TC32GENIChomozygous113815288
55742789157427892CA30GENIChomozygous114205623
55742800257428003TC46GENIChomozygous113815290
55742814957428150TC39GENIChomozygous114205624
55742837157428372AT61GENIChomozygous114205625
55742846257428463CT47GENICpossibly homozygous114205626