chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152796907827969079CT32GENIChomozygous142486792
152796911327969114GC32GENIChomozygous142486793
152796912027969121AC32GENIChomozygous142486794
152796972527969726GA23GENIChomozygous142486795
152796985627969857CT15GENIChomozygous142486796
152797017227970173GA20GENIChomozygous142486797
152797030027970301GA24GENIChomozygous142486798
152797134427971345GT23GENIChomozygous142486799
152797136927971369AGAC25GENICpossibly homozygous142460085
152797153127971532TC35GENIChomozygous142486800
152797171027971711G32GENIChomozygous142460086
152797214027972141GT20GENIChomozygous142486801
152797220427972205TC23GENIChomozygous142486802
152797230127972301A26GENIChomozygous142460087
152797270527972706TG11GENIChomozygous142486803
152797296227972963TC25GENIChomozygous142486804
152797410827974109AG28GENIChomozygous142486805
152797414127974142GA24GENIChomozygous142486806
152797421827974219CA23GENIChomozygous142486807
152797728427977284AGAA16GENIChomozygous142460088
152797763227977633CT34GENIChomozygous142486808