chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152796907827969079CT21GENIChomozygous142486792
152796911327969114GC19GENIChomozygous142486793
152796912027969121AC19GENIChomozygous142486794
152796972527969726GA24GENIChomozygous142486795
152796985627969857CT11GENIChomozygous142486796
152797017227970173GA19GENIChomozygous142486797
152797030027970301GA23GENIChomozygous142486798
152797134427971345GT16GENIChomozygous142486799
152797136927971369AGAC13GENIChomozygous142460085
152797153127971532TC24GENIChomozygous142486800
152797171027971711G13GENIChomozygous142460086
152797214027972141GT18GENIChomozygous142486801
152797220427972205TC20GENIChomozygous142486802
152797230127972301A14GENIChomozygous142460087
152797270527972706TG20GENIChomozygous142486803
152797296227972963TC20GENIChomozygous142486804
152797410827974109AG19GENIChomozygous142486805
152797414127974142GA24GENIChomozygous142486806
152797421827974219CA20GENIChomozygous142486807
152797728427977284AGAA20GENIChomozygous142460088
152797763227977633CT20GENIChomozygous142486808