chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152796907827969079CT55GENIChomozygous142486792
152796911327969114GC51GENIChomozygous142486793
152796912027969121AC49GENIChomozygous142486794
152796972527969726GA74GENICpossibly homozygous142486795
152796985627969857CT43GENIChomozygous142486796
152797017227970173GA55GENICpossibly homozygous142486797
152797030027970301GA64GENIChomozygous142486798
152797134427971345GT52GENIChomozygous142486799
152797136927971369AGAC37GENICpossibly homozygous142460085
152797153127971532TC66GENIChomozygous142486800
152797171027971711G70GENIChomozygous142460086
152797214027972141GT61GENICpossibly homozygous142486801
152797220427972205TC59GENIChomozygous142486802
152797230127972301A53GENIChomozygous142460087
152797270527972706TG73GENIChomozygous142486803
152797296227972963TC69GENIChomozygous142486804
152797410827974109AG56GENIChomozygous142486805
152797414127974142GA62GENIChomozygous142486806
152797421827974219CA68GENIChomozygous142486807
152797728427977284AGAA57GENIChomozygous142460088
152797763227977633CT56GENIChomozygous142486808