chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183659726236597263TA32GENIChomozygous110726381
183660081636600817TC24GENIChomozygous110726383
183660629736606298CT30GENIChomozygous119522341
183660953236609533AG28GENIChomozygous110726385
183661210236612103AT21GENIChomozygous110726387
183661367536613676T25GENICpossibly homozygous130603160
183661372936613730GA22GENIChomozygous119522345
183661832336618324TC24GENIChomozygous110461993
183660081536600816T24GENIChomozygous134252304
183661066036610660GTGTGT7GENIChomozygous134252305
183660203436602034A23GENIChomozygous129530356
183660449236604493CT28GENIChomozygous110461987
183660922236609223GA19GENIChomozygous110461988
183661035036610351AG16GENIChomozygous110461990
183661540636615407CA29GENIChomozygous110461991
183661547136615472GA30GENIChomozygous110461992
183660490536604907TG17GENICheterozygous135056579
183662043736620438TG25GENIChomozygous110726389
183662674336626744GA21GENIChomozygous110461996
183662943336629434T18GENIChomozygous131956527
183662969236629693TG27GENIChomozygous110461997
183663033936630339A21GENIChomozygous134252306
183663149736631498AG30GENIChomozygous110461998
183663251336632514TC23GENIChomozygous110462000
183663347736633478T31GENIChomozygous132914011
183664080636640807AT30GENIChomozygous110462004
183664864736648648GA21GENIChomozygous110462006
183665051336650514TA27GENIChomozygous110462007
183665698836656989CT21GENIChomozygous110462008
183664478836644789A25GENIChomozygous131756149