chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107079127870791279TG29GENIChomozygous116799373
107079132970791330GA33GENIChomozygous116628458
107079251270792513GA31GENIChomozygous116628462
107079256870792569GC31GENIChomozygous116628464
107079321770793218GA25GENIChomozygous116799377
107079363070793631TC26GENIChomozygous116628466
107079395970793960GA23GENIChomozygous116628470
107079431270794313TC30GENIChomozygous117083012
107079431670794317TC30GENIChomozygous116628472
107079513470795135AC24GENIChomozygous116628476
107079618270796183CT34GENIChomozygous116628478
107079637770796378AC29GENIChomozygous116628480
107079684270796843CT22GENIChomozygous116799381
107079695470796955TC35GENIChomozygous116628484
107079719570797196CT25GENIChomozygous116628486
107079747070797471TA3GENIChomozygous117130985
107079968470799685CT21GENIChomozygous116628490
107079987170799872TA20GENIChomozygous116799385
107080018770800188GC33GENIChomozygous116799387
107080036670800367GT29GENIChomozygous116628494
107080085170800852GT18GENIChomozygous117130986
107080089870800899TC14GENIChomozygous116799389
107080118970801190GA26GENIChomozygous116628496
107080129970801300GA27GENIChomozygous116799391
107080196670801967TA24GENIChomozygous116799393
107080207970802080GC8GENIChomozygous116799395
107080214870802149AG11GENIChomozygous116799397
107080231770802318CT26GENIChomozygous116799399
107080240670802407TC26GENIChomozygous116799401
107080266570802666GA40GENIChomozygous116799403