chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148448294284482943GT32GENIChomozygous113605956
148448324884483249AG31GENIChomozygous113605957
148448361184483612TA32GENIChomozygous113680161
148448431884484319TC28GENIChomozygous118766041
148448486684484867TC40GENICpossibly homozygous113605958
148448582684485827CT42GENIChomozygous113680163
148448588484485885CT42GENIChomozygous113605959
148448656984486570AG16GENIChomozygous113680165
148448716984487170TC22GENIChomozygous113605960
148448726984487270GA33GENIChomozygous113605961
148448772484487725GA39GENIChomozygous113605962
148448909084489091AG41GENIChomozygous113605963
148448968084489681TC37GENIChomozygous113605964
148448990284489903AG42GENIChomozygous113605965
148449008084490081AG34GENIChomozygous113605966
148449248884492489TC35GENIChomozygous113605967
148449320084493201TG12GENIChomozygous118766042
148449451184494512AT50GENIChomozygous113605968
148449523084495231GA34GENIChomozygous113605969
148449656184496562GA16GENICpossibly homozygous113605970
148449839384498394CT35GENIChomozygous113605971
148449856384498564AT19GENIChomozygous113605972
148449968384499684AC41GENIChomozygous113605973