chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191139050611390507GA8GENIChomozygous119688554
191139716311397164TG17GENIChomozygous109995131
191140310011403101CT17GENIChomozygous109995138
191140482811404829GT15GENIChomozygous109995140
191140483011404831GC14GENIChomozygous109995142
191140700111407002AG4GENIChomozygous109995144
191140808211408083CT18GENIChomozygous109995146
191140953111409532AG31GENIChomozygous109995148
191141024611410247CT13GENIChomozygous109995149
191141038511410386TG16GENIChomozygous109995151
191141164611411647AG19GENIChomozygous109636578
191141264111412642TC8GENIChomozygous109995153
191141312411413125GA10GENIChomozygous109995155
191141539011415391GC7GENIChomozygous109995157
191141539211415393CA9GENIChomozygous109636585
191141592811415929GT15GENIChomozygous109995159
191141614311416144TC11GENIChomozygous109995161
191141618111416182CT24GENIChomozygous109995163
191141624111416242CG23GENIChomozygous109995165
191141805511418056CT15GENIChomozygous109995167
191141822311418224AG14GENIChomozygous109995169
191141863311418634GC17GENIChomozygous109995171
191141962611419627TC18GENIChomozygous109995173
191141859211418593CT20GENIChomozygous110005541
191140595011405951GT3GENICheterozygous125331880
191141486911414870TC19GENIChomozygous125331881
191141199011411991CT15GENIChomozygous110077334
191141693911416940GT19GENIChomozygous110005539