chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106319746463197465AG14GENIChomozygous884045103
106319884363198844GA18GENIChomozygous884045104
106319929563199296TC20GENIChomozygous884045105
106320144063201441AG12GENIChomozygous884045106
106320210063202101CT16GENIChomozygous884045107
106320257063202571CT21GENIChomozygous884045108
106320483863204839CT12GENIChomozygous884045109
106320638863206389CA13GENIChomozygous884045110
106320740263207403TC30GENIChomozygous884045111
106320944563209446GA20GENIChomozygous884045112
106321088363210884AG21GENIChomozygous884045113
106321177063211771CA19GENIChomozygous884045114
106321187963211880AG11GENIChomozygous884045115
106321262863212629GT12GENIChomozygous884045116
106321277263212773CT24GENIChomozygous884045117
106321285363212854CA9GENIChomozygous884045118
106321424663214247AC16GENIChomozygous884045119
106321489363214894AG5GENICheterozygous884045120
106321500463215005AG8GENICheterozygous884045121
106321531563215316CT17GENIChomozygous884045122
106321659663216597GT19GENIChomozygous884045123
106322010063220101GA16GENIChomozygous884045124
106322053363220534AC22GENIChomozygous884045125
106322179163221792GA26GENIChomozygous884045126
106322228463222285TC9GENICheterozygous884045127
106322373363223734CT17GENIChomozygous884045128
106322630663226307CT23GENIChomozygous884045129
106322706763227068GA16GENIChomozygous884045130
106322744663227447AG7GENICheterozygous884045131
106322853463228535AT13GENIChomozygous884045132
106323056563230566TC29GENIChomozygous884045133
106323086463230865CT16GENIChomozygous884045134
106323130863231309CT25GENIChomozygous884045135
106323314163233142CT20GENIChomozygous884045136
106323765663237657GA17GENIChomozygous884045137
106323883063238831TA24GENIChomozygous884045138
106323907163239072CT29GENIChomozygous884045139
106323914963239150GC26GENIChomozygous884045140