chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1248456720248456721AG10GENIChomozygous108604122
1248456962248456963AC10GENIChomozygous108604123
1248458707248458708TG5GENIChomozygous108604125
1248459015248459016AG8GENIChomozygous108604126
1248461407248461408GC2GENIChomozygous108604127
1248461523248461524AT5GENIChomozygous108604131
1248461980248461981CT8GENIChomozygous108604136
1248461989248461990CT7GENIChomozygous108604137
1248462326248462327AG10GENIChomozygous108604138
1248462364248462365AT8GENIChomozygous108604139
1248462512248462513CG16GENIChomozygous108604140
1248462582248462583CT16GENIChomozygous108604141
1248462618248462619AG14GENIChomozygous108604142
1248462790248462791TG15GENIChomozygous108604143
1248462902248462903TA11GENIChomozygous108604144
1248463020248463021CT7GENIChomozygous108604145
1248463230248463231GA13GENIChomozygous108604146
1248463359248463360GC7GENIChomozygous108604147
1248470793248470794GA12GENIChomozygous108604155
1248471708248471709GA7GENICpossibly homozygous108604156
1248471924248471925GA7GENIChomozygous108604157
1248472123248472124TC8GENIChomozygous108604158
1248472268248472269AG9GENIChomozygous108604159
1248472383248472384AT9GENIChomozygous108604160
1248472443248472444GA8GENIChomozygous108604161
1248472754248472755TC14GENIChomozygous108604162
1248472864248472865AG15GENIChomozygous108604163
1248472935248472936CT17GENIChomozygous108604164
1248473034248473035AG16GENIChomozygous108604165
1248473307248473308GA12GENIChomozygous108604166
1248473343248473344CT9GENIChomozygous108604167