chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104566055945660560CT4GENIChomozygous116584147
104566174145661742TC18GENIChomozygous116584149
104566330245663303TC16GENIChomozygous116584151
104566377545663776AG21GENIChomozygous116584153
104566434445664345CT21GENIChomozygous116584157
104566442745664428TC20GENIChomozygous116584159
104566585345665854TC13GENIChomozygous116584161
104566615345666154GA17GENIChomozygous116584163
104566797845667979GA28GENIChomozygous116584167
104566828945668290TC14GENIChomozygous116584169
104566845345668454AG14GENIChomozygous116584171
104566913645669137TC23GENIChomozygous116584173
104566927245669273AG18GENIChomozygous116584175
104566987345669874GA16GENIChomozygous116584177
104567218545672186AC8GENIChomozygous116877283
104567350245673503TC21GENIChomozygous116584179
104567381745673818CA17GENIChomozygous116877285
104567463345674634AG17GENIChomozygous116584183
104567561045675611AG12GENIChomozygous117178148
104567659045676591AG15GENIChomozygous116584185
104567668745676688AG24GENIChomozygous116584187
104567699645676997AG13GENIChomozygous116771880
104567832145678322TA8GENIChomozygous116584191
104567899645678997TG22GENIChomozygous116584193
104567918145679182GA14GENIChomozygous116771882
104567935845679359TC24GENIChomozygous116771884
104567990445679905AG31GENIChomozygous116771886
104568056945680570CT30GENIChomozygous116771888
104568497545684976CT23GENIChomozygous116771890
104568515945685160GT31GENIChomozygous116771892