chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106319929563199296TC33GENIChomozygous953065138
106320144063201441AG15GENIChomozygous953065139
106320170563201706TG21GENIChomozygous953065140
106320210063202101CT31GENIChomozygous953065141
106320212263202123CT31GENIChomozygous953065142
106320343363203434AC35GENIChomozygous953065143
106320638863206389CA18GENIChomozygous953065144
106320740263207403TC43GENIChomozygous953065145
106320841363208414CT18GENIChomozygous953065146
106320944563209446GA22GENIChomozygous953065147
106321088363210884AG21GENIChomozygous953065148
106321177063211771CA27GENIChomozygous953065149
106321255663212557TG21GENIChomozygous953065150
106321347063213471AG27GENIChomozygous953065151
106321424663214247AC31GENIChomozygous953065152
106321530763215308GA24GENIChomozygous953065153
106321844863218449TC29GENIChomozygous953065154
106322053363220534AC32GENIChomozygous953065155
106322265963222660CT35GENIChomozygous953065156
106322320863223209GA22GENIChomozygous953065157
106322627363226274CT16GENIChomozygous953065158
106322853463228535AT21GENIChomozygous953065159
106323056563230566TC27GENICpossibly homozygous953065160
106323109163231092GA28GENIChomozygous953065161
106323130863231309CT24GENIChomozygous953065162
106323314163233142CT22GENIChomozygous953065163