chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171565313215653133GA24GENIChomozygous64688224
171565566315655664GC35GENIChomozygous64298111
171566062615660627GA15GENICpossibly homozygous64688226
171566493215664933TC26GENICpossibly homozygous64688228
171566518715665188TC20GENIChomozygous64298123
171566547415665475GT21GENIChomozygous64298125
171566554315665544CG28GENIChomozygous64298127
171566555115665552CT29GENIChomozygous64298129
171566557315665574GT30GENIChomozygous64298131
171566565315665654AG26GENIChomozygous64298133
171566570915665710CT31GENIChomozygous64298135
171566576415665765GC27GENIChomozygous64298137
171566651315666514GA30GENIChomozygous64298139
171566654315666544AG30GENIChomozygous64298141
171566671215666713GA25GENIChomozygous64298143
171566675115666752TG20GENICpossibly homozygous64298145
171566689315666894GA23GENIChomozygous64298151
171566696015666961CT34GENIChomozygous64298153
171566704015667041TC30GENIChomozygous64298155
171566721415667215TG30GENIChomozygous64298157
171566737015667371TC16GENIChomozygous64298159
171566744515667446AG21GENIChomozygous64298161
171566749215667493GT24GENIChomozygous64298163
171566756915667570AG17GENIChomozygous64298165
171566765315667654GT24GENIChomozygous64298167
171566774315667744AG27GENIChomozygous64298169
171566785215667853AG31GENIChomozygous64298171
171566795515667956GA28GENIChomozygous64298173
171566847815668479TC20GENIChomozygous64298175