chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171565313215653133GA18GENIChomozygous64688224
171565566315655664GC14GENIChomozygous64298111
171566062615660627GA15GENIChomozygous64688226
171566493215664933TC18GENIChomozygous64688228
171566518715665188TC21GENIChomozygous64298123
171566547415665475GT16GENIChomozygous64298125
171566554315665544CG19GENIChomozygous64298127
171566555115665552CT11GENIChomozygous64298129
171566557315665574GT13GENIChomozygous64298131
171566565315665654AG14GENIChomozygous64298133
171566570915665710CT11GENIChomozygous64298135
171566576415665765GC13GENIChomozygous64298137
171566651315666514GA10GENIChomozygous64298139
171566654315666544AG13GENIChomozygous64298141
171566671215666713GA21GENIChomozygous64298143
171566689315666894GA25GENIChomozygous64298151
171566696015666961CT16GENIChomozygous64298153
171566704015667041TC24GENIChomozygous64298155
171566721415667215TG17GENIChomozygous64298157
171566737015667371TC16GENIChomozygous64298159
171566744515667446AG23GENIChomozygous64298161
171566749215667493GT12GENIChomozygous64298163
171566756915667570AG21GENIChomozygous64298165
171566765315667654GT31GENIChomozygous64298167
171566774315667744AG25GENIChomozygous64298169
171566785215667853AG17GENIChomozygous64298171
171566795515667956GA14GENIChomozygous64298173
171566836515668366GT7GENIChomozygous64990201
171566847815668479TC10GENIChomozygous64298175
171566835615668358GG12GENICheterozygous65256209
171565496915654969ACT16GENICheterozygous65578206