chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171565313215653133GA29GENIChomozygous64688224
171565566315655664GC27GENIChomozygous64298111
171566062615660627GA17GENIChomozygous64688226
171566493215664933TC21GENIChomozygous64688228
171566518715665188TC17GENIChomozygous64298123
171566547415665475GT29GENIChomozygous64298125
171566554315665544CG24GENIChomozygous64298127
171566555115665552CT27GENIChomozygous64298129
171566557315665574GT23GENIChomozygous64298131
171566565315665654AG13GENIChomozygous64298133
171566570915665710CT10GENIChomozygous64298135
171566576415665765GC23GENIChomozygous64298137
171566651315666514GA19GENIChomozygous64298139
171566654315666544AG14GENIChomozygous64298141
171566671215666713GA20GENIChomozygous64298143
171566675115666752TG19GENIChomozygous64298145
171566689315666894GA12GENIChomozygous64298151
171566696015666961CT11GENIChomozygous64298153
171566704015667041TC9GENIChomozygous64298155
171566721415667215TG20GENIChomozygous64298157
171566737015667371TC24GENIChomozygous64298159
171566744515667446AG18GENIChomozygous64298161
171566749215667493GT17GENIChomozygous64298163
171566756915667570AG20GENIChomozygous64298165
171566765315667654GT20GENIChomozygous64298167
171566774315667744AG21GENIChomozygous64298169
171566785215667853AG19GENIChomozygous64298171
171566795515667956GA13GENIChomozygous64298173
171566847815668479TC16GENIChomozygous64298175