chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171565313215653133GA39GENIChomozygous64688224
171565566315655664GC26GENIChomozygous64298111
171566062615660627GA24GENIChomozygous64688226
171566493215664933TC26GENIChomozygous64688228
171566518715665188TC18GENIChomozygous64298123
171566547415665475GT29GENIChomozygous64298125
171566554315665544CG20GENICpossibly homozygous64298127
171566555115665552CT17GENIChomozygous64298129
171566557315665574GT21GENIChomozygous64298131
171566565315665654AG20GENIChomozygous64298133
171566570915665710CT27GENIChomozygous64298135
171566576415665765GC27GENIChomozygous64298137
171566651315666514GA31GENIChomozygous64298139
171566654315666544AG33GENIChomozygous64298141
171566671215666713GA14GENIChomozygous64298143
171566679015666791CA6GENIChomozygous64298149
171566689315666894GA16GENIChomozygous64298151
171566696015666961CT25GENICpossibly homozygous64298153
171566704015667041TC14GENIChomozygous64298155
171566721415667215TG16GENIChomozygous64298157
171566737015667371TC30GENIChomozygous64298159
171566744515667446AG21GENIChomozygous64298161
171566749215667493GT23GENIChomozygous64298163
171566756915667570AG34GENIChomozygous64298165
171566765315667654GT30GENICpossibly homozygous64298167
171566774315667744AG23GENIChomozygous64298169
171566785215667853AG20GENIChomozygous64298171
171566795515667956GA34GENIChomozygous64298173
171566847815668479TC20GENIChomozygous64298175
171566836515668366GT16GENICpossibly homozygous64990201
171566679615666797AG8GENIChomozygous64990200