chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171565433315654334GA31GENIChomozygous64298105
171565470215654703GA22GENIChomozygous64298107
171565505815655059CT26GENIChomozygous64298109
171565566315655664GC32GENIChomozygous64298111
171565786215657863AT21GENIChomozygous64298113
171565813315658134AG20GENIChomozygous64298115
171566013515660136AG26GENIChomozygous64298117
171566471815664719GA25GENIChomozygous64298119
171566511815665119TG24GENIChomozygous64298121
171566518715665188TC22GENIChomozygous64298123
171566547415665475GT16GENIChomozygous64298125
171566554315665544CG18GENIChomozygous64298127
171566555115665552CT19GENIChomozygous64298129
171566557315665574GT24GENIChomozygous64298131
171566565315665654AG20GENIChomozygous64298133
171566570915665710CT27GENIChomozygous64298135
171566576415665765GC24GENIChomozygous64298137
171566651315666514GA26GENIChomozygous64298139
171566654315666544AG26GENIChomozygous64298141
171566671215666713GA24GENIChomozygous64298143
171566675115666752TG20GENIChomozygous64298145
171566689315666894GA22GENIChomozygous64298151
171566696015666961CT18GENIChomozygous64298153
171566704015667041TC27GENIChomozygous64298155
171566721415667215TG30GENICpossibly homozygous64298157
171566737015667371TC28GENIChomozygous64298159
171566744515667446AG23GENIChomozygous64298161
171566749215667493GT25GENIChomozygous64298163
171566756915667570AG26GENIChomozygous64298165
171566765315667654GT24GENIChomozygous64298167
171566774315667744AG22GENIChomozygous64298169
171566785215667853AG26GENIChomozygous64298171
171566795515667956GA25GENIChomozygous64298173
171566847815668479TC14GENIChomozygous64298175