chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1276689252276689253AT14GENIChomozygous120477625
1276691336276691337GT28GENIChomozygous108659246
1276691342276691343GC30GENIChomozygous108659247
1276697393276697394AG24GENIChomozygous108659249
1276697861276697862AG15GENIChomozygous108659250
1276699831276699832CA5GENIChomozygous120496314
1276700789276700790TC39GENIChomozygous108659251
1276701347276701348TG22GENIChomozygous108659252
1276702945276702946TA26GENIChomozygous108659253
1276705492276705493GT21GENIChomozygous108659254
1276710202276710203TC14GENIChomozygous120477626
1276713258276713259GC35GENIChomozygous108659258
1276715216276715217CT25GENIChomozygous108659260
1276715609276715610GA9GENIChomozygous108804252
1276718914276718915GA19GENIChomozygous108659261
1276719582276719583AG31GENIChomozygous108659262
1276719839276719840GA23GENIChomozygous108659263
1276722109276722110AG4GENIChomozygous120819000
1276722111276722112CT1GENIChomozygous120608611
1276722112276722113CT1GENIChomozygous120819001
1276723194276723195AG14GENIChomozygous108659267
1276724995276724996TC29GENIChomozygous108659268
1276725766276725767AC13GENIChomozygous108659269
1276725768276725769AC12GENIChomozygous108659270
1276727355276727356AG21GENIChomozygous108659271
1276729368276729369TG16GENIChomozygous108659272
1276710203276710204CT15GENIChomozygous109221110