chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1223120597223120598C-19GENIChomozygous61097866
1223121902223121903GA27GENIChomozygous61597527
1223122554223122555GT19GENIChomozygous61597528
1223123776223123777TG28GENIChomozygous61097869
1223124115223124116AG20GENIChomozygous61097871
1223125643223125644TC19GENIChomozygous61097873
1223126214223126215AG23GENIChomozygous61097875
1223130406223130407GC14GENIChomozygous61097881
1223130851223130852TC17GENIChomozygous61097882
1223131822223131823TG23GENIChomozygous61097884
1223132966223132967AATTT19GENICheterozygous61597529
1223132966223132967AATT19GENICheterozygous61597530
1223132966223132967AAT19GENICheterozygous62102380
1223137194223137195AG23GENIChomozygous61097892
1223138572223138573GGGTTT9GENIChomozygous61097893
1223138679223138680TC22GENIChomozygous61097894
1223140309223140310G-16GENIChomozygous61597531
1223141086223141087TTC16GENIChomozygous61597532