chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1223120597223120598C-21GENICpossibly homozygous61097866
1223121902223121903GA25GENIChomozygous61597527
1223122554223122555GT21GENIChomozygous61597528
1223123776223123777TG16GENIChomozygous61097869
1223124115223124116AG7GENIChomozygous61097871
1223125643223125644TC15GENICpossibly homozygous61097873
1223126214223126215AG10GENICheterozygous61097875
1223128540223128541CT8GENIChomozygous62630135
1223130406223130407GC15GENIChomozygous61097881
1223130851223130852TC11GENIChomozygous61097882
1223131822223131823TG19GENIChomozygous61097884
1223137194223137195AG4GENICheterozygous61097892
1223138572223138573GGGTTT3GENICheterozygous61097893
1223138679223138680TC12GENIChomozygous61097894
1223140309223140310G-2GENICheterozygous61597531
1223141086223141087TTC1GENIChomozygous61597532