chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226742681226742682GA11GENIChomozygous121186883
1226743093226743094TC14GENIChomozygous109450919
1226746931226746932AG21GENIChomozygous108998270
1226749604226749605GA7GENIChomozygous121186885
1226751389226751390CT35GENICpossibly homozygous121186887
1226755885226755886AG10GENIChomozygous121186888
1226757112226757113TC11GENIChomozygous121186889
1226757227226757228AT27GENIChomozygous108558912
1226757310226757311TC18GENIChomozygous108558913
1226757752226757753TC12GENIChomozygous108558914
1226757929226757930GT19GENIChomozygous109450953
1226763249226763250TC25GENIChomozygous108558924
1226765457226765458GA14GENIChomozygous121186896
1226766750226766751TC21GENIChomozygous108558934
1226767457226767458CT10GENIChomozygous109450954
1226767853226767854CG18GENIChomozygous108558936
1226769530226769531GA9GENIChomozygous121186898
1226771141226771142TC21GENIChomozygous108998279
1226772062226772063AG14GENIChomozygous108558939
1226773595226773596TC17GENIChomozygous108998281
1226758603226758604TC9GENICheterozygous125535499