chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212232675212232676AG29GENIChomozygous801731878
1212246839212246840TC31GENICpossibly homozygous801731879
1212246883212246884GT34GENIChomozygous801731880
1212246939212246940CG24GENIChomozygous801731881
1212252432212252433TG24GENIChomozygous801731882
1212261270212261271AG27GENICheterozygous801731883
1212262916212262917AC9GENIChomozygous801731884
1212262936212262937TG7GENIChomozygous801731885
1212263032212263033TG13GENIChomozygous801731886
1212263077212263078AC12GENIChomozygous801731887
1212263129212263130AG14GENIChomozygous801731888
1212264037212264038GT30GENIChomozygous801731889
1212274307212274308GT26GENIChomozygous801731890
1212275738212275739AC17GENIChomozygous801731891
1212275844212275845CA27GENIChomozygous801731892
1212276381212276382CT20GENIChomozygous801731893