chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141058117410581175AG25GENIChomozygous113962639
141058118910581190GC22GENIChomozygous114083210
141058199610581997T29GENIChomozygous129124265
141058354010583544TACT21GENIChomozygous129124266
141058532910585330AT18GENIChomozygous113338318
141058238410582385CA27GENIChomozygous113338313
141058143510581436AG20GENIChomozygous113338309
141058353110583532CG23GENIChomozygous113338317
141058276510582766G12GENIChomozygous134240633
141058300310583004GC22GENIChomozygous113940856
141058493010584931CT21GENIChomozygous113940858
141058579310585794GA16GENIChomozygous113338320
141058580510585805C15GENIChomozygous129124267
141058592510585926GA10GENIChomozygous113940860
141058649110586492CT10GENIChomozygous113338322
141058797710587978T16GENICheterozygous134240634
141058628210586283GA29GENIChomozygous113783748
141058652610586527TC11GENIChomozygous113338324
141058702210587023CT13GENIChomozygous113338326
141058998210589982T22GENICpossibly homozygous134240635
141059093510590936CA17GENIChomozygous113849039
141059126210591262GT14GENIChomozygous129124268
141059196810591969GA29GENIChomozygous113940862
141059274110592742CA15GENIChomozygous113338356
141059412610594127GA23GENIChomozygous113940864
141059591910595920CG11GENIChomozygous113849043
141059750410597505GA15GENIChomozygous113940866
141058626910586270GA28GENIChomozygous118675779