chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157267568157267569C-42GENICheterozygous57960271
4157269675157269676CT24GENIChomozygous57960274
4157269917157269918GC22GENIChomozygous58164641
4157270131157270132CT22GENIChomozygous58164643
4157270307157270308CA10GENIChomozygous57960280
4157270729157270730TA26GENIChomozygous57533730
4157270857157270858GA18GENIChomozygous58164645
4157270998157270999GT12GENIChomozygous57960283
4157273359157273361AA--7GENIChomozygous57533736
4157273381157273382TG7GENIChomozygous57533738
4157273416157273417CCA10GENIChomozygous58164647
4157273559157273565ACACAC------5GENIChomozygous58348847
4157274416157274417GA13GENIChomozygous57533746
4157274468157274469AG11GENIChomozygous57960298
4157274544157274545GC20GENIChomozygous58164649
4157274820157274821TC9GENIChomozygous57533748
4157275477157275478GT13GENIChomozygous57533750
4157275873157275874TC12GENIChomozygous57533752
4157276089157276090CT7GENIChomozygous57533754
4157276887157276888AAAC20GENICheterozygous57533758
4157276887157276888AAACACAC20GENICheterozygous58407906
4157277027157277028TTACAC16GENICheterozygous57533762
4157277027157277028TTACACAC16GENICpossibly homozygous58348849
4157277710157277711T-7GENIChomozygous57533766
4157278192157278195AAG---11GENIChomozygous57960319
4157278686157278687AG6GENIChomozygous57533770
4157278859157278860AC5GENIChomozygous58164651
4157279885157279886AT12GENIChomozygous57533780
4157280260157280261GA17GENIChomozygous58164653
4157280955157280956TC6GENIChomozygous58164655
4157276887157276888AAACAC20GENICheterozygous56996730