chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157267568157267569C-32GENICheterozygous57960271
4157269675157269676CT18GENIChomozygous57960274
4157269917157269918GC21GENIChomozygous58164641
4157270131157270132CT10GENIChomozygous58164643
4157270307157270308CA5GENIChomozygous57960280
4157270729157270730TA16GENIChomozygous57533730
4157270857157270858GA8GENIChomozygous58164645
4157270998157270999GT17GENIChomozygous57960283
4157273359157273361AA--6GENIChomozygous57533736
4157273381157273382TG7GENIChomozygous57533738
4157273416157273417CCA8GENIChomozygous58164647
4157273559157273565ACACAC------1GENIChomozygous58348847
4157274416157274417GA18GENIChomozygous57533746
4157274468157274469AG20GENIChomozygous57960298
4157274544157274545GC20GENIChomozygous58164649
4157274820157274821TC9GENIChomozygous57533748
4157275477157275478GT21GENIChomozygous57533750
4157275873157275874TC31GENIChomozygous57533752
4157276089157276090CT19GENIChomozygous57533754
4157276887157276888AAAC10GENICheterozygous57533758
4157276887157276888AAACACAC10GENICheterozygous58407906
4157277027157277028TTACAC7GENICheterozygous57533762
4157277027157277028TTACACAC7GENICheterozygous58348849
4157277710157277711T-7GENIChomozygous57533766
4157278192157278195AAG---19GENIChomozygous57960319
4157278686157278687AG5GENIChomozygous57533770
4157278859157278860AC5GENIChomozygous58164651
4157279885157279886AT24GENIChomozygous57533780
4157280260157280261GA13GENIChomozygous58164653
4157280955157280956TC7GENIChomozygous58164655
4157276887157276888AAACAC10GENICheterozygous56996730