chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224572733224572734CT19GENIChomozygous640925756
4224573209224573210TC17GENIChomozygous640925757
4224573259224573261TG--14GENIChomozygous751583919
4224573304224573305TG9GENIChomozygous640925758
4224573816224573817TTC12GENICheterozygous751583921
4224573816224573817TTCC12GENICheterozygous751583922
4224574455224574456TC23GENIChomozygous640925759
4224575209224575210TC13GENIChomozygous640925760
4224575442224575443T-18GENIChomozygous751583923
4224575513224575525TCTCTCTCTCTC------------9GENIChomozygous751583924
4224575578224575579AG10GENICpossibly homozygous640925761
4224575699224575700GGA10GENIChomozygous751583926
4224575702224575703AT10GENIChomozygous640925762
4224575703224575704CCTTATGAGTGT10GENIChomozygous751583927
4224575704224575705CT10GENIChomozygous640925763
4224576326224576327AC25GENIChomozygous640925764
4224576402224576403GA22GENIChomozygous640925765
4224576561224576562TG23GENIChomozygous640925766
4224576594224576595AT24GENIChomozygous640925767
4224576851224576852AG22GENIChomozygous640925768
4224577057224577058CCA11GENIChomozygous751583928
4224577254224577255AG16GENIChomozygous640925769
4224577762224577766ACAG----22GENIChomozygous751583929
4224578284224578285A-18GENIChomozygous751583930
4224578306224578307AAAG18GENIChomozygous751583931
4224578387224578388AG20GENIChomozygous640925770
4224579990224579991TG9GENIChomozygous640925771
4224580805224580806GC14GENIChomozygous640925772