chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101669543916695440GA15GENIChomozygous116738897
101669549316695494GA16GENIChomozygous116738898
101669591016695911AC35GENIChomozygous116499819
101670001916700020GA28GENIChomozygous116738899
101670002516700026AG24GENIChomozygous116499823
101670048116700482GA31GENIChomozygous116499829
101670238916702390GA29GENIChomozygous116738900
101670274716702748GC25GENIChomozygous116738901
101670281616702817TC27GENIChomozygous116738902
101670404316704044TC22GENIChomozygous116499839
101670673116706732AG23GENIChomozygous116738903
101670856516708566TA30GENIChomozygous116499849
101670909916709100TA27GENIChomozygous116738904
101671021816710219CT17GENIChomozygous116738905
101671164016711641AT24GENIChomozygous116499851
101671225016712251CT25GENIChomozygous116738906
101671238916712390GA33GENIChomozygous116738907
101671253516712536CA30GENIChomozygous116499853
101671783016717831AG25GENIChomozygous116738908
101671787116717872GA31GENIChomozygous116738909
101672270516722706TA18GENIChomozygous116738910
101672321216723213AG25GENIChomozygous116738911
101673106216731063TC41GENIChomozygous116738912
101673239416732395GA25GENIChomozygous116738913
101671635916716360TA30GENICpossibly homozygous116861021
101673804516738046GT28GENIChomozygous116738915
101673812916738130CG29GENIChomozygous116738916
101673862616738627TC26GENIChomozygous117053223
101673998416739985TC25GENICpossibly homozygous116738917
101674020816740209GT41GENIChomozygous116738918
101674099616740997CT34GENIChomozygous116738919
101674242216742423CT27GENIChomozygous116738920
101674523216745233AG30GENIChomozygous116738921
101674622716746228TA4GENIChomozygous117163453
101674951116749512AT8GENICheterozygous117191344
101674992316749924TC26GENIChomozygous116499873
101674624416746245CG2GENIChomozygous117365308