chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2104593345104593346GC19GENIChomozygous109959919
2104593580104593581TC23GENIChomozygous109959921
2104593724104593725CT15GENIChomozygous109959925
2104593865104593866GT7GENIChomozygous109959927
2104593958104593959AT16GENIChomozygous109959929
2104594093104594094AC20GENIChomozygous110579420
2104594156104594157AG15GENIChomozygous109959933
2104594810104594811CT12GENIChomozygous109959939
2104594362104594363CT30GENIChomozygous109959935
2104594758104594759GA13GENIChomozygous109959937
2104594853104594854TG20GENIChomozygous109959941
2104595205104595206CA10GENIChomozygous109959945