chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2104593345104593346GC17GENIChomozygous109959919
2104593580104593581TC12GENIChomozygous109959921
2104593581104593582GA11GENIChomozygous109959923
2104593724104593725CT15GENIChomozygous109959925
2104593865104593866GT8GENIChomozygous109959927
2104593958104593959AT15GENIChomozygous109959929
2104594137104594138TA22GENIChomozygous109959931
2104594156104594157AG25GENIChomozygous109959933
2104594362104594363CT40GENIChomozygous109959935
2104594758104594759GA28GENIChomozygous109959937
2104594810104594811CT25GENIChomozygous109959939
2104594853104594854TG18GENIChomozygous109959941