chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108951140889511409TC11GENIChomozygous116902691
108951145089511451TC4GENIChomozygous116820211
108951145989511460GT4GENIChomozygous116902693
108951193689511937GA6GENIChomozygous117020502
108951236089512361AG14GENIChomozygous116902695
108951248589512486GA7GENIChomozygous117020503
108951265989512660GA18GENICheterozygous116950580
108951270589512706TC13GENIChomozygous116902697
108951278589512786TA10GENIChomozygous116902699
108951283589512836CT17GENIChomozygous116902701
108951300789513008TC18GENIChomozygous116902703
108951307289513073CT21GENIChomozygous116902705
108951406089514061GA14GENIChomozygous116902707
108951411089514111GA20GENIChomozygous116902709
108951531689515317CA20GENIChomozygous116902711
108951547489515475GT13GENICheterozygous116902713
108951715389517154TG4GENIChomozygous116902717
108951773789517738GA16GENIChomozygous116902719
108951958089519581GA21GENIChomozygous116902721
108952000989520010GA4GENIChomozygous116902723
108952295389522954GA22GENIChomozygous116675647
108952435689524357AC5GENIChomozygous116675653
108952562889525629GA11GENIChomozygous116902725
108952614789526148AG11GENIChomozygous116675661