chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108951140889511409TC20GENIChomozygous116902691
108951145089511451TC20GENIChomozygous116820211
108951145989511460GT21GENIChomozygous116902693
108951236089512361AG13GENIChomozygous116902695
108951265989512660GA13GENIChomozygous116950580
108951270589512706TC17GENIChomozygous116902697
108951278589512786TA16GENIChomozygous116902699
108951283589512836CT15GENIChomozygous116902701
108951300789513008TC25GENIChomozygous116902703
108951307289513073CT30GENIChomozygous116902705
108951406089514061GA30GENIChomozygous116902707
108951411089514111GA25GENIChomozygous116902709
108951531689515317CA30GENIChomozygous116902711
108951547489515475GT22GENIChomozygous116902713
108951715389517154TG24GENIChomozygous116902717
108951773789517738GA32GENICpossibly homozygous116902719
108951958089519581GA17GENIChomozygous116902721
108952000989520010GA7GENIChomozygous116902723
108952295389522954GA20GENIChomozygous116675647
108952435689524357AC28GENIChomozygous116675653
108952562889525629GA25GENIChomozygous116902725
108952614789526148AG18GENIChomozygous116675661
108951673689516737GT6GENIChomozygous117068467