chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4126376792126376793TC32GENIChomozygous112826127
4126376972126376973AT23GENIChomozygous112826129
4126377405126377406GA20GENIChomozygous113301815
4126384009126384010TC26GENIChomozygous113301817
4126384668126384669TC26GENIChomozygous113301818
4126385446126385447AC22GENIChomozygous113301819
4126385814126385815TC24GENIChomozygous113301820
4126385975126385976GA28GENIChomozygous113301821
4126386539126386540AG30GENIChomozygous113301822
4126388576126388577GA16GENIChomozygous113301823
4126389136126389137AG13GENIChomozygous113301824
4126389323126389324CT6GENIChomozygous113301825
4126389326126389327CT4GENIChomozygous113301826
4126390242126390243AG27GENIChomozygous113301827
4126390389126390390CT33GENIChomozygous119280352
4126391330126391331GA41GENIChomozygous113301828
4126393846126393847GC23GENICpossibly homozygous113301829
4126394116126394117AG22GENIChomozygous113301830
4126394351126394352GA23GENIChomozygous113301831
4126394470126394471GC34GENIChomozygous113301832
4126394985126394986GA25GENIChomozygous113301833
4126395165126395166CT23GENIChomozygous113301834
4126395189126395190GC25GENIChomozygous113301835
4126395271126395272CA22GENIChomozygous113301836
4126399943126399944GA20GENIChomozygous113301838