chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42908238829082389TC11GENIChomozygous113001826
42908241029082411TG18GENIChomozygous113001828
42908342329083424AG22GENIChomozygous113001830
42908389229083893GA16GENIChomozygous113001832
42908396929083970AC27GENIChomozygous113001834
42908416329084164TC22GENICpossibly homozygous113001836
42908420829084209GC23GENIChomozygous113001838
42908542629085427TC15GENIChomozygous113001840
42908591929085920CT20GENICpossibly homozygous113001842
42908638629086387GA7GENICpossibly homozygous113001844
42908694829086949TC32GENIChomozygous113001858
42908751829087519TC20GENIChomozygous113001860
42908866129088662CA22GENIChomozygous113001862
42908938629089387TC24GENIChomozygous113001864
42908960829089609GT25GENIChomozygous113001866
42909002929090030TC19GENIChomozygous113001868
42909020829090209GA8GENIChomozygous113001870
42909060229090603TA25GENICpossibly homozygous113001872
42909131529091316GA25GENIChomozygous113001874
42909142229091423CT15GENIChomozygous113001876
42909145829091459AG18GENIChomozygous113001878