chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41616203216162033AG40GENIChomozygous112522826
41616207916162080AC43GENIChomozygous112522828
41616240116162402TA28GENIChomozygous112522830
41616253716162538GT20GENIChomozygous112522832
41616286316162864TC15GENIChomozygous112522836
41616300416163005CT33GENIChomozygous112522838
41616349216163493CT27GENIChomozygous112522840
41616374316163744AG19GENIChomozygous112522842
41616378816163789CT27GENIChomozygous112522844
41616431716164318GA24GENIChomozygous112522846
41616436916164370GA26GENIChomozygous112522848
41616448416164485AG30GENIChomozygous112522850
41616493316164934CT36GENIChomozygous112522854
41616517116165172TC26GENIChomozygous112522856
41616523416165235GA26GENIChomozygous112522858
41616535416165355CG22GENIChomozygous112522860
41616538516165386AG21GENIChomozygous112522862
41616556116165562CT19GENIChomozygous112522864
41616565516165656CG24GENIChomozygous112522868
41616573216165733GA38GENIChomozygous112522870
41616575016165751AG36GENIChomozygous112522872
41616576716165768CT37GENIChomozygous112522874
41616579016165791TC35GENIChomozygous112522876
41616592216165923CT31GENIChomozygous112522878
41616639316166394TC27GENIChomozygous112522880
41616663016166631GA38GENIChomozygous112522882
41616700316167004AG31GENIChomozygous112522884
41616755016167551CT25GENICpossibly homozygous112522886
41617011516170116GA20GENIChomozygous112522888
41617754616177547TA17GENIChomozygous112522892
41617902316179024TC15GENIChomozygous112522894
41617921616179217GT28GENIChomozygous112522896