chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102739748227397483CT12GENIChomozygous116532870
102739763227397633CT22GENIChomozygous116532872
102739769027397691CG18GENIChomozygous116532874
102739813927398140AT18GENIChomozygous116532876
102739819627398197GA17GENIChomozygous116532878
102739862427398625CT16GENIChomozygous116532880
102739869327398694GA16GENIChomozygous116924079
102740021727400218AT14GENIChomozygous116532882
102740133427401335TC26GENIChomozygous116532884
102740148927401490CT18GENIChomozygous116532886
102740187827401879TC8GENIChomozygous117075809
102740193327401934CT17GENIChomozygous116749691
102740197327401974CT18GENIChomozygous117055227
102740210227402103CA17GENIChomozygous117001030
102740327527403276GA20GENIChomozygous116532888
102740354527403546CA14GENICpossibly homozygous116532890
102740412827404129AT7GENIChomozygous116532892
102740413027404131GC7GENIChomozygous116532894
102740416827404169GT8GENIChomozygous116532896
102740495327404954GC10GENIChomozygous116532898
102740578427405785GC18GENIChomozygous116532900
102740585127405852TC10GENIChomozygous116532902
102740621427406215AG10GENIChomozygous116532904
102740675627406757AT18GENIChomozygous116532906
102740734927407350CT33GENIChomozygous116864619
102740817027408171AG22GENIChomozygous116532908
102740893427408935TA16GENIChomozygous116532910
102740952427409525GC20GENIChomozygous116532912
102741076127410762TC26GENIChomozygous116532914
102741098227410983TC26GENIChomozygous116532916
102741130227411303TA17GENIChomozygous116532918
102741137827411379TC17GENIChomozygous116532920