chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135214853952148540AG23GENIChomozygous944926917
135214870352148704CT16GENIChomozygous944926918
135214918652149187AG34GENIChomozygous944926919
135214990952149910CT20GENIChomozygous944926920
135215095952150960AG29GENIChomozygous944926921
135215112652151127TC24GENIChomozygous944926922
135215133752151338TC19GENIChomozygous944926923
135215171052151711TC21GENIChomozygous944926924
135215176652151767GC21GENIChomozygous944926925
135215446352154464GA31GENIChomozygous944926926
135215819552158196GA20GENIChomozygous944926927
135215849452158495AG33GENIChomozygous944926928
135215854152158542CT21GENIChomozygous944926929
135216064252160643GA15GENIChomozygous944926930
135216247352162474AC30GENIChomozygous944926931
135216424752164248AG27GENIChomozygous944926932
135216606152166062GA29GENIChomozygous944926933
135216838452168385AG31GENIChomozygous944926934
135216892752168928TC24GENIChomozygous944926935
135216961752169618CT28GENIChomozygous944926936
135217104252171043CA34GENIChomozygous944926937
135217594652175947CG28GENIChomozygous944926938
135218016752180168GA24GENIChomozygous944926939
135218051152180512TC26GENIChomozygous944926940
135218057952180580CT32GENIChomozygous944926941
135218064952180650AG28GENIChomozygous944926942
135218193752181938GA29GENIChomozygous944926943
135218320652183207TC18GENIChomozygous944926944
135218398652183987CT26GENIChomozygous944926945
135218474752184748AG36GENIChomozygous944926946
135218508852185089AG22GENIChomozygous944926947
135218509752185098TC23GENIChomozygous944926948
135218531852185319CT29GENIChomozygous944926949
135218550052185501GC13GENIChomozygous944926950
135218647552186476GT10GENIChomozygous944926951
135218669352186694TC8GENIChomozygous944926952
135218670552186706AG8GENIChomozygous944926953
135218748652187487GA25GENIChomozygous944926954
135218861952188620AC24GENIChomozygous944926955
135218926052189261GC16GENIChomozygous944926956
135218970052189701TC27GENIChomozygous944926957
135218982852189829TG27GENIChomozygous944926958