chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71241004612410047TC25GENIChomozygous53790877
71241042112410422CT16GENIChomozygous54630294
71241150612411507TC14GENIChomozygous53790887
71241154412411545GGAAAAAAAA5GENIChomozygous54954908
71241170712411708GA22GENIChomozygous53790888
71241170812411709TG22GENIChomozygous54630296
71241217912412180TC28GENIChomozygous53790889
71241239012412391AAG22GENICpossibly homozygous54630298
71241302612413027CT40GENIChomozygous53790892
71241400912414010AT34GENIChomozygous53790894
71241435912414362GGG---25GENIChomozygous53790895
71241592812415929CT35GENIChomozygous54630300
71241594812415949GT37GENIChomozygous54630302
71241634612416347GT13GENIChomozygous53790897
71241635912416360CA11GENIChomozygous53790898
71241155612411557GA10GENIChomozygous54884983
71241111512411116TTGTTGAG6GENIChomozygous55071061
71241116212411163CCGGCTGT29GENIChomozygous55071063