chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5111817433111817434AG17GENICpossibly homozygous56051945
5111817554111817555TC26GENIChomozygous55640419
5111817599111817600GA21GENICpossibly homozygous56051946
5111818340111818341AG15GENIChomozygous55640420
5111818740111818741GT39GENICpossibly homozygous56051947
5111819024111819025GGCC3GENIChomozygous56051948
5111819249111819250TA19GENIChomozygous56051949
5111820163111820164CCT25GENIChomozygous56051950
5111820859111820860CT7GENIChomozygous56051951
5111820965111820966GGT20GENIChomozygous56051952
5111820979111820991TGTGTGTGTGTG------------5GENIChomozygous56051953
5111821143111821144AG20GENIChomozygous55640425
5111822415111822416GGA17GENIChomozygous56051954
5111822445111822446G-33GENIChomozygous56051955
5111822449111822450C-36GENIChomozygous56051956
5111823630111823632TT--20GENIChomozygous56120374
5111822780111822781AG26GENIChomozygous56051958
5111822984111822985T-22GENIChomozygous56051959
5111823036111823037CT22GENIChomozygous56051960
5111823793111823794GGC18GENIChomozygous56051962
5111824267111824268AG19GENIChomozygous56051963
5111824411111824412TTTGTG16GENIChomozygous55640433
5111824961111824962CCT15GENICpossibly homozygous56051964