chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122593874125938742GA20GENIChomozygous50144100
122593883625938837AATGC12GENIChomozygous50144102
122593998025939981CG18GENIChomozygous50144104
122594019925940200CT17GENIChomozygous50144106
122594180225941803TA9GENIChomozygous50144110
122594184725941848AG8GENIChomozygous50144112
122594193025941931AG8GENIChomozygous50589463
122594208725942088TG24GENIChomozygous50144120
122594232925942330TC14GENIChomozygous50144122
122594235325942354GT16GENIChomozygous50372608
122594286625942867TC18GENIChomozygous50144126
122594316625943167CT17GENIChomozygous50144128
122594346025943466AAAAAG------8GENIChomozygous50144130
122594351825943519AG12GENIChomozygous50144132
122594381225943813CT16GENIChomozygous50144136
122594382625943827TA10GENIChomozygous50144138
122594385325943854CA9GENIChomozygous50144140
122594385725943858TC8GENIChomozygous50144142
122594446725944469CA--20GENIChomozygous50372609
122594488625944887G-21GENIChomozygous50144152
122594504225945043AC17GENIChomozygous50144154
122594508125945082CG10GENIChomozygous50372611
122594510325945104CT9GENIChomozygous50372613
122594516825945169CA16GENIChomozygous50144156
122594532525945326CT11GENIChomozygous50372615
122594543825945439TA18GENIChomozygous50144158
122594608425946085TC11GENIChomozygous50144162
122594631625946317AC17GENIChomozygous50144168
122594654725946548TA17GENIChomozygous50144170
122594747425947475TC25GENIChomozygous50144174
122594845625948457AG21GENIChomozygous50144178
122594873325948734CT14GENIChomozygous50372617
122594905525949056CT21GENIChomozygous50372619
122594907525949076CT22GENIChomozygous50144182