chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185527684455276845AG19GENIChomozygous46608170
185527688955276890TG23GENICpossibly homozygous46608171
185527699755276998GA18GENIChomozygous46608172
185527798155277982AG19GENIChomozygous46608174
185527809855278099TC29GENICpossibly homozygous46608175
185527812855278129TC25GENIChomozygous46608177
185527822455278225GA29GENIChomozygous46608178
185527823055278231CG28GENIChomozygous46608180
185527917355279175CT--24GENIChomozygous46608182
185527918155279182CA26GENIChomozygous46608183
185527931255279313AG23GENIChomozygous46608185
185527940555279406AC32GENIChomozygous46608186
185527982655279828CT--10GENICheterozygous46608188
185527982755279828T-10GENICheterozygous46608189
185528015555280156CCTA30GENIChomozygous46608190
185528037755280378GA29GENIChomozygous46608192
185528038455280385GC26GENIChomozygous46608193
185528049255280493AG24GENIChomozygous46608195
185528087855280879CT21GENIChomozygous46608201
185528090255280903CT25GENIChomozygous46608203
185528120455281205CT30GENIChomozygous46608204
185528138655281387AT37GENIChomozygous46608206