chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183085946030859461AT40GENICpossibly homozygous110321172
183086037330860374TG21GENIChomozygous110321174
183086043330860434AG40GENICpossibly homozygous110321176
183093690230936903TG27GENIChomozygous110321527
183093782730937828TG15GENIChomozygous119487741
183096153930961540TC20GENIChomozygous110457556
183096154130961542AC21GENIChomozygous110457557
183096157030961571TG53GENIChomozygous110457558
183096183030961831CT36GENIChomozygous110589448
183096199330961994CA37GENIChomozygous110457559
183096230530962306GC31GENIChomozygous110589450
183096233330962334TC31GENIChomozygous110589452
183096239730962398TC31GENIChomozygous110812324
183096338130963382CA21GENIChomozygous119487744
183096234830962349CT31GENIChomozygous110769875
183095356430953565GT40GENICpossibly homozygous119558987