chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105559752555597526TC18GENIChomozygous116602635
105559780155597802CT19GENIChomozygous116602637
105559791655597917CT19GENIChomozygous116602639
105560169455601695CT23GENIChomozygous116602641
105560190555601906AG20GENIChomozygous116602643
105560191655601917CT21GENIChomozygous116602645
105560629455606295CT19GENIChomozygous116602651
105561294355612944CT31GENIChomozygous116602661
105560894155608942CT17GENIChomozygous116602653
105560970955609710GA25GENIChomozygous116602655
105561221355612214CT27GENIChomozygous116602657
105561265455612655CT21GENIChomozygous116602659
105561321655613217TC19GENICpossibly homozygous116602663
105561332355613324GA13GENIChomozygous116602665
105561526655615267GA18GENIChomozygous116602667
105561686655616867CT22GENIChomozygous116602669