chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181788215217882153GT34GENIChomozygous110289765
181789195617891957CT22GENIChomozygous110289769
181789301517893016CT32GENIChomozygous110289771
181789349817893499CG33GENIChomozygous110289773
181789367117893672TC38GENIChomozygous110289775
181789375517893756GC31GENIChomozygous110289777
181789628017896281CT38GENIChomozygous110289779
181789713217897133GA29GENIChomozygous110289781
181789842917898430CA24GENIChomozygous110289783
181789844317898444GT24GENIChomozygous110289785
181789844717898448CT20GENIChomozygous110289787
181789845117898452CT20GENIChomozygous110289789
181789845517898456CT22GENIChomozygous110289791
181789845717898458CT21GENIChomozygous110289793
181789846517898466CT25GENIChomozygous110289795
181790063217900633CT25GENIChomozygous110289797
181790090217900903TC35GENIChomozygous110289799
181790174717901748TG27GENIChomozygous110289801
181790295617902957AG22GENIChomozygous110289803
181790359917903600AT23GENIChomozygous110289807
181790364517903646TC26GENIChomozygous110289809
181790365317903654TC26GENIChomozygous110289811
181790373017903731GA37GENIChomozygous110289813
181790388117903882AG46GENIChomozygous110577314
181790390317903904GT43GENIChomozygous110577316
181790463717904638TC22GENIChomozygous110289817
181790574017905741GA28GENIChomozygous110289819
181790779117907792GA37GENIChomozygous110289821
181790789217907893TC28GENIChomozygous110289823
181790913317909134TC32GENIChomozygous110289825
181790917017909171GA36GENIChomozygous110289827
181790960717909608AG26GENIChomozygous110289829
181791048517910486AT24GENIChomozygous110289831
181791234217912343CA25GENIChomozygous110289833
181791284417912845GA27GENIChomozygous110289835