chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2213416712213416713AG22GENIChomozygous885632894
2213416980213416981CT21GENIChomozygous885632895
2213417719213417720AG16GENIChomozygous885632896
2213418216213418217AG19GENICpossibly homozygous885632897
2213418378213418379CT12GENIChomozygous885632898
2213418392213418393CT19GENIChomozygous885632899
2213418663213418664GA17GENIChomozygous885632900
2213418791213418792TG18GENIChomozygous885632901
2213419466213419467AG19GENIChomozygous885632902
2213419576213419577TA22GENIChomozygous885632903
2213419613213419614TC18GENIChomozygous885632904
2213419705213419706CT11GENIChomozygous885632905
2213420315213420316TC22GENIChomozygous885632906
2213423220213423221TA19GENIChomozygous885632907
2213423280213423281GA32GENIChomozygous885632908
2213423372213423373GA17GENIChomozygous885632909
2213423398213423399TC22GENIChomozygous885632910
2213423816213423817GA23GENIChomozygous885632911
2213423902213423903GA23GENIChomozygous885632912