chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8130120530130120531AG17GENIChomozygous116724660
8130120581130120582GA15GENIChomozygous116724661
8130120680130120681GT18GENIChomozygous116724662
8130120697130120698CA19GENIChomozygous116724663
8130120847130120848AG17GENIChomozygous116724664
8130121116130121117CG24GENIChomozygous116724665
8130121305130121306GT12GENIChomozygous116724666
8130122325130122326AG19GENIChomozygous116724668
8130122465130122466CT19GENIChomozygous116724669
8130122957130122958CA30GENIChomozygous116724670
8130123073130123074AG32GENIChomozygous116724671
8130123309130123310GA30GENIChomozygous116724672
8130123529130123530GA29GENIChomozygous116724673
8130123547130123548CT27GENIChomozygous116724674
8130124110130124111TC16GENIChomozygous116724675
8130124162130124163AC19GENIChomozygous116724676
8130124594130124595TC29GENIChomozygous116724677
8130124720130124721AT17GENIChomozygous116724678
8130124734130124735TC19GENIChomozygous116724679
8130125544130125545GA31GENIChomozygous116724680
8130126053130126054CG10GENIChomozygous116724681
8130127107130127108TG19GENIChomozygous116724682
8130127420130127421GA27GENIChomozygous116724683