chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8130120530130120531AG15GENIChomozygous116724660
8130120581130120582GA21GENIChomozygous116724661
8130120680130120681GT23GENIChomozygous116724662
8130120697130120698CA25GENIChomozygous116724663
8130120847130120848AG12GENIChomozygous116724664
8130121116130121117CG13GENIChomozygous116724665
8130121305130121306GT31GENIChomozygous116724666
8130122325130122326AG25GENIChomozygous116724668
8130122465130122466CT28GENIChomozygous116724669
8130122957130122958CA22GENICpossibly homozygous116724670
8130123073130123074AG18GENIChomozygous116724671
8130123309130123310GA24GENIChomozygous116724672
8130123529130123530GA18GENIChomozygous116724673
8130123547130123548CT19GENIChomozygous116724674
8130124110130124111TC12GENIChomozygous116724675
8130124162130124163AC20GENIChomozygous116724676
8130124594130124595TC21GENIChomozygous116724677
8130124720130124721AT19GENIChomozygous116724678
8130124734130124735TC19GENIChomozygous116724679
8130125544130125545GA26GENIChomozygous116724680
8130126053130126054CG11GENIChomozygous116724681
8130127107130127108TG14GENIChomozygous116724682
8130127420130127421GA23GENIChomozygous116724683