chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8130120530130120531AG29GENIChomozygous116724660
8130120581130120582GA27GENIChomozygous116724661
8130120680130120681GT24GENIChomozygous116724662
8130120697130120698CA34GENIChomozygous116724663
8130120847130120848AG11GENIChomozygous116724664
8130121116130121117CG21GENIChomozygous116724665
8130121305130121306GT28GENIChomozygous116724666
8130121948130121949CT19GENIChomozygous116724667
8130122325130122326AG24GENIChomozygous116724668
8130122465130122466CT24GENIChomozygous116724669
8130122957130122958CA26GENIChomozygous116724670
8130123073130123074AG22GENIChomozygous116724671
8130123309130123310GA27GENIChomozygous116724672
8130123529130123530GA46GENIChomozygous116724673
8130123547130123548CT38GENIChomozygous116724674
8130123791130123792CT34GENIChomozygous117955664
8130124110130124111TC24GENIChomozygous116724675
8130124162130124163AC24GENIChomozygous116724676
8130124720130124721AT22GENIChomozygous116724678
8130124734130124735TC18GENIChomozygous116724679
8130125544130125545GA28GENIChomozygous116724680
8130127107130127108TG12GENIChomozygous116724682
8130127420130127421GA21GENIChomozygous116724683