chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8130120530130120531AG19GENIChomozygous116724660
8130120581130120582GA17GENIChomozygous116724661
8130120646130120647GA4GENICheterozygous117007037
8130120680130120681GT11GENIChomozygous116724662
8130120697130120698CA8GENIChomozygous116724663
8130120847130120848AG6GENIChomozygous116724664
8130120995130120996GA8GENIChomozygous116902104
8130121116130121117CG9GENIChomozygous116724665
8130121305130121306GT14GENIChomozygous116724666
8130121948130121949CT6GENICheterozygous116724667
8130122325130122326AG21GENIChomozygous116724668
8130122465130122466CT21GENIChomozygous116724669
8130122957130122958CA17GENIChomozygous116724670
8130123073130123074AG11GENIChomozygous116724671
8130123309130123310GA9GENIChomozygous116724672
8130123529130123530GA14GENIChomozygous116724673
8130123547130123548CT12GENIChomozygous116724674
8130123791130123792CT7GENICheterozygous117955664
8130124110130124111TC15GENIChomozygous116724675
8130124162130124163AC16GENIChomozygous116724676
8130124594130124595TC10GENICheterozygous116724677
8130124720130124721AT16GENIChomozygous116724678
8130124734130124735TC8GENIChomozygous116724679
8130125544130125545GA16GENIChomozygous116724680
8130127107130127108TG15GENIChomozygous116724682
8130127420130127421GA15GENIChomozygous116724683