chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8130120530130120531AG25GENIChomozygous116724660
8130120581130120582GA18GENIChomozygous116724661
8130120680130120681GT12GENIChomozygous116724662
8130120697130120698CA15GENIChomozygous116724663
8130120847130120848AG24GENIChomozygous116724664
8130121116130121117CG15GENIChomozygous116724665
8130121305130121306GT22GENIChomozygous116724666
8130122325130122326AG28GENIChomozygous116724668
8130122465130122466CT19GENIChomozygous116724669
8130121572130121575AGA10GENIChomozygous128648239
8130120646130120646AACA17GENIChomozygous128648237
8130120992130120992TGCA19GENIChomozygous128648238
8130122957130122958CA25GENIChomozygous116724670
8130123073130123074AG35GENIChomozygous116724671
8130123309130123310GA27GENIChomozygous116724672
8130123529130123530GA26GENIChomozygous116724673
8130123547130123548CT30GENIChomozygous116724674
8130124110130124111TC25GENIChomozygous116724675
8130124162130124163AC25GENIChomozygous116724676
8130124448130124448CCAT21GENIChomozygous128648241
8130124594130124595TC22GENIChomozygous116724677
8130124720130124721AT20GENIChomozygous116724678
8130124734130124735TC23GENIChomozygous116724679
8130125544130125545GA16GENIChomozygous116724680
8130126053130126054CG13GENIChomozygous116724681
8130126788130126803CCATCCTTGCCCTAG23GENIChomozygous128648242
8130127107130127108TG19GENIChomozygous116724682
8130127420130127421GA21GENIChomozygous116724683