chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264776922264776923TC22GENIChomozygous108636598
1264777765264777766TG5GENIChomozygous108636599
1264778310264778311AG11GENIChomozygous108636600
1264784648264784649AG17GENIChomozygous108636601
1264786025264786026AG15GENIChomozygous108636602
1264786617264786618GT13GENIChomozygous108636603
1264789833264789834CT31GENIChomozygous108636605
1264790085264790086AG15GENIChomozygous108636606
1264790733264790734GA24GENIChomozygous108636607
1264791605264791606GA17GENIChomozygous108636608
1264791845264791846GA22GENIChomozygous108636609
1264793054264793055AC11GENIChomozygous108636610
1264794355264794356GC18GENIChomozygous108636613
1264794610264794611AG17GENIChomozygous108636614