chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264776922264776923TC18GENIChomozygous108636598
1264777765264777766TG9GENIChomozygous108636599
1264778310264778311AG9GENIChomozygous108636600
1264784648264784649AG17GENIChomozygous108636601
1264786025264786026AG6GENIChomozygous108636602
1264786617264786618GT19GENIChomozygous108636603
1264789833264789834CT30GENIChomozygous108636605
1264790085264790086AG25GENIChomozygous108636606
1264790733264790734GA21GENIChomozygous108636607
1264791605264791606GA19GENIChomozygous108636608
1264791845264791846GA16GENIChomozygous108636609
1264793054264793055AC15GENIChomozygous108636610
1264794355264794356GC38GENIChomozygous108636613
1264794610264794611AG19GENIChomozygous108636614