chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264776922264776923TC30GENIChomozygous108636598
1264777765264777766TG27GENIChomozygous108636599
1264778310264778311AG28GENIChomozygous108636600
1264784648264784649AG26GENIChomozygous108636601
1264786025264786026AG25GENIChomozygous108636602
1264789306264789307TC31GENIChomozygous108636604
1264789833264789834CT26GENIChomozygous108636605
1264790085264790086AG28GENIChomozygous108636606
1264790733264790734GA15GENIChomozygous108636607
1264791605264791606GA26GENIChomozygous108636608
1264791845264791846GA10GENIChomozygous108636609
1264793054264793055AC26GENIChomozygous108636610
1264793258264793259GA13GENIChomozygous108783489
1264793283264793284CT24GENIChomozygous108636612
1264794355264794356GC21GENIChomozygous108636613
1264794610264794611AG30GENIChomozygous108636614