chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1247502531247502532CT19GENIChomozygous109017655
1247503300247503301AC31GENIChomozygous108775547
1247503323247503324CT27GENIChomozygous108775548
1247503327247503328CT28GENIChomozygous108775549
1247505170247505171AC33GENIChomozygous108602890
1247505282247505283CT19GENIChomozygous108602891
1247505976247505977TA23GENIChomozygous108602892
1247508430247508431GT23GENIChomozygous108602898
1247510104247510105CG23GENIChomozygous108602899
1247511468247511469AG38GENIChomozygous108602902
1247511571247511572AG28GENIChomozygous108602903
1247512289247512290TC12GENIChomozygous108602904
1247513612247513613CA24GENIChomozygous109017659
1247514372247514373GA25GENIChomozygous109017660
1247514378247514379GA32GENIChomozygous108602907