chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1247502531247502532CT21GENIChomozygous109017655
1247503300247503301AC23GENIChomozygous108775547
1247503323247503324CT24GENIChomozygous108775548
1247503327247503328CT24GENIChomozygous108775549
1247505170247505171AC24GENIChomozygous108602890
1247505282247505283CT18GENIChomozygous108602891
1247505976247505977TA26GENIChomozygous108602892
1247508430247508431GT26GENIChomozygous108602898
1247509726247509727AC36GENIChomozygous109017657
1247511468247511469AG27GENIChomozygous108602902
1247511571247511572AG29GENIChomozygous108602903
1247512289247512290TC24GENIChomozygous108602904
1247513612247513613CA33GENIChomozygous109017659
1247514372247514373GA20GENIChomozygous109017660
1247514378247514379GA19GENIChomozygous108602907