chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204739979847399799TC20GENIChomozygous109316843
204739985247399853GC12GENIChomozygous109346916
204739985947399860GC11GENIChomozygous109346918
204741839847418399AG18GENIChomozygous109382059
204741840047418401CA18GENIChomozygous109405018
204741857347418574CT15GENIChomozygous109276512
204741857447418575TA15GENIChomozygous109382061
204741895847418959TA15GENIChomozygous109212450
204741944947419450CT33GENIChomozygous109276514
204741945547419456CT30GENIChomozygous109276516
204741952047419521TC25GENIChomozygous109212452
204741968247419683GC16GENIChomozygous109346926
204741986047419861AT27GENIChomozygous109276517
204741986147419862TA27GENIChomozygous109276519
204741988447419885TC31GENIChomozygous109276521