chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4176510009176510010TC20GENIChomozygous112963990
4176510250176510250G19GENIChomozygous128107904
4176510303176510304AG21GENIChomozygous112963992
4176510625176510626GA26GENIChomozygous113222359
4176510956176510957TC21GENIChomozygous112963994
4176512076176512077TG15GENIChomozygous113222360
4176513229176513237TCTATCTA14GENIChomozygous128107906
4176514188176514189CA9GENIChomozygous113248658
4176515128176515129TC18GENIChomozygous113222361
4176515131176515132GA18GENIChomozygous113222362
4176516152176516153G24GENIChomozygous128107908
4176517892176517893AG21GENIChomozygous112964014