Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
GRHL2	gene	GRHL2	Expert Review Red;Wessex and West Midlands GLH	Congenital fibrosis of the extraocular muscles		Ophthalmology	Unknown	congenital fibrosis of extraocular muscles, MONDO:0007614				29110737		False	1	0;0;100	2.3	False		ENSG00000083307	ENSG00000083307	HGNC:2799													
TUBB2B	gene	TUBB2B	Expert Review Red;Literature;Wessex and West Midlands GLH	Congenital fibrosis of the extraocular muscles		Ophthalmology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	congenital fibrosis of extraocular muscles, MONDO:0007614				23001566;11425694		False	1	0;50;50	2.3	False		ENSG00000137285	ENSG00000137285	HGNC:30829