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
WDR36	gene	WDR36	Expert Review Red;Victorian Clinical Genetics Services	Glaucoma congenital		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Glaucoma 1, open angle, G, MIM# 609887			Glaucoma;HP:0000501	15677485;18172102;20813748		False	1	0;50;50	1.12	False		ENSG00000134987	ENSG00000134987	HGNC:30696													
PITX2 upstream regulatory region	region		Literature;Literature	Glaucoma congenital		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Axenfeld-Rieger syndrome, MONDO:0019187			Glaucoma;HP:0000501	PMID: 20881290, 28911203, 14991915, 9480756		False	1	100;0;0	1.12	False					4			110875898	111624359						70	cnv_loss	PITX2 upstream regulatory region