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
COCH	gene	COCH	Emory Genetics Laboratory;Expert Review Green;Literature;Other;Radboud University Medical Center, Nijmegen;UKGTN	Familial Meniere Disease	Other hearing and ear disorders	Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Deafness, autosomal dominant 9, 601369;cochlear-vestibular dysfunction				28787010;9806553;10400989;14512963;14704763;26758463		False	3	100;0;0	1.4	False	Other - please provide details in the comments	ENSG00000100473	ENSG00000100473	HGNC:2180