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
CBFB	gene	CBFB	Expert Review Green;Literature;NHS GMS	Cleidocranial Dysplasia		Musculoskeletal	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cleidocranial dysplasia 2, OMIM:620099;cleidocranial dysplasia 2, MONDO:0859307				36241386		False	3	100;0;0	2.3	False		ENSG00000067955	ENSG00000067955	HGNC:1539													
RUNX2	gene	RUNX2	Expert Review Green;NHS GMS	Cleidocranial Dysplasia		Musculoskeletal	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cleidocranial dysplasia, OMIM:119600;cleidocranial dysplasia 1, MONDO:0007340						False	3	100;0;0	2.3	False		ENSG00000124813	ENSG00000124813	HGNC:10472