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
EGLN2	gene	EGLN2	Expert Review Red;Literature	Hereditary Erythrocytosis		Haematology	Unknown	Familial erythrocytosis				22274579		False	1	0;0;0	2.17	False		ENSG00000269858	ENSG00000269858	HGNC:14660													
EGLN3	gene	EGLN3	Expert Review Red;Literature	Hereditary Erythrocytosis		Haematology	Unknown	Familial erythrocytosis				22274579		False	1	0;0;0	2.17	False		ENSG00000129521	ENSG00000129521	HGNC:14661													
HIF1A	gene	HIF1A	Literature	Hereditary Erythrocytosis		Haematology	Unknown	Familial erythrocytosis				22274579		False	1	0;0;0	2.17	False		ENSG00000100644	ENSG00000100644	HGNC:4910													
PKLR	gene	PKLR	Literature	Hereditary Erythrocytosis		Haematology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Adenosine triphosphate, elevated, of erythrocytes, OMIM:102900				22274579;9090535;4160306;14300761;7426754		False	1	0;0;0	2.17	False		ENSG00000143627	ENSG00000143627	HGNC:9020