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
ANK2	gene	ANK2	Expert list;Expert Review Red;South West GLH	Catecholaminergic polymorphic VT		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	catecholaminergic polymorphic ventricular tachycardia, MONDO:0017990						False	1	0;50;50	5.3	False		ENSG00000145362	ENSG00000145362	HGNC:493													
KCNE1	gene	KCNE1	Literature;South West GLH	Catecholaminergic polymorphic VT		Cardiology	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	catecholaminergic polymorphic ventricular tachycardia, MONDO:0017990				16818210; doi:10. 1007/ s12265-016-9673-5		False	1	0;0;100	5.3	False		ENSG00000180509	ENSG00000180509	HGNC:6240													
KCNJ2	gene	KCNJ2	Expert list;North West GLH;South West GLH;UKGTN	Catecholaminergic polymorphic VT		Cardiology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	catecholaminergic polymorphic ventricular tachycardia, MONDO:0017990				27761157		False	1	0;0;100	5.3	False		ENSG00000123700	ENSG00000123700	HGNC:6263