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
CDKN1C	gene	CDKN1C	Expert Review Green	Wilms tumour with features suggestive of predisposition		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)	Beckwith-Wiedemann syndrome, OMIM:130650				10424812		False	3	0;0;0	1.5	False		ENSG00000129757	ENSG00000129757	HGNC:1786													
CTR9	gene	CTR9	Expert Review Green	Wilms tumour with features suggestive of predisposition		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Familial Wilms tumor				25099282;29292210		False	3	0;0;0	1.5	False		ENSG00000198730	ENSG00000198730	HGNC:16850													
REST	gene	REST	Expert Review Green	Wilms tumour with features suggestive of predisposition		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Wilms tumor 6, susceptibility to}, OMIM:616806				26551668		False	3	0;0;0	1.5	False		ENSG00000084093	ENSG00000084093	HGNC:9966													
TRIM28	gene	TRIM28	Expert Review Green	Wilms tumour with features suggestive of predisposition		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Wilms tumor 7, OMIM:621332				30885698;29912901;30694527		False	3	0;0;0	1.5	False		ENSG00000130726	ENSG00000130726	HGNC:16384													
WT1	gene	WT1	Expert Review Green	Wilms tumour with features suggestive of predisposition		Inherited cancer	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Wilms tumor, type 1, OMIM:194070				15483024		False	3	0;0;0	1.5	False		ENSG00000184937	ENSG00000184937	HGNC:12796