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
CANVAS_ACAGG	str	RFC1	Expert Review Amber;Literature	Repeat Disorders			BIALLELIC, autosomal or pseudoautosomal	Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome;fasciculations;elevated serum creatine kinase levels;denervation				33237689;32694621;33103729		False	2	0;100;0	0.168	True		ENSG00000035928	ENSG00000035928	HGNC:9969	4	39350045	39350103	39348425	39348483	ACAGG	0	400					
CCD	str	RUNX2	Expert Review Amber;Expert list	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cleidocranial dysplasia MIM#119600				9182765;33811808;20560987;26220009;25852448		False	2	0;100;0	0.168	True		ENSG00000124813	ENSG00000124813	HGNC:10472	6	45390488	45390538	45422751	45422801	GCN	18	20					
DMD	str	DMD	Expert Review Amber;Literature	Repeat Disorders			X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Duchenne muscular dystrophy MIM#310200;Becker muscular dystrophy MIM#300376				27417533;36048237		False	2	0;100;0	0.168	True		ENSG00000198947	ENSG00000198947	HGNC:2928	X	31302674	31302722	31284557	31284605	GAA	33	59					
FAME7	str	RAPGEF2	Expert Review Amber;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Epilepsy, familial adult myoclonic, 7 MIM#618075				29507423;30351492;33791773		False	2	0;100;0	0.168	True		ENSG00000109756	ENSG00000109756	HGNC:16854	4	160263679	160263768	159342527	159342616	TTTCA	0	1					
FRA12A	str	DIP2B	Expert Review Amber;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Mental retardation, FRA12A type MIM#136630				17236128		False	2	0;100;0	0.168	True		ENSG00000066084	ENSG00000066084	HGNC:29284	12	50898787	50898807	50505004	50505024	CGG	23	280					
FRA2A	str	AFF3	Expert Review Amber;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental delay				24763282		False	2	0;100;0	0.168	True		ENSG00000144218	ENSG00000144218	HGNC:6473	2	100721262	100721285	100104800	100104823	CGG	20	300					
FRA7A	str	ZNF713	Expert Review Amber;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Autism spectrum disorder				25196122		False	2	0;100;0	0.168	True		ENSG00000178665	ENSG00000178665	HGNC:22043	7	55955295	55955330	55887602	55887637	CGG	22	450					
SCA_THAP11_CAG	str	THAP11	Expert Review Amber;Other	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Spinocerebellar ataxia 51, MIM#	620947"				15368101;24677642;34165550;38113319		False	2	0;100;0	0.168	True		ENSG00000168286	ENSG00000168286	HGNC:23194	16	67876766	67876853	67842863	67842950	CAG	39	47