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
FAME1_TTTGA	str	SAMD12	Expert Review Red;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	familial cortical myoclonic tremor with epilepsy				31483537		False	1	0;0;100	0.168	True		ENSG00000177570	ENSG00000177570	HGNC:31750	8	119379055	119379157	118366816	118366918	TTTGA	0	100					
FAME4	str	YEATS2	Expert Review Red;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Epilepsy, myoclonic, familial adult, 4 MIM#615127				31539032		False	1	0;0;100	0.168	True		ENSG00000163872	ENSG00000163872	HGNC:25489	3	183429976	183430010	183712188	183712222	TTTCA	0	192					
FAME6	str	TNRC6A	Expert Review Red;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Epilepsy, familial adult myoclonic, 6 MIM#618074				29507423		False	1	0;0;100	0.168	True		ENSG00000090905	ENSG00000090905	HGNC:11969	16	24624761	24624850	24613440	24613529	TTTCA	0	1					
FRA11A	str	C11orf80	Expert Review Red;Literature	Repeat Disorders			Unknown	Intellectual disability				18160775;453198		False	1	0;0;100	0.168	True		ENSG00000173715	ENSG00000173715	HGNC:26197	11	66512291	66512316	66744820	66744845	CGG	11	500					
FRA11B	str	CBL	Expert Review Red;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Jacobsen syndrome MIM#147791				7881408;7603564;9508241;9927483;10767345;11076037;19267933		False	1	0;100;0	0.168	True		ENSG00000110395	ENSG00000110395	HGNC:1541	11	119076999	119077032	119206289	119206322	CCG	79	101					
FRAXF	str	TMEM185A	Expert Review Red;Literature	Repeat Disorders			X-LINKED: hemizygous mutation in males, biallelic mutations in females	Intellectual disability				7874164;10094554;8651274		False	1	0;0;100	0.168	True		-	-	HGNC:17125	X	148713390	148713437	149631714	149631781	GCC	29	900					
NIPA1	str	NIPA1	Expert Review Red;Literature	Repeat Disorders			Unknown	Amyotrophic lateral sclerosis				30342764;22378146		False	1	100;0;0	0.168	True		ENSG00000170113	ENSG00000170113	HGNC:17043	15	23086366	23086390	22786677	22786701	GCG	8	9					
OPML1	str	NUTM2B-AS1	Expert Review Red;Literature	Repeat Disorders			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Oculopharyngeal myopathy with leukoencephalopathy 1 MIM#618637				31332380		False	1	0;0;100	0.168	True		ENSG00000225484	ENSG00000225484	HGNC:51204	10	81586142	81586159	79826386	79826403	CCG	16	35					
VACTERLX	str	ZIC3	Expert Review Red;Literature	Repeat Disorders			X-LINKED: hemizygous mutation in males, biallelic mutations in females	VACTERL association, X-linked MIM#314390				20452998;32639022		False	1	0;0;100	0.168	True		ENSG00000156925	ENSG00000156925	HGNC:12874	X	136648986	136649015	137566827	137566856	GCC	10	11