Variant report

Variant	esv3412984
Chromosome Location	chr5:8799001-8836347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:122)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:122 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:8829150-8830091	IMR90	lung:	n/a	n/a
2	CEBPB	chr5:8829356-8829645	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr5:8829354-8829743	A549	lung:	n/a	n/a
4	CEBPB	chr5:8829325-8829661	A549	lung:	n/a	n/a
5	CEBPB	chr5:8829277-8829744	MCF-7	breast:	n/a	n/a
6	CEBPB	chr5:8829269-8829715	MCF-7	breast:	n/a	n/a
7	CEBPB	chr5:8829251-8829779	A549	lung:	n/a	n/a
8	CTCF	chr5:8829680-8829830	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr5:8829560-8829710	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr5:8829723-8829763	ProgFib	skin:	n/a	n/a
11	CTCF	chr5:8829060-8829210	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr5:8829540-8829690	AG09319	gingival:	n/a	n/a
13	CTCF	chr5:8828400-8828550	GM12867	blood:	n/a	n/a
14	E2F4	chr5:8833069-8833204	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr5:8829337-8829737	MCF10A-Er-Src	breast:	n/a	n/a
16	EP300	chr5:8829211-8830116	SK-N-SH	brain:	n/a	n/a
17	EP300	chr5:8829126-8830190	SK-N-SH	brain:	n/a	n/a
18	EP300	chr5:8829296-8830074	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr5:8829352-8829832	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr5:8829238-8829935	SK-N-SH	brain:	n/a	n/a
21	FOS	chr5:8829324-8830014	MCF10A-Er-Src	breast:	n/a	chr5:8829513-8829524
22	FOS	chr5:8829312-8829900	MCF10A-Er-Src	breast:	n/a	chr5:8829513-8829524
23	FOS	chr5:8825434-8825534	MCF10A-Er-Src	breast:	n/a	chr5:8825450-8825459 chr5:8825437-8825447 chr5:8825453-8825461 chr5:8825437-8825447 chr5:8825437-8825447 chr5:8825450-8825457
24	FOS	chr5:8825436-8825518	MCF10A-Er-Src	breast:	n/a	chr5:8825450-8825459 chr5:8825437-8825447 chr5:8825453-8825461 chr5:8825437-8825447 chr5:8825437-8825447 chr5:8825450-8825457
25	FOS	chr5:8829241-8830471	HUVEC	blood vessel:	n/a	chr5:8829513-8829524
26	FOS	chr5:8829335-8829825	MCF10A-Er-Src	breast:	n/a	chr5:8829513-8829524
27	FOS	chr5:8832894-8832952	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr5:8831662-8831691	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr5:8828732-8828926	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr5:8829332-8830423	MCF10A-Er-Src	breast:	n/a	chr5:8829513-8829524
31	FOSL2	chr5:8829390-8829696	A549	lung:	n/a	n/a
32	FOSL2	chr5:8829197-8830168	SK-N-SH	brain:	n/a	n/a
33	FOSL2	chr5:8829268-8829914	SK-N-SH	brain:	n/a	n/a
34	FOSL2	chr5:8829322-8829848	A549	lung:	n/a	n/a
35	FOSL2	chr5:8829270-8829801	MCF-7	breast:	n/a	n/a
36	FOSL2	chr5:8807708-8808183	SK-N-SH	brain:	n/a	n/a
37	GATA2	chr5:8829084-8829977	HUVEC	blood vessel:	n/a	n/a
38	GATA3	chr5:8829250-8829713	MCF-7	breast:	n/a	n/a
39	GATA3	chr5:8829268-8829864	MCF-7	breast:	n/a	n/a
40	GATA3	chr5:8829231-8830287	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr5:8829119-8830269	SK-N-SH	brain:	n/a	n/a
42	JUND	chr5:8829261-8830043	SK-N-SH	brain:	n/a	n/a
43	JUND	chr5:8829176-8830031	SK-N-SH	brain:	n/a	n/a
44	JUND	chr5:8807820-8808145	SK-N-SH	brain:	n/a	n/a
45	JUND	chr5:8828838-8830163	SK-N-SH	brain:	n/a	n/a
46	JUND	chr5:8829256-8829799	MCF-7	breast:	n/a	n/a
47	MAFK	chr5:8801943-8801959	HepG2	liver:	n/a	n/a
48	MAFK	chr5:8829244-8830027	IMR90	lung:	n/a	n/a
49	MAFK	chr5:8824447-8824631	HepG2	liver:	n/a	chr5:8824610-8824624 chr5:8824611-8824622 chr5:8824611-8824622 chr5:8824447-8824458 chr5:8824612-8824623 chr5:8824612-8824623 chr5:8824611-8824627
50	MAX	chr5:8829258-8829853	SK-N-SH	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:8827420-8827470	Jurkat	blood:	n/a
2	chr5:8827420-8827470	AG04449	skin:	fetal
3	chr5:8827420-8827470	HNPCEpiC	eye:	n/a
4	chr5:8827420-8827470	HL-60	blood:	n/a
5	chr5:8827420-8827470	SKMC	muscle:	n/a
6	chr5:8827420-8827470	A549	lung:	n/a
7	chr5:8827420-8827470	HEEpiC	esophagus:	n/a
8	chr5:8827420-8827470	PFSK-1	brain:	n/a
9	chr5:8827420-8827470	BJ	skin:	n/a
10	chr5:8827420-8827470	T-47D	breast:	n/a
11	chr5:8827420-8827470	Hepatocyte	liver:	n/a
12	chr5:8827420-8827470	RPTEC	kidney:	n/a
13	chr5:8827420-8827470	AoSMC	blood vessel:	n/a
14	chr5:8827420-8827470	GM12878	blood:	n/a
15	chr5:8827420-8827470	SK-N-MC	brain:	n/a
16	chr5:8827420-8827470	HCF	heart:	n/a
17	chr5:8827420-8827470	GM12891	blood:	n/a
18	chr5:8827420-8827470	AG09319	gingival:	n/a
19	chr5:8827420-8827470	HMEC	breast:	n/a
20	chr5:8827420-8827470	GM12892	blood:	n/a
21	chr5:8827420-8827470	HAEpiC	amniotic membrane:	n/a
22	chr5:8827420-8827470	Hela-S3	cervix:	n/a
23	chr5:8827420-8827470	NT2-D1	testis:	n/a
24	chr5:8827420-8827470	U87	brain:	n/a
25	chr5:8827420-8827470	PANC-1	pancreas:	n/a
26	chr5:8827420-8827470	GM06990	blood:	n/a
27	chr5:8827420-8827470	HRCEpiC	kidney:	n/a
28	chr5:8827420-8827470	CMK	blood:	n/a
29	chr5:8827420-8827470	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:8827420-8827470	MCF10A-Er-Src	breast:	n/a
31	chr5:8827420-8827470	ovcar-3	ovarian:	n/a
32	chr5:8827420-8827470	AG04450	lung:	fetal
33	chr5:8827420-8827470	K562	blood:	n/a
34	chr5:8827420-8827470	HCT-116	colon:	n/a
35	chr5:8827420-8827470	NH-A	brain:	n/a
36	chr5:8827420-8827470	NB4	blood:	n/a
37	chr5:8827420-8827470	Caco-2	colon:	n/a
38	chr5:8827420-8827470	HIPEpiC	eye:	n/a
39	chr5:8827420-8827470	NHBE	bronchial:	n/a
40	chr5:8827420-8827470	ProgFib	skin:	n/a
41	chr5:8827420-8827470	HepG2	liver:	n/a
42	chr5:8827420-8827470	GM19239	blood:	n/a
43	chr5:8827420-8827470	LNCaP	prostate:	n/a
44	chr5:8827420-8827470	AG10803	skin:	n/a
45	chr5:8827420-8827470	HCPEpiC	choroid plexus:	n/a
46	chr5:8827420-8827470	AG09309	skin:	n/a
47	chr5:8827420-8827470	HUVEC	blood vessel:	n/a
48	chr5:8827420-8827470	BE2_C	brain:	n/a
49	chr5:8827420-8827470	H1-hESC	embryonic stem cell:	embryo
50	chr5:8827420-8827470	HEK293	kidney:	embryo

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:8835943..8838709-chr5:8839327..8841124,2	K562	blood:
2	chr5:8813846..8815581-chr6:26020851..26022665,2	MCF-7	breast:
3	chr5:8814813..8817316-chr5:8819047..8821909,2	K562	blood:
4	chr5:8827451..8829541-chr5:8836393..8838184,2	K562	blood:
5	chr5:8814813..8817316-chr5:8819047..8821909,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA5A-1	chr5:8835495-8835535	XLOC_004729

No data

Variant related genes	Relation type
ENSG00000250198	TF binding region
ENSG00000250198	CpG island
ENSG00000250198	chromatin interactions
ENSG00000196176	chromatin interactions
FOXO1	miRNA target sites

Extended variants
information (count: 1283 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57169216	chr5:8800412-8800413	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565378497	chr5:8800448-8800449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534327166	chr5:8800510-8800511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554520851	chr5:8800519-8800520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73035694	chr5:8800546-8800547	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs543220932	chr5:8800570-8800571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184235333	chr5:8800603-8800604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370602098	chr5:8800629-8800630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576454146	chr5:8800670-8800671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs199756156	chr5:8800671-8800672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200054061	chr5:8800674-8800675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78654001	chr5:8800685-8800686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370641223	chr5:8800687-8800688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565385655	chr5:8800698-8800699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527635921	chr5:8800713-8800714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3094308	chr5:8800724-8800725	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs561388552	chr5:8800768-8800769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141744734	chr5:8800770-8800771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550083347	chr5:8800825-8800826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76340898	chr5:8800836-8800837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150552105	chr5:8800859-8800860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371024068	chr5:8800905-8800906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551815141	chr5:8800998-8800999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140079727	chr5:8801025-8801026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79489509	chr5:8801030-8801031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548186011	chr5:8801031-8801032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs386685297	chr5:8801062-8801063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78633407	chr5:8801063-8801064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528184014	chr5:8801117-8801118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371050641	chr5:8801129-8801130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376047130	chr5:8801161-8801162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78894336	chr5:8801180-8801181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567717431	chr5:8801181-8801182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142039177	chr5:8801186-8801187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375004569	chr5:8801231-8801232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527479651	chr5:8801245-8801246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572588144	chr5:8801271-8801272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs3094307	chr5:8801377-8801378	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs371156274	chr5:8801414-8801415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146315002	chr5:8801434-8801435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139500159	chr5:8801467-8801468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544136981	chr5:8801483-8801484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11134330	chr5:8801537-8801538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145926300	chr5:8801538-8801539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11742945	chr5:8801543-8801544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374197289	chr5:8801547-8801548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200738652	chr5:8801548-8801549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377304722	chr5:8801549-8801550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs151055919	chr5:8801582-8801583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368541406	chr5:8801588-8801589	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:8800400-8801600	Enhancers	Dnd41	blood
2	chr5:8805800-8806200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:8805800-8825200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr5:8806000-8806400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr5:8811400-8812200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:8812200-8813200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:8812600-8813200	Enhancers	Dnd41	blood
8	chr5:8813200-8813600	Flanking Active TSS	Dnd41	blood
9	chr5:8813200-8814600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr5:8813200-8814800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:8813400-8813600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:8813600-8814400	Enhancers	Dnd41	blood
13	chr5:8813600-8825400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:8813800-8814000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:8814000-8814600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr5:8814000-8814600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr5:8814000-8814800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:8814200-8814600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:8814200-8815000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr5:8814600-8814800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:8815800-8816200	ZNF genes & repeats	Pancreas	Pancrea
22	chr5:8825000-8825200	Enhancers	Placenta Amnion	Placenta Amnion
23	chr5:8825000-8828000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:8825000-8830000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:8825000-8830600	Enhancers	NHEK	skin
26	chr5:8825200-8825400	Enhancers	Brain Substantia Nigra	brain
27	chr5:8825200-8825800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:8825200-8825800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:8825200-8825800	Enhancers	NH-A	brain
30	chr5:8825200-8826000	Enhancers	Brain Angular Gyrus	brain
31	chr5:8825200-8826200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr5:8825200-8826200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr5:8825200-8826200	Enhancers	HSMM	muscle
34	chr5:8825200-8826400	Enhancers	NHDF-Ad	bronchial
35	chr5:8825200-8826600	Enhancers	NHLF	lung
36	chr5:8825200-8827400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr5:8825200-8827400	Enhancers	Osteobl	bone
38	chr5:8825200-8827800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr5:8825200-8829000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:8825200-8830000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:8825200-8830200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr5:8825200-8830200	Enhancers	HMEC	breast
43	chr5:8825400-8826600	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr5:8825400-8827400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:8825400-8830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:8825400-8831000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:8825600-8825800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr5:8825600-8825800	Enhancers	Small Intestine	intestine
49	chr5:8825600-8826400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr5:8825600-8826600	Weak transcription	Brain Substantia Nigra	brain

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