Variant report

Variant	nsv880591
Chromosome Location	chr5:35859863-35870588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCLAF1	chr5:35863329-35863608	GM12878	blood:	n/a	n/a
2	CEBPB	chr5:35861728-35862124	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr5:35870200-35870350	GM12873	blood:	n/a	n/a
4	CTCF	chr5:35862080-35862230	AG04450	lung:	n/a	n/a
5	CUX1	chr5:35863196-35863432	GM12878	blood:	n/a	chr5:35863333-35863349 chr5:35863318-35863327
6	EBF1	chr5:35862270-35862529	GM12878	blood:	n/a	n/a
7	EBF1	chr5:35863323-35863629	GM12878	blood:	n/a	n/a
8	EBF1	chr5:35863451-35863485	GM12878	blood:	n/a	n/a
9	EP300	chr5:35862443-35862509	GM12878	blood:	n/a	n/a
10	EP300	chr5:35864109-35864272	GM12878	blood:	n/a	n/a
11	EP300	chr5:35863294-35863638	GM12878	blood:	n/a	n/a
12	FOS	chr5:35861820-35862275	Hela-S3	cervix:	n/a	n/a
13	GATA3	chr5:35861750-35862077	MCF-7	breast:	n/a	chr5:35861801-35861811
14	GTF2F1	chr5:35861264-35861308	H1-hESC	embryonic stem cell:	n/a	n/a
15	IKZF1	chr5:35869869-35870028	GM12878	blood:	n/a	n/a
16	MAX	chr5:35863332-35863711	NB4	blood:	n/a	chr5:35863557-35863567
17	MAX	chr5:35861744-35862385	Hela-S3	cervix:	n/a	n/a
18	MAX	chr5:35869891-35870211	GM12878	blood:	n/a	n/a
19	MAX	chr5:35863301-35863792	MCF-7	breast:	n/a	chr5:35863557-35863567
20	MAX	chr5:35863352-35863681	GM12878	blood:	n/a	chr5:35863557-35863567
21	MYC	chr5:35868979-35869083	MCF-7	breast:	n/a	n/a
22	NR2F2	chr5:35863272-35863764	MCF-7	breast:	n/a	n/a
23	PAX5	chr5:35869971-35870315	GM12878	blood:	n/a	chr5:35870188-35870206
24	PAX5	chr5:35870056-35870311	GM12878	blood:	n/a	chr5:35870188-35870206
25	POLR2A	chr5:35869009-35869016	A549	lung:	n/a	n/a
26	POLR2A	chr5:35869030-35869128	A549	lung:	n/a	n/a
27	POLR2A	chr5:35860880-35861046	ProgFib	skin:	n/a	n/a
28	POLR2A	chr5:35866320-35866652	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr5:35868968-35869003	A549	lung:	n/a	n/a
30	POLR2A	chr5:35862069-35862242	ProgFib	skin:	n/a	n/a
31	POLR2A	chr5:35869145-35869154	A549	lung:	n/a	n/a
32	POLR2A	chr5:35860571-35860771	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr5:35868945-35869177	ProgFib	skin:	n/a	n/a
34	POLR2A	chr5:35859922-35860034	ProgFib	skin:	n/a	n/a
35	POLR2A	chr5:35863620-35863624	MCF10A-Er-Src	breast:	n/a	n/a
36	RAD21	chr5:35861840-35862229	Hela-S3	cervix:	n/a	n/a
37	RCOR1	chr5:35861758-35862373	Hela-S3	cervix:	n/a	n/a
38	REST	chr5:35861846-35862234	PFSK-1	brain:	n/a	n/a
39	RFX5	chr5:35861829-35862375	Hela-S3	cervix:	n/a	n/a
40	RUNX3	chr5:35863223-35863629	GM12878	blood:	n/a	n/a
41	RUNX3	chr5:35862305-35862628	GM12878	blood:	n/a	n/a
42	SPI1	chr5:35863341-35863713	HL-60	blood:	n/a	chr5:35863506-35863519
43	SPI1	chr5:35863374-35863686	GM12891	blood:	n/a	chr5:35863506-35863519
44	SPI1	chr5:35863346-35863628	GM12878	blood:	n/a	chr5:35863506-35863519
45	SPI1	chr5:35863360-35863694	HL-60	blood:	n/a	chr5:35863506-35863519
46	SPI1	chr5:35863247-35863737	GM12891	blood:	n/a	chr5:35863506-35863519
47	STAT3	chr5:35869993-35870156	GM12878	blood:	n/a	n/a
48	WRNIP1	chr5:35863475-35863535	GM12878	blood:	n/a	n/a
49	ZNF384	chr5:35869861-35870073	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:35860337-35860387	SAEC	small airway:	n/a
2	chr5:35860337-35860387	SK-N-MC	brain:	n/a
3	chr5:35860337-35860387	HCM	heart:	n/a
4	chr5:35860337-35860387	HEEpiC	esophagus:	n/a
5	chr5:35860337-35860387	Jurkat	blood:	n/a
6	chr5:35860337-35860387	K562	blood:	n/a
7	chr5:35860337-35860387	NT2-D1	testis:	n/a
8	chr5:35860337-35860387	Hela-S3	cervix:	n/a
9	chr5:35860337-35860387	AG04449	skin:	fetal
10	chr5:35860337-35860387	MCF-7	breast:	n/a
11	chr5:35860337-35860387	IMR90	lung:	fetal
12	chr5:35860337-35860387	SK-N-SH	brain:	n/a
13	chr5:35860337-35860387	A549	lung:	n/a
14	chr5:35860337-35860387	HRPEpiC	eye:	n/a
15	chr5:35860337-35860387	GM12892	blood:	n/a
16	chr5:35860337-35860387	HepG2	liver:	n/a
17	chr5:35860337-35860387	SK-N-SH_RA	brain:	n/a
18	chr5:35860337-35860387	NHBE	bronchial:	n/a
19	chr5:35860337-35860387	GM06990	blood:	n/a
20	chr5:35860337-35860387	AG10803	skin:	n/a
21	chr5:35860337-35860387	AG04450	lung:	fetal
22	chr5:35860337-35860387	U87	brain:	n/a
23	chr5:35860337-35860387	HRCEpiC	kidney:	n/a
24	chr5:35860337-35860387	H1-hESC	embryonic stem cell:	embryo
25	chr5:35860337-35860387	HNPCEpiC	eye:	n/a
26	chr5:35860337-35860387	CMK	blood:	n/a
27	chr5:35860337-35860387	NB4	blood:	n/a
28	chr5:35860337-35860387	AG09309	skin:	n/a
29	chr5:35860337-35860387	PrEC	prostate:	n/a
30	chr5:35860337-35860387	GM12878	blood:	n/a
31	chr5:35860337-35860387	ECC-1	luminal epithelium:	n/a
32	chr5:35860337-35860387	PFSK-1	brain:	n/a
33	chr5:35860337-35860387	HUVEC	blood vessel:	n/a
34	chr5:35860337-35860387	BE2_C	brain:	n/a
35	chr5:35860337-35860387	ovcar-3	ovarian:	n/a
36	chr5:35860337-35860387	T-47D	breast:	n/a
37	chr5:35860337-35860387	HEK293	kidney:	embryo
38	chr5:35860337-35860387	GM19239	blood:	n/a
39	chr5:35860337-35860387	HCF	heart:	n/a
40	chr5:35860337-35860387	GM12891	blood:	n/a
41	chr5:35860337-35860387	HRE	kidney:	n/a
42	chr5:35860337-35860387	AG09319	gingival:	n/a
43	chr5:35860337-35860387	MCF10A-Er-Src	breast:	n/a
44	chr5:35860337-35860387	NH-A	brain:	n/a
45	chr5:35860337-35860387	SKMC	muscle:	n/a
46	chr5:35860337-35860387	AoSMC	blood vessel:	n/a
47	chr5:35860337-35860387	BJ	skin:	n/a
48	chr5:35860337-35860387	HL-60	blood:	n/a
49	chr5:35860337-35860387	RPTEC	kidney:	n/a
50	chr5:35860337-35860387	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:35859166..35861325-chr5:35861673..35863431,2	MCF-7	breast:
2	chr5:35859166..35861325-chr5:35861673..35863431,2	MCF-7	breast:

No data

Variant related genes	Relation type
IL7R	TF binding region
IL7R	CpG island

Extended variants
information (count: 483 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11567701	chr5:35859863-35859864	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368702441	chr5:35859866-35859867	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs567368322	chr5:35859884-35859885	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs11567702	chr5:35859925-35859926	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs561552680	chr5:35859959-35859960	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs569806668	chr5:35859991-35859992	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs190381870	chr5:35860018-35860019	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs538636947	chr5:35860019-35860020	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs113028866	chr5:35860059-35860060	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs397843901	chr5:35860060-35860061	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs558616028	chr5:35860062-35860063	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs571957176	chr5:35860090-35860091	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs73750046	chr5:35860112-35860113	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs149588572	chr5:35860124-35860125	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs11567703	chr5:35860165-35860166	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs34227144	chr5:35860169-35860170	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs536712070	chr5:35860231-35860232	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75007333	chr5:35860239-35860240	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576155839	chr5:35860271-35860272	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544984008	chr5:35860283-35860284	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564950632	chr5:35860300-35860301	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572273454	chr5:35860319-35860320	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534093263	chr5:35860320-35860321	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540970585	chr5:35860335-35860336	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561097120	chr5:35860433-35860434	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374809718	chr5:35860435-35860436	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs80229624	chr5:35860457-35860458	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144308222	chr5:35860505-35860506	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532281338	chr5:35860523-35860524	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552168626	chr5:35860591-35860592	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1494560	chr5:35860637-35860638	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs534460984	chr5:35860658-35860659	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547786840	chr5:35860660-35860661	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376261483	chr5:35860666-35860667	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374957619	chr5:35860690-35860691	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558713317	chr5:35860710-35860711	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1494559	chr5:35860767-35860768	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs536422147	chr5:35860803-35860804	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs564259607	chr5:35860868-35860869	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148287783	chr5:35860873-35860874	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs201337361	chr5:35860909-35860910	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs199627319	chr5:35860932-35860933	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs193922646	chr5:35860936-35860937	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs200803157	chr5:35860953-35860954	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs370292681	chr5:35860958-35860959	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs140673282	chr5:35860968-35860969	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs35967524	chr5:35860975-35860976	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs373694709	chr5:35860999-35861000	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs11567704	chr5:35861003-35861004	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs200464578	chr5:35861006-35861007	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	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
Medulloblastoma	21979893	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
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Thoracic aortic aneurysm	21092924	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
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35852400-35862800	Enhancers	Hela-S3	cervix
2	chr5:35855400-35862400	Enhancers	HSMMtube	muscle
3	chr5:35856600-35860400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:35857000-35860600	Active TSS	Duodenum Mucosa	Duodenum
5	chr5:35857000-35860800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr5:35857000-35861000	Active TSS	Thymus	Thymus
7	chr5:35857000-35861200	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr5:35857000-35861400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr5:35857000-35861800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr5:35857200-35860000	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
11	chr5:35857400-35869200	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
12	chr5:35857600-35860800	Active TSS	Primary B cells from cord blood	blood
13	chr5:35857800-35866600	Transcr. at gene 5' and 3'	Dnd41	blood
14	chr5:35858000-35860000	Enhancers	HMEC	breast
15	chr5:35858000-35860000	Enhancers	NHEK	skin
16	chr5:35858000-35860200	Enhancers	NH-A	brain
17	chr5:35858000-35862600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:35858000-35862600	Enhancers	NHDF-Ad	bronchial
19	chr5:35858200-35861600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr5:35858200-35863200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:35858200-35864800	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
22	chr5:35858800-35860000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:35858800-35860200	Transcr. at gene 5' and 3'	Primary T killer memory cells from peripheral blood	blood
24	chr5:35858800-35860400	Active TSS	Small Intestine	intestine
25	chr5:35858800-35862600	Active TSS	Sigmoid Colon	Sigmoid Colon
26	chr5:35858800-35864800	Transcr. at gene 5' and 3'	Primary T helper memory cells from peripheral blood 2	blood
27	chr5:35858800-35865000	Transcr. at gene 5' and 3'	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr5:35858800-35865400	Transcr. at gene 5' and 3'	Primary T helper memory cells from peripheral blood 1	blood
29	chr5:35858800-35866600	Transcr. at gene 5' and 3'	Primary T cells fromperipheralblood	blood
30	chr5:35859000-35860000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:35859000-35860000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr5:35859000-35860000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:35859000-35860000	Transcr. at gene 5' and 3'	Primary T killer naive cells fromperipheralblood	blood
34	chr5:35859000-35860000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr5:35859000-35860000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr5:35859000-35860200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr5:35859000-35860200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:35859000-35860400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:35859000-35860400	Active TSS	Rectal Smooth Muscle	rectum
40	chr5:35859000-35860600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:35859000-35861200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr5:35859000-35862200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:35859000-35862600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr5:35859000-35864800	Transcr. at gene 5' and 3'	Primary T cells from cord blood	blood
45	chr5:35859000-35864800	Transcr. at gene 5' and 3'	Primary T helper naive cells from peripheral blood	blood
46	chr5:35859000-35865000	Transcr. at gene 5' and 3'	Primary T helper cells fromperipheralblood	blood
47	chr5:35859200-35860000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:35859200-35860000	Active TSS	Rectal Mucosa Donor 31	rectum
49	chr5:35859200-35861400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr5:35859400-35860000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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