Variant report

Variant	nsv1034853
Chromosome Location	chr5:75382047-75534981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1316)
CpG islands
(count:733)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:75517243-75517452	K562	blood:	n/a	n/a
2	ATF1	chr5:75458345-75458529	K562	blood:	n/a	n/a
3	ATF1	chr5:75515637-75515837	K562	blood:	n/a	n/a
4	ATF1	chr5:75476928-75477230	K562	blood:	n/a	n/a
5	ATF1	chr5:75442283-75442385	K562	blood:	n/a	n/a
6	ATF1	chr5:75471623-75472170	K562	blood:	n/a	n/a
7	ATF2	chr5:75474650-75475133	GM12878	blood:	n/a	n/a
8	ATF2	chr5:75394893-75395805	GM12878	blood:	n/a	n/a
9	ATF2	chr5:75476882-75477667	GM12878	blood:	n/a	n/a
10	ATF2	chr5:75476912-75477609	GM12878	blood:	n/a	n/a
11	ATF2	chr5:75474597-75475178	GM12878	blood:	n/a	n/a
12	ATF2	chr5:75471452-75472442	GM12878	blood:	n/a	n/a
13	ATF2	chr5:75394969-75395455	GM12878	blood:	n/a	n/a
14	ATF2	chr5:75471604-75472348	GM12878	blood:	n/a	n/a
15	ATF2	chr5:75483142-75483633	GM12878	blood:	n/a	n/a
16	ATF3	chr5:75471599-75472016	K562	blood:	n/a	n/a
17	BATF	chr5:75476903-75477253	GM12878	blood:	n/a	n/a
18	BATF	chr5:75395097-75395564	GM12878	blood:	n/a	n/a
19	BATF	chr5:75476907-75477562	GM12878	blood:	n/a	n/a
20	BATF	chr5:75474748-75475148	GM12878	blood:	n/a	n/a
21	BATF	chr5:75471890-75472287	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:75474738-75475112	GM12878	blood:	n/a	n/a
23	BCL11A	chr5:75476940-75477332	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:75440843-75440979	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL3	chr5:75471555-75472304	GM12878	blood:	n/a	n/a
26	BCL3	chr5:75476943-75477631	GM12878	blood:	n/a	n/a
27	BCL3	chr5:75474685-75475133	GM12878	blood:	n/a	n/a
28	BCL3	chr5:75473860-75474199	GM12878	blood:	n/a	n/a
29	BCLAF1	chr5:75476931-75477519	GM12878	blood:	n/a	n/a
30	BCLAF1	chr5:75394943-75395528	GM12878	blood:	n/a	n/a
31	BCLAF1	chr5:75470838-75471335	GM12878	blood:	n/a	n/a
32	BCLAF1	chr5:75471604-75472393	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:75471965-75472226	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:75476870-75477240	K562	blood:	n/a	n/a
35	BHLHE40	chr5:75471619-75472026	K562	blood:	n/a	n/a
36	BHLHE40	chr5:75470933-75471235	GM12878	blood:	n/a	n/a
37	BHLHE40	chr5:75515244-75515285	GM12878	blood:	n/a	n/a
38	BHLHE40	chr5:75441876-75442076	K562	blood:	n/a	n/a
39	CBX3	chr5:75471552-75472056	K562	blood:	n/a	n/a
40	CBX3	chr5:75505170-75505419	K562	blood:	n/a	n/a
41	CBX3	chr5:75476823-75477541	K562	blood:	n/a	n/a
42	CCNT2	chr5:75383757-75383903	K562	blood:	n/a	n/a
43	CCNT2	chr5:75530726-75530914	K562	blood:	n/a	n/a
44	CCNT2	chr5:75476951-75477181	K562	blood:	n/a	n/a
45	CCNT2	chr5:75471729-75471951	K562	blood:	n/a	chr5:75471940-75471949
46	CEBPB	chr5:75452257-75452426	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr5:75392152-75392229	K562	blood:	n/a	n/a
48	CEBPB	chr5:75439724-75440079	A549	lung:	n/a	chr5:75439901-75439912
49	CEBPB	chr5:75387606-75387857	IMR90	lung:	n/a	chr5:75387697-75387708
50	CEBPB	chr5:75439750-75440070	Hela-S3	cervix:	n/a	chr5:75439901-75439912

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75524056-75524106	PrEC	prostate:	n/a
2	chr5:75524056-75524106	PrEC	prostate:	n/a
3	chr5:75410147-75410197	PrEC	prostate:	n/a
4	chr5:75473201-75473251	K562	blood:	n/a
5	chr5:75469904-75469954	ProgFib	skin:	n/a
6	chr5:75472143-75472193	ProgFib	skin:	n/a
7	chr5:75472143-75472193	CMK	blood:	n/a
8	chr5:75469904-75469954	GM12892	blood:	n/a
9	chr5:75465603-75465653	Caco-2	colon:	n/a
10	chr5:75469826-75469876	NT2-D1	testis:	n/a
11	chr5:75465603-75465653	SAEC	small airway:	n/a
12	chr5:75464408-75464458	AG10803	skin:	n/a
13	chr5:75469826-75469876	AG09309	skin:	n/a
14	chr5:75524056-75524106	Caco-2	colon:	n/a
15	chr5:75524056-75524106	AG09309	skin:	n/a
16	chr5:75470039-75470089	HCM	heart:	n/a
17	chr5:75524056-75524106	HNPCEpiC	eye:	n/a
18	chr5:75473201-75473251	PANC-1	pancreas:	n/a
19	chr5:75471166-75471216	HL-60	blood:	n/a
20	chr5:75472143-75472193	GM19239	blood:	n/a
21	chr5:75384322-75384372	RPTEC	kidney:	n/a
22	chr5:75410147-75410197	HepG2	liver:	n/a
23	chr5:75469904-75469954	T-47D	breast:	n/a
24	chr5:75471166-75471216	Hepatocyte	liver:	n/a
25	chr5:75469969-75470019	NHBE	bronchial:	n/a
26	chr5:75473201-75473251	A549	lung:	n/a
27	chr5:75470039-75470089	GM19239	blood:	n/a
28	chr5:75384322-75384372	Hepatocyte	liver:	n/a
29	chr5:75470039-75470089	MCF-7	breast:	n/a
30	chr5:75410147-75410197	U87	brain:	n/a
31	chr5:75471166-75471216	HIPEpiC	eye:	n/a
32	chr5:75465603-75465653	HEEpiC	esophagus:	n/a
33	chr5:75469969-75470019	HIPEpiC	eye:	n/a
34	chr5:75465603-75465653	PANC-1	pancreas:	n/a
35	chr5:75465603-75465653	MCF-7	breast:	n/a
36	chr5:75524056-75524106	ECC-1	luminal epithelium:	n/a
37	chr5:75469826-75469876	AoSMC	blood vessel:	n/a
38	chr5:75469904-75469954	U87	brain:	n/a
39	chr5:75464408-75464458	Hela-S3	cervix:	n/a
40	chr5:75465603-75465653	AG10803	skin:	n/a
41	chr5:75469969-75470019	T-47D	breast:	n/a
42	chr5:75473201-75473251	HUVEC	blood vessel:	n/a
43	chr5:75384322-75384372	AG09309	skin:	n/a
44	chr5:75465603-75465653	AoSMC	blood vessel:	n/a
45	chr5:75465603-75465653	HIPEpiC	eye:	n/a
46	chr5:75469826-75469876	Caco-2	colon:	n/a
47	chr5:75470039-75470089	AoSMC	blood vessel:	n/a
48	chr5:75410147-75410197	HEEpiC	esophagus:	n/a
49	chr5:75524056-75524106	HRCEpiC	kidney:	n/a
50	chr5:75473201-75473251	AG09319	gingival:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75441859..75445534-chr5:75469171..75472141,3	K562	blood:
2	chr5:75369710..75371593-chr5:75472300..75473889,2	K562	blood:
3	chr5:75182130..75182669-chr5:75470688..75471450,3	MCF-7	breast:
4	chr5:75520569..75523367-chr5:75540398..75542001,2	K562	blood:
5	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:
6	chr5:75484578..75486755-chr5:75492728..75495660,2	K562	blood:
7	chr5:75011937..75013471-chr5:75474552..75477211,2	MCF-7	breast:
8	chr5:75380964..75382586-chr5:75384314..75386293,2	K562	blood:
9	chr5:75518200..75520510-chr5:75524409..75526255,2	K562	blood:
10	chr5:75370002..75370997-chr5:75470399..75471572,8	MCF-7	breast:
11	chr4:144295435..144296093-chr5:75459165..75460000,2	MCF-7	breast:
12	chr2:175960283..175962736-chr5:75428852..75431360,2	MCF-7	breast:
13	chr5:75511321..75513183-chr5:75515341..75518158,2	MCF-7	breast:
14	chr2:77243462..77244011-chr5:75510913..75511675,2	MCF-7	breast:
15	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
16	chr5:75378752..75382586-chr5:75384314..75388337,4	K562	blood:
17	chr5:75470625..75471456-chr5:75551799..75552684,5	MCF-7	breast:
18	chr5:75518200..75520510-chr5:75524409..75526255,2	K562	blood:
19	chr5:75534573..75536259-chr5:75552032..75554842,2	K562	blood:
20	chr5:75380964..75382586-chr5:75384314..75386293,2	K562	blood:
21	chr5:75469938..75472744-chr5:75476639..75478302,2	K562	blood:
22	chr5:75378752..75382586-chr5:75384314..75388337,4	K562	blood:
23	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
24	chr5:75484578..75486755-chr5:75492728..75495660,2	K562	blood:
25	chr5:75370258..75370917-chr5:75470691..75471438,2	MCF-7	breast:
26	chr5:75031130..75031721-chr5:75470748..75471418,2	MCF-7	breast:
27	chr5:75511321..75513183-chr5:75515341..75518158,2	MCF-7	breast:
28	chr5:75030911..75031730-chr5:75470555..75471416,3	MCF-7	breast:
29	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254893	TF binding region
RNA5SP186	TF binding region
ENSG00000248127	TF binding region
ENSG00000251668	TF binding region
ENSG00000254893	CpG island
RNA5SP186	CpG island
ENSG00000248127	CpG island
ENSG00000251668	CpG island
ENSG00000122012	chromatin interactions
ENSG00000252833	chromatin interactions
ENSG00000254893	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000249777	chromatin interactions
ENSG00000248127	chromatin interactions

Extended variants
information (count: 3616 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3616 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539216309	chr5:75382093-75382094	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs115196313	chr5:75382097-75382098	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376328081	chr5:75382222-75382223	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs535543530	chr5:75382240-75382241	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7712198	chr5:75382250-75382251	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555374908	chr5:75382264-75382265	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs78355803	chr5:75382267-75382268	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs541347822	chr5:75382269-75382270	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142139919	chr5:75382276-75382277	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs557043828	chr5:75382298-75382299	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs369583446	chr5:75382302-75382303	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373303980	chr5:75382304-75382305	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114668156	chr5:75382306-75382307	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs567628638	chr5:75382342-75382343	Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs112029598	chr5:75382412-75382413	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200663963	chr5:75382461-75382462	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs149294176	chr5:75382462-75382463	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs74950858	chr5:75382464-75382465	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs1160946	chr5:75382465-75382466	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs199563337	chr5:75382466-75382467	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs200704223	chr5:75382467-75382468	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs55692449	chr5:75382472-75382473	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs371650918	chr5:75382473-75382474	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs115793764	chr5:75382475-75382476	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs374986123	chr5:75382627-75382628	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs151167316	chr5:75382628-75382629	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs59554385	chr5:75383416-75383417	Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs574266246	chr5:75383502-75383503	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs541958564	chr5:75383527-75383528	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs573245540	chr5:75383544-75383545	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs527283196	chr5:75383549-75383550	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs190738966	chr5:75383820-75383821	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs550027452	chr5:75383854-75383855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs183101560	chr5:75383860-75383861	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs370786400	chr5:75384322-75384323	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs563952544	chr5:75384329-75384330	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs192558100	chr5:75384330-75384331	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs374496264	chr5:75384349-75384350	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs182110386	chr5:75384350-75384351	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs373212254	chr5:75384412-75384413	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs563202474	chr5:75384424-75384425	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529058466	chr5:75384427-75384428	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs74970894	chr5:75384434-75384435	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs30202	chr5:75384442-75384443	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs528600097	chr5:75384459-75384460	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs79780581	chr5:75384463-75384464	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs141146945	chr5:75384511-75384512	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs571577247	chr5:75384575-75384576	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs188060152	chr5:75384581-75384582	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs78610057	chr5:75384614-75384615	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75382200-75382400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
2	chr5:75383400-75383600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
3	chr5:75386000-75386200	Bivalent Enhancer	Esophagus	oesophagus
4	chr5:75393800-75395200	Enhancers	GM12878-XiMat	blood
5	chr5:75395000-75395600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr5:75395000-75395800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr5:75395000-75396400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr5:75395200-75395600	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr5:75395200-75395800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr5:75395200-75395800	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr5:75395200-75395800	Flanking Active TSS	GM12878-XiMat	blood
12	chr5:75395200-75396000	Enhancers	Primary T cells from cord blood	blood
13	chr5:75395200-75396000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr5:75395400-75395800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr5:75395400-75396000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr5:75395400-75396000	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr5:75395800-75396400	Enhancers	GM12878-XiMat	blood
18	chr5:75400000-75401800	Enhancers	Stomach Mucosa	stomach
19	chr5:75400200-75401200	Enhancers	Duodenum Mucosa	Duodenum
20	chr5:75401800-75402200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr5:75401800-75406600	Weak transcription	Stomach Mucosa	stomach
22	chr5:75406600-75409400	Enhancers	Stomach Mucosa	stomach
23	chr5:75407200-75407800	Enhancers	HUVEC	blood vessel
24	chr5:75407400-75407600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:75407600-75407800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:75407600-75407800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr5:75407800-75409800	Weak transcription	HUVEC	blood vessel
28	chr5:75408200-75408400	Enhancers	Left Ventricle	heart
29	chr5:75408200-75408400	Enhancers	Lung	lung
30	chr5:75408200-75408400	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr5:75408200-75409800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr5:75408200-75410600	Enhancers	Gastric	stomach
33	chr5:75408400-75409400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr5:75408400-75409800	Weak transcription	Lung	lung
35	chr5:75408600-75409800	Weak transcription	Left Ventricle	heart
36	chr5:75409200-75409800	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr5:75409400-75409800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr5:75409400-75410000	Flanking Active TSS	Stomach Mucosa	stomach
39	chr5:75409400-75411400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr5:75409400-75412200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:75409600-75410200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:75409600-75410400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:75409600-75410600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:75409600-75410600	Enhancers	Duodenum Mucosa	Duodenum
45	chr5:75409800-75410000	Enhancers	Brain Anterior Caudate	brain
46	chr5:75409800-75410000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
47	chr5:75409800-75410000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
48	chr5:75409800-75410000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
49	chr5:75409800-75410200	Enhancers	Adipose Nuclei	Adipose
50	chr5:75409800-75410200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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