Variant report

Variant	esv2755585
Chromosome Location	chr5:61535831-61618595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1702)
CpG islands
(count:733)
Chromatin interactive
region (count:101)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1702 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:61606306-61606906	K562	blood:	n/a	chr5:61606316-61606332 chr5:61606317-61606333
2	ARID3A	chr5:61557348-61557786	K562	blood:	n/a	n/a
3	ARID3A	chr5:61601596-61602035	K562	blood:	n/a	n/a
4	ARID3A	chr5:61616421-61616482	K562	blood:	n/a	n/a
5	ARID3A	chr5:61618221-61618789	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:61572650-61573748	K562	blood:	n/a	n/a
7	ARID3A	chr5:61602387-61602432	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:61581142-61581749	K562	blood:	n/a	n/a
9	ARID3A	chr5:61604107-61605112	K562	blood:	n/a	n/a
10	ATF1	chr5:61548385-61548659	K562	blood:	n/a	n/a
11	ATF1	chr5:61572822-61573294	K562	blood:	n/a	n/a
12	ATF1	chr5:61602787-61603228	K562	blood:	n/a	n/a
13	ATF1	chr5:61611644-61612194	K562	blood:	n/a	n/a
14	ATF1	chr5:61615299-61615590	K562	blood:	n/a	n/a
15	ATF1	chr5:61601469-61601973	K562	blood:	n/a	n/a
16	ATF1	chr5:61557325-61557825	K562	blood:	n/a	n/a
17	ATF2	chr5:61602618-61603330	GM12878	blood:	n/a	n/a
18	ATF2	chr5:61552295-61552870	GM12878	blood:	n/a	n/a
19	ATF2	chr5:61581060-61581772	GM12878	blood:	n/a	n/a
20	ATF2	chr5:61602882-61603260	GM12878	blood:	n/a	n/a
21	ATF2	chr5:61601440-61601953	GM12878	blood:	n/a	n/a
22	ATF2	chr5:61581126-61581699	GM12878	blood:	n/a	n/a
23	ATF2	chr5:61585539-61586054	GM12878	blood:	n/a	n/a
24	ATF2	chr5:61601195-61601869	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr5:61552189-61552651	GM12878	blood:	n/a	n/a
26	ATF2	chr5:61572719-61573247	GM12878	blood:	n/a	n/a
27	ATF2	chr5:61601492-61602007	GM12878	blood:	n/a	n/a
28	ATF3	chr5:61601549-61601955	K562	blood:	n/a	n/a
29	BACH1	chr5:61601831-61602559	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:61562607-61562720	K562	blood:	n/a	n/a
31	BACH1	chr5:61557393-61557887	K562	blood:	n/a	n/a
32	BACH1	chr5:61602999-61603280	K562	blood:	n/a	n/a
33	BACH1	chr5:61581356-61581733	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr5:61573590-61573604	K562	blood:	n/a	n/a
35	BATF	chr5:61572852-61573221	GM12878	blood:	n/a	n/a
36	BATF	chr5:61546763-61547085	GM12878	blood:	n/a	chr5:61546935-61546946
37	BATF	chr5:61585629-61585959	GM12878	blood:	n/a	n/a
38	BATF	chr5:61585678-61585957	GM12878	blood:	n/a	n/a
39	BATF	chr5:61581091-61581716	GM12878	blood:	n/a	n/a
40	BATF	chr5:61581190-61581653	GM12878	blood:	n/a	n/a
41	BATF	chr5:61535787-61536021	GM12878	blood:	n/a	n/a
42	BATF	chr5:61572825-61573322	GM12878	blood:	n/a	n/a
43	BATF	chr5:61546774-61547053	GM12878	blood:	n/a	chr5:61546935-61546946
44	BCL11A	chr5:61613072-61613276	GM12878	blood:	n/a	n/a
45	BCL11A	chr5:61581080-61581596	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:61546831-61547049	GM12878	blood:	n/a	n/a
47	BCL11A	chr5:61581191-61581488	GM12878	blood:	n/a	n/a
48	BCL11A	chr5:61546718-61547027	GM12878	blood:	n/a	n/a
49	BCL11A	chr5:61552251-61552596	GM12878	blood:	n/a	n/a
50	BCL11A	chr5:61572893-61573165	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61602737-61602787	BE2_C	brain:	n/a
2	chr5:61602737-61602787	BE2_C	brain:	n/a
3	chr5:61602105-61602155	NB4	blood:	n/a
4	chr5:61601647-61601697	BJ	skin:	n/a
5	chr5:61603122-61603172	HRPEpiC	eye:	n/a
6	chr5:61602105-61602155	HAEpiC	amniotic membrane:	n/a
7	chr5:61602127-61602177	HCF	heart:	n/a
8	chr5:61612144-61612194	T-47D	breast:	n/a
9	chr5:61601636-61601686	Hela-S3	cervix:	n/a
10	chr5:61602127-61602177	AoSMC	blood vessel:	n/a
11	chr5:61602127-61602177	HepG2	liver:	n/a
12	chr5:61601647-61601697	SKMC	muscle:	n/a
13	chr5:61598126-61598176	NHBE	bronchial:	n/a
14	chr5:61598126-61598176	NH-A	brain:	n/a
15	chr5:61602737-61602787	HEK293	kidney:	embryo
16	chr5:61601529-61601579	HL-60	blood:	n/a
17	chr5:61602127-61602177	GM12891	blood:	n/a
18	chr5:61602737-61602787	HUVEC	blood vessel:	n/a
19	chr5:61603122-61603172	A549	lung:	n/a
20	chr5:61601629-61601679	NHDF-neo	bronchial:	n/a
21	chr5:61602105-61602155	PFSK-1	brain:	n/a
22	chr5:61612144-61612194	PANC-1	pancreas:	n/a
23	chr5:61602737-61602787	GM12878	blood:	n/a
24	chr5:61602127-61602177	ProgFib	skin:	n/a
25	chr5:61598126-61598176	HEK293	kidney:	embryo
26	chr5:61602127-61602177	Caco-2	colon:	n/a
27	chr5:61603122-61603172	HAEpiC	amniotic membrane:	n/a
28	chr5:61598126-61598176	HRPEpiC	eye:	n/a
29	chr5:61601629-61601679	NH-A	brain:	n/a
30	chr5:61602737-61602787	HIPEpiC	eye:	n/a
31	chr5:61601647-61601697	RPTEC	kidney:	n/a
32	chr5:61598126-61598176	NT2-D1	testis:	n/a
33	chr5:61601647-61601697	A549	lung:	n/a
34	chr5:61601636-61601686	GM12878	blood:	n/a
35	chr5:61602105-61602155	PANC-1	pancreas:	n/a
36	chr5:61603122-61603172	ECC-1	luminal epithelium:	n/a
37	chr5:61612144-61612194	Caco-2	colon:	n/a
38	chr5:61602737-61602787	LNCaP	prostate:	n/a
39	chr5:61605247-61605297	HEEpiC	esophagus:	n/a
40	chr5:61601629-61601679	A549	lung:	n/a
41	chr5:61602737-61602787	HPAEpiC	pulmonary alveolar:	n/a
42	chr5:61598126-61598176	GM12892	blood:	n/a
43	chr5:61601636-61601686	CMK	blood:	n/a
44	chr5:61601647-61601697	ECC-1	luminal epithelium:	n/a
45	chr5:61601647-61601697	U87	brain:	n/a
46	chr5:61601529-61601579	ovcar-3	ovarian:	n/a
47	chr5:61602105-61602155	HCT-116	colon:	n/a
48	chr5:61601128-61601178	ovcar-3	ovarian:	n/a
49	chr5:61601636-61601686	GM06990	blood:	n/a
50	chr5:61603122-61603172	HMEC	breast:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:61567057..61569712-chr5:61601806..61604336,2	K562	blood:
2	chr5:61591655..61593210-chr5:61601094..61603116,2	K562	blood:
3	chr5:61571856..61574619-chr5:61696505..61699367,2	K562	blood:
4	chr5:61558370..61559977-chr5:61580738..61582579,2	K562	blood:
5	chr5:61604639..61607587-chr5:61647579..61650088,2	MCF-7	breast:
6	chr5:61609391..61611692-chr5:61614218..61617054,2	K562	blood:
7	chr5:61561179..61563178-chr5:61595838..61598010,2	K562	blood:
8	chr5:61593661..61595529-chr5:61600373..61601956,2	K562	blood:
9	chr5:61555924..61558214-chr5:61579881..61582380,2	K562	blood:
10	chr5:61550007..61554674-chr5:61558868..61565665,10	K562	blood:
11	chr5:61558370..61559977-chr5:61580738..61582579,2	K562	blood:
12	chr5:61560375..61564102-chr5:61592918..61596892,3	K562	blood:
13	chr5:61602098..61603608-chr5:61605633..61607272,2	MCF-7	breast:
14	chr5:61580058..61581807-chr5:61582180..61584252,2	K562	blood:
15	chr5:61560375..61564102-chr5:61592918..61596892,3	K562	blood:
16	chr5:61592874..61595599-chr5:61604099..61606788,3	K562	blood:
17	chr5:61606018..61607564-chr5:61612889..61615038,2	MCF-7	breast:
18	chr5:61601799..61604714-chr5:61698844..61701505,2	MCF-7	breast:
19	chr5:61573722..61577065-chr5:61577950..61581609,5	K562	blood:
20	chr5:61609391..61611692-chr5:61614218..61617054,2	K562	blood:
21	chr5:61551611..61555704-chr5:61555776..61558862,4	K562	blood:
22	chr5:61581120..61583166-chr5:61590441..61591948,2	MCF-7	breast:
23	chr5:61578307..61579261-chr5:61607699..61608421,2	K562	blood:
24	chr5:61561395..61563266-chr5:61628626..61630582,2	K562	blood:
25	chr5:61549033..61550848-chr5:61552778..61554762,2	K562	blood:
26	chr5:61561783..61565148-chr5:61601604..61603284,3	MCF-7	breast:
27	chr5:61555834..61558737-chr5:61608990..61611037,2	MCF-7	breast:
28	chr5:61568618..61571084-chr5:61573101..61574954,2	K562	blood:
29	chr5:61601958..61603491-chr5:61698096..61700949,2	MCF-7	breast:
30	chr5:61614359..61618770-chr5:61621420..61626796,7	K562	blood:
31	chr5:61580058..61581807-chr5:61582180..61584252,2	K562	blood:
32	chr5:61593077..61595948-chr5:61615078..61617316,2	K562	blood:
33	chr5:61593407..61596088-chr5:61596627..61599078,2	K562	blood:
34	chr5:61600400..61604450-chr5:61613587..61619204,8	MCF-7	breast:
35	chr5:61557476..61560441-chr5:61562160..61565169,3	MCF-7	breast:
36	chr5:61601759..61603415-chr5:61698105..61699743,2	K562	blood:
37	chr5:61571147..61572996-chr5:61698680..61700895,2	K562	blood:
38	chr5:61549033..61550848-chr5:61552778..61554762,2	K562	blood:
39	chr5:61560127..61563309-chr5:61603579..61607776,4	K562	blood:
40	chr5:61561722..61564557-chr5:61699479..61701538,2	K562	blood:
41	chr5:61601533..61603969-chr5:61707379..61709702,2	K562	blood:
42	chr5:61567482..61568420-chr5:61649640..61650468,3	MCF-7	breast:
43	chr10:94050798..94051586-chr5:61601516..61602145,2	Hela-S3	cervix:
44	chr5:61560127..61563609-chr5:61600323..61607787,9	K562	blood:
45	chr5:61539663..61541258-chr5:61560288..61563274,2	K562	blood:
46	chr5:61561863..61563479-chr5:61638036..61640734,2	K562	blood:
47	chr5:61541758..61543641-chr5:61554002..61556238,2	K562	blood:
48	chr5:61539494..61542163-chr5:61560247..61562435,2	K562	blood:
49	chr5:61568618..61571084-chr5:61573101..61574954,2	K562	blood:
50	chr5:61574738..61576264-chr5:61698125..61699775,2	K562	blood:

No data

Variant related genes	Relation type
KIF2A	TF binding region
KIF2A	CpG island
ENSG00000086200	chromatin interactions
ENSG00000068796	chromatin interactions
ENSG00000107864	chromatin interactions
ENSG00000265020	chromatin interactions
ENSG00000086189	chromatin interactions
ENSG00000198060	chromatin interactions
ENSG00000127948	chromatin interactions

Extended variants
information (count: 2962 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2962 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16898838	chr5:61535831-61535832	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550740416	chr5:61535837-61535838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150148524	chr5:61535863-61535864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201989938	chr5:61535899-61535900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575360490	chr5:61535908-61535909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552063664	chr5:61535959-61535960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs57426687	chr5:61536002-61536003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs397942966	chr5:61536003-61536004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200418921	chr5:61536107-61536108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201396997	chr5:61536112-61536113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs3872824	chr5:61536138-61536139	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs9942312	chr5:61536296-61536297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565504138	chr5:61536298-61536299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534538511	chr5:61536352-61536353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs9942365	chr5:61536429-61536430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187955948	chr5:61536442-61536443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192195591	chr5:61536447-61536448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9942366	chr5:61536476-61536477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574480191	chr5:61536481-61536482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537039436	chr5:61536487-61536488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574063053	chr5:61536529-61536530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556726738	chr5:61536611-61536612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576907831	chr5:61536619-61536620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546476519	chr5:61536638-61536639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369509883	chr5:61536686-61536687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112806342	chr5:61536745-61536746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3963868	chr5:61536778-61536779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573456173	chr5:61536793-61536794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4037934	chr5:61536797-61536798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542093872	chr5:61536824-61536825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559784337	chr5:61536858-61536859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs137911433	chr5:61536881-61536882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4037935	chr5:61536888-61536889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143376608	chr5:61536900-61536901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551056941	chr5:61536914-61536915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564098662	chr5:61536924-61536925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533171500	chr5:61537010-61537011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185000180	chr5:61537062-61537063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565665470	chr5:61537099-61537100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372939142	chr5:61537140-61537141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369889184	chr5:61537162-61537163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534798979	chr5:61537180-61537181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189284797	chr5:61537196-61537197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192314542	chr5:61537202-61537203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146908521	chr5:61537214-61537215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184515273	chr5:61537237-61537238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545377671	chr5:61537270-61537271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557099700	chr5:61537283-61537284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375815544	chr5:61537285-61537286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566442631	chr5:61537291-61537292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
Thoracic aortic aneurysm	21092924	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
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
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	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
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
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61531600-61536800	Weak transcription	Fetal Intestine Small	intestine
2	chr5:61531600-61537000	Weak transcription	GM12878-XiMat	blood
3	chr5:61534400-61552000	Weak transcription	Fetal Muscle Leg	muscle
4	chr5:61535600-61536600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr5:61535800-61537200	Enhancers	Pancreas	Pancrea
6	chr5:61536600-61537000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr5:61536800-61537800	Enhancers	Fetal Intestine Small	intestine
8	chr5:61537000-61537200	Enhancers	GM12878-XiMat	blood
9	chr5:61537200-61538000	Weak transcription	Pancreas	Pancrea
10	chr5:61538000-61538600	Enhancers	Pancreas	Pancrea
11	chr5:61542000-61542400	Active TSS	Placenta	Placenta
12	chr5:61543800-61544400	Enhancers	NHEK	skin
13	chr5:61544200-61544400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:61544400-61544800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:61546800-61547200	Enhancers	GM12878-XiMat	blood
16	chr5:61548200-61548400	Enhancers	K562	blood
17	chr5:61548400-61548800	Flanking Active TSS	K562	blood
18	chr5:61548800-61549000	Enhancers	K562	blood
19	chr5:61549000-61552000	Weak transcription	K562	blood
20	chr5:61549400-61551800	Enhancers	Primary T cells from cord blood	blood
21	chr5:61549800-61550000	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr5:61549800-61550800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr5:61549800-61552000	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr5:61549800-61552400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:61549800-61553800	Enhancers	Primary T cells fromperipheralblood	blood
26	chr5:61550000-61551000	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr5:61550000-61552000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr5:61550200-61550400	Enhancers	Primary hematopoietic stem cells	blood
29	chr5:61550200-61551000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr5:61550200-61552000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr5:61550200-61552200	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr5:61550400-61552000	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr5:61550800-61552000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr5:61551000-61551200	Enhancers	GM12878-XiMat	blood
35	chr5:61551000-61552000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr5:61551000-61552200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr5:61551000-61552200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr5:61551000-61552200	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr5:61551200-61552000	Weak transcription	GM12878-XiMat	blood
40	chr5:61551400-61552000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr5:61551800-61552000	Enhancers	Dnd41	blood
42	chr5:61551800-61553000	Flanking Active TSS	Primary T cells from cord blood	blood
43	chr5:61552000-61552200	Flanking Active TSS	Dnd41	blood
44	chr5:61552000-61552400	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr5:61552000-61552400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr5:61552000-61552400	Enhancers	Pancreas	Pancrea
47	chr5:61552000-61552400	Enhancers	GM12878-XiMat	blood
48	chr5:61552000-61552600	Enhancers	Fetal Intestine Small	intestine
49	chr5:61552000-61552800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr5:61552000-61552800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood

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