Variant report

Variant	nsv4897
Chromosome Location	chr5:80284196-80330223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:185)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:80285378-80285574	K562	blood:	n/a	n/a
2	CEBPB	chr5:80314559-80314721	A549	lung:	n/a	n/a
3	CEBPB	chr5:80314501-80314852	IMR90	lung:	n/a	n/a
4	CEBPB	chr5:80292435-80292627	HepG2	liver:	n/a	chr5:80292474-80292485
5	CEBPB	chr5:80286778-80287261	MCF-7	breast:	n/a	n/a
6	CEBPB	chr5:80318580-80318818	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:80286936-80287198	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:80286933-80287204	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:80286954-80287157	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr5:80284474-80284674	A549	lung:	n/a	n/a
11	CHD2	chr5:80310245-80310423	K562	blood:	n/a	n/a
12	CTCF	chr5:80316780-80316930	HMEC	breast:	n/a	n/a
13	CTCF	chr5:80296740-80296890	GM12872	blood:	n/a	n/a
14	CTCF	chr5:80316775-80316782	MCF-7	breast:	n/a	n/a
15	CTCF	chr5:80287460-80287610	BE2_C	brain:	n/a	n/a
16	CTCF	chr5:80295820-80295970	Caco-2	colon:	n/a	n/a
17	CTCF	chr5:80319160-80319310	HEK293	kidney:	n/a	n/a
18	CTCF	chr5:80295236-80295295	MCF-7	breast:	n/a	n/a
19	CTCF	chr5:80319180-80319330	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr5:80316793-80316807	MCF-7	breast:	n/a	n/a
21	CTCF	chr5:80316786-80316805	NHEK	skin:	n/a	n/a
22	CTCF	chr5:80286472-80286555	GM20000	blood:	n/a	n/a
23	E2F4	chr5:80292959-80293218	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr5:80286409-80286609	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr5:80290434-80290672	GM12878	blood:	n/a	n/a
26	EGR1	chr5:80294405-80294592	K562	blood:	n/a	n/a
27	EP300	chr5:80318674-80318766	K562	blood:	n/a	n/a
28	EP300	chr5:80288120-80288653	T-47D	breast:	n/a	n/a
29	EP300	chr5:80319468-80319708	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr5:80319322-80319707	SK-N-SH_RA	brain:	n/a	n/a
31	FOS	chr5:80316387-80316754	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr5:80286494-80287176	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:80284400-80284673	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr5:80314502-80314653	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:80316175-80316755	MCF10A-Er-Src	breast:	n/a	chr5:80316204-80316216
36	FOS	chr5:80284421-80284646	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr5:80314361-80314742	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr5:80284360-80284684	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr5:80286588-80287177	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr5:80286809-80287175	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr5:80316392-80316669	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr5:80314444-80314668	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr5:80314451-80314694	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr5:80286491-80287241	MCF10A-Er-Src	breast:	n/a	n/a
45	FOSL2	chr5:80286739-80287215	MCF-7	breast:	n/a	n/a
46	FOSL2	chr5:80286847-80287211	HepG2	liver:	n/a	n/a
47	FOXA1	chr5:80288195-80288629	T-47D	breast:	n/a	n/a
48	FOXA1	chr5:80286835-80287102	T-47D	breast:	n/a	n/a
49	FOXA1	chr5:80284337-80284764	T-47D	breast:	n/a	n/a
50	FOXA1	chr5:80325530-80325875	HepG2	liver:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:80286535-80286585	HCF	heart:	n/a
2	chr5:80286535-80286585	NHDF-neo	bronchial:	n/a
3	chr5:80286535-80286585	HCF	heart:	n/a
4	chr5:80286535-80286585	NHDF-neo	bronchial:	n/a
5	chr5:80306626-80306676	Hepatocyte	liver:	n/a
6	chr5:80286535-80286585	HCPEpiC	choroid plexus:	n/a
7	chr5:80286535-80286585	BJ	skin:	n/a
8	chr5:80306626-80306676	GM06990	blood:	n/a
9	chr5:80316822-80316872	ECC-1	luminal epithelium:	n/a
10	chr5:80286535-80286585	Caco-2	colon:	n/a
11	chr5:80316822-80316872	HUVEC	blood vessel:	n/a
12	chr5:80286535-80286585	NT2-D1	testis:	n/a
13	chr5:80316822-80316872	AoSMC	blood vessel:	n/a
14	chr5:80306626-80306676	K562	blood:	n/a
15	chr5:80316822-80316872	GM12878	blood:	n/a
16	chr5:80286535-80286585	SKMC	muscle:	n/a
17	chr5:80316822-80316872	NH-A	brain:	n/a
18	chr5:80286535-80286585	SK-N-MC	brain:	n/a
19	chr5:80316822-80316872	NB4	blood:	n/a
20	chr5:80316822-80316872	HIPEpiC	eye:	n/a
21	chr5:80286535-80286585	MCF-7	breast:	n/a
22	chr5:80316822-80316872	CMK	blood:	n/a
23	chr5:80286535-80286585	GM12878	blood:	n/a
24	chr5:80316822-80316872	PFSK-1	brain:	n/a
25	chr5:80286535-80286585	HCT-116	colon:	n/a
26	chr5:80306626-80306676	HCT-116	colon:	n/a
27	chr5:80286535-80286585	GM19239	blood:	n/a
28	chr5:80306626-80306676	SK-N-SH	brain:	n/a
29	chr5:80306626-80306676	SKMC	muscle:	n/a
30	chr5:80286535-80286585	PANC-1	pancreas:	n/a
31	chr5:80286535-80286585	SAEC	small airway:	n/a
32	chr5:80306626-80306676	ProgFib	skin:	n/a
33	chr5:80316822-80316872	HPAEpiC	pulmonary alveolar:	n/a
34	chr5:80316822-80316872	U87	brain:	n/a
35	chr5:80316822-80316872	SK-N-SH	brain:	n/a
36	chr5:80316822-80316872	AG04449	skin:	fetal
37	chr5:80306626-80306676	IMR90	lung:	fetal
38	chr5:80306626-80306676	MCF10A-Er-Src	breast:	n/a
39	chr5:80316822-80316872	NHBE	bronchial:	n/a
40	chr5:80306626-80306676	NT2-D1	testis:	n/a
41	chr5:80286535-80286585	PFSK-1	brain:	n/a
42	chr5:80316822-80316872	HEEpiC	esophagus:	n/a
43	chr5:80306626-80306676	HepG2	liver:	n/a
44	chr5:80316822-80316872	Jurkat	blood:	n/a
45	chr5:80306626-80306676	HRE	kidney:	n/a
46	chr5:80316822-80316872	GM06990	blood:	n/a
47	chr5:80286535-80286585	GM12892	blood:	n/a
48	chr5:80286535-80286585	NH-A	brain:	n/a
49	chr5:80306626-80306676	Jurkat	blood:	n/a
50	chr5:80286535-80286585	AG09309	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:51532795..51533745-chr5:80312236..80312930,2	MCF-7	breast:
2	chr5:80304567..80306339-chr5:80307173..80308776,2	MCF-7	breast:
3	chr5:80312638..80314887-chr5:80409746..80411334,2	K562	blood:
4	chr5:80304567..80306339-chr5:80307173..80308776,2	MCF-7	breast:
5	chr5:80280624..80283430-chr5:80318817..80321662,2	K562	blood:
6	chr5:80293956..80295842-chr5:80296253..80298015,2	K562	blood:
7	chr5:80309029..80312637-chr5:80313535..80317420,3	K562	blood:
8	chr5:80278839..80280543-chr5:80284483..80286829,2	K562	blood:
9	chr5:80293956..80295842-chr5:80296253..80298015,2	K562	blood:
10	chr5:80284586..80286843-chr5:80294142..80297037,2	K562	blood:
11	chr5:80284586..80286843-chr5:80294142..80297037,2	K562	blood:
12	chr5:80316222..80317107-chr5:80490719..80491566,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOT12-10	chr5:80293002-80293503	NONHSAT102429
2	lnc-ACOT12-10	chr5:80293833-80293866	NONHSAT102429

No data

Variant related genes	Relation type
RASGRF2	TF binding region
ENSG00000251001	TF binding region
RASGRF2	CpG island
ENSG00000251001	CpG island
ENSG00000113319	chromatin interactions
ENSG00000249772	chromatin interactions

Extended variants
information (count: 1935 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1935 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7731847	chr5:80284197-80284198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370629040	chr5:80284214-80284215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551001258	chr5:80284262-80284263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567523084	chr5:80284292-80284293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536597732	chr5:80284317-80284318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553197895	chr5:80284373-80284374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528827135	chr5:80284374-80284375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370270974	chr5:80284377-80284378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146075332	chr5:80284468-80284469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs80147088	chr5:80284516-80284517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140019028	chr5:80284555-80284556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558592595	chr5:80284586-80284587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575261107	chr5:80284603-80284604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185025880	chr5:80284611-80284612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149339254	chr5:80284675-80284676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144733238	chr5:80284769-80284770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs16878283	chr5:80284794-80284795	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552090820	chr5:80284802-80284803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79768500	chr5:80284816-80284817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187468804	chr5:80284835-80284836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112835387	chr5:80284840-80284841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558089353	chr5:80284865-80284866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546408158	chr5:80284875-80284876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571696624	chr5:80284883-80284884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528654212	chr5:80284885-80284886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537464246	chr5:80284888-80284889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545286439	chr5:80284988-80284989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192319787	chr5:80284991-80284992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530914499	chr5:80285013-80285014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184756077	chr5:80285037-80285038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375486586	chr5:80285053-80285054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567706343	chr5:80285074-80285075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530002685	chr5:80285111-80285112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567664849	chr5:80285112-80285113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375977497	chr5:80285203-80285204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566675447	chr5:80285215-80285216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541624	chr5:80285254-80285255	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs558483513	chr5:80285268-80285269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568929534	chr5:80285355-80285356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs407901	chr5:80285379-80285380	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs554128665	chr5:80285401-80285402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574122714	chr5:80285408-80285409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539862058	chr5:80285419-80285420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs80154446	chr5:80285426-80285427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573465723	chr5:80285428-80285429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572196590	chr5:80285432-80285433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540960863	chr5:80285444-80285445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565388220	chr5:80285516-80285517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs16878285	chr5:80285521-80285522	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs544755080	chr5:80285523-80285524	Weak transcription Enhancers	n/a	n/a	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	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
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
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80269800-80285800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:80270000-80284200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr5:80277600-80287000	Weak transcription	Right Ventricle	heart
4	chr5:80278000-80293000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr5:80281000-80284600	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr5:80281200-80284400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:80281200-80284600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr5:80281400-80284800	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr5:80281400-80284800	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr5:80281400-80285400	Enhancers	Primary T cells from cord blood	blood
11	chr5:80281400-80290800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr5:80281400-80290800	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr5:80281600-80286000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr5:80281600-80286800	Enhancers	Brain Substantia Nigra	brain
15	chr5:80282000-80284400	Enhancers	Brain Hippocampus Middle	brain
16	chr5:80282000-80287400	Enhancers	Brain Cingulate Gyrus	brain
17	chr5:80282400-80284200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr5:80282400-80285800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr5:80282400-80286800	Enhancers	Brain Angular Gyrus	brain
20	chr5:80282600-80284400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr5:80282600-80286400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr5:80282600-80286600	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr5:80282800-80284200	Enhancers	Right Atrium	heart
24	chr5:80282800-80284400	Enhancers	Primary T cells fromperipheralblood	blood
25	chr5:80283200-80285600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr5:80283400-80284600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr5:80283400-80284600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr5:80283400-80284600	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr5:80283400-80285200	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr5:80283400-80285600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr5:80283600-80284400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr5:80283600-80285000	Enhancers	Left Ventricle	heart
33	chr5:80283600-80285400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr5:80283600-80286400	Weak transcription	Adipose Nuclei	Adipose
35	chr5:80283600-80287800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr5:80283800-80284200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr5:80283800-80287800	Weak transcription	Brain Anterior Caudate	brain
38	chr5:80284000-80284200	Enhancers	Spleen	Spleen
39	chr5:80284000-80285200	Weak transcription	HepG2	liver
40	chr5:80284200-80284400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr5:80284200-80284600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr5:80284200-80284600	Enhancers	Fetal Lung	lung
43	chr5:80284200-80286600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:80284200-80287600	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr5:80284400-80284800	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr5:80284400-80285400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:80284400-80285600	Weak transcription	Brain Hippocampus Middle	brain
48	chr5:80284400-80286200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr5:80284400-80286800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:80284400-80289400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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