Variant report

Variant	esv2762571
Chromosome Location	chr5:177197955-177260330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:177225275-177225490	HepG2	liver:	n/a	n/a
2	CBX3	chr5:177209512-177209875	K562	blood:	n/a	n/a
3	CBX3	chr5:177209565-177209833	K562	blood:	n/a	n/a
4	CEBPB	chr5:177198236-177198491	A549	lung:	n/a	chr5:177198345-177198358
5	CEBPB	chr5:177198235-177198496	IMR90	lung:	n/a	chr5:177198345-177198358
6	CEBPB	chr5:177198402-177198415	K562	blood:	n/a	n/a
7	CTCF	chr5:177225393-177225521	Hela-S3	cervix:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
8	CTCF	chr5:177225300-177225450	K562	blood:	n/a	chr5:177225342-177225350
9	CTCF	chr5:177236175-177236436	K562	blood:	n/a	chr5:177236292-177236310
10	CTCF	chr5:177236147-177236467	Fibrobl	skin:	n/a	chr5:177236292-177236310
11	CTCF	chr5:177236158-177236464	A549	lung:	n/a	chr5:177236292-177236310
12	CTCF	chr5:177225305-177225518	H1-hESC	embryonic stem cell:	n/a	chr5:177225459-177225472 chr5:177225456-177225474 chr5:177225342-177225350
13	CTCF	chr5:177210682-177210778	LNCaP	prostate:	n/a	n/a
14	CTCF	chr5:177236555-177236657	GM10248	blood:	n/a	n/a
15	CTCF	chr5:177235967-177236003	LNCaP	prostate:	n/a	n/a
16	CTCF	chr5:177236244-177236379	GM20000	blood:	n/a	chr5:177236292-177236310
17	CTCF	chr5:177224162-177224265	Pancreas_OC	pancreas:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
18	CTCF	chr5:177224163-177224258	GM19240	blood:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
19	CTCF	chr5:177224147-177224263	GM12892	blood:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
20	CTCF	chr5:177225431-177225623	K562	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
21	CTCF	chr5:177211281-177211328	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr5:177236174-177236465	Hela-S3	cervix:	n/a	chr5:177236292-177236310
23	CTCF	chr5:177224140-177224290	SAEC	small airway:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
24	CTCF	chr5:177236502-177236645	GM19240	blood:	n/a	chr5:177236545-177236558
25	CTCF	chr5:177224108-177224269	NHEK	skin:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
26	CTCF	chr5:177225352-177225561	A549	lung:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
27	CTCF	chr5:177224097-177224284	MCF-7	breast:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
28	CTCF	chr5:177225412-177225515	Fibrobl	skin:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
29	CTCF	chr5:177224286-177224332	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr5:177236130-177236590	NHEK	skin:	n/a	chr5:177236545-177236558 chr5:177236292-177236310
31	CTCF	chr5:177236594-177236669	GM13976	blood:	n/a	n/a
32	CTCF	chr5:177225378-177225486	HepG2	liver:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
33	CTCF	chr5:177225370-177225536	NHEK	skin:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
34	CTCF	chr5:177225336-177225548	Spleen_OC	spleen:	n/a	chr5:177225459-177225472 chr5:177225456-177225474 chr5:177225342-177225350
35	CTCF	chr5:177208101-177208143	GM13976	blood:	n/a	n/a
36	CTCF	chr5:177225118-177225177	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:177225388-177225550	GM19240	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
38	CTCF	chr5:177236135-177236618	MCF-7	breast:	n/a	chr5:177236545-177236558 chr5:177236292-177236310
39	CTCF	chr5:177224147-177224244	GM12891	blood:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
40	CTCF	chr5:177236202-177236382	GM10248	blood:	n/a	chr5:177236292-177236310
41	CTCF	chr5:177225390-177225511	Medullo	brain:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
42	CTCF	chr5:177224174-177224224	GM10248	blood:	n/a	chr5:177224201-177224219
43	CTCF	chr5:177224113-177224272	GM19239	blood:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
44	CTCF	chr5:177225373-177225536	MCF-7	breast:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
45	CTCF	chr5:177224144-177224240	Hela-S3	cervix:	n/a	chr5:177224201-177224219 chr5:177224227-177224235
46	CTCF	chr5:177236154-177236465	LNCaP	prostate:	n/a	chr5:177236292-177236310
47	CTCF	chr5:177225441-177225502	GM10266	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
48	CTCF	chr5:177225394-177225551	GM12878	blood:	n/a	chr5:177225459-177225472 chr5:177225456-177225474
49	CTCF	chr5:177236675-177236756	GM19239	blood:	n/a	n/a
50	CTCF	chr5:177225300-177225450	HepG2	liver:	n/a	chr5:177225342-177225350

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177212760-177212810	K562	blood:	n/a
2	chr5:177209947-177209997	AG09319	gingival:	n/a
3	chr5:177225404-177225454	BE2_C	brain:	n/a
4	chr5:177212760-177212810	SKMC	muscle:	n/a
5	chr5:177234437-177234487	HPAEpiC	pulmonary alveolar:	n/a
6	chr5:177234437-177234487	HL-60	blood:	n/a
7	chr5:177234437-177234487	MCF-7	breast:	n/a
8	chr5:177209285-177209335	AoSMC	blood vessel:	n/a
9	chr5:177212760-177212810	SAEC	small airway:	n/a
10	chr5:177209285-177209335	NH-A	brain:	n/a
11	chr5:177225404-177225454	LNCaP	prostate:	n/a
12	chr5:177225404-177225454	HUVEC	blood vessel:	n/a
13	chr5:177210257-177210307	Hela-S3	cervix:	n/a
14	chr5:177209285-177209335	HIPEpiC	eye:	n/a
15	chr5:177210257-177210307	HCF	heart:	n/a
16	chr5:177212760-177212810	GM12892	blood:	n/a
17	chr5:177212760-177212810	HRCEpiC	kidney:	n/a
18	chr5:177209285-177209335	PFSK-1	brain:	n/a
19	chr5:177209285-177209335	MCF-7	breast:	n/a
20	chr5:177212760-177212810	SK-N-SH_RA	brain:	n/a
21	chr5:177209947-177209997	T-47D	breast:	n/a
22	chr5:177234437-177234487	ProgFib	skin:	n/a
23	chr5:177234437-177234487	K562	blood:	n/a
24	chr5:177225404-177225454	T-47D	breast:	n/a
25	chr5:177210257-177210307	ProgFib	skin:	n/a
26	chr5:177234437-177234487	HAEpiC	amniotic membrane:	n/a
27	chr5:177234437-177234487	Hepatocyte	liver:	n/a
28	chr5:177209285-177209335	LNCaP	prostate:	n/a
29	chr5:177225404-177225454	ECC-1	luminal epithelium:	n/a
30	chr5:177209285-177209335	HAEpiC	amniotic membrane:	n/a
31	chr5:177212760-177212810	GM12891	blood:	n/a
32	chr5:177225404-177225454	SK-N-SH	brain:	n/a
33	chr5:177210257-177210307	HCPEpiC	choroid plexus:	n/a
34	chr5:177209285-177209335	SK-N-SH_RA	brain:	n/a
35	chr5:177209947-177209997	AG04450	lung:	fetal
36	chr5:177209947-177209997	SAEC	small airway:	n/a
37	chr5:177209947-177209997	LNCaP	prostate:	n/a
38	chr5:177234437-177234487	H1-hESC	embryonic stem cell:	embryo
39	chr5:177234437-177234487	IMR90	lung:	fetal
40	chr5:177209947-177209997	HIPEpiC	eye:	n/a
41	chr5:177225404-177225454	AG04450	lung:	fetal
42	chr5:177234437-177234487	GM12878	blood:	n/a
43	chr5:177212760-177212810	HCM	heart:	n/a
44	chr5:177209947-177209997	AG10803	skin:	n/a
45	chr5:177225404-177225454	K562	blood:	n/a
46	chr5:177234437-177234487	HRE	kidney:	n/a
47	chr5:177210257-177210307	AoSMC	blood vessel:	n/a
48	chr5:177234437-177234487	HCPEpiC	choroid plexus:	n/a
49	chr5:177225404-177225454	GM19239	blood:	n/a
50	chr5:177225404-177225454	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177034180..177035059-chr5:177223760..177224507,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM193B-7	chr5:177207450-177207505	NONHSAT105465
2	lnc-FAM193B-7	chr5:177207450-177207505	NONHSAT105468
3	lnc-FAM193B-7	chr5:177206498-177206718	NONHSAT105467
4	lnc-FAM193B-7	chr5:177208586-177208685	NONHSAT105467
5	lnc-FAM193B-7	chr5:177209744-177209814	NONHSAT105468
6	lnc-FAM193B-7	chr5:177210285-177210365	NONHSAT105465
7	lnc-FAM193B-7	chr5:177206557-177206718	NONHSAT105468
8	lnc-FAM193B-7	chr5:177207450-177207505	NONHSAT105467

Variant related genes	Relation type
FAM153A	TF binding region
ENSG00000248943	TF binding region
ENSG00000249109	TF binding region
ENSG00000170089	TF binding region
FAM153A	CpG island
ENSG00000248943	CpG island
ENSG00000249109	CpG island
ENSG00000170089	CpG island
ENSG00000027847	chromatin interactions

Extended variants
information (count: 682 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:682 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7378862	chr5:177206205-177206206	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs548243758	chr5:177206271-177206272	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375854522	chr5:177206285-177206286	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs369066147	chr5:177206290-177206291	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs35016924	chr5:177206291-177206292	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs199984889	chr5:177206292-177206293	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs181910081	chr5:177206309-177206310	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs201560125	chr5:177206627-177206628	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs62399974	chr5:177206712-177206713	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs62399975	chr5:177206714-177206715	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs572922280	chr5:177209038-177209039	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs540197868	chr5:177209053-177209054	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs377646207	chr5:177209097-177209098	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs565044983	chr5:177209114-177209115	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs191273776	chr5:177209254-177209255	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs376066678	chr5:177209321-177209322	Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs532638292	chr5:177209323-177209324	Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs550936410	chr5:177209350-177209351	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs28450227	chr5:177209382-177209383	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs530356456	chr5:177209431-177209432	Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs62399978	chr5:177209510-177209511	Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs28588700	chr5:177209585-177209586	Active TSS Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs75196305	chr5:177209661-177209662	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs111419142	chr5:177209662-177209663	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs79321202	chr5:177209671-177209672	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs28594523	chr5:177209681-177209682	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200447169	chr5:177209689-177209690	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs28624801	chr5:177209700-177209701	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs181125595	chr5:177209777-177209778	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs371953256	chr5:177209787-177209788	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs375396375	chr5:177209824-177209825	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs375550869	chr5:177209902-177209903	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs548923138	chr5:177210186-177210187	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567135885	chr5:177210198-177210199	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs186642627	chr5:177210219-177210220	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs191446343	chr5:177210229-177210230	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs183187198	chr5:177210233-177210234	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs527281021	chr5:177210239-177210240	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs187861779	chr5:177210269-177210270	Active TSS Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	mRNA abundance
40	rs562906567	chr5:177210575-177210576	Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs549054764	chr5:177211297-177211298	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs560770588	chr5:177211744-177211745	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs370324818	chr5:177212772-177212773	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs369541195	chr5:177218422-177218423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530941605	chr5:177218428-177218429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549087140	chr5:177218446-177218447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373427274	chr5:177218466-177218467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568621817	chr5:177218467-177218468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183890557	chr5:177218498-177218499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537398649	chr5:177218505-177218506	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Autism	20841430	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177209000-177209800	Active TSS	Primary T helper cells PMA-I stimulated	--
2	chr5:177209400-177209600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr5:177209400-177209600	Enhancers	Pancreas	Pancrea
4	chr5:177209400-177209800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr5:177209400-177209800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
6	chr5:177209400-177210200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:177209400-177210400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
8	chr5:177209400-177210400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
9	chr5:177209400-177210600	Active TSS	Ovary	ovary
10	chr5:177209600-177209800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:177209600-177209800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr5:177209600-177210400	Active TSS	Primary T cells fromperipheralblood	blood
13	chr5:177209800-177210400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:177210000-177210400	Active TSS	Brain Angular Gyrus	brain
15	chr5:177210000-177210600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:177218400-177218600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr5:177218600-177220800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr5:177220800-177222400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr5:177221400-177221800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr5:177221400-177221800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr5:177221400-177221800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr5:177221400-177221800	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr5:177221400-177222600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr5:177221400-177222600	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr5:177221400-177222800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr5:177221600-177222000	Enhancers	Primary T cells fromperipheralblood	blood
27	chr5:177221800-177235600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr5:177222000-177222400	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr5:177222400-177222600	Enhancers	Primary T cells fromperipheralblood	blood
30	chr5:177222400-177230400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr5:177222600-177226400	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr5:177222600-177227400	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr5:177222800-177225400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr5:177226000-177227200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr5:177227400-177227800	Enhancers	Primary T cells fromperipheralblood	blood
36	chr5:177227800-177229000	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr5:177228600-177229600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr5:177229000-177229400	Enhancers	Primary T cells fromperipheralblood	blood
39	chr5:177229400-177234200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr5:177230400-177231000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr5:177231000-177231400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr5:177231200-177231400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr5:177231400-177231600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr5:177231400-177235600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr5:177231600-177235400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr5:177232200-177232400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr5:177232400-177233000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr5:177232400-177235600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr5:177233000-177235400	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr5:177233000-177235800	Weak transcription	Primary T helper cells PMA-I stimulated	--

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