Variant report

Variant	esv1839807
Chromosome Location	chr6:79532610-79606615
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:904)
CpG islands
(count:1037)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:904 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:79576806-79577041	K562	blood:	n/a	n/a
2	ARID3A	chr6:79575799-79575832	K562	blood:	n/a	n/a
3	ARID3A	chr6:79577598-79577777	K562	blood:	n/a	n/a
4	ATF2	chr6:79577087-79577782	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:79576934-79577738	GM12878	blood:	n/a	n/a
6	ATF2	chr6:79577022-79577772	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr6:79576885-79577787	GM12878	blood:	n/a	n/a
8	ATF3	chr6:79577395-79577639	K562	blood:	n/a	n/a
9	ATF3	chr6:79577371-79577697	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:79577206-79577978	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:79552837-79552927	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:79577037-79577147	K562	blood:	n/a	n/a
13	BCLAF1	chr6:79576821-79577785	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:79577157-79577772	K562	blood:	n/a	chr6:79577246-79577262
15	BHLHE40	chr6:79576822-79577745	GM12878	blood:	n/a	chr6:79577246-79577262
16	BRCA1	chr6:79577448-79577864	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr6:79577109-79577326	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr6:79577623-79577681	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr6:79576917-79577316	K562	blood:	n/a	n/a
20	CBX3	chr6:79577390-79577772	K562	blood:	n/a	n/a
21	CCNT2	chr6:79577088-79577612	K562	blood:	n/a	n/a
22	CEBPB	chr6:79577027-79577929	H1-hESC	embryonic stem cell:	n/a	chr6:79577904-79577917
23	CEBPB	chr6:79556229-79556482	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:79577090-79577939	HepG2	liver:	n/a	chr6:79577904-79577917
25	CEBPB	chr6:79606057-79606218	A549	lung:	n/a	chr6:79606120-79606131
26	CEBPB	chr6:79606013-79606288	K562	blood:	n/a	chr6:79606120-79606131
27	CEBPB	chr6:79577057-79577817	MCF-7	breast:	n/a	n/a
28	CEBPB	chr6:79606013-79606234	HepG2	liver:	n/a	chr6:79606120-79606131
29	CEBPB	chr6:79576983-79577921	Hela-S3	cervix:	n/a	chr6:79577904-79577917
30	CEBPB	chr6:79571201-79571456	MCF-7	breast:	n/a	n/a
31	CEBPB	chr6:79576937-79577829	K562	blood:	n/a	n/a
32	CHD1	chr6:79577672-79578053	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr6:79576919-79577235	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr6:79577430-79577442	K562	blood:	n/a	n/a
35	CHD2	chr6:79577019-79577828	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr6:79577660-79577766	K562	blood:	n/a	n/a
37	CHD2	chr6:79577215-79577380	HepG2	liver:	n/a	n/a
38	CHD2	chr6:79576913-79577825	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr6:79576921-79577144	K562	blood:	n/a	n/a
40	CHD2	chr6:79576791-79577749	GM12878	blood:	n/a	n/a
41	CREB1	chr6:79576938-79577843	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr6:79577060-79577825	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr6:79577301-79577815	K562	blood:	n/a	n/a
44	CREB1	chr6:79576734-79577856	GM12878	blood:	n/a	n/a
45	CREB1	chr6:79576952-79577838	HepG2	liver:	n/a	n/a
46	CREB1	chr6:79577086-79577740	A549	lung:	n/a	n/a
47	CREB1	chr6:79577243-79577854	K562	blood:	n/a	n/a
48	CTBP2	chr6:79576808-79577846	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr6:79571260-79571410	GM12864	blood:	n/a	n/a
50	CTCF	chr6:79577640-79577790	AG10803	skin:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:79577260-79577310	MCF-7	breast:	n/a
2	chr6:79576994-79577044	HAEpiC	amniotic membrane:	n/a
3	chr6:79580466-79580516	BJ	skin:	n/a
4	chr6:79577801-79577851	A549	lung:	n/a
5	chr6:79577232-79577282	MCF-7	breast:	n/a
6	chr6:79577691-79577741	K562	blood:	n/a
7	chr6:79577007-79577057	MCF10A-Er-Src	breast:	n/a
8	chr6:79577640-79577690	AG09319	gingival:	n/a
9	chr6:79577069-79577119	IMR90	lung:	fetal
10	chr6:79577110-79577160	HMEC	breast:	n/a
11	chr6:79577177-79577227	CMK	blood:	n/a
12	chr6:79577110-79577160	HEEpiC	esophagus:	n/a
13	chr6:79577177-79577227	HCT-116	colon:	n/a
14	chr6:79577232-79577282	AG04449	skin:	fetal
15	chr6:79576851-79576901	MCF-7	breast:	n/a
16	chr6:79576881-79576931	PFSK-1	brain:	n/a
17	chr6:79577232-79577282	HEEpiC	esophagus:	n/a
18	chr6:79577007-79577057	MCF-7	breast:	n/a
19	chr6:79577195-79577245	ovcar-3	ovarian:	n/a
20	chr6:79574843-79574893	MCF10A-Er-Src	breast:	n/a
21	chr6:79574843-79574893	HepG2	liver:	n/a
22	chr6:79577691-79577741	LNCaP	prostate:	n/a
23	chr6:79577007-79577057	HepG2	liver:	n/a
24	chr6:79577177-79577227	HUVEC	blood vessel:	n/a
25	chr6:79577195-79577245	Caco-2	colon:	n/a
26	chr6:79577110-79577160	ECC-1	luminal epithelium:	n/a
27	chr6:79577069-79577119	RPTEC	kidney:	n/a
28	chr6:79577691-79577741	AoSMC	blood vessel:	n/a
29	chr6:79577007-79577057	ProgFib	skin:	n/a
30	chr6:79576881-79576931	GM19239	blood:	n/a
31	chr6:79577691-79577741	HNPCEpiC	eye:	n/a
32	chr6:79574843-79574893	BE2_C	brain:	n/a
33	chr6:79577069-79577119	K562	blood:	n/a
34	chr6:79574843-79574893	HMEC	breast:	n/a
35	chr6:79577110-79577160	SKMC	muscle:	n/a
36	chr6:79577640-79577690	HCM	heart:	n/a
37	chr6:79576994-79577044	Hepatocyte	liver:	n/a
38	chr6:79577640-79577690	SKMC	muscle:	n/a
39	chr6:79577232-79577282	NH-A	brain:	n/a
40	chr6:79577175-79577225	HNPCEpiC	eye:	n/a
41	chr6:79577691-79577741	HepG2	liver:	n/a
42	chr6:79576851-79576901	ProgFib	skin:	n/a
43	chr6:79580466-79580516	K562	blood:	n/a
44	chr6:79577801-79577851	Hepatocyte	liver:	n/a
45	chr6:79577069-79577119	Caco-2	colon:	n/a
46	chr6:79577110-79577160	MCF10A-Er-Src	breast:	n/a
47	chr6:79577801-79577851	RPTEC	kidney:	n/a
48	chr6:79576851-79576901	GM12878	blood:	n/a
49	chr6:79576994-79577044	AoSMC	blood vessel:	n/a
50	chr6:79577801-79577851	AG04449	skin:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:79543127..79545015-chr6:79546486..79548944,2	K562	blood:
2	chr6:79584398..79586825-chr6:79590482..79592953,2	K562	blood:
3	chr6:79576198..79578688-chr6:79580398..79583072,2	K562	blood:
4	chr6:79595328..79597841-chr6:79600985..79603258,2	K562	blood:
5	chr6:79568772..79571138-chr6:79573163..79575541,2	K562	blood:
6	chr6:79543127..79545015-chr6:79546486..79548944,2	K562	blood:
7	chr6:79575390..79577053-chr6:79941953..79944016,2	K562	blood:
8	chr6:79537385..79538965-chr6:79541996..79544293,2	K562	blood:
9	chr6:79537385..79538965-chr6:79541996..79544293,2	K562	blood:
10	chr6:79575800..79578597-chr6:79786334..79789260,2	MCF-7	breast:
11	chr6:79576198..79578688-chr6:79580398..79583072,2	K562	blood:
12	chr6:79577837..79581410-chr6:79582821..79585860,5	K562	blood:
13	chr6:79572341..79575161-chr6:79575433..79577660,3	K562	blood:
14	chr6:79583511..79586825-chr6:79590200..79593930,3	K562	blood:
15	chr6:79583511..79586825-chr6:79590200..79593930,3	K562	blood:
16	chr6:79558999..79561726-chr6:79563730..79565524,2	K562	blood:
17	chr6:79576248..79579264-chr6:79581167..79583899,3	MCF-7	breast:
18	chr6:79584398..79586825-chr6:79590482..79592953,2	K562	blood:
19	chr6:79558999..79561726-chr6:79563730..79565524,2	K562	blood:
20	chr6:79595328..79597841-chr6:79600985..79603258,2	K562	blood:
21	chr6:79568772..79571138-chr6:79573163..79575541,2	K562	blood:
22	chr5:442727..443641-chr6:79590567..79591067,2	NB4	blood:

No data

Variant related genes	Relation type
IRAK1BP1	TF binding region
IRAK1BP1	CpG island
ENSG00000270362	chromatin interactions
ENSG00000221990	chromatin interactions
ENSG00000146247	chromatin interactions
ENSG00000146243	chromatin interactions
ENSG00000180104	chromatin interactions

Extended variants
information (count: 2412 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2412 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191892735	chr6:79539000-79539001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143406102	chr6:79539011-79539012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577754452	chr6:79539014-79539015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185768436	chr6:79539107-79539108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188634799	chr6:79539113-79539114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74910873	chr6:79539123-79539124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573757622	chr6:79539132-79539133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9343838	chr6:79539150-79539151	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs574933195	chr6:79539153-79539154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559295352	chr6:79539189-79539190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147151772	chr6:79539200-79539201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551777320	chr6:79539229-79539230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192779506	chr6:79539260-79539261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184218962	chr6:79539287-79539288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140350958	chr6:79539324-79539325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569780287	chr6:79539339-79539340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535513057	chr6:79539358-79539359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144315681	chr6:79539384-79539385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573820075	chr6:79539602-79539603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200223540	chr6:79539628-79539629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs80001607	chr6:79539632-79539633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34962848	chr6:79539633-79539634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34665735	chr6:79539639-79539640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397737457	chr6:79539640-79539641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201839084	chr6:79539641-79539642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542696529	chr6:79539662-79539663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188848928	chr6:79539685-79539686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573151571	chr6:79539689-79539690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545338774	chr6:79539691-79539692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35366557	chr6:79539695-79539696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191737285	chr6:79539718-79539719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531198324	chr6:79539770-79539771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113573548	chr6:79539776-79539777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561443304	chr6:79539802-79539803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368160194	chr6:79539849-79539850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150044965	chr6:79539858-79539859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184013264	chr6:79539876-79539877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373823048	chr6:79539927-79539928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561505333	chr6:79539962-79539963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs117566796	chr6:79540004-79540005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564306276	chr6:79540019-79540020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189097595	chr6:79540020-79540021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551317188	chr6:79540022-79540023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79770313	chr6:79540031-79540032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537326426	chr6:79540042-79540043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556766344	chr6:79540050-79540051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575102365	chr6:79540097-79540098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531758840	chr6:79540106-79540107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs16890324	chr6:79540109-79540110	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs536393222	chr6:79540134-79540135	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79539000-79539400	Enhancers	Hela-S3	cervix
2	chr6:79539600-79540200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr6:79539600-79541000	Enhancers	Rectal Mucosa Donor 29	rectum
4	chr6:79539600-79542000	Enhancers	Duodenum Mucosa	Duodenum
5	chr6:79540000-79540200	Enhancers	Fetal Intestine Small	intestine
6	chr6:79540200-79541200	Weak transcription	Fetal Intestine Small	intestine
7	chr6:79540200-79541400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:79540400-79542000	Enhancers	Fetal Intestine Large	intestine
9	chr6:79540600-79541600	Enhancers	Ovary	ovary
10	chr6:79540800-79541600	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr6:79541000-79541600	Enhancers	Pancreas	Pancrea
12	chr6:79541000-79542800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr6:79541200-79541400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:79541200-79542000	Enhancers	Brain Angular Gyrus	brain
15	chr6:79541200-79542000	Enhancers	Brain Cingulate Gyrus	brain
16	chr6:79541200-79542000	Enhancers	Brain Hippocampus Middle	brain
17	chr6:79541200-79542000	Enhancers	Right Atrium	heart
18	chr6:79541200-79542400	Enhancers	Fetal Intestine Small	intestine
19	chr6:79541400-79541600	Enhancers	Aorta	Aorta
20	chr6:79541400-79542000	Enhancers	Brain Substantia Nigra	brain
21	chr6:79541400-79542000	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr6:79541400-79542200	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr6:79541400-79542400	Enhancers	Left Ventricle	heart
24	chr6:79541400-79542400	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr6:79541400-79542800	Enhancers	HSMMtube	muscle
26	chr6:79541400-79543000	Enhancers	Fetal Heart	heart
27	chr6:79541600-79542000	Weak transcription	Pancreas	Pancrea
28	chr6:79541600-79542000	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr6:79541600-79542200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr6:79541600-79542200	Weak transcription	Ovary	ovary
31	chr6:79541600-79542600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr6:79542000-79542200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:79542000-79542400	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr6:79542000-79542600	Enhancers	Pancreas	Pancrea
35	chr6:79542000-79546400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr6:79542200-79542400	Enhancers	Ovary	ovary
37	chr6:79542800-79546200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr6:79546000-79546600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:79546200-79546600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:79546200-79547000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr6:79546400-79546800	Enhancers	Brain Cingulate Gyrus	brain
42	chr6:79548200-79548400	Enhancers	HSMMtube	muscle
43	chr6:79550600-79551200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr6:79550600-79551600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr6:79550600-79552800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:79550600-79554000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr6:79550600-79554000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr6:79550800-79551000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr6:79551200-79552200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr6:79551200-79554000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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