Variant report

Variant	esv3385640
Chromosome Location	chr6:71997681-71999879
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:379)
CpG islands
(count:489)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:71998373-71998481	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr6:71997741-71997991	GM12878	blood:	n/a	n/a
3	BCL11A	chr6:71997761-71998058	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:71998494-71998737	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:71997710-71998207	GM12878	blood:	n/a	n/a
6	BRCA1	chr6:71999239-71999620	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr6:71997992-71998249	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr6:71998354-71998725	K562	blood:	n/a	n/a
9	CEBPB	chr6:71997872-71998666	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:71999833-72000643	Hela-S3	cervix:	n/a	chr6:72000467-72000478
11	CHD1	chr6:71998399-71998744	GM12878	blood:	n/a	n/a
12	CHD1	chr6:71998606-71999437	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr6:71997852-71998706	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr6:71997795-71998257	GM12878	blood:	n/a	n/a
15	CREB1	chr6:71997993-71998698	A549	lung:	n/a	n/a
16	CTBP2	chr6:71997949-71998546	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr6:71998440-71998590	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr6:71998453-71998586	Medullo	brain:	n/a	n/a
19	CTCF	chr6:71998420-71998570	NHEK	skin:	n/a	n/a
20	CTCF	chr6:71998417-71998607	GM12891	blood:	n/a	n/a
21	CTCF	chr6:71998400-71998614	ProgFib	skin:	n/a	n/a
22	CTCF	chr6:71998440-71998590	GM12869	blood:	n/a	n/a
23	CTCF	chr6:71998440-71998590	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr6:71998420-71998570	GM12865	blood:	n/a	n/a
25	CTCF	chr6:71998319-71998676	IMR90	lung:	n/a	chr6:71998393-71998406 chr6:71998368-71998377
26	CTCF	chr6:71998440-71998590	GM12866	blood:	n/a	n/a
27	CTCF	chr6:71998421-71998660	HepG2	liver:	n/a	n/a
28	CTCF	chr6:71998451-71998585	GM13976	blood:	n/a	n/a
29	CTCF	chr6:71998410-71998622	NHEK	skin:	n/a	n/a
30	CTCF	chr6:71998420-71998570	SAEC	small airway:	n/a	n/a
31	CTCF	chr6:71998840-71998990	GM12866	blood:	n/a	chr6:71998968-71998981
32	CTCF	chr6:71998420-71998570	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr6:71998425-71998630	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:71998455-71998626	Lung_OC	lung:	n/a	n/a
35	CTCF	chr6:71998380-71998530	BJ	skin:	n/a	chr6:71998393-71998406
36	CTCF	chr6:71998400-71998550	HEK293	kidney:	n/a	n/a
37	CTCF	chr6:71998391-71998672	T-47D	breast:	n/a	chr6:71998393-71998406
38	CTCF	chr6:71998380-71998530	HCT-116	colon:	n/a	chr6:71998393-71998406
39	CTCF	chr6:71998520-71998670	HepG2	liver:	n/a	n/a
40	CTCF	chr6:71998429-71998609	GM20000	blood:	n/a	n/a
41	CTCF	chr6:71998360-71998510	GM12864	blood:	n/a	chr6:71998393-71998406 chr6:71998368-71998377
42	CTCF	chr6:71998455-71998573	LNCaP	prostate:	n/a	n/a
43	CTCF	chr6:71998420-71998570	HPF	lung:	n/a	n/a
44	CTCF	chr6:71998420-71998570	HAc	cerebellar:	n/a	n/a
45	CTCF	chr6:71998480-71998630	GM12867	blood:	n/a	n/a
46	CTCF	chr6:71998340-71998490	GM12875	blood:	n/a	chr6:71998393-71998406 chr6:71998368-71998377
47	CTCF	chr6:71998840-71998990	GM12865	blood:	n/a	chr6:71998968-71998981
48	CTCF	chr6:71998354-71998641	H1-hESC	embryonic stem cell:	n/a	chr6:71998393-71998406 chr6:71998368-71998377
49	CTCF	chr6:71998420-71998570	AG04449	skin:	n/a	n/a
50	CTCF	chr6:71998437-71998589	H1-hESC	embryonic stem cell:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:71999108-71999158	HNPCEpiC	eye:	n/a
2	chr6:71999108-71999158	HNPCEpiC	eye:	n/a
3	chr6:71998145-71998195	HPAEpiC	pulmonary alveolar:	n/a
4	chr6:71998145-71998195	AG04449	skin:	fetal
5	chr6:71998385-71998435	PFSK-1	brain:	n/a
6	chr6:71999105-71999155	HCF	heart:	n/a
7	chr6:71998597-71998647	BE2_C	brain:	n/a
8	chr6:71999385-71999435	HCPEpiC	choroid plexus:	n/a
9	chr6:71998398-71998448	HMEC	breast:	n/a
10	chr6:71999385-71999435	HCM	heart:	n/a
11	chr6:71998385-71998435	PANC-1	pancreas:	n/a
12	chr6:71998597-71998647	Jurkat	blood:	n/a
13	chr6:71998385-71998435	AG09319	gingival:	n/a
14	chr6:71999062-71999112	GM12878	blood:	n/a
15	chr6:71998597-71998647	HepG2	liver:	n/a
16	chr6:71999062-71999112	AoSMC	blood vessel:	n/a
17	chr6:71999105-71999155	HAEpiC	amniotic membrane:	n/a
18	chr6:71998597-71998647	AG10803	skin:	n/a
19	chr6:71998145-71998195	NHBE	bronchial:	n/a
20	chr6:71999062-71999112	PANC-1	pancreas:	n/a
21	chr6:71998597-71998647	PANC-1	pancreas:	n/a
22	chr6:71998385-71998435	MCF10A-Er-Src	breast:	n/a
23	chr6:71999385-71999435	NHDF-neo	bronchial:	n/a
24	chr6:71998145-71998195	U87	brain:	n/a
25	chr6:71999108-71999158	GM12891	blood:	n/a
26	chr6:71998145-71998195	BJ	skin:	n/a
27	chr6:71998385-71998435	U87	brain:	n/a
28	chr6:71998385-71998435	BJ	skin:	n/a
29	chr6:71998597-71998647	HRE	kidney:	n/a
30	chr6:71998145-71998195	HEK293	kidney:	embryo
31	chr6:71998597-71998647	GM06990	blood:	n/a
32	chr6:71998145-71998195	HMEC	breast:	n/a
33	chr6:71998597-71998647	Hepatocyte	liver:	n/a
34	chr6:71998597-71998647	HMEC	breast:	n/a
35	chr6:71998385-71998435	HEEpiC	esophagus:	n/a
36	chr6:71999062-71999112	LNCaP	prostate:	n/a
37	chr6:71998398-71998448	A549	lung:	n/a
38	chr6:71999105-71999155	K562	blood:	n/a
39	chr6:71999062-71999112	HRE	kidney:	n/a
40	chr6:71998145-71998195	LNCaP	prostate:	n/a
41	chr6:71999385-71999435	Hela-S3	cervix:	n/a
42	chr6:71999105-71999155	SK-N-SH	brain:	n/a
43	chr6:71998597-71998647	PFSK-1	brain:	n/a
44	chr6:71999385-71999435	RPTEC	kidney:	n/a
45	chr6:71999062-71999112	HEEpiC	esophagus:	n/a
46	chr6:71998597-71998647	MCF10A-Er-Src	breast:	n/a
47	chr6:71999385-71999435	SKMC	muscle:	n/a
48	chr6:71999062-71999112	SAEC	small airway:	n/a
49	chr6:71998145-71998195	AG09309	skin:	n/a
50	chr6:71998145-71998195	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:71997812..71999868-chr6:72020711..72023495,2	MCF-7	breast:

No data

Variant related genes	Relation type
OGFRL1	TF binding region
ENSG00000232295	TF binding region
OGFRL1	CpG island
ENSG00000232295	CpG island
ENSG00000232295	chromatin interactions

Extended variants
information (count: 67 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:67 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560967044	chr6:71997686-71997687	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs186667716	chr6:71997726-71997727	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs536018024	chr6:71997729-71997730	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs554181600	chr6:71997755-71997756	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs190824811	chr6:71997795-71997796	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs553603278	chr6:71997799-71997800	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs143789687	chr6:71997822-71997823	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs546088227	chr6:71997890-71997891	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564581183	chr6:71997983-71997984	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs182643965	chr6:71997997-71997998	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs185543093	chr6:71998023-71998024	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs6913383	chr6:71998031-71998032	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs529863981	chr6:71998070-71998071	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548400030	chr6:71998108-71998109	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs560366265	chr6:71998114-71998115	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190251500	chr6:71998131-71998132	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527631947	chr6:71998139-71998140	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs6935796	chr6:71998162-71998163	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs570867124	chr6:71998166-71998167	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs116039266	chr6:71998198-71998199	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs182162213	chr6:71998222-71998223	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs568504710	chr6:71998224-71998225	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535560449	chr6:71998258-71998259	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554395015	chr6:71998283-71998284	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546110366	chr6:71998412-71998413	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562615714	chr6:71998422-71998423	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557984940	chr6:71998550-71998551	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs576453463	chr6:71998624-71998625	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544160797	chr6:71998651-71998652	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs376036358	chr6:71998654-71998655	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs368114977	chr6:71998724-71998725	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs555871898	chr6:71998769-71998770	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112585190	chr6:71998778-71998779	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs541556627	chr6:71998796-71998797	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs560427561	chr6:71998799-71998800	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs527442325	chr6:71998894-71998895	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546121672	chr6:71998941-71998942	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564341804	chr6:71998952-71998953	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531620075	chr6:71998955-71998956	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs550180995	chr6:71999041-71999042	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs139728781	chr6:71999046-71999047	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs146979013	chr6:71999070-71999071	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529430421	chr6:71999084-71999085	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs76452774	chr6:71999145-71999146	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs12190948	chr6:71999150-71999151	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs7741988	chr6:71999242-71999243	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs187918937	chr6:71999349-71999350	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7756709	chr6:71999351-71999352	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs191907750	chr6:71999354-71999355	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs556169538	chr6:71999384-71999385	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20409316	CNVD

Chromatin state (count:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71988400-71997800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:71991600-71997800	Weak transcription	Lung	lung
3	chr6:71992000-71997800	Weak transcription	Esophagus	oesophagus
4	chr6:71994200-71997800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:71994800-71997800	Weak transcription	Gastric	stomach
6	chr6:71996800-71997800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:71996800-71997800	Enhancers	Fetal Thymus	thymus
8	chr6:71996800-71997800	Enhancers	Stomach Mucosa	stomach
9	chr6:71996800-71998000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr6:71996800-71998200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr6:71997000-71997800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr6:71997000-71997800	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr6:71997000-71997800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr6:71997000-71997800	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr6:71997000-71997800	Enhancers	HMEC	breast
16	chr6:71997000-71998000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:71997000-71998000	Flanking Active TSS	NHDF-Ad	bronchial
18	chr6:71997000-71998400	Flanking Active TSS	Primary B cells from cord blood	blood
19	chr6:71997000-71998400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:71997000-71999800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr6:71997000-72002000	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr6:71997200-71997800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr6:71997200-71997800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr6:71997200-71997800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:71997200-71997800	Flanking Active TSS	Brain Cingulate Gyrus	brain
26	chr6:71997200-71997800	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr6:71997200-71997800	Enhancers	Fetal Muscle Leg	muscle
28	chr6:71997200-71997800	Enhancers	HSMM	muscle
29	chr6:71997200-71998400	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr6:71997200-71998400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:71997200-72000400	Active TSS	A549	lung
32	chr6:71997400-71997800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr6:71997400-71997800	Enhancers	Colonic Mucosa	Colon
34	chr6:71997400-71997800	Enhancers	Fetal Stomach	stomach
35	chr6:71997400-71997800	Enhancers	Right Ventricle	heart
36	chr6:71997400-71998000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:71997400-71998000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr6:71997400-71998000	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr6:71997400-71998000	Flanking Active TSS	Brain Angular Gyrus	brain
40	chr6:71997400-71998000	Enhancers	Small Intestine	intestine
41	chr6:71997400-71998200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
42	chr6:71997400-71998200	Flanking Active TSS	Primary B cells from peripheral blood	blood
43	chr6:71997400-71998200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:71997400-71998200	Flanking Active TSS	Colon Smooth Muscle	Colon
45	chr6:71997400-71998200	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr6:71997400-71998400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr6:71997400-71999400	Active TSS	Brain Anterior Caudate	brain
48	chr6:71997400-72000000	Active TSS	Rectal Smooth Muscle	rectum
49	chr6:71997400-72000400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr6:71997600-71997800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

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