Variant report

Variant	nsv886034
Chromosome Location	chr6:66450739-66622346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:394)
CpG islands
(count:489)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:394 , 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	BATF	chr6:66586611-66586861	GM12878	blood:	n/a	n/a
2	BCL3	chr6:66528842-66529413	A549	lung:	n/a	n/a
3	CEBPB	chr6:66545603-66545935	MCF-7	breast:	n/a	n/a
4	CEBPB	chr6:66528925-66529488	A549	lung:	n/a	n/a
5	CEBPB	chr6:66612801-66613079	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr6:66622288-66622567	HepG2	liver:	n/a	n/a
7	CEBPB	chr6:66614206-66614285	H1-hESC	embryonic stem cell:	n/a	chr6:66614263-66614274
8	CEBPB	chr6:66529301-66529561	A549	lung:	n/a	n/a
9	CEBPB	chr6:66490682-66491041	A549	lung:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
10	CEBPB	chr6:66516355-66516697	HepG2	liver:	n/a	chr6:66516524-66516535
11	CEBPB	chr6:66578271-66578511	A549	lung:	n/a	chr6:66578345-66578356
12	CEBPB	chr6:66561620-66562087	MCF-7	breast:	n/a	n/a
13	CEBPB	chr6:66614129-66614403	HepG2	liver:	n/a	chr6:66614263-66614274
14	CEBPB	chr6:66516356-66516600	A549	lung:	n/a	chr6:66516524-66516535
15	CEBPB	chr6:66587515-66587847	HepG2	liver:	n/a	chr6:66587664-66587673 chr6:66587662-66587675 chr6:66587663-66587674 chr6:66587664-66587673 chr6:66587664-66587673 chr6:66587662-66587675 chr6:66587662-66587673 chr6:66587664-66587673
16	CEBPB	chr6:66567548-66567824	A549	lung:	n/a	chr6:66567667-66567678
17	CEBPB	chr6:66612899-66613087	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr6:66561662-66562163	MCF-7	breast:	n/a	n/a
19	CEBPB	chr6:66490610-66490962	A549	lung:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
20	CEBPB	chr6:66578188-66578534	HepG2	liver:	n/a	chr6:66578345-66578356
21	CEBPB	chr6:66516368-66516688	IMR90	lung:	n/a	chr6:66516524-66516535
22	CEBPB	chr6:66490606-66490975	HepG2	liver:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
23	CEBPB	chr6:66567524-66567835	HepG2	liver:	n/a	chr6:66567667-66567678
24	CEBPB	chr6:66567638-66567691	H1-hESC	embryonic stem cell:	n/a	chr6:66567667-66567678
25	CEBPB	chr6:66490621-66490964	K562	blood:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
26	CEBPB	chr6:66490661-66490950	H1-hESC	embryonic stem cell:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
27	CEBPB	chr6:66567522-66567838	IMR90	lung:	n/a	chr6:66567667-66567678
28	CEBPB	chr6:66567639-66567742	K562	blood:	n/a	chr6:66567667-66567678
29	CEBPB	chr6:66490602-66490966	IMR90	lung:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
30	CHD2	chr6:66571590-66571683	HepG2	liver:	n/a	n/a
31	CHD2	chr6:66486288-66486596	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr6:66457784-66457814	GM13976	blood:	n/a	n/a
33	CTCF	chr6:66504547-66504840	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:66456383-66456463	MCF-7	breast:	n/a	n/a
35	CTCF	chr6:66486297-66486582	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:66486325-66486500	HepG2	liver:	n/a	n/a
37	CTCF	chr6:66504554-66504853	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:66504625-66504814	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:66486366-66486522	HepG2	liver:	n/a	n/a
40	CTCF	chr6:66486380-66486530	BE2_C	brain:	n/a	n/a
41	CTCF	chr6:66454700-66454850	GM12869	blood:	n/a	n/a
42	CTCF	chr6:66486400-66486550	BE2_C	brain:	n/a	n/a
43	CTCF	chr6:66486360-66486510	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr6:66486419-66486467	GM12878	blood:	n/a	n/a
45	CTCF	chr6:66536340-66536490	GM12869	blood:	n/a	n/a
46	CTCF	chr6:66482150-66482169	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:66486320-66486470	HPF	lung:	n/a	n/a
48	CTCF	chr6:66486360-66486510	HEK293	kidney:	n/a	n/a
49	CTCF	chr6:66486360-66486510	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr6:66558120-66558270	BE2_C	brain:	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	chr6:66493769-66493819	ovcar-3	ovarian:	n/a
2	chr6:66493769-66493819	ovcar-3	ovarian:	n/a
3	chr6:66493769-66493819	HL-60	blood:	n/a
4	chr6:66496346-66496396	GM12891	blood:	n/a
5	chr6:66493769-66493819	HEK293	kidney:	embryo
6	chr6:66497746-66497796	CMK	blood:	n/a
7	chr6:66497746-66497796	HUVEC	blood vessel:	n/a
8	chr6:66498734-66498784	AG10803	skin:	n/a
9	chr6:66493769-66493819	GM12891	blood:	n/a
10	chr6:66496955-66497005	ovcar-3	ovarian:	n/a
11	chr6:66498032-66498082	ECC-1	luminal epithelium:	n/a
12	chr6:66493769-66493819	Hela-S3	cervix:	n/a
13	chr6:66496346-66496396	RPTEC	kidney:	n/a
14	chr6:66498734-66498784	HRPEpiC	eye:	n/a
15	chr6:66497885-66497935	T-47D	breast:	n/a
16	chr6:66493769-66493819	HEEpiC	esophagus:	n/a
17	chr6:66493769-66493819	PrEC	prostate:	n/a
18	chr6:66493769-66493819	SKMC	muscle:	n/a
19	chr6:66497586-66497636	HRPEpiC	eye:	n/a
20	chr6:66497746-66497796	HAEpiC	amniotic membrane:	n/a
21	chr6:66498032-66498082	BE2_C	brain:	n/a
22	chr6:66498734-66498784	HCF	heart:	n/a
23	chr6:66497885-66497935	HepG2	liver:	n/a
24	chr6:66496955-66497005	BJ	skin:	n/a
25	chr6:66497885-66497935	Hela-S3	cervix:	n/a
26	chr6:66496346-66496396	HCF	heart:	n/a
27	chr6:66497746-66497796	GM12878	blood:	n/a
28	chr6:66498734-66498784	CMK	blood:	n/a
29	chr6:66496955-66497005	NT2-D1	testis:	n/a
30	chr6:66496346-66496396	HIPEpiC	eye:	n/a
31	chr6:66497885-66497935	HRPEpiC	eye:	n/a
32	chr6:66498032-66498082	HUVEC	blood vessel:	n/a
33	chr6:66497586-66497636	H1-hESC	embryonic stem cell:	embryo
34	chr6:66498032-66498082	AG09319	gingival:	n/a
35	chr6:66497586-66497636	K562	blood:	n/a
36	chr6:66496346-66496396	SKMC	muscle:	n/a
37	chr6:66498734-66498784	MCF-7	breast:	n/a
38	chr6:66493769-66493819	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:66497885-66497935	HRE	kidney:	n/a
40	chr6:66498734-66498784	Caco-2	colon:	n/a
41	chr6:66498734-66498784	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:66497885-66497935	HEEpiC	esophagus:	n/a
43	chr6:66497586-66497636	U87	brain:	n/a
44	chr6:66498734-66498784	HIPEpiC	eye:	n/a
45	chr6:66497746-66497796	HRPEpiC	eye:	n/a
46	chr6:66498734-66498784	GM12891	blood:	n/a
47	chr6:66493769-66493819	Caco-2	colon:	n/a
48	chr6:66496955-66497005	HRCEpiC	kidney:	n/a
49	chr6:66496346-66496396	HCM	heart:	n/a
50	chr6:66497885-66497935	NT2-D1	testis:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:66470336..66472055-chr6:66477425..66479118,2	MCF-7	breast:
2	chr6:66519719..66521224-chr6:66523574..66525753,2	MCF-7	breast:
3	chr6:66515870..66517560-chr6:66518458..66521035,2	MCF-7	breast:
4	chr6:66515870..66517560-chr6:66518458..66521035,2	MCF-7	breast:
5	chr6:66470336..66472055-chr6:66477425..66479118,2	MCF-7	breast:
6	chr6:66519719..66521224-chr6:66523574..66525753,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EYS-3	chr6:66547135-66547298	NONHSAT113376
2	lnc-EYS-3	chr6:66546777-66547055	NONHSAT113376

No data

Variant related genes	Relation type
SLC25A51P1	TF binding region
ADH5P4	TF binding region
SLC25A51P1	CpG island
ADH5P4	CpG island

Extended variants
information (count: 1049 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1049 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190146648	chr6:66456232-66456233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144117372	chr6:66456233-66456234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548388925	chr6:66456234-66456235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561022730	chr6:66456238-66456239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182768348	chr6:66456255-66456256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186856606	chr6:66456267-66456268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191993498	chr6:66456285-66456286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79920717	chr6:66456289-66456290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552471860	chr6:66456296-66456297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565996372	chr6:66456297-66456298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2636129	chr6:66456318-66456319	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs2636130	chr6:66456319-66456320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554835415	chr6:66456327-66456328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574874912	chr6:66456349-66456350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532227554	chr6:66456360-66456361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150558892	chr6:66456361-66456362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557435822	chr6:66456362-66456363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373592453	chr6:66456363-66456364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547250317	chr6:66456372-66456373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12526256	chr6:66456442-66456443	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs62409474	chr6:66456443-66456444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs551452819	chr6:66456464-66456465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569596924	chr6:66456474-66456475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573235102	chr6:66456496-66456497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541998015	chr6:66456507-66456508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562189936	chr6:66456526-66456527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535113683	chr6:66456588-66456589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149686037	chr6:66456599-66456600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560359656	chr6:66470280-66470281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560240529	chr6:66470300-66470301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9453394	chr6:66470303-66470304	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs9453395	chr6:66470306-66470307	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs151250177	chr6:66470328-66470329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531917334	chr6:66470363-66470364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570973793	chr6:66470394-66470395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9360152	chr6:66470416-66470417	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs145348045	chr6:66470417-66470418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539122867	chr6:66470433-66470434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546681839	chr6:66470437-66470438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147651336	chr6:66470462-66470463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532030202	chr6:66470472-66470473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542250073	chr6:66470534-66470535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555227081	chr6:66470571-66470572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575188331	chr6:66470590-66470591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189420662	chr6:66470631-66470632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142254913	chr6:66470636-66470637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4492179	chr6:66470669-66470670	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs540339739	chr6:66470681-66470682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560584172	chr6:66470682-66470683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181019493	chr6:66470703-66470704	Enhancers	n/a	n/a	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	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
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	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
Cancer	20164919	CNVD
Retinitis pigmentosa	21519034	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66456200-66456600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:66470200-66470600	Enhancers	A549	lung
3	chr6:66470200-66471000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:66470200-66473000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:66475000-66475200	Bivalent Enhancer	Fetal Heart	heart
6	chr6:66475200-66477800	Enhancers	Fetal Heart	heart
7	chr6:66476400-66476600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr6:66479000-66479200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr6:66481600-66482200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:66481600-66482200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:66481800-66482000	Enhancers	Gastric	stomach
12	chr6:66481800-66482200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:66482000-66482400	ZNF genes & repeats	Gastric	stomach
14	chr6:66483800-66484600	Enhancers	Fetal Heart	heart
15	chr6:66486200-66486400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr6:66486200-66486800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:66486200-66486800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr6:66496800-66497000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:66497200-66497600	Enhancers	Placenta	Placenta
20	chr6:66497600-66498000	Active TSS	Placenta	Placenta
21	chr6:66500000-66501200	Enhancers	Fetal Stomach	stomach
22	chr6:66500400-66501000	Enhancers	Fetal Lung	lung
23	chr6:66515200-66515600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:66522000-66523000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:66522200-66523000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:66526600-66528600	Enhancers	A549	lung
27	chr6:66528600-66529200	Flanking Active TSS	A549	lung
28	chr6:66529200-66529400	Enhancers	A549	lung
29	chr6:66529400-66529600	Flanking Active TSS	A549	lung
30	chr6:66529600-66530400	Enhancers	A549	lung
31	chr6:66536400-66536800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:66567000-66567400	Active TSS	Primary T cells from cord blood	blood
33	chr6:66567200-66567400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:66583200-66583800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr6:66583200-66583800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr6:66583200-66585000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:66583200-66585400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:66583400-66584600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:66583400-66584800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr6:66583600-66584200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:66583600-66585000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr6:66584400-66586800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:66585000-66586200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr6:66586200-66586400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr6:66602600-66602800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr6:66602800-66604600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:66609800-66610400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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