Variant report

Variant	nsv886038
Chromosome Location	chr6:66528177-67054961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:915)
CpG islands
(count:733)
Chromatin interactive
region (count:27)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:915 , 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	ATF2	chr6:66759094-66759332	GM12878	blood:	n/a	n/a
2	ATF2	chr6:66758631-66759010	GM12878	blood:	n/a	n/a
3	BACH1	chr6:66648198-66648208	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:66631918-66632340	GM12878	blood:	n/a	n/a
5	BATF	chr6:66631968-66632296	GM12878	blood:	n/a	n/a
6	BATF	chr6:66758953-66759296	GM12878	blood:	n/a	n/a
7	BATF	chr6:66760290-66760499	GM12878	blood:	n/a	chr6:66760390-66760401
8	BATF	chr6:66586611-66586861	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:66999794-67000063	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr6:66758646-66758963	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:66631997-66632283	GM12878	blood:	n/a	n/a
12	BCL11A	chr6:66631888-66632357	GM12878	blood:	n/a	n/a
13	BCL3	chr6:66631951-66632190	GM12878	blood:	n/a	n/a
14	BCL3	chr6:66528842-66529413	A549	lung:	n/a	n/a
15	BCLAF1	chr6:66631985-66632241	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:66900743-66901106	HepG2	liver:	n/a	n/a
17	BHLHE40	chr6:66719831-66719935	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:66632014-66632283	GM12878	blood:	n/a	n/a
19	CBX3	chr6:67017402-67017708	K562	blood:	n/a	n/a
20	CBX3	chr6:66883594-66883743	K562	blood:	n/a	n/a
21	CEBPB	chr6:66567639-66567742	K562	blood:	n/a	chr6:66567667-66567678
22	CEBPB	chr6:66545603-66545935	MCF-7	breast:	n/a	n/a
23	CEBPB	chr6:66622288-66622567	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:66813960-66814254	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr6:66869914-66870326	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:66997596-66997806	IMR90	lung:	n/a	chr6:66997640-66997651 chr6:66997661-66997672
27	CEBPB	chr6:66567522-66567838	IMR90	lung:	n/a	chr6:66567667-66567678
28	CEBPB	chr6:66701577-66701831	A549	lung:	n/a	chr6:66701690-66701701
29	CEBPB	chr6:66909130-66909176	H1-hESC	embryonic stem cell:	n/a	chr6:66909154-66909167
30	CEBPB	chr6:66799687-66799916	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:66578271-66578511	A549	lung:	n/a	chr6:66578345-66578356
32	CEBPB	chr6:66528925-66529488	A549	lung:	n/a	n/a
33	CEBPB	chr6:66711119-66711450	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:66765930-66766246	HepG2	liver:	n/a	chr6:66766074-66766085
35	CEBPB	chr6:66711140-66711453	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr6:66799727-66799937	A549	lung:	n/a	n/a
37	CEBPB	chr6:66529301-66529561	A549	lung:	n/a	n/a
38	CEBPB	chr6:66614129-66614403	HepG2	liver:	n/a	chr6:66614263-66614274
39	CEBPB	chr6:66947001-66947336	HepG2	liver:	n/a	chr6:66947231-66947240 chr6:66947229-66947240
40	CEBPB	chr6:66795134-66795326	HepG2	liver:	n/a	chr6:66795236-66795247
41	CEBPB	chr6:66997543-66997824	HepG2	liver:	n/a	chr6:66997640-66997651 chr6:66997661-66997672
42	CEBPB	chr6:66953294-66953525	HepG2	liver:	n/a	chr6:66953405-66953416
43	CEBPB	chr6:66792843-66793170	Hela-S3	cervix:	n/a	chr6:66792993-66793004
44	CEBPB	chr6:66952854-66953044	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr6:66578188-66578534	HepG2	liver:	n/a	chr6:66578345-66578356
46	CEBPB	chr6:66792839-66793182	IMR90	lung:	n/a	chr6:66792993-66793004
47	CEBPB	chr6:66976521-66976629	A549	lung:	n/a	n/a
48	CEBPB	chr6:66567548-66567824	A549	lung:	n/a	chr6:66567667-66567678
49	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
50	CEBPB	chr6:66701556-66701859	HepG2	liver:	n/a	chr6:66701690-66701701

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66804704-66804754	ProgFib	skin:	n/a
2	chr6:66804704-66804754	ProgFib	skin:	n/a
3	chr6:66804704-66804754	Caco-2	colon:	n/a
4	chr6:66804631-66804681	Caco-2	colon:	n/a
5	chr6:66819090-66819140	GM12892	blood:	n/a
6	chr6:66804704-66804754	NB4	blood:	n/a
7	chr6:66804261-66804311	HEK293	kidney:	embryo
8	chr6:66999374-66999424	HCT-116	colon:	n/a
9	chr6:66819090-66819140	MCF10A-Er-Src	breast:	n/a
10	chr6:66804631-66804681	HRPEpiC	eye:	n/a
11	chr6:66804631-66804681	ProgFib	skin:	n/a
12	chr6:66709543-66709593	NH-A	brain:	n/a
13	chr6:66709543-66709593	HMEC	breast:	n/a
14	chr6:67041119-67041169	AG10803	skin:	n/a
15	chr6:66708681-66708731	ECC-1	luminal epithelium:	n/a
16	chr6:67041119-67041169	HUVEC	blood vessel:	n/a
17	chr6:66708681-66708731	BE2_C	brain:	n/a
18	chr6:66804261-66804311	HMEC	breast:	n/a
19	chr6:66708681-66708731	GM12892	blood:	n/a
20	chr6:66804261-66804311	HCF	heart:	n/a
21	chr6:66709543-66709593	ProgFib	skin:	n/a
22	chr6:66999374-66999424	PrEC	prostate:	n/a
23	chr6:66804830-66804880	AG09309	skin:	n/a
24	chr6:66709459-66709509	NH-A	brain:	n/a
25	chr6:66999374-66999424	U87	brain:	n/a
26	chr6:66709543-66709593	H1-hESC	embryonic stem cell:	embryo
27	chr6:66804261-66804311	NHDF-neo	bronchial:	n/a
28	chr6:66804704-66804754	AG04449	skin:	fetal
29	chr6:67041119-67041169	ovcar-3	ovarian:	n/a
30	chr6:66804631-66804681	HCT-116	colon:	n/a
31	chr6:66708570-66708620	GM12891	blood:	n/a
32	chr6:66708681-66708731	HNPCEpiC	eye:	n/a
33	chr6:66804261-66804311	NH-A	brain:	n/a
34	chr6:66804631-66804681	GM19239	blood:	n/a
35	chr6:66804830-66804880	HRCEpiC	kidney:	n/a
36	chr6:66804830-66804880	HCF	heart:	n/a
37	chr6:66708570-66708620	HNPCEpiC	eye:	n/a
38	chr6:66804261-66804311	AG09319	gingival:	n/a
39	chr6:66804631-66804681	HMEC	breast:	n/a
40	chr6:66804261-66804311	NT2-D1	testis:	n/a
41	chr6:66804261-66804311	Jurkat	blood:	n/a
42	chr6:66800878-66800928	HRE	kidney:	n/a
43	chr6:66709459-66709509	MCF10A-Er-Src	breast:	n/a
44	chr6:66800878-66800928	ECC-1	luminal epithelium:	n/a
45	chr6:66709543-66709593	HRE	kidney:	n/a
46	chr6:66708681-66708731	HEK293	kidney:	embryo
47	chr6:66804830-66804880	ECC-1	luminal epithelium:	n/a
48	chr6:66999374-66999424	ECC-1	luminal epithelium:	n/a
49	chr6:66708570-66708620	IMR90	lung:	fetal
50	chr6:66709459-66709509	HAEpiC	amniotic membrane:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:149614783..149615556-chr6:66750597..66751356,2	MCF-7	breast:
2	chr6:66834810..66837020-chr6:68592934..68595671,2	K562	blood:
3	chr6:66666961..66669216-chr6:66669694..66671348,2	MCF-7	breast:
4	chr6:67008436..67009111-chr6:67048434..67049041,2	MCF-7	breast:
5	chr16:75498580..75499130-chr6:66933180..66934026,2	MCF-7	breast:
6	chr6:66753689..66755338-chr6:66756434..66758951,2	K562	blood:
7	chr6:66890125..66893594-chr6:66896979..66900309,4	MCF-7	breast:
8	chr6:66753689..66755338-chr6:66756434..66758951,2	K562	blood:
9	chr6:66774856..66776961-chr6:66781125..66783110,2	MCF-7	breast:
10	chr6:66920773..66922637-chr6:66924312..66926863,2	K562	blood:
11	chr6:66697645..66699348-chr6:66753143..66756102,2	K562	blood:
12	chr6:66920773..66922637-chr6:66924312..66926863,2	K562	blood:
13	chr6:66890125..66893594-chr6:66896979..66900309,4	MCF-7	breast:
14	chr6:66774856..66776961-chr6:66781125..66783110,2	MCF-7	breast:
15	chr6:66677113..66678881-chr6:66726026..66728195,2	K562	blood:
16	chr6:66677113..66678881-chr6:66726026..66728195,2	K562	blood:
17	chr6:66831523..66833173-chr6:66834003..66836411,2	K562	blood:
18	chr6:66666961..66669216-chr6:66669694..66671348,2	MCF-7	breast:
19	chr6:66677113..66680051-chr6:66725985..66728195,2	K562	blood:
20	chr6:66890023..66892025-chr6:66894680..66896595,2	K562	blood:
21	chr6:66831523..66833173-chr6:66834003..66836411,2	K562	blood:
22	chr6:66677113..66680051-chr6:66725985..66728195,2	K562	blood:
23	chr6:67008436..67009111-chr6:67048434..67049041,2	MCF-7	breast:
24	chr6:66697645..66699348-chr6:66753143..66756102,2	K562	blood:
25	chr6:67008535..67010196-chr6:67047890..67049548,2	MCF-7	breast:
26	chr6:67008535..67010196-chr6:67047890..67049548,2	MCF-7	breast:
27	chr6:66890023..66892025-chr6:66894680..66896595,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EYS-3	chr6:66547135-66547298	NONHSAT113376
2	lnc-PHF3-4	chr6:66844838-66844945	XLOC_005336
3	lnc-PHF3-4	chr6:66858257-66858338	XLOC_005336
4	lnc-PHF3-4	chr6:66845987-66846228	XLOC_005336
5	lnc-PHF3-4	chr6:66886174-66886208	XLOC_005336
6	lnc-EYS-3	chr6:66546777-66547055	NONHSAT113376
7	lnc-PHF3-4	chr6:66848830-66848991	XLOC_005336

No data

Variant related genes	Relation type
NUFIP1P	TF binding region
ADH5P4	TF binding region
NUFIP1P	CpG island
ADH5P4	CpG island
ENSG00000261717	chromatin interactions
ENSG00000166822	chromatin interactions

Extended variants
information (count: 6683 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:6683 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4299807	chr6:66528177-66528178	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541863840	chr6:66528184-66528185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374310459	chr6:66528207-66528208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4585540	chr6:66528260-66528261	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs530485939	chr6:66528274-66528275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4318861	chr6:66528299-66528300	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs564353974	chr6:66528309-66528310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539995048	chr6:66528310-66528311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533303427	chr6:66528347-66528348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184293929	chr6:66528352-66528353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35854702	chr6:66528385-66528386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566613620	chr6:66528430-66528431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558689562	chr6:66528446-66528447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549421730	chr6:66528456-66528457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569031219	chr6:66528479-66528480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537827740	chr6:66528542-66528543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189032917	chr6:66528577-66528578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145128892	chr6:66528587-66528588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534558014	chr6:66528598-66528599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533207343	chr6:66528599-66528600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17506908	chr6:66528633-66528634	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs574139093	chr6:66528658-66528659	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs542869664	chr6:66528677-66528678	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs142252856	chr6:66528694-66528695	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs369549875	chr6:66528695-66528696	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs17416004	chr6:66528700-66528701	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs544214522	chr6:66528713-66528714	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs35925081	chr6:66528795-66528796	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs9445587	chr6:66528807-66528808	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs540477754	chr6:66528828-66528829	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs541795269	chr6:66528859-66528860	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs10498836	chr6:66528870-66528871	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs193200198	chr6:66528871-66528872	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs548792643	chr6:66528889-66528890	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs568994319	chr6:66528901-66528902	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs571511127	chr6:66528964-66528965	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs112439056	chr6:66528978-66528979	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs9445588	chr6:66529001-66529002	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs185372821	chr6:66529018-66529019	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs9445589	chr6:66529019-66529020	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs9445590	chr6:66529038-66529039	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs567888937	chr6:66529076-66529077	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs371088404	chr6:66529089-66529090	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs536834218	chr6:66529098-66529099	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs577019453	chr6:66529135-66529136	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs9453425	chr6:66529175-66529176	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs13213214	chr6:66529201-66529202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537890539	chr6:66529249-66529250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9445591	chr6:66529257-66529258	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577530997	chr6:66529261-66529262	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66526600-66528600	Enhancers	A549	lung
2	chr6:66528600-66529200	Flanking Active TSS	A549	lung
3	chr6:66529200-66529400	Enhancers	A549	lung
4	chr6:66529400-66529600	Flanking Active TSS	A549	lung
5	chr6:66529600-66530400	Enhancers	A549	lung
6	chr6:66536400-66536800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:66567000-66567400	Active TSS	Primary T cells from cord blood	blood
8	chr6:66567200-66567400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:66583200-66583800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:66583200-66583800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr6:66583200-66585000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:66583200-66585400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr6:66583400-66584600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:66583400-66584800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr6:66583600-66584200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:66583600-66585000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:66584400-66586800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:66585000-66586200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr6:66586200-66586400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr6:66602600-66602800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr6:66602800-66604600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:66609800-66610400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr6:66622600-66623000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:66633600-66634000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr6:66633600-66634000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:66634000-66634400	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr6:66634000-66634800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr6:66634400-66636000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr6:66634800-66635000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr6:66635000-66635400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr6:66635400-66635800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr6:66635600-66636000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:66635600-66636000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:66635600-66636200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:66640000-66640200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:66640200-66641400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:66640200-66641600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:66641600-66641800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr6:66641800-66645200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr6:66645200-66645600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:66647400-66647800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr6:66647400-66647800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr6:66647400-66648400	Enhancers	Ovary	ovary
44	chr6:66647800-66648200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:66647800-66648200	Enhancers	Fetal Muscle Leg	muscle
46	chr6:66648200-66648400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:66648400-66653400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:66648400-66653600	Weak transcription	Ovary	ovary
49	chr6:66649000-66649200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:66649200-66650400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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