Variant report

Variant	nsv886032
Chromosome Location	chr6:66278575-66622346
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	BACH1	chr6:66284867-66284905	K562	blood:	n/a	n/a
2	BACH1	chr6:66297779-66297795	K562	blood:	n/a	n/a
3	BATF	chr6:66356413-66356758	GM12878	blood:	n/a	n/a
4	BATF	chr6:66586611-66586861	GM12878	blood:	n/a	n/a
5	BCL3	chr6:66528842-66529413	A549	lung:	n/a	n/a
6	BRCA1	chr6:66378211-66378498	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr6:66324927-66325066	K562	blood:	n/a	n/a
8	CEBPB	chr6:66288426-66288597	HepG2	liver:	n/a	chr6:66288554-66288565
9	CEBPB	chr6:66404594-66404863	HepG2	liver:	n/a	chr6:66404777-66404786 chr6:66404777-66404786 chr6:66404777-66404786
10	CEBPB	chr6:66343306-66343713	MCF-7	breast:	n/a	chr6:66343568-66343579 chr6:66343530-66343541
11	CEBPB	chr6:66336830-66337334	A549	lung:	n/a	chr6:66337098-66337109
12	CEBPB	chr6:66343281-66343819	MCF-7	breast:	n/a	chr6:66343568-66343579 chr6:66343530-66343541
13	CEBPB	chr6:66567522-66567838	IMR90	lung:	n/a	chr6:66567667-66567678
14	CEBPB	chr6:66614129-66614403	HepG2	liver:	n/a	chr6:66614263-66614274
15	CEBPB	chr6:66336957-66337259	H1-hESC	embryonic stem cell:	n/a	chr6:66337098-66337109
16	CEBPB	chr6:66561662-66562163	MCF-7	breast:	n/a	n/a
17	CEBPB	chr6:66347922-66348400	MCF-7	breast:	n/a	n/a
18	CEBPB	chr6:66343413-66343709	HepG2	liver:	n/a	chr6:66343568-66343579 chr6:66343530-66343541
19	CEBPB	chr6:66567524-66567835	HepG2	liver:	n/a	chr6:66567667-66567678
20	CEBPB	chr6:66490606-66490975	HepG2	liver:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
21	CEBPB	chr6:66614206-66614285	H1-hESC	embryonic stem cell:	n/a	chr6:66614263-66614274
22	CEBPB	chr6:66305546-66305732	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr6:66404649-66404900	K562	blood:	n/a	chr6:66404777-66404786 chr6:66404777-66404786 chr6:66404777-66404786
24	CEBPB	chr6:66490661-66490950	H1-hESC	embryonic stem cell:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
25	CEBPB	chr6:66378201-66378540	MCF-7	breast:	n/a	n/a
26	CEBPB	chr6:66305457-66305787	A549	lung:	n/a	n/a
27	CEBPB	chr6:66336963-66337249	ECC-1	luminal epithelium:	n/a	chr6:66337098-66337109
28	CEBPB	chr6:66404609-66404903	IMR90	lung:	n/a	chr6:66404777-66404786 chr6:66404777-66404786 chr6:66404777-66404786
29	CEBPB	chr6:66622288-66622567	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:66490610-66490962	A549	lung:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
31	CEBPB	chr6:66348020-66348319	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:66528925-66529488	A549	lung:	n/a	n/a
33	CEBPB	chr6:66336928-66337275	MCF-7	breast:	n/a	chr6:66337098-66337109
34	CEBPB	chr6:66343407-66343718	Hela-S3	cervix:	n/a	chr6:66343568-66343579 chr6:66343530-66343541
35	CEBPB	chr6:66490602-66490966	IMR90	lung:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
36	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
37	CEBPB	chr6:66578188-66578534	HepG2	liver:	n/a	chr6:66578345-66578356
38	CEBPB	chr6:66529301-66529561	A549	lung:	n/a	n/a
39	CEBPB	chr6:66561620-66562087	MCF-7	breast:	n/a	n/a
40	CEBPB	chr6:66612801-66613079	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr6:66305442-66305793	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr6:66336926-66337285	A549	lung:	n/a	chr6:66337098-66337109
43	CEBPB	chr6:66516368-66516688	IMR90	lung:	n/a	chr6:66516524-66516535
44	CEBPB	chr6:66348053-66348238	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:66578271-66578511	A549	lung:	n/a	chr6:66578345-66578356
46	CEBPB	chr6:66490621-66490964	K562	blood:	n/a	chr6:66490776-66490789 chr6:66490777-66490788
47	CEBPB	chr6:66378100-66379021	MCF-7	breast:	n/a	n/a
48	CEBPB	chr6:66336928-66337282	K562	blood:	n/a	chr6:66337098-66337109
49	CEBPB	chr6:66378284-66378484	A549	lung:	n/a	n/a
50	CEBPB	chr6:66336913-66337289	HepG2	liver:	n/a	chr6:66337098-66337109

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66337526-66337576	Jurkat	blood:	n/a
2	chr6:66493769-66493819	HCM	heart:	n/a
3	chr6:66498032-66498082	H1-hESC	embryonic stem cell:	embryo
4	chr6:66337526-66337576	Jurkat	blood:	n/a
5	chr6:66493769-66493819	HCM	heart:	n/a
6	chr6:66498032-66498082	H1-hESC	embryonic stem cell:	embryo
7	chr6:66360569-66360619	K562	blood:	n/a
8	chr6:66497586-66497636	HMEC	breast:	n/a
9	chr6:66337526-66337576	SAEC	small airway:	n/a
10	chr6:66360569-66360619	HMEC	breast:	n/a
11	chr6:66493769-66493819	HIPEpiC	eye:	n/a
12	chr6:66497586-66497636	AG10803	skin:	n/a
13	chr6:66498032-66498082	SAEC	small airway:	n/a
14	chr6:66497586-66497636	RPTEC	kidney:	n/a
15	chr6:66279436-66279486	HEEpiC	esophagus:	n/a
16	chr6:66497746-66497796	HRCEpiC	kidney:	n/a
17	chr6:66496955-66497005	NH-A	brain:	n/a
18	chr6:66497586-66497636	MCF-7	breast:	n/a
19	chr6:66497746-66497796	NB4	blood:	n/a
20	chr6:66496955-66497005	SK-N-SH	brain:	n/a
21	chr6:66498032-66498082	PANC-1	pancreas:	n/a
22	chr6:66279436-66279486	Jurkat	blood:	n/a
23	chr6:66497586-66497636	AG09309	skin:	n/a
24	chr6:66360569-66360619	AG04450	lung:	fetal
25	chr6:66360569-66360619	HRE	kidney:	n/a
26	chr6:66497586-66497636	ProgFib	skin:	n/a
27	chr6:66497746-66497796	NHDF-neo	bronchial:	n/a
28	chr6:66497586-66497636	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:66496955-66497005	NHDF-neo	bronchial:	n/a
30	chr6:66498032-66498082	SK-N-MC	brain:	n/a
31	chr6:66496955-66497005	ProgFib	skin:	n/a
32	chr6:66497885-66497935	HRPEpiC	eye:	n/a
33	chr6:66496346-66496396	HPAEpiC	pulmonary alveolar:	n/a
34	chr6:66496346-66496396	AG09319	gingival:	n/a
35	chr6:66496955-66497005	HRE	kidney:	n/a
36	chr6:66497746-66497796	HL-60	blood:	n/a
37	chr6:66337526-66337576	AG10803	skin:	n/a
38	chr6:66337526-66337576	HCT-116	colon:	n/a
39	chr6:66497586-66497636	HRE	kidney:	n/a
40	chr6:66493769-66493819	GM12891	blood:	n/a
41	chr6:66360569-66360619	H1-hESC	embryonic stem cell:	embryo
42	chr6:66496955-66497005	K562	blood:	n/a
43	chr6:66498734-66498784	H1-hESC	embryonic stem cell:	embryo
44	chr6:66496955-66497005	HRPEpiC	eye:	n/a
45	chr6:66496955-66497005	NB4	blood:	n/a
46	chr6:66498032-66498082	SK-N-SH	brain:	n/a
47	chr6:66493769-66493819	IMR90	lung:	fetal
48	chr6:66497746-66497796	U87	brain:	n/a
49	chr6:66497586-66497636	GM12891	blood:	n/a
50	chr6:66337526-66337576	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:66249610..66251834-chr6:66299808..66302442,2	K562	blood:
2	chr6:66291419..66293216-chr6:66300613..66302642,2	K562	blood:
3	chr6:66389053..66391661-chr6:66392622..66394298,2	MCF-7	breast:
4	chr15:48090306..48091135-chr6:66342198..66342838,2	MCF-7	breast:
5	chr6:66515870..66517560-chr6:66518458..66521035,2	MCF-7	breast:
6	chr6:66389053..66391661-chr6:66392622..66394298,2	MCF-7	breast:
7	chr6:66366176..66367861-chr6:66369902..66372494,2	K562	blood:
8	chr6:66298118..66300419-chr6:66305829..66308285,2	K562	blood:
9	chr6:66470336..66472055-chr6:66477425..66479118,2	MCF-7	breast:
10	chr6:66344295..66347269-chr6:66347639..66350147,2	MCF-7	breast:
11	chr6:66470336..66472055-chr6:66477425..66479118,2	MCF-7	breast:
12	chr6:66519719..66521224-chr6:66523574..66525753,2	MCF-7	breast:
13	chr6:66291419..66293216-chr6:66300613..66302642,2	K562	blood:
14	chr6:66515870..66517560-chr6:66518458..66521035,2	MCF-7	breast:
15	chr6:66366176..66367861-chr6:66369902..66372494,2	K562	blood:
16	chr6:66344295..66347269-chr6:66347639..66350147,2	MCF-7	breast:
17	chr3:189034137..189034728-chr6:66401890..66402666,2	MCF-7	breast:
18	chr6:66519719..66521224-chr6:66523574..66525753,2	MCF-7	breast:
19	chr6:66298118..66300419-chr6:66305829..66308285,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EYS-3	chr6:66546777-66547055	NONHSAT113376
2	lnc-EYS-3	chr6:66547135-66547298	NONHSAT113376
3	lnc-LGSN-7	chr6:66349671-66349785	NONHSAT113373
4	lnc-LGSN-7	chr6:66417028-66417107	NONHSAT113373

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

Extended variants
information (count: 2653 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2653 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13203580	chr6:66278575-66278576	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371416135	chr6:66278684-66278685	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs543514935	chr6:66278689-66278690	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs572562049	chr6:66278730-66278731	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs200118563	chr6:66278736-66278737	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs544677679	chr6:66278790-66278791	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs532495720	chr6:66278816-66278817	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs552147372	chr6:66278869-66278870	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs565778738	chr6:66278917-66278918	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs571118717	chr6:66279011-66279012	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs528721378	chr6:66279013-66279014	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs151147959	chr6:66279039-66279040	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs9345653	chr6:66279074-66279075	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs113181467	chr6:66279084-66279085	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs568536268	chr6:66279090-66279091	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs188722110	chr6:66279113-66279114	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs557307126	chr6:66279134-66279135	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs569747973	chr6:66279137-66279138	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs538778050	chr6:66279138-66279139	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs115700369	chr6:66279180-66279181	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs193283874	chr6:66279227-66279228	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs182573693	chr6:66279250-66279251	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs554861338	chr6:66279254-66279255	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs574675546	chr6:66279294-66279295	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs186800071	chr6:66279451-66279452	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs563188693	chr6:66279510-66279511	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532462194	chr6:66279521-66279522	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs9345654	chr6:66279535-66279536	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs114782750	chr6:66279541-66279542	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs72880484	chr6:66279617-66279618	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191517463	chr6:66279619-66279620	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376469132	chr6:66279638-66279639	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531139430	chr6:66279642-66279643	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551152716	chr6:66279654-66279655	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571064961	chr6:66279692-66279693	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9363398	chr6:66279704-66279705	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs183998309	chr6:66279722-66279723	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187280591	chr6:66279788-66279789	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192869561	chr6:66279838-66279839	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554293813	chr6:66279840-66279841	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574670267	chr6:66279841-66279842	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543390696	chr6:66279842-66279843	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185392985	chr6:66279844-66279845	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149243786	chr6:66279846-66279847	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144416941	chr6:66279905-66279906	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559439079	chr6:66279916-66279917	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533591628	chr6:66279949-66279950	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148405086	chr6:66279973-66279974	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542184891	chr6:66280008-66280009	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9360137	chr6:66280020-66280021	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Dyslexia	22102821	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
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66276800-66278600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr6:66277400-66279200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr6:66277400-66279200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr6:66277600-66278600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr6:66277600-66279600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:66278000-66278800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr6:66278000-66279400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:66278200-66279000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr6:66278400-66278800	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr6:66278600-66279000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr6:66278600-66279000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr6:66278600-66279000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr6:66278800-66279000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr6:66278800-66279600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr6:66278800-66279800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:66278800-66280400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:66278800-66280600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr6:66279000-66279200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:66279000-66279200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:66279000-66279200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr6:66279000-66280200	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr6:66279200-66279600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr6:66279200-66279600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr6:66279200-66279600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr6:66279200-66279600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr6:66279200-66280400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr6:66279400-66280800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:66279600-66280400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:66279600-66281000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr6:66279600-66281000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr6:66279600-66281600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr6:66279600-66281600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr6:66280200-66280400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr6:66280400-66281000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr6:66280400-66281200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr6:66280400-66281200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:66281000-66281600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr6:66281000-66281800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr6:66281600-66281800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr6:66281800-66282000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr6:66282000-66282200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr6:66283400-66283800	ZNF genes & repeats	Gastric	stomach
43	chr6:66286800-66287200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr6:66287200-66287400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
45	chr6:66308200-66308400	Active TSS	K562	blood
46	chr6:66311400-66313400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr6:66312400-66313200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:66312600-66313000	Enhancers	Fetal Stomach	stomach
49	chr6:66312600-66313200	Enhancers	Fetal Lung	lung
50	chr6:66318800-66321400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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