Variant report

Variant	esv2758058
Chromosome Location	chr6:63706622-63985889
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	ARID3A	chr6:63982331-63982659	HepG2	liver:	n/a	n/a
2	BACH1	chr6:63732724-63732911	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:63807248-63807450	GM12878	blood:	n/a	n/a
4	BATF	chr6:63824630-63824797	GM12878	blood:	n/a	n/a
5	BATF	chr6:63807210-63807411	GM12878	blood:	n/a	n/a
6	BATF	chr6:63824586-63824792	GM12878	blood:	n/a	n/a
7	BATF	chr6:63946532-63946753	GM12878	blood:	n/a	n/a
8	BATF	chr6:63934113-63934324	GM12878	blood:	n/a	n/a
9	BATF	chr6:63971782-63972019	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:63806476-63806656	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:63807120-63807515	GM12878	blood:	n/a	n/a
12	BCL11A	chr6:63807199-63807405	GM12878	blood:	n/a	n/a
13	BCL11A	chr6:63824585-63824882	GM12878	blood:	n/a	chr6:63824743-63824752
14	BHLHE40	chr6:63806449-63806803	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:63807126-63807476	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:63946547-63946562	GM12878	blood:	n/a	n/a
17	CBX3	chr6:63913525-63913779	K562	blood:	n/a	n/a
18	CEBPB	chr6:63924655-63924850	K562	blood:	n/a	n/a
19	CEBPB	chr6:63955408-63955727	K562	blood:	n/a	chr6:63955575-63955586
20	CEBPB	chr6:63768494-63768848	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr6:63733591-63733961	Hela-S3	cervix:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
22	CEBPB	chr6:63895946-63896205	HepG2	liver:	n/a	chr6:63896069-63896080 chr6:63896030-63896041
23	CEBPB	chr6:63733606-63733992	MCF-7	breast:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
24	CEBPB	chr6:63855172-63855480	H1-hESC	embryonic stem cell:	n/a	chr6:63855308-63855319
25	CEBPB	chr6:63749108-63749358	HepG2	liver:	n/a	chr6:63749218-63749229 chr6:63749198-63749209
26	CEBPB	chr6:63946520-63946863	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr6:63955402-63955758	IMR90	lung:	n/a	chr6:63955575-63955586
28	CEBPB	chr6:63749043-63749369	Hela-S3	cervix:	n/a	chr6:63749218-63749229 chr6:63749198-63749209
29	CEBPB	chr6:63855226-63855456	HepG2	liver:	n/a	chr6:63855308-63855319
30	CEBPB	chr6:63772020-63772183	HepG2	liver:	n/a	chr6:63772099-63772110
31	CEBPB	chr6:63955435-63955746	H1-hESC	embryonic stem cell:	n/a	chr6:63955575-63955586
32	CEBPB	chr6:63749086-63749369	A549	lung:	n/a	chr6:63749218-63749229 chr6:63749198-63749209
33	CEBPB	chr6:63764073-63764237	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr6:63808099-63808450	HepG2	liver:	n/a	chr6:63808261-63808272 chr6:63808261-63808274 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808274 chr6:63808263-63808272
35	CEBPB	chr6:63955441-63955717	HepG2	liver:	n/a	chr6:63955575-63955586
36	CEBPB	chr6:63959876-63960242	A549	lung:	n/a	chr6:63959990-63960001
37	CEBPB	chr6:63808146-63808432	A549	lung:	n/a	chr6:63808261-63808272 chr6:63808261-63808274 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808274 chr6:63808263-63808272
38	CEBPB	chr6:63808130-63808451	IMR90	lung:	n/a	chr6:63808261-63808272 chr6:63808261-63808274 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808274 chr6:63808263-63808272
39	CEBPB	chr6:63738543-63738654	K562	blood:	n/a	chr6:63738589-63738600
40	CEBPB	chr6:63738461-63738743	IMR90	lung:	n/a	chr6:63738589-63738600
41	CEBPB	chr6:63955402-63955745	A549	lung:	n/a	chr6:63955575-63955586
42	CEBPB	chr6:63738434-63738741	HepG2	liver:	n/a	chr6:63738589-63738600
43	CEBPB	chr6:63955353-63955771	HepG2	liver:	n/a	chr6:63955575-63955586
44	CEBPB	chr6:63955392-63955791	Hela-S3	cervix:	n/a	chr6:63955575-63955586
45	CEBPB	chr6:63925110-63925404	HepG2	liver:	n/a	chr6:63925265-63925274
46	CEBPB	chr6:63733609-63733862	HepG2	liver:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
47	CEBPD	chr6:63924639-63924885	K562	blood:	n/a	n/a
48	CHD2	chr6:63946825-63946865	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr6:63776140-63776577	GM12878	blood:	n/a	n/a
50	CTCF	chr6:63776040-63776190	GM12866	blood:	n/a	chr6:63776156-63776165 chr6:63776155-63776176 chr6:63776153-63776171

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63921394-63921444	SAEC	small airway:	n/a
2	chr6:63940486-63940536	ovcar-3	ovarian:	n/a
3	chr6:63921394-63921444	SAEC	small airway:	n/a
4	chr6:63940486-63940536	ovcar-3	ovarian:	n/a
5	chr6:63921501-63921551	SK-N-MC	brain:	n/a
6	chr6:63984054-63984104	PrEC	prostate:	n/a
7	chr6:63947428-63947478	HAEpiC	amniotic membrane:	n/a
8	chr6:63762988-63763038	AG04450	lung:	fetal
9	chr6:63762988-63763038	PANC-1	pancreas:	n/a
10	chr6:63762988-63763038	GM12892	blood:	n/a
11	chr6:63873476-63873526	PrEC	prostate:	n/a
12	chr6:63762988-63763038	ECC-1	luminal epithelium:	n/a
13	chr6:63709255-63709305	Hepatocyte	liver:	n/a
14	chr6:63874234-63874284	GM06990	blood:	n/a
15	chr6:63709255-63709305	GM12878	blood:	n/a
16	chr6:63940486-63940536	MCF-7	breast:	n/a
17	chr6:63709255-63709305	HCT-116	colon:	n/a
18	chr6:63984054-63984104	T-47D	breast:	n/a
19	chr6:63709255-63709305	AoSMC	blood vessel:	n/a
20	chr6:63947428-63947478	AG09319	gingival:	n/a
21	chr6:63940138-63940188	SKMC	muscle:	n/a
22	chr6:63940138-63940188	T-47D	breast:	n/a
23	chr6:63873476-63873526	SK-N-SH_RA	brain:	n/a
24	chr6:63940138-63940188	MCF-7	breast:	n/a
25	chr6:63873476-63873526	MCF10A-Er-Src	breast:	n/a
26	chr6:63873809-63873859	HNPCEpiC	eye:	n/a
27	chr6:63984054-63984104	GM12891	blood:	n/a
28	chr6:63940486-63940536	K562	blood:	n/a
29	chr6:63873476-63873526	CMK	blood:	n/a
30	chr6:63947428-63947478	NB4	blood:	n/a
31	chr6:63709255-63709305	GM06990	blood:	n/a
32	chr6:63984054-63984104	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:63762988-63763038	MCF10A-Er-Src	breast:	n/a
34	chr6:63921394-63921444	PrEC	prostate:	n/a
35	chr6:63921501-63921551	HUVEC	blood vessel:	n/a
36	chr6:63873476-63873526	MCF-7	breast:	n/a
37	chr6:63873809-63873859	SK-N-SH_RA	brain:	n/a
38	chr6:63985112-63985162	HEEpiC	esophagus:	n/a
39	chr6:63762988-63763038	HCPEpiC	choroid plexus:	n/a
40	chr6:63921394-63921444	HRE	kidney:	n/a
41	chr6:63762988-63763038	HCM	heart:	n/a
42	chr6:63874234-63874284	HAEpiC	amniotic membrane:	n/a
43	chr6:63709255-63709305	PFSK-1	brain:	n/a
44	chr6:63940486-63940536	PrEC	prostate:	n/a
45	chr6:63984054-63984104	HCF	heart:	n/a
46	chr6:63921458-63921508	BE2_C	brain:	n/a
47	chr6:63940138-63940188	AG09319	gingival:	n/a
48	chr6:63985112-63985162	A549	lung:	n/a
49	chr6:63940138-63940188	NHDF-neo	bronchial:	n/a
50	chr6:63947428-63947478	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:63971090..63973718-chr6:63975676..63978605,2	K562	blood:
2	chr6:63726588..63729343-chr6:63730639..63732811,2	K562	blood:
3	chr6:63971090..63973718-chr6:63975676..63978605,2	K562	blood:
4	chr6:63948917..63949801-chr6:64200742..64201532,2	MCF-7	breast:
5	chr6:63831166..63831711-chr6:63982020..63982633,2	MCF-7	breast:
6	chr6:63981136..63982738-chr6:63987932..63990563,2	MCF-7	breast:
7	chr6:63935123..63936664-chr6:63993478..63995873,2	MCF-7	breast:
8	chr6:63775743..63776456-chr6:63981994..63982859,3	MCF-7	breast:
9	chr6:63775743..63776456-chr6:63981994..63982859,3	MCF-7	breast:
10	chr6:63831166..63831711-chr6:63982020..63982633,2	MCF-7	breast:
11	chr6:63601380..63602369-chr6:63983063..63983726,2	MCF-7	breast:
12	chr6:63726588..63729343-chr6:63730639..63732811,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKBP1C-1	chr6:63937390-63937648	NONHSAT113340

Variant related genes	Relation type
FKBP1C	TF binding region
SPTLC1P3	TF binding region
ENSG00000217477	TF binding region
ENSG00000218520	TF binding region
FKBP1C	CpG island
SPTLC1P3	CpG island
ENSG00000217477	CpG island
ENSG00000218520	CpG island

Extended variants
information (count: 5396 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:5396 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565075796	chr6:63707705-63707706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76328809	chr6:63707772-63707773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187584684	chr6:63707793-63707794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570476730	chr6:63707835-63707836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534303251	chr6:63707838-63707839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs201082166	chr6:63707845-63707846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574410594	chr6:63707874-63707875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374834145	chr6:63707902-63707903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556745557	chr6:63707905-63707906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146585865	chr6:63707923-63707924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192419630	chr6:63707937-63707938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73448320	chr6:63707939-63707940	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558760089	chr6:63707940-63707941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577202923	chr6:63707943-63707944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138782414	chr6:63707961-63707962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368388581	chr6:63707962-63707963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73448322	chr6:63707986-63707987	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs546693770	chr6:63708021-63708022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563914977	chr6:63708034-63708035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560562096	chr6:63708066-63708067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35773626	chr6:63708075-63708076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149306273	chr6:63708088-63708089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552280367	chr6:63708208-63708209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6933463	chr6:63708250-63708251	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs528158250	chr6:63708251-63708252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546188956	chr6:63708252-63708253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567676270	chr6:63708253-63708254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184511646	chr6:63708258-63708259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557538806	chr6:63708270-63708271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6907025	chr6:63708322-63708323	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs536840026	chr6:63708325-63708326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539241232	chr6:63708345-63708346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557899708	chr6:63708364-63708365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6907045	chr6:63708367-63708368	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs541468576	chr6:63708368-63708369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74566340	chr6:63708378-63708379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540135281	chr6:63708383-63708384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370422195	chr6:63708396-63708397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188909368	chr6:63708406-63708407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148072473	chr6:63708451-63708452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192934676	chr6:63708459-63708460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184567599	chr6:63708542-63708543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73448323	chr6:63708571-63708572	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs555261109	chr6:63708590-63708591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567763247	chr6:63708595-63708596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528835838	chr6:63708623-63708624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550495567	chr6:63708639-63708640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113118722	chr6:63708644-63708645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78585903	chr6:63708648-63708649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113787628	chr6:63708649-63708650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Acute lymphoblastic leukemia	20435627	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
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
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63707600-63709600	Enhancers	Fetal Heart	heart
2	chr6:63707800-63708400	Enhancers	Fetal Intestine Large	intestine
3	chr6:63707800-63708600	Enhancers	Fetal Intestine Small	intestine
4	chr6:63708000-63708200	Enhancers	HepG2	liver
5	chr6:63708200-63709200	Weak transcription	HepG2	liver
6	chr6:63708400-63709600	Weak transcription	Fetal Intestine Large	intestine
7	chr6:63708600-63709000	Weak transcription	Fetal Intestine Small	intestine
8	chr6:63708600-63710200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr6:63708600-63710200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr6:63708800-63709000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr6:63708800-63710000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:63708800-63710200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:63708800-63710200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:63708800-63710600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:63709000-63709600	Enhancers	Fetal Intestine Small	intestine
16	chr6:63709000-63709800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr6:63709000-63710000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:63709000-63710000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:63709000-63710000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:63709000-63710200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr6:63709000-63710200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:63709000-63710200	Enhancers	HMEC	breast
23	chr6:63709000-63710200	Enhancers	NHEK	skin
24	chr6:63709000-63710600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr6:63709000-63710600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr6:63709200-63709800	Enhancers	HepG2	liver
27	chr6:63709600-63710000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:63709600-63710000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:63709600-63710000	Flanking Active TSS	Fetal Heart	heart
30	chr6:63709600-63710000	Enhancers	Fetal Intestine Large	intestine
31	chr6:63709600-63710800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:63710000-63710400	Enhancers	Fetal Heart	heart
33	chr6:63710600-63720600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr6:63720400-63722600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr6:63720600-63721600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr6:63720600-63722400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr6:63721200-63721800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr6:63721200-63722600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr6:63721400-63722200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:63721800-63722400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:63722200-63722400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:63722200-63724000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:63722400-63722600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:63722400-63724000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr6:63722600-63724000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr6:63722600-63724000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr6:63722600-63746000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:63724000-63724400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr6:63724000-63724400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:63724000-63724400	Enhancers	HUES48 Cell Line	embryonic stem cell

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