Variant report

Variant	esv2757182
Chromosome Location	chr6:81265495-81304211
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	CEBPB	chr6:81283814-81284092	HepG2	liver:	n/a	n/a
2	CTCF	chr6:81302360-81302510	AG09319	gingival:	n/a	n/a
3	CTCF	chr6:81269680-81269830	GM12870	blood:	n/a	chr6:81269821-81269830
4	CTCF	chr6:81290440-81290590	HPF	lung:	n/a	n/a
5	CTCF	chr6:81296515-81296546	ProgFib	skin:	n/a	n/a
6	CTCF	chr6:81269780-81269930	HEK293	kidney:	n/a	chr6:81269810-81269831 chr6:81269821-81269830
7	CTCF	chr6:81269800-81269950	HepG2	liver:	n/a	chr6:81269810-81269831 chr6:81269821-81269830
8	CTCF	chr6:81272958-81273253	GM12878	blood:	n/a	n/a
9	CTCF	chr6:81269810-81269849	H1-hESC	embryonic stem cell:	n/a	chr6:81269810-81269831 chr6:81269821-81269830
10	CTCF	chr6:81296493-81296551	K562	blood:	n/a	n/a
11	CTCF	chr6:81269788-81269865	MCF-7	breast:	n/a	chr6:81269810-81269831 chr6:81269821-81269830
12	EP300	chr6:81275533-81275699	GM12878	blood:	n/a	n/a
13	EP300	chr6:81276274-81276343	GM12878	blood:	n/a	n/a
14	FOS	chr6:81287562-81287818	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr6:81287611-81287762	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr6:81274152-81274265	MCF10A-Er-Src	breast:	n/a	chr6:81274216-81274228 chr6:81274217-81274226 chr6:81274218-81274225 chr6:81274218-81274227 chr6:81274217-81274227 chr6:81274218-81274226 chr6:81274232-81274241 chr6:81274219-81274230
17	FOSL2	chr6:81304129-81304661	SK-N-SH	brain:	n/a	n/a
18	FOXA1	chr6:81283057-81283344	HepG2	liver:	n/a	n/a
19	FOXA2	chr6:81282864-81283514	A549	lung:	n/a	n/a
20	GATA3	chr6:81288808-81288975	SH-SY5Y	brain:	n/a	n/a
21	GATA3	chr6:81304124-81304790	SK-N-SH	brain:	n/a	chr6:81304545-81304554 chr6:81304660-81304667
22	GATA3	chr6:81297613-81297813	SH-SY5Y	brain:	n/a	n/a
23	GATA3	chr6:81304085-81304761	SK-N-SH	brain:	n/a	chr6:81304545-81304554 chr6:81304660-81304667
24	GATA3	chr6:81276353-81276920	SK-N-SH	brain:	n/a	chr6:81276678-81276689
25	GATA3	chr6:81276466-81276760	SH-SY5Y	brain:	n/a	chr6:81276678-81276689
26	IRF1	chr6:81274044-81274179	K562	blood:	n/a	n/a
27	JUN	chr6:81274114-81274349	HepG2	liver:	n/a	chr6:81274216-81274228 chr6:81274217-81274226 chr6:81274218-81274225 chr6:81274218-81274227 chr6:81274217-81274227 chr6:81274218-81274226 chr6:81274232-81274241 chr6:81274219-81274230
28	JUND	chr6:81274056-81274392	HepG2	liver:	n/a	chr6:81274216-81274228 chr6:81274217-81274226 chr6:81274218-81274225 chr6:81274218-81274227 chr6:81274217-81274227 chr6:81274218-81274226 chr6:81274232-81274241 chr6:81274216-81274227 chr6:81274219-81274230
29	JUND	chr6:81283122-81283245	HepG2	liver:	n/a	n/a
30	KAP1	chr6:81295985-81296357	HEK293	kidney:	n/a	n/a
31	MAFK	chr6:81288271-81288399	HepG2	liver:	n/a	chr6:81288322-81288333 chr6:81288321-81288332 chr6:81288320-81288334 chr6:81288317-81288332
32	MAFK	chr6:81265935-81266126	HepG2	liver:	n/a	n/a
33	MAZ	chr6:81266760-81266776	Hela-S3	cervix:	n/a	n/a
34	MXI1	chr6:81266014-81266065	H1-hESC	embryonic stem cell:	n/a	n/a
35	MYC	chr6:81273980-81274180	MCF10A-Er-Src	breast:	n/a	n/a
36	MYC	chr6:81284534-81284625	MCF10A-Er-Src	breast:	n/a	n/a
37	NFYB	chr6:81270935-81271246	GM12878	blood:	n/a	n/a
38	PBX3	chr6:81304133-81304621	SK-N-SH	brain:	n/a	n/a
39	POLR2A	chr6:81289918-81289954	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr6:81296204-81296212	MCF-7	breast:	n/a	n/a
41	POLR2A	chr6:81288199-81288217	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr6:81265763-81265794	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr6:81283197-81283216	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr6:81283093-81283265	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr6:81288194-81288637	H1-neurons	neurons:	n/a	n/a
46	POLR2A	chr6:81274539-81274550	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr6:81288837-81289336	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr6:81301602-81301757	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr6:81288885-81289293	H1-neurons	neurons:	n/a	n/a
50	POLR2A	chr6:81283010-81283548	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:81283368-81283418	ovcar-3	ovarian:	n/a
2	chr6:81283368-81283418	ovcar-3	ovarian:	n/a
3	chr6:81283368-81283418	HEEpiC	esophagus:	n/a
4	chr6:81283368-81283418	HCF	heart:	n/a
5	chr6:81283368-81283418	GM06990	blood:	n/a
6	chr6:81283368-81283418	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:81283368-81283418	MCF-7	breast:	n/a
8	chr6:81283368-81283418	SAEC	small airway:	n/a
9	chr6:81283368-81283418	GM12891	blood:	n/a
10	chr6:81283368-81283418	HCPEpiC	choroid plexus:	n/a
11	chr6:81283368-81283418	Hepatocyte	liver:	n/a
12	chr6:81283368-81283418	ECC-1	luminal epithelium:	n/a
13	chr6:81283368-81283418	ProgFib	skin:	n/a
14	chr6:81283368-81283418	HMEC	breast:	n/a
15	chr6:81283368-81283418	PANC-1	pancreas:	n/a
16	chr6:81283368-81283418	NHBE	bronchial:	n/a
17	chr6:81283368-81283418	HUVEC	blood vessel:	n/a
18	chr6:81283368-81283418	H1-hESC	embryonic stem cell:	embryo
19	chr6:81283368-81283418	A549	lung:	n/a
20	chr6:81283368-81283418	BJ	skin:	n/a
21	chr6:81283368-81283418	SKMC	muscle:	n/a
22	chr6:81283368-81283418	Caco-2	colon:	n/a
23	chr6:81283368-81283418	HRCEpiC	kidney:	n/a
24	chr6:81283368-81283418	IMR90	lung:	fetal
25	chr6:81283368-81283418	AG10803	skin:	n/a
26	chr6:81283368-81283418	Jurkat	blood:	n/a
27	chr6:81283368-81283418	HAEpiC	amniotic membrane:	n/a
28	chr6:81283368-81283418	AG04449	skin:	fetal
29	chr6:81283368-81283418	GM12892	blood:	n/a
30	chr6:81283368-81283418	AG09309	skin:	n/a
31	chr6:81283368-81283418	HRE	kidney:	n/a
32	chr6:81283368-81283418	PFSK-1	brain:	n/a
33	chr6:81283368-81283418	NH-A	brain:	n/a
34	chr6:81283368-81283418	HNPCEpiC	eye:	n/a
35	chr6:81283368-81283418	SK-N-SH	brain:	n/a
36	chr6:81283368-81283418	HIPEpiC	eye:	n/a
37	chr6:81283368-81283418	NB4	blood:	n/a
38	chr6:81283368-81283418	BE2_C	brain:	n/a
39	chr6:81283368-81283418	MCF10A-Er-Src	breast:	n/a
40	chr6:81283368-81283418	HepG2	liver:	n/a
41	chr6:81283368-81283418	SK-N-SH_RA	brain:	n/a
42	chr6:81283368-81283418	HCT-116	colon:	n/a
43	chr6:81283368-81283418	AoSMC	blood vessel:	n/a
44	chr6:81283368-81283418	GM19239	blood:	n/a
45	chr6:81283368-81283418	U87	brain:	n/a
46	chr6:81283368-81283418	SK-N-MC	brain:	n/a
47	chr6:81283368-81283418	AG04450	lung:	fetal
48	chr6:81283368-81283418	GM12878	blood:	n/a
49	chr6:81283368-81283418	NHDF-neo	bronchial:	n/a
50	chr6:81283368-81283418	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr6:81298968..81300811-chr6:81302050..81303773,2	MCF-7	breast:
2	chr6:81254930..81257563-chr6:81262833..81265650,2	K562	blood:
3	chr6:81298968..81300811-chr6:81302050..81303773,2	MCF-7	breast:
4	chr6:81266263..81267805-chr6:81274227..81276426,2	MCF-7	breast:
5	chr6:81264062..81265646-chr6:81268549..81270670,2	MCF-7	breast:
6	chr6:81264062..81265646-chr6:81268549..81270670,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000216352	TF binding region
ENSG00000216352	CpG island
ENSG00000216352	chromatin interactions

Extended variants
information (count: 771 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9449067	chr6:81265495-81265496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563348747	chr6:81265536-81265537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142661089	chr6:81265555-81265556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575623285	chr6:81265575-81265576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538341798	chr6:81265583-81265584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10806194	chr6:81265682-81265683	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs574682953	chr6:81265790-81265791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540472849	chr6:81265849-81265850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560391984	chr6:81265886-81265887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577500378	chr6:81265899-81265900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146894210	chr6:81265940-81265941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562525005	chr6:81265950-81265951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531259266	chr6:81265952-81265953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548312212	chr6:81265991-81265992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183180297	chr6:81266030-81266031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549031219	chr6:81266033-81266034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368058948	chr6:81266058-81266059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527462982	chr6:81266157-81266158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187108667	chr6:81266163-81266164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114536572	chr6:81266190-81266191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192971256	chr6:81266216-81266217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183086052	chr6:81266248-81266249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78675833	chr6:81266271-81266272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145909040	chr6:81266324-81266325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78964996	chr6:81266347-81266348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537893795	chr6:81266419-81266420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139057630	chr6:81266439-81266440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs953499	chr6:81266456-81266457	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs149337296	chr6:81266490-81266491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34573475	chr6:81266492-81266493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534110926	chr6:81266498-81266499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553959754	chr6:81266501-81266502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569844604	chr6:81266534-81266535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs953498	chr6:81266538-81266539	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs953500	chr6:81266567-81266568	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs529035642	chr6:81266570-81266571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187735912	chr6:81266593-81266594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527401061	chr6:81266597-81266598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541200760	chr6:81266607-81266608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564311857	chr6:81266611-81266612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72903917	chr6:81266712-81266713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs2322842	chr6:81266744-81266745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs144736429	chr6:81266770-81266771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531576097	chr6:81266801-81266802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs557925759	chr6:81266852-81266853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548211084	chr6:81266861-81266862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192357384	chr6:81266862-81266863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534048711	chr6:81266893-81266894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201174046	chr6:81266917-81266918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs13200991	chr6:81266919-81266920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Breast cancer	16272173	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
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81261000-81266400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:81264600-81267400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:81265400-81267400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:81266800-81267600	Enhancers	Brain Germinal Matrix	brain
5	chr6:81267400-81267800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:81267400-81267800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr6:81267400-81268000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:81276000-81277400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr6:81276400-81276800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr6:81283200-81283600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr6:81283200-81283600	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr6:81283200-81283800	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr6:81287600-81287800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:81287800-81288000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:81287800-81288800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr6:81288200-81288400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:81288400-81289400	Enhancers	HSMM	muscle
18	chr6:81288800-81289000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr6:81288800-81289200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr6:81288800-81289200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr6:81288800-81289200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:81288800-81289200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:81288800-81289200	Enhancers	Adipose Nuclei	Adipose
24	chr6:81294800-81317000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:81301600-81303000	Enhancers	Fetal Lung	lung
26	chr6:81302200-81302600	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr6:81304200-81304800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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