Variant report

Variant	esv2759435
Chromosome Location	chr6:66354388-66453548
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	BATF	chr6:66356413-66356758	GM12878	blood:	n/a	n/a
2	BRCA1	chr6:66378211-66378498	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr6:66404687-66404887	H1-hESC	embryonic stem cell:	n/a	chr6:66404777-66404786 chr6:66404777-66404786 chr6:66404777-66404786
4	CEBPB	chr6:66439123-66439443	HepG2	liver:	n/a	chr6:66439271-66439280 chr6:66439269-66439282 chr6:66439269-66439280
5	CEBPB	chr6:66378100-66379021	MCF-7	breast:	n/a	n/a
6	CEBPB	chr6:66404649-66404900	K562	blood:	n/a	chr6:66404777-66404786 chr6:66404777-66404786 chr6:66404777-66404786
7	CEBPB	chr6:66404594-66404863	HepG2	liver:	n/a	chr6:66404777-66404786 chr6:66404777-66404786 chr6:66404777-66404786
8	CEBPB	chr6:66404609-66404903	IMR90	lung:	n/a	chr6:66404777-66404786 chr6:66404777-66404786 chr6:66404777-66404786
9	CEBPB	chr6:66378201-66378540	MCF-7	breast:	n/a	n/a
10	CEBPB	chr6:66378284-66378484	A549	lung:	n/a	n/a
11	CEBPB	chr6:66378133-66378823	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr6:66378232-66378500	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr6:66410644-66410670	Lung_OC	lung:	n/a	n/a
14	CTCF	chr6:66364626-66364816	GM12878	blood:	n/a	n/a
15	CTCF	chr6:66413711-66413749	Spleen_OC	spleen:	n/a	n/a
16	E2F4	chr6:66372812-66373062	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr6:66374651-66374848	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr6:66440655-66440816	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr6:66387670-66387870	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr6:66408749-66408935	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr6:66385463-66385562	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr6:66416771-66417877	SK-N-SH	brain:	n/a	n/a
23	EP300	chr6:66378131-66378599	Hela-S3	cervix:	n/a	chr6:66378554-66378563
24	EP300	chr6:66377155-66377761	Hela-S3	cervix:	n/a	n/a
25	EP300	chr6:66381681-66382294	MCF-7	breast:	n/a	n/a
26	EP300	chr6:66416982-66417333	SK-N-SH_RA	brain:	n/a	n/a
27	FOS	chr6:66395517-66395831	MCF10A-Er-Src	breast:	n/a	chr6:66395682-66395689 chr6:66395679-66395691 chr6:66395680-66395690 chr6:66395681-66395690 chr6:66395681-66395689
28	FOS	chr6:66378237-66378484	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr6:66445352-66445653	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr6:66381906-66382098	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr6:66395537-66395830	MCF10A-Er-Src	breast:	n/a	chr6:66395682-66395689 chr6:66395679-66395691 chr6:66395680-66395690 chr6:66395681-66395690 chr6:66395681-66395689
32	FOS	chr6:66377261-66377599	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr6:66389290-66389457	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr6:66378160-66378544	MCF10A-Er-Src	breast:	n/a	chr6:66378533-66378542
35	FOS	chr6:66378222-66378569	MCF10A-Er-Src	breast:	n/a	chr6:66378533-66378542 chr6:66378556-66378563 chr6:66378555-66378563 chr6:66378555-66378563
36	FOS	chr6:66377299-66377498	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:66389200-66389458	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:66445346-66445655	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr6:66377279-66377457	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr6:66378242-66378532	MCF10A-Er-Src	breast:	n/a	n/a
41	FOXA1	chr6:66421704-66421924	T-47D	breast:	n/a	n/a
42	FOXA1	chr6:66381820-66382237	T-47D	breast:	n/a	chr6:66381971-66381983
43	FOXA1	chr6:66381819-66382312	T-47D	breast:	n/a	chr6:66381971-66381983
44	FOXA1	chr6:66416372-66416623	HepG2	liver:	n/a	chr6:66416405-66416417
45	FOXA2	chr6:66378163-66378471	A549	lung:	n/a	n/a
46	FOXA2	chr6:66416409-66416701	A549	lung:	n/a	n/a
47	FOXA2	chr6:66381910-66382288	A549	lung:	n/a	chr6:66381971-66381983
48	GATA3	chr6:66381613-66382389	MCF-7	breast:	n/a	n/a
49	GATA3	chr6:66399966-66400276	T-47D	breast:	n/a	n/a
50	GATA3	chr6:66417270-66417611	SH-SY5Y	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66360569-66360619	RPTEC	kidney:	n/a
2	chr6:66360569-66360619	A549	lung:	n/a
3	chr6:66360569-66360619	HRE	kidney:	n/a
4	chr6:66360569-66360619	SAEC	small airway:	n/a
5	chr6:66360569-66360619	HCF	heart:	n/a
6	chr6:66360569-66360619	K562	blood:	n/a
7	chr6:66360569-66360619	HNPCEpiC	eye:	n/a
8	chr6:66360569-66360619	HMEC	breast:	n/a
9	chr6:66360569-66360619	NH-A	brain:	n/a
10	chr6:66360569-66360619	NHDF-neo	bronchial:	n/a
11	chr6:66360569-66360619	Hela-S3	cervix:	n/a
12	chr6:66360569-66360619	AG04450	lung:	fetal
13	chr6:66360569-66360619	AG10803	skin:	n/a
14	chr6:66360569-66360619	HCT-116	colon:	n/a
15	chr6:66360569-66360619	GM12878	blood:	n/a
16	chr6:66360569-66360619	MCF-7	breast:	n/a
17	chr6:66360569-66360619	Hepatocyte	liver:	n/a
18	chr6:66360569-66360619	ProgFib	skin:	n/a
19	chr6:66360569-66360619	ECC-1	luminal epithelium:	n/a
20	chr6:66360569-66360619	AG09319	gingival:	n/a
21	chr6:66360569-66360619	HCPEpiC	choroid plexus:	n/a
22	chr6:66360569-66360619	SK-N-SH	brain:	n/a
23	chr6:66360569-66360619	AG09309	skin:	n/a
24	chr6:66360569-66360619	CMK	blood:	n/a
25	chr6:66360569-66360619	Jurkat	blood:	n/a
26	chr6:66360569-66360619	MCF10A-Er-Src	breast:	n/a
27	chr6:66360569-66360619	IMR90	lung:	fetal
28	chr6:66360569-66360619	SKMC	muscle:	n/a
29	chr6:66360569-66360619	AoSMC	blood vessel:	n/a
30	chr6:66360569-66360619	BJ	skin:	n/a
31	chr6:66360569-66360619	Caco-2	colon:	n/a
32	chr6:66360569-66360619	ovcar-3	ovarian:	n/a
33	chr6:66360569-66360619	PrEC	prostate:	n/a
34	chr6:66360569-66360619	H1-hESC	embryonic stem cell:	embryo
35	chr6:66360569-66360619	GM12891	blood:	n/a
36	chr6:66360569-66360619	HAEpiC	amniotic membrane:	n/a
37	chr6:66360569-66360619	NHBE	bronchial:	n/a
38	chr6:66360569-66360619	HUVEC	blood vessel:	n/a
39	chr6:66360569-66360619	HepG2	liver:	n/a
40	chr6:66360569-66360619	U87	brain:	n/a
41	chr6:66360569-66360619	HIPEpiC	eye:	n/a
42	chr6:66360569-66360619	GM12892	blood:	n/a
43	chr6:66360569-66360619	PANC-1	pancreas:	n/a
44	chr6:66360569-66360619	GM19239	blood:	n/a
45	chr6:66360569-66360619	HEK293	kidney:	embryo
46	chr6:66360569-66360619	SK-N-SH_RA	brain:	n/a
47	chr6:66360569-66360619	SK-N-MC	brain:	n/a
48	chr6:66360569-66360619	HRCEpiC	kidney:	n/a
49	chr6:66360569-66360619	HL-60	blood:	n/a
50	chr6:66360569-66360619	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:66366176..66367861-chr6:66369902..66372494,2	K562	blood:
2	chr3:189034137..189034728-chr6:66401890..66402666,2	MCF-7	breast:
3	chr6:66366176..66367861-chr6:66369902..66372494,2	K562	blood:
4	chr6:66389053..66391661-chr6:66392622..66394298,2	MCF-7	breast:
5	chr6:66389053..66391661-chr6:66392622..66394298,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGSN-7	chr6:66417028-66417107	NONHSAT113373

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

Extended variants
information (count: 1093 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1093 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560652103	chr6:66359449-66359450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34442579	chr6:66359561-66359562	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549617275	chr6:66359593-66359594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557736588	chr6:66359595-66359596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561729466	chr6:66359606-66359607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371486624	chr6:66359664-66359665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186939954	chr6:66359665-66359666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189169907	chr6:66359724-66359725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548652410	chr6:66359813-66359814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201070330	chr6:66359824-66359825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550259727	chr6:66359840-66359841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181889713	chr6:66359847-66359848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375961345	chr6:66359852-66359853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539341740	chr6:66359876-66359877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1387795	chr6:66359969-66359970	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184973219	chr6:66359972-66359973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372197879	chr6:66359973-66359974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149595267	chr6:66359990-66359991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144269889	chr6:66360007-66360008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544894421	chr6:66360044-66360045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189779691	chr6:66360104-66360105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181021779	chr6:66360162-66360163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557858907	chr6:66360176-66360177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538974720	chr6:66360201-66360202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373344209	chr6:66360202-66360203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1387796	chr6:66360228-66360229	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186430568	chr6:66360240-66360241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560737655	chr6:66360258-66360259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9342493	chr6:66360262-66360263	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543200158	chr6:66360309-66360310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563076859	chr6:66360313-66360314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191379754	chr6:66360325-66360326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140032485	chr6:66360439-66360440	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs563905300	chr6:66360464-66360465	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs532915511	chr6:66360477-66360478	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs560866305	chr6:66360484-66360485	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs183640391	chr6:66360491-66360492	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs566390060	chr6:66360500-66360501	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs529155948	chr6:66360519-66360520	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs528167039	chr6:66360548-66360549	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs548766390	chr6:66360553-66360554	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs546311691	chr6:66360570-66360571	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs34342497	chr6:66360574-66360575	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs569076453	chr6:66360645-66360646	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs72884129	chr6:66360668-66360669	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs558257678	chr6:66360682-66360683	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs571670421	chr6:66360718-66360719	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs534146142	chr6:66360737-66360738	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs16897002	chr6:66360753-66360754	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs35743268	chr6:66360823-66360824	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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66359400-66360200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr6:66359600-66360600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr6:66359600-66360800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:66359600-66361600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:66359800-66360600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr6:66360000-66360400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr6:66360400-66360800	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr6:66374000-66375200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:66377000-66379000	Enhancers	Hela-S3	cervix
10	chr6:66377200-66377600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:66377200-66378000	Enhancers	Fetal Lung	lung
12	chr6:66379000-66381600	Weak transcription	Hela-S3	cervix
13	chr6:66381400-66382000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:66381600-66382200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:66381600-66382200	Enhancers	Hela-S3	cervix
16	chr6:66381600-66383600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:66390800-66391000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr6:66390800-66391200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr6:66390800-66391800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:66391400-66392000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:66392800-66393800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:66393800-66396000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:66396000-66396200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:66396200-66396600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:66399600-66400400	Enhancers	Placenta	Placenta
26	chr6:66401800-66402200	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr6:66402200-66403400	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr6:66403600-66403800	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr6:66408400-66408800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:66408800-66409200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:66409200-66412000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr6:66410000-66411000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:66410000-66411200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr6:66410400-66411000	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr6:66410600-66411000	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr6:66411000-66411400	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr6:66411400-66412800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr6:66412800-66413600	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr6:66413600-66413800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr6:66413800-66414000	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr6:66413800-66414800	Enhancers	A549	lung
42	chr6:66414000-66414400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr6:66414400-66414800	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr6:66414800-66415200	Weak transcription	A549	lung
45	chr6:66414800-66415400	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr6:66415000-66415200	Enhancers	Fetal Intestine Small	intestine
47	chr6:66415000-66415600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:66415200-66415400	Enhancers	A549	lung
49	chr6:66415400-66416400	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr6:66415400-66416400	Weak transcription	A549	lung

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