Variant report

Variant	esv3474351
Chromosome Location	chr6:160934480-160943642
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	chr6:160941091-160941256	K562	blood:	n/a	n/a
2	ATF1	chr6:160940084-160940220	K562	blood:	n/a	n/a
3	ATF1	chr6:160940904-160941516	K562	blood:	n/a	n/a
4	ATF3	chr6:160940946-160941476	K562	blood:	n/a	n/a
5	BACH1	chr6:160941035-160941235	K562	blood:	n/a	n/a
6	BACH1	chr6:160935033-160935067	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:160940850-160941885	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr6:160940915-160941246	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:160940935-160941885	K562	blood:	n/a	n/a
10	BRCA1	chr6:160941054-160941056	HepG2	liver:	n/a	n/a
11	CBX3	chr6:160940830-160941997	K562	blood:	n/a	n/a
12	CCNT2	chr6:160941162-160941792	K562	blood:	n/a	n/a
13	CEBPB	chr6:160940705-160941430	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr6:160940932-160941245	GM12878	blood:	n/a	n/a
15	CHD2	chr6:160941080-160941330	HepG2	liver:	n/a	chr6:160941315-160941325
16	CHD2	chr6:160940986-160941246	K562	blood:	n/a	n/a
17	CHD2	chr6:160940982-160941419	H1-hESC	embryonic stem cell:	n/a	chr6:160941315-160941325
18	CREB1	chr6:160940937-160941803	K562	blood:	n/a	n/a
19	CREB1	chr6:160941042-160941586	GM12878	blood:	n/a	n/a
20	CREB1	chr6:160940978-160941746	A549	lung:	n/a	n/a
21	CREB1	chr6:160940843-160941578	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr6:160940883-160941885	K562	blood:	n/a	n/a
23	CREB1	chr6:160940795-160942010	HepG2	liver:	n/a	n/a
24	CREB1	chr6:160940937-160941696	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr6:160940925-160941230	MCF-7	breast:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
26	CTCF	chr6:160940980-160941130	A549	lung:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
27	CTCF	chr6:160940789-160941324	HepG2	liver:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
28	CTCF	chr6:160941560-160941710	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr6:160941600-160941750	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr6:160941306-160941311	NHEK	skin:	n/a	n/a
31	CTCF	chr6:160941432-160941757	HepG2	liver:	n/a	n/a
32	CTCF	chr6:160941590-160941674	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:160940917-160941228	NHEK	skin:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
34	CTCF	chr6:160940889-160941219	A549	lung:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
35	CTCF	chr6:160941000-160941150	GM12869	blood:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
36	CTCF	chr6:160941000-160941150	HepG2	liver:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
37	CTCF	chr6:160940920-160941070	BE2_C	brain:	n/a	n/a
38	CTCF	chr6:160940940-160941090	GM12867	blood:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
39	CTCF	chr6:160940960-160941110	NHDF-neo	bronchial:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
40	CTCF	chr6:160940832-160941801	K562	blood:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
41	CTCF	chr6:160941327-160941364	NHEK	skin:	n/a	n/a
42	CTCF	chr6:160940960-160941110	HFF-Myc	foreskin:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
43	CTCF	chr6:160941560-160941710	HepG2	liver:	n/a	n/a
44	CTCF	chr6:160941588-160941640	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:160940980-160941130	GM12875	blood:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
46	CTCF	chr6:160941020-160941170	GM12870	blood:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
47	CTCF	chr6:160940960-160941110	RPTEC	kidney:	n/a	chr6:160941059-160941077 chr6:160941061-160941082 chr6:160941062-160941075
48	CTCF	chr6:160941460-160941610	GM12865	blood:	n/a	n/a
49	CTCF	chr6:160941700-160941850	GM06990	blood:	n/a	n/a
50	CTCF	chr6:160941520-160941670	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:160940320-160940370	HCPEpiC	choroid plexus:	n/a
2	chr6:160940320-160940370	HCPEpiC	choroid plexus:	n/a
3	chr6:160941119-160941169	GM19239	blood:	n/a
4	chr6:160941119-160941169	ECC-1	luminal epithelium:	n/a
5	chr6:160940320-160940370	AG09319	gingival:	n/a
6	chr6:160941119-160941169	U87	brain:	n/a
7	chr6:160940606-160940656	ProgFib	skin:	n/a
8	chr6:160941119-160941169	HCM	heart:	n/a
9	chr6:160941119-160941169	GM06990	blood:	n/a
10	chr6:160941119-160941169	AG10803	skin:	n/a
11	chr6:160940606-160940656	PANC-1	pancreas:	n/a
12	chr6:160940606-160940656	GM19239	blood:	n/a
13	chr6:160940606-160940656	GM12891	blood:	n/a
14	chr6:160941119-160941169	LNCaP	prostate:	n/a
15	chr6:160940320-160940370	AG04449	skin:	fetal
16	chr6:160940320-160940370	HepG2	liver:	n/a
17	chr6:160940320-160940370	AoSMC	blood vessel:	n/a
18	chr6:160940606-160940656	HCF	heart:	n/a
19	chr6:160940606-160940656	BJ	skin:	n/a
20	chr6:160941119-160941169	HUVEC	blood vessel:	n/a
21	chr6:160941119-160941169	NHDF-neo	bronchial:	n/a
22	chr6:160940606-160940656	MCF10A-Er-Src	breast:	n/a
23	chr6:160941119-160941169	HIPEpiC	eye:	n/a
24	chr6:160941119-160941169	HEEpiC	esophagus:	n/a
25	chr6:160940606-160940656	HMEC	breast:	n/a
26	chr6:160941119-160941169	NH-A	brain:	n/a
27	chr6:160940606-160940656	T-47D	breast:	n/a
28	chr6:160941119-160941169	NB4	blood:	n/a
29	chr6:160940606-160940656	SKMC	muscle:	n/a
30	chr6:160941119-160941169	HMEC	breast:	n/a
31	chr6:160940320-160940370	CMK	blood:	n/a
32	chr6:160941119-160941169	IMR90	lung:	fetal
33	chr6:160940606-160940656	HRCEpiC	kidney:	n/a
34	chr6:160940320-160940370	NHBE	bronchial:	n/a
35	chr6:160940320-160940370	A549	lung:	n/a
36	chr6:160940320-160940370	Jurkat	blood:	n/a
37	chr6:160940320-160940370	AG10803	skin:	n/a
38	chr6:160940320-160940370	NHDF-neo	bronchial:	n/a
39	chr6:160940606-160940656	GM06990	blood:	n/a
40	chr6:160940320-160940370	GM12892	blood:	n/a
41	chr6:160941119-160941169	GM12891	blood:	n/a
42	chr6:160941119-160941169	PFSK-1	brain:	n/a
43	chr6:160940606-160940656	Hepatocyte	liver:	n/a
44	chr6:160941119-160941169	K562	blood:	n/a
45	chr6:160940606-160940656	HAEpiC	amniotic membrane:	n/a
46	chr6:160941119-160941169	SKMC	muscle:	n/a
47	chr6:160940320-160940370	SAEC	small airway:	n/a
48	chr6:160940320-160940370	PANC-1	pancreas:	n/a
49	chr6:160941119-160941169	HNPCEpiC	eye:	n/a
50	chr6:160940606-160940656	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:160940535..160941592-chr6:161088101..161089900,7	K562	blood:
2	chr6:160918427..160920098-chr6:160939899..160941930,2	K562	blood:
3	chr6:160939489..160941375-chr6:160998330..161000013,2	K562	blood:
4	chr6:160940089..160942020-chr6:161411986..161414301,2	MCF-7	breast:
5	chr6:160940571..160941215-chr6:160954967..160955505,2	K562	blood:
6	chr6:160940997..160941666-chr6:160999443..161000039,2	K562	blood:
7	chr6:160940621..160941316-chr6:161413631..161414342,2	MCF-7	breast:
8	chr6:160940670..160941542-chr6:161088487..161089076,2	MCF-7	breast:
9	chr6:160475075..160476994-chr6:160939802..160942570,2	K562	blood:
10	chr6:160941041..160942817-chr6:161087432..161089515,2	K562	blood:
11	chr6:160940613..160941580-chr6:160954987..160955524,2	MCF-7	breast:
12	chr6:160939583..160942817-chr6:161087432..161090286,3	K562	blood:

Variant related genes	Relation type
LPAL2	TF binding region
LPAL2	CpG island
ENSG00000272841	chromatin interactions
ENSG00000085511	chromatin interactions

Extended variants
information (count: 369 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151181359	chr6:160934525-160934526	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555041661	chr6:160934540-160934541	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572240927	chr6:160934552-160934553	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79302936	chr6:160934570-160934571	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113587997	chr6:160934585-160934586	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553169138	chr6:160934589-160934590	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs3123632	chr6:160934608-160934609	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374178338	chr6:160934652-160934653	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558619688	chr6:160934663-160934664	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575175294	chr6:160934666-160934667	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543891125	chr6:160934686-160934687	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76544410	chr6:160934690-160934691	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542494101	chr6:160934697-160934698	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529406767	chr6:160934729-160934730	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529704234	chr6:160934757-160934758	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3127570	chr6:160934825-160934826	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs560264282	chr6:160934858-160934859	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs60331973	chr6:160934911-160934912	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs552828744	chr6:160934925-160934926	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs191099298	chr6:160934989-160934990	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs61643720	chr6:160935056-160935057	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs548638177	chr6:160935084-160935085	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs56223728	chr6:160935112-160935113	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs147097011	chr6:160935123-160935124	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs569302110	chr6:160935162-160935163	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs566649874	chr6:160935166-160935167	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs111642218	chr6:160935168-160935169	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs538503008	chr6:160935185-160935186	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531813260	chr6:160935190-160935191	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs201009606	chr6:160935195-160935196	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs201785478	chr6:160935198-160935199	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs59598264	chr6:160935199-160935200	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs61247836	chr6:160935270-160935271	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs575481701	chr6:160935271-160935272	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200860588	chr6:160935282-160935283	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs79223078	chr6:160935286-160935287	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs386707829	chr6:160935287-160935288	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs554114341	chr6:160935289-160935290	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs201436289	chr6:160935291-160935292	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs182867903	chr6:160935314-160935315	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs56787824	chr6:160935330-160935331	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs551458048	chr6:160935342-160935343	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs57018537	chr6:160935401-160935402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs58731916	chr6:160935426-160935427	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs546109929	chr6:160935522-160935523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563181930	chr6:160935563-160935564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531877531	chr6:160935575-160935576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186696321	chr6:160935590-160935591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150273744	chr6:160935604-160935605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138677410	chr6:160935610-160935611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Coronary artery disease	17160897	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Coronary Disease	20032323	CNVD
Coronary Disease	20335594	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:160932600-160934800	Weak transcription	HepG2	liver
2	chr6:160933600-160940400	Weak transcription	Liver	Liver
3	chr6:160934400-160934600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:160934400-160935200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:160934400-160935200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr6:160934600-160935200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:160934600-160941000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:160934800-160935200	Enhancers	HepG2	liver
9	chr6:160935200-160940200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:160935200-160940600	Weak transcription	HepG2	liver
11	chr6:160935200-160941000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:160938600-160941000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr6:160938800-160940400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr6:160939200-160939400	Enhancers	Primary T cells fromperipheralblood	blood
15	chr6:160939200-160939600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr6:160939200-160939600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr6:160939200-160939800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
18	chr6:160939200-160940600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr6:160939200-160940600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:160939400-160939600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:160939400-160940000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr6:160939400-160940600	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr6:160939600-160940000	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr6:160939600-160940000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr6:160939600-160940800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:160939800-160940400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr6:160939800-160940400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:160940000-160940200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr6:160940000-160940200	Enhancers	A549	lung
30	chr6:160940000-160940600	Enhancers	Primary T cells fromperipheralblood	blood
31	chr6:160940000-160940600	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr6:160940000-160940800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:160940200-160940400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:160940200-160940400	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr6:160940200-160940400	Enhancers	K562	blood
36	chr6:160940200-160940600	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr6:160940200-160940600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:160940200-160940600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr6:160940200-160940800	Enhancers	Brain Anterior Caudate	brain
40	chr6:160940200-160940800	Enhancers	Fetal Muscle Trunk	muscle
41	chr6:160940200-160942000	Active TSS	A549	lung
42	chr6:160940400-160940600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:160940400-160940600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr6:160940400-160940600	Enhancers	NHEK	skin
45	chr6:160940400-160940800	Bivalent Enhancer	Primary T cells from cord blood	blood
46	chr6:160940400-160940800	Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr6:160940400-160940800	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr6:160940400-160940800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr6:160940400-160940800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr6:160940400-160940800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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