Variant report

Variant	esv3378121
Chromosome Location	chr6:160877757-160956624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1152)
CpG islands
(count:612)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:160955292-160955569	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:160928482-160928884	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:160931229-160931590	K562	blood:	n/a	n/a
4	ARID3A	chr6:160941091-160941256	K562	blood:	n/a	n/a
5	ATF1	chr6:160882814-160882854	K562	blood:	n/a	n/a
6	ATF1	chr6:160927073-160927273	K562	blood:	n/a	n/a
7	ATF1	chr6:160945426-160945566	K562	blood:	n/a	n/a
8	ATF1	chr6:160931236-160931585	K562	blood:	n/a	n/a
9	ATF1	chr6:160940084-160940220	K562	blood:	n/a	n/a
10	ATF1	chr6:160883569-160883793	K562	blood:	n/a	n/a
11	ATF1	chr6:160928438-160928591	K562	blood:	n/a	n/a
12	ATF1	chr6:160940904-160941516	K562	blood:	n/a	n/a
13	ATF2	chr6:160883429-160884072	GM12878	blood:	n/a	n/a
14	ATF2	chr6:160883329-160884055	GM12878	blood:	n/a	n/a
15	ATF3	chr6:160940946-160941476	K562	blood:	n/a	n/a
16	ATF3	chr6:160888615-160888846	K562	blood:	n/a	n/a
17	BACH1	chr6:160935033-160935067	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:160941035-160941235	K562	blood:	n/a	n/a
19	BACH1	chr6:160931275-160931591	K562	blood:	n/a	n/a
20	BACH1	chr6:160931323-160931490	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:160940850-160941885	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr6:160944262-160944500	GM12878	blood:	n/a	chr6:160944395-160944406
23	BATF	chr6:160883436-160883842	GM12878	blood:	n/a	chr6:160883629-160883640
24	BATF	chr6:160897968-160898303	GM12878	blood:	n/a	n/a
25	BATF	chr6:160898046-160898402	GM12878	blood:	n/a	n/a
26	BATF	chr6:160944230-160944583	GM12878	blood:	n/a	chr6:160944395-160944406
27	BATF	chr6:160883431-160883829	GM12878	blood:	n/a	chr6:160883629-160883640
28	BCL11A	chr6:160883450-160883926	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:160883590-160883885	GM12878	blood:	n/a	n/a
30	BCL3	chr6:160876547-160877846	A549	lung:	n/a	n/a
31	BCL3	chr6:160883527-160883893	GM12878	blood:	n/a	n/a
32	BCL3	chr6:160883519-160883857	GM12878	blood:	n/a	n/a
33	BCL3	chr6:160876688-160877931	A549	lung:	n/a	n/a
34	BCLAF1	chr6:160940915-160941246	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:160883465-160883847	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:160883570-160883877	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:160931382-160931516	K562	blood:	n/a	n/a
38	BHLHE40	chr6:160931968-160932306	HepG2	liver:	n/a	n/a
39	BHLHE40	chr6:160940935-160941885	K562	blood:	n/a	n/a
40	BRCA1	chr6:160955143-160955360	HepG2	liver:	n/a	n/a
41	BRCA1	chr6:160955576-160955723	HepG2	liver:	n/a	n/a
42	BRCA1	chr6:160941054-160941056	HepG2	liver:	n/a	n/a
43	CBX3	chr6:160940830-160941997	K562	blood:	n/a	n/a
44	CCNT2	chr6:160931329-160931529	K562	blood:	n/a	n/a
45	CCNT2	chr6:160941162-160941792	K562	blood:	n/a	n/a
46	CEBPB	chr6:160908810-160908931	HepG2	liver:	n/a	chr6:160908899-160908910 chr6:160908898-160908909 chr6:160908898-160908911
47	CEBPB	chr6:160886816-160887005	HepG2	liver:	n/a	chr6:160886959-160886970
48	CEBPB	chr6:160894808-160895059	HepG2	liver:	n/a	chr6:160894925-160894936
49	CEBPB	chr6:160886846-160887076	A549	lung:	n/a	chr6:160886959-160886970
50	CEBPB	chr6:160932568-160932717	K562	blood:	n/a	chr6:160932612-160932623 chr6:160932612-160932625

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:160955178-160955228	NB4	blood:	n/a
2	chr6:160952713-160952763	HMEC	breast:	n/a
3	chr6:160955178-160955228	NB4	blood:	n/a
4	chr6:160952713-160952763	HMEC	breast:	n/a
5	chr6:160940320-160940370	T-47D	breast:	n/a
6	chr6:160885486-160885536	HCM	heart:	n/a
7	chr6:160908522-160908572	HCPEpiC	choroid plexus:	n/a
8	chr6:160952713-160952763	H1-hESC	embryonic stem cell:	embryo
9	chr6:160940606-160940656	SAEC	small airway:	n/a
10	chr6:160955178-160955228	U87	brain:	n/a
11	chr6:160940320-160940370	NHDF-neo	bronchial:	n/a
12	chr6:160886239-160886289	Jurkat	blood:	n/a
13	chr6:160932670-160932720	HRCEpiC	kidney:	n/a
14	chr6:160932709-160932759	MCF-7	breast:	n/a
15	chr6:160955178-160955228	GM12891	blood:	n/a
16	chr6:160955178-160955228	AoSMC	blood vessel:	n/a
17	chr6:160940606-160940656	PANC-1	pancreas:	n/a
18	chr6:160952713-160952763	SK-N-MC	brain:	n/a
19	chr6:160940320-160940370	HepG2	liver:	n/a
20	chr6:160885486-160885536	AoSMC	blood vessel:	n/a
21	chr6:160908522-160908572	HEK293	kidney:	embryo
22	chr6:160940606-160940656	HIPEpiC	eye:	n/a
23	chr6:160886239-160886289	HRPEpiC	eye:	n/a
24	chr6:160940606-160940656	A549	lung:	n/a
25	chr6:160908522-160908572	Caco-2	colon:	n/a
26	chr6:160932709-160932759	HCT-116	colon:	n/a
27	chr6:160940320-160940370	AG10803	skin:	n/a
28	chr6:160908522-160908572	HepG2	liver:	n/a
29	chr6:160952713-160952763	ProgFib	skin:	n/a
30	chr6:160885486-160885536	H1-hESC	embryonic stem cell:	embryo
31	chr6:160940606-160940656	HRCEpiC	kidney:	n/a
32	chr6:160886239-160886289	SK-N-SH	brain:	n/a
33	chr6:160940320-160940370	BJ	skin:	n/a
34	chr6:160885486-160885536	HAEpiC	amniotic membrane:	n/a
35	chr6:160932670-160932720	SAEC	small airway:	n/a
36	chr6:160955178-160955228	ovcar-3	ovarian:	n/a
37	chr6:160885486-160885536	ovcar-3	ovarian:	n/a
38	chr6:160908522-160908572	AoSMC	blood vessel:	n/a
39	chr6:160885486-160885536	GM06990	blood:	n/a
40	chr6:160941119-160941169	GM06990	blood:	n/a
41	chr6:160885486-160885536	GM19239	blood:	n/a
42	chr6:160952713-160952763	GM19239	blood:	n/a
43	chr6:160941119-160941169	GM12878	blood:	n/a
44	chr6:160932709-160932759	SKMC	muscle:	n/a
45	chr6:160952713-160952763	NB4	blood:	n/a
46	chr6:160886239-160886289	Caco-2	colon:	n/a
47	chr6:160885486-160885536	RPTEC	kidney:	n/a
48	chr6:160932670-160932720	NT2-D1	testis:	n/a
49	chr6:160932670-160932720	H1-hESC	embryonic stem cell:	embryo
50	chr6:160955178-160955228	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:160918427..160920098-chr6:160939899..160941930,2	K562	blood:
2	chr6:160915674..160918470-chr6:160928618..160930503,2	K562	blood:
3	chr6:160940613..160941580-chr6:160954987..160955524,2	MCF-7	breast:
4	chr6:160559138..160559777-chr6:160954950..160955755,2	K562	blood:
5	chr6:160940670..160941542-chr6:161088487..161089076,2	MCF-7	breast:
6	chr6:160876492..160879466-chr6:160895352..160897823,2	K562	blood:
7	chr6:160876492..160879466-chr6:160895352..160897823,2	K562	blood:
8	chr6:160876699..160877379-chr6:160954968..160955609,2	K562	blood:
9	chr6:160940621..160941316-chr6:161413631..161414342,2	MCF-7	breast:
10	chr6:160940571..160941215-chr6:160954967..160955505,2	K562	blood:
11	chr6:160940997..160941666-chr6:160999443..161000039,2	K562	blood:
12	chr6:160940613..160941580-chr6:160954987..160955524,2	MCF-7	breast:
13	chr6:160939489..160941375-chr6:160998330..161000013,2	K562	blood:
14	chr6:160939583..160942817-chr6:161087432..161090286,3	K562	blood:
15	chr6:160918427..160920098-chr6:160939899..160941930,2	K562	blood:
16	chr6:160940571..160941215-chr6:160954967..160955505,2	K562	blood:
17	chr6:160475075..160476994-chr6:160939802..160942570,2	K562	blood:
18	chr6:160915674..160918470-chr6:160928618..160930503,2	K562	blood:
19	chr6:160284403..160284908-chr6:160954965..160955519,2	K562	blood:
20	chr6:160940089..160942020-chr6:161411986..161414301,2	MCF-7	breast:
21	chr6:160919688..160921620-chr6:160926024..160927581,2	K562	blood:
22	chr6:160876378..160878345-chr6:160878761..160881634,2	K562	blood:
23	chr6:160954972..160955719-chr6:161088699..161089595,2	MCF-7	breast:
24	chr6:160940535..160941592-chr6:161088101..161089900,7	K562	blood:
25	chr6:160919688..160921620-chr6:160926024..160927581,2	K562	blood:
26	chr6:160941041..160942817-chr6:161087432..161089515,2	K562	blood:
27	chr6:160876378..160878345-chr6:160878761..160881634,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPA-6	chr6:160902420-160903851	NONHSAT115906
2	lnc-LPA-6	chr6:160904377-160904406	NONHSAT115906

No data

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

Extended variants
information (count: 3309 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3309 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56410748	chr6:160877757-160877758	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs56190014	chr6:160877760-160877761	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs56299651	chr6:160877763-160877764	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs386707822	chr6:160877767-160877768	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs56076041	chr6:160877769-160877770	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201970557	chr6:160877772-160877773	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376242300	chr6:160877775-160877776	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368582097	chr6:160877789-160877790	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372618716	chr6:160877790-160877791	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs56252654	chr6:160877794-160877795	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs55774412	chr6:160877800-160877801	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs55769008	chr6:160877801-160877802	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs55748808	chr6:160877810-160877811	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10945671	chr6:160877817-160877818	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10945672	chr6:160877820-160877821	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377035116	chr6:160877825-160877826	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201116311	chr6:160877826-160877827	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370358194	chr6:160877827-160877828	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111318123	chr6:160877828-160877829	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112958296	chr6:160877830-160877831	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188397997	chr6:160877846-160877847	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111821130	chr6:160877847-160877848	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112275381	chr6:160877865-160877866	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199554257	chr6:160877869-160877870	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372241381	chr6:160877872-160877873	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111243301	chr6:160877876-160877877	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200809972	chr6:160877899-160877900	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111259762	chr6:160877908-160877909	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371372456	chr6:160877918-160877919	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570966242	chr6:160877929-160877930	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201786674	chr6:160877933-160877934	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182895783	chr6:160877951-160877952	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556485107	chr6:160877961-160877962	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569703771	chr6:160877972-160877973	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62440433	chr6:160877985-160877986	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76018427	chr6:160878006-160878007	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555500809	chr6:160878057-160878058	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572469598	chr6:160878077-160878078	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149565105	chr6:160878078-160878079	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553888156	chr6:160878091-160878092	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189754059	chr6:160878113-160878114	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560348770	chr6:160878180-160878181	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562807119	chr6:160878220-160878221	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576083156	chr6:160878284-160878285	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61345061	chr6:160878291-160878292	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113580890	chr6:160878311-160878312	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374934993	chr6:160878315-160878316	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113070933	chr6:160878450-160878451	Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143266951	chr6:160878455-160878456	Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148337847	chr6:160878460-160878461	Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Follicular lymphoma	20505157	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
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	19459884	CNVD
Hearing loss	19459884	CNVD
Microcephaly	19459884	CNVD
Coronary artery disease	17160897	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	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
Non-syndromic sensorineural hearing loss	18451855	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
Autism	21865298	CNVD
Schizophrenia	23813976	CNVD
Carotid artery disease	21127300	CNVD

Chromatin state (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:160863600-160882800	Weak transcription	Gastric	stomach
2	chr6:160866600-160883800	Weak transcription	Spleen	Spleen
3	chr6:160867000-160877800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:160876600-160877800	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr6:160876600-160882600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr6:160876600-160882600	Enhancers	Dnd41	blood
7	chr6:160876600-160882800	Enhancers	Primary T cells fromperipheralblood	blood
8	chr6:160876600-160882800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:160876600-160883000	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr6:160876800-160877800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr6:160876800-160877800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr6:160876800-160877800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr6:160876800-160877800	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr6:160876800-160878000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr6:160876800-160878000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr6:160876800-160883800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr6:160877000-160877800	Enhancers	Primary B cells from peripheral blood	blood
18	chr6:160877000-160878200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:160877200-160879000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:160877200-160879200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr6:160877200-160882600	Weak transcription	Osteobl	bone
22	chr6:160877400-160878200	Weak transcription	Placenta	Placenta
23	chr6:160877400-160878600	Weak transcription	A549	lung
24	chr6:160877400-160879600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr6:160877400-160882200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr6:160877400-160882200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr6:160877400-160882600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr6:160877400-160882800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:160877400-160882800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:160877400-160882800	Weak transcription	NHLF	lung
31	chr6:160877400-160883800	Weak transcription	Pancreas	Pancrea
32	chr6:160877400-160884000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr6:160877600-160879200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr6:160877600-160883400	Strong transcription	Liver	Liver
35	chr6:160877800-160878200	Weak transcription	Primary B cells from peripheral blood	blood
36	chr6:160877800-160878800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr6:160877800-160878800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr6:160877800-160878800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr6:160877800-160879000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr6:160877800-160879400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr6:160878000-160878400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr6:160878000-160878400	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr6:160878200-160878400	Enhancers	Placenta	Placenta
44	chr6:160878200-160879200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr6:160878200-160885000	Enhancers	Primary B cells from peripheral blood	blood
46	chr6:160878400-160878600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
47	chr6:160878400-160879200	Weak transcription	Placenta	Placenta
48	chr6:160878400-160882800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:160878400-160882800	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr6:160878600-160879600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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