Variant report

Variant	nsv427767
Chromosome Location	chr6:130875056-131008620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:990)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:990 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:130996306-130996584	K562	blood:	n/a	n/a
2	ATF2	chr6:130897025-130897525	GM12878	blood:	n/a	n/a
3	ATF2	chr6:130945114-130945717	GM12878	blood:	n/a	n/a
4	ATF2	chr6:130946799-130947649	GM12878	blood:	n/a	n/a
5	ATF2	chr6:130954017-130954448	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:130914348-130914708	GM12878	blood:	n/a	n/a
7	ATF2	chr6:130945152-130945633	GM12878	blood:	n/a	n/a
8	ATF2	chr6:130954092-130954462	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr6:130946838-130947649	GM12878	blood:	n/a	n/a
10	ATF2	chr6:130897079-130897454	GM12878	blood:	n/a	n/a
11	ATF2	chr6:130882294-130882744	GM12878	blood:	n/a	n/a
12	ATF3	chr6:130937020-130937183	K562	blood:	n/a	n/a
13	ATF3	chr6:130947082-130947308	K562	blood:	n/a	n/a
14	ATF3	chr6:130937020-130937339	GM12878	blood:	n/a	n/a
15	BACH1	chr6:131006798-131006819	K562	blood:	n/a	n/a
16	BATF	chr6:130998434-130998722	GM12878	blood:	n/a	n/a
17	BATF	chr6:130943366-130943635	GM12878	blood:	n/a	n/a
18	BATF	chr6:130945222-130945603	GM12878	blood:	n/a	chr6:130945401-130945412
19	BATF	chr6:130885163-130885395	GM12878	blood:	n/a	chr6:130885286-130885297
20	BATF	chr6:130885156-130885417	GM12878	blood:	n/a	chr6:130885286-130885297
21	BATF	chr6:130941434-130941664	GM12878	blood:	n/a	n/a
22	BATF	chr6:130914374-130914653	GM12878	blood:	n/a	chr6:130914550-130914561
23	BATF	chr6:130943375-130943649	GM12878	blood:	n/a	n/a
24	BATF	chr6:130897115-130897445	GM12878	blood:	n/a	n/a
25	BATF	chr6:130914392-130914685	GM12878	blood:	n/a	chr6:130914550-130914561
26	BATF	chr6:130946902-130947726	GM12878	blood:	n/a	chr6:130947703-130947713 chr6:130947516-130947526 chr6:130947179-130947189
27	BATF	chr6:130945201-130945571	GM12878	blood:	n/a	chr6:130945401-130945412
28	BATF	chr6:130941435-130941683	GM12878	blood:	n/a	n/a
29	BATF	chr6:130946973-130947315	GM12878	blood:	n/a	chr6:130947179-130947189
30	BCL11A	chr6:130954087-130954378	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr6:130897117-130897465	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:130945213-130945570	GM12878	blood:	n/a	n/a
33	BCL11A	chr6:130954119-130954419	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr6:130946925-130947330	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:130945232-130945531	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:130897119-130897435	GM12878	blood:	n/a	n/a
37	BCL11A	chr6:130946969-130947280	GM12878	blood:	n/a	n/a
38	BCL3	chr6:130946900-130947346	GM12878	blood:	n/a	n/a
39	BCL3	chr6:130946972-130947231	GM12878	blood:	n/a	n/a
40	BCL3	chr6:130945162-130945635	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:130897084-130897598	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:130945164-130945584	GM12878	blood:	n/a	n/a
43	BCLAF1	chr6:130946878-130947334	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:130941455-130941841	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:130945272-130945534	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:130897123-130897536	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:130991405-130991633	HepG2	liver:	n/a	n/a
48	CBX3	chr6:130938783-130939209	HCT-116	colon:	n/a	n/a
49	CBX3	chr6:130922854-130924345	HCT-116	colon:	n/a	n/a
50	CBX3	chr6:130946938-130947892	HCT-116	colon:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:130992677-130992727	HL-60	blood:	n/a
2	chr6:130992677-130992727	NHBE	bronchial:	n/a
3	chr6:130992677-130992727	AoSMC	blood vessel:	n/a
4	chr6:130992677-130992727	HNPCEpiC	eye:	n/a
5	chr6:130992677-130992727	HPAEpiC	pulmonary alveolar:	n/a
6	chr6:130992677-130992727	ovcar-3	ovarian:	n/a
7	chr6:130992677-130992727	AG09309	skin:	n/a
8	chr6:130992677-130992727	PFSK-1	brain:	n/a
9	chr6:130992677-130992727	SKMC	muscle:	n/a
10	chr6:130992677-130992727	LNCaP	prostate:	n/a
11	chr6:130992677-130992727	ProgFib	skin:	n/a
12	chr6:130992677-130992727	ECC-1	luminal epithelium:	n/a
13	chr6:130992677-130992727	AG04449	skin:	fetal
14	chr6:130992677-130992727	NH-A	brain:	n/a
15	chr6:130992677-130992727	GM12891	blood:	n/a
16	chr6:130992677-130992727	GM19239	blood:	n/a
17	chr6:130992677-130992727	HMEC	breast:	n/a
18	chr6:130992677-130992727	RPTEC	kidney:	n/a
19	chr6:130992677-130992727	GM06990	blood:	n/a
20	chr6:130992677-130992727	HRE	kidney:	n/a
21	chr6:130992677-130992727	GM12892	blood:	n/a
22	chr6:130992677-130992727	AG09319	gingival:	n/a
23	chr6:130992677-130992727	BE2_C	brain:	n/a
24	chr6:130992677-130992727	HEK293	kidney:	embryo
25	chr6:130992677-130992727	HCF	heart:	n/a
26	chr6:130992677-130992727	CMK	blood:	n/a
27	chr6:130992677-130992727	HepG2	liver:	n/a
28	chr6:130992677-130992727	HCPEpiC	choroid plexus:	n/a
29	chr6:130992677-130992727	HCM	heart:	n/a
30	chr6:130992677-130992727	Caco-2	colon:	n/a
31	chr6:130992677-130992727	AG10803	skin:	n/a
32	chr6:130992677-130992727	GM12878	blood:	n/a
33	chr6:130992677-130992727	H1-hESC	embryonic stem cell:	embryo
34	chr6:130992677-130992727	HCT-116	colon:	n/a
35	chr6:130992677-130992727	AG04450	lung:	fetal
36	chr6:130992677-130992727	SK-N-MC	brain:	n/a
37	chr6:130992677-130992727	MCF10A-Er-Src	breast:	n/a
38	chr6:130992677-130992727	HRPEpiC	eye:	n/a
39	chr6:130992677-130992727	HAEpiC	amniotic membrane:	n/a
40	chr6:130992677-130992727	A549	lung:	n/a
41	chr6:130992677-130992727	IMR90	lung:	fetal
42	chr6:130992677-130992727	Hepatocyte	liver:	n/a
43	chr6:130992677-130992727	U87	brain:	n/a
44	chr6:130992677-130992727	K562	blood:	n/a
45	chr6:130992677-130992727	HIPEpiC	eye:	n/a
46	chr6:130992677-130992727	NB4	blood:	n/a
47	chr6:130992677-130992727	Jurkat	blood:	n/a
48	chr6:130992677-130992727	SK-N-SH	brain:	n/a
49	chr6:130992677-130992727	HUVEC	blood vessel:	n/a
50	chr6:130992677-130992727	PrEC	prostate:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:130987487..130989823-chr6:130991661..130995786,3	K562	blood:
2	chr6:130990956..130992945-chr6:130994542..130996616,2	K562	blood:
3	chr6:130994751..130996672-chr6:131006100..131008606,2	K562	blood:
4	chr6:130614666..130615631-chr6:130996925..130997908,2	MCF-7	breast:
5	chr6:130885144..130887510-chr6:130925182..130927047,2	K562	blood:
6	chr6:130876811..130878612-chr6:130880460..130883120,2	K562	blood:
7	chr6:130986671..130988987-chr6:130993431..130995786,2	K562	blood:
8	chr6:130990956..130992945-chr6:130994542..130996616,2	K562	blood:
9	chr6:130987487..130989823-chr6:130991661..130995786,3	K562	blood:
10	chr6:130986671..130988987-chr6:130993431..130995786,2	K562	blood:
11	chr6:130928750..130930789-chr6:130933145..130935900,2	K562	blood:
12	chr6:130643519..130644361-chr6:130996843..130997590,3	MCF-7	breast:
13	chr6:130994751..130996672-chr6:131006100..131008606,2	K562	blood:
14	chr17:56708616..56709251-chr6:130881822..130882325,2	MCF-7	breast:
15	chr6:130885144..130887510-chr6:130925182..130927047,2	K562	blood:
16	chr6:130928750..130930789-chr6:130933145..130935900,2	K562	blood:
17	chr6:130873679..130876307-chr6:130911669..130914160,2	K562	blood:
18	chr6:130873679..130876307-chr6:130911669..130914160,2	K562	blood:
19	chr6:130876811..130878612-chr6:130880460..130883120,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPB41L2-3	chr6:130947013-130947226	NONHSAT114905
2	lnc-TMEM200A-1	chr6:130917300-130917756	NONHSAT114904
3	lnc-EPB41L2-3	chr6:130935087-130935225	NONHSAT114905

No data

Variant related genes	Relation type
ENSG00000202438	TF binding region
ENSG00000202438	CpG island
ENSG00000212195	chromatin interactions

Extended variants
information (count: 4946 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4946 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548491534	chr6:130878216-130878217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116578140	chr6:130878245-130878246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs527940319	chr6:130878384-130878385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112955670	chr6:130878400-130878401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78057355	chr6:130878406-130878407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565170763	chr6:130878426-130878427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532326867	chr6:130878432-130878433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150329076	chr6:130878445-130878446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547322701	chr6:130878452-130878453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538260872	chr6:130878476-130878477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186550542	chr6:130878498-130878499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191726505	chr6:130878503-130878504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112919884	chr6:130878518-130878519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10872372	chr6:130878565-130878566	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs111801826	chr6:130878576-130878577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535992678	chr6:130878594-130878595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373685497	chr6:130878627-130878628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572207266	chr6:130878674-130878675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539324309	chr6:130878702-130878703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138015568	chr6:130878703-130878704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111971784	chr6:130878739-130878740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575965788	chr6:130878741-130878742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542990895	chr6:130878742-130878743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545925206	chr6:130878746-130878747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182382575	chr6:130878790-130878791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149504781	chr6:130878795-130878796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144089125	chr6:130878807-130878808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138754089	chr6:130878835-130878836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549078197	chr6:130878864-130878865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141862285	chr6:130878867-130878868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112072254	chr6:130878868-130878869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187497725	chr6:130878874-130878875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115712045	chr6:130878876-130878877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112034625	chr6:130878880-130878881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146046770	chr6:130878895-130878896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376308400	chr6:130878901-130878902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192019528	chr6:130878925-130878926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568483027	chr6:130878933-130878934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113452780	chr6:130878941-130878942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535531113	chr6:130878942-130878943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561212286	chr6:130878972-130878973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185787063	chr6:130879049-130879050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190465145	chr6:130879088-130879089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372971180	chr6:130879097-130879098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569438441	chr6:130879116-130879117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575925260	chr6:130879133-130879134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536988148	chr6:130879154-130879155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11154594	chr6:130879168-130879169	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs538031322	chr6:130879175-130879176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556492427	chr6:130879195-130879196	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	22495311	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
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Brain cancer	19584924	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:130878200-130879400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr6:130878800-130879200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:130879000-130879400	Enhancers	Fetal Stomach	stomach
4	chr6:130879200-130881400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:130879400-130881400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr6:130880000-130882200	Enhancers	HSMMtube	muscle
7	chr6:130880200-130882000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:130880400-130880600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr6:130880400-130881200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:130880400-130882200	Enhancers	NH-A	brain
11	chr6:130880600-130881600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr6:130880600-130881800	Enhancers	Osteobl	bone
13	chr6:130881000-130882000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr6:130881200-130882200	Enhancers	HSMM	muscle
15	chr6:130881400-130881800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:130881400-130881800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr6:130881600-130882200	Enhancers	Muscle Satellite Cultured Cells	--
18	chr6:130881600-130882400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr6:130882000-130882600	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr6:130882000-130882600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr6:130882000-130883000	Enhancers	Primary T cells from cord blood	blood
22	chr6:130882000-130883000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:130882000-130883000	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr6:130882000-130883200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:130882200-130882600	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr6:130882200-130883000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr6:130882200-130883000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr6:130882200-130883200	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:130882200-130883400	Weak transcription	HSMMtube	muscle
30	chr6:130882400-130882800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr6:130882400-130883000	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr6:130882600-130894400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr6:130882800-130884400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr6:130883400-130883600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:130883400-130883600	Enhancers	HSMMtube	muscle
36	chr6:130884600-130884800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr6:130893800-130894000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr6:130893800-130896800	Enhancers	Dnd41	blood
39	chr6:130894200-130894400	Enhancers	Thymus	Thymus
40	chr6:130894200-130897200	Enhancers	Primary T cells from cord blood	blood
41	chr6:130894200-130899000	Enhancers	Fetal Thymus	thymus
42	chr6:130894400-130895400	Weak transcription	Thymus	Thymus
43	chr6:130894400-130896000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr6:130894400-130896800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr6:130894400-130897000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr6:130894400-130897200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr6:130894600-130897000	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr6:130895000-130897000	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr6:130895200-130895400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:130895200-130900000	Enhancers	Primary T helper cells fromperipheralblood	blood

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