Variant report

Variant	nsv886674
Chromosome Location	chr6:132613798-132694751
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:830)
CpG islands
(count:0)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:132654701-132655804	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:132621513-132621801	HepG2	liver:	n/a	n/a
3	ATF2	chr6:132686637-132687239	GM12878	blood:	n/a	n/a
4	ATF2	chr6:132686605-132687324	GM12878	blood:	n/a	n/a
5	BACH1	chr6:132632147-132632218	K562	blood:	n/a	n/a
6	BACH1	chr6:132675964-132676231	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:132669416-132669559	K562	blood:	n/a	n/a
8	BATF	chr6:132686396-132687158	GM12878	blood:	n/a	n/a
9	BATF	chr6:132686648-132687157	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:132686385-132687090	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:132686307-132687173	GM12878	blood:	n/a	n/a
12	BCL3	chr6:132686719-132687169	GM12878	blood:	n/a	n/a
13	BCLAF1	chr6:132686404-132687116	GM12878	blood:	n/a	n/a
14	BCLAF1	chr6:132686377-132687257	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:132687693-132688000	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:132686511-132687167	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:132644876-132645139	HepG2	liver:	n/a	n/a
18	BHLHE40	chr6:132655418-132655780	HepG2	liver:	n/a	n/a
19	BHLHE40	chr6:132654736-132655147	HepG2	liver:	n/a	n/a
20	BRCA1	chr6:132635606-132635625	GM12878	blood:	n/a	n/a
21	BRCA1	chr6:132621688-132621954	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:132613952-132614196	IMR90	lung:	n/a	chr6:132614070-132614081
23	CEBPB	chr6:132628351-132628446	A549	lung:	n/a	n/a
24	CEBPB	chr6:132686566-132687289	GM12878	blood:	n/a	n/a
25	CEBPB	chr6:132690116-132690385	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:132641147-132641459	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:132690189-132690346	A549	lung:	n/a	n/a
28	CEBPB	chr6:132690072-132690440	IMR90	lung:	n/a	n/a
29	CEBPB	chr6:132628257-132628522	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:132626997-132627270	A549	lung:	n/a	chr6:132627104-132627115
31	CEBPB	chr6:132658420-132658603	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:132690695-132691034	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:132627029-132627259	IMR90	lung:	n/a	chr6:132627104-132627115
34	CEBPB	chr6:132670542-132670742	HepG2	liver:	n/a	chr6:132670687-132670698
35	CEBPB	chr6:132685397-132685723	HepG2	liver:	n/a	chr6:132685557-132685568
36	CEBPB	chr6:132686823-132687093	GM12878	blood:	n/a	n/a
37	CEBPB	chr6:132621578-132621786	A549	lung:	n/a	n/a
38	CEBPB	chr6:132621554-132621860	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr6:132613945-132614231	HepG2	liver:	n/a	chr6:132614070-132614081
40	CEBPB	chr6:132643603-132643926	IMR90	lung:	n/a	n/a
41	CEBPB	chr6:132628354-132628565	IMR90	lung:	n/a	n/a
42	CEBPB	chr6:132626929-132627262	HepG2	liver:	n/a	chr6:132627104-132627115
43	CEBPB	chr6:132670681-132670736	IMR90	lung:	n/a	chr6:132670687-132670698
44	CHD1	chr6:132621373-132622005	IMR90	lung:	n/a	n/a
45	CHD2	chr6:132655427-132655673	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr6:132686495-132687096	GM12878	blood:	n/a	n/a
47	CHD2	chr6:132657678-132657720	HepG2	liver:	n/a	n/a
48	CTCF	chr6:132621580-132621730	AG09309	skin:	n/a	chr6:132621655-132621671 chr6:132621657-132621670 chr6:132621654-132621672 chr6:132621656-132621677
49	CTCF	chr6:132621580-132621730	GM12878	blood:	n/a	chr6:132621655-132621671 chr6:132621657-132621670 chr6:132621654-132621672 chr6:132621656-132621677
50	CTCF	chr6:132621436-132621888	GM12878	blood:	n/a	chr6:132621655-132621671 chr6:132621657-132621670 chr6:132621654-132621672 chr6:132621656-132621677

No data

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:132649643..132651250-chr6:132662888..132664788,2	MCF-7	breast:
2	chr6:132600817..132602327-chr6:132613911..132616035,2	K562	blood:
3	chr6:132613610..132615905-chr6:132619619..132622099,2	K562	blood:
4	chr6:132621208..132622414-chr6:132713427..132714582,10	MCF-7	breast:
5	chr6:132687277..132689536-chr6:132691486..132694409,3	K562	blood:
6	6:132269655-132282174..6:132614342-132616667	H1-hESC	embryonic stem cell:	embryo
7	chr6:132621360..132622167-chr6:132713670..132714516,2	MCF-7	breast:
8	chr6:132653758..132656591-chr6:132657655..132660147,2	K562	blood:
9	chr6:132603488..132605263-chr6:132623712..132625367,2	K562	blood:
10	6:132646256-132647474..6:132647474-132649464	GM12878	blood:
11	6:132182612-132191683..6:132614342-132616667	H1-hESC	embryonic stem cell:	embryo
12	chr6:132600758..132601636-chr6:132619204..132619917,2	K562	blood:
13	chr6:132687277..132689201-chr6:132691486..132694409,2	K562	blood:
14	chr6:132621089..132622122-chr6:132804970..132805985,5	MCF-7	breast:
15	chr20:49346564..49349230-chr6:132633452..132636150,2	MCF-7	breast:
16	chr6:132600727..132601573-chr6:132618032..132618974,2	MCF-7	breast:
17	chr6:132684501..132686095-chr6:132688658..132690202,2	K562	blood:
18	6:132243347-132257249..6:132641847-132646256	Hela-S3	cervix:
19	chr6:132684114..132687099-chr6:132691049..132693602,3	MCF-7	breast:
20	chr6:132649643..132651250-chr6:132662888..132664788,2	MCF-7	breast:
21	6:132282174-132286019..6:132641847-132646256	GM12878	blood:
22	chr6:132613610..132615905-chr6:132619619..132622099,2	K562	blood:
23	chr6:132612822..132613346-chr6:132621640..132622145,2	K562	blood:
24	6:132218210-132218634..6:132641847-132646256	H1-hESC	embryonic stem cell:	embryo
25	chr6:132621505..132622229-chr6:132805066..132805735,3	MCF-7	breast:
26	chr20:52349507..52351793-chr6:132662386..132665362,2	MCF-7	breast:
27	6:132317180-132317980..6:132641847-132646256	K562	blood:
28	chr6:132684501..132686095-chr6:132688658..132690202,2	K562	blood:
29	chr6:132653758..132656591-chr6:132657655..132660147,2	K562	blood:
30	chr6:132687277..132689201-chr6:132691486..132694409,2	K562	blood:
31	chr6:132600647..132601321-chr6:132619115..132620190,4	MCF-7	breast:
32	chr6:132684114..132687099-chr6:132691049..132693602,3	MCF-7	breast:
33	chr6:132600387..132601705-chr6:132618997..132620734,23	MCF-7	breast:
34	6:132232580-132243347..6:132641847-132646256	GM12878	blood:
35	6:132182612-132191683..6:132619491-132621769	Hela-S3	cervix:
36	chr6:132600646..132601168-chr6:132616048..132617057,3	MCF-7	breast:
37	chr6:131206668..131207174-chr6:132619578..132620094,2	K562	blood:
38	chr6:132687277..132689536-chr6:132691486..132694409,3	K562	blood:
39	chr6:132621231..132622212-chr6:132805003..132805993,9	K562	blood:
40	chr6:132600489..132601319-chr6:132621500..132622187,2	MCF-7	breast:
41	6:132269655-132282174..6:132619491-132621769	Hela-S3	cervix:
42	chr6:132618961..132619982-chr6:132805082..132805920,3	MCF-7	breast:
43	chr6:132651937..132652448-chr8:134519934..134520831,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MOXD1	hsa-miR-21-5p	chr6:132617234-132617254
2	MOXD1	hsa-miR-21-5p	chr6:132617206-132617227

Variant related genes	Relation type
MOXD1	TF binding region
ENSG00000118523	chromatin interactions
ENSG00000197594	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000079931	chromatin interactions
ENSG00000227220	chromatin interactions

Extended variants
information (count: 3133 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3133 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17061146	chr6:132613798-132613799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558989790	chr6:132613808-132613809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528193798	chr6:132613835-132613836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551090284	chr6:132613879-132613880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571405263	chr6:132613915-132613916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538529688	chr6:132613978-132613979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536889985	chr6:132613984-132613985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556325513	chr6:132614015-132614016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578040228	chr6:132614018-132614019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372156760	chr6:132614024-132614025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376393742	chr6:132614047-132614048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536611578	chr6:132614054-132614055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138015537	chr6:132614063-132614064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566897683	chr6:132614070-132614071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554277137	chr6:132614136-132614137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79149731	chr6:132614145-132614146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367696337	chr6:132614164-132614165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558823308	chr6:132614197-132614198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117202003	chr6:132614200-132614201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544481974	chr6:132614201-132614202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9483432	chr6:132614269-132614270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs542490871	chr6:132614280-132614281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574808460	chr6:132614303-132614304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182521718	chr6:132614335-132614336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377300484	chr6:132614350-132614351	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs377157275	chr6:132614358-132614359	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs149091753	chr6:132614368-132614369	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs186912274	chr6:132614370-132614371	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs528110322	chr6:132614371-132614372	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs115108989	chr6:132614419-132614420	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs9483433	chr6:132614494-132614495	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs114611185	chr6:132614499-132614500	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs550512704	chr6:132614526-132614527	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs567520067	chr6:132614551-132614552	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs531553274	chr6:132614560-132614561	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs73544038	chr6:132614636-132614637	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543663008	chr6:132614673-132614674	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs546948144	chr6:132614701-132614702	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs564543140	chr6:132614734-132614735	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs148282017	chr6:132614741-132614742	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs143825108	chr6:132614757-132614758	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs373213599	chr6:132614765-132614766	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs147258689	chr6:132614783-132614784	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569260968	chr6:132614804-132614805	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs139041485	chr6:132614811-132614812	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs554886132	chr6:132614884-132614885	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs376470169	chr6:132614901-132614902	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs574719808	chr6:132614923-132614924	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs143069443	chr6:132614936-132614937	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs192517110	chr6:132614956-132614957	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	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
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132610800-132614400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:132611000-132625600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:132611200-132617000	Weak transcription	NHDF-Ad	bronchial
4	chr6:132612200-132616000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr6:132612600-132626400	Weak transcription	Fetal Stomach	stomach
6	chr6:132614400-132619000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:132615000-132617000	Weak transcription	Fetal Kidney	kidney
8	chr6:132615400-132617200	Weak transcription	Osteobl	bone
9	chr6:132615600-132618000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:132615800-132635400	Weak transcription	Fetal Lung	lung
11	chr6:132616000-132616400	Strong transcription	Cortex derived primary cultured neurospheres	brain
12	chr6:132616200-132620400	Weak transcription	Esophagus	oesophagus
13	chr6:132616200-132625200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr6:132616400-132617200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr6:132616600-132625200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr6:132617000-132618400	Strong transcription	Fetal Kidney	kidney
17	chr6:132617000-132618800	Strong transcription	NHDF-Ad	bronchial
18	chr6:132617200-132618400	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr6:132617200-132618600	Strong transcription	Osteobl	bone
20	chr6:132617200-132627600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:132617400-132617600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:132617600-132619000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:132617600-132619200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:132617600-132626200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:132618000-132619000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr6:132618200-132619000	Enhancers	Brain Hippocampus Middle	brain
27	chr6:132618400-132618600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
28	chr6:132618400-132631600	Weak transcription	Fetal Kidney	kidney
29	chr6:132618600-132624600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr6:132618600-132626200	Weak transcription	Osteobl	bone
31	chr6:132618800-132620400	Enhancers	Brain Cingulate Gyrus	brain
32	chr6:132618800-132634600	Weak transcription	NHDF-Ad	bronchial
33	chr6:132619000-132620200	Weak transcription	Brain Hippocampus Middle	brain
34	chr6:132619000-132622800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:132619000-132625200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:132620200-132620400	Enhancers	Brain Hippocampus Middle	brain
37	chr6:132622800-132623000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:132623000-132623200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:132623200-132625200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:132624000-132624600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:132624600-132625800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:132624600-132627800	Strong transcription	Cortex derived primary cultured neurospheres	brain
43	chr6:132625000-132627600	Weak transcription	Fetal Brain Female	brain
44	chr6:132625200-132625800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:132625200-132626800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr6:132625200-132627000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:132625200-132627800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:132625600-132625800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:132625800-132626000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:132625800-132626200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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