Variant report

Variant	nsv604668
Chromosome Location	chr6:132687248-132731358
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	chr6:132714073-132714255	HepG2	liver:	n/a	n/a
2	ATF2	chr6:132726180-132726820	GM12878	blood:	n/a	n/a
3	ATF2	chr6:132686605-132687324	GM12878	blood:	n/a	n/a
4	ATF2	chr6:132725318-132726038	GM12878	blood:	n/a	n/a
5	ATF2	chr6:132726247-132726788	GM12878	blood:	n/a	n/a
6	BACH1	chr6:132722976-132723047	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:132720843-132721071	GM12878	blood:	n/a	chr6:132720978-132720988 chr6:132720977-132720988
8	BATF	chr6:132725461-132726107	GM12878	blood:	n/a	n/a
9	BATF	chr6:132726394-132726656	GM12878	blood:	n/a	chr6:132726513-132726524
10	BATF	chr6:132725365-132726168	GM12878	blood:	n/a	n/a
11	BATF	chr6:132720900-132721132	GM12878	blood:	n/a	chr6:132720978-132720988 chr6:132720977-132720988
12	BATF	chr6:132726358-132726658	GM12878	blood:	n/a	chr6:132726513-132726524
13	BCL11A	chr6:132726395-132726555	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:132726405-132726655	GM12878	blood:	n/a	n/a
15	BCL3	chr6:132726291-132726676	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:132686377-132687257	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:132687693-132688000	GM12878	blood:	n/a	n/a
18	CEBPB	chr6:132690695-132691034	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:132723045-132723232	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr6:132690189-132690346	A549	lung:	n/a	n/a
21	CEBPB	chr6:132712797-132713343	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:132686566-132687289	GM12878	blood:	n/a	n/a
23	CEBPB	chr6:132690072-132690440	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:132714044-132714199	A549	lung:	n/a	n/a
25	CEBPB	chr6:132701614-132701856	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:132690116-132690385	HepG2	liver:	n/a	n/a
27	CHD2	chr6:132722886-132722923	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:132713470-132713473	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr6:132726260-132726777	GM12878	blood:	n/a	n/a
30	CTBP2	chr6:132721722-132723412	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr6:132722513-132722640	GM19240	blood:	n/a	chr6:132722572-132722585 chr6:132722596-132722609
32	CTCF	chr6:132714040-132714190	HepG2	liver:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
33	CTCF	chr6:132714047-132714241	GM12878	blood:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
34	CTCF	chr6:132714040-132714190	SK-N-SH_RA	brain:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
35	CTCF	chr6:132722600-132722750	GM12872	blood:	n/a	chr6:132722723-132722736 chr6:132722729-132722742
36	CTCF	chr6:132688848-132688909	GM13977	blood:	n/a	n/a
37	CTCF	chr6:132722543-132722662	ProgFib	skin:	n/a	chr6:132722572-132722585 chr6:132722596-132722609
38	CTCF	chr6:132713879-132714278	HCT-116	colon:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
39	CTCF	chr6:132688852-132688968	Medullo	brain:	n/a	n/a
40	CTCF	chr6:132722685-132722812	GM12892	blood:	n/a	chr6:132722723-132722736 chr6:132722729-132722742
41	CTCF	chr6:132713926-132714287	HepG2	liver:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
42	CTCF	chr6:132722560-132722710	AG09319	gingival:	n/a	chr6:132722572-132722585 chr6:132722596-132722609
43	CTCF	chr6:132714040-132714190	HCPEpiC	choroid plexus:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
44	CTCF	chr6:132714080-132714230	AG04450	lung:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
45	CTCF	chr6:132714120-132714270	NHEK	skin:	n/a	n/a
46	CTCF	chr6:132714300-132714450	HMEC	breast:	n/a	n/a
47	CTCF	chr6:132714060-132714210	HPAF	blood vessel:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
48	CTCF	chr6:132714080-132714230	BJ	skin:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
49	CTCF	chr6:132714040-132714190	GM12865	blood:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132
50	CTCF	chr6:132714020-132714170	GM12867	blood:	n/a	chr6:132714112-132714133 chr6:132714117-132714135 chr6:132714119-132714132

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:132696379-132696429	Hela-S3	cervix:	n/a
2	chr6:132696379-132696429	Hela-S3	cervix:	n/a
3	chr6:132697112-132697162	AG04449	skin:	fetal
4	chr6:132722664-132722714	T-47D	breast:	n/a
5	chr6:132722822-132722872	RPTEC	kidney:	n/a
6	chr6:132722810-132722860	Hela-S3	cervix:	n/a
7	chr6:132697112-132697162	NB4	blood:	n/a
8	chr6:132697112-132697162	HL-60	blood:	n/a
9	chr6:132719721-132719771	PANC-1	pancreas:	n/a
10	chr6:132719721-132719771	Jurkat	blood:	n/a
11	chr6:132723164-132723214	HRE	kidney:	n/a
12	chr6:132725393-132725443	HCM	heart:	n/a
13	chr6:132722045-132722095	SK-N-MC	brain:	n/a
14	chr6:132722664-132722714	NT2-D1	testis:	n/a
15	chr6:132725393-132725443	PrEC	prostate:	n/a
16	chr6:132722822-132722872	ProgFib	skin:	n/a
17	chr6:132722664-132722714	HEK293	kidney:	embryo
18	chr6:132722778-132722828	NH-A	brain:	n/a
19	chr6:132722045-132722095	HEEpiC	esophagus:	n/a
20	chr6:132722664-132722714	HCT-116	colon:	n/a
21	chr6:132723033-132723083	HRPEpiC	eye:	n/a
22	chr6:132696379-132696429	ECC-1	luminal epithelium:	n/a
23	chr6:132722664-132722714	Caco-2	colon:	n/a
24	chr6:132722810-132722860	GM12892	blood:	n/a
25	chr6:132722315-132722365	NHBE	bronchial:	n/a
26	chr6:132719721-132719771	GM19239	blood:	n/a
27	chr6:132697112-132697162	ECC-1	luminal epithelium:	n/a
28	chr6:132722822-132722872	PANC-1	pancreas:	n/a
29	chr6:132722770-132722820	NT2-D1	testis:	n/a
30	chr6:132724047-132724097	MCF-7	breast:	n/a
31	chr6:132722770-132722820	LNCaP	prostate:	n/a
32	chr6:132722045-132722095	HEK293	kidney:	embryo
33	chr6:132724047-132724097	T-47D	breast:	n/a
34	chr6:132697112-132697162	AG04450	lung:	fetal
35	chr6:132722810-132722860	HUVEC	blood vessel:	n/a
36	chr6:132697112-132697162	HMEC	breast:	n/a
37	chr6:132722045-132722095	K562	blood:	n/a
38	chr6:132725393-132725443	Caco-2	colon:	n/a
39	chr6:132696379-132696429	T-47D	breast:	n/a
40	chr6:132722770-132722820	PFSK-1	brain:	n/a
41	chr6:132722778-132722828	H1-hESC	embryonic stem cell:	embryo
42	chr6:132696379-132696429	NT2-D1	testis:	n/a
43	chr6:132722315-132722365	AG09319	gingival:	n/a
44	chr6:132722045-132722095	SK-N-SH_RA	brain:	n/a
45	chr6:132724047-132724097	SK-N-SH_RA	brain:	n/a
46	chr6:132723164-132723214	PFSK-1	brain:	n/a
47	chr6:132697112-132697162	HIPEpiC	eye:	n/a
48	chr6:132722664-132722714	HCM	heart:	n/a
49	chr6:132722421-132722471	PrEC	prostate:	n/a
50	chr6:132722664-132722714	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:132684501..132686095-chr6:132688658..132690202,2	K562	blood:
2	chr6:132621360..132622167-chr6:132713670..132714516,2	MCF-7	breast:
3	chr6:132687277..132689536-chr6:132691486..132694409,3	K562	blood:
4	chr6:132687277..132689201-chr6:132691486..132694409,2	K562	blood:
5	chr6:132687277..132689536-chr6:132691486..132694409,3	K562	blood:
6	chr6:132600570..132601283-chr6:132713650..132714534,4	K562	blood:
7	chr6:132687277..132689201-chr6:132691486..132694409,2	K562	blood:
8	chr6:132600674..132601355-chr6:132713689..132714612,2	MCF-7	breast:
9	chr6:132621208..132622414-chr6:132713427..132714582,10	MCF-7	breast:
10	chr6:132684114..132687099-chr6:132691049..132693602,3	MCF-7	breast:

Variant related genes	Relation type
MOXD1	TF binding region
MOXD1	CpG island

Extended variants
information (count: 1693 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1693 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9373014	chr6:132687248-132687249	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17061204	chr6:132687293-132687294	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs35419950	chr6:132687314-132687315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547258775	chr6:132687318-132687319	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536044767	chr6:132687337-132687338	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560762124	chr6:132687482-132687483	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114496271	chr6:132687499-132687500	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191812253	chr6:132687511-132687512	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571185791	chr6:132687568-132687569	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530444522	chr6:132687582-132687583	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550603243	chr6:132687605-132687606	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs149438031	chr6:132687617-132687618	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs35284575	chr6:132687640-132687641	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs397824212	chr6:132687645-132687646	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs553376580	chr6:132687719-132687720	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs200289679	chr6:132687727-132687728	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs536036811	chr6:132687808-132687809	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs552777295	chr6:132687826-132687827	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs377466451	chr6:132687854-132687855	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs182203106	chr6:132687856-132687857	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs538512270	chr6:132687944-132687945	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs73780059	chr6:132687955-132687956	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs114083101	chr6:132687974-132687975	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs186789313	chr6:132687976-132687977	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs144823966	chr6:132687985-132687986	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs552745406	chr6:132687992-132687993	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs117520506	chr6:132687993-132687994	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs1338387	chr6:132688042-132688043	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs77275226	chr6:132688075-132688076	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192325480	chr6:132688117-132688118	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563042590	chr6:132688258-132688259	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530484899	chr6:132688268-132688269	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73780060	chr6:132688281-132688282	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs567333951	chr6:132688282-132688283	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529773569	chr6:132688317-132688318	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544831573	chr6:132688319-132688320	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546306387	chr6:132688321-132688322	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9483439	chr6:132688331-132688332	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs538451497	chr6:132688365-132688366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143959575	chr6:132688384-132688385	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145939795	chr6:132688402-132688403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139888674	chr6:132688434-132688435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73546086	chr6:132688485-132688486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574967610	chr6:132688576-132688577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77869788	chr6:132688615-132688616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199600541	chr6:132688661-132688662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs151203485	chr6:132688665-132688666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140269628	chr6:132688717-132688718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373107732	chr6:132688769-132688770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563187693	chr6:132688770-132688771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132677200-132688600	Weak transcription	Osteobl	bone
2	chr6:132677400-132701200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:132678600-132690400	Weak transcription	NH-A	brain
4	chr6:132679000-132690000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr6:132682000-132692200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr6:132682200-132705800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:132683600-132688000	Enhancers	Fetal Lung	lung
8	chr6:132685600-132687400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:132685600-132687800	Enhancers	Primary B cells from peripheral blood	blood
10	chr6:132685600-132688400	Enhancers	Fetal Kidney	kidney
11	chr6:132685800-132687400	Enhancers	Primary B cells from cord blood	blood
12	chr6:132686000-132687800	Weak transcription	NHDF-Ad	bronchial
13	chr6:132686600-132690200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:132686800-132687800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:132686800-132688200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:132686800-132690200	Weak transcription	HSMMtube	muscle
17	chr6:132687000-132687600	Enhancers	GM12878-XiMat	blood
18	chr6:132687000-132690200	Weak transcription	HSMM	muscle
19	chr6:132687000-132690400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:132687200-132687800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr6:132687200-132689000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:132687200-132690000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:132687400-132690400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:132687600-132687800	Enhancers	Duodenum Mucosa	Duodenum
25	chr6:132687600-132688000	Flanking Active TSS	GM12878-XiMat	blood
26	chr6:132687800-132688000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr6:132687800-132689000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:132687800-132690000	Strong transcription	NHDF-Ad	bronchial
29	chr6:132688000-132688400	Enhancers	GM12878-XiMat	blood
30	chr6:132688000-132692000	Weak transcription	Fetal Lung	lung
31	chr6:132688200-132689600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:132688400-132692000	Weak transcription	Fetal Kidney	kidney
33	chr6:132688600-132689400	Strong transcription	Osteobl	bone
34	chr6:132689000-132690200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:132689000-132690800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:132689400-132690000	Weak transcription	Osteobl	bone
37	chr6:132689600-132693600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:132690000-132690400	Genic enhancers	NHDF-Ad	bronchial
39	chr6:132690000-132690400	Enhancers	Osteobl	bone
40	chr6:132690000-132690600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr6:132690000-132690600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr6:132690200-132690600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:132690200-132690800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:132690200-132690800	Enhancers	HSMM	muscle
45	chr6:132690200-132690800	Enhancers	HSMMtube	muscle
46	chr6:132690400-132690600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr6:132690400-132690600	Enhancers	Brain Angular Gyrus	brain
48	chr6:132690400-132690600	Enhancers	NH-A	brain
49	chr6:132690400-132690600	Flanking Active TSS	NHDF-Ad	bronchial
50	chr6:132690400-132691000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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