Variant report

Variant	nsv886709
Chromosome Location	chr6:140911389-141015758
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:575)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:575 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:140962459-140962964	GM12878	blood:	n/a	n/a
2	BACH1	chr6:140931711-140931747	K562	blood:	n/a	n/a
3	BATF	chr6:140962571-140962917	GM12878	blood:	n/a	n/a
4	BATF	chr6:140957343-140957787	GM12878	blood:	n/a	n/a
5	BATF	chr6:140999274-140999525	GM12878	blood:	n/a	n/a
6	BATF	chr6:140962532-140962960	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:140962665-140962965	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:140957373-140957725	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:140962597-140962976	GM12878	blood:	n/a	n/a
10	BCL3	chr6:140923817-140924135	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:140957284-140957740	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:140962545-140962966	GM12878	blood:	n/a	n/a
13	CBX3	chr6:140948115-140948497	K562	blood:	n/a	n/a
14	CCNT2	chr6:141006502-141006618	K562	blood:	n/a	n/a
15	CEBPB	chr6:140950761-140951042	K562	blood:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
16	CEBPB	chr6:140978749-140979032	IMR90	lung:	n/a	n/a
17	CEBPB	chr6:140944453-140945069	HCT-116	colon:	n/a	chr6:140944736-140944747
18	CEBPB	chr6:140944558-140944922	A549	lung:	n/a	chr6:140944736-140944747
19	CEBPB	chr6:140950874-140950971	Hela-S3	cervix:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
20	CEBPB	chr6:140978793-140979003	K562	blood:	n/a	n/a
21	CEBPB	chr6:140950718-140951059	HepG2	liver:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
22	CEBPB	chr6:140950730-140951057	IMR90	lung:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
23	CEBPB	chr6:140950521-140950534	K562	blood:	n/a	n/a
24	CEBPB	chr6:140944593-140944912	A549	lung:	n/a	chr6:140944736-140944747
25	CEBPB	chr6:140950786-140950984	H1-hESC	embryonic stem cell:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
26	CEBPB	chr6:140950735-140950999	A549	lung:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
27	CEBPB	chr6:140928375-140928391	K562	blood:	n/a	n/a
28	CEBPB	chr6:140926256-140926456	HepG2	liver:	n/a	chr6:140926351-140926362 chr6:140926350-140926363
29	CEBPB	chr6:140944554-140945005	IMR90	lung:	n/a	chr6:140944736-140944747
30	CEBPB	chr6:140911779-140912094	IMR90	lung:	n/a	chr6:140911918-140911929 chr6:140911918-140911931 chr6:140911917-140911934 chr6:140911918-140911931 chr6:140911918-140911929 chr6:140911918-140911931
31	CEBPB	chr6:140944651-140944864	HepG2	liver:	n/a	chr6:140944736-140944747
32	CEBPB	chr6:140933530-140933696	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:140978710-140979038	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:141006378-141006630	IMR90	lung:	n/a	n/a
35	CEBPB	chr6:140944568-140944937	Hela-S3	cervix:	n/a	chr6:140944736-140944747
36	CEBPB	chr6:141006465-141006576	HepG2	liver:	n/a	n/a
37	CEBPB	chr6:140944477-140945154	HCT-116	colon:	n/a	chr6:140944736-140944747
38	CEBPB	chr6:140992588-140992943	HepG2	liver:	n/a	chr6:140992865-140992876
39	CEBPB	chr6:141005694-141005708	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr6:140923491-140924190	GM12878	blood:	n/a	n/a
41	CTCF	chr6:140993205-140993328	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr6:140971300-140971450	HMEC	breast:	n/a	n/a
43	CTCF	chr6:140971380-140971530	HVMF	connective:	n/a	n/a
44	CTCF	chr6:140993040-140993190	HCT-116	colon:	n/a	n/a
45	CTCF	chr6:140971404-140971485	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr6:140993122-140993300	HepG2	liver:	n/a	n/a
47	CTCF	chr6:140993180-140993330	GM12874	blood:	n/a	n/a
48	CTCF	chr6:140971319-140971569	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:140993180-140993330	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr6:140993190-140993292	GM10248	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:140957775-140957825	HNPCEpiC	eye:	n/a
2	chr6:140923112-140923162	AG04449	skin:	fetal
3	chr6:140957775-140957825	PANC-1	pancreas:	n/a
4	chr6:140957775-140957825	HIPEpiC	eye:	n/a
5	chr6:140923112-140923162	HMEC	breast:	n/a
6	chr6:140957775-140957825	NH-A	brain:	n/a
7	chr6:140957775-140957825	SK-N-SH	brain:	n/a
8	chr6:140923112-140923162	HCT-116	colon:	n/a
9	chr6:140957775-140957825	HCF	heart:	n/a
10	chr6:140923112-140923162	GM06990	blood:	n/a
11	chr6:140923112-140923162	ECC-1	luminal epithelium:	n/a
12	chr6:140957775-140957825	SAEC	small airway:	n/a
13	chr6:140923112-140923162	HL-60	blood:	n/a
14	chr6:140957775-140957825	HRE	kidney:	n/a
15	chr6:140923112-140923162	SK-N-SH	brain:	n/a
16	chr6:140957775-140957825	PFSK-1	brain:	n/a
17	chr6:140923112-140923162	T-47D	breast:	n/a
18	chr6:140957775-140957825	HEK293	kidney:	embryo
19	chr6:140923112-140923162	MCF10A-Er-Src	breast:	n/a
20	chr6:140923112-140923162	PrEC	prostate:	n/a
21	chr6:140957775-140957825	RPTEC	kidney:	n/a
22	chr6:140923112-140923162	PANC-1	pancreas:	n/a
23	chr6:140923112-140923162	ProgFib	skin:	n/a
24	chr6:140957775-140957825	IMR90	lung:	fetal
25	chr6:140957775-140957825	PrEC	prostate:	n/a
26	chr6:140957775-140957825	GM12891	blood:	n/a
27	chr6:140923112-140923162	AG09309	skin:	n/a
28	chr6:140957775-140957825	GM12878	blood:	n/a
29	chr6:140957775-140957825	H1-hESC	embryonic stem cell:	embryo
30	chr6:140923112-140923162	PFSK-1	brain:	n/a
31	chr6:140957775-140957825	Caco-2	colon:	n/a
32	chr6:140957775-140957825	SKMC	muscle:	n/a
33	chr6:140923112-140923162	K562	blood:	n/a
34	chr6:140957775-140957825	NB4	blood:	n/a
35	chr6:140957775-140957825	U87	brain:	n/a
36	chr6:140957775-140957825	ProgFib	skin:	n/a
37	chr6:140923112-140923162	Caco-2	colon:	n/a
38	chr6:140957775-140957825	GM06990	blood:	n/a
39	chr6:140957775-140957825	K562	blood:	n/a
40	chr6:140923112-140923162	AG09319	gingival:	n/a
41	chr6:140923112-140923162	HIPEpiC	eye:	n/a
42	chr6:140957775-140957825	Hela-S3	cervix:	n/a
43	chr6:140923112-140923162	AG10803	skin:	n/a
44	chr6:140923112-140923162	U87	brain:	n/a
45	chr6:140957775-140957825	HCPEpiC	choroid plexus:	n/a
46	chr6:140923112-140923162	AG04450	lung:	fetal
47	chr6:140923112-140923162	HUVEC	blood vessel:	n/a
48	chr6:140923112-140923162	LNCaP	prostate:	n/a
49	chr6:140957775-140957825	NHDF-neo	bronchial:	n/a
50	chr6:140957775-140957825	HAEpiC	amniotic membrane:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
2	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
3	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
4	chr6:140905860..140907615-chr6:140923172..140925767,2	K562	blood:
5	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
6	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
7	chr6:140919683..140922477-chr6:140922951..140925065,2	K562	blood:
8	chr6:139691177..139693399-chr6:140971784..140974474,2	MCF-7	breast:
9	chr6:140912649..140915188-chr6:140915453..140918177,2	K562	blood:
10	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
11	chr6:140912649..140915188-chr6:140915453..140918177,2	K562	blood:
12	chr6:140919169..140921783-chr6:140922844..140925130,2	MCF-7	breast:
13	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
14	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
15	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
16	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
17	chr6:140905427..140908857-chr6:140910975..140913769,3	K562	blood:
18	chr6:140919683..140922477-chr6:140922951..140925065,2	K562	blood:
19	chr6:140919169..140921783-chr6:140922844..140925130,2	MCF-7	breast:
20	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
21	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HECA-10	chr6:140972927-140973185	l_3279_chr6:140928454-140973185_placenta
2	lnc-HECA-10	chr6:140928455-140928491	l_3279_chr6:140928454-140973185_placenta

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4465	chr6:141004992-141005013	MIMAT0018992

No data

Variant related genes	Relation type
ENSG00000221336	TF binding region
MIR4465	TF binding region
ENSG00000221336	CpG island
MIR4465	CpG island

Extended variants
information (count: 3532 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3532 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13212274	chr6:140911389-140911390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559775193	chr6:140911429-140911430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530168345	chr6:140911436-140911437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549125074	chr6:140911441-140911442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73583513	chr6:140911503-140911504	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs544517842	chr6:140911525-140911526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7771673	chr6:140911594-140911595	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs73583516	chr6:140911628-140911629	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533110086	chr6:140911638-140911639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571616970	chr6:140911769-140911770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546481272	chr6:140911815-140911816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1336374	chr6:140911875-140911876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150198836	chr6:140911916-140911917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565734277	chr6:140911928-140911929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535986455	chr6:140911979-140911980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34229757	chr6:140912008-140912009	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs9495772	chr6:140912139-140912140	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537286526	chr6:140912140-140912141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs57272964	chr6:140912169-140912170	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs577144764	chr6:140912301-140912302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs59099315	chr6:140912340-140912341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180922381	chr6:140912363-140912364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559501057	chr6:140912366-140912367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533876003	chr6:140912379-140912380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371849384	chr6:140912392-140912393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115191533	chr6:140912420-140912421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549093518	chr6:140912465-140912466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372005359	chr6:140912493-140912494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541971070	chr6:140912531-140912532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568906975	chr6:140912686-140912687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563847207	chr6:140912690-140912691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531533918	chr6:140912726-140912727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs72981815	chr6:140912745-140912746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143428380	chr6:140917228-140917229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567277723	chr6:140917248-140917249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114806388	chr6:140917270-140917271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147154332	chr6:140917275-140917276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577849454	chr6:140917292-140917293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539190390	chr6:140917298-140917299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186233834	chr6:140917364-140917365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs6570401	chr6:140917367-140917368	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs377136041	chr6:140917369-140917370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs56356485	chr6:140917376-140917377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539924152	chr6:140920833-140920834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1336375	chr6:140920870-140920871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115006451	chr6:140920871-140920872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78703911	chr6:140920907-140920908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182697470	chr6:140921000-140921001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs557880454	chr6:140921038-140921039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577556232	chr6:140921049-140921050	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
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
Colorectal cancer	16272173	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140908200-140911400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:140908400-140912000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:140910800-140912000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:140911400-140912400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:140911400-140912400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr6:140911400-140912600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:140911600-140912600	Enhancers	NHDF-Ad	bronchial
8	chr6:140911600-140912600	Enhancers	Osteobl	bone
9	chr6:140912000-140912400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:140912000-140912600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:140912200-140912800	Enhancers	NHLF	lung
12	chr6:140917200-140917400	Enhancers	Aorta	Aorta
13	chr6:140920800-140922600	Enhancers	Fetal Lung	lung
14	chr6:140920800-140923800	Enhancers	Fetal Stomach	stomach
15	chr6:140921200-140921400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:140921400-140921600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:140921400-140922200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:140921600-140922600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:140921600-140924600	Enhancers	Osteobl	bone
20	chr6:140921800-140923800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:140922000-140923600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr6:140922200-140923800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:140922200-140924200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:140922200-140924600	Enhancers	NH-A	brain
25	chr6:140922200-140924800	Enhancers	NHDF-Ad	bronchial
26	chr6:140922600-140923000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:140922600-140923000	Weak transcription	Fetal Lung	lung
28	chr6:140922800-140924600	Enhancers	NHLF	lung
29	chr6:140923000-140923800	Enhancers	Fetal Lung	lung
30	chr6:140923000-140924000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr6:140923200-140924000	Enhancers	HSMMtube	muscle
32	chr6:140923600-140924200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:140923600-140925800	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr6:140923800-140924600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:140923800-140926000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:140924000-140926000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr6:140924200-140924800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:140924600-140925800	Weak transcription	NHLF	lung
39	chr6:140924600-140925800	Weak transcription	Osteobl	bone
40	chr6:140924600-140929400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:140925800-140926400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr6:140926000-140926200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:140926000-140926200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:140926000-140926200	Enhancers	NHLF	lung
45	chr6:140926000-140926200	Enhancers	Osteobl	bone
46	chr6:140929400-140929800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:140930400-140931400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:140930400-140931600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:140930400-140947200	Weak transcription	Placenta	Placenta
50	chr6:140930600-140931600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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