Variant report

Variant	esv33208
Chromosome Location	chr6:140957346-141057355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:141032327-141032490	K562	blood:	n/a	n/a
2	ATF2	chr6:140962459-140962964	GM12878	blood:	n/a	n/a
3	BATF	chr6:140999274-140999525	GM12878	blood:	n/a	n/a
4	BATF	chr6:140957343-140957787	GM12878	blood:	n/a	n/a
5	BATF	chr6:140962571-140962917	GM12878	blood:	n/a	n/a
6	BATF	chr6:140962532-140962960	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:140957373-140957725	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:140962665-140962965	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:140962597-140962976	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:140957284-140957740	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:141032530-141032747	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:140962545-140962966	GM12878	blood:	n/a	n/a
13	CCNT2	chr6:141006502-141006618	K562	blood:	n/a	n/a
14	CEBPB	chr6:141046985-141047253	IMR90	lung:	n/a	chr6:141047121-141047132
15	CEBPB	chr6:141005694-141005708	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr6:141006465-141006576	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:141023864-141024001	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:141006378-141006630	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:140978793-140979003	K562	blood:	n/a	n/a
20	CEBPB	chr6:140978710-140979038	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:140978749-140979032	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:140992588-140992943	HepG2	liver:	n/a	chr6:140992865-140992876
23	CEBPB	chr6:141019569-141019573	K562	blood:	n/a	n/a
24	CEBPB	chr6:141046992-141047275	HepG2	liver:	n/a	chr6:141047121-141047132
25	CTCF	chr6:140971340-140971490	NHEK	skin:	n/a	n/a
26	CTCF	chr6:140964211-140964249	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr6:140957389-140957667	GM12878	blood:	n/a	n/a
28	CTCF	chr6:140993152-140993321	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr6:140971340-140971490	HFF	foreskin:	n/a	n/a
30	CTCF	chr6:140993200-140993350	SAEC	small airway:	n/a	n/a
31	CTCF	chr6:140971340-140971490	GM12875	blood:	n/a	n/a
32	CTCF	chr6:140971332-140971561	NHEK	skin:	n/a	n/a
33	CTCF	chr6:140993100-140993250	SAEC	small airway:	n/a	n/a
34	CTCF	chr6:140993200-140993350	GM12871	blood:	n/a	n/a
35	CTCF	chr6:140993180-140993330	HEK293	kidney:	n/a	n/a
36	CTCF	chr6:140993108-140993366	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:140993040-140993190	HMEC	breast:	n/a	n/a
38	CTCF	chr6:140993080-140993230	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr6:140993180-140993398	GM12878	blood:	n/a	n/a
40	CTCF	chr6:140993206-140993275	GM19239	blood:	n/a	n/a
41	CTCF	chr6:140993140-140993290	K562	blood:	n/a	n/a
42	CTCF	chr6:140971340-140971490	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr6:140993160-140993310	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr6:140993158-140993321	K562	blood:	n/a	n/a
45	CTCF	chr6:140993100-140993250	NHEK	skin:	n/a	n/a
46	CTCF	chr6:140993114-140993467	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:140971360-140971510	HEK293	kidney:	n/a	n/a
48	CTCF	chr6:140993140-140993290	GM12865	blood:	n/a	n/a
49	CTCF	chr6:140971340-140971490	GM12874	blood:	n/a	n/a
50	CTCF	chr6:140971380-140971530	NB4	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:140957775-140957825	SK-N-SH	brain:	n/a
2	chr6:140957775-140957825	IMR90	lung:	fetal
3	chr6:140957775-140957825	HRE	kidney:	n/a
4	chr6:140957775-140957825	PFSK-1	brain:	n/a
5	chr6:140957775-140957825	GM19239	blood:	n/a
6	chr6:140957775-140957825	HIPEpiC	eye:	n/a
7	chr6:140957775-140957825	Caco-2	colon:	n/a
8	chr6:140957775-140957825	HUVEC	blood vessel:	n/a
9	chr6:140957775-140957825	AG04450	lung:	fetal
10	chr6:140957775-140957825	A549	lung:	n/a
11	chr6:140957775-140957825	BJ	skin:	n/a
12	chr6:140957775-140957825	MCF10A-Er-Src	breast:	n/a
13	chr6:140957775-140957825	SAEC	small airway:	n/a
14	chr6:140957775-140957825	PANC-1	pancreas:	n/a
15	chr6:140957775-140957825	HCF	heart:	n/a
16	chr6:140957775-140957825	Jurkat	blood:	n/a
17	chr6:140957775-140957825	SKMC	muscle:	n/a
18	chr6:140957775-140957825	NHDF-neo	bronchial:	n/a
19	chr6:140957775-140957825	K562	blood:	n/a
20	chr6:140957775-140957825	ProgFib	skin:	n/a
21	chr6:140957775-140957825	HepG2	liver:	n/a
22	chr6:140957775-140957825	AG04449	skin:	fetal
23	chr6:140957775-140957825	T-47D	breast:	n/a
24	chr6:140957775-140957825	HCM	heart:	n/a
25	chr6:140957775-140957825	PrEC	prostate:	n/a
26	chr6:140957775-140957825	HNPCEpiC	eye:	n/a
27	chr6:140957775-140957825	HEEpiC	esophagus:	n/a
28	chr6:140957775-140957825	H1-hESC	embryonic stem cell:	embryo
29	chr6:140957775-140957825	HRCEpiC	kidney:	n/a
30	chr6:140957775-140957825	AG10803	skin:	n/a
31	chr6:140957775-140957825	GM12892	blood:	n/a
32	chr6:140957775-140957825	HRPEpiC	eye:	n/a
33	chr6:140957775-140957825	AG09319	gingival:	n/a
34	chr6:140957775-140957825	Hepatocyte	liver:	n/a
35	chr6:140957775-140957825	HMEC	breast:	n/a
36	chr6:140957775-140957825	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:140957775-140957825	HCT-116	colon:	n/a
38	chr6:140957775-140957825	Hela-S3	cervix:	n/a
39	chr6:140957775-140957825	RPTEC	kidney:	n/a
40	chr6:140957775-140957825	NHBE	bronchial:	n/a
41	chr6:140957775-140957825	NB4	blood:	n/a
42	chr6:140957775-140957825	HAEpiC	amniotic membrane:	n/a
43	chr6:140957775-140957825	LNCaP	prostate:	n/a
44	chr6:140957775-140957825	HEK293	kidney:	embryo
45	chr6:140957775-140957825	ECC-1	luminal epithelium:	n/a
46	chr6:140957775-140957825	ovcar-3	ovarian:	n/a
47	chr6:140957775-140957825	MCF-7	breast:	n/a
48	chr6:140957775-140957825	SK-N-SH_RA	brain:	n/a
49	chr6:140957775-140957825	AoSMC	blood vessel:	n/a
50	chr6:140957775-140957825	AG09309	skin:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
2	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
3	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
4	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
5	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
6	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
7	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
8	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
9	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
10	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
11	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
12	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
13	chr6:139691177..139693399-chr6:140971784..140974474,2	MCF-7	breast:
14	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
15	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
16	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
17	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:

(count:1 , 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

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: 2866 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2866 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9495792	chr6:140957356-140957357	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117049227	chr6:140957369-140957370	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs552019853	chr6:140957391-140957392	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs80154377	chr6:140957414-140957415	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs571024456	chr6:140957465-140957466	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs192767764	chr6:140957472-140957473	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs116679198	chr6:140957484-140957485	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs182506756	chr6:140957490-140957491	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs141755336	chr6:140957492-140957493	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs536197315	chr6:140957503-140957504	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs557323094	chr6:140957505-140957506	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs146258847	chr6:140957554-140957555	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs35215628	chr6:140957589-140957590	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs187538054	chr6:140957616-140957617	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs79447333	chr6:140957639-140957640	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs550009214	chr6:140957641-140957642	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs191901304	chr6:140957701-140957702	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs540834301	chr6:140957717-140957718	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs538802231	chr6:140957775-140957776	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs184747622	chr6:140957776-140957777	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs190254795	chr6:140957974-140957975	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs529934081	chr6:140957978-140957979	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs541785190	chr6:140958012-140958013	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs80333807	chr6:140958026-140958027	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs1336370	chr6:140958047-140958048	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs78102074	chr6:140958117-140958118	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs76948602	chr6:140958119-140958120	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs78802408	chr6:140958121-140958122	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs552221511	chr6:140958146-140958147	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570565220	chr6:140958148-140958149	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs528656702	chr6:140958156-140958157	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs192761173	chr6:140958186-140958187	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs113978673	chr6:140958197-140958198	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536126406	chr6:140958204-140958205	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs557406794	chr6:140958226-140958227	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs569203756	chr6:140958229-140958230	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs535116697	chr6:140958248-140958249	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs148065762	chr6:140958282-140958283	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375377738	chr6:140958287-140958288	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs141610518	chr6:140958310-140958311	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs76672077	chr6:140958335-140958336	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs184466565	chr6:140958340-140958341	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs372081732	chr6:140958343-140958344	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs552726710	chr6:140958346-140958347	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs189395545	chr6:140958383-140958384	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs542072403	chr6:140958471-140958472	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs150504854	chr6:140958482-140958483	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs530478337	chr6:140958497-140958498	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs545492135	chr6:140958499-140958500	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs117086537	chr6:140958521-140958522	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Breast cancer	22522925	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140948600-140991200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:140949000-140957400	Weak transcription	Right Atrium	heart
3	chr6:140956800-140958000	Enhancers	Fetal Heart	heart
4	chr6:140956800-140958400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:140957200-140957400	Enhancers	Brain Germinal Matrix	brain
6	chr6:140957200-140957400	Enhancers	Fetal Brain Female	brain
7	chr6:140957200-140957400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr6:140957200-140958200	Active TSS	Brain Anterior Caudate	brain
9	chr6:140957400-140957600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr6:140957400-140957600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr6:140957400-140957600	Active TSS	GM12878-XiMat	blood
12	chr6:140957400-140957800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:140957400-140957800	Enhancers	Primary B cells from peripheral blood	blood
14	chr6:140957400-140957800	Enhancers	Fetal Kidney	kidney
15	chr6:140957400-140958000	Active TSS	Brain Angular Gyrus	brain
16	chr6:140957400-140958000	Flanking Active TSS	Brain Germinal Matrix	brain
17	chr6:140957400-140958000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr6:140957400-140958200	Active TSS	Brain Cingulate Gyrus	brain
19	chr6:140957400-140958200	Active TSS	Brain Hippocampus Middle	brain
20	chr6:140957400-140958200	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr6:140957400-140958200	Active TSS	Brain Substantia Nigra	brain
22	chr6:140957400-140958200	Active TSS	Right Atrium	heart
23	chr6:140957400-140958400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr6:140957400-140958400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:140957400-140958400	Flanking Active TSS	Fetal Brain Female	brain
26	chr6:140957400-140958400	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr6:140957400-140958400	Enhancers	Fetal Stomach	stomach
28	chr6:140957400-140958600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr6:140957400-140958600	Enhancers	Fetal Brain Male	brain
30	chr6:140957600-140957800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr6:140957600-140958000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:140957600-140958000	Flanking Active TSS	GM12878-XiMat	blood
33	chr6:140957600-140958200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:140957600-140958400	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr6:140957600-140958400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr6:140957600-140958600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr6:140957600-140958600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr6:140957600-140958600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr6:140957800-140958000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr6:140957800-140958200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:140957800-140958200	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr6:140957800-140958200	Active TSS	Fetal Kidney	kidney
43	chr6:140957800-140958200	Enhancers	Stomach Smooth Muscle	stomach
44	chr6:140957800-140958400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr6:140957800-140958400	Active TSS	Rectal Smooth Muscle	rectum
46	chr6:140957800-140958600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:140958000-140958200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr6:140958000-140958200	Enhancers	Brain Angular Gyrus	brain
49	chr6:140958000-140958200	Enhancers	GM12878-XiMat	blood
50	chr6:140958000-140958400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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