Variant report

Variant	nsv886712
Chromosome Location	chr6:140931435-141047572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:551)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:551 , 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	ATF1	chr6:141032327-141032490	K562	blood:	n/a	n/a
2	ATF2	chr6:140962459-140962964	GM12878	blood:	n/a	n/a
3	BACH1	chr6:140931711-140931747	K562	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	chr6:140999274-140999525	GM12878	blood:	n/a	n/a
7	BATF	chr6:140962532-140962960	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:140962597-140962976	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:140962665-140962965	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:140957373-140957725	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	BHLHE40	chr6:141032530-141032747	GM12878	blood:	n/a	n/a
14	CBX3	chr6:140948115-140948497	K562	blood:	n/a	n/a
15	CCNT2	chr6:141006502-141006618	K562	blood:	n/a	n/a
16	CEBPB	chr6:141019569-141019573	K562	blood:	n/a	n/a
17	CEBPB	chr6:140933530-140933696	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:141006465-141006576	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:141006378-141006630	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:140950718-140951059	HepG2	liver:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
21	CEBPB	chr6:140944477-140945154	HCT-116	colon:	n/a	chr6:140944736-140944747
22	CEBPB	chr6:140978749-140979032	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:141023864-141024001	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:140944453-140945069	HCT-116	colon:	n/a	chr6:140944736-140944747
25	CEBPB	chr6:141046992-141047275	HepG2	liver:	n/a	chr6:141047121-141047132
26	CEBPB	chr6:140944651-140944864	HepG2	liver:	n/a	chr6:140944736-140944747
27	CEBPB	chr6:140950521-140950534	K562	blood:	n/a	n/a
28	CEBPB	chr6:140978793-140979003	K562	blood:	n/a	n/a
29	CEBPB	chr6:140950874-140950971	Hela-S3	cervix:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
30	CEBPB	chr6:140978710-140979038	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:141005694-141005708	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr6:140992588-140992943	HepG2	liver:	n/a	chr6:140992865-140992876
33	CEBPB	chr6:140944558-140944922	A549	lung:	n/a	chr6:140944736-140944747
34	CEBPB	chr6:140950735-140950999	A549	lung:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
35	CEBPB	chr6:140944568-140944937	Hela-S3	cervix:	n/a	chr6:140944736-140944747
36	CEBPB	chr6:140944593-140944912	A549	lung:	n/a	chr6:140944736-140944747
37	CEBPB	chr6:140950786-140950984	H1-hESC	embryonic stem cell:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
38	CEBPB	chr6:140944554-140945005	IMR90	lung:	n/a	chr6:140944736-140944747
39	CEBPB	chr6:141046985-141047253	IMR90	lung:	n/a	chr6:141047121-141047132
40	CEBPB	chr6:140950730-140951057	IMR90	lung:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
41	CEBPB	chr6:140950761-140951042	K562	blood:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
42	CTCF	chr6:140971352-140971545	K562	blood:	n/a	n/a
43	CTCF	chr6:140971340-140971490	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr6:140938600-140938750	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr6:140971319-140971569	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:140993080-140993230	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr6:140993205-140993328	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr6:140993140-140993290	HMEC	breast:	n/a	n/a
49	CTCF	chr6:140993200-140993350	HMF	breast:	n/a	n/a
50	CTCF	chr6:140967765-140967791	GM10248	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	GM12892	blood:	n/a
2	chr6:140957775-140957825	NB4	blood:	n/a
3	chr6:140957775-140957825	Hepatocyte	liver:	n/a
4	chr6:140957775-140957825	SK-N-SH	brain:	n/a
5	chr6:140957775-140957825	AG04449	skin:	fetal
6	chr6:140957775-140957825	NHBE	bronchial:	n/a
7	chr6:140957775-140957825	SK-N-MC	brain:	n/a
8	chr6:140957775-140957825	BE2_C	brain:	n/a
9	chr6:140957775-140957825	MCF10A-Er-Src	breast:	n/a
10	chr6:140957775-140957825	A549	lung:	n/a
11	chr6:140957775-140957825	NH-A	brain:	n/a
12	chr6:140957775-140957825	HAEpiC	amniotic membrane:	n/a
13	chr6:140957775-140957825	RPTEC	kidney:	n/a
14	chr6:140957775-140957825	GM06990	blood:	n/a
15	chr6:140957775-140957825	LNCaP	prostate:	n/a
16	chr6:140957775-140957825	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:140957775-140957825	HCT-116	colon:	n/a
18	chr6:140957775-140957825	GM19239	blood:	n/a
19	chr6:140957775-140957825	BJ	skin:	n/a
20	chr6:140957775-140957825	HMEC	breast:	n/a
21	chr6:140957775-140957825	T-47D	breast:	n/a
22	chr6:140957775-140957825	Caco-2	colon:	n/a
23	chr6:140957775-140957825	Hela-S3	cervix:	n/a
24	chr6:140957775-140957825	SKMC	muscle:	n/a
25	chr6:140957775-140957825	HL-60	blood:	n/a
26	chr6:140957775-140957825	GM12878	blood:	n/a
27	chr6:140957775-140957825	PrEC	prostate:	n/a
28	chr6:140957775-140957825	CMK	blood:	n/a
29	chr6:140957775-140957825	K562	blood:	n/a
30	chr6:140957775-140957825	HCM	heart:	n/a
31	chr6:140957775-140957825	HEK293	kidney:	embryo
32	chr6:140957775-140957825	NT2-D1	testis:	n/a
33	chr6:140957775-140957825	SAEC	small airway:	n/a
34	chr6:140957775-140957825	HCF	heart:	n/a
35	chr6:140957775-140957825	PFSK-1	brain:	n/a
36	chr6:140957775-140957825	ovcar-3	ovarian:	n/a
37	chr6:140957775-140957825	HepG2	liver:	n/a
38	chr6:140957775-140957825	SK-N-SH_RA	brain:	n/a
39	chr6:140957775-140957825	AG10803	skin:	n/a
40	chr6:140957775-140957825	AoSMC	blood vessel:	n/a
41	chr6:140957775-140957825	NHDF-neo	bronchial:	n/a
42	chr6:140957775-140957825	MCF-7	breast:	n/a
43	chr6:140957775-140957825	ProgFib	skin:	n/a
44	chr6:140957775-140957825	H1-hESC	embryonic stem cell:	embryo
45	chr6:140957775-140957825	HNPCEpiC	eye:	n/a
46	chr6:140957775-140957825	HCPEpiC	choroid plexus:	n/a
47	chr6:140957775-140957825	HRCEpiC	kidney:	n/a
48	chr6:140957775-140957825	HUVEC	blood vessel:	n/a
49	chr6:140957775-140957825	GM12891	blood:	n/a
50	chr6:140957775-140957825	IMR90	lung:	fetal

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
2	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
3	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
4	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
5	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
6	chr6:139691177..139693399-chr6:140971784..140974474,2	MCF-7	breast:
7	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
8	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
9	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
10	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
11	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
12	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
13	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
14	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
15	chr6:140974220..140975794-chr6:140989570..140992507,2	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: 3515 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3515 , 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	rs12196606	chr6:140931435-140931436	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs528255306	chr6:140931489-140931490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529599601	chr6:140931495-140931496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546404503	chr6:140931502-140931503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139315053	chr6:140931548-140931549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10635369	chr6:140931566-140931567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34295423	chr6:140931567-140931568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374002808	chr6:140931588-140931589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs3075138	chr6:140931589-140931590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529183112	chr6:140931613-140931614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550893426	chr6:140931705-140931706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568757495	chr6:140931749-140931750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539448976	chr6:140931783-140931784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187970361	chr6:140931789-140931790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566590993	chr6:140931795-140931796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191136901	chr6:140931849-140931850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6570402	chr6:140931910-140931911	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs577358542	chr6:140931951-140931952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34256316	chr6:140931961-140931962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544566265	chr6:140932004-140932005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556862497	chr6:140932008-140932009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577935731	chr6:140932136-140932137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545419390	chr6:140932184-140932185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372743961	chr6:140932187-140932188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183312573	chr6:140932202-140932203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549206940	chr6:140932240-140932241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527783397	chr6:140932245-140932246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145485262	chr6:140932257-140932258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563745204	chr6:140932271-140932272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187732364	chr6:140932352-140932353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77454091	chr6:140932359-140932360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61263289	chr6:140932417-140932418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs192706324	chr6:140932470-140932471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184779838	chr6:140932500-140932501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs386706438	chr6:140932521-140932522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9389812	chr6:140932526-140932527	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532760052	chr6:140932546-140932547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551420579	chr6:140932552-140932553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566524053	chr6:140932613-140932614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552218052	chr6:140932734-140932735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533880010	chr6:140932739-140932740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555540564	chr6:140932778-140932779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543076780	chr6:140932779-140932780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199932383	chr6:140932811-140932812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567753268	chr6:140932832-140932833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538460077	chr6:140932840-140932841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147609098	chr6:140932930-140932931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565857678	chr6:140932964-140932965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77113621	chr6:140932965-140932966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115320822	chr6:140932967-140932968	Weak transcription	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:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140930400-140931600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:140930400-140947200	Weak transcription	Placenta	Placenta
3	chr6:140930600-140931600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:140930600-140931600	Enhancers	Fetal Heart	heart
5	chr6:140931200-140931600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:140931200-140931600	Enhancers	Ovary	ovary
7	chr6:140936800-140945000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:140941800-140942200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:140942200-140945400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:140944200-140945000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:140944400-140945200	Enhancers	NHEK	skin
12	chr6:140944400-140945400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:140944400-140945400	Enhancers	HSMM	muscle
14	chr6:140944600-140945600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr6:140944800-140945000	Enhancers	NH-A	brain
16	chr6:140944800-140945400	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr6:140944800-140945400	Enhancers	Fetal Lung	lung
18	chr6:140944800-140945600	Enhancers	Ovary	ovary
19	chr6:140944800-140945600	Enhancers	HMEC	breast
20	chr6:140945000-140945600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:140945000-140946600	Weak transcription	NH-A	brain
22	chr6:140945400-140945600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:140945600-140946200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:140945600-140946600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:140946200-140946400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:140946600-140948600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:140947000-140948200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
28	chr6:140947200-140948400	ZNF genes & repeats	Placenta	Placenta
29	chr6:140947600-140948200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr6:140947600-140948400	ZNF genes & repeats	Aorta	Aorta
31	chr6:140948200-140948400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:140948600-140991200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:140949000-140957400	Weak transcription	Right Atrium	heart
34	chr6:140954200-140954800	Enhancers	Fetal Heart	heart
35	chr6:140954800-140956800	Weak transcription	Fetal Heart	heart
36	chr6:140956600-140957200	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr6:140956800-140958000	Enhancers	Fetal Heart	heart
38	chr6:140956800-140958400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr6:140957200-140957400	Enhancers	Brain Germinal Matrix	brain
40	chr6:140957200-140957400	Enhancers	Fetal Brain Female	brain
41	chr6:140957200-140957400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr6:140957200-140958200	Active TSS	Brain Anterior Caudate	brain
43	chr6:140957400-140957600	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr6:140957400-140957600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr6:140957400-140957600	Active TSS	GM12878-XiMat	blood
46	chr6:140957400-140957800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr6:140957400-140957800	Enhancers	Primary B cells from peripheral blood	blood
48	chr6:140957400-140957800	Enhancers	Fetal Kidney	kidney
49	chr6:140957400-140958000	Active TSS	Brain Angular Gyrus	brain
50	chr6:140957400-140958000	Flanking Active TSS	Brain Germinal Matrix	brain

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