Variant report

Variant	esv3402332
Chromosome Location	chr3:134077812-134080610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:119)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:119 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr3:134070900-134094634	IMR90	lung:	n/a	chr3:134093783-134093793 chr3:134092557-134092567 chr3:134083055-134083065
2	CHD2	chr3:134079399-134079406	Hela-S3	cervix:	n/a	n/a
3	CHD2	chr3:134078914-134079037	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr3:134077263-134077818	A549	lung:	n/a	n/a
5	CTCF	chr3:134076834-134077851	HCT-116	colon:	n/a	n/a
6	CTCF	chr3:134077720-134077870	WI-38	lung:	n/a	n/a
7	EP300	chr3:134079439-134079829	T-47D	breast:	n/a	n/a
8	EP300	chr3:134075816-134077866	ECC-1	luminal epithelium:	n/a	n/a
9	FOXA1	chr3:134079402-134079777	T-47D	breast:	n/a	chr3:134079634-134079649
10	FOXA1	chr3:134079410-134079783	T-47D	breast:	n/a	chr3:134079634-134079649
11	FOXA1	chr3:134079497-134079737	HepG2	liver:	n/a	chr3:134079634-134079649
12	FOXA1	chr3:134079449-134079722	HepG2	liver:	n/a	chr3:134079634-134079649
13	FOXA1	chr3:134079381-134079735	HepG2	liver:	n/a	chr3:134079634-134079649
14	FOXA1	chr3:134078592-134078908	T-47D	breast:	n/a	n/a
15	FOXA2	chr3:134079516-134079719	HepG2	liver:	n/a	n/a
16	FOXA2	chr3:134079351-134079969	A549	lung:	n/a	n/a
17	FOXA2	chr3:134079357-134079890	A549	lung:	n/a	n/a
18	GATA3	chr3:134079478-134079850	T-47D	breast:	n/a	n/a
19	GATA3	chr3:134078444-134078820	T-47D	breast:	n/a	n/a
20	GATA3	chr3:134079433-134079846	T-47D	breast:	n/a	n/a
21	MAX	chr3:134076378-134077856	A549	lung:	n/a	n/a
22	MAX	chr3:134076273-134077872	ECC-1	luminal epithelium:	n/a	n/a
23	NFIC	chr3:134079488-134080443	ECC-1	luminal epithelium:	n/a	n/a
24	NFIC	chr3:134076423-134077891	ECC-1	luminal epithelium:	n/a	n/a
25	POLR2A	chr3:134080350-134080354	MCF-7	breast:	n/a	n/a
26	POLR2A	chr3:134077737-134079796	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr3:134075304-134077814	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr3:134079051-134079179	MCF-7	breast:	n/a	n/a
29	POLR2A	chr3:134079057-134079712	U87	brain:	n/a	n/a
30	POLR2A	chr3:134079491-134079790	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr3:134075038-134079875	ECC-1	luminal epithelium:	n/a	n/a
32	POLR2A	chr3:134079555-134079567	ProgFib	skin:	n/a	n/a
33	POLR2A	chr3:134074967-134094367	PANC-1	pancreas:	n/a	n/a
34	POLR2A	chr3:134079063-134079789	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr3:134078019-134078396	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr3:134077898-134078907	SK-N-SH	brain:	n/a	n/a
37	POLR2A	chr3:134069355-134094620	IMR90	lung:	n/a	n/a
38	POLR2A	chr3:134079946-134081898	ECC-1	luminal epithelium:	n/a	n/a
39	POLR2A	chr3:134076663-134078489	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr3:134080140-134080689	A549	lung:	n/a	n/a
41	POLR2A	chr3:134080568-134080825	HepG2	liver:	n/a	n/a
42	POLR2A	chr3:134077968-134078734	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr3:134078785-134079186	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr3:134079989-134080321	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr3:134080188-134080289	MCF-7	breast:	n/a	n/a
46	POLR2A	chr3:134079547-134079923	HepG2	liver:	n/a	n/a
47	POLR2A	chr3:134077718-134078976	U87	brain:	n/a	n/a
48	POLR2A	chr3:134079044-134079049	MCF-7	breast:	n/a	n/a
49	POLR2A	chr3:134078655-134078822	MCF-7	breast:	n/a	n/a
50	POLR2A	chr3:134078191-134078666	ProgFib	skin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:134080397-134080447	GM19239	blood:	n/a
2	chr3:134078647-134078697	Jurkat	blood:	n/a
3	chr3:134078647-134078697	NHBE	bronchial:	n/a
4	chr3:134080574-134080624	HCPEpiC	choroid plexus:	n/a
5	chr3:134078647-134078697	HCM	heart:	n/a
6	chr3:134080397-134080447	HCPEpiC	choroid plexus:	n/a
7	chr3:134080574-134080624	AG09309	skin:	n/a
8	chr3:134078647-134078697	T-47D	breast:	n/a
9	chr3:134080574-134080624	HMEC	breast:	n/a
10	chr3:134080574-134080624	NT2-D1	testis:	n/a
11	chr3:134078647-134078697	GM19239	blood:	n/a
12	chr3:134080517-134080567	GM12878	blood:	n/a
13	chr3:134078647-134078697	PFSK-1	brain:	n/a
14	chr3:134080517-134080567	NH-A	brain:	n/a
15	chr3:134078647-134078697	CMK	blood:	n/a
16	chr3:134080517-134080567	MCF-7	breast:	n/a
17	chr3:134080574-134080624	AG09319	gingival:	n/a
18	chr3:134080574-134080624	SAEC	small airway:	n/a
19	chr3:134080517-134080567	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:134080517-134080567	AoSMC	blood vessel:	n/a
21	chr3:134080517-134080567	SAEC	small airway:	n/a
22	chr3:134080574-134080624	Hela-S3	cervix:	n/a
23	chr3:134080517-134080567	HUVEC	blood vessel:	n/a
24	chr3:134080517-134080567	HMEC	breast:	n/a
25	chr3:134078647-134078697	H1-hESC	embryonic stem cell:	embryo
26	chr3:134078647-134078697	HRCEpiC	kidney:	n/a
27	chr3:134080517-134080567	Hela-S3	cervix:	n/a
28	chr3:134080397-134080447	HMEC	breast:	n/a
29	chr3:134078647-134078697	SAEC	small airway:	n/a
30	chr3:134080397-134080447	IMR90	lung:	fetal
31	chr3:134080397-134080447	HNPCEpiC	eye:	n/a
32	chr3:134080574-134080624	HEEpiC	esophagus:	n/a
33	chr3:134080574-134080624	HepG2	liver:	n/a
34	chr3:134080517-134080567	PANC-1	pancreas:	n/a
35	chr3:134080517-134080567	HCPEpiC	choroid plexus:	n/a
36	chr3:134080517-134080567	SKMC	muscle:	n/a
37	chr3:134078647-134078697	HCF	heart:	n/a
38	chr3:134080574-134080624	PANC-1	pancreas:	n/a
39	chr3:134078647-134078697	NH-A	brain:	n/a
40	chr3:134080517-134080567	AG10803	skin:	n/a
41	chr3:134078647-134078697	HUVEC	blood vessel:	n/a
42	chr3:134080517-134080567	SK-N-SH	brain:	n/a
43	chr3:134080517-134080567	HAEpiC	amniotic membrane:	n/a
44	chr3:134080517-134080567	HCT-116	colon:	n/a
45	chr3:134080397-134080447	PANC-1	pancreas:	n/a
46	chr3:134080574-134080624	GM12878	blood:	n/a
47	chr3:134080574-134080624	SK-N-SH	brain:	n/a
48	chr3:134080397-134080447	HCT-116	colon:	n/a
49	chr3:134080397-134080447	CMK	blood:	n/a
50	chr3:134080574-134080624	AG10803	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:134077067..134080470-chr3:134177227..134178995,3	MCF-7	breast:
2	chr3:134079471..134081511-chr3:134198648..134200784,2	MCF-7	breast:
3	chr3:134024307..134037207-chr3:134080573..134100993,88	MCF-7	breast:
4	chr3:134046165..134047037-chr3:134079239..134080512,3	MCF-7	breast:
5	chr3:134077016..134078829-chr3:134203979..134206355,2	MCF-7	breast:
6	chr3:134076345..134078417-chr3:134195768..134197623,2	MCF-7	breast:
7	chr3:134069007..134072370-chr3:134075638..134078854,3	K562	blood:
8	chr3:134077038..134077967-chr3:134192480..134193108,3	K562	blood:
9	chr3:134024378..134037377-chr3:134063304..134080412,83	MCF-7	breast:

No data

Variant related genes	Relation type
RPL39P5	TF binding region
RPL39P5	CpG island
ENSG00000129055	chromatin interactions
ENSG00000240006	chromatin interactions
ENSG00000214289	chromatin interactions
ENSG00000182923	chromatin interactions

Extended variants
information (count: 149 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:149 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534205300	chr3:134077856-134077857	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs199874653	chr3:134078129-134078130	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs149761638	chr3:134078137-134078138	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs372900931	chr3:134078146-134078147	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs147292735	chr3:134078147-134078148	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs556572166	chr3:134078160-134078161	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs140943062	chr3:134078174-134078175	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs543449878	chr3:134078210-134078211	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs376138663	chr3:134078213-134078214	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs375617544	chr3:134078224-134078225	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs189825181	chr3:134078225-134078226	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs557857902	chr3:134078227-134078228	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs144685493	chr3:134078229-134078230	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs577285464	chr3:134078259-134078260	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs368824669	chr3:134078278-134078279	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs147485667	chr3:134078283-134078284	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs140029062	chr3:134078284-134078285	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs142786862	chr3:134078300-134078301	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs201127105	chr3:134078368-134078369	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs76064335	chr3:134078384-134078385	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs76982430	chr3:134078385-134078386	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs540880815	chr3:134078414-134078415	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs75410942	chr3:134078433-134078434	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs528854353	chr3:134078435-134078436	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs557111746	chr3:134078440-134078441	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs562623840	chr3:134078444-134078445	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs531559186	chr3:134078466-134078467	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs551257508	chr3:134078504-134078505	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs6439478	chr3:134078566-134078567	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs527743318	chr3:134078569-134078570	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs11719057	chr3:134078580-134078581	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs567706326	chr3:134078647-134078648	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs536237757	chr3:134078676-134078677	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs556846341	chr3:134078680-134078681	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs13325929	chr3:134078694-134078695	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs561219735	chr3:134078733-134078734	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs563231405	chr3:134078743-134078744	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs570226384	chr3:134078759-134078760	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs539238348	chr3:134078827-134078828	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs558685849	chr3:134078838-134078839	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs577322168	chr3:134078861-134078862	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs148948420	chr3:134078881-134078882	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs369922508	chr3:134078899-134078900	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371137555	chr3:134078911-134078912	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs367916829	chr3:134078914-134078915	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200489847	chr3:134078915-134078916	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs147176018	chr3:134078916-134078917	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573334002	chr3:134078944-134078945	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs192757705	chr3:134078990-134078991	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs562821811	chr3:134078994-134078995	Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134069200-134090000	Genic enhancers	Fetal Muscle Trunk	muscle
2	chr3:134069400-134089800	Genic enhancers	Fetal Muscle Leg	muscle
3	chr3:134070000-134082400	Genic enhancers	Right Ventricle	heart
4	chr3:134070400-134088200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr3:134071000-134082600	Genic enhancers	NHLF	lung
6	chr3:134071000-134088800	Enhancers	Right Atrium	heart
7	chr3:134071200-134082400	Genic enhancers	Brain Substantia Nigra	brain
8	chr3:134071400-134079000	Genic enhancers	Fetal Intestine Large	intestine
9	chr3:134071600-134082200	Weak transcription	Primary T cells from cord blood	blood
10	chr3:134071600-134082800	Genic enhancers	Placenta	Placenta
11	chr3:134072000-134079000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr3:134072000-134082800	Genic enhancers	Lung	lung
13	chr3:134072200-134082400	Genic enhancers	Brain Hippocampus Middle	brain
14	chr3:134072200-134090200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr3:134072400-134091200	Genic enhancers	Spleen	Spleen
16	chr3:134072600-134080200	Weak transcription	Small Intestine	intestine
17	chr3:134072600-134082000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr3:134072600-134082200	Genic enhancers	Adipose Nuclei	Adipose
19	chr3:134072800-134081000	Genic enhancers	Placenta Amnion	Placenta Amnion
20	chr3:134072800-134082400	Genic enhancers	Brain Cingulate Gyrus	brain
21	chr3:134072800-134082600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr3:134072800-134090600	Genic enhancers	Left Ventricle	heart
23	chr3:134073000-134078400	Genic enhancers	Fetal Kidney	kidney
24	chr3:134073000-134080400	Genic enhancers	Ovary	ovary
25	chr3:134073000-134082200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:134073000-134089400	Genic enhancers	HMEC	breast
27	chr3:134073200-134078200	Genic enhancers	Fetal Lung	lung
28	chr3:134073200-134079400	Genic enhancers	Esophagus	oesophagus
29	chr3:134073200-134082000	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr3:134073200-134082200	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr3:134073400-134082200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
32	chr3:134073400-134091400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr3:134073800-134082400	Strong transcription	Sigmoid Colon	Sigmoid Colon
34	chr3:134074400-134078800	Strong transcription	Liver	Liver
35	chr3:134074400-134082600	Genic enhancers	Brain Anterior Caudate	brain
36	chr3:134074400-134089400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr3:134075000-134090400	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr3:134075200-134078000	Genic enhancers	Stomach Mucosa	stomach
39	chr3:134075200-134081000	Genic enhancers	Gastric	stomach
40	chr3:134075200-134082200	Genic enhancers	Brain Inferior Temporal Lobe	brain
41	chr3:134075200-134082400	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr3:134075200-134082800	Genic enhancers	Brain Angular Gyrus	brain
43	chr3:134075400-134079000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:134075400-134079400	Genic enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr3:134075400-134079400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr3:134075600-134079200	Genic enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr3:134075600-134079200	Genic enhancers	HepG2	liver
48	chr3:134075600-134082200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr3:134075800-134079000	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr3:134075800-134079600	Genic enhancers	ES-I3 Cell Line	embryonic stem cell

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