Variant report

Variant	rs2495391
Chromosome Location	chr1:151373200-151373201
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:58)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:58 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MTA3	chr1:151371612-151376558	GM12878	blood:	n/a	n/a
2	STAT5A	chr1:151372926-151373537	GM12878	blood:	n/a	n/a
3	POLR2A	chr1:151371549-151376573	PANC-1	pancreas:	n/a	n/a
4	POLR2A	chr1:151372349-151373207	SK-N-SH	brain:	n/a	n/a
5	POLR2A	chr1:151373176-151373557	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr1:151371387-151376022	H1-hESC	embryonic stem cell:	n/a	n/a
7	HCFC1	chr1:151371677-151373496	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr1:151372842-151374184	SK-N-SH	brain:	n/a	n/a
9	POLR2A	chr1:151372949-151373875	SK-N-MC	brain:	n/a	n/a
10	POLR2A	chr1:151373145-151373221	HUVEC	blood vessel:	n/a	n/a
11	POLR2A	chr1:151372958-151373518	ProgFib	skin:	n/a	n/a
12	POLR2A	chr1:151371538-151376015	GM12878	blood:	n/a	n/a
13	POLR2A	chr1:151371809-151374090	A549	lung:	n/a	n/a
14	PML	chr1:151373041-151374281	GM12878	blood:	n/a	n/a
15	POLR2A	chr1:151371544-151373302	HUVEC	blood vessel:	n/a	n/a
16	POLR2A	chr1:151373103-151373583	ECC-1	luminal epithelium:	n/a	n/a
17	MAZ	chr1:151371422-151373596	IMR90	lung:	n/a	n/a
18	NFATC1	chr1:151373112-151374250	GM12878	blood:	n/a	n/a
19	MXI1	chr1:151371588-151373214	IMR90	lung:	n/a	n/a
20	POLR2A	chr1:151372984-151376641	GM12892	blood:	n/a	n/a
21	POLR2A	chr1:151373157-151374165	HepG2	liver:	n/a	n/a
22	POLR2A	chr1:151373099-151373566	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr1:151371682-151376489	GM12878	blood:	n/a	n/a
24	POLR2A	chr1:151373134-151374164	GM12892	blood:	n/a	n/a
25	POLR2A	chr1:151371763-151376305	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr1:151373119-151373268	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr1:151371622-151375204	GM12878	blood:	n/a	n/a
28	POLR2A	chr1:151371703-151373380	HepG2	liver:	n/a	n/a
29	POLR2A	chr1:151371665-151373494	U87	brain:	n/a	n/a
30	POLR2A	chr1:151372916-151373376	GM12891	blood:	n/a	n/a
31	POLR2A	chr1:151371649-151374571	U87	brain:	n/a	n/a
32	POLR2A	chr1:151373084-151373313	GM12878	blood:	n/a	n/a
33	POLR2A	chr1:151371672-151376556	GM12891	blood:	n/a	n/a
34	POLR2A	chr1:151373042-151374675	HCT-116	colon:	n/a	n/a
35	POLR2A	chr1:151371734-151376573	GM12878	blood:	n/a	n/a
36	POLR2A	chr1:151371589-151376047	GM12891	blood:	n/a	n/a
37	POLR2A	chr1:151373115-151373526	HepG2	liver:	n/a	n/a
38	POLR2A	chr1:151371610-151373472	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr1:151371658-151374261	PFSK-1	brain:	n/a	n/a
40	POLR2A	chr1:151373101-151373562	HCT-116	colon:	n/a	n/a
41	POLR2A	chr1:151372726-151376013	PFSK-1	brain:	n/a	n/a
42	POLR2A	chr1:151371675-151373417	ECC-1	luminal epithelium:	n/a	n/a
43	PML	chr1:151372616-151373878	MCF-7	breast:	n/a	n/a
44	POLR2A	chr1:151371526-151376147	U87	brain:	n/a	n/a
45	POLR2A	chr1:151373129-151373539	K562	blood:	n/a	n/a
46	POLR2A	chr1:151371832-151376521	K562	blood:	n/a	n/a
47	POLR2A	chr1:151371577-151376044	GM12891	blood:	n/a	n/a
48	POLR2A	chr1:151371316-151375162	HepG2	liver:	n/a	n/a
49	POLR2A	chr1:151372415-151376594	PANC-1	pancreas:	n/a	n/a
50	POLR2A	chr1:151371617-151374076	MCF-7	breast:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151372028..151374418-chr1:151511841..151514665,2	MCF-7	breast:
2	chr1:151254429..151257729-chr1:151370560..151375073,7	MCF-7	breast:
3	chr1:151372245..151374554-chr1:151396741..151398920,2	MCF-7	breast:
4	chr1:151370719..151373828-chr1:151394792..151398021,4	MCF-7	breast:
5	chr1:151225665..151228952-chr1:151371435..151373604,4	MCF-7	breast:
6	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
7	chr1:151312120..151316742-chr1:151370081..151375586,6	MCF-7	breast:
8	chr1:151318180..151322621-chr1:151370786..151375600,7	K562	blood:
9	chr1:151252692..151257354-chr1:151370358..151373702,7	K562	blood:
10	1:151171193-151178589..1:151368336-151375897	Hela-S3	cervix:
11	chr1:151252566..151256216-chr1:151370228..151373702,9	K562	blood:
12	chr1:151318199..151320967-chr1:151371516..151373553,2	K562	blood:
13	chr1:151297425..151301136-chr1:151370895..151373723,5	MCF-7	breast:
14	chr1:151312109..151317002-chr1:151372398..151376596,7	MCF-7	breast:
15	chr1:151370811..151373589-chr1:151512732..151514796,2	K562	blood:
16	1:151368336-151375897..1:151592347-151603110	Hela-S3	cervix:
17	chr1:151252229..151256416-chr1:151370480..151373573,6	MCF-7	breast:
18	chr1:151371973..151373501-chr1:151810861..151813533,2	MCF-7	breast:
19	chr1:151372236..151373964-chr20:46129058..46130747,2	MCF-7	breast:
20	chr1:151343373..151350462-chr1:151369795..151376328,11	MCF-7	breast:
21	chr1:151371526..151374105-chr1:151428160..151432357,4	K562	blood:
22	chr1:151317450..151322791-chr1:151370457..151374000,10	MCF-7	breast:

No data

Variant related genes	Relation type
PSMB4	TF binding region
ENSG00000232671	Chromatin interaction
ENSG00000232536	Chromatin interaction
ENSG00000159352	Chromatin interaction
ENSG00000225556	Chromatin interaction
ENSG00000143373	Chromatin interaction
ENSG00000143390	Chromatin interaction
ENSG00000143393	Chromatin interaction
ENSG00000143442	Chromatin interaction
ENSG00000143367	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000143416	Chromatin interaction
ENSG00000273481	Chromatin interaction
ENSG00000206635	Chromatin interaction
ENSG00000224645	Chromatin interaction
ENSG00000143398	Chromatin interaction
ENSG00000237976	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10749663	1.00[MEX][hapmap]
rs11204824	0.84[ASW][hapmap]
rs1418822	1.00[MEX][hapmap]
rs1539494	1.00[AMR][1000 genomes]
rs1752379	1.00[MEX][hapmap]
rs2337361	1.00[MEX][hapmap]
rs2479381	1.00[AMR][1000 genomes]
rs2479384	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2479386	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2495379	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2495390	0.82[ASW][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2864115	1.00[MEX][hapmap]
rs3001839	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3001840	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap]
rs4246528	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4970952	1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4970959	1.00[MEX][hapmap]
rs6667714	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6683010	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7533032	1.00[MEX][hapmap]
rs9436030	0.90[AFR][1000 genomes]
rs9661205	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916272	chr1:150961809-151557253	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
2	esv34461	chr1:151240542-151411635	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
3	esv2753774	chr1:151240542-151411635	Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
4	nsv831581	chr1:151289151-151478605	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv872424	chr1:151325055-151413180	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv872425	chr1:151325055-151413790	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	esv2756864	chr1:151328794-151411635	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
8	esv2758969	chr1:151328794-151411635	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv872428	chr1:151329138-151395782	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
10	nsv872429	chr1:151329138-151413180	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv8380	chr1:151329887-151410346	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
12	esv2753659	chr1:151330927-151384927	Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
13	nsv824575	chr1:151331533-151408096	Enhancers Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
14	nsv463761	chr1:151333167-151404848	Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
15	nsv463772	chr1:151333167-151404848	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
16	nsv463783	chr1:151333167-151404848	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
17	nsv463794	chr1:151333167-151404848	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
18	nsv463805	chr1:151333167-151404848	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
19	nsv463816	chr1:151333167-151404848	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
20	nsv470737	chr1:151333167-151404848	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
21	nsv547849	chr1:151333167-151404848	Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
22	nsv818467	chr1:151333167-151404848	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
23	nsv463827	chr1:151333167-151413180	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
24	nsv547850	chr1:151333167-151413180	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
25	nsv1011398	chr1:151333430-151402839	Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
26	nsv872430	chr1:151334796-151413180	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
27	nsv441714	chr1:151336699-151397878	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
28	esv2753719	chr1:151337788-151373200	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
29	nsv463839	chr1:151338570-151404848	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
30	nsv547851	chr1:151338570-151404848	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
31	nsv872431	chr1:151338570-151413180	Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
32	nsv872432	chr1:151339196-151413180	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
33	nsv872433	chr1:151341417-151413180	Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
34	nsv872434	chr1:151347820-151413180	Genic enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
35	nsv872435	chr1:151351060-151413180	Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
36	nsv872436	chr1:151357333-151413180	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	32 gene(s)	inside rSNPs	diseases
37	nsv872437	chr1:151373065-151413180	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151371400-151373400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr1:151371600-151373200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:151371600-151373200	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr1:151371600-151373200	Active TSS	Left Ventricle	heart
5	chr1:151371600-151373200	Active TSS	Psoas Muscle	Psoas
6	chr1:151372000-151373200	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
7	chr1:151372000-151373400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
8	chr1:151372000-151373600	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
9	chr1:151372200-151373200	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
10	chr1:151372200-151373200	Transcr. at gene 5' and 3'	Rectal Smooth Muscle	rectum
11	chr1:151372200-151373400	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
12	chr1:151372400-151373200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:151372400-151373200	Flanking Active TSS	Liver	Liver
14	chr1:151372400-151373200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr1:151372400-151373400	Transcr. at gene 5' and 3'	Brain Substantia Nigra	brain
16	chr1:151372400-151373400	Transcr. at gene 5' and 3'	Fetal Lung	lung
17	chr1:151372400-151373600	Transcr. at gene 5' and 3'	K562	blood
18	chr1:151372400-151374000	Transcr. at gene 5' and 3'	Dnd41	blood
19	chr1:151372600-151373200	Flanking Active TSS	Primary T cells from cord blood	blood
20	chr1:151372600-151373200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr1:151372600-151373200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr1:151372600-151373200	Flanking Active TSS	Brain Angular Gyrus	brain
23	chr1:151372600-151373200	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr1:151372600-151373200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
25	chr1:151372600-151373200	Flanking Active TSS	Stomach Mucosa	stomach
26	chr1:151372600-151373200	Flanking Active TSS	Thymus	Thymus
27	chr1:151372600-151373400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
28	chr1:151372800-151373200	Transcr. at gene 5' and 3'	Cortex derived primary cultured neurospheres	brain
29	chr1:151372800-151373200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:151372800-151373200	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
31	chr1:151372800-151373200	Flanking Active TSS	Gastric	stomach
32	chr1:151372800-151373200	Enhancers	Placenta Amnion	Placenta Amnion
33	chr1:151372800-151373200	Flanking Active TSS	Right Atrium	heart
34	chr1:151372800-151373200	Flanking Active TSS	HepG2	liver
35	chr1:151372800-151373200	Flanking Active TSS	HMEC	breast
36	chr1:151372800-151373200	Flanking Active TSS	HUVEC	blood vessel
37	chr1:151372800-151373400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr1:151372800-151373400	Enhancers	Fetal Heart	heart
39	chr1:151372800-151373400	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
40	chr1:151372800-151373400	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
41	chr1:151372800-151373600	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:151372800-151373600	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
43	chr1:151372800-151373600	Transcr. at gene 5' and 3'	Brain Cingulate Gyrus	brain
44	chr1:151372800-151373600	Transcr. at gene 5' and 3'	Brain Inferior Temporal Lobe	brain
45	chr1:151372800-151373600	Enhancers	Small Intestine	intestine
46	chr1:151372800-151373800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:151372800-151373800	Weak transcription	Aorta	Aorta
48	chr1:151372800-151373800	Transcr. at gene 5' and 3'	NHEK	skin
49	chr1:151372800-151374000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:151372800-151374200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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