Variant report

Variant	rs2784041
Chromosome Location	chr9:139686556-139686557
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:180)
CpG islands
(count:0)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:180 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:139686071-139686652	H1-hESC	embryonic stem cell:	n/a	n/a
2	SMC3	chr9:139686125-139686580	HepG2	liver:	n/a	n/a
3	CTCF	chr9:139686156-139686583	HUVEC	blood vessel:	n/a	n/a
4	NR2F2	chr9:139685958-139686657	K562	blood:	n/a	n/a
5	CTCF	chr9:139686136-139686605	A549	lung:	n/a	n/a
6	TAF7	chr9:139686115-139686595	H1-hESC	embryonic stem cell:	n/a	n/a
7	RAD21	chr9:139686087-139686696	A549	lung:	n/a	n/a
8	CTCF	chr9:139686420-139686570	NHDF-neo	bronchial:	n/a	n/a
9	MAZ	chr9:139685084-139686634	K562	blood:	n/a	chr9:139685649-139685659
10	CTCF	chr9:139686088-139686623	MCF-7	breast:	n/a	n/a
11	IRF4	chr9:139686145-139686587	GM12878	blood:	n/a	n/a
12	CTCF	chr9:139686069-139686618	GM19238	blood:	n/a	n/a
13	MAZ	chr9:139685066-139686591	GM12878	blood:	n/a	chr9:139685649-139685659
14	BCL3	chr9:139685791-139686679	A549	lung:	n/a	n/a
15	CTCF	chr9:139686088-139686648	T-47D	breast:	n/a	n/a
16	CTCF	chr9:139686121-139686597	GM10248	blood:	n/a	n/a
17	E2F6	chr9:139685539-139686588	H1-hESC	embryonic stem cell:	n/a	chr9:139685648-139685657 chr9:139685786-139685795
18	CTCF	chr9:139686211-139686569	HepG2	liver:	n/a	n/a
19	CTCF	chr9:139686145-139686613	ECC-1	luminal epithelium:	n/a	n/a
20	FOSL2	chr9:139685990-139686571	A549	lung:	n/a	n/a
21	RAD21	chr9:139686175-139686664	H1-hESC	embryonic stem cell:	n/a	n/a
22	SIN3AK20	chr9:139686116-139686579	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr9:139686095-139686620	Gliobla	brain:	n/a	n/a
24	ZNF143	chr9:139686128-139686683	K562	blood:	n/a	n/a
25	MXI1	chr9:139685040-139687172	IMR90	lung:	n/a	chr9:139687092-139687101 chr9:139687090-139687099
26	ZNF143	chr9:139686090-139686632	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAX	chr9:139685123-139686599	H1-hESC	embryonic stem cell:	n/a	chr9:139685649-139685659
28	CTCF	chr9:139686145-139686621	K562	blood:	n/a	n/a
29	RAD21	chr9:139686174-139686559	IMR90	lung:	n/a	n/a
30	ELF1	chr9:139686293-139686834	K562	blood:	n/a	n/a
31	YY1	chr9:139686070-139686710	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr9:139686091-139686692	K562	blood:	n/a	n/a
33	RAD21	chr9:139686411-139686563	K562	blood:	n/a	n/a
34	CTCF	chr9:139686160-139686557	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr9:139686440-139686590	GM12870	blood:	n/a	n/a
36	ZEB1	chr9:139685736-139686616	GM12878	blood:	n/a	n/a
37	CREB1	chr9:139685027-139687281	HepG2	liver:	n/a	n/a
38	POLR2A	chr9:139685597-139686930	HL-60	blood:	n/a	n/a
39	MXI1	chr9:139686290-139686572	K562	blood:	n/a	n/a
40	CTCF	chr9:139686280-139686570	HCM	heart:	n/a	n/a
41	NANOG	chr9:139686193-139686619	H1-hESC	embryonic stem cell:	n/a	n/a
42	PML	chr9:139685596-139686580	GM12878	blood:	n/a	n/a
43	TAF1	chr9:139686011-139686600	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr9:139686117-139686626	GM12878	blood:	n/a	n/a
45	CTCF	chr9:139686155-139686578	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr9:139686029-139686604	GM10266	blood:	n/a	n/a
47	RAD21	chr9:139686133-139686618	H1-hESC	embryonic stem cell:	n/a	n/a
48	FOXM1	chr9:139686088-139686675	GM12878	blood:	n/a	n/a
49	E2F4	chr9:139684865-139686664	MCF10A-Er-Src	breast:	n/a	chr9:139685648-139685657 chr9:139685786-139685795
50	SP1	chr9:139686178-139686562	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:139683536..139687591-chr9:139921894..139924460,4	MCF-7	breast:
2	chr9:139683659..139687292-chr9:139920616..139923884,4	MCF-7	breast:
3	chr9:139683448..139687043-chr9:139724439..139728151,3	MCF-7	breast:
4	chr9:139685742..139688116-chr9:140148155..140149665,2	K562	blood:
5	chr9:139682366..139684711-chr9:139686192..139687800,2	K562	blood:
6	chr9:139684658..139687578-chr9:139740553..139743920,5	K562	blood:
7	chr9:139684238..139687578-chr9:139742280..139744165,4	K562	blood:
8	chr9:139683825..139687268-chr9:139871414..139874835,3	K562	blood:
9	chr9:139621035..139624561-chr9:139681529..139687287,9	K562	blood:
10	chr9:139621216..139622875-chr9:139685230..139687360,2	MCF-7	breast:
11	chr9:139685378..139687271-chr9:139915052..139917495,3	MCF-7	breast:
12	chr9:139377008..139379859-chr9:139684453..139686903,3	MCF-7	breast:
13	chr9:139685391..139688312-chr9:139795592..139798395,3	MCF-7	breast:
14	chr9:139685199..139687807-chr9:139878255..139880218,2	MCF-7	breast:
15	chr9:139685893..139687788-chr9:139748071..139750238,2	K562	blood:
16	chr9:139684892..139687578-chr9:139837356..139841601,5	MCF-7	breast:
17	chr9:139684091..139686797-chr9:139779339..139782193,3	K562	blood:
18	chr9:139684839..139687692-chr9:140133379..140136351,2	K562	blood:
19	chr9:139655064..139662123-chr9:139682792..139687315,8	K562	blood:
20	chr9:139620499..139624602-chr9:139683512..139688148,14	K562	blood:
21	chr9:139684641..139688491-chr9:139944424..139947811,3	K562	blood:
22	chr9:139655316..139662123-chr9:139682792..139687315,9	K562	blood:
23	chr9:139685272..139687236-chr9:139783437..139786045,2	MCF-7	breast:
24	chr9:139684091..139687398-chr9:139780288..139782193,3	K562	blood:
25	chr9:139686320..139689132-chr9:139920712..139922686,2	K562	blood:
26	chr9:139685305..139687370-chr9:139885305..139886970,2	MCF-7	breast:
27	chr9:139685972..139686767-chr9:139929631..139930328,4	MCF-7	breast:
28	chr9:139685184..139687112-chr9:139923073..139925089,2	K562	blood:
29	chr9:139685045..139687775-chr9:139838528..139840680,3	MCF-7	breast:
30	chr9:139683956..139686805-chr9:139759476..139762269,2	K562	blood:
31	chr9:139682478..139689029-chr9:139739017..139745111,14	MCF-7	breast:
32	chr9:139685870..139687386-chr9:139979656..139982069,2	MCF-7	breast:
33	chr9:139685272..139686894-chr9:139719097..139721634,2	K562	blood:
34	chr9:139684905..139687555-chr9:139781430..139784355,2	MCF-7	breast:
35	chr9:139684580..139687679-chr9:139885169..139891093,6	MCF-7	breast:
36	chr9:139683838..139686879-chr9:140133317..140137174,3	MCF-7	breast:
37	chr9:139684319..139687155-chr9:139837681..139840267,3	K562	blood:
38	chr9:139685326..139687361-chr9:139939628..139942072,2	MCF-7	breast:
39	chr9:139681106..139687354-chr9:139701145..139707280,8	K562	blood:
40	chr9:139685015..139687198-chr9:139901432..139904187,2	MCF-7	breast:
41	chr9:139682195..139706361-chr9:139728316..139752024,110	MCF-7	breast:

No data

Variant related genes	Relation type
CCDC183	TF binding region
ENSG00000177984	Chromatin interaction
ENSG00000054148	Chromatin interaction
ENSG00000177943	Chromatin interaction
ENSG00000196642	Chromatin interaction
ENSG00000107331	Chromatin interaction
ENSG00000265806	Chromatin interaction
ENSG00000213213	Chromatin interaction
ENSG00000228544	Chromatin interaction
ENSG00000188229	Chromatin interaction
ENSG00000232434	Chromatin interaction
ENSG00000188986	Chromatin interaction
ENSG00000196366	Chromatin interaction
ENSG00000127191	Chromatin interaction
ENSG00000214402	Chromatin interaction
ENSG00000177239	Chromatin interaction
ENSG00000169583	Chromatin interaction
ENSG00000107281	Chromatin interaction
ENSG00000176919	Chromatin interaction
ENSG00000233016	Chromatin interaction
ENSG00000107223	Chromatin interaction
ENSG00000159069	Chromatin interaction
ENSG00000236394	Chromatin interaction
ENSG00000266507	Chromatin interaction
ENSG00000107317	Chromatin interaction
ENSG00000268996	Chromatin interaction
ENSG00000148362	Chromatin interaction
ENSG00000180539	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1055995	0.94[CHD][hapmap];0.93[GIH][hapmap]
rs10781516	1.00[CHB][hapmap];0.87[CHD][hapmap]
rs11789783	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2248077	0.89[CHB][hapmap];0.87[CHD][hapmap]
rs2297722	1.00[CHB][hapmap];0.87[CHD][hapmap];0.82[GIH][hapmap]
rs2492307	1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2498193	0.87[EUR][1000 genomes]
rs2498195	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2784035	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2784036	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2784037	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2784038	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2784039	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2784040	0.92[CEU][hapmap];0.90[CHB][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784044	0.90[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2784045	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2784046	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2784047	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2784048	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2784049	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784050	1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784051	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784052	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2784053	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2784054	1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784055	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.97[TSI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784056	1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784057	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784059	0.83[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[GIH][hapmap];0.97[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784060	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2784065	1.00[CHB][hapmap]
rs2784070	0.89[CHB][hapmap];0.87[CHD][hapmap]
rs2811736	0.89[CHB][hapmap]
rs2811767	0.89[EUR][1000 genomes]
rs2811768	1.00[CHB][hapmap];0.87[CHD][hapmap];0.81[TSI][hapmap]
rs2811769	1.00[CHB][hapmap]
rs2811777	1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2811778	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2811779	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2811781	0.82[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2811782	0.86[ASN][1000 genomes]
rs2811783	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2811784	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2811785	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2811786	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.97[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2811788	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35342663	0.86[ASN][1000 genomes]
rs4880140	1.00[CHB][hapmap];0.87[CHD][hapmap]
rs4880142	1.00[CHB][hapmap];0.86[CHD][hapmap]
rs4880143	0.90[CHB][hapmap];0.87[CHD][hapmap]
rs57277737	0.86[ASN][1000 genomes]
rs62581399	0.94[ASN][1000 genomes]
rs62581400	0.86[ASN][1000 genomes]
rs7852010	0.82[CEU][hapmap];0.81[CHB][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9411234	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9411237	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9411285	1.00[CHB][hapmap]
rs9411286	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9411287	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1849811	chr9:138939662-139755001	Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	323 gene(s)	inside rSNPs	diseases
2	esv1822553	chr9:138967205-139755539	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	323 gene(s)	inside rSNPs	diseases
3	esv1851120	chr9:139101947-139711758	Bivalent Enhancer Weak transcription Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	275 gene(s)	inside rSNPs	diseases
4	nsv430118	chr9:139101947-139795504	Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	299 gene(s)	inside rSNPs	diseases
5	nsv540342	chr9:139218422-139973312	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	317 gene(s)	inside rSNPs	diseases
6	esv2758204	chr9:139252829-139826485	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	270 gene(s)	inside rSNPs	diseases
7	esv2759720	chr9:139252829-139826485	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS 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 lncRNA miRNA miRNA target site	270 gene(s)	inside rSNPs	diseases
8	nsv469918	chr9:139254317-140068342	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	341 gene(s)	inside rSNPs	diseases
9	esv1799492	chr9:139341612-139711758	Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	216 gene(s)	inside rSNPs	diseases
10	nsv540346	chr9:139360142-140164011	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	471 gene(s)	inside rSNPs	diseases
11	nsv894386	chr9:139376426-139693992	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	208 gene(s)	inside rSNPs	diseases
12	nsv1039149	chr9:139376829-139991102	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	303 gene(s)	inside rSNPs	diseases
13	esv1829857	chr9:139385438-139760041	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
14	esv1819204	chr9:139388365-139758238	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
15	esv1803979	chr9:139395473-139979276	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
16	esv1831778	chr9:139395473-139979276	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	267 gene(s)	inside rSNPs	diseases
17	esv1821575	chr9:139395473-140068342	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases
18	esv2422220	chr9:139478587-140244550	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	454 gene(s)	inside rSNPs	diseases
19	nsv894409	chr9:139483954-139860264	Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	209 gene(s)	inside rSNPs	diseases
20	nsv894422	chr9:139487092-139776400	Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
21	nsv894432	chr9:139522101-139869914	Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	205 gene(s)	inside rSNPs	diseases
22	nsv894440	chr9:139544437-139841512	Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	194 gene(s)	inside rSNPs	diseases
23	nsv894441	chr9:139544437-139860264	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	201 gene(s)	inside rSNPs	diseases
24	nsv894442	chr9:139544437-140462099	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
25	nsv540348	chr9:139550414-139687876	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
26	nsv894450	chr9:139598108-139776400	Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	130 gene(s)	inside rSNPs	diseases
27	nsv894451	chr9:139598108-139995065	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
28	nsv894452	chr9:139598108-140523429	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
29	nsv894454	chr9:139607966-139904037	Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	172 gene(s)	inside rSNPs	diseases
30	nsv894455	chr9:139607966-140411547	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	417 gene(s)	inside rSNPs	diseases
31	nsv1051605	chr9:139620105-139728697	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
32	nsv540350	chr9:139620105-139728697	Bivalent Enhancer Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
33	nsv818738	chr9:139634495-139904037	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	126 gene(s)	inside rSNPs	diseases
34	nsv466681	chr9:139647074-139693992	Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
35	nsv615982	chr9:139647074-139693992	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
36	nsv894457	chr9:139650448-139776400	Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	79 gene(s)	inside rSNPs	diseases
37	nsv540351	chr9:139664948-139703627	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
38	nsv523639	chr9:139669111-139690144	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
39	nsv894458	chr9:139683224-139776400	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	77 gene(s)	inside rSNPs	diseases
40	nsv894459	chr9:139683224-139787453	Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	80 gene(s)	inside rSNPs	diseases
41	nsv894460	chr9:139683224-139810595	Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
42	nsv894461	chr9:139683224-139860264	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
43	nsv894462	chr9:139683224-140274164	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	353 gene(s)	inside rSNPs	diseases
44	nsv894463	chr9:139683224-140411547	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139685200-139686600	Active TSS	iPS-18 Cell Line	embryonic stem cell
2	chr9:139685200-139686600	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr9:139685200-139686600	Active TSS	Muscle Satellite Cultured Cells	--
4	chr9:139685200-139686600	Active TSS	HSMMtube	muscle
5	chr9:139685200-139686800	Enhancers	Fetal Brain Male	brain
6	chr9:139685200-139687000	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr9:139685600-139686800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:139685600-139688200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr9:139685800-139686600	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr9:139685800-139686600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:139685800-139686600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:139685800-139686600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
13	chr9:139685800-139686600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr9:139685800-139686600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr9:139685800-139686600	Active TSS	Fetal Intestine Large	intestine
16	chr9:139685800-139686600	Flanking Active TSS	Fetal Muscle Trunk	muscle
17	chr9:139685800-139686600	Active TSS	Right Atrium	heart
18	chr9:139685800-139686600	Active TSS	K562	blood
19	chr9:139685800-139686600	Active TSS	NHDF-Ad	bronchial
20	chr9:139685800-139686800	Active TSS	H1 Cell Line	embryonic stem cell
21	chr9:139685800-139686800	Active TSS	H9 Cell Line	embryonic stem cell
22	chr9:139685800-139686800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:139685800-139686800	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr9:139685800-139686800	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr9:139685800-139686800	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr9:139685800-139686800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr9:139685800-139686800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr9:139685800-139686800	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr9:139685800-139686800	Flanking Active TSS	Fetal Thymus	thymus
30	chr9:139685800-139686800	Active TSS	Ovary	ovary
31	chr9:139685800-139686800	Active TSS	A549	lung
32	chr9:139685800-139686800	Flanking Active TSS	Dnd41	blood
33	chr9:139685800-139687000	Flanking Active TSS	Primary hematopoietic stem cells	blood
34	chr9:139685800-139687000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr9:139685800-139687000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr9:139685800-139687000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:139685800-139687000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr9:139685800-139687000	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr9:139685800-139687000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr9:139685800-139687200	Flanking Active TSS	HMEC	breast
41	chr9:139686000-139686600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr9:139686000-139686600	Flanking Active TSS	Liver	Liver
43	chr9:139686000-139686600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr9:139686000-139686600	Flanking Active TSS	Fetal Muscle Leg	muscle
45	chr9:139686000-139686600	Flanking Active TSS	Placenta	Placenta
46	chr9:139686000-139686600	Flanking Active TSS	Rectal Smooth Muscle	rectum
47	chr9:139686000-139686600	Flanking Active TSS	HUVEC	blood vessel
48	chr9:139686000-139686800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr9:139686000-139686800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr9:139686000-139686800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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