Variant report

Variant	rs2511058
Chromosome Location	chr11:67231745-67231746
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr11:67231294-67232159	A549	lung:	n/a	n/a
2	ELK4	chr11:67231431-67232072	Hela-S3	cervix:	n/a	n/a
3	E2F6	chr11:67231453-67232474	K562	blood:	n/a	n/a
4	TBP	chr11:67231376-67232614	K562	blood:	n/a	n/a
5	RCOR1	chr11:67231444-67232088	K562	blood:	n/a	n/a
6	E2F6	chr11:67231275-67232598	A549	lung:	n/a	chr11:67232506-67232518
7	POLR2A	chr11:67231297-67232989	MCF-7	breast:	n/a	n/a
8	POLR2A	chr11:67231062-67233381	U87	brain:	n/a	n/a
9	SMARCC1	chr11:67231363-67232168	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr11:67231448-67232585	PFSK-1	brain:	n/a	n/a
11	FOS	chr11:67231387-67231782	MCF10A-Er-Src	breast:	n/a	chr11:67231574-67231586 chr11:67231576-67231584 chr11:67231577-67231584 chr11:67231575-67231585
12	POLR2A	chr11:67231338-67232767	MCF-7	breast:	n/a	n/a
13	MAZ	chr11:67231352-67232730	Hela-S3	cervix:	n/a	chr11:67232504-67232514
14	POLR2A	chr11:67231613-67232621	GM15510	blood:	n/a	n/a
15	POLR2A	chr11:67231335-67232531	K562	blood:	n/a	n/a
16	POLR2A	chr11:67231612-67232685	GM18951	blood:	n/a	n/a
17	GTF2F1	chr11:67231254-67232475	Hela-S3	cervix:	n/a	n/a
18	ETS1	chr11:67231337-67231878	A549	lung:	n/a	n/a
19	ELF1	chr11:67231392-67231763	A549	lung:	n/a	n/a
20	GTF2F1	chr11:67231568-67232504	K562	blood:	n/a	n/a
21	POLR2A	chr11:67231134-67233282	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr11:67231269-67232526	HCT-116	colon:	n/a	n/a
23	POLR2A	chr11:67231239-67233047	HUVEC	blood vessel:	n/a	n/a
24	FOS	chr11:67231420-67231758	MCF10A-Er-Src	breast:	n/a	chr11:67231574-67231586 chr11:67231576-67231584 chr11:67231577-67231584 chr11:67231575-67231585
25	POLR2A	chr11:67230621-67232134	K562	blood:	n/a	n/a
26	FOSL2	chr11:67231308-67231834	HepG2	liver:	n/a	chr11:67231574-67231586 chr11:67231576-67231584 chr11:67231573-67231584 chr11:67231577-67231584 chr11:67231575-67231585
27	NR3C1	chr11:67231397-67231784	A549	lung:	n/a	chr11:67231600-67231614
28	NR3C1	chr11:67231317-67231782	A549	lung:	n/a	chr11:67231600-67231614 chr11:67231359-67231372
29	HMGN3	chr11:67231363-67232600	K562	blood:	n/a	chr11:67231577-67231586
30	MAX	chr11:67231377-67232448	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr11:67231318-67232087	K562	blood:	n/a	n/a
32	POLR2A	chr11:67231005-67233381	U87	brain:	n/a	n/a
33	POLR2A	chr11:67231324-67231815	A549	lung:	n/a	n/a
34	RUNX3	chr11:67231542-67232621	GM12878	blood:	n/a	n/a
35	FOS	chr11:67231387-67231762	MCF10A-Er-Src	breast:	n/a	chr11:67231574-67231586 chr11:67231576-67231584 chr11:67231577-67231584 chr11:67231575-67231585
36	POLR2A	chr11:67231187-67232640	HL-60	blood:	n/a	n/a
37	POLR2A	chr11:67230571-67233333	K562	blood:	n/a	n/a
38	CCNT2	chr11:67231397-67232858	K562	blood:	n/a	chr11:67231594-67231603 chr11:67231588-67231597
39	POLR2A	chr11:67231249-67233279	GM12892	blood:	n/a	n/a
40	HDAC2	chr11:67231479-67231745	K562	blood:	n/a	n/a
41	ZBTB7A	chr11:67231635-67232844	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr11:67231237-67233021	K562	blood:	n/a	n/a
43	SIN3AK20	chr11:67230555-67233239	MCF-7	breast:	n/a	n/a
44	JUND	chr11:67231262-67232674	MCF-7	breast:	n/a	chr11:67231574-67231586 chr11:67232170-67232179 chr11:67231576-67231584 chr11:67231577-67231584 chr11:67231575-67231585
45	MTA3	chr11:67231543-67233221	GM12878	blood:	n/a	n/a
46	TBP	chr11:67231348-67232500	Hela-S3	cervix:	n/a	n/a
47	PML	chr11:67231331-67232609	MCF-7	breast:	n/a	chr11:67231577-67231586
48	POLR2A	chr11:67231407-67233007	Raji	blood:	n/a	n/a
49	CREB1	chr11:67231255-67231825	A549	lung:	n/a	n/a
50	MYC	chr11:67231481-67232409	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67231460..67232161-chr16:56965623..56966449,2	Hela-S3	cervix:
2	chr11:67231740..67232557-chr5:79783790..79784496,2	Hela-S3	cervix:
3	chr11:67231400..67232240-chr12:27932856..27933621,2	Hela-S3	cervix:
4	chr11:67201799..67203957-chr11:67229051..67231861,3	K562	blood:
5	chr11:67175949..67181191-chr11:67230601..67234346,6	K562	blood:
6	chr11:67119569..67122629-chr11:67231645..67234377,4	MCF-7	breast:
7	chr11:67231739..67232585-chr7:6120356..6121094,2	NB4	blood:
8	chr11:67230622..67232854-chr11:67248914..67251189,3	MCF-7	breast:
9	chr11:67159952..67162907-chr11:67231636..67233328,2	K562	blood:
10	chr11:67230145..67233819-chr11:67248914..67252066,4	K562	blood:
11	chr11:67218019..67220766-chr11:67230531..67233882,3	K562	blood:
12	chr11:67231244..67235869-chr11:67255079..67259378,6	MCF-7	breast:
13	chr1:16840048..16841042-chr11:67231498..67232010,2	Hela-S3	cervix:
14	chr11:67231354..67231981-chr5:139487346..139487980,2	Hela-S3	cervix:
15	chr11:67229953..67232204-chr6:151995538..151997819,2	MCF-7	breast:
16	chr11:67215208..67219901-chr11:67230573..67236211,5	K562	blood:
17	chr11:67231620..67232535-chr12:46776564..46777258,2	Hela-S3	cervix:
18	chr11:67121023..67122771-chr11:67229925..67232799,2	K562	blood:
19	chr11:67231087..67233865-chr11:67375187..67377797,2	K562	blood:
20	chr11:66626403..66628670-chr11:67229720..67232252,2	K562	blood:
21	chr11:67160326..67163213-chr11:67229848..67232719,2	MCF-7	breast:
22	chr11:67230107..67238941-chr11:67268499..67277838,23	MCF-7	breast:
23	chr11:67231198..67233116-chr11:67249356..67252066,3	K562	blood:
24	chr11:67204954..67212426-chr11:67228820..67232211,6	K562	blood:
25	chr11:67221211..67222819-chr11:67229683..67232141,2	K562	blood:
26	chr11:67166766..67171737-chr11:67231413..67236466,7	K562	blood:
27	chr11:67187592..67190127-chr11:67230614..67234165,3	K562	blood:
28	chr11:67231069..67231753-chr20:30192471..30193342,2	Hela-S3	cervix:
29	chr11:67231016..67231782-chr3:141059446..141059946,2	Hela-S3	cervix:
30	chr11:67231368..67232079-chr20:57464161..57464673,2	Hela-S3	cervix:
31	chr11:67051198..67053837-chr11:67230277..67232997,2	MCF-7	breast:
32	chr11:67194291..67197631-chr11:67229995..67233154,6	K562	blood:
33	chr11:67229962..67234772-chr11:67234827..67242516,28	K562	blood:
34	chr11:67225990..67228470-chr11:67230116..67233017,3	K562	blood:

Variant related genes	Relation type
ENSG00000270169	TF binding region
ENSG00000175634	Chromatin interaction
ENSG00000206652	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000051108	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000087448	Chromatin interaction
ENSG00000253024	Chromatin interaction
ENSG00000167792	Chromatin interaction
ENSG00000175514	Chromatin interaction
ENSG00000185129	Chromatin interaction
ENSG00000152380	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000213402	Chromatin interaction
ENSG00000249042	Chromatin interaction
ENSG00000172725	Chromatin interaction
ENSG00000255949	Chromatin interaction
ENSG00000125968	Chromatin interaction
ENSG00000175544	Chromatin interaction
ENSG00000173599	Chromatin interaction
ENSG00000231704	Chromatin interaction
ENSG00000269913	Chromatin interaction
ENSG00000087460	Chromatin interaction
ENSG00000173020	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000172531	Chromatin interaction

Extended variants
information (count: 138 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10896175	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227796	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227804	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11821703	1.00[EUR][1000 genomes]
rs12288316	1.00[EUR][1000 genomes]
rs12293606	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1382089	1.00[EUR][1000 genomes]
rs1618605	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1620333	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1624189	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1625032	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1625892	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1630068	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1632616	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638558	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638559	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638560	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638561	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638562	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638563	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638570	1.00[EUR][1000 genomes]
rs1638572	1.00[EUR][1000 genomes]
rs1638575	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638576	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638577	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638581	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638584	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638585	0.90[AMR][1000 genomes]
rs1638587	1.00[EUR][1000 genomes]
rs1790729	1.00[EUR][1000 genomes]
rs1790730	1.00[EUR][1000 genomes]
rs1790734	1.00[EUR][1000 genomes]
rs1790736	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790741	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790743	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790744	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790745	1.00[EUR][1000 genomes]
rs1790749	1.00[EUR][1000 genomes]
rs1790750	1.00[EUR][1000 genomes]
rs1790754	1.00[EUR][1000 genomes]
rs1790756	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790763	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790764	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790765	1.00[EUR][1000 genomes]
rs1824712	1.00[EUR][1000 genomes]
rs2054409	1.00[EUR][1000 genomes]
rs2447590	1.00[EUR][1000 genomes]
rs2447591	1.00[EUR][1000 genomes]
rs2447597	1.00[EUR][1000 genomes]
rs2511059	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514013	1.00[EUR][1000 genomes]
rs2514014	1.00[EUR][1000 genomes]
rs2514015	1.00[EUR][1000 genomes]
rs2514024	1.00[EUR][1000 genomes]
rs2514045	1.00[EUR][1000 genomes]
rs2514064	1.00[EUR][1000 genomes]
rs2514259	0.97[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2514262	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514263	1.00[EUR][1000 genomes]
rs2885171	1.00[EUR][1000 genomes]
rs3016861	1.00[EUR][1000 genomes]
rs35363135	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36052107	1.00[EUR][1000 genomes]
rs56050553	1.00[EUR][1000 genomes]
rs56102510	1.00[EUR][1000 genomes]
rs56405884	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57047868	1.00[EUR][1000 genomes]
rs57134963	1.00[EUR][1000 genomes]
rs57748654	1.00[EUR][1000 genomes]
rs57749415	1.00[EUR][1000 genomes]
rs57757103	1.00[EUR][1000 genomes]
rs57955602	1.00[EUR][1000 genomes]
rs58999825	1.00[EUR][1000 genomes]
rs59500232	1.00[EUR][1000 genomes]
rs596431	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs596944	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs601363	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60136955	1.00[EUR][1000 genomes]
rs602220	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60251934	1.00[EUR][1000 genomes]
rs602720	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs604540	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60521870	1.00[EUR][1000 genomes]
rs611697	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61282424	1.00[EUR][1000 genomes]
rs61429992	1.00[EUR][1000 genomes]
rs61610719	1.00[EUR][1000 genomes]
rs618633	1.00[EUR][1000 genomes]
rs641081	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6591267	1.00[EUR][1000 genomes]
rs7104627	1.00[EUR][1000 genomes]
rs7121803	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7124630	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73490545	1.00[EUR][1000 genomes]
rs73490554	1.00[EUR][1000 genomes]
rs73501797	1.00[EUR][1000 genomes]
rs73501800	1.00[EUR][1000 genomes]
rs73506004	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506015	1.00[EUR][1000 genomes]
rs73506054	1.00[EUR][1000 genomes]
rs73506056	1.00[EUR][1000 genomes]
rs73506069	1.00[EUR][1000 genomes]
rs73506074	1.00[EUR][1000 genomes]
rs743679	1.00[EUR][1000 genomes]
rs7934566	1.00[EUR][1000 genomes]
rs7941752	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7947114	1.00[EUR][1000 genomes]
rs8191436	1.00[EUR][1000 genomes]
rs8191446	1.00[EUR][1000 genomes]
rs8191449	1.00[EUR][1000 genomes]
rs949250	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949251	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949252	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949253	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949254	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949255	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
3	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
4	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
5	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
6	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
7	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription 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 lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
8	esv1798859	chr11:67139954-67272983	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer 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	154 gene(s)	inside rSNPs	diseases
9	nsv897805	chr11:67155210-67283891	ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
10	nsv897806	chr11:67155210-67294308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
11	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer 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	176 gene(s)	inside rSNPs	diseases
12	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
13	nsv897809	chr11:67156875-67276235	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
14	nsv555254	chr11:67164495-67288594	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' 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	146 gene(s)	inside rSNPs	diseases
15	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
16	nsv897813	chr11:67175692-67283891	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
17	nsv521723	chr11:67175692-67311258	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
18	nsv468604	chr11:67186000-67283891	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
19	nsv555256	chr11:67186000-67283891	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
20	nsv527056	chr11:67207426-67294308	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS 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	115 gene(s)	inside rSNPs	diseases
21	esv1813337	chr11:67217703-67235815	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
22	nsv983155	chr11:67220251-67251432	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67211800-67232000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:67227400-67231800	Enhancers	Primary B cells from cord blood	blood
3	chr11:67228400-67231800	Weak transcription	Brain Germinal Matrix	brain
4	chr11:67230000-67231800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:67230000-67231800	Enhancers	Placenta	Placenta
6	chr11:67230600-67231800	Enhancers	Pancreas	Pancrea
7	chr11:67230600-67231800	Enhancers	Spleen	Spleen
8	chr11:67230600-67232000	Enhancers	Stomach Mucosa	stomach
9	chr11:67230600-67232200	Enhancers	Small Intestine	intestine
10	chr11:67230800-67231800	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr11:67230800-67232200	Flanking Active TSS	K562	blood
12	chr11:67230800-67232400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr11:67231000-67231800	Enhancers	Primary T cells fromperipheralblood	blood
14	chr11:67231000-67231800	Enhancers	Fetal Thymus	thymus
15	chr11:67231000-67232200	Flanking Active TSS	Hela-S3	cervix
16	chr11:67231200-67231800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr11:67231200-67231800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr11:67231200-67231800	Genic enhancers	Right Atrium	heart
19	chr11:67231200-67231800	Enhancers	HUVEC	blood vessel
20	chr11:67231200-67231800	Enhancers	NHEK	skin
21	chr11:67231200-67232000	Enhancers	NHDF-Ad	bronchial
22	chr11:67231200-67232200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr11:67231200-67232200	Enhancers	HMEC	breast
24	chr11:67231200-67233000	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr11:67231400-67231800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr11:67231400-67231800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr11:67231400-67231800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:67231400-67231800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr11:67231400-67231800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr11:67231400-67231800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr11:67231400-67231800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr11:67231400-67231800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr11:67231400-67231800	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr11:67231400-67231800	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr11:67231400-67231800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr11:67231400-67231800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr11:67231400-67231800	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr11:67231400-67231800	Flanking Active TSS	Brain Anterior Caudate	brain
39	chr11:67231400-67231800	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr11:67231400-67231800	Enhancers	Right Ventricle	heart
41	chr11:67231400-67231800	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr11:67231400-67232000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:67231400-67232000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:67231400-67232000	Flanking Active TSS	Colonic Mucosa	Colon
45	chr11:67231400-67232000	Flanking Active TSS	Lung	lung
46	chr11:67231400-67232000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr11:67231400-67232000	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr11:67231400-67232000	Flanking Active TSS	A549	lung
49	chr11:67231400-67232000	Enhancers	HSMMtube	muscle
50	chr11:67231400-67232200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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