Variant report

Variant	rs35363135
Chromosome Location	chr11:67196049-67196050
allele	A/G
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	RCOR1	chr11:67195714-67196093	Hela-S3	cervix:	n/a	n/a
2	ZNF143	chr11:67195557-67196100	H1-hESC	embryonic stem cell:	n/a	chr11:67195818-67195836 chr11:67195818-67195827 chr11:67195820-67195829 chr11:67195734-67195749
3	YY1	chr11:67195584-67196199	NT2-D1	testis:	n/a	chr11:67195846-67195868 chr11:67195849-67195857 chr11:67195845-67195857
4	MAX	chr11:67195577-67196286	ECC-1	luminal epithelium:	n/a	n/a
5	MYC	chr11:67195750-67196099	HUVEC	blood vessel:	n/a	n/a
6	SRF	chr11:67195691-67196170	H1-hESC	embryonic stem cell:	n/a	n/a
7	HA-E2F1	chr11:67195436-67196325	MCF-7	breast:	n/a	n/a
8	POLR2A	chr11:67195041-67197253	GM12892	blood:	n/a	n/a
9	POLR2A	chr11:67195323-67197285	GM12891	blood:	n/a	n/a
10	POLR2A	chr11:67195750-67196203	K562	blood:	n/a	n/a
11	TAF1	chr11:67195816-67196120	GM12892	blood:	n/a	n/a
12	E2F4	chr11:67195713-67196191	MCF10A-Er-Src	breast:	n/a	n/a
13	POLR2A	chr11:67195448-67196369	HUVEC	blood vessel:	n/a	n/a
14	CEBPD	chr11:67195698-67196118	HepG2	liver:	n/a	n/a
15	GABPA	chr11:67195590-67196152	SK-N-SH	brain:	n/a	n/a
16	POLR2A	chr11:67195855-67196180	A549	lung:	n/a	n/a
17	PBX3	chr11:67195661-67196244	A549	lung:	n/a	chr11:67195960-67195969
18	POLR2A	chr11:67195602-67196218	K562	blood:	n/a	n/a
19	POLR2A	chr11:67195406-67196934	GM12878	blood:	n/a	n/a
20	POLR2A	chr11:67195769-67196192	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr11:67195319-67196550	K562	blood:	n/a	n/a
22	FOS	chr11:67195688-67196057	MCF10A-Er-Src	breast:	n/a	n/a
23	CREB1	chr11:67195082-67196845	HepG2	liver:	n/a	n/a
24	SRF	chr11:67195438-67196408	HCT-116	colon:	n/a	n/a
25	POU2F2	chr11:67195415-67196296	GM12878	blood:	n/a	n/a
26	TAF1	chr11:67195692-67196191	HepG2	liver:	n/a	n/a
27	POLR2A	chr11:67195673-67196190	HCT-116	colon:	n/a	n/a
28	POLR2A	chr11:67195635-67196761	K562	blood:	n/a	n/a
29	ELK1	chr11:67195434-67196112	GM12878	blood:	n/a	n/a
30	ATF3	chr11:67195657-67196160	H1-hESC	embryonic stem cell:	n/a	chr11:67195902-67195915 chr11:67195913-67195922 chr11:67195904-67195914 chr11:67195903-67195923 chr11:67195902-67195913 chr11:67195902-67195913
31	POLR2A	chr11:67195546-67196294	U87	brain:	n/a	n/a
32	SRF	chr11:67195682-67196139	K562	blood:	n/a	n/a
33	CTCF	chr11:67195757-67196069	GM12878	blood:	n/a	n/a
34	YY1	chr11:67195385-67196428	A549	lung:	n/a	chr11:67195846-67195868 chr11:67195849-67195857 chr11:67195845-67195857
35	MAX	chr11:67195591-67196277	ECC-1	luminal epithelium:	n/a	n/a
36	POLR2A	chr11:67195661-67196203	A549	lung:	n/a	n/a
37	PBX3	chr11:67195759-67196093	GM12878	blood:	n/a	chr11:67195960-67195969
38	RFX5	chr11:67195725-67196081	HepG2	liver:	n/a	n/a
39	ZNF274	chr11:67195832-67196228	K562	blood:	n/a	n/a
40	ZNF263	chr11:67195569-67197264	HEK293-T-REx	kidney:	n/a	n/a
41	ELF1	chr11:67195443-67196255	MCF-7	breast:	n/a	chr11:67196147-67196159
42	POU2F2	chr11:67195527-67196211	GM12891	blood:	n/a	n/a
43	GABPA	chr11:67195600-67196221	A549	lung:	n/a	n/a
44	ZNF143	chr11:67195501-67196117	K562	blood:	n/a	chr11:67195818-67195836 chr11:67195818-67195827 chr11:67195820-67195829 chr11:67195734-67195749
45	MAZ	chr11:67195494-67196132	GM12878	blood:	n/a	n/a
46	SRF	chr11:67195295-67196371	MCF-7	breast:	n/a	n/a
47	POLR2A	chr11:67195542-67196290	U87	brain:	n/a	n/a
48	CHD2	chr11:67195557-67196389	GM12878	blood:	n/a	n/a
49	ATF3	chr11:67195454-67196229	K562	blood:	n/a	chr11:67195902-67195915 chr11:67195913-67195922 chr11:67195904-67195914 chr11:67195903-67195923 chr11:67195902-67195913 chr11:67195902-67195913
50	TBP	chr11:67195670-67196169	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67194291..67197631-chr11:67229995..67233154,6	K562	blood:
2	chr10:6244775..6245295-chr11:67195896..67196459,2	Hela-S3	cervix:
3	chr11:67195918..67196419-chr12:6643261..6644093,2	Hela-S3	cervix:
4	chr11:67168861..67169503-chr11:67195685..67196520,2	Hela-S3	cervix:
5	chr11:67196018..67196797-chr12:7052980..7053791,2	HCT-116	colon:
6	chr11:67195808..67196470-chr19:3366580..3367564,2	Hela-S3	cervix:
7	chr11:67195924..67196428-chr16:67969687..67970420,2	NB4	blood:
8	chr11:67195909..67196678-chr14:35873287..35873888,2	Hela-S3	cervix:
9	chr11:67194364..67200337-chr11:67272800..67277654,9	MCF-7	breast:
10	chr11:67195874..67196504-chr6:27114693..27115280,2	Hela-S3	cervix:
11	chr11:33279068..33280061-chr11:67195914..67196832,2	Hela-S3	cervix:
12	chr11:62608635..62609568-chr11:67195953..67196834,2	NB4	blood:
13	chr11:67195686..67198461-chr11:67271538..67273445,2	K562	blood:
14	chr11:67195785..67196556-chr20:30192761..30193301,2	Hela-S3	cervix:
15	chr11:67195661..67196414-chr14:92587537..92588307,2	Hela-S3	cervix:
16	chr11:67195659..67197780-chr5:130970138..130971644,2	MCF-7	breast:
17	chr11:67195896..67196549-chr15:81292682..81293568,2	Hela-S3	cervix:

Variant related genes	Relation type
RPS6KB2	TF binding region
ENSG00000272173	Chromatin interaction
ENSG00000141905	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000110422	Chromatin interaction
ENSG00000100906	Chromatin interaction
ENSG00000170525	Chromatin interaction
ENSG00000111678	Chromatin interaction
ENSG00000183648	Chromatin interaction
ENSG00000111640	Chromatin interaction
ENSG00000205220	Chromatin interaction
ENSG00000140406	Chromatin interaction
ENSG00000158987	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000165934	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000261884	Chromatin interaction
ENSG00000125968	Chromatin interaction
ENSG00000110697	Chromatin interaction

Extended variants
information (count: 130 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10896175	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227796	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227804	1.00[EUR][1000 genomes]
rs12293606	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1382089	1.00[EUR][1000 genomes]
rs1618605	0.90[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	0.90[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	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638559	0.92[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	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638562	0.95[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	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638577	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638581	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638584	0.90[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	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790741	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790743	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790744	0.99[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	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790763	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790764	0.96[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]
rs2447590	1.00[EUR][1000 genomes]
rs2447591	1.00[EUR][1000 genomes]
rs2511058	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2511059	0.90[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]
rs2514064	1.00[EUR][1000 genomes]
rs2514259	0.90[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]
rs3016861	1.00[EUR][1000 genomes]
rs56050553	1.00[EUR][1000 genomes]
rs56102510	1.00[EUR][1000 genomes]
rs56405884	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57047868	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]
rs596431	0.88[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	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60136955	1.00[EUR][1000 genomes]
rs602220	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60251934	1.00[EUR][1000 genomes]
rs602720	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs604540	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60521870	1.00[EUR][1000 genomes]
rs60751057	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]
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	0.92[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]
rs7941752	0.92[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	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949251	0.93[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	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949254	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949255	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 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	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	nsv897810	chr11:67166310-67196237	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
18	nsv897811	chr11:67166984-67218909	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
19	nsv897812	chr11:67174597-67198887	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
20	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
21	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
22	esv1847460	chr11:67182600-67219337	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
23	nsv524096	chr11:67186000-67224988	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
24	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
25	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

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67195000-67196600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr11:67195000-67196800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:67195200-67196400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:67195200-67196400	Active TSS	Fetal Brain Female	brain
5	chr11:67195200-67196400	Active TSS	Spleen	Spleen
6	chr11:67195200-67196600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:67195200-67196600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:67195200-67196600	Active TSS	Ovary	ovary
9	chr11:67195200-67196600	Active TSS	Psoas Muscle	Psoas
10	chr11:67195200-67196600	Active TSS	A549	lung
11	chr11:67195200-67196600	Active TSS	GM12878-XiMat	blood
12	chr11:67195200-67196600	Active TSS	NHLF	lung
13	chr11:67195200-67196800	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr11:67195200-67196800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
15	chr11:67195200-67197000	Active TSS	H9 Cell Line	embryonic stem cell
16	chr11:67195200-67197000	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr11:67195200-67197000	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr11:67195200-67197200	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr11:67195200-67197200	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr11:67195400-67196400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr11:67195400-67196400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:67195400-67196400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:67195400-67196400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:67195400-67196400	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
25	chr11:67195400-67196400	Active TSS	Brain Anterior Caudate	brain
26	chr11:67195400-67196400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr11:67195400-67196400	Active TSS	Colonic Mucosa	Colon
28	chr11:67195400-67196400	Active TSS	Esophagus	oesophagus
29	chr11:67195400-67196400	Active TSS	Gastric	stomach
30	chr11:67195400-67196400	Active TSS	Left Ventricle	heart
31	chr11:67195400-67196400	Active TSS	Rectal Smooth Muscle	rectum
32	chr11:67195400-67196400	Active TSS	Right Ventricle	heart
33	chr11:67195400-67196400	Active TSS	Stomach Mucosa	stomach
34	chr11:67195400-67196400	Active TSS	Osteobl	bone
35	chr11:67195400-67196600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr11:67195400-67196600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:67195400-67196600	Active TSS	Aorta	Aorta
38	chr11:67195400-67196600	Active TSS	Colon Smooth Muscle	Colon
39	chr11:67195400-67196600	Active TSS	Lung	lung
40	chr11:67195400-67196600	Active TSS	Sigmoid Colon	Sigmoid Colon
41	chr11:67195400-67196600	Active TSS	Thymus	Thymus
42	chr11:67195400-67196600	Active TSS	HMEC	breast
43	chr11:67195400-67196800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr11:67195400-67196800	Active TSS	Fetal Kidney	kidney
45	chr11:67195400-67197000	Active TSS	NHDF-Ad	bronchial
46	chr11:67195400-67197200	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr11:67195600-67196200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:67195600-67196200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr11:67195600-67196200	Active TSS	Primary monocytes fromperipheralblood	blood
50	chr11:67195600-67196200	Active TSS	Primary B cells from peripheral blood	blood

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