Variant report

Variant	esv3328878
Chromosome Location	chr11:66107076-66111474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:244)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:55 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr11:66108680-66109648	GM12878	blood:	n/a	n/a
2	BCL3	chr11:66109145-66109615	GM12878	blood:	n/a	n/a
3	CTCF	chr11:66108240-66108390	WERI-Rb-1	eye:	n/a	n/a
4	CTCF	chr11:66108240-66108390	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr11:66108298-66108353	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAFF	chr11:66107390-66107547	HepG2	liver:	n/a	chr11:66107424-66107442
7	MAFK	chr11:66110623-66110923	IMR90	lung:	n/a	n/a
8	MAFK	chr11:66107381-66107493	HepG2	liver:	n/a	chr11:66107427-66107438 chr11:66107425-66107439 chr11:66107426-66107437 chr11:66107427-66107438
9	MAFK	chr11:66110781-66110790	HepG2	liver:	n/a	n/a
10	MYC	chr11:66109180-66109375	MCF-7	breast:	n/a	n/a
11	NFATC1	chr11:66109060-66109602	GM12878	blood:	n/a	n/a
12	PBX3	chr11:66109135-66109504	GM12878	blood:	n/a	n/a
13	POLR2A	chr11:66110576-66110583	HepG2	liver:	n/a	n/a
14	POLR2A	chr11:66110358-66110363	K562	blood:	n/a	n/a
15	POLR2A	chr11:66109212-66109232	MCF-7	breast:	n/a	n/a
16	POLR2A	chr11:66109065-66110007	GM12892	blood:	n/a	n/a
17	POLR2A	chr11:66109346-66109738	K562	blood:	n/a	n/a
18	POLR2A	chr11:66111117-66111310	HepG2	liver:	n/a	n/a
19	POLR2A	chr11:66110057-66110293	K562	blood:	n/a	n/a
20	POLR2A	chr11:66110596-66110740	HepG2	liver:	n/a	n/a
21	POLR2A	chr11:66108956-66109539	GM12892	blood:	n/a	n/a
22	POLR2A	chr11:66109391-66109392	MCF-7	breast:	n/a	n/a
23	POLR2A	chr11:66107756-66107927	GM12878	blood:	n/a	n/a
24	POLR2A	chr11:66107317-66107659	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:66109062-66109496	GM12891	blood:	n/a	n/a
26	POLR2A	chr11:66108382-66108507	K562	blood:	n/a	n/a
27	POLR2A	chr11:66107395-66107487	HepG2	liver:	n/a	n/a
28	POLR2A	chr11:66109213-66109536	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:66106389-66107246	K562	blood:	n/a	n/a
30	POLR2A	chr11:66110330-66110401	HepG2	liver:	n/a	n/a
31	POLR2A	chr11:66108704-66110024	GM12878	blood:	n/a	n/a
32	POLR2A	chr11:66109150-66109456	MCF-7	breast:	n/a	n/a
33	POLR2A	chr11:66108915-66108928	K562	blood:	n/a	n/a
34	POLR2A	chr11:66109125-66109487	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr11:66108711-66108892	GM12878	blood:	n/a	n/a
36	POLR2A	chr11:66109282-66109634	K562	blood:	n/a	n/a
37	POLR2A	chr11:66109368-66109369	MCF-7	breast:	n/a	n/a
38	POLR2A	chr11:66108952-66109595	GM12892	blood:	n/a	n/a
39	POLR2A	chr11:66109193-66109201	K562	blood:	n/a	n/a
40	POLR2A	chr11:66108960-66109694	HepG2	liver:	n/a	n/a
41	POLR2A	chr11:66108929-66109127	K562	blood:	n/a	n/a
42	POLR2A	chr11:66108142-66108218	K562	blood:	n/a	n/a
43	POLR2A	chr11:66106948-66107184	K562	blood:	n/a	n/a
44	POLR2A	chr11:66109143-66109148	MCF-7	breast:	n/a	n/a
45	POLR2A	chr11:66110953-66111277	IMR90	lung:	n/a	n/a
46	POLR2A	chr11:66111256-66111481	K562	blood:	n/a	n/a
47	POLR2A	chr11:66110407-66110522	HepG2	liver:	n/a	n/a
48	POLR2A	chr11:66109801-66109950	K562	blood:	n/a	n/a
49	POLR2A	chr11:66109157-66109210	MCF-7	breast:	n/a	n/a
50	POLR2A	chr11:66109309-66109333	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:66109018-66109068	GM06990	blood:	n/a
2	chr11:66108893-66108943	HNPCEpiC	eye:	n/a
3	chr11:66109162-66109212	NT2-D1	testis:	n/a
4	chr11:66108473-66108523	GM06990	blood:	n/a
5	chr11:66109018-66109068	GM19239	blood:	n/a
6	chr11:66109018-66109068	ECC-1	luminal epithelium:	n/a
7	chr11:66108893-66108943	HRE	kidney:	n/a
8	chr11:66109162-66109212	MCF10A-Er-Src	breast:	n/a
9	chr11:66109162-66109212	Hepatocyte	liver:	n/a
10	chr11:66109018-66109068	HCF	heart:	n/a
11	chr11:66109018-66109068	PrEC	prostate:	n/a
12	chr11:66109018-66109068	HL-60	blood:	n/a
13	chr11:66108893-66108943	U87	brain:	n/a
14	chr11:66108893-66108943	HUVEC	blood vessel:	n/a
15	chr11:66108893-66108943	H1-hESC	embryonic stem cell:	embryo
16	chr11:66108893-66108943	HCF	heart:	n/a
17	chr11:66108473-66108523	K562	blood:	n/a
18	chr11:66108893-66108943	PrEC	prostate:	n/a
19	chr11:66108893-66108943	MCF-7	breast:	n/a
20	chr11:66109018-66109068	PFSK-1	brain:	n/a
21	chr11:66109162-66109212	AG10803	skin:	n/a
22	chr11:66108473-66108523	Jurkat	blood:	n/a
23	chr11:66108473-66108523	H1-hESC	embryonic stem cell:	embryo
24	chr11:66109018-66109068	HEK293	kidney:	embryo
25	chr11:66108473-66108523	HRE	kidney:	n/a
26	chr11:66109162-66109212	Jurkat	blood:	n/a
27	chr11:66109162-66109212	HCF	heart:	n/a
28	chr11:66109018-66109068	HUVEC	blood vessel:	n/a
29	chr11:66109162-66109212	ECC-1	luminal epithelium:	n/a
30	chr11:66108893-66108943	HCPEpiC	choroid plexus:	n/a
31	chr11:66109162-66109212	GM12892	blood:	n/a
32	chr11:66109162-66109212	ovcar-3	ovarian:	n/a
33	chr11:66109018-66109068	AG09309	skin:	n/a
34	chr11:66108473-66108523	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:66109162-66109212	HAEpiC	amniotic membrane:	n/a
36	chr11:66108473-66108523	NHDF-neo	bronchial:	n/a
37	chr11:66108893-66108943	HCM	heart:	n/a
38	chr11:66109162-66109212	SK-N-MC	brain:	n/a
39	chr11:66109018-66109068	HRE	kidney:	n/a
40	chr11:66108893-66108943	HAEpiC	amniotic membrane:	n/a
41	chr11:66108893-66108943	SAEC	small airway:	n/a
42	chr11:66108893-66108943	HRCEpiC	kidney:	n/a
43	chr11:66109018-66109068	HepG2	liver:	n/a
44	chr11:66108473-66108523	HNPCEpiC	eye:	n/a
45	chr11:66108893-66108943	NB4	blood:	n/a
46	chr11:66108473-66108523	GM12892	blood:	n/a
47	chr11:66108473-66108523	HAEpiC	amniotic membrane:	n/a
48	chr11:66108893-66108943	GM12892	blood:	n/a
49	chr11:66108473-66108523	AoSMC	blood vessel:	n/a
50	chr11:66109162-66109212	AG04449	skin:	fetal

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:66077296..66081246-chr11:66109722..66112526,4	K562	blood:
2	chr11:66056831..66061115-chr11:66109718..66114909,6	MCF-7	breast:
3	chr11:66054162..66056937-chr11:66109546..66111530,2	K562	blood:
4	chr11:66103854..66118324-chr11:66119048..66141728,55	K562	blood:
5	chr11:66097476..66098221-chr11:66111385..66111891,2	K562	blood:
6	chr11:66056885..66058669-chr11:66106452..66107991,2	K562	blood:
7	chr11:66108764..66111622-chr11:66204863..66206886,2	K562	blood:
8	chr11:66079011..66083261-chr11:66109999..66114385,7	MCF-7	breast:
9	chr11:66105926..66107634-chr11:66113963..66115693,2	K562	blood:
10	chr11:66108426..66118730-chr11:66133678..66141000,25	MCF-7	breast:
11	chr11:66111080..66113877-chr17:56707692..56710441,2	MCF-7	breast:
12	chr11:66084372..66086380-chr11:66109864..66112582,2	MCF-7	breast:
13	chr11:66108839..66110813-chr11:66110934..66112585,3	K562	blood:
14	chr11:65625352..65628744-chr11:66111177..66113723,3	K562	blood:
15	chr11:66092468..66094191-chr11:66107437..66109172,2	K562	blood:
16	chr11:66105229..66107921-chr11:66137845..66140826,3	MCF-7	breast:
17	chr11:66108839..66110813-chr11:66110934..66112585,3	K562	blood:
18	chr11:66043530..66045792-chr11:66110035..66112602,2	MCF-7	breast:
19	chr11:66048984..66050928-chr11:66106089..66108288,2	MCF-7	breast:

No data

Variant related genes	Relation type
BRMS1	TF binding region
ENSG00000255468	TF binding region
RIN1	TF binding region
BRMS1	CpG island
ENSG00000255468	CpG island
RIN1	CpG island
ENSG00000174871	chromatin interactions
ENSG00000174744	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000174807	chromatin interactions
ENSG00000174669	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000174547	chromatin interactions
ENSG00000255468	chromatin interactions
ENSG00000179292	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000254452	chromatin interactions
ENSG00000254458	chromatin interactions
ENSG00000174684	chromatin interactions

Extended variants
information (count: 248 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:248 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574045921	chr11:66107082-66107083	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs1784031	chr11:66107121-66107122	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs1784032	chr11:66107131-66107132	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs1784033	chr11:66107135-66107136	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs12286121	chr11:66107158-66107159	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs1785634	chr11:66107190-66107191	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs75928472	chr11:66107191-66107192	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs1784034	chr11:66107196-66107197	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs373113172	chr11:66107224-66107225	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs533552583	chr11:66107238-66107239	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs77391993	chr11:66107240-66107241	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs2016960	chr11:66107320-66107321	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs571190611	chr11:66107328-66107329	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs146694647	chr11:66107361-66107362	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs112569767	chr11:66107374-66107375	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs567023944	chr11:66107422-66107423	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs536068138	chr11:66107428-66107429	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs555865388	chr11:66107450-66107451	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs545888606	chr11:66107453-66107454	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs575717527	chr11:66107481-66107482	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs537983993	chr11:66107482-66107483	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs558120997	chr11:66107493-66107494	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs577993152	chr11:66107521-66107522	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs1785633	chr11:66107527-66107528	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs183317843	chr11:66107540-66107541	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs115148520	chr11:66107543-66107544	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs188771254	chr11:66107555-66107556	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs562569436	chr11:66107556-66107557	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs374809325	chr11:66107571-66107572	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs369071599	chr11:66107604-66107605	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs373539734	chr11:66107623-66107624	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs376902794	chr11:66107635-66107636	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs531419407	chr11:66107648-66107649	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs145163737	chr11:66107662-66107663	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs377478442	chr11:66107665-66107666	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs141305456	chr11:66107673-66107674	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs1784035	chr11:66107674-66107675	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs373982938	chr11:66107691-66107692	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs202046882	chr11:66107692-66107693	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs58024886	chr11:66107709-66107710	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs192653592	chr11:66107711-66107712	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376664227	chr11:66107736-66107737	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549534128	chr11:66107752-66107753	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs569386544	chr11:66107794-66107795	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs538331730	chr11:66107815-66107816	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs557972014	chr11:66107823-66107824	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs577925977	chr11:66107839-66107840	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs576880335	chr11:66107845-66107846	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs553621951	chr11:66107886-66107887	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs573575625	chr11:66107921-66107922	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66098400-66108800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:66103600-66107600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:66104200-66107800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:66104200-66109000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr11:66104400-66107200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr11:66104400-66107800	Enhancers	HMEC	breast
7	chr11:66104400-66110400	Strong transcription	Dnd41	blood
8	chr11:66104600-66107200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:66104600-66108200	Weak transcription	Stomach Mucosa	stomach
10	chr11:66104600-66109000	Weak transcription	Fetal Kidney	kidney
11	chr11:66104600-66109800	Strong transcription	Colonic Mucosa	Colon
12	chr11:66104600-66109800	Strong transcription	Lung	lung
13	chr11:66104600-66110000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:66104600-66110400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr11:66104600-66110400	Strong transcription	Fetal Intestine Large	intestine
16	chr11:66104600-66110400	Strong transcription	Right Ventricle	heart
17	chr11:66104600-66110800	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr11:66104600-66111600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr11:66104800-66107800	Weak transcription	HepG2	liver
20	chr11:66104800-66108800	Strong transcription	Gastric	stomach
21	chr11:66104800-66109600	Strong transcription	Brain Substantia Nigra	brain
22	chr11:66104800-66109600	Strong transcription	Rectal Smooth Muscle	rectum
23	chr11:66104800-66109800	Strong transcription	Left Ventricle	heart
24	chr11:66104800-66110000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr11:66104800-66110000	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr11:66104800-66110000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr11:66104800-66110400	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr11:66104800-66110800	Strong transcription	Adipose Nuclei	Adipose
29	chr11:66104800-66110800	Strong transcription	Brain Cingulate Gyrus	brain
30	chr11:66104800-66110800	Weak transcription	Psoas Muscle	Psoas
31	chr11:66104800-66111000	Strong transcription	Primary T cells from cord blood	blood
32	chr11:66104800-66111200	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr11:66104800-66111200	Strong transcription	Placenta	Placenta
34	chr11:66105000-66107200	Genic enhancers	Esophagus	oesophagus
35	chr11:66105000-66107400	Strong transcription	Stomach Smooth Muscle	stomach
36	chr11:66105000-66109000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr11:66105000-66109600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr11:66105000-66109800	Strong transcription	Liver	Liver
39	chr11:66105000-66110000	Strong transcription	H9 Cell Line	embryonic stem cell
40	chr11:66105000-66110000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr11:66105000-66110400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:66105000-66110600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:66105000-66111000	Strong transcription	Duodenum Mucosa	Duodenum
44	chr11:66105000-66111000	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr11:66105000-66111200	Strong transcription	Fetal Intestine Small	intestine
46	chr11:66105200-66109800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
47	chr11:66105200-66110000	Strong transcription	Brain Hippocampus Middle	brain
48	chr11:66105200-66110400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr11:66105200-66110400	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr11:66105200-66110600	Strong transcription	Primary B cells from peripheral blood	blood

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