Variant report

Variant	nsv896949
Chromosome Location	chr11:5711177-5722444
allele	n/a
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	ATF1	chr11:5711871-5712078	K562	blood:	n/a	n/a
2	ATF2	chr11:5710628-5711278	GM12878	blood:	n/a	n/a
3	BACH1	chr11:5710876-5711199	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr11:5710864-5711209	GM12878	blood:	n/a	n/a
5	BCLAF1	chr11:5710594-5711294	GM12878	blood:	n/a	chr11:5710965-5710974
6	BHLHE40	chr11:5710647-5712219	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:5711515-5711857	K562	blood:	n/a	n/a
8	CEBPB	chr11:5722438-5722817	Hela-S3	cervix:	n/a	chr11:5722580-5722591
9	CEBPB	chr11:5710867-5711240	H1-hESC	embryonic stem cell:	n/a	chr11:5711132-5711145
10	CEBPB	chr11:5710576-5712088	GM12878	blood:	n/a	chr11:5711132-5711145
11	CEBPB	chr11:5722409-5722861	A549	lung:	n/a	chr11:5722580-5722591
12	CEBPD	chr11:5711490-5711861	K562	blood:	n/a	n/a
13	CHD1	chr11:5710750-5712282	GM12878	blood:	n/a	n/a
14	CHD1	chr11:5713674-5713792	GM12878	blood:	n/a	n/a
15	CHD1	chr11:5711150-5711375	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr11:5713601-5713801	GM12878	blood:	n/a	n/a
17	CHD2	chr11:5712913-5713066	GM12878	blood:	n/a	n/a
18	CHD2	chr11:5710705-5711373	GM12878	blood:	n/a	n/a
19	CTCF	chr11:5711120-5711270	GM12873	blood:	n/a	n/a
20	CTCF	chr11:5720036-5720236	GM12878	blood:	n/a	n/a
21	CUX1	chr11:5710287-5711959	GM12878	blood:	n/a	chr11:5710472-5710486 chr11:5710328-5710342
22	E2F4	chr11:5719481-5719584	MCF10A-Er-Src	breast:	n/a	n/a
23	EBF1	chr11:5721748-5721859	GM12878	blood:	n/a	n/a
24	EBF1	chr11:5713369-5713703	GM12878	blood:	n/a	n/a
25	EBF1	chr11:5719845-5720160	GM12878	blood:	n/a	n/a
26	EBF1	chr11:5710636-5711711	GM12878	blood:	n/a	chr11:5710914-5710924
27	ELF1	chr11:5710760-5711193	GM12878	blood:	n/a	n/a
28	ELK1	chr11:5712132-5712200	GM12878	blood:	n/a	n/a
29	EP300	chr11:5710546-5711204	GM12878	blood:	n/a	n/a
30	EP300	chr11:5713234-5713239	GM12878	blood:	n/a	n/a
31	EP300	chr11:5713417-5713422	K562	blood:	n/a	n/a
32	EP300	chr11:5710710-5711223	GM12878	blood:	n/a	n/a
33	EP300	chr11:5712958-5712972	GM12878	blood:	n/a	n/a
34	EP300	chr11:5712674-5712776	K562	blood:	n/a	n/a
35	FOXM1	chr11:5710650-5711441	GM12878	blood:	n/a	n/a
36	GATA1	chr11:5711249-5713169	PBDE	blood:	n/a	chr11:5712979-5712986 chr11:5712979-5712986 chr11:5712083-5712095 chr11:5712979-5712986 chr11:5712975-5712991 chr11:5712085-5712092 chr11:5712085-5712094
37	GATA2	chr11:5711112-5712342	HUVEC	blood vessel:	n/a	chr11:5712083-5712095 chr11:5712085-5712092 chr11:5712085-5712094
38	GATA3	chr11:5711340-5712394	SK-N-SH	brain:	n/a	chr11:5712083-5712095 chr11:5712085-5712092 chr11:5712085-5712094
39	GATA3	chr11:5712933-5713109	SH-SY5Y	brain:	n/a	chr11:5712979-5712986 chr11:5712979-5712986 chr11:5712979-5712986 chr11:5712975-5712991
40	GTF2F1	chr11:5710929-5711296	H1-hESC	embryonic stem cell:	n/a	n/a
41	IKZF1	chr11:5711465-5712245	GM12878	blood:	n/a	n/a
42	IRF1	chr11:5713402-5713493	K562	blood:	n/a	n/a
43	IRF1	chr11:5710647-5711177	K562	blood:	n/a	chr11:5710983-5710996 chr11:5710964-5710974 chr11:5710960-5710974 chr11:5710978-5710991 chr11:5710982-5710996
44	IRF1	chr11:5711525-5712188	K562	blood:	n/a	chr11:5712032-5712044 chr11:5712033-5712043 chr11:5712032-5712043 chr11:5712027-5712044 chr11:5712033-5712047 chr11:5712032-5712044 chr11:5712029-5712043
45	IRF3	chr11:5712931-5713053	GM12878	blood:	n/a	n/a
46	JUN	chr11:5710803-5711268	H1-hESC	embryonic stem cell:	n/a	chr11:5710859-5710869 chr11:5710859-5710869
47	JUND	chr11:5710788-5711278	H1-hESC	embryonic stem cell:	n/a	chr11:5710859-5710869 chr11:5710859-5710869
48	KAP1	chr11:5710777-5711900	U2OS	brain:	n/a	n/a
49	MAFK	chr11:5715353-5715483	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAFK	chr11:5721162-5721343	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5716255-5716305	MCF-7	breast:	n/a
2	chr11:5716255-5716305	GM06990	blood:	n/a
3	chr11:5716255-5716305	HCF	heart:	n/a
4	chr11:5716255-5716305	AG09309	skin:	n/a
5	chr11:5716255-5716305	GM19239	blood:	n/a
6	chr11:5716255-5716305	SK-N-SH_RA	brain:	n/a
7	chr11:5716255-5716305	AG10803	skin:	n/a
8	chr11:5716255-5716305	Caco-2	colon:	n/a
9	chr11:5716255-5716305	H1-hESC	embryonic stem cell:	embryo
10	chr11:5716255-5716305	RPTEC	kidney:	n/a
11	chr11:5716255-5716305	HRCEpiC	kidney:	n/a
12	chr11:5716255-5716305	Hela-S3	cervix:	n/a
13	chr11:5716255-5716305	PANC-1	pancreas:	n/a
14	chr11:5716255-5716305	ECC-1	luminal epithelium:	n/a
15	chr11:5716255-5716305	HIPEpiC	eye:	n/a
16	chr11:5716255-5716305	U87	brain:	n/a
17	chr11:5716255-5716305	BJ	skin:	n/a
18	chr11:5716255-5716305	GM12891	blood:	n/a
19	chr11:5716255-5716305	Jurkat	blood:	n/a
20	chr11:5716255-5716305	HUVEC	blood vessel:	n/a
21	chr11:5716255-5716305	HRE	kidney:	n/a
22	chr11:5716255-5716305	HCT-116	colon:	n/a
23	chr11:5716255-5716305	SAEC	small airway:	n/a
24	chr11:5716255-5716305	GM12892	blood:	n/a
25	chr11:5716255-5716305	A549	lung:	n/a
26	chr11:5716255-5716305	NH-A	brain:	n/a
27	chr11:5716255-5716305	SKMC	muscle:	n/a
28	chr11:5716255-5716305	HEEpiC	esophagus:	n/a
29	chr11:5716255-5716305	HEK293	kidney:	embryo
30	chr11:5716255-5716305	AoSMC	blood vessel:	n/a
31	chr11:5716255-5716305	MCF10A-Er-Src	breast:	n/a
32	chr11:5716255-5716305	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:5716255-5716305	HCPEpiC	choroid plexus:	n/a
34	chr11:5716255-5716305	PrEC	prostate:	n/a
35	chr11:5716255-5716305	GM12878	blood:	n/a
36	chr11:5716255-5716305	ovcar-3	ovarian:	n/a
37	chr11:5716255-5716305	HL-60	blood:	n/a
38	chr11:5716255-5716305	SK-N-MC	brain:	n/a
39	chr11:5716255-5716305	PFSK-1	brain:	n/a
40	chr11:5716255-5716305	AG09319	gingival:	n/a
41	chr11:5716255-5716305	IMR90	lung:	fetal
42	chr11:5716255-5716305	BE2_C	brain:	n/a
43	chr11:5716255-5716305	HepG2	liver:	n/a
44	chr11:5716255-5716305	LNCaP	prostate:	n/a
45	chr11:5716255-5716305	SK-N-SH	brain:	n/a
46	chr11:5716255-5716305	HNPCEpiC	eye:	n/a
47	chr11:5716255-5716305	NB4	blood:	n/a
48	chr11:5716255-5716305	K562	blood:	n/a
49	chr11:5716255-5716305	HCM	heart:	n/a
50	chr11:5716255-5716305	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:4988858-5002113..11:5707362-5712027	Hela-S3	cervix:
2	chr11:5706176..5707758-chr11:5710825..5713115,2	K562	blood:
3	11:5087036-5092291..11:5721056-5732713	K562	blood:
4	11:4957178-4961904..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
5	11:5349791-5355747..11:5714465-5718134	GM12878	blood:
6	chr11:5721533..5723837-chr11:5757099..5760021,2	K562	blood:
7	11:5714465-5718134..11:5720889-5721056	Hela-S3	cervix:
8	11:4988858-5002113..11:5714465-5718134	Hela-S3	cervix:
9	11:4988858-5002113..11:5721056-5732713	Hela-S3	cervix:
10	11:5488942-5494633..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
11	11:5033143-5038367..11:5721056-5732713	GM12878	blood:
12	chr11:5700598..5702290-chr11:5720300..5722601,2	K562	blood:
13	11:5586716-5591774..11:5721056-5732713	GM12878	blood:
14	11:5033143-5038367..11:5714465-5718134	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HBG2-1	chr11:5717300-5718052	NONHSAT017688

Variant related genes	Relation type
TRIM5	TF binding region
TRIM22	TF binding region
TRIM5	CpG island
TRIM22	CpG island
ENSG00000227023	chromatin interactions
ENSG00000236359	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000181023	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000233646	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000230484	chromatin interactions
ENSG00000273085	chromatin interactions
ENSG00000225003	chromatin interactions

Extended variants
information (count: 565 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7129909	chr11:5711177-5711178	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7935494	chr11:5711197-5711198	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs565335593	chr11:5711264-5711265	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs113928802	chr11:5711309-5711310	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs181306107	chr11:5711322-5711323	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs563964241	chr11:5711351-5711352	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs569367928	chr11:5711421-5711422	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs576940754	chr11:5711455-5711456	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs140428907	chr11:5711513-5711514	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs536137789	chr11:5711546-5711547	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs185174685	chr11:5711578-5711579	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs369435868	chr11:5711669-5711670	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs578222982	chr11:5711696-5711697	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs556120745	chr11:5711734-5711735	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs142052212	chr11:5711769-5711770	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs552889477	chr11:5711773-5711774	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs35926783	chr11:5711791-5711792	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs559503586	chr11:5711814-5711815	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs78853815	chr11:5711820-5711821	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs151147170	chr11:5711847-5711848	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs576421426	chr11:5711905-5711906	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs75935256	chr11:5711964-5711965	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs34668644	chr11:5711995-5711996	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs117002722	chr11:5712006-5712007	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs577669175	chr11:5712014-5712015	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs547282784	chr11:5712024-5712025	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs559183270	chr11:5712037-5712038	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs529646811	chr11:5712078-5712079	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs35652173	chr11:5712189-5712190	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs191111790	chr11:5712219-5712220	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73402272	chr11:5712240-5712241	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs1995162	chr11:5712260-5712261	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs550378334	chr11:5712296-5712297	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571746491	chr11:5712318-5712319	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539181869	chr11:5712331-5712332	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs550509771	chr11:5712342-5712343	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183780361	chr11:5712386-5712387	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566348456	chr11:5712407-5712408	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536657853	chr11:5712415-5712416	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554985124	chr11:5712438-5712439	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576507476	chr11:5712475-5712476	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543547520	chr11:5712524-5712525	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6578678	chr11:5712525-5712526	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs4625503	chr11:5712526-5712527	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540783112	chr11:5712538-5712539	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559247171	chr11:5712559-5712560	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529905170	chr11:5712561-5712562	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541459606	chr11:5712565-5712566	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563116904	chr11:5712566-5712567	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs146834269	chr11:5712583-5712584	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	23613489	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5707200-5712200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:5710200-5711200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr11:5710200-5714000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:5710400-5712400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:5710400-5714000	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr11:5710400-5714000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
7	chr11:5710400-5714000	Active TSS	Duodenum Smooth Muscle	Duodenum
8	chr11:5710400-5714000	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr11:5710600-5711200	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr11:5710600-5711200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:5710600-5711200	Enhancers	Fetal Stomach	stomach
12	chr11:5710600-5711400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr11:5710600-5711600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:5710600-5712400	Active TSS	Aorta	Aorta
15	chr11:5710600-5712400	Flanking Active TSS	HUVEC	blood vessel
16	chr11:5710600-5712600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
17	chr11:5710600-5712800	Active TSS	NHDF-Ad	bronchial
18	chr11:5710600-5713000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:5710600-5713000	Active TSS	GM12878-XiMat	blood
20	chr11:5710600-5713000	Active TSS	HSMM	muscle
21	chr11:5710600-5713400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
22	chr11:5710600-5713600	Active TSS	Brain Anterior Caudate	brain
23	chr11:5710600-5713600	Active TSS	Thymus	Thymus
24	chr11:5710600-5713800	Active TSS	Primary T cells fromperipheralblood	blood
25	chr11:5710600-5713800	Flanking Active TSS	Primary hematopoietic stem cells	blood
26	chr11:5710600-5713800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:5710600-5713800	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr11:5710600-5714000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:5710600-5714000	Active TSS	Right Atrium	heart
30	chr11:5710800-5711200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:5710800-5711200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:5710800-5711200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr11:5710800-5711200	Active TSS	Duodenum Mucosa	Duodenum
34	chr11:5710800-5711400	Flanking Active TSS	Fetal Kidney	kidney
35	chr11:5710800-5711400	Active TSS	Fetal Lung	lung
36	chr11:5710800-5711400	Enhancers	A549	lung
37	chr11:5710800-5711800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr11:5710800-5711800	Active TSS	Fetal Brain Male	brain
39	chr11:5710800-5711800	Enhancers	K562	blood
40	chr11:5710800-5711800	Flanking Active TSS	NHEK	skin
41	chr11:5710800-5712000	Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr11:5710800-5712200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:5710800-5712200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr11:5710800-5712200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr11:5710800-5712200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr11:5710800-5712200	Active TSS	Fetal Muscle Trunk	muscle
47	chr11:5710800-5712200	Active TSS	Stomach Mucosa	stomach
48	chr11:5710800-5712200	Active TSS	HSMMtube	muscle
49	chr11:5710800-5712400	Active TSS	H1 Cell Line	embryonic stem cell
50	chr11:5710800-5712400	Active TSS	Brain Angular Gyrus	brain

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