Variant report

Variant	nsv613942
Chromosome Location	chr9:26722736-26789975
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	ARID3A	chr9:26746655-26746928	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:26744401-26744755	HepG2	liver:	n/a	n/a
3	ATF1	chr9:26779126-26779512	K562	blood:	n/a	n/a
4	ATF2	chr9:26746311-26747148	GM12878	blood:	n/a	n/a
5	BACH1	chr9:26746447-26747018	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr9:26746185-26747145	GM12878	blood:	n/a	n/a
7	BRCA1	chr9:26779130-26779354	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr9:26746522-26747086	HCT-116	colon:	n/a	n/a
9	CBX3	chr9:26746383-26747096	HCT-116	colon:	n/a	n/a
10	CEBPB	chr9:26737005-26737170	A549	lung:	n/a	n/a
11	CEBPB	chr9:26778913-26779621	HCT-116	colon:	n/a	chr9:26779217-26779228
12	CEBPB	chr9:26723642-26723933	MCF-7	breast:	n/a	n/a
13	CEBPB	chr9:26772178-26772489	IMR90	lung:	n/a	chr9:26772321-26772332
14	CEBPB	chr9:26727767-26728072	HepG2	liver:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
15	CEBPB	chr9:26779098-26779379	A549	lung:	n/a	chr9:26779217-26779228
16	CEBPB	chr9:26723709-26723857	HepG2	liver:	n/a	n/a
17	CEBPB	chr9:26727899-26727940	H1-hESC	embryonic stem cell:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
18	CEBPB	chr9:26747699-26748040	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr9:26772174-26772358	HepG2	liver:	n/a	chr9:26772321-26772332
20	CEBPB	chr9:26723563-26723907	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr9:26727749-26728064	K562	blood:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
22	CEBPB	chr9:26779021-26779569	HCT-116	colon:	n/a	chr9:26779217-26779228
23	CEBPB	chr9:26779131-26779393	HepG2	liver:	n/a	chr9:26779217-26779228
24	CEBPB	chr9:26746742-26746968	MCF-7	breast:	n/a	n/a
25	CEBPB	chr9:26727788-26728098	A549	lung:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
26	CEBPB	chr9:26727783-26728067	IMR90	lung:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
27	CEBPB	chr9:26779040-26779491	Hela-S3	cervix:	n/a	chr9:26779217-26779228
28	CHD1	chr9:26746419-26746824	GM12878	blood:	n/a	n/a
29	CHD2	chr9:26748166-26748203	HepG2	liver:	n/a	n/a
30	CHD2	chr9:26723518-26723804	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr9:26746691-26747084	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr9:26723554-26723861	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr9:26744431-26744664	GM10266	blood:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
34	CTCF	chr9:26723600-26723750	GM12872	blood:	n/a	n/a
35	CTCF	chr9:26723595-26723769	GM13976	blood:	n/a	n/a
36	CTCF	chr9:26744500-26744650	HCPEpiC	choroid plexus:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
37	CTCF	chr9:26748506-26748865	K562	blood:	n/a	n/a
38	CTCF	chr9:26723600-26723750	GM12869	blood:	n/a	n/a
39	CTCF	chr9:26723580-26723730	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr9:26723620-26723770	GM12871	blood:	n/a	n/a
41	CTCF	chr9:26723620-26723770	HCT-116	colon:	n/a	n/a
42	CTCF	chr9:26744520-26744670	HMEC	breast:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
43	CTCF	chr9:26723600-26723750	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr9:26744480-26744630	HL-60	blood:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
45	CTCF	chr9:26748540-26748690	BE2_C	brain:	n/a	n/a
46	CTCF	chr9:26744463-26744691	ECC-1	luminal epithelium:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
47	CTCF	chr9:26744440-26744590	K562	blood:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
48	CTCF	chr9:26723600-26723750	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr9:26744480-26744630	GM12866	blood:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
50	CTCF	chr9:26723420-26723570	HFF-Myc	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:26761746-26761796	HPAEpiC	pulmonary alveolar:	n/a
2	chr9:26761746-26761796	GM12892	blood:	n/a
3	chr9:26761746-26761796	SK-N-MC	brain:	n/a
4	chr9:26761746-26761796	NB4	blood:	n/a
5	chr9:26761746-26761796	U87	brain:	n/a
6	chr9:26761746-26761796	Jurkat	blood:	n/a
7	chr9:26761746-26761796	GM12878	blood:	n/a
8	chr9:26761746-26761796	GM12891	blood:	n/a
9	chr9:26761746-26761796	NT2-D1	testis:	n/a
10	chr9:26761746-26761796	HEEpiC	esophagus:	n/a
11	chr9:26761746-26761796	HUVEC	blood vessel:	n/a
12	chr9:26761746-26761796	T-47D	breast:	n/a
13	chr9:26761746-26761796	SK-N-SH	brain:	n/a
14	chr9:26761746-26761796	RPTEC	kidney:	n/a
15	chr9:26761746-26761796	AG09319	gingival:	n/a
16	chr9:26761746-26761796	NHDF-neo	bronchial:	n/a
17	chr9:26761746-26761796	HRE	kidney:	n/a
18	chr9:26761746-26761796	NHBE	bronchial:	n/a
19	chr9:26761746-26761796	A549	lung:	n/a
20	chr9:26761746-26761796	HCF	heart:	n/a
21	chr9:26761746-26761796	HL-60	blood:	n/a
22	chr9:26761746-26761796	HRCEpiC	kidney:	n/a
23	chr9:26761746-26761796	AG04449	skin:	fetal
24	chr9:26761746-26761796	HCT-116	colon:	n/a
25	chr9:26761746-26761796	IMR90	lung:	fetal
26	chr9:26761746-26761796	ovcar-3	ovarian:	n/a
27	chr9:26761746-26761796	Hepatocyte	liver:	n/a
28	chr9:26761746-26761796	HIPEpiC	eye:	n/a
29	chr9:26761746-26761796	HAEpiC	amniotic membrane:	n/a
30	chr9:26761746-26761796	K562	blood:	n/a
31	chr9:26761746-26761796	HMEC	breast:	n/a
32	chr9:26761746-26761796	HepG2	liver:	n/a
33	chr9:26761746-26761796	H1-hESC	embryonic stem cell:	embryo
34	chr9:26761746-26761796	PANC-1	pancreas:	n/a
35	chr9:26761746-26761796	ECC-1	luminal epithelium:	n/a
36	chr9:26761746-26761796	GM06990	blood:	n/a
37	chr9:26761746-26761796	AoSMC	blood vessel:	n/a
38	chr9:26761746-26761796	HEK293	kidney:	embryo
39	chr9:26761746-26761796	SAEC	small airway:	n/a
40	chr9:26761746-26761796	PFSK-1	brain:	n/a
41	chr9:26761746-26761796	LNCaP	prostate:	n/a
42	chr9:26761746-26761796	BE2_C	brain:	n/a
43	chr9:26761746-26761796	HCM	heart:	n/a
44	chr9:26761746-26761796	AG04450	lung:	fetal
45	chr9:26761746-26761796	AG09309	skin:	n/a
46	chr9:26761746-26761796	Hela-S3	cervix:	n/a
47	chr9:26761746-26761796	PrEC	prostate:	n/a
48	chr9:26761746-26761796	GM19239	blood:	n/a
49	chr9:26761746-26761796	ProgFib	skin:	n/a
50	chr9:26761746-26761796	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:26751819..26753348-chr9:26754776..26757194,2	MCF-7	breast:
2	chr9:26744529..26745078-chr9:26976174..26976879,2	K562	blood:
3	chr9:26744400..26745094-chr9:26856160..26856966,3	MCF-7	breast:
4	chr9:26744169..26744992-chr9:26856156..26857045,4	MCF-7	breast:
5	chr9:26762229..26764985-chr9:26768189..26769709,2	MCF-7	breast:
6	chr9:26744400..26745007-chr9:26975049..26975918,2	MCF-7	breast:
7	chr9:26751819..26753348-chr9:26754776..26757194,2	MCF-7	breast:
8	chr9:26723206..26723920-chr9:26975181..26975897,2	K562	blood:
9	chr9:26758275..26760056-chr9:26761242..26763572,2	K562	blood:
10	chr9:26762229..26764985-chr9:26768189..26769709,2	MCF-7	breast:
11	chr9:26758275..26760056-chr9:26761242..26763572,2	K562	blood:
12	chr9:26745009..26745599-chr9:26856133..26856633,2	MCF-7	breast:
13	chr9:26722378..26723174-chr9:26856170..26856819,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000254261	TF binding region
ENSG00000254261	CpG island
ENSG00000096872	chromatin interactions

Extended variants
information (count: 1929 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1929 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7045601	chr9:26722736-26722737	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537568485	chr9:26722756-26722757	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs549480452	chr9:26722769-26722770	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs567726071	chr9:26722813-26722814	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs116213277	chr9:26722824-26722825	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs115237736	chr9:26722834-26722835	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs10812450	chr9:26722838-26722839	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs201079418	chr9:26722848-26722849	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs539312382	chr9:26722866-26722867	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs557181086	chr9:26722876-26722877	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs576077037	chr9:26722900-26722901	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs575412638	chr9:26722966-26722967	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs114060829	chr9:26723001-26723002	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs561463559	chr9:26723004-26723005	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs183746880	chr9:26723026-26723027	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs139831032	chr9:26723110-26723111	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559291084	chr9:26723123-26723124	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs572722539	chr9:26723152-26723153	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs74311904	chr9:26723167-26723168	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs140967407	chr9:26723183-26723184	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs186926997	chr9:26723199-26723200	Weak transcription Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs193008181	chr9:26723205-26723206	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs144100493	chr9:26723232-26723233	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs111474045	chr9:26723250-26723251	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs543027122	chr9:26723256-26723257	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs370874958	chr9:26723266-26723267	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs7035173	chr9:26723273-26723274	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs374580668	chr9:26723286-26723287	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs567767270	chr9:26723310-26723311	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs535078908	chr9:26723333-26723334	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs546720365	chr9:26723334-26723335	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs7018883	chr9:26723349-26723350	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113174856	chr9:26723362-26723363	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs147338423	chr9:26723372-26723373	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs2043465	chr9:26723380-26723381	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs575499425	chr9:26723400-26723401	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs536469473	chr9:26723439-26723440	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs532142402	chr9:26723442-26723443	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs554702991	chr9:26723465-26723466	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs573695336	chr9:26723501-26723502	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
41	rs10967494	chr9:26723522-26723523	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs141012181	chr9:26723570-26723571	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
43	rs577549400	chr9:26723590-26723591	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs544984674	chr9:26723629-26723630	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs11791320	chr9:26723658-26723659	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs4531131	chr9:26723702-26723703	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs562685535	chr9:26723724-26723725	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs111816026	chr9:26723759-26723760	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs541887858	chr9:26723780-26723781	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs547051897	chr9:26723784-26723785	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26720600-26726600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:26721600-26723400	Enhancers	Brain Germinal Matrix	brain
3	chr9:26722200-26723000	Enhancers	Fetal Lung	lung
4	chr9:26722200-26723600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr9:26722200-26723800	Enhancers	Duodenum Mucosa	Duodenum
6	chr9:26722400-26723000	Enhancers	Fetal Brain Female	brain
7	chr9:26722400-26723400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr9:26722600-26722800	Enhancers	Fetal Stomach	stomach
9	chr9:26722600-26723000	Bivalent Enhancer	Brain Hippocampus Middle	brain
10	chr9:26722800-26723000	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr9:26722800-26723200	Enhancers	Brain Anterior Caudate	brain
12	chr9:26722800-26723600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr9:26723000-26723400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:26723000-26723400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr9:26723000-26723400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:26723000-26723800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
17	chr9:26723000-26723800	Active TSS	Fetal Brain Female	brain
18	chr9:26723000-26724000	Active TSS	Duodenum Smooth Muscle	Duodenum
19	chr9:26723200-26723400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr9:26723200-26723600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr9:26723200-26723600	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr9:26723200-26723600	Active TSS	Fetal Kidney	kidney
23	chr9:26723200-26723800	Active TSS	Brain Anterior Caudate	brain
24	chr9:26723200-26723800	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr9:26723400-26723600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr9:26723400-26723600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr9:26723400-26723600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr9:26723400-26723800	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr9:26723400-26723800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr9:26723400-26723800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:26723400-26723800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:26723400-26723800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr9:26723400-26723800	Active TSS	Brain Germinal Matrix	brain
34	chr9:26723400-26723800	Flanking Bivalent TSS/Enh	A549	lung
35	chr9:26723400-26724000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr9:26723400-26724000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr9:26723600-26723800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr9:26723600-26723800	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr9:26723600-26723800	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
40	chr9:26723600-26723800	Enhancers	Colon Smooth Muscle	Colon
41	chr9:26723600-26724000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:26723600-26724000	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr9:26723600-26724000	Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr9:26723600-26724000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr9:26723600-26724000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:26723600-26724000	Enhancers	Small Intestine	intestine
47	chr9:26723800-26724000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr9:26723800-26724000	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr9:26723800-26724000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr9:26723800-26724000	Enhancers	Cortex derived primary cultured neurospheres	brain

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