Variant report

Variant	nsv1015623
Chromosome Location	chr9:21579110-21694039
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1180)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1180 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:21591377-21592439	A549	lung:	n/a	n/a
2	ATF3	chr9:21684629-21685479	HCT-116	colon:	n/a	n/a
3	ATF3	chr9:21605330-21606023	A549	lung:	n/a	chr9:21605662-21605675
4	ATF3	chr9:21677574-21678317	A549	lung:	n/a	n/a
5	ATF3	chr9:21615994-21616769	A549	lung:	n/a	n/a
6	ATF3	chr9:21684623-21685773	A549	lung:	n/a	n/a
7	ATF3	chr9:21684624-21685507	HCT-116	colon:	n/a	n/a
8	ATF3	chr9:21615943-21616582	A549	lung:	n/a	n/a
9	ATF3	chr9:21677553-21678303	HCT-116	colon:	n/a	n/a
10	ATF3	chr9:21677783-21678297	A549	lung:	n/a	n/a
11	ATF3	chr9:21591469-21592177	A549	lung:	n/a	n/a
12	BACH1	chr9:21591580-21592070	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:21678040-21678111	H1-hESC	embryonic stem cell:	n/a	chr9:21678050-21678064
14	BCL3	chr9:21682728-21683550	A549	lung:	n/a	n/a
15	BCL3	chr9:21605304-21606082	A549	lung:	n/a	n/a
16	BCL3	chr9:21684389-21685850	A549	lung:	n/a	chr9:21684825-21684834 chr9:21684554-21684563 chr9:21685100-21685109
17	BCL3	chr9:21580109-21581261	A549	lung:	n/a	n/a
18	BCL3	chr9:21615855-21616733	A549	lung:	n/a	n/a
19	BCL3	chr9:21589622-21592324	A549	lung:	n/a	chr9:21591639-21591648 chr9:21590038-21590047
20	BCL3	chr9:21591457-21592217	A549	lung:	n/a	chr9:21591639-21591648
21	BCL3	chr9:21684674-21685858	A549	lung:	n/a	chr9:21684825-21684834 chr9:21685100-21685109
22	BCL3	chr9:21681396-21682102	A549	lung:	n/a	n/a
23	BCL3	chr9:21677389-21678468	A549	lung:	n/a	chr9:21677552-21677561 chr9:21678052-21678061 chr9:21678053-21678062
24	BHLHE40	chr9:21581460-21581801	A549	lung:	n/a	chr9:21581610-21581619 chr9:21581609-21581618 chr9:21581603-21581624 chr9:21581609-21581618
25	BRCA1	chr9:21580257-21581211	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr9:21681494-21682052	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr9:21595046-21595052	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr9:21591202-21592001	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr9:21615858-21616712	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr9:21611650-21612393	HCT-116	colon:	n/a	n/a
31	CBX3	chr9:21666059-21666421	HCT-116	colon:	n/a	n/a
32	CBX3	chr9:21677415-21678415	HCT-116	colon:	n/a	n/a
33	CBX3	chr9:21591058-21592382	HCT-116	colon:	n/a	n/a
34	CBX3	chr9:21684614-21685498	HCT-116	colon:	n/a	chr9:21685011-21685022
35	CEBPB	chr9:21682935-21684052	A549	lung:	n/a	n/a
36	CEBPB	chr9:21689903-21690545	A549	lung:	n/a	chr9:21690345-21690356
37	CEBPB	chr9:21688699-21689081	Hela-S3	cervix:	n/a	chr9:21688804-21688817
38	CEBPB	chr9:21684543-21685510	A549	lung:	n/a	n/a
39	CEBPB	chr9:21681594-21682064	A549	lung:	n/a	n/a
40	CEBPB	chr9:21688158-21689185	A549	lung:	n/a	chr9:21688804-21688817
41	CEBPB	chr9:21689876-21690833	IMR90	lung:	n/a	chr9:21690345-21690356
42	CEBPB	chr9:21591570-21591954	ECC-1	luminal epithelium:	n/a	chr9:21591752-21591763
43	CEBPB	chr9:21689826-21690456	Hela-S3	cervix:	n/a	chr9:21690345-21690356
44	CEBPB	chr9:21616056-21616702	IMR90	lung:	n/a	n/a
45	CEBPB	chr9:21591588-21591945	H1-hESC	embryonic stem cell:	n/a	chr9:21591752-21591763
46	CEBPB	chr9:21605321-21606117	A549	lung:	n/a	chr9:21605728-21605741
47	CEBPB	chr9:21586009-21586633	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:21591218-21592190	HCT-116	colon:	n/a	chr9:21591752-21591763
49	CEBPB	chr9:21591625-21591969	MCF-7	breast:	n/a	chr9:21591752-21591763
50	CEBPB	chr9:21681626-21682119	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21687953-21688003	Hela-S3	cervix:	n/a
2	chr9:21687953-21688003	HNPCEpiC	eye:	n/a
3	chr9:21687953-21688003	GM19239	blood:	n/a
4	chr9:21687953-21688003	SKMC	muscle:	n/a
5	chr9:21687953-21688003	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:21687953-21688003	HL-60	blood:	n/a
7	chr9:21687953-21688003	GM12878	blood:	n/a
8	chr9:21687953-21688003	LNCaP	prostate:	n/a
9	chr9:21687953-21688003	HAEpiC	amniotic membrane:	n/a
10	chr9:21687953-21688003	PFSK-1	brain:	n/a
11	chr9:21687953-21688003	Caco-2	colon:	n/a
12	chr9:21687953-21688003	HRE	kidney:	n/a
13	chr9:21687953-21688003	BJ	skin:	n/a
14	chr9:21687953-21688003	RPTEC	kidney:	n/a
15	chr9:21687953-21688003	ProgFib	skin:	n/a
16	chr9:21687953-21688003	A549	lung:	n/a
17	chr9:21687953-21688003	HCM	heart:	n/a
18	chr9:21687953-21688003	AG10803	skin:	n/a
19	chr9:21687953-21688003	U87	brain:	n/a
20	chr9:21687953-21688003	BE2_C	brain:	n/a
21	chr9:21687953-21688003	T-47D	breast:	n/a
22	chr9:21687953-21688003	SK-N-MC	brain:	n/a
23	chr9:21687953-21688003	IMR90	lung:	fetal
24	chr9:21687953-21688003	SAEC	small airway:	n/a
25	chr9:21687953-21688003	SK-N-SH	brain:	n/a
26	chr9:21687953-21688003	MCF10A-Er-Src	breast:	n/a
27	chr9:21687953-21688003	HEK293	kidney:	embryo
28	chr9:21687953-21688003	HIPEpiC	eye:	n/a
29	chr9:21687953-21688003	NT2-D1	testis:	n/a
30	chr9:21687953-21688003	AG09319	gingival:	n/a
31	chr9:21687953-21688003	AG09309	skin:	n/a
32	chr9:21687953-21688003	HCT-116	colon:	n/a
33	chr9:21687953-21688003	NHBE	bronchial:	n/a
34	chr9:21687953-21688003	NHDF-neo	bronchial:	n/a
35	chr9:21687953-21688003	GM12892	blood:	n/a
36	chr9:21687953-21688003	NB4	blood:	n/a
37	chr9:21687953-21688003	PANC-1	pancreas:	n/a
38	chr9:21687953-21688003	AG04449	skin:	fetal
39	chr9:21687953-21688003	HepG2	liver:	n/a
40	chr9:21687953-21688003	GM12891	blood:	n/a
41	chr9:21687953-21688003	ovcar-3	ovarian:	n/a
42	chr9:21687953-21688003	PrEC	prostate:	n/a
43	chr9:21687953-21688003	HRPEpiC	eye:	n/a
44	chr9:21687953-21688003	NH-A	brain:	n/a
45	chr9:21687953-21688003	Hepatocyte	liver:	n/a
46	chr9:21687953-21688003	MCF-7	breast:	n/a
47	chr9:21687953-21688003	GM06990	blood:	n/a
48	chr9:21687953-21688003	HUVEC	blood vessel:	n/a
49	chr9:21687953-21688003	AoSMC	blood vessel:	n/a
50	chr9:21687953-21688003	HMEC	breast:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:9877764..9878356-chr9:21674606..21675106,2	Hela-S3	cervix:
2	chr9:21678019..21679658-chr9:21681885..21684334,2	MCF-7	breast:
3	chr5:150593443..150594007-chr9:21684916..21685496,2	HCT-116	colon:
4	chr11:18690057..18690608-chr9:21683732..21684232,2	HCT-116	colon:
5	chr17:37356320..37357046-chr9:21591367..21592107,2	Hela-S3	cervix:
6	chr7:110268028..110268940-chr9:21579308..21579808,2	HCT-116	colon:
7	chr9:21606867..21609575-chr9:21609641..21611330,2	MCF-7	breast:
8	chr9:21559603..21561116-chr9:21590002..21592420,2	MCF-7	breast:
9	chr9:21653463..21655344-chr9:21656269..21658699,2	MCF-7	breast:
10	chr9:21606867..21609575-chr9:21609641..21611330,2	MCF-7	breast:
11	chr9:21588453..21590122-chr9:21684881..21686548,2	MCF-7	breast:
12	chr9:21597064..21598967-chr9:21805974..21808961,2	MCF-7	breast:
13	chr9:21681458..21682986-chr9:21704343..21706212,2	MCF-7	breast:
14	chr7:45025732..45026728-chr9:21683864..21684615,2	HCT-116	colon:
15	chr9:21678019..21679658-chr9:21681885..21684334,2	MCF-7	breast:
16	chr9:21586444..21586977-chr9:21789496..21790440,2	MCF-7	breast:
17	chr6:31125893..31126847-chr9:21590881..21591539,2	Hela-S3	cervix:
18	chr9:21586208..21586976-chr9:21789155..21790210,3	MCF-7	breast:
19	chr9:21588453..21590122-chr9:21684881..21686548,2	MCF-7	breast:
20	chr9:21653463..21655344-chr9:21656269..21658699,2	MCF-7	breast:
21	chr1:26202267..26202833-chr9:21582216..21582914,2	HCT-116	colon:
22	chr1:160231834..160232484-chr9:21591140..21591940,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000227443	TF binding region
KHSRPP1	TF binding region
ENSG00000227443	CpG island
KHSRPP1	CpG island
ENSG00000137310	chromatin interactions
ENSG00000266732	chromatin interactions
ENSG00000171889	chromatin interactions
ENSG00000232956	chromatin interactions
ENSG00000204536	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000132716	chromatin interactions

Extended variants
information (count: 5510 )
Associated
traits (count: 155 )

Variant overlapped rSNPs/rCNVs (count:5510 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184586056	chr9:21579208-21579209	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs552481549	chr9:21579284-21579285	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs565658844	chr9:21579297-21579298	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs528065647	chr9:21579303-21579304	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs116041458	chr9:21579352-21579353	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs568123533	chr9:21579392-21579393	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs537152277	chr9:21579394-21579395	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs370115385	chr9:21579467-21579468	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs557268115	chr9:21579517-21579518	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs571065547	chr9:21579523-21579524	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs576880701	chr9:21579532-21579533	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs539729351	chr9:21579562-21579563	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs534373184	chr9:21579614-21579615	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs189271543	chr9:21579653-21579654	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs573220788	chr9:21579660-21579661	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs10491563	chr9:21579686-21579687	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs192624863	chr9:21579687-21579688	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs575647774	chr9:21579693-21579694	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs114351909	chr9:21579696-21579697	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs563326228	chr9:21579710-21579711	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs142297541	chr9:21579718-21579719	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs546042450	chr9:21579803-21579804	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs368747175	chr9:21579816-21579817	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs559652412	chr9:21579824-21579825	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs10965068	chr9:21579827-21579828	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs151270413	chr9:21579848-21579849	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs184327587	chr9:21579852-21579853	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530511970	chr9:21579857-21579858	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs550684407	chr9:21579881-21579882	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs7867955	chr9:21579882-21579883	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs117501779	chr9:21579893-21579894	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs553164173	chr9:21579896-21579897	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs10965069	chr9:21579922-21579923	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553233296	chr9:21579942-21579943	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs555333681	chr9:21579955-21579956	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs190404109	chr9:21579976-21579977	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs537930860	chr9:21580005-21580006	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs13283078	chr9:21580031-21580032	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs578047134	chr9:21580039-21580040	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs10757226	chr9:21580062-21580063	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs75506088	chr9:21580074-21580075	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs111627787	chr9:21580100-21580101	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs573169414	chr9:21580139-21580140	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs542183245	chr9:21580230-21580231	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs16938462	chr9:21580274-21580275	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530552829	chr9:21580351-21580352	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs550326669	chr9:21580399-21580400	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs564172707	chr9:21580419-21580420	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs566942440	chr9:21580461-21580462	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs572908695	chr9:21580496-21580497	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:155)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	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
Oral cancer	21386901	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
Breast cancer	21858162	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
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	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
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD

Chromatin state (count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21575800-21592200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:21576600-21579200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr9:21577200-21585800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr9:21577400-21579600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr9:21577800-21579200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:21577800-21579200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr9:21578000-21579200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr9:21578000-21579400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr9:21578000-21579800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:21578400-21580800	Flanking Active TSS	A549	lung
11	chr9:21578600-21579200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:21578600-21579600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
13	chr9:21578600-21579600	Enhancers	HUVEC	blood vessel
14	chr9:21578600-21579600	Flanking Active TSS	Osteobl	bone
15	chr9:21578600-21579800	Enhancers	NH-A	brain
16	chr9:21578600-21579800	Enhancers	NHEK	skin
17	chr9:21578800-21579200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr9:21578800-21579200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
19	chr9:21578800-21579200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
20	chr9:21578800-21579200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:21578800-21579200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:21578800-21579200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr9:21578800-21579200	Flanking Active TSS	Dnd41	blood
24	chr9:21578800-21579200	Active TSS	NHDF-Ad	bronchial
25	chr9:21578800-21579400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
26	chr9:21578800-21579400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
27	chr9:21578800-21579400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
28	chr9:21578800-21579400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr9:21578800-21579400	Flanking Active TSS	NHLF	lung
30	chr9:21578800-21579600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
31	chr9:21578800-21579600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr9:21578800-21579600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
33	chr9:21578800-21579600	Enhancers	Thymus	Thymus
34	chr9:21578800-21579800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr9:21578800-21579800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:21578800-21579800	Flanking Active TSS	Hela-S3	cervix
37	chr9:21579000-21579200	Active TSS	Duodenum Mucosa	Duodenum
38	chr9:21579000-21579200	Enhancers	GM12878-XiMat	blood
39	chr9:21579000-21579400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr9:21579000-21579400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr9:21579000-21579400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:21579000-21579400	Enhancers	HSMM	muscle
43	chr9:21579000-21579600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr9:21579000-21579600	Flanking Active TSS	Primary T cells from cord blood	blood
45	chr9:21579000-21579600	Enhancers	HMEC	breast
46	chr9:21579000-21580000	Enhancers	Stomach Mucosa	stomach
47	chr9:21579200-21579400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr9:21579200-21579400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr9:21579200-21579400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr9:21579200-21579400	Enhancers	Primary T cells fromperipheralblood	blood

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