Variant report

Variant	nsv892742
Chromosome Location	chr9:21589041-21707372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1109)
CpG islands
(count:122)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1109 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:21684623-21685773	A549	lung:	n/a	n/a
2	ATF3	chr9:21684629-21685479	HCT-116	colon:	n/a	n/a
3	ATF3	chr9:21677783-21678297	A549	lung:	n/a	n/a
4	ATF3	chr9:21677553-21678303	HCT-116	colon:	n/a	n/a
5	ATF3	chr9:21591469-21592177	A549	lung:	n/a	n/a
6	ATF3	chr9:21615994-21616769	A549	lung:	n/a	n/a
7	ATF3	chr9:21591377-21592439	A549	lung:	n/a	n/a
8	ATF3	chr9:21615943-21616582	A549	lung:	n/a	n/a
9	ATF3	chr9:21677574-21678317	A549	lung:	n/a	n/a
10	ATF3	chr9:21605330-21606023	A549	lung:	n/a	chr9:21605662-21605675
11	ATF3	chr9:21684624-21685507	HCT-116	colon:	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	chr9:21589622-21592324	A549	lung:	n/a	chr9:21591639-21591648 chr9:21590038-21590047
15	BCL3	chr9:21677389-21678468	A549	lung:	n/a	chr9:21677552-21677561 chr9:21678052-21678061 chr9:21678053-21678062
16	BCL3	chr9:21684389-21685850	A549	lung:	n/a	chr9:21684825-21684834 chr9:21684554-21684563 chr9:21685100-21685109
17	BCL3	chr9:21684674-21685858	A549	lung:	n/a	chr9:21684825-21684834 chr9:21685100-21685109
18	BCL3	chr9:21681396-21682102	A549	lung:	n/a	n/a
19	BCL3	chr9:21615855-21616733	A549	lung:	n/a	n/a
20	BCL3	chr9:21605304-21606082	A549	lung:	n/a	n/a
21	BCL3	chr9:21591457-21592217	A549	lung:	n/a	chr9:21591639-21591648
22	BCL3	chr9:21682728-21683550	A549	lung:	n/a	n/a
23	BRCA1	chr9:21591202-21592001	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr9:21615858-21616712	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr9:21681494-21682052	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr9:21595046-21595052	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr9:21591058-21592382	HCT-116	colon:	n/a	n/a
28	CBX3	chr9:21684614-21685498	HCT-116	colon:	n/a	chr9:21685011-21685022
29	CBX3	chr9:21666059-21666421	HCT-116	colon:	n/a	n/a
30	CBX3	chr9:21611650-21612393	HCT-116	colon:	n/a	n/a
31	CBX3	chr9:21677415-21678415	HCT-116	colon:	n/a	n/a
32	CEBPB	chr9:21677611-21678329	A549	lung:	n/a	chr9:21678215-21678223 chr9:21677685-21677698
33	CEBPB	chr9:21661722-21661869	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr9:21690214-21690414	HepG2	liver:	n/a	chr9:21690345-21690356
35	CEBPB	chr9:21684790-21685317	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:21682810-21683502	HCT-116	colon:	n/a	n/a
37	CEBPB	chr9:21681510-21682278	HCT-116	colon:	n/a	n/a
38	CEBPB	chr9:21591422-21592061	Hela-S3	cervix:	n/a	chr9:21591752-21591763
39	CEBPB	chr9:21591625-21591969	MCF-7	breast:	n/a	chr9:21591752-21591763
40	CEBPB	chr9:21685010-21685403	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:21591277-21592301	A549	lung:	n/a	chr9:21591752-21591763
42	CEBPB	chr9:21684543-21685510	A549	lung:	n/a	n/a
43	CEBPB	chr9:21674703-21675398	HCT-116	colon:	n/a	n/a
44	CEBPB	chr9:21677757-21678296	A549	lung:	n/a	chr9:21678215-21678223
45	CEBPB	chr9:21591218-21592190	HCT-116	colon:	n/a	chr9:21591752-21591763
46	CEBPB	chr9:21681626-21682119	A549	lung:	n/a	n/a
47	CEBPB	chr9:21594098-21594115	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:21591539-21592047	ECC-1	luminal epithelium:	n/a	chr9:21591752-21591763
49	CEBPB	chr9:21590350-21592281	HCT-116	colon:	n/a	chr9:21591752-21591763
50	CEBPB	chr9:21682796-21684019	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21696666-21696716	NT2-D1	testis:	n/a
2	chr9:21696666-21696716	HEK293	kidney:	embryo
3	chr9:21687953-21688003	K562	blood:	n/a
4	chr9:21696666-21696716	SK-N-MC	brain:	n/a
5	chr9:21696666-21696716	GM12891	blood:	n/a
6	chr9:21687953-21688003	HCF	heart:	n/a
7	chr9:21696666-21696716	AG10803	skin:	n/a
8	chr9:21696666-21696716	HAEpiC	amniotic membrane:	n/a
9	chr9:21687953-21688003	AG10803	skin:	n/a
10	chr9:21696666-21696716	PrEC	prostate:	n/a
11	chr9:21696666-21696716	ovcar-3	ovarian:	n/a
12	chr9:21696666-21696716	SAEC	small airway:	n/a
13	chr9:21687953-21688003	AG09319	gingival:	n/a
14	chr9:21687953-21688003	ovcar-3	ovarian:	n/a
15	chr9:21687953-21688003	HUVEC	blood vessel:	n/a
16	chr9:21687953-21688003	HCM	heart:	n/a
17	chr9:21687953-21688003	HepG2	liver:	n/a
18	chr9:21687953-21688003	HNPCEpiC	eye:	n/a
19	chr9:21687953-21688003	BE2_C	brain:	n/a
20	chr9:21687953-21688003	T-47D	breast:	n/a
21	chr9:21696666-21696716	HRPEpiC	eye:	n/a
22	chr9:21687953-21688003	HEEpiC	esophagus:	n/a
23	chr9:21687953-21688003	PrEC	prostate:	n/a
24	chr9:21696666-21696716	HNPCEpiC	eye:	n/a
25	chr9:21687953-21688003	ProgFib	skin:	n/a
26	chr9:21687953-21688003	HIPEpiC	eye:	n/a
27	chr9:21687953-21688003	H1-hESC	embryonic stem cell:	embryo
28	chr9:21696666-21696716	NHBE	bronchial:	n/a
29	chr9:21687953-21688003	MCF-7	breast:	n/a
30	chr9:21696666-21696716	HCPEpiC	choroid plexus:	n/a
31	chr9:21687953-21688003	CMK	blood:	n/a
32	chr9:21687953-21688003	SK-N-MC	brain:	n/a
33	chr9:21696666-21696716	PFSK-1	brain:	n/a
34	chr9:21696666-21696716	HRCEpiC	kidney:	n/a
35	chr9:21687953-21688003	SK-N-SH_RA	brain:	n/a
36	chr9:21696666-21696716	SKMC	muscle:	n/a
37	chr9:21687953-21688003	SKMC	muscle:	n/a
38	chr9:21687953-21688003	Jurkat	blood:	n/a
39	chr9:21696666-21696716	Caco-2	colon:	n/a
40	chr9:21687953-21688003	AG04450	lung:	fetal
41	chr9:21696666-21696716	NH-A	brain:	n/a
42	chr9:21696666-21696716	LNCaP	prostate:	n/a
43	chr9:21687953-21688003	PFSK-1	brain:	n/a
44	chr9:21687953-21688003	GM19239	blood:	n/a
45	chr9:21687953-21688003	A549	lung:	n/a
46	chr9:21696666-21696716	T-47D	breast:	n/a
47	chr9:21696666-21696716	BE2_C	brain:	n/a
48	chr9:21687953-21688003	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:21696666-21696716	GM19239	blood:	n/a
50	chr9:21696666-21696716	RPTEC	kidney:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTAP-5	chr9:21699313-21699569	NONHSAT130395

No data

Variant related genes	Relation type
ENSG00000227443	TF binding region
KHSRPP1	TF binding region
RN7SL151P	TF binding region
ENSG00000227443	CpG island
KHSRPP1	CpG island
RN7SL151P	CpG island
ENSG00000266732	chromatin interactions
ENSG00000132716	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000204536	chromatin interactions
ENSG00000137310	chromatin interactions
ENSG00000232956	chromatin interactions
ENSG00000171889	chromatin interactions

Extended variants
information (count: 5803 )
Associated
traits (count: 159 )

Variant overlapped rSNPs/rCNVs (count:5803 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2123340	chr9:21589041-21589042	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536384548	chr9:21589084-21589085	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs16938468	chr9:21589129-21589130	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs576737360	chr9:21589152-21589153	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs77235987	chr9:21589174-21589175	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs564617591	chr9:21589230-21589231	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs559259716	chr9:21589247-21589248	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs572786772	chr9:21589253-21589254	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs541019777	chr9:21589280-21589281	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs74733441	chr9:21589293-21589294	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs185561339	chr9:21589312-21589313	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs57703006	chr9:21589422-21589423	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs367558439	chr9:21589434-21589435	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs4977728	chr9:21589457-21589458	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs189578099	chr9:21589507-21589508	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs148878056	chr9:21589541-21589542	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs571163805	chr9:21589543-21589544	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs376211482	chr9:21589580-21589581	Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs143602474	chr9:21589607-21589608	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs547065789	chr9:21589618-21589619	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs553835126	chr9:21589620-21589621	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs374039963	chr9:21589638-21589639	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs567286440	chr9:21589664-21589665	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs182768196	chr9:21589671-21589672	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs556265168	chr9:21589679-21589680	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs569782214	chr9:21589699-21589700	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs539194646	chr9:21589707-21589708	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs138236338	chr9:21589710-21589711	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs572645694	chr9:21589722-21589723	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs549582783	chr9:21589777-21589778	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs554645037	chr9:21589794-21589795	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs111351097	chr9:21589846-21589847	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs543468640	chr9:21589892-21589893	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs377294328	chr9:21589910-21589911	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs370027170	chr9:21589945-21589946	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs143822241	chr9:21589962-21589963	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs146419848	chr9:21589976-21589977	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs139057511	chr9:21589979-21589980	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs564782068	chr9:21590028-21590029	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187685373	chr9:21590046-21590047	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143071454	chr9:21590073-21590074	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369234146	chr9:21590092-21590093	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs60647530	chr9:21590127-21590128	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529655694	chr9:21590146-21590147	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549810589	chr9:21590178-21590179	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116702448	chr9:21590307-21590308	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538785948	chr9:21590318-21590319	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs552788995	chr9:21590335-21590336	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576663597	chr9:21590390-21590391	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566291712	chr9:21590406-21590407	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:159)

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
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21575800-21592200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:21579400-21590800	Weak transcription	HSMM	muscle
3	chr9:21579600-21589400	Weak transcription	HUVEC	blood vessel
4	chr9:21580000-21594800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr9:21583200-21591400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr9:21584800-21589400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:21585800-21589600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr9:21586000-21589400	Enhancers	HMEC	breast
9	chr9:21586200-21589400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:21586400-21589600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:21586400-21590200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:21586600-21589400	Weak transcription	NHLF	lung
13	chr9:21586800-21589200	Weak transcription	NHDF-Ad	bronchial
14	chr9:21586800-21589400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:21587000-21590400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:21587400-21589400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr9:21588600-21590000	Flanking Active TSS	A549	lung
18	chr9:21588800-21589400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr9:21588800-21589600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:21588800-21589600	Transcr. at gene 5' and 3'	NHEK	skin
21	chr9:21588800-21590400	Enhancers	Osteobl	bone
22	chr9:21589000-21589200	Enhancers	NH-A	brain
23	chr9:21589000-21589400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr9:21589000-21591000	Flanking Active TSS	Hela-S3	cervix
25	chr9:21589200-21590800	Enhancers	NHDF-Ad	bronchial
26	chr9:21589200-21591400	Flanking Active TSS	NH-A	brain
27	chr9:21589400-21589600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr9:21589400-21589600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr9:21589400-21589600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr9:21589400-21589600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr9:21589400-21590000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr9:21589400-21590000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:21589400-21590000	Flanking Active TSS	HMEC	breast
34	chr9:21589400-21590000	Enhancers	NHLF	lung
35	chr9:21589400-21590600	Enhancers	HUVEC	blood vessel
36	chr9:21589400-21591600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:21589400-21592200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
38	chr9:21589600-21589800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr9:21589600-21589800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr9:21589600-21590400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr9:21589600-21590400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr9:21589600-21590600	Flanking Active TSS	NHEK	skin
43	chr9:21589600-21590800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr9:21589600-21590800	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr9:21589600-21591400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr9:21589600-21593000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr9:21589800-21590000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:21589800-21590000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr9:21589800-21590200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr9:21590000-21590200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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