Variant report

Variant	nsv892743
Chromosome Location	chr9:21675545-21772064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1051)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1051 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:21709533-21709820	HepG2	liver:	n/a	n/a
2	ATF2	chr9:21751899-21752360	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr9:21761267-21761735	GM12878	blood:	n/a	n/a
4	ATF2	chr9:21761271-21761724	GM12878	blood:	n/a	n/a
5	ATF3	chr9:21684624-21685507	HCT-116	colon:	n/a	n/a
6	ATF3	chr9:21677783-21678297	A549	lung:	n/a	n/a
7	ATF3	chr9:21677574-21678317	A549	lung:	n/a	n/a
8	ATF3	chr9:21684623-21685773	A549	lung:	n/a	n/a
9	ATF3	chr9:21677553-21678303	HCT-116	colon:	n/a	n/a
10	ATF3	chr9:21684629-21685479	HCT-116	colon:	n/a	n/a
11	BACH1	chr9:21678040-21678111	H1-hESC	embryonic stem cell:	n/a	chr9:21678050-21678064
12	BATF	chr9:21711502-21711771	GM12878	blood:	n/a	chr9:21711661-21711672
13	BATF	chr9:21711462-21711794	GM12878	blood:	n/a	chr9:21711661-21711672
14	BATF	chr9:21761304-21761682	GM12878	blood:	n/a	n/a
15	BATF	chr9:21761251-21761742	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:21761331-21761649	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:21761371-21761656	GM12878	blood:	n/a	n/a
18	BCL3	chr9:21677389-21678468	A549	lung:	n/a	chr9:21677552-21677561 chr9:21678052-21678061 chr9:21678053-21678062
19	BCL3	chr9:21681396-21682102	A549	lung:	n/a	n/a
20	BCL3	chr9:21682728-21683550	A549	lung:	n/a	n/a
21	BCL3	chr9:21684389-21685850	A549	lung:	n/a	chr9:21684825-21684834 chr9:21684554-21684563 chr9:21685100-21685109
22	BCL3	chr9:21684674-21685858	A549	lung:	n/a	chr9:21684825-21684834 chr9:21685100-21685109
23	BCLAF1	chr9:21761256-21761703	GM12878	blood:	n/a	n/a
24	BRCA1	chr9:21681494-21682052	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr9:21745003-21745115	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr9:21684614-21685498	HCT-116	colon:	n/a	chr9:21685011-21685022
27	CBX3	chr9:21709389-21709975	HCT-116	colon:	n/a	n/a
28	CBX3	chr9:21677415-21678415	HCT-116	colon:	n/a	n/a
29	CBX3	chr9:21754643-21755240	HCT-116	colon:	n/a	n/a
30	CBX3	chr9:21754761-21755206	HCT-116	colon:	n/a	n/a
31	CEBPB	chr9:21684543-21685510	A549	lung:	n/a	n/a
32	CEBPB	chr9:21764848-21764960	H1-hESC	embryonic stem cell:	n/a	chr9:21764909-21764922
33	CEBPB	chr9:21747167-21747482	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:21688699-21689081	Hela-S3	cervix:	n/a	chr9:21688804-21688817
35	CEBPB	chr9:21681511-21682494	A549	lung:	n/a	n/a
36	CEBPB	chr9:21684790-21685317	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:21764205-21764405	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr9:21681610-21682016	IMR90	lung:	n/a	n/a
39	CEBPB	chr9:21729211-21729269	IMR90	lung:	n/a	n/a
40	CEBPB	chr9:21677757-21678296	A549	lung:	n/a	chr9:21678215-21678223
41	CEBPB	chr9:21747100-21747545	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr9:21677490-21678343	HCT-116	colon:	n/a	chr9:21678215-21678223 chr9:21677685-21677698
43	CEBPB	chr9:21702033-21702278	A549	lung:	n/a	chr9:21702179-21702190 chr9:21702179-21702188
44	CEBPB	chr9:21711413-21712016	HCT-116	colon:	n/a	n/a
45	CEBPB	chr9:21769460-21769564	A549	lung:	n/a	n/a
46	CEBPB	chr9:21681626-21682119	A549	lung:	n/a	n/a
47	CEBPB	chr9:21744934-21745234	A549	lung:	n/a	n/a
48	CEBPB	chr9:21764797-21765276	IMR90	lung:	n/a	chr9:21764909-21764922
49	CEBPB	chr9:21681594-21682064	A549	lung:	n/a	n/a
50	CEBPB	chr9:21711549-21711834	IMR90	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	NHBE	bronchial:	n/a
2	chr9:21696666-21696716	AG04449	skin:	fetal
3	chr9:21696666-21696716	PFSK-1	brain:	n/a
4	chr9:21696666-21696716	GM12878	blood:	n/a
5	chr9:21696666-21696716	CMK	blood:	n/a
6	chr9:21696666-21696716	K562	blood:	n/a
7	chr9:21687953-21688003	NHDF-neo	bronchial:	n/a
8	chr9:21696666-21696716	HRPEpiC	eye:	n/a
9	chr9:21687953-21688003	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:21696666-21696716	MCF10A-Er-Src	breast:	n/a
11	chr9:21687953-21688003	HCT-116	colon:	n/a
12	chr9:21687953-21688003	A549	lung:	n/a
13	chr9:21696666-21696716	T-47D	breast:	n/a
14	chr9:21696666-21696716	Jurkat	blood:	n/a
15	chr9:21687953-21688003	HRPEpiC	eye:	n/a
16	chr9:21687953-21688003	GM06990	blood:	n/a
17	chr9:21696666-21696716	BJ	skin:	n/a
18	chr9:21687953-21688003	LNCaP	prostate:	n/a
19	chr9:21687953-21688003	ECC-1	luminal epithelium:	n/a
20	chr9:21696666-21696716	HCPEpiC	choroid plexus:	n/a
21	chr9:21687953-21688003	AG09309	skin:	n/a
22	chr9:21696666-21696716	GM12891	blood:	n/a
23	chr9:21696666-21696716	Caco-2	colon:	n/a
24	chr9:21687953-21688003	RPTEC	kidney:	n/a
25	chr9:21687953-21688003	CMK	blood:	n/a
26	chr9:21696666-21696716	HMEC	breast:	n/a
27	chr9:21687953-21688003	HAEpiC	amniotic membrane:	n/a
28	chr9:21687953-21688003	NT2-D1	testis:	n/a
29	chr9:21687953-21688003	AG09319	gingival:	n/a
30	chr9:21687953-21688003	T-47D	breast:	n/a
31	chr9:21687953-21688003	MCF10A-Er-Src	breast:	n/a
32	chr9:21696666-21696716	H1-hESC	embryonic stem cell:	embryo
33	chr9:21696666-21696716	RPTEC	kidney:	n/a
34	chr9:21696666-21696716	HEEpiC	esophagus:	n/a
35	chr9:21687953-21688003	GM12891	blood:	n/a
36	chr9:21687953-21688003	HEEpiC	esophagus:	n/a
37	chr9:21687953-21688003	AoSMC	blood vessel:	n/a
38	chr9:21687953-21688003	SK-N-SH	brain:	n/a
39	chr9:21687953-21688003	HRCEpiC	kidney:	n/a
40	chr9:21687953-21688003	HCM	heart:	n/a
41	chr9:21696666-21696716	AG09319	gingival:	n/a
42	chr9:21696666-21696716	A549	lung:	n/a
43	chr9:21687953-21688003	PANC-1	pancreas:	n/a
44	chr9:21696666-21696716	NH-A	brain:	n/a
45	chr9:21696666-21696716	NB4	blood:	n/a
46	chr9:21696666-21696716	AoSMC	blood vessel:	n/a
47	chr9:21687953-21688003	NH-A	brain:	n/a
48	chr9:21696666-21696716	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:21687953-21688003	HEK293	kidney:	embryo
50	chr9:21687953-21688003	HepG2	liver:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:21678019..21679658-chr9:21681885..21684334,2	MCF-7	breast:
2	chr9:21588453..21590122-chr9:21684881..21686548,2	MCF-7	breast:
3	chr7:45025732..45026728-chr9:21683864..21684615,2	HCT-116	colon:
4	chr5:150593443..150594007-chr9:21684916..21685496,2	HCT-116	colon:
5	chr9:21681458..21682986-chr9:21704343..21706212,2	MCF-7	breast:
6	chr11:93474769..93475337-chr9:21707894..21708478,2	HCT-116	colon:
7	chr9:21709315..21710109-chr9:21789136..21789898,2	MCF-7	breast:
8	chr9:21678019..21679658-chr9:21681885..21684334,2	MCF-7	breast:
9	chr9:21681458..21682986-chr9:21704343..21706212,2	MCF-7	breast:
10	chr9:21747038..21749658-chr9:21801876..21803848,2	MCF-7	breast:
11	chr9:21709125..21709738-chr9:21789173..21789997,3	MCF-7	breast:
12	chr11:18690057..18690608-chr9:21683732..21684232,2	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
KHSRPP1	TF binding region
RN7SL151P	TF binding region
KHSRPP1	CpG island
RN7SL151P	CpG island
ENSG00000264545	chromatin interactions
ENSG00000099810	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000232956	chromatin interactions
ENSG00000166012	chromatin interactions

Extended variants
information (count: 4305 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:4305 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1377195	chr9:21675545-21675546	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148780566	chr9:21675559-21675560	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs377059497	chr9:21675624-21675625	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs543726009	chr9:21675627-21675628	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs563674939	chr9:21675645-21675646	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs142448309	chr9:21675663-21675664	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs16938530	chr9:21675670-21675671	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs73649930	chr9:21675692-21675693	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs528527694	chr9:21675704-21675705	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs548682053	chr9:21675707-21675708	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs560884903	chr9:21675708-21675709	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs151332834	chr9:21675714-21675715	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs7021741	chr9:21675716-21675717	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs374071590	chr9:21675717-21675718	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs570013012	chr9:21675755-21675756	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs538630568	chr9:21675765-21675766	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs187073734	chr9:21675777-21675778	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs565683431	chr9:21675823-21675824	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs534395138	chr9:21675833-21675834	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs554667193	chr9:21675839-21675840	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs574921080	chr9:21675866-21675867	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs537681787	chr9:21675933-21675934	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs141879961	chr9:21675937-21675938	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs145730817	chr9:21675943-21675944	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs546088437	chr9:21675964-21675965	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs191601229	chr9:21675979-21675980	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs1377196	chr9:21676042-21676043	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs541942395	chr9:21676054-21676055	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562237057	chr9:21676063-21676064	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs182530860	chr9:21676103-21676104	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs553668043	chr9:21676122-21676123	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs558943450	chr9:21676126-21676127	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs147773831	chr9:21676138-21676139	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs117484426	chr9:21676151-21676152	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs532401753	chr9:21676153-21676154	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs187896105	chr9:21676167-21676168	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs16938531	chr9:21676187-21676188	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534651379	chr9:21676194-21676195	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs141182772	chr9:21676209-21676210	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs538358368	chr9:21676217-21676218	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs4275302	chr9:21676221-21676222	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs150336062	chr9:21676233-21676234	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs557083197	chr9:21676238-21676239	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs55689357	chr9:21676256-21676257	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs10965098	chr9:21676273-21676274	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs2039584	chr9:21676295-21676296	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs543132329	chr9:21676297-21676298	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs117811787	chr9:21676314-21676315	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs193005513	chr9:21676320-21676321	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs183355571	chr9:21676330-21676331	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:161)

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
Barrett''s syndrome	19417022	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Breast cancer	17142309	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Gastrointestinal stromal cancer	20877625	CNVD

Chromatin state (count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21673000-21679400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr9:21674200-21677600	Enhancers	HMEC	breast
3	chr9:21674200-21678200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:21674400-21677600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:21674600-21676600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:21674600-21677400	Enhancers	NHEK	skin
7	chr9:21674600-21677600	Enhancers	NHDF-Ad	bronchial
8	chr9:21674800-21676800	Enhancers	Hela-S3	cervix
9	chr9:21674800-21677400	Enhancers	HUVEC	blood vessel
10	chr9:21674800-21677600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr9:21675000-21675600	Enhancers	NH-A	brain
12	chr9:21675000-21676400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr9:21675000-21677400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr9:21675000-21677600	Enhancers	Osteobl	bone
15	chr9:21675200-21675800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:21675200-21676200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr9:21675400-21676600	Enhancers	NHLF	lung
18	chr9:21675400-21676800	Flanking Active TSS	A549	lung
19	chr9:21675600-21677600	Weak transcription	NH-A	brain
20	chr9:21675800-21677600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:21676200-21678600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr9:21676400-21676800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr9:21676600-21677000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr9:21676600-21677400	Weak transcription	NHLF	lung
25	chr9:21676800-21677200	Weak transcription	Hela-S3	cervix
26	chr9:21676800-21677400	Enhancers	A549	lung
27	chr9:21676800-21677600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr9:21677000-21677200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:21677000-21677200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:21677000-21677200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:21677200-21677400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:21677200-21677400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr9:21677200-21679200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr9:21677200-21684600	Enhancers	Hela-S3	cervix
35	chr9:21677400-21677600	Enhancers	NHLF	lung
36	chr9:21677400-21677800	Flanking Active TSS	A549	lung
37	chr9:21677400-21678000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr9:21677400-21678200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:21677400-21678200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr9:21677400-21678200	Flanking Active TSS	NHEK	skin
41	chr9:21677400-21678600	Flanking Active TSS	HUVEC	blood vessel
42	chr9:21677600-21677800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr9:21677600-21677800	Enhancers	NH-A	brain
44	chr9:21677600-21677800	Flanking Active TSS	NHLF	lung
45	chr9:21677600-21678000	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr9:21677600-21678000	Flanking Active TSS	HMEC	breast
47	chr9:21677600-21678200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr9:21677600-21678200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr9:21677600-21678200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr9:21677600-21678200	Flanking Active TSS	NHDF-Ad	bronchial

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