Variant report

Variant	nsv892734
Chromosome Location	chr9:21108817-21323089
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	chr9:21318485-21318626	HepG2	liver:	n/a	n/a
2	ATF2	chr9:21295176-21295511	GM12878	blood:	n/a	n/a
3	BATF	chr9:21213980-21214258	GM12878	blood:	n/a	n/a
4	BATF	chr9:21160171-21160535	GM12878	blood:	n/a	n/a
5	BATF	chr9:21183393-21183622	GM12878	blood:	n/a	n/a
6	BATF	chr9:21268139-21268356	GM12878	blood:	n/a	n/a
7	BATF	chr9:21214009-21214242	GM12878	blood:	n/a	n/a
8	BATF	chr9:21236050-21236328	GM12878	blood:	n/a	n/a
9	BATF	chr9:21195452-21195727	GM12878	blood:	n/a	n/a
10	BATF	chr9:21160236-21160531	GM12878	blood:	n/a	n/a
11	BATF	chr9:21183391-21183669	GM12878	blood:	n/a	n/a
12	BATF	chr9:21154272-21154547	GM12878	blood:	n/a	n/a
13	BATF	chr9:21154219-21154564	GM12878	blood:	n/a	n/a
14	BATF	chr9:21195481-21195714	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:21236105-21236278	GM12878	blood:	n/a	chr9:21236181-21236190
16	BCL11A	chr9:21295273-21295487	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:21183431-21183637	GM12878	blood:	n/a	chr9:21183522-21183531
18	BCL11A	chr9:21213999-21214266	GM12878	blood:	n/a	chr9:21214111-21214120
19	BCL11A	chr9:21154322-21154533	GM12878	blood:	n/a	chr9:21154420-21154429
20	BCL11A	chr9:21295247-21295511	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:21195389-21195749	GM12878	blood:	n/a	chr9:21195583-21195592
22	BCL11A	chr9:21195471-21195683	GM12878	blood:	n/a	chr9:21195583-21195592
23	BCL11A	chr9:21294961-21295244	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:21213900-21214291	GM12878	blood:	n/a	chr9:21214111-21214120
25	BCL11A	chr9:21236007-21236322	GM12878	blood:	n/a	chr9:21236181-21236190
26	BCLAF1	chr9:21110892-21111373	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:21295038-21295518	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:21118951-21119419	GM12878	blood:	n/a	chr9:21119195-21119204 chr9:21119196-21119205 chr9:21119196-21119205
29	BHLHE40	chr9:21318322-21318601	GM12878	blood:	n/a	n/a
30	BHLHE40	chr9:21235842-21236001	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:21121811-21122218	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:21121132-21121436	GM12878	blood:	n/a	n/a
33	BHLHE40	chr9:21195256-21195293	GM12878	blood:	n/a	n/a
34	BRCA1	chr9:21136902-21136913	GM12878	blood:	n/a	n/a
35	BRCA1	chr9:21235836-21236005	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr9:21144902-21144907	GM12878	blood:	n/a	n/a
37	CBX3	chr9:21294177-21294800	HCT-116	colon:	n/a	n/a
38	CBX3	chr9:21294159-21294859	HCT-116	colon:	n/a	n/a
39	CEBPB	chr9:21308626-21308922	IMR90	lung:	n/a	n/a
40	CEBPB	chr9:21317430-21317630	A549	lung:	n/a	chr9:21317548-21317561 chr9:21317549-21317560
41	CEBPB	chr9:21119156-21119446	IMR90	lung:	n/a	chr9:21119276-21119287 chr9:21119276-21119289
42	CEBPB	chr9:21316276-21316754	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr9:21115193-21115428	MCF-7	breast:	n/a	n/a
44	CEBPB	chr9:21155145-21155376	HepG2	liver:	n/a	chr9:21155248-21155261 chr9:21155248-21155261 chr9:21155250-21155259 chr9:21155250-21155259 chr9:21155250-21155259
45	CEBPB	chr9:21176035-21176261	A549	lung:	n/a	chr9:21176156-21176169 chr9:21176156-21176169 chr9:21176158-21176167 chr9:21176233-21176244 chr9:21176231-21176244 chr9:21176156-21176167 chr9:21176157-21176168
46	CEBPB	chr9:21308602-21308919	A549	lung:	n/a	n/a
47	CEBPB	chr9:21154074-21154382	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:21317437-21317710	IMR90	lung:	n/a	chr9:21317548-21317561 chr9:21317549-21317560
49	CEBPB	chr9:21317500-21317694	HepG2	liver:	n/a	chr9:21317548-21317561 chr9:21317549-21317560
50	CEBPB	chr9:21175999-21176288	IMR90	lung:	n/a	chr9:21176156-21176169 chr9:21176156-21176169 chr9:21176158-21176167 chr9:21176233-21176244 chr9:21176231-21176244 chr9:21176156-21176167 chr9:21176157-21176168

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21239944-21239994	IMR90	lung:	fetal
2	chr9:21239944-21239994	Caco-2	colon:	n/a
3	chr9:21241233-21241283	HRCEpiC	kidney:	n/a
4	chr9:21202213-21202263	HCM	heart:	n/a
5	chr9:21241233-21241283	PFSK-1	brain:	n/a
6	chr9:21187344-21187394	MCF10A-Er-Src	breast:	n/a
7	chr9:21241233-21241283	AoSMC	blood vessel:	n/a
8	chr9:21187344-21187394	MCF-7	breast:	n/a
9	chr9:21187344-21187394	HUVEC	blood vessel:	n/a
10	chr9:21239944-21239994	T-47D	breast:	n/a
11	chr9:21241233-21241283	AG10803	skin:	n/a
12	chr9:21239944-21239994	Jurkat	blood:	n/a
13	chr9:21187344-21187394	HRE	kidney:	n/a
14	chr9:21241233-21241283	HNPCEpiC	eye:	n/a
15	chr9:21202213-21202263	SKMC	muscle:	n/a
16	chr9:21239944-21239994	HIPEpiC	eye:	n/a
17	chr9:21202213-21202263	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:21187344-21187394	HL-60	blood:	n/a
19	chr9:21187344-21187394	Hela-S3	cervix:	n/a
20	chr9:21239944-21239994	BE2_C	brain:	n/a
21	chr9:21202213-21202263	HL-60	blood:	n/a
22	chr9:21241233-21241283	HEEpiC	esophagus:	n/a
23	chr9:21202213-21202263	HNPCEpiC	eye:	n/a
24	chr9:21241233-21241283	ECC-1	luminal epithelium:	n/a
25	chr9:21202213-21202263	SK-N-SH_RA	brain:	n/a
26	chr9:21241233-21241283	AG04449	skin:	fetal
27	chr9:21239944-21239994	Hepatocyte	liver:	n/a
28	chr9:21187344-21187394	BJ	skin:	n/a
29	chr9:21202213-21202263	HCPEpiC	choroid plexus:	n/a
30	chr9:21241233-21241283	ProgFib	skin:	n/a
31	chr9:21241233-21241283	HCF	heart:	n/a
32	chr9:21187344-21187394	NH-A	brain:	n/a
33	chr9:21241233-21241283	NH-A	brain:	n/a
34	chr9:21187344-21187394	HEEpiC	esophagus:	n/a
35	chr9:21239944-21239994	AG04450	lung:	fetal
36	chr9:21202213-21202263	Jurkat	blood:	n/a
37	chr9:21239944-21239994	HL-60	blood:	n/a
38	chr9:21239944-21239994	MCF-7	breast:	n/a
39	chr9:21187344-21187394	AG04450	lung:	fetal
40	chr9:21241233-21241283	LNCaP	prostate:	n/a
41	chr9:21239944-21239994	SKMC	muscle:	n/a
42	chr9:21239944-21239994	HCM	heart:	n/a
43	chr9:21241233-21241283	T-47D	breast:	n/a
44	chr9:21202213-21202263	HRE	kidney:	n/a
45	chr9:21202213-21202263	GM12891	blood:	n/a
46	chr9:21187344-21187394	SK-N-SH_RA	brain:	n/a
47	chr9:21241233-21241283	BE2_C	brain:	n/a
48	chr9:21202213-21202263	HUVEC	blood vessel:	n/a
49	chr9:21239944-21239994	AG09319	gingival:	n/a
50	chr9:21239944-21239994	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:21150083..21152339-chr9:21152667..21154547,2	MCF-7	breast:
2	chr9:21130782..21132489-chr9:21132879..21134890,3	MCF-7	breast:
3	chr9:21318010..21319069-chr9:21395893..21396720,4	MCF-7	breast:
4	chr9:21150083..21152339-chr9:21152667..21154547,2	MCF-7	breast:
5	chr9:20682614..20684265-chr9:21107460..21109454,2	MCF-7	breast:
6	chr9:21317987..21318804-chr9:21455380..21456013,2	MCF-7	breast:
7	chr9:21078514..21079405-chr9:21110637..21111248,3	MCF-7	breast:
8	chr9:21318056..21318697-chrX:104999680..105000200,2	MCF-7	breast:
9	chr9:21253305..21254010-chr9:21318409..21318973,2	MCF-7	breast:
10	chr9:21318068..21318780-chr9:21789413..21789937,2	MCF-7	breast:
11	chr9:21317956..21318799-chr9:21455067..21455992,4	MCF-7	breast:
12	chr9:21130782..21132489-chr9:21132879..21134890,3	MCF-7	breast:
13	chr9:21253305..21254010-chr9:21318409..21318973,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNA5-1	chr9:21277687-21278562	NONHSAT130376
2	lnc-IFNA8-3	chr9:21321299-21321826	NONHSAT130379
3	lnc-IFNA5-1	chr9:21278049-21278618	NONHSAT130377
4	lnc-IFNA4-2	chr9:21178588-21179187	NONHSAT130372
5	lnc-IFNA10-1	chr9:21209188-21209778	NONHSAT130374
6	lnc-IFNA17-1	chr9:21231265-21231852	NONHSAT130375
7	lnc-IFNA4-1	chr9:21190653-21191243	NONHSAT130373
8	lnc-KLHL9-1	chr9:21321195-21321632	NONHSAT130378

Variant related genes	Relation type
ENSG00000199635	TF binding region
IFNA20P	TF binding region
IFNA5	TF binding region
IFNA7	TF binding region
IFNA21	TF binding region
IFNWP15	TF binding region
IFNWP9	TF binding region
IFNA14	TF binding region
IFNA17	TF binding region
IFNWP18	TF binding region
IFNA16	TF binding region
IFNA4	TF binding region
IFNA22P	TF binding region
IFNW1	TF binding region
IFNA10	TF binding region
IFNWP5	TF binding region
ENSG00000199635	CpG island
IFNA20P	CpG island
IFNA5	CpG island
IFNA7	CpG island
IFNA21	CpG island
IFNWP15	CpG island
IFNWP9	CpG island
IFNA14	CpG island
IFNA17	CpG island
IFNWP18	CpG island
IFNA16	CpG island
IFNA4	CpG island
IFNA22P	CpG island
IFNW1	CpG island
IFNA10	CpG island
IFNWP5	CpG island
ENSG00000261696	chromatin interactions
ENSG00000188352	chromatin interactions
ENSG00000238271	chromatin interactions
ENSG00000227071	chromatin interactions

Extended variants
information (count: 5205 )
Associated
traits (count: 159 )

Variant overlapped rSNPs/rCNVs (count:5205 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2113718	chr9:21108817-21108818	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs180963856	chr9:21108827-21108828	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs532397846	chr9:21108839-21108840	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs187009605	chr9:21108849-21108850	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs565926886	chr9:21108862-21108863	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs534786976	chr9:21108908-21108909	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs548731245	chr9:21108957-21108958	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149706155	chr9:21109024-21109025	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs537464028	chr9:21109028-21109029	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs557276415	chr9:21109032-21109033	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145578364	chr9:21109047-21109048	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs540173191	chr9:21109074-21109075	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs554932045	chr9:21109152-21109153	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs553369713	chr9:21109181-21109182	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs7859885	chr9:21109188-21109189	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541985905	chr9:21109288-21109289	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs192304421	chr9:21109345-21109346	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs574151648	chr9:21109361-21109362	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543061607	chr9:21109371-21109372	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs182029828	chr9:21109424-21109425	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs557031056	chr9:21110814-21110815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143259131	chr9:21110831-21110832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539443147	chr9:21110836-21110837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192490227	chr9:21110866-21110867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185050542	chr9:21110896-21110897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542191430	chr9:21110917-21110918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187448772	chr9:21110939-21110940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566270043	chr9:21110949-21110950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575411987	chr9:21110982-21110983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538193581	chr9:21111211-21111212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141470210	chr9:21111227-21111228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150446788	chr9:21111279-21111280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138465580	chr9:21111286-21111287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577858385	chr9:21111354-21111355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551633756	chr9:21111382-21111383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570535518	chr9:21111393-21111394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368643515	chr9:21111416-21111417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192252823	chr9:21111437-21111438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372103433	chr9:21111453-21111454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553099905	chr9:21111502-21111503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs28606605	chr9:21111514-21111515	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs184603673	chr9:21111523-21111524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189878335	chr9:21111540-21111541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553970804	chr9:21111573-21111574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544407522	chr9:21111592-21111593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564169309	chr9:21111596-21111597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577767333	chr9:21111650-21111651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540358037	chr9:21111690-21111691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560195586	chr9:21111704-21111705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529261740	chr9:21111775-21111776	Enhancers	n/a	n/a	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
Glioblastoma multiforme	21525872	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Cancer	20581869	CNVD
XY gonadal dysgenesis	20685758	CNVD
Non-small cell lung cancer	16651412	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Oral cancer	22144094	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:813 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21110800-21111000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr9:21111200-21112400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:21112400-21112600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:21112400-21112600	Enhancers	Fetal Lung	lung
5	chr9:21112800-21114000	Weak transcription	Fetal Lung	lung
6	chr9:21114000-21114400	Enhancers	Fetal Lung	lung
7	chr9:21114200-21114800	Enhancers	Placenta Amnion	Placenta Amnion
8	chr9:21114400-21119000	Weak transcription	Fetal Lung	lung
9	chr9:21114800-21118800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr9:21118400-21118800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr9:21118600-21119000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr9:21118600-21119400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr9:21118600-21121400	Enhancers	Primary hematopoietic stem cells	blood
14	chr9:21118800-21119000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr9:21118800-21119200	Enhancers	Right Atrium	heart
16	chr9:21118800-21119400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr9:21118800-21119800	Enhancers	GM12878-XiMat	blood
18	chr9:21118800-21120400	Enhancers	Placenta Amnion	Placenta Amnion
19	chr9:21118800-21120600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr9:21118800-21120600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr9:21118800-21121200	Enhancers	Placenta	Placenta
22	chr9:21119000-21119400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr9:21119000-21119600	Enhancers	Primary T cells from cord blood	blood
24	chr9:21119000-21119800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:21119000-21119800	Enhancers	Fetal Lung	lung
26	chr9:21119000-21119800	Enhancers	Dnd41	blood
27	chr9:21119000-21120400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr9:21119200-21119600	Enhancers	Adipose Nuclei	Adipose
29	chr9:21119200-21119600	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr9:21119400-21119800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr9:21119400-21119800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr9:21119400-21119800	Enhancers	Fetal Thymus	thymus
33	chr9:21119400-21119800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr9:21119600-21119800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr9:21119600-21123400	Weak transcription	Adipose Nuclei	Adipose
36	chr9:21119800-21120000	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr9:21119800-21120400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr9:21119800-21120600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr9:21119800-21120800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr9:21119800-21120800	Weak transcription	Dnd41	blood
41	chr9:21119800-21121400	Weak transcription	GM12878-XiMat	blood
42	chr9:21119800-21121800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:21120400-21121400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr9:21120600-21121200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr9:21120800-21121800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr9:21120800-21122200	Enhancers	Dnd41	blood
47	chr9:21121200-21121400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr9:21121400-21121600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr9:21121400-21122600	Enhancers	GM12878-XiMat	blood
50	chr9:21121800-21122200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood

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