Variant report

Variant	nsv1032466
Chromosome Location	chr9:21052069-21243756
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	ATF2	chr9:21096158-21096906	GM12878	blood:	n/a	n/a
2	ATF2	chr9:21096241-21096694	GM12878	blood:	n/a	n/a
3	ATF3	chr9:21096343-21096742	GM12878	blood:	n/a	n/a
4	BACH1	chr9:21070100-21070522	H1-hESC	embryonic stem cell:	n/a	chr9:21070284-21070298
5	BATF	chr9:21183393-21183622	GM12878	blood:	n/a	n/a
6	BATF	chr9:21160171-21160535	GM12878	blood:	n/a	n/a
7	BATF	chr9:21195481-21195714	GM12878	blood:	n/a	n/a
8	BATF	chr9:21195452-21195727	GM12878	blood:	n/a	n/a
9	BATF	chr9:21183391-21183669	GM12878	blood:	n/a	n/a
10	BATF	chr9:21236050-21236328	GM12878	blood:	n/a	n/a
11	BATF	chr9:21213980-21214258	GM12878	blood:	n/a	n/a
12	BATF	chr9:21214009-21214242	GM12878	blood:	n/a	n/a
13	BATF	chr9:21154272-21154547	GM12878	blood:	n/a	n/a
14	BATF	chr9:21154219-21154564	GM12878	blood:	n/a	n/a
15	BATF	chr9:21160236-21160531	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:21213999-21214266	GM12878	blood:	n/a	chr9:21214111-21214120
17	BCL11A	chr9:21154322-21154533	GM12878	blood:	n/a	chr9:21154420-21154429
18	BCL11A	chr9:21213900-21214291	GM12878	blood:	n/a	chr9:21214111-21214120
19	BCL11A	chr9:21236007-21236322	GM12878	blood:	n/a	chr9:21236181-21236190
20	BCL11A	chr9:21195389-21195749	GM12878	blood:	n/a	chr9:21195583-21195592
21	BCL11A	chr9:21183431-21183637	GM12878	blood:	n/a	chr9:21183522-21183531
22	BCL11A	chr9:21195471-21195683	GM12878	blood:	n/a	chr9:21195583-21195592
23	BCL11A	chr9:21236105-21236278	GM12878	blood:	n/a	chr9:21236181-21236190
24	BCLAF1	chr9:21110892-21111373	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:21121132-21121436	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:21235842-21236001	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:21061272-21061492	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	chr9:21195256-21195293	GM12878	blood:	n/a	n/a
30	BHLHE40	chr9:21121811-21122218	GM12878	blood:	n/a	n/a
31	BRCA1	chr9:21235836-21236005	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr9:21136902-21136913	GM12878	blood:	n/a	n/a
33	BRCA1	chr9:21144902-21144907	GM12878	blood:	n/a	n/a
34	CEBPB	chr9:21096210-21096670	HCT-116	colon:	n/a	chr9:21096515-21096526
35	CEBPB	chr9:21172249-21172496	A549	lung:	n/a	chr9:21172346-21172357
36	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
37	CEBPB	chr9:21072981-21073212	A549	lung:	n/a	n/a
38	CEBPB	chr9:21096269-21096712	MCF-7	breast:	n/a	chr9:21096515-21096526
39	CEBPB	chr9:21115135-21115583	MCF-7	breast:	n/a	n/a
40	CEBPB	chr9:21119199-21119424	Hela-S3	cervix:	n/a	chr9:21119276-21119287 chr9:21119276-21119289
41	CEBPB	chr9:21096311-21096675	IMR90	lung:	n/a	chr9:21096515-21096526
42	CEBPB	chr9:21095672-21095870	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr9:21155119-21155340	A549	lung:	n/a	chr9:21155248-21155261 chr9:21155248-21155261 chr9:21155250-21155259 chr9:21155250-21155259 chr9:21155250-21155259
44	CEBPB	chr9:21096226-21096728	HCT-116	colon:	n/a	chr9:21096515-21096526
45	CEBPB	chr9:21096160-21097105	GM12878	blood:	n/a	chr9:21096805-21096813 chr9:21096515-21096526
46	CEBPB	chr9:21115193-21115428	MCF-7	breast:	n/a	n/a
47	CEBPB	chr9:21094881-21095125	A549	lung:	n/a	n/a
48	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
49	CEBPB	chr9:21096317-21096625	ECC-1	luminal epithelium:	n/a	chr9:21096515-21096526
50	CEBPB	chr9:21096269-21096738	MCF-7	breast:	n/a	chr9:21096515-21096526

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:21187344-21187394	GM12892	blood:	n/a
2	chr9:21241233-21241283	SK-N-SH_RA	brain:	n/a
3	chr9:21241233-21241283	HCT-116	colon:	n/a
4	chr9:21202213-21202263	SK-N-MC	brain:	n/a
5	chr9:21187344-21187394	LNCaP	prostate:	n/a
6	chr9:21202213-21202263	HPAEpiC	pulmonary alveolar:	n/a
7	chr9:21241233-21241283	NB4	blood:	n/a
8	chr9:21202213-21202263	MCF10A-Er-Src	breast:	n/a
9	chr9:21202213-21202263	AG04449	skin:	fetal
10	chr9:21202213-21202263	AoSMC	blood vessel:	n/a
11	chr9:21241233-21241283	AG04450	lung:	fetal
12	chr9:21187344-21187394	GM12878	blood:	n/a
13	chr9:21187344-21187394	Jurkat	blood:	n/a
14	chr9:21241233-21241283	AG04449	skin:	fetal
15	chr9:21202213-21202263	PrEC	prostate:	n/a
16	chr9:21239944-21239994	HL-60	blood:	n/a
17	chr9:21187344-21187394	MCF-7	breast:	n/a
18	chr9:21241233-21241283	HCF	heart:	n/a
19	chr9:21241233-21241283	PrEC	prostate:	n/a
20	chr9:21239944-21239994	HEK293	kidney:	embryo
21	chr9:21202213-21202263	ProgFib	skin:	n/a
22	chr9:21202213-21202263	PANC-1	pancreas:	n/a
23	chr9:21187344-21187394	ECC-1	luminal epithelium:	n/a
24	chr9:21241233-21241283	GM12891	blood:	n/a
25	chr9:21241233-21241283	HAEpiC	amniotic membrane:	n/a
26	chr9:21239944-21239994	NH-A	brain:	n/a
27	chr9:21241233-21241283	HRPEpiC	eye:	n/a
28	chr9:21241233-21241283	GM06990	blood:	n/a
29	chr9:21202213-21202263	PFSK-1	brain:	n/a
30	chr9:21187344-21187394	BJ	skin:	n/a
31	chr9:21202213-21202263	SKMC	muscle:	n/a
32	chr9:21202213-21202263	NB4	blood:	n/a
33	chr9:21202213-21202263	HCM	heart:	n/a
34	chr9:21202213-21202263	MCF-7	breast:	n/a
35	chr9:21239944-21239994	HNPCEpiC	eye:	n/a
36	chr9:21239944-21239994	HUVEC	blood vessel:	n/a
37	chr9:21202213-21202263	Jurkat	blood:	n/a
38	chr9:21239944-21239994	AG04449	skin:	fetal
39	chr9:21241233-21241283	SKMC	muscle:	n/a
40	chr9:21202213-21202263	NT2-D1	testis:	n/a
41	chr9:21187344-21187394	Hela-S3	cervix:	n/a
42	chr9:21241233-21241283	NHBE	bronchial:	n/a
43	chr9:21187344-21187394	HAEpiC	amniotic membrane:	n/a
44	chr9:21241233-21241283	SK-N-MC	brain:	n/a
45	chr9:21241233-21241283	BJ	skin:	n/a
46	chr9:21239944-21239994	PrEC	prostate:	n/a
47	chr9:21239944-21239994	SK-N-SH_RA	brain:	n/a
48	chr9:21187344-21187394	HRE	kidney:	n/a
49	chr9:21241233-21241283	H1-hESC	embryonic stem cell:	embryo
50	chr9:21239944-21239994	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:21076953..21079185-chr9:21106248..21108735,2	MCF-7	breast:
2	chr9:21150083..21152339-chr9:21152667..21154547,2	MCF-7	breast:
3	chr9:21044579..21046540-chr9:21053460..21056237,2	MCF-7	breast:
4	chr9:21068380..21070778-chr9:21072335..21074314,2	MCF-7	breast:
5	chr9:21068380..21070778-chr9:21072335..21074314,2	MCF-7	breast:
6	chr9:21150083..21152339-chr9:21152667..21154547,2	MCF-7	breast:
7	chr17:72800948..72803891-chr9:21084620..21086617,2	MCF-7	breast:
8	chr9:21076953..21079185-chr9:21106248..21108735,2	MCF-7	breast:
9	chr9:21078514..21079405-chr9:21110637..21111248,3	MCF-7	breast:
10	chr9:21078514..21079405-chr9:21110637..21111248,3	MCF-7	breast:
11	chr9:21130782..21132489-chr9:21132879..21134890,3	MCF-7	breast:
12	chr9:20682614..20684265-chr9:21107460..21109454,2	MCF-7	breast:
13	chr9:21046351..21048535-chr9:21050216..21052104,2	MCF-7	breast:
14	chr9:21130782..21132489-chr9:21132879..21134890,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNA17-1	chr9:21231265-21231852	NONHSAT130375
2	lnc-IFNA4-1	chr9:21190653-21191243	NONHSAT130373
3	lnc-IFNB1-1	chr9:21058770-21059322	NONHSAT130369
4	lnc-IFNA4-2	chr9:21178588-21179187	NONHSAT130372
5	lnc-IFNA10-1	chr9:21209188-21209778	NONHSAT130374
6	lnc-KIAA1797-1	chr9:21106542-21106835	NONHSAT130370

Variant related genes	Relation type
ENSG00000199635	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
IFNW1	TF binding region
IFNNP1	TF binding region
IFNA10	TF binding region
IFNB1	TF binding region
IFNWP5	TF binding region
IFNWP4	TF binding region
ENSG00000199635	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
IFNW1	CpG island
IFNNP1	CpG island
IFNA10	CpG island
IFNB1	CpG island
IFNWP5	CpG island
IFNWP4	CpG island
ENSG00000188352	chromatin interactions
ENSG00000227071	chromatin interactions
ENSG00000225027	chromatin interactions
ENSG00000171855	chromatin interactions

Extended variants
information (count: 5393 )
Associated
traits (count: 159 )

Variant overlapped rSNPs/rCNVs (count:5393 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578262200	chr9:21052176-21052177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540920316	chr9:21052226-21052227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541274096	chr9:21052270-21052271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560702991	chr9:21052275-21052276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559565620	chr9:21052311-21052312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74899761	chr9:21052336-21052337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183308110	chr9:21052462-21052463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561787816	chr9:21052477-21052478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530432681	chr9:21052525-21052526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574867765	chr9:21052526-21052527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141530823	chr9:21052557-21052558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189153147	chr9:21052600-21052601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79963666	chr9:21052639-21052640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78424713	chr9:21052654-21052655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533095711	chr9:21052656-21052657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79529832	chr9:21052657-21052658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10811458	chr9:21052663-21052664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs114358268	chr9:21052668-21052669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12375575	chr9:21052705-21052706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535606267	chr9:21052709-21052710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540392613	chr9:21052714-21052715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10811459	chr9:21052797-21052798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs192839370	chr9:21052809-21052810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558225405	chr9:21052823-21052824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185328185	chr9:21052833-21052834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146195523	chr9:21052841-21052842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187801113	chr9:21052874-21052875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577076947	chr9:21052899-21052900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554479171	chr9:21052913-21052914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574167250	chr9:21052920-21052921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10120242	chr9:21052926-21052927	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs35204598	chr9:21052928-21052929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561630824	chr9:21052937-21052938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575343487	chr9:21052940-21052941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543892538	chr9:21052941-21052942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191671457	chr9:21052944-21052945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532742788	chr9:21052946-21052947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546509027	chr9:21052956-21052957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560357091	chr9:21052963-21052964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs137915927	chr9:21053030-21053031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10114868	chr9:21053044-21053045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs564483318	chr9:21053046-21053047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141683386	chr9:21053087-21053088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551884701	chr9:21053141-21053142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150554304	chr9:21053168-21053169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534148229	chr9:21053191-21053192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528760193	chr9:21053195-21053196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530089732	chr9:21053233-21053234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554177614	chr9:21053243-21053244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79074474	chr9:21053245-21053246	Weak transcription	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
early-passage human iPS cells	21368824	CNVD
XY gonadal dysgenesis	20685758	CNVD
Non-small cell lung cancer	16651412	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21048200-21053800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr9:21048400-21060400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr9:21050600-21052800	Weak transcription	Aorta	Aorta
4	chr9:21051800-21052200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr9:21053800-21054400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr9:21054400-21059600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr9:21055000-21055200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr9:21055200-21060800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr9:21056000-21059000	Weak transcription	Primary T cells from cord blood	blood
10	chr9:21056600-21057400	Enhancers	A549	lung
11	chr9:21057000-21057400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr9:21057200-21057400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:21057400-21060600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:21059000-21059200	Enhancers	Primary T cells from cord blood	blood
15	chr9:21059200-21059400	Enhancers	Fetal Thymus	thymus
16	chr9:21059200-21059600	Weak transcription	Primary T cells from cord blood	blood
17	chr9:21059200-21062600	Enhancers	Dnd41	blood
18	chr9:21059400-21060600	Weak transcription	Fetal Thymus	thymus
19	chr9:21059600-21061200	Enhancers	Primary T cells from cord blood	blood
20	chr9:21059600-21061800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr9:21060000-21061800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:21060400-21061200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr9:21060400-21061800	Enhancers	Primary hematopoietic stem cells	blood
24	chr9:21060400-21061800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr9:21060400-21062400	Enhancers	NHDF-Ad	bronchial
26	chr9:21060600-21061400	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr9:21060600-21061400	Enhancers	Primary T cells fromperipheralblood	blood
28	chr9:21060600-21061400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr9:21060600-21061400	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr9:21060600-21061400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr9:21060600-21061400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr9:21060600-21061400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:21060600-21061400	Enhancers	Fetal Thymus	thymus
34	chr9:21060600-21061600	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr9:21060600-21061600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr9:21060600-21061600	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr9:21060600-21063000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:21060800-21061400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr9:21060800-21061600	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr9:21060800-21061600	Enhancers	GM12878-XiMat	blood
41	chr9:21061000-21061400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:21061000-21061600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr9:21061200-21061600	Flanking Active TSS	Primary T cells from cord blood	blood
44	chr9:21061200-21061600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr9:21061200-21061600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr9:21061400-21062400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr9:21061400-21063800	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr9:21061600-21062200	Enhancers	Primary T cells from cord blood	blood
49	chr9:21062400-21062600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr9:21062600-21069800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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