Variant report

Variant	nsv1029889
Chromosome Location	chr9:22118046-22161828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:104)
LncRNA
region (count:166)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:21994827..21996468-chr9:22135173..22136965,2	MCF-7	breast:
2	chr9:22110189..22115240-chr9:22131461..22136615,6	MCF-7	breast:
3	chr9:22117626..22120036-chr9:22123513..22125253,2	MCF-7	breast:
4	chr9:22007857..22010391-chr9:22129225..22130795,2	MCF-7	breast:
5	chr9:21993620..21995506-chr9:22141634..22143434,2	MCF-7	breast:
6	chr9:21801828..21804335-chr9:22143883..22147019,3	MCF-7	breast:
7	chr9:22132234..22134475-chr9:22237338..22238952,2	MCF-7	breast:
8	chr9:22103217..22103971-chr9:22136513..22137057,2	MCF-7	breast:
9	chr9:21993916..21996141-chr9:22137153..22139167,2	MCF-7	breast:
10	chr9:22118293..22119936-chr9:22134631..22137538,2	MCF-7	breast:
11	chr9:22123972..22126695-chr9:22237756..22240192,3	MCF-7	breast:
12	chr9:22144326..22149025-chr9:22156385..22160476,6	MCF-7	breast:
13	chr9:22113925..22116012-chr9:22117761..22119700,2	MCF-7	breast:
14	chr9:22006677..22008959-chr9:22118289..22120923,3	MCF-7	breast:
15	chr9:22085206..22088406-chr9:22135474..22138114,4	MCF-7	breast:
16	chr9:22155649..22159842-chr9:22208995..22214201,6	MCF-7	breast:
17	chr9:22136976..22138844-chr9:22139980..22142402,4	MCF-7	breast:
18	chr9:22146078..22148525-chr9:22216609..22218568,2	MCF-7	breast:
19	chr9:22117118..22121296-chr9:22132550..22137842,5	MCF-7	breast:
20	chr9:22118013..22119873-chr9:22212335..22214736,2	MCF-7	breast:
21	chr9:21802572..21804265-chr9:22133803..22136293,3	MCF-7	breast:
22	chr9:22134738..22136588-chr9:22241376..22243783,2	MCF-7	breast:
23	chr9:22139895..22144660-chr9:22144670..22148571,6	MCF-7	breast:
24	chr9:22139628..22142458-chr9:22215449..22217635,2	MCF-7	breast:
25	chr9:22137683..22139589-chr9:22148553..22150930,2	MCF-7	breast:
26	chr9:22131413..22138789-chr9:22206819..22215785,18	MCF-7	breast:
27	chr9:22133614..22136264-chr9:22136467..22138356,2	MCF-7	breast:
28	chr9:22134290..22136074-chr9:22199654..22202617,2	MCF-7	breast:
29	chr9:22139653..22143239-chr9:22209012..22211720,3	MCF-7	breast:
30	chr9:22117390..22119557-chr9:22241595..22244405,2	MCF-7	breast:
31	chr9:22128437..22130493-chr9:22144310..22146528,2	MCF-7	breast:
32	chr9:22008766..22011345-chr9:22133491..22135206,2	MCF-7	breast:
33	chr9:22124882..22127392-chr9:22128921..22130490,2	MCF-7	breast:
34	chr9:22137856..22139797-chr9:22230437..22233157,2	MCF-7	breast:
35	chr9:22123951..22126513-chr9:22237605..22240050,3	MCF-7	breast:
36	chr9:22117727..22120443-chr9:22236352..22239028,4	MCF-7	breast:
37	chr9:22139895..22144660-chr9:22144670..22148571,6	MCF-7	breast:
38	chr9:22131104..22132900-chr9:22134723..22136356,2	MCF-7	breast:
39	chr9:22080912..22082747-chr9:22118308..22120981,2	MCF-7	breast:
40	chr9:21810736..21813520-chr9:22127525..22130440,2	MCF-7	breast:
41	chr9:22134989..22139400-chr9:22207897..22213962,14	MCF-7	breast:
42	chr9:22123237..22127319-chr9:22132072..22135694,5	MCF-7	breast:
43	chr9:22117114..22119217-chr9:22236717..22238636,2	MCF-7	breast:
44	chr9:22116649..22120343-chr9:22129230..22133367,5	MCF-7	breast:
45	chr9:22124882..22127392-chr9:22128921..22130490,2	MCF-7	breast:
46	chr9:22102619..22105197-chr9:22133745..22136663,3	MCF-7	breast:
47	chr9:22106401..22111630-chr9:22133940..22138604,9	MCF-7	breast:
48	chr9:21801068..21804766-chr9:22124826..22127661,4	MCF-7	breast:
49	chr9:22102592..22104298-chr9:22138020..22139528,2	MCF-7	breast:
50	chr9:21813942..21814572-chr9:22119265..22120234,3	MCF-7	breast:

(count:166 , 50 per page) page: 1 2 3 4

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
2	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
3	lnc-MTAP-1	chr9:22118643-22118766	NONHSAT130423
4	lnc-MTAP-1	chr9:22120503-22121094	ENSG00000240498.2
5	lnc-MTAP-1	chr9:22120199-22120409	NR_003529
6	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
7	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
8	lnc-MTAP-1	chr9:22118643-22118766	ENSG00000240498.2
9	lnc-MTAP-1	chr9:22118643-22118766	ENSG00000240498.2
10	lnc-MTAP-1	chr9:22118643-22118766	ENSG00000240498.2
11	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
12	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
13	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
14	lnc-MTAP-1	chr9:22120199-22120409	NONHSAT130420
15	lnc-MTAP-1	chr9:22119497-22121116	NONHSAT130433
16	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
17	lnc-MTAP-1	chr9:22118643-22118766	ENSG00000240498.2
18	lnc-MTAP-1	chr9:22118643-22118701	ENSG00000240498.2
19	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
20	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
21	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
22	lnc-MTAP-1	chr9:22120503-22121093	NONHSAT130422
23	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
24	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
25	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
26	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
27	lnc-MTAP-1	chr9:22118643-22118766	NONHSAT130420
28	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
29	lnc-MTAP-1	chr9:22123175-22124037	NONHSAT130429
30	lnc-MTAP-1	chr9:22118643-22118766	ENSG00000240498.2
31	lnc-MTAP-1	chr9:22118643-22118701	ENSG00000240498.2
32	lnc-MTAP-1	chr9:22120199-22120409	NONHSAT130425
33	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
34	lnc-MTAP-1	chr9:22120199-22120409	NONHSAT130419
35	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
36	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
37	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
38	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
39	lnc-MTAP-1	chr9:22120199-22120409	ENSG00000240498.2
40	lnc-MTAP-1	chr9:22120503-22121096	ENSG00000240498.2
41	lnc-MTAP-1	chr9:22120503-22121093	NONHSAT130419
42	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
43	lnc-MTAP-1	chr9:22118643-22118766	ENSG00000240498.2
44	lnc-MTAP-1	chr9:22120503-22120645	ENSG00000240498.2
45	lnc-MTAP-1	chr9:22127325-22128078	NONHSAT130433
46	lnc-MTAP-1	chr9:22120503-22121096	NONHSAT130421
47	lnc-MTAP-1	chr9:22120503-22120571	ENSG00000240498.2
48	lnc-MTAP-1	chr9:22120503-22121093	NR_003529
49	lnc-MTAP-1	chr9:22118643-22118766	ENSG00000240498.2
50	lnc-MTAP-1	chr9:22120503-22121094	ENSG00000240498.2

No data

Variant related genes	Relation type
ENSG00000240498	chromatin interactions
ENSG00000264545	chromatin interactions
ENSG00000099810	chromatin interactions
ENSG00000147883	chromatin interactions
ENSG00000236921	chromatin interactions
ENSG00000229298	chromatin interactions
ENSG00000266446	chromatin interactions
ENSG00000147889	chromatin interactions
ADIPOR1	lncRNA
TMEM258	lncRNA
CDKN2B	lncRNA
CARD8	lncRNA
VAMP3	lncRNA

Extended variants
information (count: 2202 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:2202 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544499419	chr9:22118046-22118047	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs17761446	chr9:22118102-22118103	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533126670	chr9:22118103-22118104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs576249105	chr9:22118112-22118113	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs144724677	chr9:22118114-22118115	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs72654266	chr9:22118170-22118171	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs528982398	chr9:22118196-22118197	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs192660975	chr9:22118210-22118211	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs568812099	chr9:22118233-22118234	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs537468919	chr9:22118236-22118237	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs183419640	chr9:22118248-22118249	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs192295201	chr9:22118257-22118258	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs10627766	chr9:22118259-22118260	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs35899222	chr9:22118260-22118261	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs557995126	chr9:22118288-22118289	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs539719475	chr9:22118293-22118294	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs377179793	chr9:22118302-22118303	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs146731444	chr9:22118315-22118316	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs534076918	chr9:22118372-22118373	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs7854631	chr9:22118378-22118379	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs576515377	chr9:22118394-22118395	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs199788163	chr9:22118424-22118425	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs545341652	chr9:22118444-22118445	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs368228793	chr9:22118460-22118461	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs183385857	chr9:22118467-22118468	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs80292119	chr9:22118470-22118471	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs4977758	chr9:22118481-22118482	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs576479970	chr9:22118506-22118507	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs544118631	chr9:22118513-22118514	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs72654267	chr9:22118519-22118520	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs564333313	chr9:22118535-22118536	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs562010760	chr9:22118539-22118540	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs578002564	chr9:22118607-22118608	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs540209707	chr9:22118613-22118614	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs115811252	chr9:22118639-22118640	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs529104471	chr9:22118696-22118697	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
37	rs564348858	chr9:22118725-22118726	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs562459207	chr9:22118748-22118749	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
39	rs531166355	chr9:22118799-22118800	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs367717288	chr9:22118805-22118806	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs72654268	chr9:22118819-22118820	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs188068805	chr9:22118864-22118865	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs4977759	chr9:22118885-22118886	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs140375388	chr9:22118895-22118896	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs371579649	chr9:22118949-22118950	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs534210633	chr9:22118958-22118959	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs547812761	chr9:22118964-22118965	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs528272967	chr9:22118984-22118985	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs567828288	chr9:22119001-22119002	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs536470693	chr9:22119009-22119010	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:160)

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
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	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Cancer	20581869	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Barrett''s syndrome	19417022	CNVD
Cancer	20164920	CNVD
Breast cancer	17142309	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung adenocarcinoma	17982442	CNVD
Acute myeloid leukemia	21251322	CNVD
Burkitt''s lymphoma	19759907	CNVD
Oral cancer	21386901	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22097800-22122400	Weak transcription	Dnd41	blood
2	chr9:22113400-22119800	Weak transcription	Small Intestine	intestine
3	chr9:22115000-22119600	Enhancers	NHLF	lung
4	chr9:22116200-22119600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:22116400-22119800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:22116600-22118200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:22116600-22118400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr9:22116600-22118400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:22116600-22119000	Enhancers	NHDF-Ad	bronchial
10	chr9:22116600-22119400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:22116600-22119400	Enhancers	HSMM	muscle
12	chr9:22116600-22119600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:22116600-22119800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:22116600-22119800	Enhancers	Osteobl	bone
15	chr9:22116600-22120400	Enhancers	Fetal Intestine Small	intestine
16	chr9:22116800-22119000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr9:22116800-22119000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr9:22116800-22119600	Enhancers	Muscle Satellite Cultured Cells	--
19	chr9:22117000-22118600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr9:22117200-22118200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:22117200-22118400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr9:22117200-22118800	Enhancers	HepG2	liver
23	chr9:22117200-22119000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr9:22117200-22119000	Enhancers	HSMMtube	muscle
25	chr9:22117200-22119600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:22117200-22119800	Enhancers	NHEK	skin
27	chr9:22117200-22120400	Enhancers	Fetal Intestine Large	intestine
28	chr9:22117400-22118200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr9:22117400-22118200	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr9:22117400-22118200	Enhancers	Esophagus	oesophagus
31	chr9:22117400-22118200	Enhancers	Ovary	ovary
32	chr9:22117400-22118200	Bivalent Enhancer	Pancreas	Pancrea
33	chr9:22117400-22118400	Enhancers	Colonic Mucosa	Colon
34	chr9:22117400-22118600	Flanking Active TSS	Hela-S3	cervix
35	chr9:22117400-22119200	Enhancers	Placenta Amnion	Placenta Amnion
36	chr9:22117400-22119400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr9:22117400-22119800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr9:22117400-22120000	Enhancers	Stomach Mucosa	stomach
39	chr9:22117600-22118200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr9:22117600-22118200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr9:22117600-22118200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr9:22117600-22118200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr9:22117600-22118200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr9:22117600-22118200	Enhancers	Gastric	stomach
45	chr9:22117600-22118200	Enhancers	Left Ventricle	heart
46	chr9:22117600-22118200	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr9:22117600-22118200	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr9:22117600-22118200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
49	chr9:22117600-22118400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr9:22117600-22118400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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