Variant report

Variant	nsv1031340
Chromosome Location	chr9:15163004-15332769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1910)
CpG islands
(count:671)
Chromatin interactive
region (count:57)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1910 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15265977-15266099	K562	blood:	n/a	n/a
2	ARID3A	chr9:15306129-15306386	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15232084-15232341	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15307077-15307551	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:15277823-15278394	HepG2	liver:	n/a	chr9:15278078-15278094
6	ARID3A	chr9:15280121-15280547	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:15205864-15206291	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:15232148-15232279	K562	blood:	n/a	n/a
9	ARID3A	chr9:15211631-15211737	K562	blood:	n/a	n/a
10	ARID3A	chr9:15211512-15211813	HepG2	liver:	n/a	n/a
11	ATF1	chr9:15232104-15232252	K562	blood:	n/a	n/a
12	ATF1	chr9:15220876-15221098	K562	blood:	n/a	n/a
13	ATF1	chr9:15287263-15287635	K562	blood:	n/a	n/a
14	ATF1	chr9:15293783-15294043	K562	blood:	n/a	n/a
15	ATF1	chr9:15268609-15268879	K562	blood:	n/a	n/a
16	ATF1	chr9:15299673-15299858	K562	blood:	n/a	n/a
17	BACH1	chr9:15216138-15216193	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr9:15328555-15328874	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr9:15328520-15328827	K562	blood:	n/a	n/a
20	BACH1	chr9:15306339-15306925	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr9:15228358-15228733	GM12878	blood:	n/a	n/a
22	BATF	chr9:15228348-15228763	GM12878	blood:	n/a	n/a
23	BATF	chr9:15180159-15180457	GM12878	blood:	n/a	n/a
24	BATF	chr9:15306084-15306387	GM12878	blood:	n/a	n/a
25	BATF	chr9:15299577-15299867	GM12878	blood:	n/a	chr9:15299785-15299794
26	BCL3	chr9:15268317-15268573	GM12878	blood:	n/a	n/a
27	BCL3	chr9:15293395-15293760	GM12878	blood:	n/a	n/a
28	BCL3	chr9:15331480-15331831	GM12878	blood:	n/a	n/a
29	BCL3	chr9:15268365-15268698	GM12878	blood:	n/a	chr9:15268606-15268614
30	BCL3	chr9:15331510-15331929	GM12878	blood:	n/a	n/a
31	BCLAF1	chr9:15299556-15300027	GM12878	blood:	n/a	chr9:15299645-15299654
32	BHLHE40	chr9:15253812-15254120	HepG2	liver:	n/a	n/a
33	BHLHE40	chr9:15307178-15307437	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:15318021-15318086	K562	blood:	n/a	n/a
35	BHLHE40	chr9:15232167-15232259	K562	blood:	n/a	n/a
36	BHLHE40	chr9:15306190-15306323	K562	blood:	n/a	n/a
37	BHLHE40	chr9:15315454-15315624	K562	blood:	n/a	n/a
38	BHLHE40	chr9:15307159-15307687	K562	blood:	n/a	n/a
39	BRCA1	chr9:15307498-15307506	HepG2	liver:	n/a	n/a
40	BRCA1	chr9:15295906-15296187	GM12878	blood:	n/a	n/a
41	BRCA1	chr9:15299127-15299177	GM12878	blood:	n/a	n/a
42	CBX3	chr9:15323298-15323578	K562	blood:	n/a	n/a
43	CCNT2	chr9:15307181-15307674	K562	blood:	n/a	n/a
44	CEBPB	chr9:15305916-15306307	HepG2	liver:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
45	CEBPB	chr9:15307099-15307605	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:15305873-15306429	MCF-7	breast:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
47	CEBPB	chr9:15308517-15308964	IMR90	lung:	n/a	n/a
48	CEBPB	chr9:15305937-15306278	K562	blood:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
49	CEBPB	chr9:15243971-15244366	IMR90	lung:	n/a	n/a
50	CEBPB	chr9:15239698-15240120	HepG2	liver:	n/a	chr9:15239852-15239863 chr9:15239934-15239947

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15307376-15307426	RPTEC	kidney:	n/a
2	chr9:15232701-15232751	GM06990	blood:	n/a
3	chr9:15310979-15311029	Hela-S3	cervix:	n/a
4	chr9:15307873-15307923	HAEpiC	amniotic membrane:	n/a
5	chr9:15310979-15311029	GM12891	blood:	n/a
6	chr9:15232701-15232751	GM19239	blood:	n/a
7	chr9:15232867-15232917	SKMC	muscle:	n/a
8	chr9:15307376-15307426	AG09319	gingival:	n/a
9	chr9:15183958-15184008	H1-hESC	embryonic stem cell:	embryo
10	chr9:15305873-15305923	NH-A	brain:	n/a
11	chr9:15307376-15307426	AoSMC	blood vessel:	n/a
12	chr9:15232701-15232751	HepG2	liver:	n/a
13	chr9:15310979-15311029	GM19239	blood:	n/a
14	chr9:15307873-15307923	HepG2	liver:	n/a
15	chr9:15307873-15307923	GM12892	blood:	n/a
16	chr9:15232701-15232751	T-47D	breast:	n/a
17	chr9:15232867-15232917	LNCaP	prostate:	n/a
18	chr9:15232867-15232917	HIPEpiC	eye:	n/a
19	chr9:15310979-15311029	AG04450	lung:	fetal
20	chr9:15305873-15305923	PANC-1	pancreas:	n/a
21	chr9:15305873-15305923	Hela-S3	cervix:	n/a
22	chr9:15232867-15232917	BE2_C	brain:	n/a
23	chr9:15183958-15184008	HUVEC	blood vessel:	n/a
24	chr9:15305873-15305923	RPTEC	kidney:	n/a
25	chr9:15232701-15232751	HIPEpiC	eye:	n/a
26	chr9:15306337-15306387	GM19239	blood:	n/a
27	chr9:15183958-15184008	BJ	skin:	n/a
28	chr9:15306736-15306786	SK-N-SH	brain:	n/a
29	chr9:15307376-15307426	HepG2	liver:	n/a
30	chr9:15307376-15307426	NH-A	brain:	n/a
31	chr9:15310979-15311029	HRCEpiC	kidney:	n/a
32	chr9:15232014-15232064	Hela-S3	cervix:	n/a
33	chr9:15232014-15232064	HCT-116	colon:	n/a
34	chr9:15232867-15232917	NH-A	brain:	n/a
35	chr9:15310979-15311029	HCT-116	colon:	n/a
36	chr9:15232701-15232751	HNPCEpiC	eye:	n/a
37	chr9:15232014-15232064	AG04449	skin:	fetal
38	chr9:15307376-15307426	NT2-D1	testis:	n/a
39	chr9:15232867-15232917	SK-N-SH_RA	brain:	n/a
40	chr9:15232014-15232064	K562	blood:	n/a
41	chr9:15232014-15232064	MCF10A-Er-Src	breast:	n/a
42	chr9:15232867-15232917	HCF	heart:	n/a
43	chr9:15306337-15306387	NT2-D1	testis:	n/a
44	chr9:15232701-15232751	MCF-7	breast:	n/a
45	chr9:15310979-15311029	MCF10A-Er-Src	breast:	n/a
46	chr9:15232867-15232917	HUVEC	blood vessel:	n/a
47	chr9:15306337-15306387	Jurkat	blood:	n/a
48	chr9:15183958-15184008	ProgFib	skin:	n/a
49	chr9:15306337-15306387	Hela-S3	cervix:	n/a
50	chr9:15183958-15184008	K562	blood:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:15255737..15258644-chr9:15264903..15266791,2	MCF-7	breast:
2	chr9:15276823..15279769-chr9:15280291..15283089,2	MCF-7	breast:
3	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
4	chr9:15277443..15278337-chr9:15356714..15357650,2	MCF-7	breast:
5	chr9:15235538..15237507-chr9:117160951..117163548,2	MCF-7	breast:
6	chr9:15277682..15279519-chr9:15415467..15418240,3	MCF-7	breast:
7	chr9:15290133..15292362-chr9:15306023..15308672,3	MCF-7	breast:
8	chr9:15306135..15309581-chr9:15420818..15425516,6	MCF-7	breast:
9	chr9:15240990..15244433-chr9:15303373..15307437,3	MCF-7	breast:
10	chr9:15211245..15212139-chr9:15416585..15417547,5	MCF-7	breast:
11	chr9:15332011..15334775-chr9:15347128..15349228,2	MCF-7	breast:
12	chr9:15163944..15166887-chr9:15170115..15173415,3	K562	blood:
13	chr9:15305128..15307154-chr9:15417021..15419951,2	MCF-7	breast:
14	chr9:15180910..15183220-chr9:15227592..15229851,2	MCF-7	breast:
15	chr9:15277764..15278338-chr9:15416698..15417388,2	MCF-7	breast:
16	chr9:15306963..15308773-chr9:15314988..15318754,3	MCF-7	breast:
17	chr9:15273274..15274780-chr9:15289457..15291065,2	K562	blood:
18	chr9:15178556..15180974-chr9:15188192..15191171,2	MCF-7	breast:
19	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:
20	chr9:15273681..15276030-chr9:15420461..15422928,2	MCF-7	breast:
21	chr9:15253671..15255824-chr9:15255883..15257422,2	MCF-7	breast:
22	chr9:15275279..15280411-chr9:15305554..15308797,6	MCF-7	breast:
23	chr9:15281113..15283116-chr9:15421375..15424271,2	MCF-7	breast:
24	chr9:15238862..15241119-chr9:15243843..15246423,2	MCF-7	breast:
25	chr9:15276373..15278004-chr9:15420785..15422574,2	MCF-7	breast:
26	chr9:15211338..15211919-chr9:15356761..15357369,2	MCF-7	breast:
27	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
28	chr9:15285917..15290029-chr9:15305142..15308889,4	MCF-7	breast:
29	chr9:15163944..15166887-chr9:15170115..15173415,3	K562	blood:
30	chr9:15298942..15301605-chr9:15420446..15422025,2	MCF-7	breast:
31	chr9:15218010..15219971-chr9:15288500..15290967,2	MCF-7	breast:
32	chr9:15211153..15211795-chr9:15417051..15417568,2	K562	blood:
33	chr9:15278015..15280577-chr9:15305865..15308821,3	MCF-7	breast:
34	chr9:15238862..15241119-chr9:15243843..15246423,2	MCF-7	breast:
35	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:
36	chr9:15218010..15219971-chr9:15288500..15290967,2	MCF-7	breast:
37	chr9:15305088..15306661-chr9:15415103..15416933,2	MCF-7	breast:
38	chr9:15281310..15283636-chr9:15305576..15307784,3	MCF-7	breast:
39	chr9:15283042..15284645-chr9:15287369..15289731,2	K562	blood:
40	chr9:15242669..15244431-chr9:15422825..15424488,2	MCF-7	breast:
41	chr9:15293831..15297894-chr9:15305171..15308300,4	MCF-7	breast:
42	chr9:15211127..15212104-chr9:15232089..15232692,4	MCF-7	breast:
43	chr9:15283111..15284924-chr9:15291453..15293765,2	MCF-7	breast:
44	chr9:15206033..15209018-chr9:15421767..15424540,2	MCF-7	breast:
45	chr9:15283111..15284924-chr9:15291453..15293765,2	MCF-7	breast:
46	chr9:15273274..15274780-chr9:15289457..15291065,2	K562	blood:
47	chr9:15255737..15258644-chr9:15264903..15266791,2	MCF-7	breast:
48	chr15:94585854..94588550-chr9:15169410..15171976,2	K562	blood:
49	chr9:15283042..15284645-chr9:15287369..15289731,2	K562	blood:
50	chr9:15285882..15288246-chr9:15510557..15512091,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSIP1-3	chr9:15224358-15224503	NONHSAT130261
2	lnc-PSIP1-3	chr9:15225915-15226010	NONHSAT130261
3	lnc-PSIP1-3	chr9:15232230-15232442	NONHSAT130261
4	lnc-PSIP1-3	chr9:15214136-15214247	NONHSAT130261
5	lnc-TTC39B-1	chr9:15163622-15166031	NONHSAT130260

No data

Variant related genes	Relation type
TTC39B	TF binding region
TTC39B	CpG island
ENSG00000263817	chromatin interactions
ENSG00000164985	chromatin interactions
ENSG00000155158	chromatin interactions
ENSG00000164975	chromatin interactions

Extended variants
information (count: 8006 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:8006 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544467564	chr9:15163009-15163010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73646007	chr9:15163015-15163016	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs144655348	chr9:15163059-15163060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545586215	chr9:15163062-15163063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564244683	chr9:15163067-15163068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556769120	chr9:15163069-15163070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528189060	chr9:15163107-15163108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540459915	chr9:15163114-15163115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561851522	chr9:15163116-15163117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113888965	chr9:15163131-15163132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576715227	chr9:15163170-15163171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189431085	chr9:15163270-15163271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562746223	chr9:15163277-15163278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111679434	chr9:15163299-15163300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149189217	chr9:15163350-15163351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567002980	chr9:15163410-15163411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542305360	chr9:15163486-15163487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562203915	chr9:15163494-15163495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2800580	chr9:15163509-15163510	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs549181181	chr9:15163539-15163540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567491482	chr9:15163577-15163578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538152444	chr9:15163588-15163589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143398784	chr9:15163708-15163709	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs578178811	chr9:15163711-15163712	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs34707096	chr9:15163715-15163716	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs541443966	chr9:15163747-15163748	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs118148138	chr9:15163791-15163792	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs115082395	chr9:15163806-15163807	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs368045917	chr9:15163943-15163944	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs564210105	chr9:15163948-15163949	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs181752168	chr9:15164011-15164012	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs186883790	chr9:15164036-15164037	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs375119973	chr9:15164058-15164059	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs376286600	chr9:15164061-15164062	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs78855268	chr9:15164063-15164064	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs191325676	chr9:15164151-15164152	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs533074604	chr9:15164153-15164154	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs559912328	chr9:15164157-15164158	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs181172278	chr9:15164161-15164162	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs185962464	chr9:15164183-15164184	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs112813553	chr9:15164193-15164194	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs370822489	chr9:15164231-15164232	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs569471067	chr9:15164237-15164238	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs148364961	chr9:15164243-15164244	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs190874363	chr9:15164245-15164246	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs567528798	chr9:15164258-15164259	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs538086594	chr9:15164261-15164262	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs550102068	chr9:15164282-15164283	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs571933821	chr9:15164300-15164301	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs538946912	chr9:15164318-15164319	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
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
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	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
Intellectual disability	22102821	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
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:3487 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15155600-15181400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr9:15156200-15185400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr9:15156400-15171200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:15156600-15194200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr9:15156800-15169000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr9:15156800-15170200	Weak transcription	Esophagus	oesophagus
7	chr9:15156800-15170800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr9:15156800-15173800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr9:15156800-15175600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:15156800-15181600	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:15156800-15190400	Weak transcription	Brain Anterior Caudate	brain
12	chr9:15156800-15211800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr9:15158600-15168000	Weak transcription	Liver	Liver
14	chr9:15158800-15168000	Weak transcription	Aorta	Aorta
15	chr9:15159000-15166600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr9:15159000-15170800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr9:15159000-15177000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:15159000-15211200	Weak transcription	HMEC	breast
19	chr9:15159200-15168000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:15159200-15169000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:15159200-15205800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:15161000-15169000	Weak transcription	Fetal Intestine Large	intestine
23	chr9:15161200-15181400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr9:15161800-15163400	Enhancers	Fetal Stomach	stomach
25	chr9:15161800-15165800	Weak transcription	Primary T cells from cord blood	blood
26	chr9:15162000-15170200	Weak transcription	Ovary	ovary
27	chr9:15162000-15181600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:15162000-15183800	Weak transcription	Fetal Intestine Small	intestine
29	chr9:15162200-15163400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr9:15162200-15163400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:15162400-15163200	Enhancers	Fetal Kidney	kidney
32	chr9:15162600-15164400	Enhancers	Fetal Brain Male	brain
33	chr9:15162800-15168000	Weak transcription	Fetal Brain Female	brain
34	chr9:15162800-15193000	Weak transcription	Spleen	Spleen
35	chr9:15163000-15163200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr9:15163000-15163200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:15163000-15168000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr9:15163000-15175200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr9:15163000-15233000	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr9:15163200-15176000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr9:15163200-15185400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr9:15163200-15186800	Weak transcription	Fetal Kidney	kidney
43	chr9:15163400-15165200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:15163400-15179000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr9:15163400-15181400	Weak transcription	Fetal Stomach	stomach
46	chr9:15163800-15185200	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr9:15164000-15170600	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr9:15164200-15169000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr9:15164200-15170400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr9:15164400-15178400	Weak transcription	Fetal Brain Male	brain

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