Variant report

Variant	nsv893572
Chromosome Location	chr9:94891778-94944778
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2028)
CpG islands
(count:366)
Chromatin interactive
region (count:80)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2028 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:94896337-94896492	K562	blood:	n/a	n/a
2	ARID3A	chr9:94900919-94901145	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:94909300-94909532	K562	blood:	n/a	n/a
4	ARID3A	chr9:94942313-94942427	K562	blood:	n/a	n/a
5	ARID3A	chr9:94901677-94901732	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:94902761-94902764	K562	blood:	n/a	n/a
7	ATF1	chr9:94909518-94909853	K562	blood:	n/a	n/a
8	ATF3	chr9:94943111-94943445	K562	blood:	n/a	n/a
9	ATF3	chr9:94943166-94943487	K562	blood:	n/a	n/a
10	ATF3	chr9:94896213-94896454	K562	blood:	n/a	n/a
11	ATF3	chr9:94909505-94909796	K562	blood:	n/a	n/a
12	BACH1	chr9:94900416-94900651	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:94896169-94896625	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:94943166-94943481	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr9:94909593-94909878	GM12878	blood:	n/a	chr9:94909709-94909720 chr9:94909710-94909720
16	BATF	chr9:94927786-94928028	GM12878	blood:	n/a	n/a
17	BATF	chr9:94927779-94928116	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:94909551-94909891	GM12878	blood:	n/a	n/a
19	BCLAF1	chr9:94902534-94902978	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:94916779-94916993	K562	blood:	n/a	n/a
21	BHLHE40	chr9:94942933-94943560	K562	blood:	n/a	n/a
22	BHLHE40	chr9:94896217-94896518	K562	blood:	n/a	n/a
23	BHLHE40	chr9:94900440-94900613	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:94910089-94910116	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:94900446-94901149	HepG2	liver:	n/a	n/a
26	BHLHE40	chr9:94896281-94896527	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:94909275-94910098	K562	blood:	n/a	n/a
28	BHLHE40	chr9:94902613-94902968	K562	blood:	n/a	n/a
29	BHLHE40	chr9:94900414-94900591	K562	blood:	n/a	n/a
30	BHLHE40	chr9:94909669-94909786	GM12878	blood:	n/a	n/a
31	BRCA1	chr9:94896280-94896529	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr9:94909221-94910068	K562	blood:	n/a	n/a
33	CBX3	chr9:94943809-94944283	K562	blood:	n/a	n/a
34	CBX3	chr9:94927353-94927571	K562	blood:	n/a	n/a
35	CBX3	chr9:94893300-94893666	K562	blood:	n/a	n/a
36	CBX3	chr9:94927288-94927657	K562	blood:	n/a	n/a
37	CBX3	chr9:94942797-94943657	K562	blood:	n/a	n/a
38	CBX3	chr9:94902536-94902959	K562	blood:	n/a	n/a
39	CCNT2	chr9:94933312-94933386	K562	blood:	n/a	n/a
40	CEBPB	chr9:94909344-94909851	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:94909522-94909833	K562	blood:	n/a	n/a
42	CEBPB	chr9:94900960-94901140	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:94937374-94937563	K562	blood:	n/a	n/a
44	CEBPB	chr9:94914008-94914678	MCF-7	breast:	n/a	chr9:94914193-94914210
45	CEBPB	chr9:94909616-94909718	K562	blood:	n/a	n/a
46	CEBPB	chr9:94909121-94909127	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr9:94900895-94901236	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:94943302-94943374	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:94909350-94909799	A549	lung:	n/a	n/a
50	CEBPB	chr9:94914022-94914600	IMR90	lung:	n/a	chr9:94914193-94914210

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:94903088-94903138	MCF-7	breast:	n/a
2	chr9:94903573-94903623	MCF10A-Er-Src	breast:	n/a
3	chr9:94902753-94902803	ProgFib	skin:	n/a
4	chr9:94902753-94902803	HMEC	breast:	n/a
5	chr9:94897483-94897533	NHBE	bronchial:	n/a
6	chr9:94897483-94897533	GM06990	blood:	n/a
7	chr9:94903088-94903138	HEK293	kidney:	embryo
8	chr9:94903088-94903138	HIPEpiC	eye:	n/a
9	chr9:94903573-94903623	ProgFib	skin:	n/a
10	chr9:94900583-94900633	Jurkat	blood:	n/a
11	chr9:94900583-94900633	LNCaP	prostate:	n/a
12	chr9:94903573-94903623	HEK293	kidney:	embryo
13	chr9:94903573-94903623	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:94903088-94903138	ECC-1	luminal epithelium:	n/a
15	chr9:94902753-94902803	NHBE	bronchial:	n/a
16	chr9:94903088-94903138	HepG2	liver:	n/a
17	chr9:94902753-94902803	BE2_C	brain:	n/a
18	chr9:94903088-94903138	HRCEpiC	kidney:	n/a
19	chr9:94897483-94897533	AG10803	skin:	n/a
20	chr9:94902753-94902803	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:94897483-94897533	RPTEC	kidney:	n/a
22	chr9:94897483-94897533	IMR90	lung:	fetal
23	chr9:94900583-94900633	MCF-7	breast:	n/a
24	chr9:94897483-94897533	NH-A	brain:	n/a
25	chr9:94902753-94902803	NB4	blood:	n/a
26	chr9:94903088-94903138	GM19239	blood:	n/a
27	chr9:94895189-94895239	AG04449	skin:	fetal
28	chr9:94897483-94897533	MCF-7	breast:	n/a
29	chr9:94895189-94895239	AoSMC	blood vessel:	n/a
30	chr9:94902753-94902803	Jurkat	blood:	n/a
31	chr9:94900583-94900633	PrEC	prostate:	n/a
32	chr9:94903088-94903138	HEEpiC	esophagus:	n/a
33	chr9:94903573-94903623	AG04449	skin:	fetal
34	chr9:94900583-94900633	HCT-116	colon:	n/a
35	chr9:94902753-94902803	HCT-116	colon:	n/a
36	chr9:94900583-94900633	T-47D	breast:	n/a
37	chr9:94900583-94900633	BE2_C	brain:	n/a
38	chr9:94903088-94903138	Caco-2	colon:	n/a
39	chr9:94900583-94900633	RPTEC	kidney:	n/a
40	chr9:94903088-94903138	AG04449	skin:	fetal
41	chr9:94902753-94902803	AG04450	lung:	fetal
42	chr9:94900583-94900633	K562	blood:	n/a
43	chr9:94903573-94903623	NHBE	bronchial:	n/a
44	chr9:94897483-94897533	ovcar-3	ovarian:	n/a
45	chr9:94902753-94902803	SK-N-SH_RA	brain:	n/a
46	chr9:94897483-94897533	Hela-S3	cervix:	n/a
47	chr9:94895189-94895239	HNPCEpiC	eye:	n/a
48	chr9:94903573-94903623	IMR90	lung:	fetal
49	chr9:94900583-94900633	NHBE	bronchial:	n/a
50	chr9:94903088-94903138	PFSK-1	brain:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:94902223..94905302-chr9:94908199..94910430,4	MCF-7	breast:
2	chr9:94903732..94905881-chr9:94913415..94915626,3	MCF-7	breast:
3	chr9:94909350..94911414-chr9:94915017..94917948,2	K562	blood:
4	chr9:94900325..94903739-chr9:94909399..94912070,4	MCF-7	breast:
5	chr8:82692841..82693496-chr9:94896066..94896862,2	MCF-7	breast:
6	chr9:94902503..94903236-chr9:95396725..95397397,2	MCF-7	breast:
7	chr9:94934989..94939332-chr9:94939467..94943300,4	MCF-7	breast:
8	chr9:94899950..94900862-chr9:95004789..95005404,2	MCF-7	breast:
9	chr9:94931746..94933333-chr9:94938554..94941076,2	MCF-7	breast:
10	chr9:94914353..94916544-chr9:94926663..94928953,2	K562	blood:
11	chr9:94907222..94909546-chr9:94910880..94913844,2	K562	blood:
12	chr9:94921403..94923643-chr9:94939810..94941774,2	MCF-7	breast:
13	chr9:94906006..94908675-chr9:94917827..94919493,2	MCF-7	breast:
14	chr9:94895102..94897917-chr9:95001636..95003511,2	K562	blood:
15	chr9:94920054..94922956-chr9:94923750..94925745,3	K562	blood:
16	chr9:94912447..94914532-chr9:94951103..94952987,2	MCF-7	breast:
17	chr9:94899946..94902668-chr9:94908231..94910049,3	K562	blood:
18	chr9:94907081..94909170-chr9:94913018..94916076,3	MCF-7	breast:
19	chr9:94896533..94899071-chr9:94912382..94914127,2	MCF-7	breast:
20	chr9:94900325..94903739-chr9:94909399..94912070,4	MCF-7	breast:
21	chr9:94895931..94896458-chr9:95396736..95397637,2	MCF-7	breast:
22	chr9:94899264..94900077-chr9:95004607..95005252,2	MCF-7	breast:
23	chr1:202153463..202154431-chr9:94896000..94897129,6	MCF-7	breast:
24	chr9:94938776..94941220-chr9:95002439..95005177,2	K562	blood:
25	chr9:94885307..94887334-chr9:94894826..94896515,2	MCF-7	breast:
26	chr9:94903732..94905881-chr9:94913415..94915626,3	MCF-7	breast:
27	chr9:94939871..94945930-chr9:94946587..94952427,7	K562	blood:
28	chr9:94872521..94875047-chr9:94923668..94925543,2	K562	blood:
29	chr9:94939916..94941677-chr9:94943459..94945410,2	K562	blood:
30	chr9:94921403..94923643-chr9:94939810..94941774,2	MCF-7	breast:
31	chr1:117477349..117478025-chr9:94902653..94903339,2	MCF-7	breast:
32	chr9:94923505..94925174-chr9:94927166..94928893,2	K562	blood:
33	chr9:94902342..94903195-chr9:95004476..95005483,4	MCF-7	breast:
34	chr9:94896262..94897893-chr9:95004270..95006052,2	K562	blood:
35	chr9:94902262..94903203-chr9:95396707..95397642,2	K562	blood:
36	chr9:94877231..94877871-chr9:94896353..94897283,2	MCF-7	breast:
37	chr9:94897533..94900717-chr9:94902765..94904749,3	MCF-7	breast:
38	chr9:94931746..94933333-chr9:94938554..94941076,2	MCF-7	breast:
39	chr9:94923018..94924668-chr9:95056057..95058529,2	K562	blood:
40	chr9:94897363..94901349-chr9:95056061..95059787,4	K562	blood:
41	chr9:94907081..94909170-chr9:94913018..94916076,3	MCF-7	breast:
42	chr9:94902180..94903465-chr9:95004247..95005390,7	MCF-7	breast:
43	chr9:94896533..94899071-chr9:94912382..94914127,2	MCF-7	breast:
44	chr9:94899508..94902437-chr9:95003923..95007845,5	MCF-7	breast:
45	chr9:94909662..94911780-chr9:94913646..94915674,2	K562	blood:
46	chr9:94907697..94909675-chr9:94998713..95001365,2	K562	blood:
47	chr9:94909200..94911052-chr9:95430848..95432803,2	K562	blood:
48	chr9:94902223..94905302-chr9:94908199..94910430,4	MCF-7	breast:
49	chr9:94931765..94935481-chr9:94937705..94941450,3	K562	blood:
50	chr9:94909662..94911780-chr9:94913646..94915674,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CENPP-3	chr9:94919969-94920155	ENSG00000225511
2	lnc-CENPP-3	chr9:94909994-94910064	XLOC_007458
3	lnc-CENPP-3	chr9:94910204-94910588	XLOC_007458
4	lnc-CENPP-3	chr9:94907167-94907313	NONHSAT133169
5	lnc-CENPP-3	chr9:94907167-94907301	NONHSAT133168
6	lnc-CENPP-3	chr9:94909446-94910419	NONHSAT133169
7	lnc-CENPP-3	chr9:94910204-94910588	XLOC_007458
8	lnc-CENPP-3	chr9:94914876-94914911	ENSG00000225511
9	lnc-CENPP-3	chr9:94915019-94915146	ENSG00000225511
10	lnc-SPTLC1-5	chr9:94921483-94921700	NONHSAT133179
11	lnc-CENPP-3	chr9:94907223-94907313	ENSG00000225511
12	lnc-CENPP-3	chr9:94910204-94910588	ENSG00000225511
13	lnc-CENPP-3	chr9:94906427-94906849	NONHSAT133169
14	lnc-SPTLC1-4	chr9:94908151-94908605	NONHSAT133172
15	lnc-CENPP-3	chr9:94904101-94904386	NONHSAT133168
16	lnc-CENPP-3	chr9:94918392-94918571	ENSG00000225511
17	lnc-CENPP-3	chr9:94909874-94909955	XLOC_007458
18	lnc-CENPP-3	chr9:94920383-94920492	ENSG00000225511
19	lnc-CENPP-9	chr9:94897025-94897245	NONHSAT133157
20	lnc-CENPP-3	chr9:94920616-94920770	ENSG00000225511
21	lnc-CENPP-9	chr9:94896483-94896529	NONHSAT133157

No data

Variant related genes	Relation type
ENSG00000238996	TF binding region
BEND3P2	TF binding region
ENSG00000236717	TF binding region
ENSG00000234537	TF binding region
LINC00475	TF binding region
ENSG00000238996	CpG island
BEND3P2	CpG island
ENSG00000236717	CpG island
ENSG00000234537	CpG island
LINC00475	CpG island
ENSG00000127080	chromatin interactions
ENSG00000090054	chromatin interactions
ENSG00000196305	chromatin interactions
ENSG00000198000	chromatin interactions
ENSG00000225511	chromatin interactions
ENSG00000238996	chromatin interactions
ENSG00000224809	chromatin interactions
ENSG00000240791	chromatin interactions
ENSG00000188312	chromatin interactions
ENSG00000227321	chromatin interactions
E2F3	miRNA target sites
CCND1	miRNA target sites
CCND2	miRNA target sites
MYCN	miRNA target sites

Extended variants
information (count: 2078 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10992241	chr9:94891778-94891779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561714939	chr9:94891910-94891911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187057567	chr9:94891972-94891973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190779732	chr9:94891975-94891976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75857610	chr9:94892091-94892092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150566248	chr9:94892092-94892093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76356132	chr9:94892095-94892096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539228331	chr9:94892133-94892134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139494919	chr9:94892206-94892207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566585263	chr9:94892208-94892209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181474597	chr9:94892228-94892229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555335987	chr9:94892231-94892232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573735026	chr9:94892267-94892268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538512669	chr9:94892282-94892283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145131709	chr9:94892338-94892339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs578210457	chr9:94892341-94892342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186058759	chr9:94892402-94892403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556170549	chr9:94892403-94892404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141668928	chr9:94892454-94892455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560672421	chr9:94892466-94892467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544916148	chr9:94892504-94892505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149205623	chr9:94892505-94892506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76731127	chr9:94892513-94892514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375864663	chr9:94892514-94892515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572972732	chr9:94892523-94892524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540371602	chr9:94892524-94892525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545373589	chr9:94892533-94892534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190071413	chr9:94892566-94892567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550571024	chr9:94892582-94892583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182394079	chr9:94892625-94892626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368063945	chr9:94892639-94892640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111889306	chr9:94892645-94892646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549826544	chr9:94892660-94892661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566374082	chr9:94892661-94892662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568117294	chr9:94892665-94892666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140907509	chr9:94892669-94892670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527668916	chr9:94892703-94892704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142386386	chr9:94892717-94892718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10739926	chr9:94892772-94892773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186573717	chr9:94892775-94892776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539389340	chr9:94892811-94892812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10992242	chr9:94892814-94892815	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs117269948	chr9:94892827-94892828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540309351	chr9:94892836-94892837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146735473	chr9:94892855-94892856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113817642	chr9:94892864-94892865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs28808581	chr9:94892873-94892874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28817656	chr9:94892874-94892875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59731126	chr9:94892935-94892936	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs190675563	chr9:94892949-94892950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94878200-94896400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:94894000-94896800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr9:94894800-94895000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:94894800-94895200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:94894800-94897000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
6	chr9:94895000-94895200	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr9:94895000-94900200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr9:94895200-94896200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr9:94895200-94896200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr9:94895800-94896000	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr9:94895800-94896200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr9:94895800-94896400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:94896000-94896200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr9:94896000-94896200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
15	chr9:94896000-94896200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr9:94896000-94896200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
17	chr9:94896000-94896200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr9:94896000-94896200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr9:94896000-94896200	Enhancers	Brain Angular Gyrus	brain
20	chr9:94896000-94896200	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr9:94896000-94896200	Enhancers	Brain Cingulate Gyrus	brain
22	chr9:94896000-94896200	Enhancers	Brain Substantia Nigra	brain
23	chr9:94896000-94896200	Enhancers	Colonic Mucosa	Colon
24	chr9:94896000-94896200	Bivalent Enhancer	Fetal Brain Male	brain
25	chr9:94896000-94896200	Enhancers	Fetal Kidney	kidney
26	chr9:94896000-94896200	Enhancers	Hela-S3	cervix
27	chr9:94896000-94896200	Flanking Bivalent TSS/Enh	HepG2	liver
28	chr9:94896000-94896400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr9:94896000-94896400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
30	chr9:94896000-94896400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:94896000-94896400	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr9:94896000-94896400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr9:94896000-94896400	Bivalent Enhancer	Adipose Nuclei	Adipose
34	chr9:94896000-94896400	Enhancers	Fetal Heart	heart
35	chr9:94896000-94896400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
36	chr9:94896000-94896400	Enhancers	NHDF-Ad	bronchial
37	chr9:94896000-94896600	Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr9:94896000-94896600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr9:94896000-94896600	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr9:94896000-94896600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
41	chr9:94896000-94896600	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr9:94896000-94896600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
43	chr9:94896000-94896600	Enhancers	Pancreas	Pancrea
44	chr9:94896000-94896600	Active TSS	A549	lung
45	chr9:94896000-94896600	Enhancers	Dnd41	blood
46	chr9:94896000-94896600	Enhancers	K562	blood
47	chr9:94896000-94896600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
48	chr9:94896000-94896800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:94896000-94896800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:94896000-94896800	Enhancers	Primary T helper cells PMA-I stimulated	--

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