Variant report

Variant	nsv892691
Chromosome Location	chr9:18519699-18805483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1240)
CpG islands
(count:611)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:3)

(count:1240 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:18705112-18705234	K562	blood:	n/a	n/a
2	ARID3A	chr9:18669020-18669356	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:18622195-18622391	HepG2	liver:	n/a	n/a
4	ATF2	chr9:18768932-18769740	GM12878	blood:	n/a	n/a
5	ATF2	chr9:18768817-18769760	GM12878	blood:	n/a	n/a
6	BACH1	chr9:18606813-18606827	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:18708496-18708726	H1-hESC	embryonic stem cell:	n/a	chr9:18708633-18708647
8	BATF	chr9:18768878-18769670	GM12878	blood:	n/a	n/a
9	BATF	chr9:18768943-18769625	GM12878	blood:	n/a	n/a
10	BCL11A	chr9:18768921-18769607	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:18768959-18769211	GM12878	blood:	n/a	n/a
12	BCL3	chr9:18768916-18769623	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:18791280-18791295	K562	blood:	n/a	n/a
14	BHLHE40	chr9:18768912-18769756	GM12878	blood:	n/a	n/a
15	BRCA1	chr9:18658837-18659489	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr9:18574188-18574199	GM12878	blood:	n/a	n/a
17	CEBPB	chr9:18699795-18700171	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:18658554-18659633	Hela-S3	cervix:	n/a	chr9:18659245-18659262
19	CEBPB	chr9:18756477-18756591	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr9:18596985-18597185	HepG2	liver:	n/a	chr9:18597079-18597090
21	CEBPB	chr9:18631140-18631424	IMR90	lung:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
22	CEBPB	chr9:18799545-18800030	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr9:18591842-18592151	A549	lung:	n/a	chr9:18591978-18591989
24	CEBPB	chr9:18798153-18798439	IMR90	lung:	n/a	n/a
25	CEBPB	chr9:18638458-18639249	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:18526744-18527111	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:18631227-18631419	K562	blood:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
28	CEBPB	chr9:18607910-18608198	HepG2	liver:	n/a	chr9:18608045-18608056
29	CEBPB	chr9:18544401-18544745	IMR90	lung:	n/a	chr9:18544557-18544570
30	CEBPB	chr9:18668962-18669337	MCF-7	breast:	n/a	n/a
31	CEBPB	chr9:18707184-18707437	IMR90	lung:	n/a	chr9:18707297-18707314
32	CEBPB	chr9:18756278-18756653	HepG2	liver:	n/a	chr9:18756457-18756468
33	CEBPB	chr9:18591830-18592160	HepG2	liver:	n/a	chr9:18591978-18591989
34	CEBPB	chr9:18756363-18756643	Hela-S3	cervix:	n/a	chr9:18756457-18756468
35	CEBPB	chr9:18785708-18785903	IMR90	lung:	n/a	chr9:18785873-18785884
36	CEBPB	chr9:18526755-18527079	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:18532530-18532635	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr9:18756385-18756534	HepG2	liver:	n/a	chr9:18756457-18756468
39	CEBPB	chr9:18631285-18631331	A549	lung:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
40	CEBPB	chr9:18526754-18527079	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:18668980-18669271	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr9:18526762-18527049	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:18580228-18580540	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr9:18756340-18756695	A549	lung:	n/a	chr9:18756457-18756468
45	CEBPB	chr9:18756230-18756707	IMR90	lung:	n/a	chr9:18756457-18756468
46	CEBPB	chr9:18544465-18544730	Hela-S3	cervix:	n/a	chr9:18544557-18544570
47	CEBPB	chr9:18632787-18632970	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:18591831-18592127	IMR90	lung:	n/a	chr9:18591978-18591989
49	CEBPB	chr9:18526773-18527003	A549	lung:	n/a	n/a
50	CEBPB	chr9:18631153-18631463	HepG2	liver:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18776340-18776390	HIPEpiC	eye:	n/a
2	chr9:18776340-18776390	HIPEpiC	eye:	n/a
3	chr9:18776340-18776390	RPTEC	kidney:	n/a
4	chr9:18706865-18706915	A549	lung:	n/a
5	chr9:18770966-18771016	SKMC	muscle:	n/a
6	chr9:18770966-18771016	U87	brain:	n/a
7	chr9:18706865-18706915	HCT-116	colon:	n/a
8	chr9:18706865-18706915	Hela-S3	cervix:	n/a
9	chr9:18776940-18776990	AG09319	gingival:	n/a
10	chr9:18770966-18771016	HRE	kidney:	n/a
11	chr9:18770966-18771016	Caco-2	colon:	n/a
12	chr9:18706865-18706915	AG10803	skin:	n/a
13	chr9:18776940-18776990	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:18777683-18777733	BJ	skin:	n/a
15	chr9:18727406-18727456	ovcar-3	ovarian:	n/a
16	chr9:18793879-18793929	HepG2	liver:	n/a
17	chr9:18706865-18706915	BJ	skin:	n/a
18	chr9:18777555-18777605	HEK293	kidney:	embryo
19	chr9:18776340-18776390	AG04450	lung:	fetal
20	chr9:18777683-18777733	NB4	blood:	n/a
21	chr9:18622331-18622381	T-47D	breast:	n/a
22	chr9:18727406-18727456	SKMC	muscle:	n/a
23	chr9:18776940-18776990	HCT-116	colon:	n/a
24	chr9:18793879-18793929	NB4	blood:	n/a
25	chr9:18727406-18727456	SK-N-SH_RA	brain:	n/a
26	chr9:18777555-18777605	HCT-116	colon:	n/a
27	chr9:18605667-18605717	ProgFib	skin:	n/a
28	chr9:18777555-18777605	Hela-S3	cervix:	n/a
29	chr9:18777683-18777733	HCPEpiC	choroid plexus:	n/a
30	chr9:18776340-18776390	HRCEpiC	kidney:	n/a
31	chr9:18776340-18776390	AG09309	skin:	n/a
32	chr9:18605667-18605717	GM19239	blood:	n/a
33	chr9:18776340-18776390	IMR90	lung:	fetal
34	chr9:18776940-18776990	Jurkat	blood:	n/a
35	chr9:18777555-18777605	T-47D	breast:	n/a
36	chr9:18727406-18727456	NT2-D1	testis:	n/a
37	chr9:18793879-18793929	HUVEC	blood vessel:	n/a
38	chr9:18776340-18776390	ovcar-3	ovarian:	n/a
39	chr9:18770966-18771016	HepG2	liver:	n/a
40	chr9:18776940-18776990	ovcar-3	ovarian:	n/a
41	chr9:18776940-18776990	GM06990	blood:	n/a
42	chr9:18770966-18771016	HMEC	breast:	n/a
43	chr9:18793879-18793929	HAEpiC	amniotic membrane:	n/a
44	chr9:18622331-18622381	AoSMC	blood vessel:	n/a
45	chr9:18776340-18776390	HCF	heart:	n/a
46	chr9:18776940-18776990	SK-N-SH_RA	brain:	n/a
47	chr9:18777683-18777733	HepG2	liver:	n/a
48	chr9:18777555-18777605	AG04450	lung:	fetal
49	chr9:18777555-18777605	NB4	blood:	n/a
50	chr9:18605667-18605717	CMK	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:18734493..18736072-chr9:18736528..18738186,2	MCF-7	breast:
2	chr9:18777312..18778984-chr9:18781193..18784128,2	K562	blood:
3	chr9:18254776..18255758-chr9:18790832..18791755,3	MCF-7	breast:
4	chr21:39358274..39359037-chr9:18704805..18705621,2	MCF-7	breast:
5	chr9:18762802..18765724-chr9:18766149..18769161,3	K562	blood:
6	chr9:18725510..18728390-chr9:18733590..18735848,2	MCF-7	breast:
7	chr9:18745157..18747160-chr9:18747921..18750231,2	MCF-7	breast:
8	chr9:18722180..18723810-chr9:18726997..18728852,2	K562	blood:
9	chr9:18745157..18747160-chr9:18747921..18750231,2	MCF-7	breast:
10	chr2:126575127..126575844-chr9:18665491..18666183,2	MCF-7	breast:
11	chr9:18769799..18772875-chr9:18776003..18779587,3	K562	blood:
12	chr9:18552353..18554750-chr9:18819699..18822182,2	MCF-7	breast:
13	chr9:18733967..18736858-chr9:18739933..18741976,3	MCF-7	breast:
14	chr9:18769799..18772875-chr9:18776003..18779587,3	K562	blood:
15	chr8:61562599..61565494-chr9:18702295..18704681,2	MCF-7	breast:
16	chr9:18662167..18665769-chr9:18669383..18672936,3	MCF-7	breast:
17	chr9:18791200..18791746-chr9:19457106..19458088,3	K562	blood:
18	chr9:18662167..18665769-chr9:18669383..18672936,3	MCF-7	breast:
19	chr9:18762802..18765724-chr9:18766149..18769161,3	K562	blood:
20	chr9:18733967..18736858-chr9:18739933..18741976,3	MCF-7	breast:
21	chr9:18725510..18728390-chr9:18733590..18735848,2	MCF-7	breast:
22	chr9:18705469..18707872-chr9:18709248..18712015,2	MCF-7	breast:
23	chr9:18722180..18723810-chr9:18726997..18728852,2	K562	blood:
24	chr9:18770497..18772251-chr9:18783540..18785289,2	K562	blood:
25	chr9:18777312..18778984-chr9:18781193..18784128,2	K562	blood:
26	chr9:18770497..18772251-chr9:18783540..18785289,2	K562	blood:
27	chr9:18734493..18736072-chr9:18736528..18738186,2	MCF-7	breast:
28	chr9:18377972..18379506-chr9:18518837..18521140,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM154A-3	chr9:18717972-18718524	NONHSAT130313
2	lnc-RRAGA-3	chr9:18651145-18651448	NONHSAT130312

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3152-5p	chr9:18573314-18573335	MIMAT0019207
hsa-miR-3152-3p	chr9:18573348-18573369	MIMAT0015025

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ADAMTSL1	hsa-miR-25-3p	chr9:18681248-18681269
2	ADAMTSL1	hsa-miR-132-3p	chr9:18684803-18684824
3	ADAMTSL1	hsa-miR-25-3p	chr9:18681336-18681357

Variant related genes	Relation type
RN7SKP258	TF binding region
ADAMTSL1	TF binding region
MIR3152	TF binding region
ENSG00000236857	TF binding region
RN7SKP258	CpG island
ADAMTSL1	CpG island
MIR3152	CpG island
ENSG00000236857	CpG island
ENSG00000178031	chromatin interactions

Extended variants
information (count: 13328 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:13328 , 50 per page) page: 1 2 3 4 5 6 7 ... 267

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1341061	chr9:18519699-18519700	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573625525	chr9:18519704-18519705	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187794930	chr9:18519708-18519709	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111898747	chr9:18519718-18519719	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10810976	chr9:18519730-18519731	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs574128242	chr9:18519767-18519768	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1341060	chr9:18519768-18519769	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs12554156	chr9:18519784-18519785	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559536202	chr9:18519801-18519802	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577281262	chr9:18519809-18519810	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184211901	chr9:18519814-18519815	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142283395	chr9:18519839-18519840	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs151238593	chr9:18519858-18519859	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548992411	chr9:18519860-18519861	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529989893	chr9:18519889-18519890	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189062543	chr9:18519936-18519937	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561166267	chr9:18519972-18519973	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192402210	chr9:18519996-18519997	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370379844	chr9:18520045-18520046	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549907905	chr9:18520074-18520075	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367864635	chr9:18520075-18520076	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185747199	chr9:18520092-18520093	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10963623	chr9:18520116-18520117	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs74545057	chr9:18520124-18520125	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534522500	chr9:18520130-18520131	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555804998	chr9:18520131-18520132	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189429495	chr9:18520198-18520199	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538068414	chr9:18520206-18520207	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12336626	chr9:18520260-18520261	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs116556358	chr9:18520283-18520284	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544696334	chr9:18520291-18520292	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575434833	chr9:18520305-18520306	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73644231	chr9:18520307-18520308	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571686017	chr9:18520371-18520372	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370194736	chr9:18520374-18520375	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542581205	chr9:18520395-18520396	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180728338	chr9:18520399-18520400	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531586803	chr9:18520452-18520453	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543298720	chr9:18520477-18520478	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565064080	chr9:18520528-18520529	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140397168	chr9:18520548-18520549	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150363220	chr9:18520578-18520579	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10963624	chr9:18520591-18520592	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs527698045	chr9:18520611-18520612	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138201620	chr9:18520645-18520646	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567870643	chr9:18520675-18520676	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7041523	chr9:18520679-18520680	Enhancers Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs556522876	chr9:18520687-18520688	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571494242	chr9:18520701-18520702	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7041646	chr9:18520705-18520706	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Ovarian cancer	19835627	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20841430	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2456 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18501600-18520400	Weak transcription	Fetal Stomach	stomach
2	chr9:18502800-18520400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr9:18506800-18519800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr9:18510600-18533000	Weak transcription	NHDF-Ad	bronchial
5	chr9:18513800-18520600	Weak transcription	NH-A	brain
6	chr9:18517400-18519800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:18519200-18521000	Enhancers	Osteobl	bone
8	chr9:18519200-18521400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:18519400-18533600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr9:18519600-18521200	Genic enhancers	HSMM	muscle
11	chr9:18519600-18521400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:18519800-18521000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr9:18519800-18521400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:18520000-18520800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:18520000-18521000	Enhancers	Fetal Lung	lung
16	chr9:18520400-18520800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr9:18520400-18520800	Enhancers	Fetal Muscle Leg	muscle
18	chr9:18520400-18520800	Enhancers	HSMMtube	muscle
19	chr9:18520400-18521200	Enhancers	Fetal Stomach	stomach
20	chr9:18520600-18520800	Enhancers	NH-A	brain
21	chr9:18520800-18533200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr9:18521000-18521800	Weak transcription	Osteobl	bone
23	chr9:18521000-18529000	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr9:18521200-18522400	Strong transcription	HSMM	muscle
25	chr9:18521400-18521800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:18521800-18522200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:18521800-18522400	Strong transcription	Osteobl	bone
28	chr9:18522200-18530400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:18522400-18529200	Weak transcription	HSMM	muscle
30	chr9:18522400-18533200	Weak transcription	Osteobl	bone
31	chr9:18526200-18527400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr9:18526800-18527400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr9:18526800-18527600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr9:18527000-18527400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr9:18527000-18527400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr9:18529000-18529600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr9:18529200-18529400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr9:18529200-18529400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:18529200-18530400	Strong transcription	HSMM	muscle
40	chr9:18529400-18531200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:18529600-18530800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr9:18529600-18533200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr9:18529600-18533200	Weak transcription	NHLF	lung
44	chr9:18529800-18534200	Weak transcription	HUVEC	blood vessel
45	chr9:18530400-18531600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr9:18530400-18531600	Genic enhancers	HSMM	muscle
47	chr9:18530800-18531600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:18530800-18531600	Enhancers	Fetal Heart	heart
49	chr9:18531000-18531200	Weak transcription	Aorta	Aorta
50	chr9:18531200-18531400	Enhancers	Aorta	Aorta

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