Variant report

Variant	nsv831491
Chromosome Location	chr9:794113-974142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1834)
CpG islands
(count:1954)
Chromatin interactive
region (count:88)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:893752-894467	GM12878	blood:	n/a	n/a
2	ATF2	chr9:859288-859680	GM12878	blood:	n/a	n/a
3	ATF2	chr9:880676-881163	GM12878	blood:	n/a	n/a
4	ATF2	chr9:859161-859692	GM12878	blood:	n/a	n/a
5	ATF2	chr9:893794-894511	GM12878	blood:	n/a	n/a
6	ATF2	chr9:840342-840725	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:880645-881171	GM12878	blood:	n/a	n/a
8	BACH1	chr9:971010-971040	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:908830-909208	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:972119-972583	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:801698-801802	H1-hESC	embryonic stem cell:	n/a	chr9:801716-801730
12	BACH1	chr9:919938-919953	K562	blood:	n/a	n/a
13	BACH1	chr9:971586-971900	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:969420-970114	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:841437-841715	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr9:800791-801012	GM12878	blood:	n/a	n/a
17	BATF	chr9:893792-894397	GM12878	blood:	n/a	n/a
18	BATF	chr9:903869-904086	GM12878	blood:	n/a	n/a
19	BATF	chr9:808690-808887	GM12878	blood:	n/a	n/a
20	BATF	chr9:847470-847844	GM12878	blood:	n/a	n/a
21	BATF	chr9:847504-847840	GM12878	blood:	n/a	n/a
22	BATF	chr9:893858-894326	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:840410-840568	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr9:859287-859598	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:903913-904168	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:880682-881185	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:893880-894376	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:899799-900118	GM12878	blood:	n/a	n/a
29	BCL11A	chr9:899421-899798	GM12878	blood:	n/a	n/a
30	BCL11A	chr9:880773-881159	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:808677-809119	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:899392-899596	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL11A	chr9:859277-859643	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:893909-894335	GM12878	blood:	n/a	n/a
35	BCL3	chr9:893869-894422	GM12878	blood:	n/a	n/a
36	BCL3	chr9:893884-894319	GM12878	blood:	n/a	n/a
37	BCLAF1	chr9:893713-894423	GM12878	blood:	n/a	n/a
38	BCLAF1	chr9:893770-894413	GM12878	blood:	n/a	n/a
39	BHLHE40	chr9:875266-875944	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:893926-894026	K562	blood:	n/a	n/a
41	BHLHE40	chr9:880679-881199	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:859004-859714	GM12878	blood:	n/a	n/a
43	BHLHE40	chr9:893810-894528	GM12878	blood:	n/a	n/a
44	BHLHE40	chr9:960866-961066	GM12878	blood:	n/a	n/a
45	BHLHE40	chr9:852632-852864	GM12878	blood:	n/a	n/a
46	BHLHE40	chr9:899445-900212	GM12878	blood:	n/a	n/a
47	BRCA1	chr9:893893-894341	GM12878	blood:	n/a	n/a
48	BRCA1	chr9:968034-968190	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr9:856522-856717	A549	lung:	n/a	n/a
50	CEBPB	chr9:935358-935835	MCF-7	breast:	n/a	n/a

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:973184-973234	AG04450	lung:	fetal
2	chr9:857563-857613	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:973184-973234	AG04450	lung:	fetal
4	chr9:857563-857613	HPAEpiC	pulmonary alveolar:	n/a
5	chr9:969544-969594	T-47D	breast:	n/a
6	chr9:841636-841686	NHBE	bronchial:	n/a
7	chr9:842799-842849	HRE	kidney:	n/a
8	chr9:841340-841390	AG10803	skin:	n/a
9	chr9:857563-857613	HEK293	kidney:	embryo
10	chr9:839126-839176	HMEC	breast:	n/a
11	chr9:899635-899685	HCM	heart:	n/a
12	chr9:842799-842849	HCPEpiC	choroid plexus:	n/a
13	chr9:842914-842964	NH-A	brain:	n/a
14	chr9:972622-972672	NB4	blood:	n/a
15	chr9:970379-970429	AG09309	skin:	n/a
16	chr9:839126-839176	HepG2	liver:	n/a
17	chr9:839126-839176	NT2-D1	testis:	n/a
18	chr9:969473-969523	HIPEpiC	eye:	n/a
19	chr9:843748-843798	AG04450	lung:	fetal
20	chr9:841559-841609	Hela-S3	cervix:	n/a
21	chr9:899635-899685	HNPCEpiC	eye:	n/a
22	chr9:839126-839176	BE2_C	brain:	n/a
23	chr9:970654-970704	AG04449	skin:	fetal
24	chr9:845427-845477	H1-hESC	embryonic stem cell:	embryo
25	chr9:842914-842964	K562	blood:	n/a
26	chr9:970379-970429	K562	blood:	n/a
27	chr9:970882-970932	Jurkat	blood:	n/a
28	chr9:970379-970429	AG04450	lung:	fetal
29	chr9:841340-841390	MCF10A-Er-Src	breast:	n/a
30	chr9:970605-970655	HEEpiC	esophagus:	n/a
31	chr9:839557-839607	SK-N-SH_RA	brain:	n/a
32	chr9:843179-843229	SAEC	small airway:	n/a
33	chr9:839557-839607	AoSMC	blood vessel:	n/a
34	chr9:970297-970347	AG04450	lung:	fetal
35	chr9:839557-839607	NHDF-neo	bronchial:	n/a
36	chr9:973198-973248	AG10803	skin:	n/a
37	chr9:841559-841609	HIPEpiC	eye:	n/a
38	chr9:841340-841390	HEK293	kidney:	embryo
39	chr9:970605-970655	IMR90	lung:	fetal
40	chr9:971480-971530	NB4	blood:	n/a
41	chr9:972622-972672	HCF	heart:	n/a
42	chr9:972622-972672	CMK	blood:	n/a
43	chr9:969544-969594	Caco-2	colon:	n/a
44	chr9:843748-843798	U87	brain:	n/a
45	chr9:841636-841686	HCM	heart:	n/a
46	chr9:841340-841390	MCF-7	breast:	n/a
47	chr9:841636-841686	PFSK-1	brain:	n/a
48	chr9:973198-973248	GM12892	blood:	n/a
49	chr9:973198-973248	HEK293	kidney:	embryo
50	chr9:841340-841390	GM12878	blood:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:893619..895667-chr9:1001274..1003528,2	MCF-7	breast:
2	chr9:879492..881659-chr9:881684..884926,3	MCF-7	breast:
3	chr9:875320..878036-chr9:881518..883087,2	MCF-7	breast:
4	chr9:347478..348338-chr9:806313..807172,2	MCF-7	breast:
5	chr17:56708820..56710571-chr9:890436..893377,2	MCF-7	breast:
6	chr9:968342..970313-chr9:973554..975096,2	K562	blood:
7	chr9:931185..932724-chr9:947067..948621,2	MCF-7	breast:
8	chr9:889496..890427-chr9:998557..999062,2	MCF-7	breast:
9	chr9:873202..875175-chr9:876431..878577,2	K562	blood:
10	chr9:923145..924947-chr9:928055..930388,2	MCF-7	breast:
11	chr9:893739..894732-chr9:1008819..1009733,5	MCF-7	breast:
12	chr9:891442..893609-chr9:898111..900604,2	MCF-7	breast:
13	chr9:826413..827016-chr9:1004866..1005745,2	MCF-7	breast:
14	chr9:968342..970313-chr9:973554..975096,2	K562	blood:
15	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
16	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
17	chr9:879356..881162-chr9:885762..888045,2	K562	blood:
18	chr9:846543..848941-chr9:858349..860587,2	K562	blood:
19	chr9:931185..932724-chr9:947067..948621,2	MCF-7	breast:
20	chr9:893937..894571-chr9:1000555..1001318,2	MCF-7	breast:
21	chr9:900039..901541-chr9:989164..991359,2	MCF-7	breast:
22	chr9:967263..969449-chr9:973261..974895,2	MCF-7	breast:
23	chr9:962191..965396-chr9:970150..972525,3	MCF-7	breast:
24	chr9:893903..894431-chr9:1004790..1005383,2	K562	blood:
25	chr9:937368..939632-chr9:940406..941967,2	MCF-7	breast:
26	chr9:879356..881162-chr9:885762..888045,2	K562	blood:
27	chr9:852085..854136-chr9:910104..912950,2	K562	blood:
28	chr9:846543..848941-chr9:858349..860587,2	K562	blood:
29	chr9:962191..965396-chr9:970150..972525,3	MCF-7	breast:
30	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
31	chr9:845876..848526-chr9:868544..871068,2	MCF-7	breast:
32	chr9:947744..949483-chr9:965915..968744,2	MCF-7	breast:
33	chr9:893523..894096-chr9:1008794..1009361,2	MCF-7	breast:
34	chr9:950930..953777-chr9:967112..968787,2	MCF-7	breast:
35	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
36	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
37	chr9:891599..892777-chr9:998523..999622,4	MCF-7	breast:
38	chr9:971648..973169-chr9:976261..977886,2	MCF-7	breast:
39	chr9:796752..799581-chr9:806597..809420,2	MCF-7	breast:
40	chr9:959751..962676-chr9:970259..973174,2	K562	blood:
41	chr9:887794..889918-chr9:1005357..1008295,2	MCF-7	breast:
42	chr9:893804..894399-chr9:1008894..1009774,3	K562	blood:
43	chr9:952441..954452-chr9:976112..977840,2	K562	blood:
44	chr9:953799..955412-chr9:960065..962028,2	MCF-7	breast:
45	chr9:829461..831177-chr9:832230..834782,2	MCF-7	breast:
46	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
47	chr9:843269..845393-chr9:851272..854140,2	MCF-7	breast:
48	chr9:959751..962676-chr9:970259..973174,2	K562	blood:
49	chr9:801986..804534-chr9:805350..807829,2	MCF-7	breast:
50	chr9:953799..955412-chr9:960065..962028,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-9	chr9:959154-959514	uc_247_-
2	lnc-DMRT3-2	chr9:964189-964410	uc_248_+
3	lnc-C9orf66-10	chr9:964189-964410	uc_248_-
4	lnc-DMRT3-3	chr9:959154-959514	uc_247_+

No data

Variant related genes	Relation type
DMRT3	TF binding region
DMRT1	TF binding region
DMRT3	CpG island
DMRT1	CpG island
ENSG00000212195	chromatin interactions
ENSG00000107104	chromatin interactions
ENSG00000064218	chromatin interactions
ENSG00000252991	chromatin interactions

Extended variants
information (count: 6019 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:6019 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549543627	chr9:794114-794115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562959646	chr9:794142-794143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377075500	chr9:794143-794144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187979645	chr9:794154-794155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78306724	chr9:794166-794167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534241588	chr9:794191-794192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548053828	chr9:794197-794198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566161165	chr9:794199-794200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577372967	chr9:794212-794213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535080040	chr9:794239-794240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs60707479	chr9:794249-794250	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs182003585	chr9:794254-794255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537503185	chr9:794314-794315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557692527	chr9:794334-794335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577749009	chr9:794338-794339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75525900	chr9:794361-794362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554029390	chr9:794374-794375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574121632	chr9:794383-794384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149985351	chr9:794401-794402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544206087	chr9:794402-794403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78082422	chr9:794403-794404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562823431	chr9:794452-794453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531864168	chr9:794456-794457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545449207	chr9:794498-794499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184628084	chr9:794511-794512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145145126	chr9:794564-794565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141308373	chr9:794567-794568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145036323	chr9:794611-794612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530291720	chr9:794664-794665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146811174	chr9:794704-794705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564006209	chr9:794715-794716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568488003	chr9:794721-794722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537575033	chr9:794732-794733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs16924003	chr9:794761-794762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs78098293	chr9:794773-794774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533978715	chr9:794786-794787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2370199	chr9:794813-794814	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs3084797	chr9:794816-794817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397839353	chr9:794820-794821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573985875	chr9:794851-794852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560041286	chr9:794883-794884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34512581	chr9:794884-794885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141037830	chr9:794904-794905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556612041	chr9:794952-794953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181795831	chr9:794977-794978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113286625	chr9:794985-794986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34813878	chr9:795022-795023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565377071	chr9:795050-795051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527921667	chr9:795058-795059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4740911	chr9:795065-795066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	21272361	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-small cell lung cancer	16651412	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:1164 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:792600-795800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:793400-798400	Weak transcription	HepG2	liver
3	chr9:794600-809600	Weak transcription	Right Atrium	heart
4	chr9:795800-796000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:796000-796200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:798400-799400	Enhancers	HepG2	liver
7	chr9:800400-801400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:800400-801400	Enhancers	HUVEC	blood vessel
9	chr9:800400-801600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr9:800400-802000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr9:800400-802400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr9:800600-800800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:800600-801400	Enhancers	NHEK	skin
14	chr9:800600-802800	Enhancers	NH-A	brain
15	chr9:801000-801400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:801000-801600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr9:801000-801800	Enhancers	Hela-S3	cervix
18	chr9:801000-802000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr9:801200-802400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr9:801200-802400	Enhancers	Fetal Kidney	kidney
21	chr9:801200-802400	Enhancers	Osteobl	bone
22	chr9:801400-801600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:801400-801600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr9:801400-802200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr9:801400-802400	Flanking Active TSS	NHEK	skin
26	chr9:801400-802800	Enhancers	HMEC	breast
27	chr9:801400-803600	Flanking Active TSS	HUVEC	blood vessel
28	chr9:801600-801800	Enhancers	Duodenum Mucosa	Duodenum
29	chr9:801600-802000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr9:801600-802000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr9:801600-802000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:801600-802200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr9:801600-802600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr9:801800-802200	Active TSS	Aorta	Aorta
35	chr9:801800-802400	Weak transcription	Hela-S3	cervix
36	chr9:802000-802400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr9:802000-802400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr9:802000-802400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr9:802000-802400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr9:802000-802400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr9:802000-802600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr9:802200-805000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr9:802400-802600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr9:802400-802600	Enhancers	Hela-S3	cervix
45	chr9:802400-802800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr9:802400-802800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr9:802400-802800	Enhancers	NHEK	skin
48	chr9:802400-803000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr9:802600-802800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:802600-805000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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