Variant report

Variant	nsv892629
Chromosome Location	chr9:15516375-15634326
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1536)
CpG islands
(count:488)
Chromatin interactive
region (count:25)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15552151-15552649	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15606729-15607013	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15552687-15552948	K562	blood:	n/a	n/a
4	ARID3A	chr9:15529836-15529927	K562	blood:	n/a	n/a
5	ATF1	chr9:15606159-15606277	K562	blood:	n/a	n/a
6	ATF2	chr9:15552023-15553562	H1-hESC	embryonic stem cell:	n/a	chr9:15552396-15552403
7	ATF2	chr9:15552934-15553370	GM12878	blood:	n/a	n/a
8	ATF2	chr9:15552105-15553502	GM12878	blood:	n/a	chr9:15552396-15552403
9	ATF2	chr9:15529514-15530431	GM12878	blood:	n/a	n/a
10	ATF2	chr9:15531390-15531836	GM12878	blood:	n/a	n/a
11	ATF2	chr9:15552008-15553342	H1-hESC	embryonic stem cell:	n/a	chr9:15552396-15552403
12	ATF2	chr9:15529444-15530413	GM12878	blood:	n/a	n/a
13	ATF3	chr9:15587162-15587411	K562	blood:	n/a	n/a
14	BACH1	chr9:15533280-15533522	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:15552248-15553824	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr9:15613003-15613305	GM12878	blood:	n/a	chr9:15613158-15613169
17	BATF	chr9:15531423-15531671	GM12878	blood:	n/a	n/a
18	BATF	chr9:15529561-15530461	GM12878	blood:	n/a	n/a
19	BATF	chr9:15612994-15613254	GM12878	blood:	n/a	chr9:15613158-15613169
20	BATF	chr9:15527023-15527263	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:15529515-15530437	GM12878	blood:	n/a	n/a
22	BCL11A	chr9:15529908-15530305	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:15529591-15529894	GM12878	blood:	n/a	n/a
24	BCL3	chr9:15529570-15530149	GM12878	blood:	n/a	n/a
25	BCL3	chr9:15529482-15530374	GM12878	blood:	n/a	n/a
26	BCLAF1	chr9:15552224-15553528	GM12878	blood:	n/a	chr9:15552861-15552874 chr9:15552858-15552871 chr9:15553084-15553093 chr9:15552986-15552999
27	BCLAF1	chr9:15529456-15530507	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:15552208-15553359	HepG2	liver:	n/a	n/a
29	BHLHE40	chr9:15529542-15530441	GM12878	blood:	n/a	n/a
30	BHLHE40	chr9:15531576-15531579	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:15553594-15553760	K562	blood:	n/a	n/a
32	BHLHE40	chr9:15552719-15553088	K562	blood:	n/a	n/a
33	BHLHE40	chr9:15552022-15553397	GM12878	blood:	n/a	n/a
34	BRCA1	chr9:15552718-15553410	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr9:15552681-15553468	GM12878	blood:	n/a	n/a
36	BRCA1	chr9:15552798-15553456	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr9:15553012-15553375	HepG2	liver:	n/a	n/a
38	BRCA1	chr9:15533324-15533607	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr9:15554639-15554686	GM12878	blood:	n/a	n/a
40	CBX3	chr9:15552616-15553168	K562	blood:	n/a	n/a
41	CCNT2	chr9:15553242-15553567	K562	blood:	n/a	n/a
42	CCNT2	chr9:15552710-15553034	K562	blood:	n/a	n/a
43	CEBPB	chr9:15543068-15543387	IMR90	lung:	n/a	n/a
44	CEBPB	chr9:15552145-15552651	A549	lung:	n/a	n/a
45	CEBPB	chr9:15550618-15550810	A549	lung:	n/a	chr9:15550693-15550704 chr9:15550673-15550686 chr9:15550695-15550704
46	CEBPB	chr9:15532813-15533531	H1-hESC	embryonic stem cell:	n/a	chr9:15533019-15533030 chr9:15532971-15532982
47	CEBPB	chr9:15552552-15553376	GM12878	blood:	n/a	n/a
48	CEBPB	chr9:15519057-15519305	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr9:15552214-15552605	K562	blood:	n/a	n/a
50	CEBPB	chr9:15528863-15529007	HepG2	liver:	n/a	chr9:15528955-15528966

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15553181-15553231	AoSMC	blood vessel:	n/a
2	chr9:15552606-15552656	T-47D	breast:	n/a
3	chr9:15553069-15553119	GM19239	blood:	n/a
4	chr9:15552606-15552656	BJ	skin:	n/a
5	chr9:15553286-15553336	PrEC	prostate:	n/a
6	chr9:15527817-15527867	HIPEpiC	eye:	n/a
7	chr9:15553451-15553501	LNCaP	prostate:	n/a
8	chr9:15553069-15553119	NHBE	bronchial:	n/a
9	chr9:15552606-15552656	AG04449	skin:	fetal
10	chr9:15552606-15552656	HepG2	liver:	n/a
11	chr9:15553069-15553119	SAEC	small airway:	n/a
12	chr9:15553060-15553110	RPTEC	kidney:	n/a
13	chr9:15553060-15553110	HCT-116	colon:	n/a
14	chr9:15553181-15553231	MCF-7	breast:	n/a
15	chr9:15553181-15553231	HRPEpiC	eye:	n/a
16	chr9:15553451-15553501	HIPEpiC	eye:	n/a
17	chr9:15527817-15527867	HAEpiC	amniotic membrane:	n/a
18	chr9:15553060-15553110	SKMC	muscle:	n/a
19	chr9:15553451-15553501	NH-A	brain:	n/a
20	chr9:15553060-15553110	SK-N-MC	brain:	n/a
21	chr9:15553451-15553501	HUVEC	blood vessel:	n/a
22	chr9:15552206-15552256	HUVEC	blood vessel:	n/a
23	chr9:15553286-15553336	SK-N-SH_RA	brain:	n/a
24	chr9:15552606-15552656	HUVEC	blood vessel:	n/a
25	chr9:15552606-15552656	PrEC	prostate:	n/a
26	chr9:15527817-15527867	AG09309	skin:	n/a
27	chr9:15553069-15553119	PFSK-1	brain:	n/a
28	chr9:15553069-15553119	HRE	kidney:	n/a
29	chr9:15553286-15553336	PANC-1	pancreas:	n/a
30	chr9:15553451-15553501	PrEC	prostate:	n/a
31	chr9:15527817-15527867	HMEC	breast:	n/a
32	chr9:15552206-15552256	AG04450	lung:	fetal
33	chr9:15553286-15553336	A549	lung:	n/a
34	chr9:15553069-15553119	AG04450	lung:	fetal
35	chr9:15553181-15553231	AG04449	skin:	fetal
36	chr9:15527817-15527867	HCT-116	colon:	n/a
37	chr9:15552206-15552256	HEK293	kidney:	embryo
38	chr9:15552206-15552256	NHBE	bronchial:	n/a
39	chr9:15553451-15553501	SK-N-SH_RA	brain:	n/a
40	chr9:15552206-15552256	H1-hESC	embryonic stem cell:	embryo
41	chr9:15552206-15552256	HCF	heart:	n/a
42	chr9:15553069-15553119	MCF-7	breast:	n/a
43	chr9:15553069-15553119	HEK293	kidney:	embryo
44	chr9:15553060-15553110	HCM	heart:	n/a
45	chr9:15552606-15552656	HRE	kidney:	n/a
46	chr9:15553451-15553501	HCT-116	colon:	n/a
47	chr9:15553181-15553231	GM12878	blood:	n/a
48	chr9:15553060-15553110	Hela-S3	cervix:	n/a
49	chr9:15553181-15553231	AG09309	skin:	n/a
50	chr9:15553181-15553231	SKMC	muscle:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:15510264..15513012-chr9:15513420..15518300,5	K562	blood:
2	chr9:15510875..15512396-chr9:15551516..15553319,2	MCF-7	breast:
3	chr9:15508603..15511423-chr9:15563063..15564927,2	MCF-7	breast:
4	chr9:15548082..15550677-chr9:15551279..15553386,2	MCF-7	breast:
5	chr9:15540944..15543831-chr9:15548082..15550784,2	MCF-7	breast:
6	chr3:5020895..5021614-chr9:15552897..15553484,2	Hela-S3	cervix:
7	chr9:15509655..15511884-chr9:15514283..15517212,3	MCF-7	breast:
8	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:
9	chr9:15551939..15552527-chr9:15606365..15606962,2	MCF-7	breast:
10	chr9:15511224..15513667-chr9:15516724..15518268,2	K562	blood:
11	chr9:15551939..15552527-chr9:15606365..15606962,2	MCF-7	breast:
12	chr9:15570769..15573187-chr9:15586351..15588425,2	MCF-7	breast:
13	chr9:15509144..15511285-chr9:15608383..15610950,2	MCF-7	breast:
14	chr9:15512114..15513693-chr9:15523609..15526046,2	MCF-7	breast:
15	chr9:15421567..15424446-chr9:15606338..15608598,2	MCF-7	breast:
16	chr11:61559649..61560247-chr9:15552431..15552962,2	Hela-S3	cervix:
17	chr9:15510403..15512119-chr9:15516919..15518617,2	MCF-7	breast:
18	chr9:15551543..15553297-chr9:15600119..15601625,2	MCF-7	breast:
19	chr9:15551936..15552629-chr9:15619996..15620642,2	MCF-7	breast:
20	chr9:15509318..15512022-chr9:15550389..15555494,9	MCF-7	breast:
21	chr9:15538062..15540509-chr9:15552565..15554442,2	MCF-7	breast:
22	chr9:15540944..15543831-chr9:15548082..15550784,2	MCF-7	breast:
23	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:
24	chr9:15551936..15552629-chr9:15619996..15620642,2	MCF-7	breast:
25	chr9:15540367..15542446-chr9:15551493..15554062,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSIP1-2	chr9:15525782-15526079	NONHSAT130270
2	lnc-SNAPC3-3	chr9:15563976-15564022	NONHSAT130275
3	lnc-C9orf93-3	chr9:15550639-15551154	NONHSAT130274
4	lnc-SNAPC3-4	chr9:15588353-15588613	NONHSAT130276
5	lnc-SNAPC3-3	chr9:15553289-15553604	NONHSAT130275

No data

Variant related genes	Relation type
FTH1P12	TF binding region
RN7SL98P	TF binding region
RNU6-246P	TF binding region
CCDC171	TF binding region
HMGN2P16	TF binding region
FTH1P12	CpG island
RN7SL98P	CpG island
RNU6-246P	CpG island
CCDC171	CpG island
HMGN2P16	CpG island
ENSG00000168496	chromatin interactions
ENSG00000231376	chromatin interactions
ENSG00000134107	chromatin interactions
ENSG00000207601	chromatin interactions
ENSG00000164985	chromatin interactions
ENSG00000164975	chromatin interactions
ENSG00000164989	chromatin interactions
ENSG00000134825	chromatin interactions

Extended variants
information (count: 6022 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6022 , 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	rs7857933	chr9:15516375-15516376	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140442806	chr9:15516397-15516398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541199614	chr9:15516438-15516439	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs10962050	chr9:15516443-15516444	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571147826	chr9:15516470-15516471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537144410	chr9:15516479-15516480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs60439308	chr9:15516494-15516495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75275124	chr9:15516524-15516525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370986734	chr9:15516526-15516527	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527332787	chr9:15516529-15516530	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs10962051	chr9:15516587-15516588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556733163	chr9:15516603-15516604	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182160350	chr9:15516631-15516632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567391190	chr9:15516711-15516712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537420927	chr9:15516768-15516769	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138183513	chr9:15516774-15516775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186321026	chr9:15516794-15516795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149512969	chr9:15516806-15516807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368223752	chr9:15516931-15516932	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs149748841	chr9:15516932-15516933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs55974827	chr9:15516955-15516956	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538432939	chr9:15516968-15516969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540056216	chr9:15516971-15516972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10962053	chr9:15517001-15517002	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573688421	chr9:15517014-15517015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75740972	chr9:15517015-15517016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561151345	chr9:15517065-15517066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs57849124	chr9:15517088-15517089	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs12006227	chr9:15517096-15517097	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs542403529	chr9:15517122-15517123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554747278	chr9:15517135-15517136	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576507403	chr9:15517136-15517137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543449786	chr9:15517161-15517162	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138651578	chr9:15517182-15517183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190717274	chr9:15517202-15517203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577571501	chr9:15517220-15517221	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374296692	chr9:15517270-15517271	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541748052	chr9:15517279-15517280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs553026028	chr9:15517286-15517287	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148550358	chr9:15517386-15517387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559952865	chr9:15517389-15517390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181684044	chr9:15517390-15517391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541780594	chr9:15517394-15517395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560817958	chr9:15517409-15517410	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73408340	chr9:15517434-15517435	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549473756	chr9:15517469-15517470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs533408263	chr9:15517489-15517490	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570916516	chr9:15517505-15517506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186024733	chr9:15517511-15517512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs149796744	chr9:15517543-15517544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15513400-15521800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:15513600-15516600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:15513600-15521400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:15513800-15521400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr9:15514600-15521200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr9:15521200-15521600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:15521200-15521800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr9:15521200-15522000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:15521400-15521800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr9:15521400-15523000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:15521800-15522000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:15521800-15522200	Enhancers	Primary hematopoietic stem cells	blood
13	chr9:15521800-15522400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr9:15521800-15522400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr9:15522000-15522600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr9:15522400-15522600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr9:15522600-15522800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr9:15523000-15528200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr9:15524400-15525800	Enhancers	HUVEC	blood vessel
20	chr9:15525000-15525400	Enhancers	Brain Angular Gyrus	brain
21	chr9:15528400-15528800	Enhancers	GM12878-XiMat	blood
22	chr9:15528800-15529000	Flanking Active TSS	GM12878-XiMat	blood
23	chr9:15529000-15529600	Enhancers	GM12878-XiMat	blood
24	chr9:15529600-15530200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr9:15529600-15530400	Flanking Active TSS	GM12878-XiMat	blood
26	chr9:15529800-15530200	Enhancers	Primary B cells from peripheral blood	blood
27	chr9:15529800-15530200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr9:15529800-15530200	Enhancers	Fetal Thymus	thymus
29	chr9:15530200-15532800	Weak transcription	Fetal Thymus	thymus
30	chr9:15530400-15533400	Enhancers	GM12878-XiMat	blood
31	chr9:15532400-15533400	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr9:15532600-15532800	Enhancers	Placenta	Placenta
33	chr9:15532600-15533000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr9:15532600-15533400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr9:15532800-15533000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr9:15532800-15533400	Enhancers	Primary T cells fromperipheralblood	blood
37	chr9:15532800-15533400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr9:15532800-15533400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr9:15532800-15533400	Flanking Active TSS	Placenta	Placenta
40	chr9:15532800-15533400	Enhancers	Fetal Thymus	thymus
41	chr9:15533200-15533400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr9:15535800-15536200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:15536200-15536400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr9:15541800-15542200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr9:15541800-15542400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr9:15541800-15542400	Enhancers	Fetal Kidney	kidney
47	chr9:15541800-15542400	Enhancers	Fetal Lung	lung
48	chr9:15541800-15542600	Enhancers	A549	lung
49	chr9:15542000-15543800	Enhancers	Fetal Stomach	stomach
50	chr9:15542200-15544000	Enhancers	Primary neutrophils fromperipheralblood	blood

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