Variant report

Variant	nsv982157
Chromosome Location	chr9:6712980-6727674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:244)
Chromatin interactive
region (count:17)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6714320-6714869	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6716174-6716454	HepG2	liver:	n/a	n/a
3	ATF2	chr9:6722727-6723186	GM12878	blood:	n/a	n/a
4	ATF2	chr9:6715890-6716329	GM12878	blood:	n/a	chr9:6716129-6716140
5	ATF2	chr9:6722741-6723673	GM12878	blood:	n/a	n/a
6	ATF2	chr9:6715844-6716527	GM12878	blood:	n/a	chr9:6716129-6716140
7	BATF	chr9:6723227-6723565	GM12878	blood:	n/a	n/a
8	BATF	chr9:6722711-6723091	GM12878	blood:	n/a	n/a
9	BCL11A	chr9:6723143-6723561	GM12878	blood:	n/a	n/a
10	BCL11A	chr9:6722699-6723018	GM12878	blood:	n/a	n/a
11	BCL3	chr9:6726224-6726550	GM12878	blood:	n/a	n/a
12	BCLAF1	chr9:6723281-6723701	GM12878	blood:	n/a	n/a
13	BCLAF1	chr9:6715879-6716683	GM12878	blood:	n/a	chr9:6716073-6716086 chr9:6716320-6716329 chr9:6716213-6716221
14	BHLHE40	chr9:6715913-6716873	GM12878	blood:	n/a	chr9:6716419-6716428 chr9:6716413-6716434 chr9:6716417-6716430 chr9:6716418-6716427 chr9:6716419-6716428
15	BHLHE40	chr9:6723433-6723669	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:6715802-6716907	HepG2	liver:	n/a	chr9:6716419-6716428 chr9:6716413-6716434 chr9:6716417-6716430 chr9:6716418-6716427 chr9:6716419-6716428
17	BRCA1	chr9:6716101-6716288	HepG2	liver:	n/a	n/a
18	BRCA1	chr9:6715949-6716503	GM12878	blood:	n/a	n/a
19	CEBPB	chr9:6714351-6714473	K562	blood:	n/a	n/a
20	CEBPB	chr9:6714282-6714602	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:6715249-6715433	HepG2	liver:	n/a	chr9:6715355-6715366
22	CEBPB	chr9:6715189-6715515	HepG2	liver:	n/a	chr9:6715355-6715366
23	CEBPB	chr9:6715155-6715503	MCF-7	breast:	n/a	chr9:6715355-6715366
24	CEBPB	chr9:6716043-6716801	GM12878	blood:	n/a	n/a
25	CEBPB	chr9:6715903-6716177	K562	blood:	n/a	chr9:6715961-6715972
26	CEBPB	chr9:6714003-6714628	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:6717843-6717863	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr9:6715856-6716204	HepG2	liver:	n/a	chr9:6715961-6715972
29	CEBPB	chr9:6715203-6715509	K562	blood:	n/a	chr9:6715355-6715366
30	CEBPB	chr9:6715701-6716620	MCF-7	breast:	n/a	chr9:6715961-6715972
31	CEBPB	chr9:6715714-6716369	MCF-7	breast:	n/a	chr9:6715961-6715972
32	CEBPB	chr9:6713984-6714106	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:6722676-6723593	GM12878	blood:	n/a	n/a
34	CEBPB	chr9:6715178-6715580	MCF-7	breast:	n/a	chr9:6715355-6715366
35	CEBPB	chr9:6715972-6716139	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:6715250-6715507	HepG2	liver:	n/a	chr9:6715355-6715366
37	CEBPD	chr9:6715839-6716389	HepG2	liver:	n/a	n/a
38	CEBPD	chr9:6715250-6715476	HepG2	liver:	n/a	n/a
39	CHD1	chr9:6715863-6716902	GM12878	blood:	n/a	chr9:6716397-6716407
40	CHD2	chr9:6716019-6716635	GM12878	blood:	n/a	chr9:6716397-6716407
41	CHD2	chr9:6716158-6716218	HepG2	liver:	n/a	n/a
42	CREB1	chr9:6715825-6716816	GM12878	blood:	n/a	chr9:6716128-6716141
43	CREB1	chr9:6715603-6716792	HepG2	liver:	n/a	chr9:6716128-6716141
44	CREB1	chr9:6715971-6716209	A549	lung:	n/a	chr9:6716128-6716141
45	CREB1	chr9:6715851-6716369	A549	lung:	n/a	chr9:6716128-6716141
46	CREB1	chr9:6715700-6716756	HepG2	liver:	n/a	chr9:6716128-6716141
47	CTCF	chr9:6716175-6716244	MCF-7	breast:	n/a	n/a
48	CTCF	chr9:6716700-6716850	A549	lung:	n/a	n/a
49	CTCF	chr9:6716157-6716565	GM12878	blood:	n/a	n/a
50	CTCF	chr9:6716287-6716306	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6715032-6715082	HL-60	blood:	n/a
2	chr9:6715032-6715082	T-47D	breast:	n/a
3	chr9:6715032-6715082	K562	blood:	n/a
4	chr9:6716007-6716057	BJ	skin:	n/a
5	chr9:6716007-6716057	SKMC	muscle:	n/a
6	chr9:6716480-6716530	HUVEC	blood vessel:	n/a
7	chr9:6716417-6716467	GM12892	blood:	n/a
8	chr9:6716480-6716530	AG04449	skin:	fetal
9	chr9:6716480-6716530	SKMC	muscle:	n/a
10	chr9:6716480-6716530	HRPEpiC	eye:	n/a
11	chr9:6716007-6716057	Caco-2	colon:	n/a
12	chr9:6716417-6716467	HCF	heart:	n/a
13	chr9:6716007-6716057	HRCEpiC	kidney:	n/a
14	chr9:6716007-6716057	CMK	blood:	n/a
15	chr9:6716007-6716057	PANC-1	pancreas:	n/a
16	chr9:6716480-6716530	HepG2	liver:	n/a
17	chr9:6715032-6715082	ECC-1	luminal epithelium:	n/a
18	chr9:6715032-6715082	ProgFib	skin:	n/a
19	chr9:6715032-6715082	ovcar-3	ovarian:	n/a
20	chr9:6716417-6716467	Hela-S3	cervix:	n/a
21	chr9:6715032-6715082	HRE	kidney:	n/a
22	chr9:6715032-6715082	Hepatocyte	liver:	n/a
23	chr9:6716417-6716467	LNCaP	prostate:	n/a
24	chr9:6716417-6716467	HepG2	liver:	n/a
25	chr9:6716417-6716467	HAEpiC	amniotic membrane:	n/a
26	chr9:6716480-6716530	AG09309	skin:	n/a
27	chr9:6716007-6716057	HL-60	blood:	n/a
28	chr9:6716417-6716467	NT2-D1	testis:	n/a
29	chr9:6716007-6716057	NH-A	brain:	n/a
30	chr9:6716417-6716467	NHDF-neo	bronchial:	n/a
31	chr9:6716007-6716057	SK-N-SH	brain:	n/a
32	chr9:6716417-6716467	SAEC	small airway:	n/a
33	chr9:6716417-6716467	NH-A	brain:	n/a
34	chr9:6716007-6716057	ECC-1	luminal epithelium:	n/a
35	chr9:6716417-6716467	HNPCEpiC	eye:	n/a
36	chr9:6716007-6716057	Hela-S3	cervix:	n/a
37	chr9:6716480-6716530	MCF-7	breast:	n/a
38	chr9:6716007-6716057	HCPEpiC	choroid plexus:	n/a
39	chr9:6715032-6715082	HCF	heart:	n/a
40	chr9:6715032-6715082	Jurkat	blood:	n/a
41	chr9:6715032-6715082	AG09319	gingival:	n/a
42	chr9:6716480-6716530	HNPCEpiC	eye:	n/a
43	chr9:6716480-6716530	PFSK-1	brain:	n/a
44	chr9:6716007-6716057	HUVEC	blood vessel:	n/a
45	chr9:6715032-6715082	H1-hESC	embryonic stem cell:	embryo
46	chr9:6715032-6715082	HAEpiC	amniotic membrane:	n/a
47	chr9:6716480-6716530	Hela-S3	cervix:	n/a
48	chr9:6716007-6716057	PFSK-1	brain:	n/a
49	chr9:6716480-6716530	AG10803	skin:	n/a
50	chr9:6716007-6716057	HEK293	kidney:	embryo

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6702847..6705575-chr9:6714326..6717882,7	MCF-7	breast:
2	chr9:6681423..6683704-chr9:6710640..6713020,2	MCF-7	breast:
3	chr9:6711589..6718151-chr9:6755774..6759657,12	MCF-7	breast:
4	chr9:6714844..6717578-chr9:6754943..6759087,4	MCF-7	breast:
5	chr9:6702551..6705246-chr9:6715022..6717677,6	MCF-7	breast:
6	chr9:6722888..6726785-chr9:6754807..6757177,3	K562	blood:
7	chr1:100503108..100504085-chr9:6716038..6716673,2	NB4	blood:
8	chr9:6713012..6714984-chr9:6718479..6720574,2	K562	blood:
9	chr9:6715258..6717463-chr9:6718537..6720528,2	MCF-7	breast:
10	chr2:32389334..32390859-chr9:6713099..6716031,2	MCF-7	breast:
11	chr14:51410899..51411829-chr9:6715512..6716484,2	HCT-116	colon:
12	chr9:6715258..6717463-chr9:6718537..6720528,2	MCF-7	breast:
13	chr9:6725196..6728190-chr9:6756447..6759048,2	MCF-7	breast:
14	chr9:6714309..6715981-chr9:6723655..6726584,2	MCF-7	breast:
15	chr9:6714309..6715981-chr9:6723655..6726584,2	MCF-7	breast:
16	chr21:41708247..41710641-chr9:6714300..6715810,2	MCF-7	breast:
17	chr9:6716286..6718322-chr9:6724305..6726614,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-1	chr9:6726503-6726619	ENSG00000225489.2
2	lnc-KDM4C-1	chr9:6716196-6716315	NONHSAT130158
3	lnc-KDM4C-1	chr9:6719071-6719154	ENSG00000225489.1
4	lnc-KDM4C-1	chr9:6719071-6719154	ENSG00000225489.2
5	lnc-KDM4C-1	chr9:6716183-6716616	NONHSAT130157
6	lnc-KDM4C-1	chr9:6717873-6719234	NONHSAT130157
7	lnc-KDM4C-1	chr9:6713527-6713630	NONHSAT130154
8	lnc-KDM4C-1	chr9:6723527-6723630	ENSG00000225489.1
9	lnc-KDM4C-1	chr9:6726946-6727438	ENSG00000225489.2
10	lnc-KDM4C-1	chr9:6716548-6716616	ENSG00000225489.1
11	lnc-KDM4C-1	chr9:6726503-6726619	ENSG00000225489.1
12	lnc-KDM4C-1	chr9:6716946-6717438	NONHSAT130156
13	lnc-KDM4C-1	chr9:6716503-6716619	NONHSAT130156
14	lnc-KDM4C-1	chr9:6717873-6718149	NONHSAT130158
15	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.1
16	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.1
17	lnc-KDM4C-1	chr9:6718965-6718981	ENSG00000225489.2
18	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.2
19	lnc-KDM4C-1	chr9:6719068-6719154	ENSG00000225489.1
20	lnc-KDM4C-1	chr9:6726946-6727438	ENSG00000225489.1
21	lnc-KDM4C-1	chr9:6717873-6718981	ENSG00000225489.1
22	lnc-KDM4C-1	chr9:6718810-6718981	ENSG00000225489.1
23	lnc-KDM4C-1	chr9:6719071-6719370	ENSG00000225489.1

No data

Variant related genes	Relation type
ENSG00000225489	TF binding region
KDM4C	TF binding region
ENSG00000225489	CpG island
KDM4C	CpG island
ENSG00000100504	chromatin interactions
ENSG00000225489	chromatin interactions
ENSG00000229611	chromatin interactions
ENSG00000156875	chromatin interactions
ENSG00000272716	chromatin interactions
ENSG00000107077	chromatin interactions

Extended variants
information (count: 806 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182088949	chr9:6712998-6712999	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs34862838	chr9:6713074-6713075	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs34087434	chr9:6713095-6713096	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs78130862	chr9:6713096-6713097	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541192040	chr9:6713099-6713100	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs150286241	chr9:6713110-6713111	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs137949397	chr9:6713111-6713112	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs536143112	chr9:6713133-6713134	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs13296663	chr9:6713143-6713144	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs10119869	chr9:6713145-6713146	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs531686171	chr9:6713158-6713159	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs150029365	chr9:6713166-6713167	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs376908142	chr9:6713167-6713168	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs550091341	chr9:6713211-6713212	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs35630035	chr9:6713219-6713220	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs149483106	chr9:6713224-6713225	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs10116086	chr9:6713237-6713238	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs10116109	chr9:6713300-6713301	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs144699192	chr9:6713305-6713306	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs537380741	chr9:6713306-6713307	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs545695141	chr9:6713374-6713375	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574219021	chr9:6713419-6713420	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs535032786	chr9:6713442-6713443	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs559141073	chr9:6713443-6713444	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138655922	chr9:6713446-6713447	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs10975793	chr9:6713448-6713449	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs367799290	chr9:6713460-6713461	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs187634456	chr9:6713479-6713480	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs34880774	chr9:6713482-6713483	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs570066762	chr9:6713483-6713484	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs191989242	chr9:6713486-6713487	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs547381631	chr9:6713524-6713525	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs10975794	chr9:6713527-6713528	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533096737	chr9:6713663-6713664	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs72697543	chr9:6713672-6713673	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs569940967	chr9:6713678-6713679	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs537267246	chr9:6713685-6713686	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs549128412	chr9:6713690-6713691	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs146249284	chr9:6713695-6713696	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs536337186	chr9:6713699-6713700	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs116245718	chr9:6713708-6713709	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs115010856	chr9:6713718-6713719	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs148470018	chr9:6713720-6713721	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs557469354	chr9:6713732-6713733	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs182715557	chr9:6713757-6713758	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs141793378	chr9:6713761-6713762	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs62568247	chr9:6713788-6713789	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs555233526	chr9:6713791-6713792	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs573884947	chr9:6713811-6713812	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs10975795	chr9:6713856-6713857	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	21346763	CNVD
early-passage human iPS cells	21368824	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6706400-6714200	Weak transcription	HepG2	liver
2	chr9:6711800-6715800	Weak transcription	NH-A	brain
3	chr9:6711800-6716400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr9:6712000-6715800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:6712200-6714400	Weak transcription	Fetal Intestine Large	intestine
6	chr9:6712200-6715800	Weak transcription	NHLF	lung
7	chr9:6712400-6715400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr9:6712600-6715400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:6712800-6715600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr9:6713600-6715600	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr9:6714200-6714600	Enhancers	HepG2	liver
12	chr9:6714400-6714600	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr9:6714400-6714600	Enhancers	Fetal Intestine Large	intestine
14	chr9:6714600-6714800	Enhancers	A549	lung
15	chr9:6714600-6714800	Flanking Active TSS	HepG2	liver
16	chr9:6714600-6715200	Enhancers	Liver	Liver
17	chr9:6714600-6715600	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr9:6714600-6715600	Weak transcription	Fetal Intestine Large	intestine
19	chr9:6714800-6715200	Enhancers	HepG2	liver
20	chr9:6715000-6715400	Enhancers	Pancreas	Pancrea
21	chr9:6715200-6715400	Flanking Active TSS	Liver	Liver
22	chr9:6715200-6715600	Enhancers	Placenta	Placenta
23	chr9:6715200-6715600	Enhancers	Stomach Mucosa	stomach
24	chr9:6715200-6715600	Enhancers	GM12878-XiMat	blood
25	chr9:6715200-6715800	Flanking Active TSS	HepG2	liver
26	chr9:6715400-6715600	Enhancers	Primary B cells from cord blood	blood
27	chr9:6715400-6715600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:6715400-6715600	Enhancers	Duodenum Mucosa	Duodenum
29	chr9:6715400-6715600	Enhancers	Fetal Intestine Small	intestine
30	chr9:6715400-6715600	Weak transcription	Lung	lung
31	chr9:6715400-6715600	Active TSS	Rectal Mucosa Donor 29	rectum
32	chr9:6715400-6715800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr9:6715400-6716000	Active TSS	Rectal Mucosa Donor 31	rectum
34	chr9:6715400-6716600	Active TSS	Liver	Liver
35	chr9:6715400-6717200	Active TSS	Pancreas	Pancrea
36	chr9:6715600-6715800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:6715600-6715800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr9:6715600-6715800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr9:6715600-6715800	Enhancers	Primary B cells from peripheral blood	blood
40	chr9:6715600-6715800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
41	chr9:6715600-6715800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr9:6715600-6715800	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr9:6715600-6715800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr9:6715600-6715800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr9:6715600-6715800	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr9:6715600-6715800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr9:6715600-6715800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr9:6715600-6715800	Enhancers	Esophagus	oesophagus
49	chr9:6715600-6715800	Flanking Active TSS	Fetal Intestine Large	intestine
50	chr9:6715600-6715800	Flanking Active TSS	Fetal Intestine Small	intestine

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