Variant report

Variant	nsv1030626
Chromosome Location	chr9:14786215-14853681
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:14797561-14797747	K562	blood:	n/a	n/a
2	ATF3	chr9:14846813-14847157	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr9:14812818-14813170	GM12878	blood:	n/a	n/a
4	BHLHE40	chr9:14822708-14823063	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:14831736-14831957	K562	blood:	n/a	n/a
6	CEBPB	chr9:14799090-14799366	MCF-7	breast:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
7	CEBPB	chr9:14799051-14799431	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
8	CEBPB	chr9:14799044-14799407	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
9	CEBPB	chr9:14799112-14799348	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
10	CEBPB	chr9:14799070-14799407	IMR90	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
11	CEBPB	chr9:14799137-14799326	Hela-S3	cervix:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
12	CEBPB	chr9:14799109-14799362	H1-hESC	embryonic stem cell:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
13	CEBPB	chr9:14799087-14799406	A549	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
14	CEBPB	chr9:14799060-14799419	K562	blood:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
15	CEBPB	chr9:14799005-14799390	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
16	CEBPB	chr9:14827792-14827904	IMR90	lung:	n/a	chr9:14827827-14827838
17	CEBPB	chr9:14827709-14827960	HepG2	liver:	n/a	chr9:14827827-14827838
18	CEBPD	chr9:14799130-14799332	HepG2	liver:	n/a	n/a
19	CHD2	chr9:14846857-14847057	HepG2	liver:	n/a	n/a
20	CHD2	chr9:14846832-14847123	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr9:14818253-14818267	GM12878	blood:	n/a	n/a
22	CREB1	chr9:14846723-14847119	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr9:14831931-14832025	K562	blood:	n/a	n/a
24	CTCF	chr9:14846880-14847030	GM06990	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
25	CTCF	chr9:14846900-14847050	NHEK	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
26	CTCF	chr9:14788040-14788190	GM06990	blood:	n/a	n/a
27	CTCF	chr9:14846860-14847010	GM12870	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
28	CTCF	chr9:14846799-14847116	GM12878	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
29	CTCF	chr9:14831900-14832050	AG09319	gingival:	n/a	n/a
30	CTCF	chr9:14846880-14847030	GM12870	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
31	CTCF	chr9:14846838-14847067	LNCaP	prostate:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
32	CTCF	chr9:14846761-14847136	ECC-1	luminal epithelium:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
33	CTCF	chr9:14846880-14847030	GM12875	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
34	CTCF	chr9:14847245-14847309	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr9:14851051-14851083	Fibrobl	skin:	n/a	n/a
36	CTCF	chr9:14846860-14847010	K562	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
37	CTCF	chr9:14846860-14847010	Caco-2	colon:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
38	CTCF	chr9:14846823-14847039	A549	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
39	CTCF	chr9:14846793-14847113	A549	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
40	CTCF	chr9:14846900-14847050	SK-N-SH_RA	brain:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
41	CTCF	chr9:14846751-14847075	K562	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
42	CTCF	chr9:14846880-14847030	Hela-S3	cervix:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
43	CTCF	chr9:14847640-14847790	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr9:14846880-14847030	GM12871	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
45	CTCF	chr9:14846688-14847074	HCT-116	colon:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
46	CTCF	chr9:14846745-14847152	H1-hESC	embryonic stem cell:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
47	CTCF	chr9:14847198-14847287	GM12878	blood:	n/a	n/a
48	CTCF	chr9:14846631-14847328	SK-N-SH	brain:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
49	CTCF	chr9:14846900-14847050	AG04449	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
50	CTCF	chr9:14846765-14847137	SK-N-SH_RA	brain:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14838752-14838802	HCT-116	colon:	n/a
2	chr9:14838752-14838802	HCT-116	colon:	n/a
3	chr9:14838752-14838802	HEEpiC	esophagus:	n/a
4	chr9:14838752-14838802	HNPCEpiC	eye:	n/a
5	chr9:14838752-14838802	A549	lung:	n/a
6	chr9:14838752-14838802	HEK293	kidney:	embryo
7	chr9:14838752-14838802	SK-N-MC	brain:	n/a
8	chr9:14838752-14838802	LNCaP	prostate:	n/a
9	chr9:14838752-14838802	Jurkat	blood:	n/a
10	chr9:14838752-14838802	GM19239	blood:	n/a
11	chr9:14838752-14838802	HRCEpiC	kidney:	n/a
12	chr9:14838752-14838802	AG10803	skin:	n/a
13	chr9:14838752-14838802	HMEC	breast:	n/a
14	chr9:14838752-14838802	AG09309	skin:	n/a
15	chr9:14838752-14838802	HL-60	blood:	n/a
16	chr9:14838752-14838802	PANC-1	pancreas:	n/a
17	chr9:14838752-14838802	T-47D	breast:	n/a
18	chr9:14838752-14838802	SK-N-SH	brain:	n/a
19	chr9:14838752-14838802	H1-hESC	embryonic stem cell:	embryo
20	chr9:14838752-14838802	ovcar-3	ovarian:	n/a
21	chr9:14838752-14838802	HepG2	liver:	n/a
22	chr9:14838752-14838802	NH-A	brain:	n/a
23	chr9:14838752-14838802	IMR90	lung:	fetal
24	chr9:14838752-14838802	AG09319	gingival:	n/a
25	chr9:14838752-14838802	HIPEpiC	eye:	n/a
26	chr9:14838752-14838802	U87	brain:	n/a
27	chr9:14838752-14838802	ProgFib	skin:	n/a
28	chr9:14838752-14838802	NHBE	bronchial:	n/a
29	chr9:14838752-14838802	SK-N-SH_RA	brain:	n/a
30	chr9:14838752-14838802	BJ	skin:	n/a
31	chr9:14838752-14838802	GM12878	blood:	n/a
32	chr9:14838752-14838802	Hela-S3	cervix:	n/a
33	chr9:14838752-14838802	Hepatocyte	liver:	n/a
34	chr9:14838752-14838802	MCF-7	breast:	n/a
35	chr9:14838752-14838802	GM12892	blood:	n/a
36	chr9:14838752-14838802	HUVEC	blood vessel:	n/a
37	chr9:14838752-14838802	NB4	blood:	n/a
38	chr9:14838752-14838802	AG04450	lung:	fetal
39	chr9:14838752-14838802	PFSK-1	brain:	n/a
40	chr9:14838752-14838802	CMK	blood:	n/a
41	chr9:14838752-14838802	GM06990	blood:	n/a
42	chr9:14838752-14838802	PrEC	prostate:	n/a
43	chr9:14838752-14838802	HCPEpiC	choroid plexus:	n/a
44	chr9:14838752-14838802	Caco-2	colon:	n/a
45	chr9:14838752-14838802	BE2_C	brain:	n/a
46	chr9:14838752-14838802	ECC-1	luminal epithelium:	n/a
47	chr9:14838752-14838802	NHDF-neo	bronchial:	n/a
48	chr9:14838752-14838802	MCF10A-Er-Src	breast:	n/a
49	chr9:14838752-14838802	HAEpiC	amniotic membrane:	n/a
50	chr9:14838752-14838802	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
2	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
3	chr9:14785127..14787393-chr9:14791653..14793787,2	MCF-7	breast:
4	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
5	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
6	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
7	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
8	chr4:48089025..48089740-chr9:14788684..14789184,2	MCF-7	breast:
9	chr9:14846510..14847037-chr9:15142689..15143560,2	MCF-7	breast:
10	chr9:14691985..14694492-chr9:14845348..14847282,2	MCF-7	breast:
11	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:

Variant related genes	Relation type
RNU6-1260P	TF binding region
FREM1	TF binding region
RNU6-1260P	CpG island
FREM1	CpG island
ENSG00000251960	chromatin interactions
ENSG00000164946	chromatin interactions
ENSG00000175893	chromatin interactions

Extended variants
information (count: 3431 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3431 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141075534	chr9:14786222-14786223	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs150193952	chr9:14786241-14786242	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs191587501	chr9:14786242-14786243	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs36103644	chr9:14786337-14786338	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs34003527	chr9:14786338-14786339	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10810241	chr9:14786401-14786402	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571769841	chr9:14786403-14786404	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs183725625	chr9:14786417-14786418	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188900335	chr9:14786418-14786419	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566172085	chr9:14786475-14786476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541542754	chr9:14786492-14786493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536925720	chr9:14786655-14786656	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs193228220	chr9:14786699-14786700	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs76904131	chr9:14786700-14786701	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs57207087	chr9:14786703-14786704	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs555788891	chr9:14786770-14786771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577657669	chr9:14786774-14786775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544809627	chr9:14786782-14786783	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560273420	chr9:14786799-14786800	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572168743	chr9:14786832-14786833	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542906747	chr9:14786859-14786860	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs76853298	chr9:14786862-14786863	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs530679119	chr9:14786873-14786874	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531688543	chr9:14786878-14786879	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185240623	chr9:14786881-14786882	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs72711305	chr9:14786887-14786888	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs532618712	chr9:14786891-14786892	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs547599859	chr9:14786896-14786897	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs566232122	chr9:14786900-14786901	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141940245	chr9:14786905-14786906	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529205315	chr9:14786913-14786914	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs570012405	chr9:14786921-14786922	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12685522	chr9:14786962-14786963	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs78651545	chr9:14786981-14786982	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577593773	chr9:14787012-14787013	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538698294	chr9:14787014-14787015	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs553600524	chr9:14787019-14787020	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs190088381	chr9:14787022-14787023	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs181282545	chr9:14787046-14787047	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs376784032	chr9:14787049-14787050	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs528126641	chr9:14787085-14787086	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561111737	chr9:14787088-14787089	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1546135	chr9:14787156-14787157	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs72711307	chr9:14787175-14787176	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184144778	chr9:14787192-14787193	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550342774	chr9:14787197-14787198	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532420322	chr9:14787198-14787199	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368920162	chr9:14787211-14787212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188498406	chr9:14787214-14787215	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs145721589	chr9:14787225-14787226	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14745000-14809800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr9:14748800-14790000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:14755800-14812400	Weak transcription	Pancreas	Pancrea
4	chr9:14758400-14793400	Weak transcription	Aorta	Aorta
5	chr9:14764800-14809600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:14766600-14787400	Weak transcription	Fetal Intestine Large	intestine
7	chr9:14768600-14808800	Weak transcription	Fetal Intestine Small	intestine
8	chr9:14773400-14796400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr9:14776200-14794000	Weak transcription	Fetal Stomach	stomach
10	chr9:14779200-14798600	Strong transcription	Fetal Kidney	kidney
11	chr9:14779800-14789000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr9:14779800-14853200	Weak transcription	Placenta	Placenta
13	chr9:14780400-14795800	Weak transcription	Left Ventricle	heart
14	chr9:14780400-14843200	Weak transcription	Fetal Heart	heart
15	chr9:14782000-14822000	Weak transcription	Fetal Brain Male	brain
16	chr9:14782200-14790400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:14782800-14822000	Weak transcription	Rectal Smooth Muscle	rectum
18	chr9:14783600-14800200	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr9:14784000-14787400	Weak transcription	Colon Smooth Muscle	Colon
20	chr9:14784400-14791400	Weak transcription	Fetal Muscle Leg	muscle
21	chr9:14784600-14790800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr9:14785200-14786800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr9:14785200-14786800	Weak transcription	Fetal Lung	lung
24	chr9:14785200-14786800	Weak transcription	Psoas Muscle	Psoas
25	chr9:14785200-14787400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr9:14785200-14787600	Weak transcription	Adipose Nuclei	Adipose
27	chr9:14785400-14787600	Weak transcription	Fetal Muscle Trunk	muscle
28	chr9:14785800-14791000	Strong transcription	HepG2	liver
29	chr9:14786600-14789400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr9:14786800-14787000	Enhancers	Psoas Muscle	Psoas
31	chr9:14786800-14787200	Strong transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr9:14786800-14814400	Strong transcription	Fetal Lung	lung
33	chr9:14787200-14793800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr9:14787400-14789000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr9:14787400-14789200	Strong transcription	Colon Smooth Muscle	Colon
36	chr9:14787400-14789400	Strong transcription	Fetal Intestine Large	intestine
37	chr9:14787600-14789400	Strong transcription	Adipose Nuclei	Adipose
38	chr9:14787600-14792000	Strong transcription	Fetal Muscle Trunk	muscle
39	chr9:14788400-14806800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr9:14789000-14789200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:14789000-14790800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr9:14789200-14791000	Weak transcription	Colon Smooth Muscle	Colon
43	chr9:14789200-14793400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr9:14789400-14790200	Weak transcription	Adipose Nuclei	Adipose
45	chr9:14789400-14809200	Weak transcription	Fetal Intestine Large	intestine
46	chr9:14790000-14790400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr9:14790200-14797800	Strong transcription	Adipose Nuclei	Adipose
48	chr9:14790400-14793600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr9:14790400-14795400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr9:14790800-14791800	Strong transcription	Duodenum Mucosa	Duodenum

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