Variant report

Variant	nsv564058
Chromosome Location	chr14:24771285-24786976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1202)
CpG islands
(count:1770)
Chromatin interactive
region (count:48)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1202 , 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	chr14:24784983-24785016	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24777039-24777664	HepG2	liver:	n/a	n/a
3	ATF2	chr14:24777259-24777715	GM12878	blood:	n/a	n/a
4	ATF2	chr14:24779960-24780363	GM12878	blood:	n/a	n/a
5	BACH1	chr14:24785917-24785970	K562	blood:	n/a	n/a
6	BACH1	chr14:24786387-24786769	K562	blood:	n/a	n/a
7	BCL3	chr14:24786422-24787200	A549	lung:	n/a	n/a
8	BCLAF1	chr14:24779845-24780355	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:24786588-24786776	K562	blood:	n/a	n/a
10	BHLHE40	chr14:24785136-24785858	K562	blood:	n/a	n/a
11	BHLHE40	chr14:24776793-24777630	HepG2	liver:	n/a	n/a
12	BHLHE40	chr14:24777276-24777647	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:24784770-24785588	HepG2	liver:	n/a	n/a
14	BHLHE40	chr14:24779894-24780243	GM12878	blood:	n/a	n/a
15	BRCA1	chr14:24776937-24777590	HepG2	liver:	n/a	n/a
16	BRCA1	chr14:24777441-24777582	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr14:24784878-24784996	HepG2	liver:	n/a	n/a
18	BRCA1	chr14:24777421-24777475	GM12878	blood:	n/a	n/a
19	BRCA1	chr14:24780021-24780028	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr14:24781168-24781368	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr14:24785340-24785746	K562	blood:	n/a	n/a
22	CCNT2	chr14:24785060-24785896	K562	blood:	n/a	n/a
23	CEBPB	chr14:24784312-24784703	HepG2	liver:	n/a	chr14:24784600-24784613 chr14:24784601-24784612 chr14:24784600-24784611 chr14:24784600-24784611
24	CEBPB	chr14:24781032-24781414	IMR90	lung:	n/a	chr14:24781217-24781228
25	CEBPB	chr14:24784439-24784779	HepG2	liver:	n/a	chr14:24784600-24784613 chr14:24784601-24784612 chr14:24784600-24784611 chr14:24784600-24784611
26	CEBPB	chr14:24781010-24781410	Hela-S3	cervix:	n/a	chr14:24781217-24781228
27	CEBPB	chr14:24781109-24781339	K562	blood:	n/a	chr14:24781217-24781228
28	CEBPB	chr14:24785033-24785161	K562	blood:	n/a	n/a
29	CEBPB	chr14:24784433-24784790	HepG2	liver:	n/a	chr14:24784600-24784613 chr14:24784601-24784612 chr14:24784600-24784611 chr14:24784600-24784611
30	CEBPB	chr14:24781034-24781401	HepG2	liver:	n/a	chr14:24781217-24781228
31	CEBPB	chr14:24777053-24777544	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:24781071-24781464	MCF-7	breast:	n/a	chr14:24781217-24781228
33	CEBPB	chr14:24781068-24781394	A549	lung:	n/a	chr14:24781217-24781228
34	CEBPD	chr14:24776940-24777406	HepG2	liver:	n/a	n/a
35	CEBPD	chr14:24776820-24777631	HepG2	liver:	n/a	n/a
36	CHD1	chr14:24777388-24777479	GM12878	blood:	n/a	n/a
37	CHD2	chr14:24785096-24785617	HepG2	liver:	n/a	n/a
38	CHD2	chr14:24780379-24780469	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr14:24776991-24777659	HepG2	liver:	n/a	n/a
40	CHD2	chr14:24777577-24777769	K562	blood:	n/a	n/a
41	CHD2	chr14:24785451-24785651	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr14:24779921-24780035	GM12878	blood:	n/a	n/a
43	CHD2	chr14:24777364-24777888	GM12878	blood:	n/a	n/a
44	CHD2	chr14:24784643-24784671	HepG2	liver:	n/a	n/a
45	CHD2	chr14:24785103-24785208	K562	blood:	n/a	n/a
46	CHD2	chr14:24785588-24785687	K562	blood:	n/a	n/a
47	CHD2	chr14:24786501-24786579	K562	blood:	n/a	n/a
48	CTCF	chr14:24779920-24780070	GM12865	blood:	n/a	n/a
49	CTCF	chr14:24785400-24785550	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr14:24779940-24780090	GM12875	blood:	n/a	n/a

(count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24780825-24780875	Hela-S3	cervix:	n/a
2	chr14:24780825-24780875	Hela-S3	cervix:	n/a
3	chr14:24776700-24776750	Jurkat	blood:	n/a
4	chr14:24773029-24773079	HRE	kidney:	n/a
5	chr14:24785488-24785538	HRE	kidney:	n/a
6	chr14:24781937-24781987	AoSMC	blood vessel:	n/a
7	chr14:24781881-24781931	MCF10A-Er-Src	breast:	n/a
8	chr14:24779793-24779843	HNPCEpiC	eye:	n/a
9	chr14:24779959-24780009	MCF-7	breast:	n/a
10	chr14:24780691-24780741	BE2_C	brain:	n/a
11	chr14:24777910-24777960	Jurkat	blood:	n/a
12	chr14:24780734-24780784	NHBE	bronchial:	n/a
13	chr14:24780926-24780976	ProgFib	skin:	n/a
14	chr14:24780825-24780875	HCPEpiC	choroid plexus:	n/a
15	chr14:24785488-24785538	NHDF-neo	bronchial:	n/a
16	chr14:24777803-24777853	BE2_C	brain:	n/a
17	chr14:24780926-24780976	RPTEC	kidney:	n/a
18	chr14:24785488-24785538	GM12891	blood:	n/a
19	chr14:24780890-24780940	HRPEpiC	eye:	n/a
20	chr14:24777803-24777853	NHBE	bronchial:	n/a
21	chr14:24773029-24773079	H1-hESC	embryonic stem cell:	embryo
22	chr14:24780926-24780976	BE2_C	brain:	n/a
23	chr14:24780557-24780607	HIPEpiC	eye:	n/a
24	chr14:24785933-24785983	GM12891	blood:	n/a
25	chr14:24785488-24785538	GM12892	blood:	n/a
26	chr14:24785933-24785983	AG09309	skin:	n/a
27	chr14:24779959-24780009	GM06990	blood:	n/a
28	chr14:24777910-24777960	NT2-D1	testis:	n/a
29	chr14:24779400-24779450	AG09309	skin:	n/a
30	chr14:24781881-24781931	Jurkat	blood:	n/a
31	chr14:24784787-24784837	HAEpiC	amniotic membrane:	n/a
32	chr14:24779400-24779450	RPTEC	kidney:	n/a
33	chr14:24779793-24779843	Hepatocyte	liver:	n/a
34	chr14:24777878-24777928	ProgFib	skin:	n/a
35	chr14:24779959-24780009	NT2-D1	testis:	n/a
36	chr14:24779793-24779843	RPTEC	kidney:	n/a
37	chr14:24777910-24777960	RPTEC	kidney:	n/a
38	chr14:24777878-24777928	HIPEpiC	eye:	n/a
39	chr14:24779793-24779843	K562	blood:	n/a
40	chr14:24780404-24780454	SKMC	muscle:	n/a
41	chr14:24781937-24781987	CMK	blood:	n/a
42	chr14:24785488-24785538	NH-A	brain:	n/a
43	chr14:24780557-24780607	NT2-D1	testis:	n/a
44	chr14:24780890-24780940	SK-N-MC	brain:	n/a
45	chr14:24785847-24785897	SKMC	muscle:	n/a
46	chr14:24778279-24778329	AG10803	skin:	n/a
47	chr14:24781881-24781931	HRCEpiC	kidney:	n/a
48	chr14:24777708-24777758	AG04449	skin:	fetal
49	chr14:24784787-24784837	AoSMC	blood vessel:	n/a
50	chr14:24780926-24780976	ECC-1	luminal epithelium:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24766804..24771569-chr14:24898237..24903800,5	MCF-7	breast:
2	chr14:24681085..24682828-chr14:24772928..24775361,2	MCF-7	breast:
3	chr14:24654479..24657858-chr14:24783212..24786979,3	K562	blood:
4	chr14:24769506..24771314-chr14:24788379..24791495,3	K562	blood:
5	chr14:24785903..24787847-chr14:24833580..24835158,2	MCF-7	breast:
6	chr14:24684779..24685489-chr14:24777283..24777942,2	MCF-7	breast:
7	chr14:24778683..24780646-chr14:24900996..24904566,3	K562	blood:
8	chr14:24710202..24713274-chr14:24777163..24780691,4	K562	blood:
9	chr14:24784144..24786069-chr14:24899565..24901293,2	K562	blood:
10	chr14:24784156..24786411-chr14:24902043..24903972,2	MCF-7	breast:
11	chr14:24766841..24768982-chr14:24770722..24773085,2	MCF-7	breast:
12	chr14:24740917..24742571-chr14:24770385..24772196,2	K562	blood:
13	chr14:24740443..24742571-chr14:24769665..24772196,4	K562	blood:
14	chr14:24774171..24777503-chr14:24780795..24784046,4	K562	blood:
15	chr14:24769087..24772179-chr14:24900488..24904117,5	K562	blood:
16	chr14:24783396..24785005-chr14:24908424..24911111,2	K562	blood:
17	chr14:24769037..24771886-chr14:24904413..24906460,2	MCF-7	breast:
18	chr14:24770771..24773074-chr14:24835790..24837584,2	MCF-7	breast:
19	chr14:24767332..24771774-chr14:24910139..24913002,7	MCF-7	breast:
20	chr14:24781460..24810019-chr14:24892340..24914262,110	MCF-7	breast:
21	chr14:24774171..24777503-chr14:24780795..24784046,4	K562	blood:
22	chr14:24682270..24687913-chr14:24764870..24771791,12	MCF-7	breast:
23	chr14:24765570..24768951-chr14:24773362..24777339,4	K562	blood:
24	chr14:24605250..24607686-chr14:24782564..24785003,2	K562	blood:
25	chr14:24786484..24789445-chr14:24867448..24869110,2	K562	blood:
26	chr14:24702582..24706480-chr14:24770203..24773016,3	K562	blood:
27	chr14:24655120..24666858-chr14:24765577..24776253,24	MCF-7	breast:
28	chr14:24773182..24775572-chr14:24899600..24904217,4	MCF-7	breast:
29	chr14:24781177..24783367-chr14:24784569..24786396,2	K562	blood:
30	chr14:24778484..24781723-chr14:24903121..24905574,3	MCF-7	breast:
31	chr14:24711592..24713123-chr14:24785220..24787593,2	K562	blood:
32	chr14:24767097..24775014-chr14:24779936..24787049,14	MCF-7	breast:
33	chr14:24775299..24777826-chr14:24904340..24907258,3	MCF-7	breast:
34	chr14:24772236..24774305-chr14:24778506..24780366,3	K562	blood:
35	chr14:24769074..24771139-chr14:24772218..24774623,3	K562	blood:
36	chr14:24779448..24783163-chr14:24897934..24900807,3	MCF-7	breast:
37	chr14:24769018..24771644-chr14:24778129..24781269,3	K562	blood:
38	chr14:24772771..24774909-chr14:24909093..24912015,2	MCF-7	breast:
39	chr14:24701050..24707093-chr14:24765824..24771703,7	K562	blood:
40	chr14:24682923..24685133-chr14:24776691..24778395,2	MCF-7	breast:
41	chr14:24710493..24713129-chr14:24782481..24785147,3	K562	blood:
42	chr14:24785563..24788287-chr14:24805710..24808640,2	MCF-7	breast:
43	chr14:24768871..24772362-chr14:24798723..24803416,4	MCF-7	breast:
44	chr14:24680927..24686311-chr14:24766466..24771455,6	K562	blood:
45	chr14:24681591..24684402-chr14:24776273..24778851,2	K562	blood:
46	chr14:24767097..24775014-chr14:24779936..24787049,14	MCF-7	breast:
47	chr14:24769018..24771644-chr14:24778129..24781269,3	K562	blood:
48	chr14:24610521..24612373-chr14:24774882..24776542,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADCY4-3	chr14:24779293-24779754	NONHSAT036045
2	lnc-ADCY4-3	chr14:24779855-24779924	NONHSAT036045

No data

Variant related genes	Relation type
NOP9	TF binding region
ENSG00000272658	TF binding region
DHRS1	TF binding region
CIDEB	TF binding region
LTB4R2	TF binding region
LTB4R	TF binding region
NOP9	CpG island
ENSG00000272658	CpG island
DHRS1	CpG island
CIDEB	CpG island
LTB4R2	CpG island
LTB4R	CpG island
ENSG00000100938	chromatin interactions
ENSG00000157379	chromatin interactions
ENSG00000258973	chromatin interactions
ENSG00000259522	chromatin interactions
ENSG00000213903	chromatin interactions
ENSG00000213920	chromatin interactions
ENSG00000100968	chromatin interactions
ENSG00000129559	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000254505	chromatin interactions
ENSG00000196497	chromatin interactions
ENSG00000100445	chromatin interactions
ENSG00000255526	chromatin interactions
ENSG00000092010	chromatin interactions
ENSG00000129465	chromatin interactions
ENSG00000254692	chromatin interactions
ENSG00000272658	chromatin interactions
ENSG00000213906	chromatin interactions
ENSG00000100926	chromatin interactions
ENSG00000196943	chromatin interactions
ENSG00000100908	chromatin interactions
ENSG00000100441	chromatin interactions
ENSG00000205978	chromatin interactions
ENSG00000136305	chromatin interactions
ENSG00000129467	chromatin interactions
ENSG00000139899	chromatin interactions
ENSG00000260669	chromatin interactions
ENSG00000100949	chromatin interactions

Extended variants
information (count: 702 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4280164	chr14:24771285-24771286	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs143592319	chr14:24771292-24771293	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
3	rs76058592	chr14:24771293-24771294	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
4	rs370074153	chr14:24771316-24771317	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
5	rs373980463	chr14:24771342-24771343	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
6	rs576680834	chr14:24771348-24771349	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
7	rs552303131	chr14:24771370-24771371	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
8	rs369868962	chr14:24771401-24771402	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
9	rs201894673	chr14:24771442-24771443	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
10	rs182491838	chr14:24771450-24771451	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
11	rs149379909	chr14:24771480-24771481	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
12	rs537212196	chr14:24771500-24771501	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
13	rs144755501	chr14:24771506-24771507	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
14	rs200425444	chr14:24771514-24771515	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
15	rs371219756	chr14:24771539-24771540	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
16	rs573854331	chr14:24771544-24771545	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
17	rs139514138	chr14:24771551-24771552	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
18	rs374151715	chr14:24771570-24771571	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
19	rs142793921	chr14:24771597-24771598	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
20	rs202195425	chr14:24771599-24771600	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
21	rs375215967	chr14:24771600-24771601	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
22	rs200480319	chr14:24771613-24771614	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
23	rs555787431	chr14:24771644-24771645	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
24	rs572516828	chr14:24771668-24771669	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
25	rs55791955	chr14:24771705-24771706	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
26	rs193265829	chr14:24771739-24771740	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
27	rs568969166	chr14:24771803-24771804	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs941506	chr14:24771843-24771844	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs150294176	chr14:24771867-24771868	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs374836123	chr14:24771877-24771878	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs529576422	chr14:24771883-24771884	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs185368760	chr14:24771957-24771958	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
33	rs369112161	chr14:24772024-24772025	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs137954149	chr14:24772048-24772049	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs149001969	chr14:24772056-24772057	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs74896700	chr14:24772088-24772089	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs188737767	chr14:24772124-24772125	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs369221455	chr14:24772143-24772144	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs536770684	chr14:24772176-24772177	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs373638907	chr14:24772204-24772205	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs567386929	chr14:24772235-24772236	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs372781354	chr14:24772236-24772237	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs375671972	chr14:24772243-24772244	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs536540961	chr14:24772290-24772291	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs369481973	chr14:24772310-24772311	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs372920925	chr14:24772339-24772340	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs201976440	chr14:24772341-24772342	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs147123517	chr14:24772373-24772374	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs201037901	chr14:24772390-24772391	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs368982560	chr14:24772405-24772406	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24770000-24771400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:24770000-24773000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:24770200-24771400	Genic enhancers	Placenta	Placenta
4	chr14:24770200-24771400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr14:24770200-24772600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr14:24770200-24773000	Weak transcription	Psoas Muscle	Psoas
7	chr14:24770200-24777000	Strong transcription	Primary T cells fromperipheralblood	blood
8	chr14:24770200-24778600	Strong transcription	Fetal Stomach	stomach
9	chr14:24770200-24779400	Weak transcription	Right Atrium	heart
10	chr14:24770400-24771600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr14:24770400-24775400	Genic enhancers	Duodenum Mucosa	Duodenum
12	chr14:24770400-24775600	Genic enhancers	Liver	Liver
13	chr14:24770400-24775600	Genic enhancers	Fetal Intestine Small	intestine
14	chr14:24770400-24775800	Strong transcription	A549	lung
15	chr14:24770400-24777000	Strong transcription	Brain Cingulate Gyrus	brain
16	chr14:24770400-24778800	Weak transcription	Fetal Heart	heart
17	chr14:24770400-24782000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr14:24770600-24771600	Genic enhancers	Dnd41	blood
19	chr14:24770600-24775600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr14:24770600-24776200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:24770600-24776400	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr14:24770600-24776400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr14:24770600-24776400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr14:24770600-24776400	Strong transcription	Fetal Thymus	thymus
25	chr14:24770600-24776600	Strong transcription	H1 Cell Line	embryonic stem cell
26	chr14:24770600-24776600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr14:24770600-24776600	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr14:24770600-24776800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr14:24770600-24776800	Strong transcription	Brain Germinal Matrix	brain
30	chr14:24770600-24777000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr14:24770600-24777000	Strong transcription	Primary B cells from peripheral blood	blood
32	chr14:24770600-24777000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:24770600-24777000	Strong transcription	Ovary	ovary
34	chr14:24770600-24777000	Strong transcription	HMEC	breast
35	chr14:24770600-24777200	Strong transcription	Brain Hippocampus Middle	brain
36	chr14:24770600-24777200	Strong transcription	Fetal Muscle Leg	muscle
37	chr14:24770600-24777400	Strong transcription	Colon Smooth Muscle	Colon
38	chr14:24770600-24778000	Strong transcription	Thymus	Thymus
39	chr14:24770600-24781800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:24770600-24781800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr14:24770800-24771400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:24770800-24771600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:24770800-24773000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr14:24770800-24773200	Strong transcription	Spleen	Spleen
45	chr14:24770800-24773400	Strong transcription	K562	blood
46	chr14:24770800-24773600	Strong transcription	NHDF-Ad	bronchial
47	chr14:24770800-24775200	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr14:24770800-24775600	Strong transcription	Gastric	stomach
49	chr14:24770800-24775600	Strong transcription	Stomach Mucosa	stomach
50	chr14:24770800-24775600	Strong transcription	Osteobl	bone

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