Variant report

Variant	nsv597254
Chromosome Location	chr5:14661675-14664951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:547)
CpG islands
(count:366)
Chromatin interactive
region (count:28)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:14664658-14664818	K562	blood:	n/a	n/a
2	ARID3A	chr5:14664457-14664978	HepG2	liver:	n/a	n/a
3	ATF1	chr5:14664316-14664943	K562	blood:	n/a	n/a
4	ATF2	chr5:14663624-14664414	GM12878	blood:	n/a	n/a
5	ATF2	chr5:14663721-14664765	GM12878	blood:	n/a	n/a
6	ATF3	chr5:14664495-14664880	A549	lung:	n/a	chr5:14664784-14664804
7	ATF3	chr5:14664343-14664885	K562	blood:	n/a	chr5:14664784-14664804
8	BACH1	chr5:14664715-14664915	K562	blood:	n/a	n/a
9	BACH1	chr5:14664379-14665689	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr5:14664157-14664883	A549	lung:	n/a	chr5:14664655-14664668 chr5:14664626-14664639 chr5:14664393-14664402 chr5:14664622-14664635
11	BCLAF1	chr5:14663776-14665079	GM12878	blood:	n/a	chr5:14664655-14664668 chr5:14664626-14664639 chr5:14664393-14664402 chr5:14664622-14664635
12	BCLAF1	chr5:14663727-14665699	GM12878	blood:	n/a	chr5:14664655-14664668 chr5:14664626-14664639 chr5:14664393-14664402 chr5:14664622-14664635
13	BHLHE40	chr5:14664101-14665031	K562	blood:	n/a	chr5:14664652-14664668
14	BHLHE40	chr5:14664029-14665027	GM12878	blood:	n/a	chr5:14664652-14664668
15	BHLHE40	chr5:14664233-14664949	HepG2	liver:	n/a	chr5:14664652-14664668
16	BRCA1	chr5:14664414-14664747	GM12878	blood:	n/a	n/a
17	BRCA1	chr5:14664191-14664537	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr5:14664447-14664954	HepG2	liver:	n/a	n/a
19	BRCA1	chr5:14664024-14664178	GM12878	blood:	n/a	n/a
20	BRCA1	chr5:14663757-14664910	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr5:14664248-14664997	K562	blood:	n/a	n/a
22	CCNT2	chr5:14664031-14665452	K562	blood:	n/a	chr5:14665153-14665162 chr5:14664291-14664300
23	CEBPB	chr5:14664328-14664555	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:14664077-14664870	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:14663253-14663484	K562	blood:	n/a	chr5:14663374-14663385
26	CEBPB	chr5:14664386-14664910	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr5:14663270-14663403	HepG2	liver:	n/a	chr5:14663374-14663385
28	CEBPB	chr5:14664630-14664636	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPD	chr5:14664417-14664995	HepG2	liver:	n/a	n/a
30	CHD1	chr5:14663829-14665056	GM12878	blood:	n/a	n/a
31	CHD1	chr5:14664137-14664572	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr5:14664422-14664939	K562	blood:	n/a	n/a
33	CHD2	chr5:14664306-14664701	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr5:14664461-14664892	HepG2	liver:	n/a	n/a
35	CHD2	chr5:14663825-14664954	GM12878	blood:	n/a	n/a
36	CHD2	chr5:14663994-14665033	Hela-S3	cervix:	n/a	n/a
37	CREB1	chr5:14664156-14665207	GM12878	blood:	n/a	n/a
38	CREB1	chr5:14664289-14665082	ECC-1	luminal epithelium:	n/a	n/a
39	CREB1	chr5:14664162-14665117	HepG2	liver:	n/a	n/a
40	CREB1	chr5:14664199-14664994	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr5:14664222-14665165	HepG2	liver:	n/a	n/a
42	CREB1	chr5:14664480-14664973	A549	lung:	n/a	n/a
43	CREB1	chr5:14664262-14665161	A549	lung:	n/a	n/a
44	CREB1	chr5:14664280-14665015	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr5:14664264-14665058	K562	blood:	n/a	n/a
46	CREB1	chr5:14664141-14665158	K562	blood:	n/a	n/a
47	CREB1	chr5:14664498-14664994	ECC-1	luminal epithelium:	n/a	n/a
48	CTBP2	chr5:14664085-14665388	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr5:14664260-14664410	Caco-2	colon:	n/a	n/a
50	CTCF	chr5:14664649-14664757	Spleen_OC	spleen:	n/a	chr5:14664671-14664689

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14662325-14662375	RPTEC	kidney:	n/a
2	chr5:14664248-14664298	PFSK-1	brain:	n/a
3	chr5:14662198-14662248	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:14664248-14664298	AG04450	lung:	fetal
5	chr5:14664487-14664537	NH-A	brain:	n/a
6	chr5:14664470-14664520	HL-60	blood:	n/a
7	chr5:14664470-14664520	ProgFib	skin:	n/a
8	chr5:14662198-14662248	HEEpiC	esophagus:	n/a
9	chr5:14664662-14664712	NT2-D1	testis:	n/a
10	chr5:14664487-14664537	GM19239	blood:	n/a
11	chr5:14662325-14662375	SKMC	muscle:	n/a
12	chr5:14664662-14664712	GM12878	blood:	n/a
13	chr5:14664662-14664712	HMEC	breast:	n/a
14	chr5:14662325-14662375	NHDF-neo	bronchial:	n/a
15	chr5:14664248-14664298	NH-A	brain:	n/a
16	chr5:14664662-14664712	HCT-116	colon:	n/a
17	chr5:14664487-14664537	IMR90	lung:	fetal
18	chr5:14664487-14664537	K562	blood:	n/a
19	chr5:14664470-14664520	GM12892	blood:	n/a
20	chr5:14664662-14664712	HRE	kidney:	n/a
21	chr5:14662325-14662375	IMR90	lung:	fetal
22	chr5:14664662-14664712	K562	blood:	n/a
23	chr5:14664662-14664712	PrEC	prostate:	n/a
24	chr5:14662198-14662248	Jurkat	blood:	n/a
25	chr5:14664248-14664298	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:14664470-14664520	NB4	blood:	n/a
27	chr5:14664662-14664712	U87	brain:	n/a
28	chr5:14664487-14664537	HRE	kidney:	n/a
29	chr5:14664487-14664537	Jurkat	blood:	n/a
30	chr5:14662325-14662375	AG09309	skin:	n/a
31	chr5:14662198-14662248	HMEC	breast:	n/a
32	chr5:14664248-14664298	AoSMC	blood vessel:	n/a
33	chr5:14662198-14662248	LNCaP	prostate:	n/a
34	chr5:14662325-14662375	SAEC	small airway:	n/a
35	chr5:14664487-14664537	HRPEpiC	eye:	n/a
36	chr5:14664487-14664537	PFSK-1	brain:	n/a
37	chr5:14664470-14664520	AG04450	lung:	fetal
38	chr5:14664248-14664298	HCPEpiC	choroid plexus:	n/a
39	chr5:14664662-14664712	AG09319	gingival:	n/a
40	chr5:14662325-14662375	Hela-S3	cervix:	n/a
41	chr5:14664248-14664298	HIPEpiC	eye:	n/a
42	chr5:14664487-14664537	SAEC	small airway:	n/a
43	chr5:14662325-14662375	HCPEpiC	choroid plexus:	n/a
44	chr5:14664662-14664712	HCPEpiC	choroid plexus:	n/a
45	chr5:14662325-14662375	K562	blood:	n/a
46	chr5:14662198-14662248	SK-N-SH_RA	brain:	n/a
47	chr5:14664662-14664712	HepG2	liver:	n/a
48	chr5:14662325-14662375	HAEpiC	amniotic membrane:	n/a
49	chr5:14664470-14664520	MCF-7	breast:	n/a
50	chr5:14662198-14662248	HIPEpiC	eye:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:14657786..14662304-chr5:14663276..14666291,7	MCF-7	breast:
2	chr5:14663911..14666053-chr5:14679468..14682192,2	MCF-7	breast:
3	chr12:121837283..121837955-chr5:14664313..14665299,2	Hela-S3	cervix:
4	chr5:14497930..14500445-chr5:14662848..14665215,2	MCF-7	breast:
5	chr1:16482022..16482600-chr5:14664854..14665513,2	Hela-S3	cervix:
6	chr5:14664160..14664958-chr5:82372800..82373613,2	Hela-S3	cervix:
7	chr16:56484857..56485398-chr5:14664111..14664803,2	Hela-S3	cervix:
8	chr1:147806219..147807143-chr5:14664370..14664996,2	Hela-S3	cervix:
9	chr19:9938591..9939096-chr5:14664436..14665121,2	Hela-S3	cervix:
10	chr17:62222968..62223765-chr5:14664311..14665257,2	Hela-S3	cervix:
11	chr2:75937399..75938318-chr5:14664189..14665128,2	Hela-S3	cervix:
12	chr10:103824761..103825626-chr5:14664698..14665242,2	Hela-S3	cervix:
13	chr3:120314958..120315682-chr5:14664161..14664669,2	Hela-S3	cervix:
14	chr5:14663431..14670152-chr5:14672054..14680588,17	K562	blood:
15	chr2:20101550..20102401-chr5:14664511..14665186,2	Hela-S3	cervix:
16	chr5:14657185..14658730-chr5:14661178..14663060,2	K562	blood:
17	chr5:14611853..14613930-chr5:14664860..14666930,2	K562	blood:
18	chr17:1620010..1621019-chr5:14664271..14665202,3	Hela-S3	cervix:
19	chr15:65588332..65589080-chr5:14664136..14664865,2	Hela-S3	cervix:
20	chr12:125398725..125399588-chr5:14664525..14665354,2	Hela-S3	cervix:
21	chr5:14664623..14665342-chr5:89705556..89706261,2	HCT-116	colon:
22	chr11:65190115..65190731-chr5:14664107..14664931,2	Hela-S3	cervix:
23	chr11:124543288..124543836-chr5:14664268..14664773,2	Hela-S3	cervix:
24	chr1:176175719..176176397-chr5:14664793..14665438,2	Hela-S3	cervix:
25	chr5:14659517..14662200-chr5:14662698..14665748,5	MCF-7	breast:
26	chr19:39935648..39936578-chr5:14664034..14664744,2	Hela-S3	cervix:
27	chr5:14660316..14662919-chr5:14663099..14665410,3	K562	blood:
28	chr5:14143682..14146659-chr5:14664431..14666395,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKH-1	chr5:14663988-14664384	ENSG00000261360.1
2	lnc-ANKH-1	chr5:14664543-14664682	ENSG00000261360.1
3	lnc-ANKH-1	chr5:14663988-14664160	ENSG00000261360.1
4	lnc-ANKH-1	chr5:14663212-14663452	ENSG00000261360.1
5	lnc-ANKH-1	chr5:14663210-14663424	ENSG00000261360.1
6	lnc-ANKH-1	chr5:14663208-14664704	NONHSAT100548

No data

Variant related genes	Relation type
ENSG00000261360	TF binding region
FAM105B	TF binding region
ENSG00000261360	CpG island
FAM105B	CpG island
ENSG00000143207	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000142627	chromatin interactions
ENSG00000166189	chromatin interactions
ENSG00000271991	chromatin interactions
ENSG00000255647	chromatin interactions
ENSG00000152422	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000110013	chromatin interactions
ENSG00000174695	chromatin interactions
ENSG00000198258	chromatin interactions
ENSG00000065518	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000183891	chromatin interactions
ENSG00000186594	chromatin interactions
ENSG00000064199	chromatin interactions
ENSG00000167005	chromatin interactions
ENSG00000261360	chromatin interactions
ENSG00000038382	chromatin interactions
ENSG00000196235	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000170633	chromatin interactions
ENSG00000154124	chromatin interactions
ENSG00000150991	chromatin interactions
ENSG00000005436	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4702043	chr5:14661675-14661676	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527615545	chr5:14661767-14661768	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552187621	chr5:14661804-14661805	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376440914	chr5:14661820-14661821	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs571658686	chr5:14661821-14661822	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs184186299	chr5:14661822-14661823	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556892725	chr5:14661825-14661826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs188840057	chr5:14661830-14661831	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs536313975	chr5:14661859-14661860	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs368792884	chr5:14661861-14661862	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370963239	chr5:14661888-14661889	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs573335115	chr5:14661892-14661893	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs153836	chr5:14661908-14661909	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs375939727	chr5:14661911-14661912	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577571516	chr5:14661940-14661941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs182590303	chr5:14661945-14661946	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs153837	chr5:14662044-14662045	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs10038397	chr5:14662045-14662046	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs541542504	chr5:14662053-14662054	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs560344566	chr5:14662070-14662071	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs4585445	chr5:14662122-14662123	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs527487680	chr5:14662126-14662127	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs549280176	chr5:14662158-14662159	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs187007265	chr5:14662163-14662164	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs564228832	chr5:14662167-14662168	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs152766	chr5:14662187-14662188	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs150062547	chr5:14662199-14662200	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs538130188	chr5:14662269-14662270	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs191909803	chr5:14662288-14662289	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs145433581	chr5:14662427-14662428	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs556824087	chr5:14662482-14662483	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs548388485	chr5:14662500-14662501	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs11952550	chr5:14662502-14662503	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534139048	chr5:14662503-14662504	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs549800834	chr5:14662574-14662575	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577631731	chr5:14662575-14662576	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs538503426	chr5:14662583-14662584	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs184519346	chr5:14662680-14662681	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs574461193	chr5:14662692-14662693	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs558882872	chr5:14662698-14662699	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs541951550	chr5:14662700-14662701	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs35743758	chr5:14662811-14662812	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs142531205	chr5:14662906-14662907	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs572062576	chr5:14662922-14662923	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189181569	chr5:14662956-14662957	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs152785	chr5:14663047-14663048	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs115226400	chr5:14663132-14663133	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549644667	chr5:14663164-14663165	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538609209	chr5:14663199-14663200	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs201540231	chr5:14663202-14663203	Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14655200-14663800	Weak transcription	Pancreas	Pancrea
2	chr5:14655600-14663400	Weak transcription	Fetal Thymus	thymus
3	chr5:14655800-14663000	Weak transcription	Dnd41	blood
4	chr5:14659400-14662200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:14659400-14663200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:14659400-14663400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr5:14659400-14663400	Weak transcription	HSMMtube	muscle
8	chr5:14659600-14661800	Enhancers	HMEC	breast
9	chr5:14659800-14662200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:14659800-14663200	Weak transcription	Fetal Muscle Leg	muscle
11	chr5:14659800-14663400	Weak transcription	Fetal Lung	lung
12	chr5:14660000-14662200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:14660000-14663200	Weak transcription	Esophagus	oesophagus
14	chr5:14660200-14663400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr5:14660600-14663200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr5:14660600-14663200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr5:14660600-14663200	Weak transcription	Colon Smooth Muscle	Colon
18	chr5:14660800-14661800	Enhancers	HUVEC	blood vessel
19	chr5:14660800-14663200	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr5:14660800-14663400	Weak transcription	Brain Anterior Caudate	brain
21	chr5:14661000-14662800	Enhancers	NHEK	skin
22	chr5:14661000-14663200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr5:14661000-14663200	Weak transcription	Liver	Liver
24	chr5:14661000-14663400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr5:14661000-14663400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:14661000-14663400	Weak transcription	Duodenum Mucosa	Duodenum
27	chr5:14661000-14663600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr5:14661000-14663600	Weak transcription	Adipose Nuclei	Adipose
29	chr5:14661000-14663600	Weak transcription	NH-A	brain
30	chr5:14661000-14663800	Weak transcription	Fetal Muscle Trunk	muscle
31	chr5:14661200-14663200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:14661200-14663200	Weak transcription	Left Ventricle	heart
33	chr5:14661200-14663400	Weak transcription	Psoas Muscle	Psoas
34	chr5:14661200-14663800	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr5:14661400-14662200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr5:14661400-14662800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr5:14661400-14663000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:14661400-14663200	Weak transcription	Primary B cells from cord blood	blood
39	chr5:14661400-14663200	Weak transcription	Primary B cells from peripheral blood	blood
40	chr5:14661400-14663200	Weak transcription	Osteobl	bone
41	chr5:14661400-14663400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:14661400-14663400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr5:14661400-14663400	Weak transcription	NHDF-Ad	bronchial
44	chr5:14661600-14662000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr5:14661600-14662000	Weak transcription	GM12878-XiMat	blood
46	chr5:14661600-14662200	Weak transcription	Primary T cells from cord blood	blood
47	chr5:14661600-14662400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:14661600-14662600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr5:14661600-14662800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr5:14661600-14663200	Weak transcription	HepG2	liver

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