Variant report

Variant	esv3322007
Chromosome Location	chr11:120079642-120084040
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	ARID3A	chr11:120081643-120081806	K562	blood:	n/a	n/a
2	ARID3A	chr11:120081640-120081840	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:120078747-120079772	HepG2	liver:	n/a	n/a
4	BACH1	chr11:120081501-120082019	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr11:120081656-120082329	K562	blood:	n/a	chr11:120081879-120081895
6	BHLHE40	chr11:120081990-120082230	HepG2	liver:	n/a	n/a
7	BHLHE40	chr11:120081336-120081979	GM12878	blood:	n/a	chr11:120081879-120081895
8	CBX3	chr11:120081994-120082290	K562	blood:	n/a	n/a
9	CBX3	chr11:120081370-120081822	K562	blood:	n/a	n/a
10	CCNT2	chr11:120081437-120082236	K562	blood:	n/a	chr11:120081574-120081583
11	CEBPB	chr11:120079326-120079865	Hela-S3	cervix:	n/a	chr11:120079660-120079673
12	CEBPB	chr11:120079487-120079867	IMR90	lung:	n/a	chr11:120079660-120079673
13	CEBPB	chr11:120081654-120082193	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:120079553-120079725	HepG2	liver:	n/a	chr11:120079660-120079673
15	CEBPB	chr11:120079488-120079815	HepG2	liver:	n/a	chr11:120079660-120079673
16	CEBPD	chr11:120081561-120081887	HepG2	liver:	n/a	n/a
17	CHD2	chr11:120079570-120079663	HepG2	liver:	n/a	n/a
18	CHD2	chr11:120081487-120081724	GM12878	blood:	n/a	chr11:120081572-120081582
19	CHD2	chr11:120081635-120081835	K562	blood:	n/a	n/a
20	CHD2	chr11:120081411-120082079	Hela-S3	cervix:	n/a	chr11:120081572-120081582
21	CHD2	chr11:120082106-120082212	K562	blood:	n/a	n/a
22	CHD2	chr11:120081438-120081626	HepG2	liver:	n/a	chr11:120081572-120081582
23	CREB1	chr11:120081437-120081979	A549	lung:	n/a	n/a
24	CREB1	chr11:120081047-120082445	HepG2	liver:	n/a	n/a
25	CTBP2	chr11:120080927-120082755	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr11:120081440-120081590	AG09319	gingival:	n/a	chr11:120081576-120081589
27	CTCF	chr11:120081780-120081930	GM12878	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
28	CTCF	chr11:120081500-120081650	RPTEC	kidney:	n/a	chr11:120081576-120081589
29	CTCF	chr11:120081660-120081810	HL-60	blood:	n/a	n/a
30	CTCF	chr11:120081440-120081590	HPAF	blood vessel:	n/a	chr11:120081576-120081589
31	CTCF	chr11:120081720-120081870	Caco-2	colon:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
32	CTCF	chr11:120081700-120081850	GM12871	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
33	CTCF	chr11:120081664-120081891	K562	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
34	CTCF	chr11:120081400-120081550	GM12865	blood:	n/a	chr11:120081439-120081448
35	CTCF	chr11:120081420-120081570	BJ	skin:	n/a	chr11:120081439-120081448
36	CTCF	chr11:120081680-120081830	AG09319	gingival:	n/a	n/a
37	CTCF	chr11:120081475-120082008	GM12878	blood:	n/a	chr11:120081834-120081850 chr11:120081576-120081589 chr11:120081835-120081848
38	CTCF	chr11:120081780-120081930	GM12864	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
39	CTCF	chr11:120081760-120081910	GM12871	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
40	CTCF	chr11:120081700-120081850	AoAF	blood vessel:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
41	CTCF	chr11:120081660-120081810	HCM	heart:	n/a	n/a
42	CTCF	chr11:120081762-120081865	GM13977	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
43	CTCF	chr11:120081420-120081570	HCPEpiC	choroid plexus:	n/a	chr11:120081439-120081448
44	CTCF	chr11:120081440-120081590	HMEC	breast:	n/a	chr11:120081576-120081589
45	CTCF	chr11:120081680-120081830	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr11:120082152-120082161	GM19238	blood:	n/a	n/a
47	CTCF	chr11:120081400-120081550	HMF	breast:	n/a	chr11:120081439-120081448
48	CTCF	chr11:120081700-120081850	HMEC	breast:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
49	CTCF	chr11:120081760-120081910	HEK293	kidney:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
50	CTCF	chr11:120080061-120080089	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:120081506-120081556	ECC-1	luminal epithelium:	n/a
2	chr11:120081506-120081556	AG09309	skin:	n/a
3	chr11:120081497-120081547	MCF10A-Er-Src	breast:	n/a
4	chr11:120081497-120081547	NHDF-neo	bronchial:	n/a
5	chr11:120081645-120081695	SKMC	muscle:	n/a
6	chr11:120082238-120082288	CMK	blood:	n/a
7	chr11:120081643-120081693	HL-60	blood:	n/a
8	chr11:120081749-120081799	MCF-7	breast:	n/a
9	chr11:120082238-120082288	HRCEpiC	kidney:	n/a
10	chr11:120081089-120081139	ovcar-3	ovarian:	n/a
11	chr11:120081749-120081799	Hela-S3	cervix:	n/a
12	chr11:120081259-120081309	HEK293	kidney:	embryo
13	chr11:120081497-120081547	HIPEpiC	eye:	n/a
14	chr11:120081143-120081193	AG04449	skin:	fetal
15	chr11:120081497-120081547	LNCaP	prostate:	n/a
16	chr11:120081645-120081695	ovcar-3	ovarian:	n/a
17	chr11:120081890-120081940	SKMC	muscle:	n/a
18	chr11:120081890-120081940	PrEC	prostate:	n/a
19	chr11:120081755-120081805	BJ	skin:	n/a
20	chr11:120081645-120081695	NB4	blood:	n/a
21	chr11:120082805-120082855	RPTEC	kidney:	n/a
22	chr11:120081890-120081940	Caco-2	colon:	n/a
23	chr11:120081645-120081695	HCF	heart:	n/a
24	chr11:120081089-120081139	H1-hESC	embryonic stem cell:	embryo
25	chr11:120081749-120081799	A549	lung:	n/a
26	chr11:120081643-120081693	AG09319	gingival:	n/a
27	chr11:120081890-120081940	IMR90	lung:	fetal
28	chr11:120081506-120081556	HCF	heart:	n/a
29	chr11:120081497-120081547	SK-N-MC	brain:	n/a
30	chr11:120081506-120081556	BE2_C	brain:	n/a
31	chr11:120082238-120082288	HRE	kidney:	n/a
32	chr11:120081497-120081547	GM12891	blood:	n/a
33	chr11:120082238-120082288	AG04449	skin:	fetal
34	chr11:120081506-120081556	SKMC	muscle:	n/a
35	chr11:120082805-120082855	HUVEC	blood vessel:	n/a
36	chr11:120081643-120081693	MCF-7	breast:	n/a
37	chr11:120081645-120081695	NHDF-neo	bronchial:	n/a
38	chr11:120081643-120081693	BE2_C	brain:	n/a
39	chr11:120082805-120082855	SK-N-SH_RA	brain:	n/a
40	chr11:120081645-120081695	AoSMC	blood vessel:	n/a
41	chr11:120081143-120081193	MCF10A-Er-Src	breast:	n/a
42	chr11:120080945-120080995	HRCEpiC	kidney:	n/a
43	chr11:120082805-120082855	NHBE	bronchial:	n/a
44	chr11:120081497-120081547	HepG2	liver:	n/a
45	chr11:120080945-120080995	U87	brain:	n/a
46	chr11:120081890-120081940	HCPEpiC	choroid plexus:	n/a
47	chr11:120081643-120081693	AG09309	skin:	n/a
48	chr11:120081643-120081693	HRPEpiC	eye:	n/a
49	chr11:120080945-120080995	NT2-D1	testis:	n/a
50	chr11:120081890-120081940	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:120080662..120083182-chr11:120083944..120086303,3	MCF-7	breast:
2	chr11:120038992..120040633-chr11:120083752..120086483,2	K562	blood:
3	chr11:120081219..120081853-chr16:30366400..30367038,2	Hela-S3	cervix:
4	chr11:120054593..120056417-chr11:120079805..120082698,2	K562	blood:
5	chr11:120038506..120040920-chr11:120082703..120085252,3	K562	blood:
6	chr11:120080610..120089931-chr11:120105398..120112199,18	K562	blood:
7	chr11:120061784..120063825-chr11:120078138..120080529,2	K562	blood:
8	chr11:120080662..120083182-chr11:120083944..120086303,3	MCF-7	breast:
9	chr11:120066886..120069148-chr11:120079541..120081080,2	K562	blood:
10	chr11:120079370..120085014-chr11:120104504..120109067,9	K562	blood:
11	chr11:120078701..120081046-chr11:120081423..120083396,2	K562	blood:

Variant related genes	Relation type
OAF	TF binding region
OAF	CpG island
ENSG00000137699	chromatin interactions
ENSG00000260219	chromatin interactions
ENSG00000176984	chromatin interactions
ENSG00000169217	chromatin interactions
ENSG00000184232	chromatin interactions
ENSG00000137709	chromatin interactions

Extended variants
information (count: 162 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:162 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185327316	chr11:120079677-120079678	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs555628892	chr11:120079678-120079679	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs573864675	chr11:120079732-120079733	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs540151833	chr11:120079733-120079734	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs151331398	chr11:120079746-120079747	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs372601871	chr11:120079790-120079791	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs477863	chr11:120079884-120079885	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs576628827	chr11:120079892-120079893	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs191120986	chr11:120079906-120079907	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs372827035	chr11:120079954-120079955	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs376578409	chr11:120079955-120079956	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs560271504	chr11:120079959-120079960	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs530978680	chr11:120079964-120079965	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs368434274	chr11:120079981-120079982	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs56815632	chr11:120079985-120079986	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs476809	chr11:120080022-120080023	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs183783833	chr11:120080029-120080030	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs528770823	chr11:120080030-120080031	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs146933298	chr11:120080063-120080064	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs571569935	chr11:120080077-120080078	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs188366563	chr11:120080095-120080096	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs551060077	chr11:120080117-120080118	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs569352671	chr11:120080142-120080143	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs137948180	chr11:120080159-120080160	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs141957777	chr11:120080176-120080177	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs567396793	chr11:120080213-120080214	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs542767810	chr11:120080218-120080219	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs554672304	chr11:120080267-120080268	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs534874284	chr11:120080318-120080319	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs530242857	chr11:120080324-120080325	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs553005024	chr11:120080325-120080326	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs192471544	chr11:120080404-120080405	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs115255720	chr11:120080484-120080485	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs556564965	chr11:120080520-120080521	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs521841	chr11:120080526-120080527	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs374392074	chr11:120080527-120080528	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs561529518	chr11:120080535-120080536	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs528681895	chr11:120080567-120080568	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs113480991	chr11:120080595-120080596	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs73584892	chr11:120080653-120080654	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532885129	chr11:120080717-120080718	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs34394186	chr11:120080771-120080772	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs550980438	chr11:120080772-120080773	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs562910643	chr11:120080808-120080809	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs113739737	chr11:120080893-120080894	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs548398671	chr11:120080920-120080921	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs543006260	chr11:120080946-120080947	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs115401280	chr11:120080992-120080993	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs368685901	chr11:120081024-120081025	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs534535534	chr11:120081027-120081028	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120075200-120081000	Enhancers	Pancreas	Pancrea
2	chr11:120076200-120080600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:120076200-120080600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:120076600-120080600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:120077000-120080600	Enhancers	Fetal Stomach	stomach
6	chr11:120077000-120080800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:120078000-120081200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr11:120078200-120080800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:120078200-120080800	Enhancers	Spleen	Spleen
10	chr11:120078400-120079800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr11:120078400-120079800	Flanking Active TSS	HepG2	liver
12	chr11:120078400-120080000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:120078400-120080000	Enhancers	Brain Substantia Nigra	brain
14	chr11:120078400-120080000	Enhancers	Left Ventricle	heart
15	chr11:120078400-120080400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:120078400-120080400	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr11:120078400-120080600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr11:120078400-120080600	Enhancers	Adipose Nuclei	Adipose
19	chr11:120078400-120080600	Enhancers	Brain Anterior Caudate	brain
20	chr11:120078400-120080600	Enhancers	Brain Hippocampus Middle	brain
21	chr11:120078400-120080600	Enhancers	Colonic Mucosa	Colon
22	chr11:120078400-120080600	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr11:120078400-120080600	Enhancers	NHDF-Ad	bronchial
24	chr11:120078400-120080800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr11:120078400-120080800	Enhancers	Brain Angular Gyrus	brain
26	chr11:120078400-120080800	Enhancers	Brain Cingulate Gyrus	brain
27	chr11:120078400-120080800	Enhancers	Fetal Intestine Small	intestine
28	chr11:120078400-120080800	Enhancers	Fetal Muscle Trunk	muscle
29	chr11:120078400-120080800	Enhancers	Ovary	ovary
30	chr11:120078400-120081000	Enhancers	Esophagus	oesophagus
31	chr11:120078400-120081000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr11:120078400-120081000	Enhancers	Small Intestine	intestine
33	chr11:120078600-120079800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
34	chr11:120078600-120079800	Enhancers	Osteobl	bone
35	chr11:120078600-120080400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr11:120078600-120080400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:120078600-120080400	Enhancers	Muscle Satellite Cultured Cells	--
38	chr11:120078600-120080400	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr11:120078600-120080400	Enhancers	Fetal Muscle Leg	muscle
40	chr11:120078600-120080600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr11:120078600-120080600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr11:120078600-120080600	Enhancers	Duodenum Mucosa	Duodenum
43	chr11:120078600-120080600	Enhancers	Hela-S3	cervix
44	chr11:120078600-120080800	Enhancers	Right Atrium	heart
45	chr11:120078600-120081000	Enhancers	HMEC	breast
46	chr11:120078600-120081000	Enhancers	HUVEC	blood vessel
47	chr11:120078800-120079800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
48	chr11:120078800-120079800	Enhancers	HSMMtube	muscle
49	chr11:120078800-120080600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:120078800-120080600	Enhancers	NHLF	lung

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