Variant report

Variant	esv3325819
Chromosome Location	chr11:120080267-120083115
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	BACH1	chr11:120081501-120082019	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr11:120081990-120082230	HepG2	liver:	n/a	n/a
5	BHLHE40	chr11:120081656-120082329	K562	blood:	n/a	chr11:120081879-120081895
6	BHLHE40	chr11:120081336-120081979	GM12878	blood:	n/a	chr11:120081879-120081895
7	CBX3	chr11:120081370-120081822	K562	blood:	n/a	n/a
8	CBX3	chr11:120081994-120082290	K562	blood:	n/a	n/a
9	CCNT2	chr11:120081437-120082236	K562	blood:	n/a	chr11:120081574-120081583
10	CEBPB	chr11:120081654-120082193	Hela-S3	cervix:	n/a	n/a
11	CEBPD	chr11:120081561-120081887	HepG2	liver:	n/a	n/a
12	CHD2	chr11:120081411-120082079	Hela-S3	cervix:	n/a	chr11:120081572-120081582
13	CHD2	chr11:120081487-120081724	GM12878	blood:	n/a	chr11:120081572-120081582
14	CHD2	chr11:120081635-120081835	K562	blood:	n/a	n/a
15	CHD2	chr11:120081438-120081626	HepG2	liver:	n/a	chr11:120081572-120081582
16	CHD2	chr11:120082106-120082212	K562	blood:	n/a	n/a
17	CREB1	chr11:120081437-120081979	A549	lung:	n/a	n/a
18	CREB1	chr11:120081047-120082445	HepG2	liver:	n/a	n/a
19	CTBP2	chr11:120080927-120082755	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr11:120081598-120082026	HepG2	liver:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
21	CTCF	chr11:120081680-120081830	AG04449	skin:	n/a	n/a
22	CTCF	chr11:120081680-120081830	AG09319	gingival:	n/a	n/a
23	CTCF	chr11:120081400-120081550	GM12865	blood:	n/a	chr11:120081439-120081448
24	CTCF	chr11:120081400-120081550	HUVEC	blood vessel:	n/a	chr11:120081439-120081448
25	CTCF	chr11:120081500-120081650	HCT-116	colon:	n/a	chr11:120081576-120081589
26	CTCF	chr11:120081895-120081898	K562	blood:	n/a	n/a
27	CTCF	chr11:120081760-120081910	HEK293	kidney:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
28	CTCF	chr11:120081800-120081950	GM12873	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
29	CTCF	chr11:120081700-120081850	HBMEC	blood vessel:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
30	CTCF	chr11:120081400-120081550	AG09319	gingival:	n/a	chr11:120081439-120081448
31	CTCF	chr11:120081660-120081810	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr11:120081540-120081690	AG04450	lung:	n/a	chr11:120081576-120081589
33	CTCF	chr11:120081420-120081570	AoAF	blood vessel:	n/a	chr11:120081439-120081448
34	CTCF	chr11:120081689-120081930	GM19238	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
35	CTCF	chr11:120081720-120081870	AG09319	gingival:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
36	CTCF	chr11:120081778-120081814	LNCaP	prostate:	n/a	n/a
37	CTCF	chr11:120081320-120081470	BJ	skin:	n/a	chr11:120081439-120081448
38	CTCF	chr11:120081710-120081950	Kidney_OC	kidney:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
39	CTCF	chr11:120081753-120081894	GM13976	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
40	CTCF	chr11:120081680-120081830	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr11:120081720-120081870	NHLF	lung:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
42	CTCF	chr11:120082036-120082040	GM19240	blood:	n/a	n/a
43	CTCF	chr11:120081740-120081890	AG10803	skin:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
44	CTCF	chr11:120081740-120081890	GM12865	blood:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
45	CTCF	chr11:120081660-120081810	HCFaa	heart:	n/a	n/a
46	CTCF	chr11:120081340-120081490	AG04449	skin:	n/a	chr11:120081439-120081448
47	CTCF	chr11:120081640-120081790	A549	lung:	n/a	n/a
48	CTCF	chr11:120081680-120081830	GM12873	blood:	n/a	n/a
49	CTCF	chr11:120081700-120081850	HUVEC	blood vessel:	n/a	chr11:120081834-120081850 chr11:120081835-120081848
50	CTCF	chr11:120081766-120081858	NHEK	skin:	n/a	chr11:120081834-120081850 chr11:120081835-120081848

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:120081506-120081556	Hepatocyte	liver:	n/a
2	chr11:120081890-120081940	ovcar-3	ovarian:	n/a
3	chr11:120081506-120081556	Hepatocyte	liver:	n/a
4	chr11:120081890-120081940	ovcar-3	ovarian:	n/a
5	chr11:120081755-120081805	HCF	heart:	n/a
6	chr11:120081890-120081940	PrEC	prostate:	n/a
7	chr11:120081143-120081193	GM19239	blood:	n/a
8	chr11:120081890-120081940	HL-60	blood:	n/a
9	chr11:120081643-120081693	GM12891	blood:	n/a
10	chr11:120081143-120081193	HRE	kidney:	n/a
11	chr11:120081645-120081695	HCF	heart:	n/a
12	chr11:120081089-120081139	Hela-S3	cervix:	n/a
13	chr11:120081089-120081139	U87	brain:	n/a
14	chr11:120080945-120080995	AG09309	skin:	n/a
15	chr11:120081506-120081556	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:120082805-120082855	IMR90	lung:	fetal
17	chr11:120082805-120082855	HEEpiC	esophagus:	n/a
18	chr11:120081643-120081693	HNPCEpiC	eye:	n/a
19	chr11:120081089-120081139	BE2_C	brain:	n/a
20	chr11:120081749-120081799	GM12878	blood:	n/a
21	chr11:120081143-120081193	GM06990	blood:	n/a
22	chr11:120080945-120080995	SK-N-SH_RA	brain:	n/a
23	chr11:120081749-120081799	CMK	blood:	n/a
24	chr11:120080945-120080995	NHDF-neo	bronchial:	n/a
25	chr11:120081643-120081693	AG10803	skin:	n/a
26	chr11:120081143-120081193	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:120081755-120081805	PANC-1	pancreas:	n/a
28	chr11:120082238-120082288	HUVEC	blood vessel:	n/a
29	chr11:120082805-120082855	MCF-7	breast:	n/a
30	chr11:120081890-120081940	CMK	blood:	n/a
31	chr11:120081497-120081547	MCF-7	breast:	n/a
32	chr11:120080945-120080995	ECC-1	luminal epithelium:	n/a
33	chr11:120081890-120081940	AG04449	skin:	fetal
34	chr11:120081497-120081547	HEK293	kidney:	embryo
35	chr11:120082805-120082855	T-47D	breast:	n/a
36	chr11:120081143-120081193	CMK	blood:	n/a
37	chr11:120081089-120081139	HMEC	breast:	n/a
38	chr11:120081259-120081309	NH-A	brain:	n/a
39	chr11:120081143-120081193	Jurkat	blood:	n/a
40	chr11:120080945-120080995	NHBE	bronchial:	n/a
41	chr11:120081497-120081547	AoSMC	blood vessel:	n/a
42	chr11:120081506-120081556	Caco-2	colon:	n/a
43	chr11:120081749-120081799	ProgFib	skin:	n/a
44	chr11:120081143-120081193	HCF	heart:	n/a
45	chr11:120081643-120081693	Caco-2	colon:	n/a
46	chr11:120082238-120082288	T-47D	breast:	n/a
47	chr11:120081506-120081556	AG10803	skin:	n/a
48	chr11:120081749-120081799	RPTEC	kidney:	n/a
49	chr11:120081089-120081139	HNPCEpiC	eye:	n/a
50	chr11:120082238-120082288	HCM	heart:	n/a

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

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

Extended variants
information (count: 98 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:98 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	rs183255862	chr11:120081055-120081056	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
25	rs546846749	chr11:120081080-120081081	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
26	rs114217933	chr11:120081152-120081153	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs78777904	chr11:120081160-120081161	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs114874993	chr11:120081165-120081166	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs574938370	chr11:120081167-120081168	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs116008980	chr11:120081223-120081224	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs116362174	chr11:120081228-120081229	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs573350517	chr11:120081294-120081295	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs372053079	chr11:120081312-120081313	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs540492075	chr11:120081320-120081321	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs374518972	chr11:120081377-120081378	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs71462037	chr11:120081388-120081389	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs397933821	chr11:120081402-120081403	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs376655523	chr11:120081403-120081404	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs199834788	chr11:120081443-120081444	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs145896216	chr11:120081463-120081464	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs56041316	chr11:120081465-120081466	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs202223979	chr11:120081468-120081469	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs138435357	chr11:120081510-120081511	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs577605006	chr11:120081516-120081517	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs544968176	chr11:120081525-120081526	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs562825402	chr11:120081526-120081527	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs571210103	chr11:120081544-120081545	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs76424512	chr11:120081700-120081701	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs557326391	chr11:120081746-120081747	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs548631734	chr11:120081763-120081764	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 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:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr11:120078400-120080400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:120078400-120080400	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr11:120078400-120080600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr11:120078400-120080600	Enhancers	Adipose Nuclei	Adipose
14	chr11:120078400-120080600	Enhancers	Brain Anterior Caudate	brain
15	chr11:120078400-120080600	Enhancers	Brain Hippocampus Middle	brain
16	chr11:120078400-120080600	Enhancers	Colonic Mucosa	Colon
17	chr11:120078400-120080600	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr11:120078400-120080600	Enhancers	NHDF-Ad	bronchial
19	chr11:120078400-120080800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr11:120078400-120080800	Enhancers	Brain Angular Gyrus	brain
21	chr11:120078400-120080800	Enhancers	Brain Cingulate Gyrus	brain
22	chr11:120078400-120080800	Enhancers	Fetal Intestine Small	intestine
23	chr11:120078400-120080800	Enhancers	Fetal Muscle Trunk	muscle
24	chr11:120078400-120080800	Enhancers	Ovary	ovary
25	chr11:120078400-120081000	Enhancers	Esophagus	oesophagus
26	chr11:120078400-120081000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr11:120078400-120081000	Enhancers	Small Intestine	intestine
28	chr11:120078600-120080400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:120078600-120080400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:120078600-120080400	Enhancers	Muscle Satellite Cultured Cells	--
31	chr11:120078600-120080400	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr11:120078600-120080400	Enhancers	Fetal Muscle Leg	muscle
33	chr11:120078600-120080600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr11:120078600-120080600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:120078600-120080600	Enhancers	Duodenum Mucosa	Duodenum
36	chr11:120078600-120080600	Enhancers	Hela-S3	cervix
37	chr11:120078600-120080800	Enhancers	Right Atrium	heart
38	chr11:120078600-120081000	Enhancers	HMEC	breast
39	chr11:120078600-120081000	Enhancers	HUVEC	blood vessel
40	chr11:120078800-120080600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr11:120078800-120080600	Enhancers	NHLF	lung
42	chr11:120078800-120080800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr11:120078800-120080800	Enhancers	Placenta	Placenta
44	chr11:120078800-120080800	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr11:120078800-120080800	Enhancers	HSMM	muscle
46	chr11:120079000-120080400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
47	chr11:120079000-120080600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:120079000-120080600	Weak transcription	Lung	lung
49	chr11:120079000-120080800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr11:120079200-120080400	Weak transcription	Brain Germinal Matrix	brain

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