Variant report

Variant	esv3370994
Chromosome Location	chr11:10471201-10473749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:274)
CpG islands
(count:672)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr11:10473141-10473311	GM12878	blood:	n/a	n/a
2	BRCA1	chr11:10472723-10472726	Hela-S3	cervix:	n/a	n/a
3	CHD1	chr11:10472559-10472877	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr11:10471337-10471338	GM12878	blood:	n/a	n/a
5	CHD2	chr11:10472462-10472925	Hela-S3	cervix:	n/a	n/a
6	CHD2	chr11:10473026-10473065	HepG2	liver:	n/a	n/a
7	CHD2	chr11:10472640-10472658	GM12878	blood:	n/a	n/a
8	CHD2	chr11:10473070-10473141	GM12878	blood:	n/a	n/a
9	CTBP2	chr11:10471474-10472989	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr11:10473100-10473250	GM12866	blood:	n/a	n/a
11	CTCF	chr11:10472770-10472886	GM10248	blood:	n/a	n/a
12	CTCF	chr11:10472780-10472930	GM12871	blood:	n/a	n/a
13	CTCF	chr11:10472160-10472310	HCPEpiC	choroid plexus:	n/a	chr11:10472176-10472189
14	CTCF	chr11:10472763-10472878	Lung_OC	lung:	n/a	n/a
15	CTCF	chr11:10472780-10472930	GM12869	blood:	n/a	n/a
16	CTCF	chr11:10472773-10472918	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr11:10472680-10472830	GM12875	blood:	n/a	n/a
18	CTCF	chr11:10472800-10472950	AG10803	skin:	n/a	n/a
19	CTCF	chr11:10472760-10472910	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr11:10472340-10472351	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr11:10472780-10472930	RPTEC	kidney:	n/a	n/a
22	CTCF	chr11:10472560-10472710	AG09319	gingival:	n/a	n/a
23	CTCF	chr11:10471900-10472050	GM12873	blood:	n/a	n/a
24	CTCF	chr11:10472760-10472910	BJ	skin:	n/a	n/a
25	CTCF	chr11:10472740-10472890	HCT-116	colon:	n/a	n/a
26	CTCF	chr11:10472780-10472930	HCM	heart:	n/a	n/a
27	CTCF	chr11:10472720-10472870	AG04450	lung:	n/a	n/a
28	CTCF	chr11:10472840-10472990	A549	lung:	n/a	n/a
29	CTCF	chr11:10472720-10472870	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr11:10472780-10472930	HPF	lung:	n/a	n/a
31	CTCF	chr11:10472770-10472860	ProgFib	skin:	n/a	n/a
32	CTCF	chr11:10472740-10472890	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr11:10472740-10472890	AG10803	skin:	n/a	n/a
34	CTCF	chr11:10472732-10472904	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:10472160-10472310	GM12873	blood:	n/a	chr11:10472176-10472189
36	CTCF	chr11:10472831-10472874	GM13976	blood:	n/a	n/a
37	CTCF	chr11:10472740-10472890	GM12865	blood:	n/a	n/a
38	CTCF	chr11:10472320-10472470	GM12871	blood:	n/a	n/a
39	CTCF	chr11:10472808-10472852	GM13977	blood:	n/a	n/a
40	CTCF	chr11:10472342-10472350	GM12892	blood:	n/a	n/a
41	CTCF	chr11:10472700-10472850	HCM	heart:	n/a	n/a
42	CTCF	chr11:10472140-10472290	GM06990	blood:	n/a	chr11:10472176-10472189
43	CTCF	chr11:10472740-10472890	GM12869	blood:	n/a	n/a
44	CTCF	chr11:10472780-10472930	GM12864	blood:	n/a	n/a
45	CTCF	chr11:10472100-10472250	SAEC	small airway:	n/a	chr11:10472176-10472189
46	CTCF	chr11:10472583-10473000	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr11:10473220-10473370	GM12871	blood:	n/a	n/a
48	CTCF	chr11:10472620-10472770	GM12875	blood:	n/a	n/a
49	CTCF	chr11:10472212-10472254	GM12892	blood:	n/a	n/a
50	CTCF	chr11:10472727-10472916	MCF-7	breast:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10473038-10473088	PFSK-1	brain:	n/a
2	chr11:10473038-10473088	PFSK-1	brain:	n/a
3	chr11:10473038-10473088	MCF10A-Er-Src	breast:	n/a
4	chr11:10472840-10472890	SKMC	muscle:	n/a
5	chr11:10472149-10472199	NHBE	bronchial:	n/a
6	chr11:10472099-10472149	H1-hESC	embryonic stem cell:	embryo
7	chr11:10472001-10472051	HEEpiC	esophagus:	n/a
8	chr11:10471371-10471421	SK-N-SH_RA	brain:	n/a
9	chr11:10473038-10473088	CMK	blood:	n/a
10	chr11:10472156-10472206	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:10472156-10472206	AG09309	skin:	n/a
12	chr11:10472159-10472209	A549	lung:	n/a
13	chr11:10472133-10472183	AG09309	skin:	n/a
14	chr11:10472159-10472209	AG04449	skin:	fetal
15	chr11:10471371-10471421	NH-A	brain:	n/a
16	chr11:10472156-10472206	NB4	blood:	n/a
17	chr11:10472840-10472890	MCF-7	breast:	n/a
18	chr11:10472149-10472199	HAEpiC	amniotic membrane:	n/a
19	chr11:10472099-10472149	PFSK-1	brain:	n/a
20	chr11:10471371-10471421	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:10471371-10471421	NHDF-neo	bronchial:	n/a
22	chr11:10472840-10472890	HCT-116	colon:	n/a
23	chr11:10471371-10471421	AG04450	lung:	fetal
24	chr11:10473038-10473088	Jurkat	blood:	n/a
25	chr11:10472840-10472890	SK-N-SH	brain:	n/a
26	chr11:10472465-10472515	HepG2	liver:	n/a
27	chr11:10472099-10472149	SKMC	muscle:	n/a
28	chr11:10472149-10472199	SK-N-MC	brain:	n/a
29	chr11:10472149-10472199	SKMC	muscle:	n/a
30	chr11:10472001-10472051	H1-hESC	embryonic stem cell:	embryo
31	chr11:10472156-10472206	HCM	heart:	n/a
32	chr11:10472099-10472149	NH-A	brain:	n/a
33	chr11:10473038-10473088	HepG2	liver:	n/a
34	chr11:10472161-10472211	BE2_C	brain:	n/a
35	chr11:10472159-10472209	HCM	heart:	n/a
36	chr11:10472161-10472211	HCF	heart:	n/a
37	chr11:10472133-10472183	SAEC	small airway:	n/a
38	chr11:10472156-10472206	PrEC	prostate:	n/a
39	chr11:10472161-10472211	HCT-116	colon:	n/a
40	chr11:10472156-10472206	ProgFib	skin:	n/a
41	chr11:10472465-10472515	HCM	heart:	n/a
42	chr11:10472133-10472183	PFSK-1	brain:	n/a
43	chr11:10472465-10472515	HAEpiC	amniotic membrane:	n/a
44	chr11:10472149-10472199	AG10803	skin:	n/a
45	chr11:10472099-10472149	AG04450	lung:	fetal
46	chr11:10472161-10472211	HEEpiC	esophagus:	n/a
47	chr11:10472149-10472199	HCF	heart:	n/a
48	chr11:10472099-10472149	T-47D	breast:	n/a
49	chr11:10471371-10471421	AG10803	skin:	n/a
50	chr11:10472840-10472890	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:10471184..10472852-chr11:10561290..10564176,2	K562	blood:
2	chr11:10469398..10472547-chr11:10473380..10477623,4	K562	blood:
3	chr11:10470733..10474944-chr11:10476648..10480616,5	MCF-7	breast:
4	chr11:10428535..10430173-chr11:10471249..10473167,2	MCF-7	breast:
5	chr11:10469398..10472547-chr11:10473380..10477623,4	K562	blood:
6	chr11:10466561..10468211-chr11:10473032..10475120,2	K562	blood:

No data

Variant related genes	Relation type
AMPD3	TF binding region
AMPD3	CpG island
ENSG00000110315	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000177112	chromatin interactions

Extended variants
information (count: 95 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7112321	chr11:10471218-10471219	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549755564	chr11:10471219-10471220	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs192070296	chr11:10471236-10471237	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs563296401	chr11:10471288-10471289	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs542575543	chr11:10471301-10471302	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs532056235	chr11:10471309-10471310	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs117982407	chr11:10471356-10471357	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs531826167	chr11:10471371-10471372	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs185353025	chr11:10471374-10471375	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs190594424	chr11:10471375-10471376	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs548003669	chr11:10471384-10471385	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs567388355	chr11:10471399-10471400	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs562822048	chr11:10471414-10471415	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs531159022	chr11:10471433-10471434	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs181942554	chr11:10471500-10471501	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs11042810	chr11:10471532-10471533	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs187412423	chr11:10471533-10471534	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs538701034	chr11:10471594-10471595	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs559190776	chr11:10471674-10471675	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs7111970	chr11:10471680-10471681	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs112396918	chr11:10471738-10471739	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs375057061	chr11:10471773-10471774	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs9300103	chr11:10471785-10471786	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs59922442	chr11:10471807-10471808	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs398015331	chr11:10471825-10471826	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs202123961	chr11:10471833-10471834	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs140973307	chr11:10471886-10471887	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs147657718	chr11:10471887-10471888	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs10590775	chr11:10471919-10471920	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs561473444	chr11:10471921-10471922	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs7937289	chr11:10471931-10471932	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs7938316	chr11:10472064-10472065	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs563278746	chr11:10472207-10472208	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	4 gene(s)	Overlapped CNVs	n/a
34	rs532117907	chr11:10472208-10472209	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	4 gene(s)	Overlapped CNVs	n/a
35	rs61891367	chr11:10472239-10472240	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559569973	chr11:10472247-10472248	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs528385857	chr11:10472263-10472264	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs547942597	chr11:10472332-10472333	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs567919603	chr11:10472352-10472353	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs536893586	chr11:10472421-10472422	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs550242052	chr11:10472427-10472428	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs570088725	chr11:10472437-10472438	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs138176008	chr11:10472438-10472439	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs558692820	chr11:10472479-10472480	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs35417007	chr11:10472493-10472494	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs398075717	chr11:10472494-10472495	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs397849293	chr11:10472495-10472496	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs572734481	chr11:10472497-10472498	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs535336026	chr11:10472499-10472500	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs555347075	chr11:10472521-10472522	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10457600-10471800	Weak transcription	NHDF-Ad	bronchial
2	chr11:10464600-10471600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:10465600-10472000	Weak transcription	Right Atrium	heart
4	chr11:10466600-10471400	Weak transcription	Spleen	Spleen
5	chr11:10467200-10471800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr11:10467400-10471400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr11:10467400-10471600	Weak transcription	Adipose Nuclei	Adipose
8	chr11:10469800-10471400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr11:10471000-10471400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr11:10471000-10471400	Enhancers	Brain Hippocampus Middle	brain
11	chr11:10471000-10471600	Enhancers	Primary B cells from cord blood	blood
12	chr11:10471000-10471600	Enhancers	Primary B cells from peripheral blood	blood
13	chr11:10471000-10471600	Enhancers	Primary T cells from cord blood	blood
14	chr11:10471000-10471600	Enhancers	Primary T cells fromperipheralblood	blood
15	chr11:10471000-10471600	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr11:10471000-10471600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr11:10471000-10471600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
18	chr11:10471000-10471600	Enhancers	Esophagus	oesophagus
19	chr11:10471000-10471800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr11:10471000-10471800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr11:10471000-10472000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr11:10471200-10471400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr11:10471200-10471400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr11:10471200-10471400	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr11:10471200-10471400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:10471200-10471400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:10471200-10471600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr11:10471200-10471600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
29	chr11:10471200-10471600	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr11:10471200-10471600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr11:10471200-10471600	Enhancers	Brain Angular Gyrus	brain
32	chr11:10471200-10471600	Enhancers	Fetal Thymus	thymus
33	chr11:10471200-10471600	Enhancers	Pancreas	Pancrea
34	chr11:10471200-10471800	Enhancers	Primary hematopoietic stem cells	blood
35	chr11:10471200-10471800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr11:10471200-10471800	Flanking Active TSS	Brain Anterior Caudate	brain
37	chr11:10471200-10472000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr11:10471200-10472200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
39	chr11:10471200-10472800	Active TSS	Brain Substantia Nigra	brain
40	chr11:10471400-10471600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr11:10471400-10471600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:10471400-10471600	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr11:10471400-10471600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr11:10471400-10471600	Enhancers	Brain Cingulate Gyrus	brain
45	chr11:10471400-10471600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr11:10471400-10471600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr11:10471400-10471600	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr11:10471400-10471800	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:10471400-10471800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:10471400-10471800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood

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