Variant report

Variant	esv1799280
Chromosome Location	chr11:17299390-17354775
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:319)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17298792-17299541	K562	blood:	n/a	n/a
2	ATF2	chr11:17315464-17316124	GM12878	blood:	n/a	n/a
3	ATF2	chr11:17319713-17320319	GM12878	blood:	n/a	n/a
4	ATF2	chr11:17315495-17315916	GM12878	blood:	n/a	n/a
5	ATF2	chr11:17319739-17320323	GM12878	blood:	n/a	n/a
6	BATF	chr11:17318396-17318651	GM12878	blood:	n/a	n/a
7	BATF	chr11:17319777-17320285	GM12878	blood:	n/a	n/a
8	BATF	chr11:17319816-17320200	GM12878	blood:	n/a	n/a
9	BATF	chr11:17315531-17315975	GM12878	blood:	n/a	n/a
10	BATF	chr11:17318368-17318670	GM12878	blood:	n/a	n/a
11	BATF	chr11:17315562-17315887	GM12878	blood:	n/a	n/a
12	BCL11A	chr11:17315561-17315939	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:17319838-17320210	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:17319811-17320210	GM12878	blood:	n/a	n/a
15	BCL3	chr11:17319744-17320237	GM12878	blood:	n/a	n/a
16	BCL3	chr11:17319803-17320138	GM12878	blood:	n/a	n/a
17	BCLAF1	chr11:17319783-17320311	GM12878	blood:	n/a	n/a
18	BCLAF1	chr11:17319803-17320210	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:17336006-17336007	HepG2	liver:	n/a	n/a
20	BHLHE40	chr11:17319916-17320153	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:17307409-17307597	K562	blood:	n/a	n/a
22	CEBPB	chr11:17319896-17320187	GM12878	blood:	n/a	n/a
23	CEBPB	chr11:17320251-17320332	A549	lung:	n/a	n/a
24	CEBPB	chr11:17335796-17336042	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:17313606-17313609	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:17302045-17302413	K562	blood:	n/a	chr11:17302231-17302242
27	CEBPB	chr11:17320225-17320412	K562	blood:	n/a	n/a
28	CEBPB	chr11:17302037-17302399	K562	blood:	n/a	chr11:17302231-17302242
29	CEBPB	chr11:17302044-17302398	HepG2	liver:	n/a	chr11:17302231-17302242
30	CEBPB	chr11:17320213-17320404	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:17304269-17304472	HepG2	liver:	n/a	chr11:17304409-17304420
32	CEBPB	chr11:17302088-17302280	A549	lung:	n/a	chr11:17302231-17302242
33	CEBPB	chr11:17335538-17336126	IMR90	lung:	n/a	n/a
34	CEBPB	chr11:17302029-17302414	Hela-S3	cervix:	n/a	chr11:17302231-17302242
35	CEBPB	chr11:17304373-17304520	A549	lung:	n/a	chr11:17304409-17304420
36	CEBPB	chr11:17319749-17320358	GM12878	blood:	n/a	n/a
37	CEBPB	chr11:17302077-17302365	IMR90	lung:	n/a	chr11:17302231-17302242
38	CEBPB	chr11:17327219-17327340	HepG2	liver:	n/a	chr11:17327224-17327235
39	CHD1	chr11:17320060-17320072	GM12878	blood:	n/a	n/a
40	CHD2	chr11:17320004-17320060	GM12878	blood:	n/a	n/a
41	CREB1	chr11:17319819-17320336	GM12878	blood:	n/a	n/a
42	CTCF	chr11:17350520-17350670	GM12866	blood:	n/a	n/a
43	CTCF	chr11:17350580-17350730	GM12864	blood:	n/a	n/a
44	CTCF	chr11:17350560-17350710	HCFaa	heart:	n/a	n/a
45	CTCF	chr11:17350520-17350670	HMF	breast:	n/a	n/a
46	CTCF	chr11:17350580-17350730	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr11:17350460-17350610	GM12865	blood:	n/a	n/a
48	CTCF	chr11:17350500-17350650	GM12865	blood:	n/a	n/a
49	CTCF	chr11:17350560-17350710	WI-38	lung:	n/a	n/a
50	CTCF	chr11:17335420-17335570	GM12869	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17300909-17300959	BE2_C	brain:	n/a
2	chr11:17300909-17300959	MCF10A-Er-Src	breast:	n/a
3	chr11:17300909-17300959	GM12891	blood:	n/a
4	chr11:17300909-17300959	NHBE	bronchial:	n/a
5	chr11:17300909-17300959	Hepatocyte	liver:	n/a
6	chr11:17300909-17300959	HL-60	blood:	n/a
7	chr11:17300909-17300959	GM12892	blood:	n/a
8	chr11:17300909-17300959	HRPEpiC	eye:	n/a
9	chr11:17300909-17300959	T-47D	breast:	n/a
10	chr11:17300909-17300959	NH-A	brain:	n/a
11	chr11:17300909-17300959	HAEpiC	amniotic membrane:	n/a
12	chr11:17300909-17300959	MCF-7	breast:	n/a
13	chr11:17300909-17300959	Hela-S3	cervix:	n/a
14	chr11:17300909-17300959	AG10803	skin:	n/a
15	chr11:17300909-17300959	U87	brain:	n/a
16	chr11:17300909-17300959	AG04450	lung:	fetal
17	chr11:17300909-17300959	AG09319	gingival:	n/a
18	chr11:17300909-17300959	K562	blood:	n/a
19	chr11:17300909-17300959	GM12878	blood:	n/a
20	chr11:17300909-17300959	ovcar-3	ovarian:	n/a
21	chr11:17300909-17300959	HUVEC	blood vessel:	n/a
22	chr11:17300909-17300959	SAEC	small airway:	n/a
23	chr11:17300909-17300959	H1-hESC	embryonic stem cell:	embryo
24	chr11:17300909-17300959	HEK293	kidney:	embryo
25	chr11:17300909-17300959	BJ	skin:	n/a
26	chr11:17300909-17300959	CMK	blood:	n/a
27	chr11:17300909-17300959	GM19239	blood:	n/a
28	chr11:17300909-17300959	A549	lung:	n/a
29	chr11:17300909-17300959	RPTEC	kidney:	n/a
30	chr11:17300909-17300959	ProgFib	skin:	n/a
31	chr11:17300909-17300959	Jurkat	blood:	n/a
32	chr11:17300909-17300959	SK-N-MC	brain:	n/a
33	chr11:17300909-17300959	NT2-D1	testis:	n/a
34	chr11:17300909-17300959	NB4	blood:	n/a
35	chr11:17300909-17300959	PANC-1	pancreas:	n/a
36	chr11:17300909-17300959	LNCaP	prostate:	n/a
37	chr11:17300909-17300959	NHDF-neo	bronchial:	n/a
38	chr11:17300909-17300959	HIPEpiC	eye:	n/a
39	chr11:17300909-17300959	HNPCEpiC	eye:	n/a
40	chr11:17300909-17300959	HCF	heart:	n/a
41	chr11:17300909-17300959	HRE	kidney:	n/a
42	chr11:17300909-17300959	SKMC	muscle:	n/a
43	chr11:17300909-17300959	PFSK-1	brain:	n/a
44	chr11:17300909-17300959	AoSMC	blood vessel:	n/a
45	chr11:17300909-17300959	HEEpiC	esophagus:	n/a
46	chr11:17300909-17300959	PrEC	prostate:	n/a
47	chr11:17300909-17300959	SK-N-SH	brain:	n/a
48	chr11:17300909-17300959	HCPEpiC	choroid plexus:	n/a
49	chr11:17300909-17300959	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:17300909-17300959	AG09309	skin:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17294885..17299963-chr11:17371989..17377835,11	K562	blood:
2	chr11:17229425..17232064-chr11:17297458..17300131,2	K562	blood:
3	chr11:17298938..17303193-chr11:17304940..17310347,8	K562	blood:
4	chr11:17296907..17298912-chr11:17352213..17353767,2	K562	blood:
5	chr11:17336111..17336712-chr4:31786899..31787441,2	MCF-7	breast:
6	chr11:17298938..17303193-chr11:17304940..17310347,8	K562	blood:
7	chr11:17305212..17308146-chr11:17308901..17311776,2	K562	blood:
8	chr11:17097827..17101102-chr11:17296839..17299555,4	K562	blood:
9	chr11:17336064..17337683-chr11:17338247..17340454,2	MCF-7	breast:
10	chr11:17336064..17337683-chr11:17338247..17340454,2	MCF-7	breast:
11	chr11:17324227..17326282-chr11:17370624..17372568,2	K562	blood:
12	chr11:17300662..17302728-chr11:17307021..17310347,3	K562	blood:
13	chr11:17297082..17301177-chr11:17313853..17317788,6	K562	blood:
14	chr11:17325618..17327534-chr11:17329034..17330695,2	K562	blood:
15	chr11:17297839..17299498-chr11:17314289..17315941,2	K562	blood:
16	chr11:17353493..17354076-chr19:10443927..10444707,2	NB4	blood:
17	chr11:17308283..17309860-chr11:17310824..17312984,2	K562	blood:
18	chr11:17326206..17329035-chr11:17373142..17375618,2	K562	blood:
19	chr11:17300662..17302728-chr11:17307021..17310347,3	K562	blood:
20	chr11:17097070..17101102-chr11:17296326..17299484,3	K562	blood:
21	chr11:17297082..17301177-chr11:17313853..17317788,6	K562	blood:
22	chr11:17305212..17308146-chr11:17308901..17311776,2	K562	blood:
23	chr11:17325618..17327534-chr11:17329034..17330695,2	K562	blood:
24	chr11:17229045..17230754-chr11:17298034..17300385,2	MCF-7	breast:
25	chr11:17296529..17299421-chr11:17301500..17303584,3	K562	blood:
26	chr11:17289797..17291811-chr11:17310885..17313618,2	MCF-7	breast:
27	chr11:17308283..17309860-chr11:17310824..17312984,2	K562	blood:
28	chr11:17293894..17295404-chr11:17299540..17302043,2	K562	blood:
29	chr11:17312629..17314667-chr11:17373506..17375869,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNJ11-5	chr11:17315881-17316560	l_439_chr11:17315763-17328093_testes
2	lnc-RP1-239B22.1.1-2	chr11:17317652-17317713	NONHSAT018223
3	lnc-RP1-239B22.1.1-2	chr11:17316872-17317014	NONHSAT018223
4	lnc-KCNJ11-5	chr11:17328921-17329034	l_439_chr11:17315763-17328093_testes
5	lnc-NUCB2-3	chr11:17353589-17356027	NONHSAT018224
6	lnc-RP1-239B22.1.1-2	chr11:17299909-17300084	NONHSAT018222
7	lnc-KCNJ11-5	chr11:17327447-17328093	l_439_chr11:17315763-17328093_testes
8	lnc-RP1-239B22.1.1-2	chr11:17304336-17304417	NONHSAT018222
9	lnc-KCNJ11-5	chr11:17329160-17329300	l_439_chr11:17315763-17328093_testes
10	lnc-RP1-239B22.1.1-2	chr11:17304337-17304490	NONHSAT018223
11	lnc-KCNJ11-5	chr11:17315764-17315875	l_439_chr11:17315763-17328093_testes

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NUCB2	hsa-miR-215-5p	chr11:17352449-17352453
2	NUCB2	hsa-miR-192-5p	chr11:17351828-17351844
3	NUCB2	hsa-miR-192-5p	chr11:17352449-17352453
4	NUCB2	hsa-miR-215-5p	chr11:17351828-17351844

Variant related genes	Relation type
NUCB2	TF binding region
NUCB2	CpG island
ENSG00000011405	chromatin interactions
ENSG00000201403	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000188211	chromatin interactions
ENSG00000070081	chromatin interactions

Extended variants
information (count: 1901 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1901 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs214082	chr11:17299390-17299391	Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376740519	chr11:17299394-17299395	Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs566215705	chr11:17299447-17299448	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs533612099	chr11:17299484-17299485	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs368191369	chr11:17299492-17299493	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs551489568	chr11:17299493-17299494	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs569798709	chr11:17299538-17299539	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs537022469	chr11:17299541-17299542	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs117253561	chr11:17299553-17299554	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs76299999	chr11:17299556-17299557	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs534876388	chr11:17299559-17299560	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs552996935	chr11:17299641-17299642	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs214081	chr11:17299654-17299655	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs188340798	chr11:17299662-17299663	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs557814773	chr11:17299687-17299688	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs576160193	chr11:17299702-17299703	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs368126965	chr11:17299715-17299716	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs375806525	chr11:17299717-17299718	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs35441492	chr11:17299740-17299741	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs11601108	chr11:17299743-17299744	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs544560590	chr11:17299761-17299762	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs214080	chr11:17299762-17299763	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs541706427	chr11:17299786-17299787	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs559834503	chr11:17299847-17299848	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs214079	chr11:17299868-17299869	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs214078	chr11:17299881-17299882	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs191293474	chr11:17299897-17299898	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs214077	chr11:17299969-17299970	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs374315197	chr11:17300013-17300014	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs560382356	chr11:17300036-17300037	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs529060358	chr11:17300089-17300090	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs202149020	chr11:17300091-17300092	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs34520227	chr11:17300137-17300138	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549105174	chr11:17300151-17300152	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs570538916	chr11:17300168-17300169	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs142295235	chr11:17300182-17300183	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs35873853	chr11:17300208-17300209	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs530586892	chr11:17300239-17300240	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs214076	chr11:17300257-17300258	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs567204983	chr11:17300267-17300268	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs556631712	chr11:17300397-17300398	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs369173212	chr11:17300402-17300403	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs214075	chr11:17300417-17300418	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs553224724	chr11:17300438-17300439	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146873713	chr11:17300510-17300511	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538427087	chr11:17300561-17300562	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs183201439	chr11:17300569-17300570	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575114983	chr11:17300655-17300656	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs61881920	chr11:17300687-17300688	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs554113933	chr11:17300695-17300696	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17297400-17299400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
2	chr11:17297400-17299400	Active TSS	Brain Angular Gyrus	brain
3	chr11:17297600-17299400	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr11:17297600-17299400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr11:17297600-17299400	Active TSS	Brain Germinal Matrix	brain
6	chr11:17297600-17299400	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr11:17297800-17299400	Active TSS	Brain Anterior Caudate	brain
8	chr11:17297800-17299400	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr11:17297800-17299400	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr11:17297800-17299400	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr11:17297800-17299400	Active TSS	NHLF	lung
12	chr11:17298000-17299400	Active TSS	Duodenum Mucosa	Duodenum
13	chr11:17298000-17299400	Active TSS	Fetal Intestine Large	intestine
14	chr11:17298000-17299400	Active TSS	Stomach Smooth Muscle	stomach
15	chr11:17298000-17299400	Active TSS	HSMMtube	muscle
16	chr11:17298000-17299400	Active TSS	NH-A	brain
17	chr11:17298000-17299600	Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr11:17298000-17299800	Active TSS	Fetal Thymus	thymus
19	chr11:17298000-17300000	Active TSS	Dnd41	blood
20	chr11:17298000-17300200	Active TSS	GM12878-XiMat	blood
21	chr11:17298000-17300800	Active TSS	Primary T cells fromperipheralblood	blood
22	chr11:17298000-17301200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
23	chr11:17298000-17302000	Active TSS	Thymus	Thymus
24	chr11:17298600-17299400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:17298600-17299400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr11:17298600-17299400	Flanking Active TSS	Adipose Nuclei	Adipose
27	chr11:17298600-17299400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr11:17298600-17299600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr11:17298600-17299800	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr11:17298800-17299400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:17298800-17299400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
32	chr11:17298800-17299400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr11:17298800-17299400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr11:17298800-17299400	Flanking Active TSS	Fetal Heart	heart
35	chr11:17298800-17299400	Flanking Active TSS	HUVEC	blood vessel
36	chr11:17298800-17299800	Flanking Active TSS	Primary T cells from cord blood	blood
37	chr11:17299000-17299400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:17299000-17299400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr11:17299000-17299400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:17299000-17299400	Flanking Active TSS	Fetal Brain Female	brain
41	chr11:17299000-17299400	Flanking Active TSS	A549	lung
42	chr11:17299000-17299400	Flanking Active TSS	NHEK	skin
43	chr11:17299000-17299600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr11:17299000-17299600	Flanking Active TSS	NHDF-Ad	bronchial
45	chr11:17299000-17300400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr11:17299000-17301000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr11:17299000-17301400	Weak transcription	Pancreas	Pancrea
48	chr11:17299000-17301600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:17299000-17302200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:17299000-17307200	Weak transcription	Left Ventricle	heart

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