Variant report

Variant	nsv975851
Chromosome Location	chr11:71278888-71295301
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	chr11:71291147-71291237	K562	blood:	n/a	n/a
2	BACH1	chr11:71291175-71291514	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr11:71288393-71289155	GM12878	blood:	n/a	n/a
4	BCL3	chr11:71288357-71289171	GM12878	blood:	n/a	n/a
5	BCL3	chr11:71281541-71282202	GM12878	blood:	n/a	n/a
6	BCL3	chr11:71281522-71282063	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:71291241-71291351	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:71291263-71291425	K562	blood:	n/a	n/a
9	CBX3	chr11:71291200-71291647	HCT-116	colon:	n/a	n/a
10	CBX3	chr11:71291105-71291464	K562	blood:	n/a	n/a
11	CEBPB	chr11:71291255-71291367	K562	blood:	n/a	n/a
12	CTCF	chr11:71291220-71291370	WERI-Rb-1	eye:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
13	CTCF	chr11:71291200-71291350	NB4	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
14	CTCF	chr11:71291220-71291370	BE2_C	brain:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
15	CTCF	chr11:71291220-71291370	HPF	lung:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
16	CTCF	chr11:71291220-71291370	HEEpiC	esophagus:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
17	CTCF	chr11:71291200-71291350	HRE	kidney:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
18	CTCF	chr11:71291220-71291370	HEK293	kidney:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
19	CTCF	chr11:71291260-71291410	WI-38	lung:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
20	CTCF	chr11:71278780-71278930	HRE	kidney:	n/a	chr11:71278817-71278838
21	CTCF	chr11:71291700-71291850	RPTEC	kidney:	n/a	n/a
22	CTCF	chr11:71291721-71291988	K562	blood:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
23	CTCF	chr11:71291137-71291439	HepG2	liver:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
24	CTCF	chr11:71291152-71291447	Gliobla	brain:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
25	CTCF	chr11:71291920-71292070	GM06990	blood:	n/a	n/a
26	CTCF	chr11:71291743-71291920	GM12878	blood:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
27	CTCF	chr11:71291104-71291517	H1-hESC	embryonic stem cell:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
28	CTCF	chr11:71291220-71291370	HCFaa	heart:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
29	CTCF	chr11:71291786-71291931	GM10266	blood:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
30	CTCF	chr11:71291804-71291968	GM10248	blood:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
31	CTCF	chr11:71290860-71291010	GM12869	blood:	n/a	n/a
32	CTCF	chr11:71291240-71291390	HEK293	kidney:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
33	CTCF	chr11:71291752-71291890	MCF-7	breast:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
34	CTCF	chr11:71291747-71291978	K562	blood:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
35	CTCF	chr11:71291680-71291830	HCT-116	colon:	n/a	n/a
36	CTCF	chr11:71291680-71291830	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr11:71291700-71291850	MCF-7	breast:	n/a	n/a
38	CTCF	chr11:71291160-71291310	GM12866	blood:	n/a	chr11:71291302-71291310
39	CTCF	chr11:71278802-71278890	MCF-7	breast:	n/a	chr11:71278817-71278838
40	CTCF	chr11:71291220-71291370	GM12865	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
41	CTCF	chr11:71291046-71291528	K562	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
42	CTCF	chr11:71291598-71291944	GM13977	blood:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
43	CTCF	chr11:71291240-71291390	HMF	breast:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
44	CTCF	chr11:71291640-71291790	GM12868	blood:	n/a	n/a
45	CTCF	chr11:71291744-71291961	Gliobla	brain:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
46	CTCF	chr11:71291680-71291830	WI-38	lung:	n/a	n/a
47	CTCF	chr11:71291721-71291968	K562	blood:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
48	CTCF	chr11:71291680-71291830	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr11:71291157-71291470	LNCaP	prostate:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
50	CTCF	chr11:71291220-71291370	GM12872	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71282370-71282420	GM12892	blood:	n/a
2	chr11:71285546-71285596	HMEC	breast:	n/a
3	chr11:71282370-71282420	GM12892	blood:	n/a
4	chr11:71285546-71285596	HMEC	breast:	n/a
5	chr11:71294819-71294869	HAEpiC	amniotic membrane:	n/a
6	chr11:71293892-71293942	HepG2	liver:	n/a
7	chr11:71282370-71282420	Jurkat	blood:	n/a
8	chr11:71288256-71288306	ProgFib	skin:	n/a
9	chr11:71288203-71288253	PFSK-1	brain:	n/a
10	chr11:71288256-71288306	NT2-D1	testis:	n/a
11	chr11:71288514-71288564	AG10803	skin:	n/a
12	chr11:71282370-71282420	AG04449	skin:	fetal
13	chr11:71282718-71282768	AG09319	gingival:	n/a
14	chr11:71293892-71293942	MCF10A-Er-Src	breast:	n/a
15	chr11:71293996-71294046	HRCEpiC	kidney:	n/a
16	chr11:71294744-71294794	HEK293	kidney:	embryo
17	chr11:71294819-71294869	H1-hESC	embryonic stem cell:	embryo
18	chr11:71285546-71285596	PFSK-1	brain:	n/a
19	chr11:71288256-71288306	BJ	skin:	n/a
20	chr11:71294605-71294655	HNPCEpiC	eye:	n/a
21	chr11:71294744-71294794	SAEC	small airway:	n/a
22	chr11:71294605-71294655	PANC-1	pancreas:	n/a
23	chr11:71285546-71285596	GM19239	blood:	n/a
24	chr11:71293996-71294046	GM12891	blood:	n/a
25	chr11:71294819-71294869	A549	lung:	n/a
26	chr11:71288256-71288306	NHDF-neo	bronchial:	n/a
27	chr11:71293892-71293942	ECC-1	luminal epithelium:	n/a
28	chr11:71293892-71293942	AoSMC	blood vessel:	n/a
29	chr11:71288514-71288564	Jurkat	blood:	n/a
30	chr11:71293184-71293234	IMR90	lung:	fetal
31	chr11:71294744-71294794	HCM	heart:	n/a
32	chr11:71294744-71294794	PrEC	prostate:	n/a
33	chr11:71293184-71293234	T-47D	breast:	n/a
34	chr11:71287919-71287969	Caco-2	colon:	n/a
35	chr11:71288203-71288253	NH-A	brain:	n/a
36	chr11:71287919-71287969	HL-60	blood:	n/a
37	chr11:71294605-71294655	HEEpiC	esophagus:	n/a
38	chr11:71288514-71288564	LNCaP	prostate:	n/a
39	chr11:71293996-71294046	AG10803	skin:	n/a
40	chr11:71293184-71293234	MCF10A-Er-Src	breast:	n/a
41	chr11:71282370-71282420	MCF-7	breast:	n/a
42	chr11:71282718-71282768	HCF	heart:	n/a
43	chr11:71288203-71288253	HL-60	blood:	n/a
44	chr11:71294744-71294794	HPAEpiC	pulmonary alveolar:	n/a
45	chr11:71288256-71288306	GM12892	blood:	n/a
46	chr11:71293184-71293234	SK-N-SH	brain:	n/a
47	chr11:71288256-71288306	HIPEpiC	eye:	n/a
48	chr11:71288256-71288306	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:71282718-71282768	SK-N-SH	brain:	n/a
50	chr11:71294605-71294655	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:71163473..71165824-chr11:71289975..71292795,2	MCF-7	breast:
2	chr11:71282448..71285837-chr11:71286010..71289392,3	MCF-7	breast:
3	chr11:71279425..71280036-chr11:71290519..71291383,2	MCF-7	breast:
4	chr11:71282448..71285837-chr11:71286010..71289392,3	MCF-7	breast:
5	chr11:71279425..71280036-chr11:71290519..71291383,2	MCF-7	breast:
6	chr11:71278406..71279386-chr11:71291430..71292089,2	MCF-7	breast:
7	chr11:71278394..71279845-chr11:71290961..71292008,7	MCF-7	breast:
8	chr11:71272055..71274887-chr11:71280546..71282110,2	K562	blood:
9	chr11:71162651..71164294-chr11:71282060..71284159,2	K562	blood:
10	chr11:71185954..71187783-chr11:71290414..71293087,2	MCF-7	breast:
11	chr11:71198072..71200599-chr11:71283906..71285709,2	MCF-7	breast:
12	chr11:71278406..71279386-chr11:71291430..71292089,2	MCF-7	breast:
13	chr11:71158604..71160379-chr11:71280505..71283180,2	MCF-7	breast:
14	chr11:71279845..71280406-chr11:71290008..71290749,2	MCF-7	breast:
15	chr11:71159116..71165503-chr11:71274687..71279227,9	MCF-7	breast:
16	chr11:71284028..71285602-chr11:71289697..71292475,2	MCF-7	breast:
17	chr11:71278628..71280477-chr11:71289049..71291000,2	MCF-7	breast:
18	chr11:71158649..71161220-chr11:71291218..71293129,2	MCF-7	breast:
19	chr11:71278628..71280477-chr11:71289049..71291000,2	MCF-7	breast:
20	chr11:71279845..71280406-chr11:71290008..71290749,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-3	chr11:71292956-71293203	NONHSAT022693
2	lnc-KRTAP5-10-1	chr11:71279726-71279980	NONHSAT022692

Variant related genes	Relation type
ENSG00000248903	TF binding region
KRTAP5-14P	TF binding region
KRTAP5-11	TF binding region
ENSG00000248903	CpG island
KRTAP5-14P	CpG island
KRTAP5-11	CpG island
ENSG00000249387	chromatin interactions
ENSG00000172893	chromatin interactions
ENSG00000254682	chromatin interactions
ENSG00000172890	chromatin interactions
ENSG00000248903	chromatin interactions

Extended variants
information (count: 966 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:966 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545411445	chr11:71278906-71278907	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs9651752	chr11:71278915-71278916	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs375413620	chr11:71278916-71278917	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs61890231	chr11:71278930-71278931	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs150780750	chr11:71278972-71278973	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs113605649	chr11:71278975-71278976	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs567469939	chr11:71278995-71278996	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs528339780	chr11:71279045-71279046	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs73530502	chr11:71279052-71279053	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs72966230	chr11:71279053-71279054	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs9651753	chr11:71279092-71279093	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs372922113	chr11:71279109-71279110	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs547988723	chr11:71279171-71279172	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs9651754	chr11:71279222-71279223	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs369024155	chr11:71279227-71279228	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs536349754	chr11:71279257-71279258	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs552946696	chr11:71279268-71279269	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs371083819	chr11:71279334-71279335	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs548707986	chr11:71279338-71279339	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs118079461	chr11:71279353-71279354	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs77442921	chr11:71279364-71279365	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7128806	chr11:71279377-71279378	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs6592210	chr11:71279388-71279389	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs181691907	chr11:71279391-71279392	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs563708028	chr11:71279395-71279396	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs575600368	chr11:71279399-71279400	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs145180756	chr11:71279411-71279412	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561405197	chr11:71279412-71279413	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs553936639	chr11:71279413-71279414	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs202023695	chr11:71279420-71279421	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs375122269	chr11:71279452-71279453	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565145099	chr11:71279465-71279466	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532448290	chr11:71279555-71279556	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs550261488	chr11:71279561-71279562	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs141919544	chr11:71279562-71279563	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs7934661	chr11:71279571-71279572	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs374747244	chr11:71279572-71279573	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs548252959	chr11:71279599-71279600	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs67700829	chr11:71279600-71279601	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs534860001	chr11:71279601-71279602	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs397962082	chr11:71279603-71279604	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs371106752	chr11:71279616-71279617	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs117175351	chr11:71279653-71279654	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs150142033	chr11:71279656-71279657	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs144202902	chr11:71279698-71279699	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs539320363	chr11:71279699-71279700	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374350043	chr11:71279725-71279726	Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs557413070	chr11:71279757-71279758	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs370246933	chr11:71279790-71279791	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs575583349	chr11:71279798-71279799	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71277000-71279200	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr11:71277200-71280400	Enhancers	Adipose Nuclei	Adipose
3	chr11:71277400-71279800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:71277600-71279000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr11:71277600-71279000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:71277600-71279800	Weak transcription	Left Ventricle	heart
7	chr11:71277600-71280400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:71277600-71281600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:71277600-71282800	Weak transcription	Fetal Intestine Small	intestine
10	chr11:71277600-71290400	Weak transcription	Right Atrium	heart
11	chr11:71278000-71279800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr11:71278200-71281600	Weak transcription	Spleen	Spleen
13	chr11:71278400-71279800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr11:71278800-71279000	Bivalent Enhancer	Fetal Stomach	stomach
15	chr11:71278800-71279000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr11:71278800-71279200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:71278800-71279400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr11:71278800-71279600	Bivalent Enhancer	HepG2	liver
19	chr11:71279000-71279400	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr11:71279000-71280200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:71279000-71280600	Enhancers	Fetal Muscle Leg	muscle
22	chr11:71279000-71281200	Enhancers	Fetal Stomach	stomach
23	chr11:71279200-71279600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr11:71279200-71280400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:71279400-71280000	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr11:71279400-71281400	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr11:71279600-71280200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr11:71279600-71280200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr11:71279600-71280200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:71279600-71280200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:71279600-71280200	Enhancers	Psoas Muscle	Psoas
32	chr11:71279600-71280200	Enhancers	Stomach Smooth Muscle	stomach
33	chr11:71279600-71280200	Flanking Bivalent TSS/Enh	HepG2	liver
34	chr11:71279600-71280400	Enhancers	Fetal Lung	lung
35	chr11:71279600-71282000	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr11:71279800-71280000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr11:71279800-71280000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr11:71279800-71280200	Enhancers	Colon Smooth Muscle	Colon
39	chr11:71279800-71280200	Enhancers	Left Ventricle	heart
40	chr11:71279800-71280400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr11:71279800-71280400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr11:71279800-71280600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr11:71280000-71280200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr11:71280000-71280200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr11:71280000-71280400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr11:71280000-71281800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr11:71280200-71280400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:71280200-71280400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:71280200-71280400	Bivalent Enhancer	HepG2	liver
50	chr11:71280200-71281800	Weak transcription	H9 Cell Line	embryonic stem cell

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