Variant report

Variant	nsv825988
Chromosome Location	chr11:71277262-71294289
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	chr11:71288357-71289171	GM12878	blood:	n/a	n/a
4	BCL3	chr11:71281541-71282202	GM12878	blood:	n/a	n/a
5	BCL3	chr11:71288393-71289155	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	chr11:71291240-71291390	GM12864	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
13	CTCF	chr11:71291600-71291750	GM12875	blood:	n/a	n/a
14	CTCF	chr11:71291680-71291830	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr11:71291220-71291370	Hela-S3	cervix:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
16	CTCF	chr11:71291820-71291970	HEEpiC	esophagus:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
17	CTCF	chr11:71291180-71291330	HAc	cerebellar:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
18	CTCF	chr11:71291137-71291439	HepG2	liver:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
19	CTCF	chr11:71291240-71291390	GM12873	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
20	CTCF	chr11:71291780-71291930	HPAF	blood vessel:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
21	CTCF	chr11:71291240-71291390	HEK293	kidney:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
22	CTCF	chr11:71291680-71291830	HCFaa	heart:	n/a	n/a
23	CTCF	chr11:71291163-71291456	GM12892	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
24	CTCF	chr11:71291171-71291447	HepG2	liver:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
25	CTCF	chr11:71278695-71278895	GM12878	blood:	n/a	chr11:71278817-71278838
26	CTCF	chr11:71291748-71291904	GM12892	blood:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
27	CTCF	chr11:71291240-71291390	WERI-Rb-1	eye:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
28	CTCF	chr11:71291240-71291390	BE2_C	brain:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
29	CTCF	chr11:71291240-71291390	GM12874	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
30	CTCF	chr11:71293080-71293230	GM12868	blood:	n/a	n/a
31	CTCF	chr11:71278768-71278811	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr11:71291560-71291710	GM12872	blood:	n/a	n/a
33	CTCF	chr11:71291154-71291463	K562	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
34	CTCF	chr11:71291220-71291370	AG10803	skin:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
35	CTCF	chr11:71289597-71289620	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr11:71291796-71292011	Spleen_OC	spleen:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
37	CTCF	chr11:71291795-71291995	Lung_OC	lung:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
38	CTCF	chr11:71290079-71290118	HepG2	liver:	n/a	n/a
39	CTCF	chr11:71292078-71292157	GM13976	blood:	n/a	n/a
40	CTCF	chr11:71291819-71291940	IMR90	lung:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
41	CTCF	chr11:71291220-71291370	GM12873	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
42	CTCF	chr11:71291220-71291370	K562	blood:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
43	CTCF	chr11:71291656-71292025	A549	lung:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
44	CTCF	chr11:71291741-71291932	ProgFib	skin:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866
45	CTCF	chr11:71291700-71291850	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr11:71291240-71291390	HVMF	connective:	n/a	chr11:71291299-71291320 chr11:71291300-71291313 chr11:71291298-71291314 chr11:71291302-71291310 chr11:71291297-71291315
47	CTCF	chr11:71291160-71291310	MCF-7	breast:	n/a	chr11:71291302-71291310
48	CTCF	chr11:71290992-71291004	GM10248	blood:	n/a	n/a
49	CTCF	chr11:71278800-71278950	HCPEpiC	choroid plexus:	n/a	chr11:71278817-71278838
50	CTCF	chr11:71291737-71291987	HepG2	liver:	n/a	chr11:71291846-71291867 chr11:71291851-71291869 chr11:71291853-71291866

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71277473-71277523	HRCEpiC	kidney:	n/a
2	chr11:71277473-71277523	HRCEpiC	kidney:	n/a
3	chr11:71285546-71285596	Hela-S3	cervix:	n/a
4	chr11:71288203-71288253	BE2_C	brain:	n/a
5	chr11:71288203-71288253	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:71285546-71285596	CMK	blood:	n/a
7	chr11:71293996-71294046	GM12891	blood:	n/a
8	chr11:71288203-71288253	SK-N-MC	brain:	n/a
9	chr11:71282370-71282420	GM06990	blood:	n/a
10	chr11:71293184-71293234	HEEpiC	esophagus:	n/a
11	chr11:71277473-71277523	AG09309	skin:	n/a
12	chr11:71282718-71282768	ECC-1	luminal epithelium:	n/a
13	chr11:71282370-71282420	SKMC	muscle:	n/a
14	chr11:71288256-71288306	AG09309	skin:	n/a
15	chr11:71288256-71288306	K562	blood:	n/a
16	chr11:71277473-71277523	HCF	heart:	n/a
17	chr11:71282370-71282420	HCM	heart:	n/a
18	chr11:71285546-71285596	Hepatocyte	liver:	n/a
19	chr11:71293996-71294046	HCF	heart:	n/a
20	chr11:71288514-71288564	AoSMC	blood vessel:	n/a
21	chr11:71288514-71288564	GM12878	blood:	n/a
22	chr11:71293892-71293942	HCT-116	colon:	n/a
23	chr11:71293996-71294046	HCPEpiC	choroid plexus:	n/a
24	chr11:71293996-71294046	PANC-1	pancreas:	n/a
25	chr11:71277473-71277523	PANC-1	pancreas:	n/a
26	chr11:71293996-71294046	PrEC	prostate:	n/a
27	chr11:71288256-71288306	RPTEC	kidney:	n/a
28	chr11:71293892-71293942	AG09309	skin:	n/a
29	chr11:71288256-71288306	Caco-2	colon:	n/a
30	chr11:71293996-71294046	GM06990	blood:	n/a
31	chr11:71293996-71294046	U87	brain:	n/a
32	chr11:71293996-71294046	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:71287919-71287969	AG10803	skin:	n/a
34	chr11:71288514-71288564	MCF-7	breast:	n/a
35	chr11:71277473-71277523	Hepatocyte	liver:	n/a
36	chr11:71288256-71288306	SKMC	muscle:	n/a
37	chr11:71293892-71293942	NHBE	bronchial:	n/a
38	chr11:71288514-71288564	A549	lung:	n/a
39	chr11:71282718-71282768	SK-N-SH_RA	brain:	n/a
40	chr11:71282718-71282768	RPTEC	kidney:	n/a
41	chr11:71288514-71288564	HRPEpiC	eye:	n/a
42	chr11:71288514-71288564	ProgFib	skin:	n/a
43	chr11:71282718-71282768	CMK	blood:	n/a
44	chr11:71287919-71287969	HRCEpiC	kidney:	n/a
45	chr11:71293892-71293942	SK-N-MC	brain:	n/a
46	chr11:71293184-71293234	HepG2	liver:	n/a
47	chr11:71288256-71288306	AoSMC	blood vessel:	n/a
48	chr11:71293892-71293942	AG10803	skin:	n/a
49	chr11:71287919-71287969	SK-N-SH_RA	brain:	n/a
50	chr11:71293996-71294046	MCF10A-Er-Src	breast:	n/a

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

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

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
ENSG00000248903	chromatin interactions
ENSG00000172893	chromatin interactions
ENSG00000172890	chromatin interactions
ENSG00000254682	chromatin interactions

Extended variants
information (count: 998 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:998 , 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	rs66487667	chr11:71277273-71277274	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187984631	chr11:71277303-71277304	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs191345688	chr11:71277365-71277366	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs73530493	chr11:71277371-71277372	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs540766043	chr11:71277387-71277388	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs73530494	chr11:71277427-71277428	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182425245	chr11:71277448-71277449	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs555948326	chr11:71277460-71277461	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs564740169	chr11:71277465-71277466	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs577810263	chr11:71277471-71277472	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs368796119	chr11:71277472-71277473	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs146914949	chr11:71277475-71277476	Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs373412632	chr11:71277476-71277477	Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs550105332	chr11:71277499-71277500	Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs148378708	chr11:71277508-71277509	Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs188235028	chr11:71277515-71277516	Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs117660730	chr11:71277531-71277532	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs543059957	chr11:71277534-71277535	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs371031116	chr11:71277540-71277541	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs192802681	chr11:71277558-71277559	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs7120471	chr11:71277598-71277599	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs532048332	chr11:71277616-71277617	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs550457064	chr11:71277628-71277629	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs71946973	chr11:71277648-71277649	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs201171826	chr11:71277651-71277652	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs75544717	chr11:71277652-71277653	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs539220182	chr11:71277665-71277666	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs530931284	chr11:71277744-71277745	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs117393523	chr11:71277777-71277778	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs536949726	chr11:71277821-71277822	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369284443	chr11:71277841-71277842	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs374056111	chr11:71277871-71277872	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs184908574	chr11:71277902-71277903	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs150461342	chr11:71277905-71277906	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs377361112	chr11:71277917-71277918	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs34678580	chr11:71277946-71277947	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs66743503	chr11:71277947-71277948	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs71272259	chr11:71277948-71277949	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs559468601	chr11:71277958-71277959	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs188225724	chr11:71277959-71277960	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs550905026	chr11:71277963-71277964	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs547659658	chr11:71277968-71277969	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546382540	chr11:71277972-71277973	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs564532435	chr11:71277980-71277981	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs11234218	chr11:71277981-71277982	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs373917868	chr11:71277983-71277984	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs73530497	chr11:71278015-71278016	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs138189121	chr11:71278016-71278017	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs373812282	chr11:71278023-71278024	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs367943244	chr11:71278026-71278027	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 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:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71274800-71277400	Weak transcription	Brain Substantia Nigra	brain
2	chr11:71275200-71277400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr11:71275400-71277600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:71276200-71277600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr11:71276400-71277400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr11:71276600-71278200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr11:71276800-71277600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr11:71277000-71277400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr11:71277000-71277400	Enhancers	HMEC	breast
10	chr11:71277000-71279200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr11:71277200-71277400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:71277200-71277600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:71277200-71277600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:71277200-71277600	Enhancers	Left Ventricle	heart
15	chr11:71277200-71277800	Enhancers	Fetal Brain Male	brain
16	chr11:71277200-71278000	Bivalent Enhancer	Fetal Stomach	stomach
17	chr11:71277200-71278200	Enhancers	Spleen	Spleen
18	chr11:71277200-71280400	Enhancers	Adipose Nuclei	Adipose
19	chr11:71277400-71277600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:71277400-71277600	Enhancers	Brain Substantia Nigra	brain
21	chr11:71277400-71277600	Enhancers	Fetal Intestine Small	intestine
22	chr11:71277400-71277600	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr11:71277400-71277600	Enhancers	Right Atrium	heart
24	chr11:71277400-71277600	Bivalent Enhancer	HMEC	breast
25	chr11:71277400-71277800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
26	chr11:71277400-71278000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr11:71277400-71278000	Enhancers	Lung	lung
28	chr11:71277400-71278400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr11:71277400-71279800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:71277600-71278000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr11:71277600-71278000	Bivalent Enhancer	HepG2	liver
32	chr11:71277600-71278200	Enhancers	H9 Cell Line	embryonic stem cell
33	chr11:71277600-71279000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr11:71277600-71279000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr11:71277600-71279800	Weak transcription	Left Ventricle	heart
36	chr11:71277600-71280400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:71277600-71281600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:71277600-71282800	Weak transcription	Fetal Intestine Small	intestine
39	chr11:71277600-71290400	Weak transcription	Right Atrium	heart
40	chr11:71277800-71278000	Enhancers	Fetal Brain Female	brain
41	chr11:71277800-71278800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr11:71278000-71278800	Enhancers	HepG2	liver
43	chr11:71278000-71279800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr11:71278200-71278800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr11:71278200-71281600	Weak transcription	Spleen	Spleen
46	chr11:71278400-71279800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr11:71278800-71279000	Bivalent Enhancer	Fetal Stomach	stomach
48	chr11:71278800-71279000	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr11:71278800-71279200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:71278800-71279400	Enhancers	H9 Cell Line	embryonic stem cell

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