Variant report

Variant	esv2757459
Chromosome Location	chr11:85436868-85473347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:322)
CpG islands
(count:855)
Chromatin interactive
region (count:81)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:322 , 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	ATF1	chr11:85437160-85437164	K562	blood:	n/a	n/a
2	ATF3	chr11:85459311-85459985	A549	lung:	n/a	n/a
3	ATF3	chr11:85437022-85437235	K562	blood:	n/a	n/a
4	BCL3	chr11:85459306-85460048	A549	lung:	n/a	n/a
5	CBX3	chr11:85436418-85437521	HCT-116	colon:	n/a	n/a
6	CBX3	chr11:85436571-85437484	HCT-116	colon:	n/a	n/a
7	CEBPB	chr11:85470952-85471285	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:85453740-85454559	HCT-116	colon:	n/a	n/a
9	CEBPB	chr11:85454000-85454341	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:85451606-85451830	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:85460565-85460818	A549	lung:	n/a	n/a
12	CEBPB	chr11:85470816-85471428	HCT-116	colon:	n/a	n/a
13	CEBPB	chr11:85450575-85450778	K562	blood:	n/a	chr11:85450662-85450673 chr11:85450663-85450674
14	CEBPB	chr11:85460646-85460756	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:85470939-85471214	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr11:85470922-85471280	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:85470917-85471335	IMR90	lung:	n/a	n/a
18	CEBPB	chr11:85459571-85460198	A549	lung:	n/a	n/a
19	CEBPB	chr11:85470946-85471251	A549	lung:	n/a	n/a
20	CEBPB	chr11:85436706-85437444	HCT-116	colon:	n/a	n/a
21	CEBPB	chr11:85436954-85437343	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:85450530-85450847	HepG2	liver:	n/a	chr11:85450662-85450673 chr11:85450663-85450674
23	CEBPB	chr11:85470887-85471251	MCF-7	breast:	n/a	n/a
24	CEBPB	chr11:85460665-85460721	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:85450526-85450834	A549	lung:	n/a	chr11:85450662-85450673 chr11:85450663-85450674
26	CEBPB	chr11:85450545-85450852	Hela-S3	cervix:	n/a	chr11:85450662-85450673 chr11:85450663-85450674
27	CEBPB	chr11:85436811-85437316	HCT-116	colon:	n/a	n/a
28	CEBPB	chr11:85459303-85459997	A549	lung:	n/a	n/a
29	CEBPB	chr11:85461891-85462184	IMR90	lung:	n/a	n/a
30	CEBPB	chr11:85457839-85458035	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:85470950-85471431	A549	lung:	n/a	n/a
32	CEBPB	chr11:85469749-85469863	A549	lung:	n/a	chr11:85469817-85469826
33	CTCF	chr11:85436740-85436890	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr11:85449920-85450070	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr11:85466000-85466150	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr11:85436720-85436870	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr11:85436860-85437010	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr11:85451342-85451412	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr11:85456750-85456789	GM20000	blood:	n/a	n/a
40	CTCF	chr11:85436820-85436970	BJ	skin:	n/a	n/a
41	CTCF	chr11:85436660-85436950	Caco-2	colon:	n/a	n/a
42	CTCF	chr11:85436720-85436870	HFF	foreskin:	n/a	n/a
43	CTCF	chr11:85446691-85446739	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:85436780-85436930	HAc	cerebellar:	n/a	n/a
45	CTCF	chr11:85468610-85468669	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr11:85436720-85436990	AG04450	lung:	n/a	n/a
47	CTCF	chr11:85436740-85436890	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr11:85437000-85437150	HCFaa	heart:	n/a	n/a
49	E2F4	chr11:85468096-85468140	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr11:85437111-85437311	MCF10A-Er-Src	breast:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:85469919-85469969	ECC-1	luminal epithelium:	n/a
2	chr11:85469919-85469969	ECC-1	luminal epithelium:	n/a
3	chr11:85469037-85469087	GM12891	blood:	n/a
4	chr11:85469919-85469969	AG04450	lung:	fetal
5	chr11:85470458-85470508	HEK293	kidney:	embryo
6	chr11:85451557-85451607	GM12892	blood:	n/a
7	chr11:85470458-85470508	PANC-1	pancreas:	n/a
8	chr11:85438947-85438997	MCF-7	breast:	n/a
9	chr11:85438818-85438868	HEK293	kidney:	embryo
10	chr11:85469117-85469167	SKMC	muscle:	n/a
11	chr11:85469037-85469087	SKMC	muscle:	n/a
12	chr11:85438818-85438868	GM12892	blood:	n/a
13	chr11:85469247-85469297	HRPEpiC	eye:	n/a
14	chr11:85438818-85438868	U87	brain:	n/a
15	chr11:85438773-85438823	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:85451557-85451607	U87	brain:	n/a
17	chr11:85469037-85469087	ProgFib	skin:	n/a
18	chr11:85438947-85438997	Hela-S3	cervix:	n/a
19	chr11:85438818-85438868	AG09319	gingival:	n/a
20	chr11:85438773-85438823	AG04449	skin:	fetal
21	chr11:85469247-85469297	Jurkat	blood:	n/a
22	chr11:85438947-85438997	K562	blood:	n/a
23	chr11:85469919-85469969	PFSK-1	brain:	n/a
24	chr11:85470458-85470508	NT2-D1	testis:	n/a
25	chr11:85438773-85438823	ECC-1	luminal epithelium:	n/a
26	chr11:85437579-85437629	HIPEpiC	eye:	n/a
27	chr11:85437579-85437629	NH-A	brain:	n/a
28	chr11:85469037-85469087	NHDF-neo	bronchial:	n/a
29	chr11:85460604-85460654	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:85438773-85438823	SKMC	muscle:	n/a
31	chr11:85470458-85470508	A549	lung:	n/a
32	chr11:85469117-85469167	SAEC	small airway:	n/a
33	chr11:85438818-85438868	AG09309	skin:	n/a
34	chr11:85472846-85472896	MCF10A-Er-Src	breast:	n/a
35	chr11:85438947-85438997	HRE	kidney:	n/a
36	chr11:85437589-85437639	BE2_C	brain:	n/a
37	chr11:85469247-85469297	HRE	kidney:	n/a
38	chr11:85460604-85460654	Hela-S3	cervix:	n/a
39	chr11:85470458-85470508	Jurkat	blood:	n/a
40	chr11:85460604-85460654	Jurkat	blood:	n/a
41	chr11:85438773-85438823	PANC-1	pancreas:	n/a
42	chr11:85453669-85453719	BJ	skin:	n/a
43	chr11:85438947-85438997	HCT-116	colon:	n/a
44	chr11:85460604-85460654	HMEC	breast:	n/a
45	chr11:85469037-85469087	HEEpiC	esophagus:	n/a
46	chr11:85469919-85469969	NHDF-neo	bronchial:	n/a
47	chr11:85437589-85437639	Caco-2	colon:	n/a
48	chr11:85437589-85437639	HCF	heart:	n/a
49	chr11:85472846-85472896	SAEC	small airway:	n/a
50	chr11:85451557-85451607	AoSMC	blood vessel:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:85445267..85447565-chr11:85447614..85449688,2	MCF-7	breast:
2	chr11:85460295..85462125-chr11:85496572..85498601,2	MCF-7	breast:
3	chr11:85448431..85450003-chr11:85541669..85543570,2	MCF-7	breast:
4	chr11:85434439..85436977-chr11:85459317..85462236,2	MCF-7	breast:
5	chr11:85445028..85447969-chr11:85452486..85454600,2	K562	blood:
6	chr11:85452340..85455544-chr11:85456750..85459606,3	K562	blood:
7	chr11:85374803..85376402-chr11:85446135..85448325,2	MCF-7	breast:
8	chr11:85445028..85447969-chr11:85452486..85454600,2	K562	blood:
9	chr11:85456882..85459698-chr17:57916750..57918708,2	MCF-7	breast:
10	chr11:85445751..85448371-chr11:85941133..85943891,2	MCF-7	breast:
11	chr11:85460961..85463869-chr11:85465217..85468287,3	MCF-7	breast:
12	chr11:85445724..85449951-chr11:85518014..85522628,5	MCF-7	breast:
13	chr11:85434348..85438681-chr11:85520824..85523815,4	MCF-7	breast:
14	chr11:85449862..85452666-chr3:62852459..62854509,2	MCF-7	breast:
15	chr11:85449141..85453316-chr11:85456820..85460896,4	MCF-7	breast:
16	chr11:85449712..85452124-chr11:85536910..85538885,2	MCF-7	breast:
17	chr11:85404945..85406929-chr11:85457970..85459498,2	MCF-7	breast:
18	chr11:85461055..85463214-chr11:85468718..85471214,2	MCF-7	breast:
19	chr11:85473245..85476644-chr11:85486524..85489414,3	MCF-7	breast:
20	chr11:85434029..85438059-chr11:85455702..85460015,5	MCF-7	breast:
21	chr11:85459682..85462503-chr11:85466829..85468700,3	MCF-7	breast:
22	chr11:85447416..85450012-chr11:85465090..85467738,2	MCF-7	breast:
23	chr11:85446235..85448098-chr11:85532932..85535818,2	MCF-7	breast:
24	chr11:85453893..85455528-chr11:85457587..85459184,2	MCF-7	breast:
25	chr11:85456923..85462918-chr11:85517727..85523482,9	MCF-7	breast:
26	chr11:85449141..85453316-chr11:85456820..85460896,4	MCF-7	breast:
27	chr11:85453675..85456598-chr11:85463651..85465546,2	MCF-7	breast:
28	chr11:85457955..85460944-chr11:85541331..85543778,2	MCF-7	breast:
29	chr11:85447416..85450012-chr11:85465090..85467738,2	MCF-7	breast:
30	chr11:85373496..85375971-chr11:85442950..85444857,2	MCF-7	breast:
31	chr11:85438614..85440584-chr11:85468892..85470720,2	MCF-7	breast:
32	chr11:85452340..85455544-chr11:85456750..85459606,3	K562	blood:
33	chr11:85456354..85459698-chr11:85460209..85463531,4	MCF-7	breast:
34	chr11:85432781..85434564-chr11:85442681..85445528,2	MCF-7	breast:
35	chr11:85457148..85461266-chr11:85520193..85525185,6	MCF-7	breast:
36	chr11:85446637..85448828-chr11:85475522..85477132,2	MCF-7	breast:
37	chr11:85453675..85456598-chr11:85463651..85465546,2	MCF-7	breast:
38	chr11:85459682..85462503-chr11:85466829..85468700,3	MCF-7	breast:
39	chr11:85339388..85341161-chr11:85467592..85470414,2	MCF-7	breast:
40	chr11:85461323..85463573-chr11:85539177..85540857,2	MCF-7	breast:
41	chr11:85444504..85447684-chr11:85505412..85508647,3	MCF-7	breast:
42	chr11:85438614..85440584-chr11:85468892..85470720,2	MCF-7	breast:
43	chr11:85470232..85472552-chr11:85473605..85477376,4	K562	blood:
44	chr11:85456354..85459698-chr11:85460209..85463531,4	MCF-7	breast:
45	chr11:85445267..85447565-chr11:85447614..85449688,2	MCF-7	breast:
46	chr11:85447296..85450521-chr11:85450822..85453106,4	MCF-7	breast:
47	chr11:85374169..85377247-chr11:85434867..85438072,3	MCF-7	breast:
48	chr11:85447296..85450521-chr11:85450822..85453106,4	MCF-7	breast:
49	chr11:85469322..85470979-chr11:85520431..85523173,2	MCF-7	breast:
50	chr11:85468435..85470460-chr11:85522182..85523762,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC89-7	chr11:85455444-85456066	expReg_chr11_8320_-
2	lnc-AP000974.1-1	chr11:85468803-85469112	NONHSAT023448
3	lnc-CCDC89-6	chr11:85452619-85452847	expReg_chr11_8315_-

No data

Variant related genes	Relation type
SYTL2	TF binding region
SYTL2	CpG island
ENSG00000171204	chromatin interactions
ENSG00000137504	chromatin interactions
ENSG00000137501	chromatin interactions
ENSG00000199004	chromatin interactions

Extended variants
information (count: 1431 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1431 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs597480	chr11:85436868-85436869	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138711024	chr11:85436875-85436876	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs377074608	chr11:85436899-85436900	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs369714015	chr11:85436910-85436911	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs375386505	chr11:85436967-85436968	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs201464962	chr11:85436979-85436980	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372685279	chr11:85436983-85436984	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs375941893	chr11:85436991-85436992	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs534962134	chr11:85436999-85437000	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs116662107	chr11:85437007-85437008	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs116047730	chr11:85437012-85437013	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs575107119	chr11:85437034-85437035	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs201305323	chr11:85437091-85437092	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs141630348	chr11:85437116-85437117	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs114177971	chr11:85437117-85437118	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs113068280	chr11:85437120-85437121	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs145374887	chr11:85437121-85437122	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs574962856	chr11:85437122-85437123	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs199651478	chr11:85437138-85437139	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs372504994	chr11:85437139-85437140	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs377007027	chr11:85437146-85437147	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs137874226	chr11:85437153-85437154	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs111770919	chr11:85437167-85437168	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs144826107	chr11:85437196-85437197	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs369096723	chr11:85437197-85437198	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs75207631	chr11:85437226-85437227	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs372983553	chr11:85437234-85437235	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs200315200	chr11:85437246-85437247	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs141925178	chr11:85437247-85437248	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs528073431	chr11:85437259-85437260	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs147296637	chr11:85437264-85437265	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs201835158	chr11:85437268-85437269	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs534314190	chr11:85437275-85437276	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs116055284	chr11:85437325-85437326	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs116639648	chr11:85437328-85437329	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs570172257	chr11:85437329-85437330	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs144700046	chr11:85437368-85437369	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs147912942	chr11:85437389-85437390	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs115240923	chr11:85437405-85437406	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs200627406	chr11:85437430-85437431	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs570895958	chr11:85437436-85437437	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs370844079	chr11:85437479-85437480	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs72947495	chr11:85437499-85437500	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs184990558	chr11:85437503-85437504	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs377311067	chr11:85437516-85437517	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs543504480	chr11:85437517-85437518	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs370586216	chr11:85437522-85437523	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs374733068	chr11:85437523-85437524	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs367860762	chr11:85437543-85437544	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568238675	chr11:85437544-85437545	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
Obesity	20622171	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	18438408	CNVD
Cancer	17440070	CNVD

Chromatin state (count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85397200-85438600	Weak transcription	Colonic Mucosa	Colon
2	chr11:85412000-85438000	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr11:85417600-85453000	Weak transcription	Gastric	stomach
4	chr11:85422600-85448600	Weak transcription	Fetal Intestine Large	intestine
5	chr11:85422800-85448200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr11:85424000-85448600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr11:85430200-85437800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr11:85430400-85437400	Weak transcription	Stomach Mucosa	stomach
9	chr11:85430400-85459000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr11:85430400-85480400	Weak transcription	Aorta	Aorta
11	chr11:85430600-85437200	Weak transcription	Fetal Kidney	kidney
12	chr11:85430600-85447000	Weak transcription	Ovary	ovary
13	chr11:85430800-85445000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr11:85430800-85447200	Weak transcription	Fetal Stomach	stomach
15	chr11:85430800-85448800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr11:85430800-85459000	Weak transcription	Fetal Muscle Trunk	muscle
17	chr11:85431000-85445200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:85431400-85451600	Weak transcription	HSMMtube	muscle
19	chr11:85431800-85437600	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr11:85431800-85466600	Weak transcription	Brain Substantia Nigra	brain
21	chr11:85432000-85460800	Weak transcription	Fetal Muscle Leg	muscle
22	chr11:85432200-85448400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr11:85433800-85448600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr11:85434000-85439400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:85434200-85439800	Strong transcription	Primary T cells from cord blood	blood
26	chr11:85434600-85437000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr11:85434600-85445000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr11:85434800-85448200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr11:85435200-85437400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr11:85435200-85439000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:85435400-85437800	Enhancers	NHLF	lung
32	chr11:85435400-85438000	Enhancers	NHDF-Ad	bronchial
33	chr11:85435400-85439000	Strong transcription	Rectal Mucosa Donor 31	rectum
34	chr11:85435400-85448600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr11:85435600-85456400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr11:85436000-85437800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr11:85436000-85438000	Enhancers	Hela-S3	cervix
38	chr11:85436200-85437800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr11:85436200-85437800	Enhancers	NH-A	brain
40	chr11:85436200-85438000	Enhancers	NHEK	skin
41	chr11:85436200-85443600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr11:85436400-85437000	Flanking Active TSS	HUVEC	blood vessel
43	chr11:85436400-85437600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr11:85436400-85437600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:85436400-85437800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:85436400-85438400	Enhancers	HMEC	breast
47	chr11:85436600-85437000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
48	chr11:85436600-85437000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr11:85436600-85437600	Enhancers	Muscle Satellite Cultured Cells	--
50	chr11:85436600-85437600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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