Variant report

Variant	esv2762927
Chromosome Location	chr11:85468051-85559618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1462)
CpG islands
(count:1405)
Chromatin interactive
region (count:150)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1462 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:85555535-85555787	K562	blood:	n/a	n/a
2	ATF3	chr11:85538936-85539647	A549	lung:	n/a	n/a
3	ATF3	chr11:85555379-85556025	A549	lung:	n/a	n/a
4	ATF3	chr11:85555342-85555951	HCT-116	colon:	n/a	n/a
5	ATF3	chr11:85538959-85539741	A549	lung:	n/a	n/a
6	ATF3	chr11:85498726-85499634	A549	lung:	n/a	n/a
7	ATF3	chr11:85555389-85555851	A549	lung:	n/a	n/a
8	ATF3	chr11:85498884-85499364	A549	lung:	n/a	n/a
9	BACH1	chr11:85515192-85515254	K562	blood:	n/a	n/a
10	BACH1	chr11:85521756-85522062	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr11:85498752-85499306	A549	lung:	n/a	n/a
12	BCL3	chr11:85555325-85555855	A549	lung:	n/a	n/a
13	BCL3	chr11:85498631-85499909	A549	lung:	n/a	chr11:85499833-85499842
14	BCL3	chr11:85538683-85540073	A549	lung:	n/a	chr11:85539231-85539240
15	BCL3	chr11:85538847-85539930	A549	lung:	n/a	chr11:85539231-85539240
16	BHLHE40	chr11:85522107-85522170	HepG2	liver:	n/a	n/a
17	BRCA1	chr11:85555495-85555815	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr11:85538848-85539772	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr11:85498881-85499728	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr11:85555108-85556044	HCT-116	colon:	n/a	n/a
21	CBX3	chr11:85538830-85539973	HCT-116	colon:	n/a	n/a
22	CBX3	chr11:85538804-85540100	HCT-116	colon:	n/a	n/a
23	CCNT2	chr11:85522083-85522159	K562	blood:	n/a	n/a
24	CEBPB	chr11:85524779-85525143	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:85524716-85525223	A549	lung:	n/a	n/a
26	CEBPB	chr11:85491001-85491592	A549	lung:	n/a	chr11:85491312-85491323
27	CEBPB	chr11:85491260-85491460	Hela-S3	cervix:	n/a	chr11:85491312-85491323
28	CEBPB	chr11:85492761-85492997	K562	blood:	n/a	n/a
29	CEBPB	chr11:85491164-85491483	HepG2	liver:	n/a	chr11:85491312-85491323
30	CEBPB	chr11:85555162-85556625	HCT-116	colon:	n/a	chr11:85555641-85555654 chr11:85556462-85556473
31	CEBPB	chr11:85541833-85542710	MCF-7	breast:	n/a	n/a
32	CEBPB	chr11:85470816-85471428	HCT-116	colon:	n/a	n/a
33	CEBPB	chr11:85492613-85493012	HCT-116	colon:	n/a	n/a
34	CEBPB	chr11:85555480-85555738	HepG2	liver:	n/a	chr11:85555641-85555654
35	CEBPB	chr11:85555367-85555870	A549	lung:	n/a	chr11:85555641-85555654
36	CEBPB	chr11:85526150-85526836	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:85507015-85507289	IMR90	lung:	n/a	chr11:85507131-85507142
38	CEBPB	chr11:85492614-85493148	MCF-7	breast:	n/a	n/a
39	CEBPB	chr11:85470922-85471280	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr11:85470952-85471285	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr11:85499533-85499776	HepG2	liver:	n/a	chr11:85499674-85499691
42	CEBPB	chr11:85555573-85555680	K562	blood:	n/a	chr11:85555641-85555654
43	CEBPB	chr11:85559597-85559966	MCF-7	breast:	n/a	n/a
44	CEBPB	chr11:85555352-85556585	Hela-S3	cervix:	n/a	chr11:85555641-85555654 chr11:85556462-85556473
45	CEBPB	chr11:85538948-85540078	HCT-116	colon:	n/a	n/a
46	CEBPB	chr11:85556210-85556638	IMR90	lung:	n/a	chr11:85556462-85556473
47	CEBPB	chr11:85470946-85471251	A549	lung:	n/a	n/a
48	CEBPB	chr11:85524897-85525124	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr11:85555284-85556156	HCT-116	colon:	n/a	chr11:85555641-85555654
50	CEBPB	chr11:85499621-85499724	H1-hESC	embryonic stem cell:	n/a	chr11:85499674-85499691

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:85472846-85472896	Caco-2	colon:	n/a
2	chr11:85522435-85522485	GM12891	blood:	n/a
3	chr11:85472846-85472896	Caco-2	colon:	n/a
4	chr11:85522435-85522485	GM12891	blood:	n/a
5	chr11:85522525-85522575	NB4	blood:	n/a
6	chr11:85469919-85469969	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:85524670-85524720	GM19239	blood:	n/a
8	chr11:85538052-85538102	BE2_C	brain:	n/a
9	chr11:85522525-85522575	HRPEpiC	eye:	n/a
10	chr11:85521839-85521889	HCF	heart:	n/a
11	chr11:85469919-85469969	A549	lung:	n/a
12	chr11:85469919-85469969	SK-N-MC	brain:	n/a
13	chr11:85522094-85522144	HAEpiC	amniotic membrane:	n/a
14	chr11:85491089-85491139	AG04450	lung:	fetal
15	chr11:85522279-85522329	HRPEpiC	eye:	n/a
16	chr11:85538052-85538102	LNCaP	prostate:	n/a
17	chr11:85522279-85522329	LNCaP	prostate:	n/a
18	chr11:85522435-85522485	HUVEC	blood vessel:	n/a
19	chr11:85521992-85522042	HRPEpiC	eye:	n/a
20	chr11:85469117-85469167	AG09309	skin:	n/a
21	chr11:85484509-85484559	CMK	blood:	n/a
22	chr11:85469919-85469969	GM12892	blood:	n/a
23	chr11:85470458-85470508	HNPCEpiC	eye:	n/a
24	chr11:85522637-85522687	SAEC	small airway:	n/a
25	chr11:85469919-85469969	NB4	blood:	n/a
26	chr11:85522295-85522345	AG04450	lung:	fetal
27	chr11:85470458-85470508	ovcar-3	ovarian:	n/a
28	chr11:85522005-85522055	AG09319	gingival:	n/a
29	chr11:85522005-85522055	HNPCEpiC	eye:	n/a
30	chr11:85522575-85522625	HepG2	liver:	n/a
31	chr11:85491089-85491139	BE2_C	brain:	n/a
32	chr11:85522094-85522144	GM06990	blood:	n/a
33	chr11:85522575-85522625	NT2-D1	testis:	n/a
34	chr11:85469247-85469297	MCF10A-Er-Src	breast:	n/a
35	chr11:85522435-85522485	GM12892	blood:	n/a
36	chr11:85491089-85491139	HNPCEpiC	eye:	n/a
37	chr11:85469247-85469297	HepG2	liver:	n/a
38	chr11:85491089-85491139	HEEpiC	esophagus:	n/a
39	chr11:85522525-85522575	Hepatocyte	liver:	n/a
40	chr11:85469037-85469087	HMEC	breast:	n/a
41	chr11:85469037-85469087	SKMC	muscle:	n/a
42	chr11:85491089-85491139	NHDF-neo	bronchial:	n/a
43	chr11:85484509-85484559	SKMC	muscle:	n/a
44	chr11:85472846-85472896	BE2_C	brain:	n/a
45	chr11:85472846-85472896	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:85522525-85522575	HCM	heart:	n/a
47	chr11:85491089-85491139	HMEC	breast:	n/a
48	chr11:85522609-85522659	ProgFib	skin:	n/a
49	chr11:85522094-85522144	HRPEpiC	eye:	n/a
50	chr11:85469247-85469297	U87	brain:	n/a

(count:150 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:85505294..85507043-chr11:85526404..85527937,2	K562	blood:
2	chr11:85468435..85470460-chr11:85522182..85523762,2	MCF-7	breast:
3	chr11:85470232..85471819-chr11:85473605..85475832,2	K562	blood:
4	chr11:85461323..85463573-chr11:85539177..85540857,2	MCF-7	breast:
5	chr11:85438614..85440584-chr11:85468892..85470720,2	MCF-7	breast:
6	chr11:85374657..85377519-chr11:85553328..85556273,3	MCF-7	breast:
7	chr11:85553949..85557231-chr11:85564538..85567553,4	MCF-7	breast:
8	chr11:85528152..85530111-chr11:85537242..85539154,2	K562	blood:
9	chr11:85433132..85435744-chr11:85522806..85525692,2	MCF-7	breast:
10	chr11:85434078..85436234-chr11:85516970..85518571,2	MCF-7	breast:
11	chr11:85520161..85523649-chr11:85564385..85567428,4	MCF-7	breast:
12	chr11:85535692..85538329-chr11:85564444..85566884,2	MCF-7	breast:
13	chr11:85519432..85524089-chr11:85553392..85557771,8	MCF-7	breast:
14	chr11:85491140..85492854-chr11:85498576..85500721,2	MCF-7	breast:
15	chr11:85306486..85307001-chr11:85536829..85537808,2	K562	blood:
16	chr11:85518792..85520429-chr11:85538920..85541767,2	K562	blood:
17	chr11:85494490..85496333-chr11:85515737..85519342,3	MCF-7	breast:
18	chr11:85457955..85460944-chr11:85541331..85543778,2	MCF-7	breast:
19	chr11:85521201..85523634-chr11:85558488..85561627,3	MCF-7	breast:
20	chr11:85547607..85549279-chr11:85549472..85552275,2	MCF-7	breast:
21	chr11:85519803..85521941-chr11:85564201..85565920,2	MCF-7	breast:
22	chr11:85433923..85435734-chr11:85518099..85520604,2	MCF-7	breast:
23	chr11:85497196..85498847-chr11:85516352..85520145,3	MCF-7	breast:
24	chr11:85483031..85484829-chr11:85489354..85491386,2	MCF-7	breast:
25	chr11:85520346..85521861-chr11:85552981..85555359,2	MCF-7	breast:
26	chr11:85371590..85374337-chr11:85533761..85535613,2	MCF-7	breast:
27	chr11:85544689..85547229-chr11:85564767..85567061,2	MCF-7	breast:
28	chr11:85469322..85470979-chr11:85520431..85523173,2	MCF-7	breast:
29	chr11:85405093..85406585-chr11:85536858..85537561,5	MCF-7	breast:
30	chr11:85488026..85490392-chr11:85537176..85539130,2	MCF-7	breast:
31	chr11:85468435..85470460-chr11:85522182..85523762,2	MCF-7	breast:
32	chr11:85428619..85430275-chr11:85519411..85522192,2	MCF-7	breast:
33	chr11:85554738..85557275-chr11:85564156..85566058,2	K562	blood:
34	chr11:85496644..85498965-chr11:85505232..85507259,2	MCF-7	breast:
35	chr11:85546125..85548288-chr11:85553041..85556244,4	MCF-7	breast:
36	chr11:85476838..85478489-chr11:85489449..85492312,2	MCF-7	breast:
37	chr11:85470232..85472552-chr11:85473605..85477376,4	K562	blood:
38	chr11:85446235..85448098-chr11:85532932..85535818,2	MCF-7	breast:
39	chr11:85542289..85542895-chr11:85555344..85556058,2	MCF-7	breast:
40	chr11:85368566..85377997-chr11:85535712..85544822,15	MCF-7	breast:
41	chr11:85547607..85549279-chr11:85549472..85552275,2	MCF-7	breast:
42	chr11:85447110..85449601-chr11:85539919..85542813,2	MCF-7	breast:
43	chr11:85497196..85498847-chr11:85516352..85520145,3	MCF-7	breast:
44	chr11:85520346..85521861-chr11:85552981..85555359,2	MCF-7	breast:
45	chr11:85452005..85453753-chr11:85496799..85498710,2	MCF-7	breast:
46	chr11:85504991..85507109-chr11:85510444..85513172,2	MCF-7	breast:
47	chr11:85373477..85376414-chr11:85531223..85532903,2	MCF-7	breast:
48	chr11:85496644..85498965-chr11:85505232..85507259,2	MCF-7	breast:
49	chr11:85546125..85548288-chr11:85553041..85556244,4	MCF-7	breast:
50	chr11:85475609..85477419-chr11:85479383..85481786,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000974.1-1	chr11:85468803-85469112	NONHSAT023448
2	lnc-AP000974.1-1	chr11:85521997-85522183	NONHSAT023448

No data

Variant related genes	Relation type
SYTL2	TF binding region
SYTL2	CpG island
ENSG00000212195	chromatin interactions
ENSG00000215504	chromatin interactions
ENSG00000073921	chromatin interactions
ENSG00000171202	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000254502	chromatin interactions
ENSG00000137501	chromatin interactions
ENSG00000150676	chromatin interactions
ENSG00000171204	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000172201	chromatin interactions
ENSG00000137504	chromatin interactions
ENSG00000150687	chromatin interactions

Extended variants
information (count: 3300 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3300 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569600432	chr11:85468063-85468064	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs531673617	chr11:85468221-85468222	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550065496	chr11:85468235-85468236	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369533137	chr11:85468253-85468254	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571375507	chr11:85468266-85468267	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201675229	chr11:85468279-85468280	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11400282	chr11:85468284-85468285	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs386374376	chr11:85468285-85468286	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs373474341	chr11:85468289-85468290	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369139678	chr11:85468290-85468291	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11501831	chr11:85468291-85468292	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs77091889	chr11:85468329-85468330	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs377754913	chr11:85468348-85468349	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370232421	chr11:85468368-85468369	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553596414	chr11:85468481-85468482	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs149210271	chr11:85468483-85468484	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs535938721	chr11:85468509-85468510	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs34851708	chr11:85468585-85468586	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554171622	chr11:85468598-85468599	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs374959762	chr11:85468616-85468617	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs376224097	chr11:85468625-85468626	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575617219	chr11:85468631-85468632	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369766248	chr11:85468650-85468651	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201770370	chr11:85468680-85468681	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs544516547	chr11:85468685-85468686	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs374660440	chr11:85468698-85468699	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149582759	chr11:85468708-85468709	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs369267760	chr11:85468762-85468763	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs535127960	chr11:85468792-85468793	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs578111232	chr11:85468793-85468794	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs11234402	chr11:85468819-85468820	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs560518938	chr11:85468829-85468830	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs527814921	chr11:85468839-85468840	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs543129010	chr11:85468880-85468881	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs181979455	chr11:85468952-85468953	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs533234089	chr11:85468985-85468986	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs186877703	chr11:85469030-85469031	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs571480461	chr11:85469048-85469049	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs532297096	chr11:85469049-85469050	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs113461390	chr11:85469051-85469052	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs139032989	chr11:85469065-85469066	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs535973232	chr11:85469087-85469088	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs190122815	chr11:85469109-85469110	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs113708708	chr11:85469114-85469115	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs536436919	chr11:85469118-85469119	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs141930606	chr11:85469174-85469175	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs145661654	chr11:85469216-85469217	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs578224944	chr11:85469218-85469219	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs545356484	chr11:85469227-85469228	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs138280694	chr11:85469248-85469249	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Lung cancer	18438408	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1845 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85430400-85480400	Weak transcription	Aorta	Aorta
2	chr11:85448000-85480600	Weak transcription	Fetal Stomach	stomach
3	chr11:85449200-85478400	Weak transcription	Right Ventricle	heart
4	chr11:85453000-85471000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:85455000-85470800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:85456800-85468600	Weak transcription	Psoas Muscle	Psoas
7	chr11:85457000-85469000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr11:85457000-85469000	Weak transcription	Gastric	stomach
9	chr11:85459400-85470600	Weak transcription	HSMM	muscle
10	chr11:85459800-85470600	Weak transcription	NHEK	skin
11	chr11:85460600-85483800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr11:85461600-85471000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr11:85461800-85468400	Weak transcription	Fetal Kidney	kidney
14	chr11:85461800-85470800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr11:85462000-85470800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr11:85462000-85470800	Weak transcription	Osteobl	bone
17	chr11:85462000-85471000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr11:85463200-85470800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:85463200-85478800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:85463400-85472400	Weak transcription	Fetal Muscle Leg	muscle
21	chr11:85463800-85470400	Weak transcription	NHDF-Ad	bronchial
22	chr11:85463800-85470800	Weak transcription	NHLF	lung
23	chr11:85464200-85468200	Bivalent Enhancer	Fetal Thymus	thymus
24	chr11:85464400-85468800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr11:85464400-85468800	Weak transcription	Fetal Lung	lung
26	chr11:85464400-85471000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:85464600-85469400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr11:85464600-85470000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr11:85464600-85470200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr11:85464600-85470800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr11:85464600-85470800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:85464600-85471800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr11:85464600-85472600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr11:85464800-85468400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:85465200-85468600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr11:85466200-85469200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr11:85466200-85469800	Enhancers	Stomach Mucosa	stomach
38	chr11:85466400-85468800	Enhancers	Fetal Intestine Large	intestine
39	chr11:85466400-85468800	Enhancers	Fetal Intestine Small	intestine
40	chr11:85466400-85469200	Enhancers	Colonic Mucosa	Colon
41	chr11:85466800-85468800	Enhancers	Small Intestine	intestine
42	chr11:85467200-85469400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr11:85467600-85468600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr11:85467600-85469400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr11:85467600-85469800	Enhancers	Duodenum Mucosa	Duodenum
46	chr11:85467600-85470200	Enhancers	Primary T cells fromperipheralblood	blood
47	chr11:85467600-85471800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:85467600-85472200	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr11:85467600-85477600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:85467800-85468200	Enhancers	HSMMtube	muscle

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