Variant report

Variant	nsv553565
Chromosome Location	chr11:16220289-16307700
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	chr11:16302822-16302846	K562	blood:	n/a	n/a
2	ARID3A	chr11:16261422-16261856	K562	blood:	n/a	n/a
3	ARID3A	chr11:16274129-16274292	K562	blood:	n/a	n/a
4	ARID3A	chr11:16283929-16284325	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:16292843-16293227	K562	blood:	n/a	n/a
6	ARID3A	chr11:16299166-16299541	K562	blood:	n/a	n/a
7	ARID3A	chr11:16274051-16274250	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:16247839-16248178	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:16225893-16226444	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:16301328-16302542	K562	blood:	n/a	chr11:16301883-16301899
11	ATF1	chr11:16301903-16302256	K562	blood:	n/a	n/a
12	ATF1	chr11:16235644-16235823	K562	blood:	n/a	n/a
13	ATF1	chr11:16220369-16220662	K562	blood:	n/a	n/a
14	ATF1	chr11:16283956-16284156	K562	blood:	n/a	n/a
15	BACH1	chr11:16273238-16273356	K562	blood:	n/a	n/a
16	BACH1	chr11:16261791-16261801	K562	blood:	n/a	n/a
17	BHLHE40	chr11:16262212-16262324	K562	blood:	n/a	n/a
18	BHLHE40	chr11:16261173-16261323	K562	blood:	n/a	n/a
19	BHLHE40	chr11:16248034-16248148	K562	blood:	n/a	n/a
20	BHLHE40	chr11:16220419-16220582	K562	blood:	n/a	n/a
21	BHLHE40	chr11:16301649-16302234	K562	blood:	n/a	n/a
22	BHLHE40	chr11:16301906-16302158	GM12878	blood:	n/a	n/a
23	CBX3	chr11:16287556-16287971	K562	blood:	n/a	n/a
24	CBX3	chr11:16287608-16287923	K562	blood:	n/a	n/a
25	CBX3	chr11:16224012-16224364	K562	blood:	n/a	n/a
26	CBX3	chr11:16269564-16270388	K562	blood:	n/a	n/a
27	CCNT2	chr11:16301921-16302409	K562	blood:	n/a	n/a
28	CEBPB	chr11:16301006-16301757	K562	blood:	n/a	chr11:16301249-16301258 chr11:16301263-16301274 chr11:16301247-16301260 chr11:16301263-16301276 chr11:16301249-16301260 chr11:16301249-16301260 chr11:16301249-16301258 chr11:16301247-16301260 chr11:16301249-16301258 chr11:16301264-16301275 chr11:16301247-16301258 chr11:16301247-16301260 chr11:16301249-16301258
29	CEBPB	chr11:16291993-16292148	K562	blood:	n/a	n/a
30	CEBPB	chr11:16287706-16287967	HepG2	liver:	n/a	chr11:16287808-16287819
31	CEBPB	chr11:16300978-16302276	K562	blood:	n/a	chr11:16301249-16301258 chr11:16301263-16301274 chr11:16301247-16301260 chr11:16301263-16301276 chr11:16301249-16301260 chr11:16301249-16301260 chr11:16301249-16301258 chr11:16301247-16301260 chr11:16301249-16301258 chr11:16302151-16302163 chr11:16301264-16301275 chr11:16301247-16301258 chr11:16301247-16301260 chr11:16301249-16301258
32	CEBPB	chr11:16255090-16255143	IMR90	lung:	n/a	n/a
33	CEBPB	chr11:16301097-16301432	HepG2	liver:	n/a	chr11:16301249-16301258 chr11:16301263-16301274 chr11:16301247-16301260 chr11:16301263-16301276 chr11:16301249-16301260 chr11:16301249-16301260 chr11:16301249-16301258 chr11:16301247-16301260 chr11:16301249-16301258 chr11:16301264-16301275 chr11:16301247-16301258 chr11:16301247-16301260 chr11:16301249-16301258
34	CEBPB	chr11:16301137-16301404	Hela-S3	cervix:	n/a	chr11:16301249-16301258 chr11:16301263-16301274 chr11:16301247-16301260 chr11:16301263-16301276 chr11:16301249-16301260 chr11:16301249-16301260 chr11:16301249-16301258 chr11:16301247-16301260 chr11:16301249-16301258 chr11:16301264-16301275 chr11:16301247-16301258 chr11:16301247-16301260 chr11:16301249-16301258
35	CEBPB	chr11:16287670-16287919	IMR90	lung:	n/a	chr11:16287808-16287819
36	CEBPB	chr11:16287647-16287968	K562	blood:	n/a	chr11:16287808-16287819
37	CEBPB	chr11:16236683-16236798	H1-hESC	embryonic stem cell:	n/a	chr11:16236707-16236718
38	CEBPB	chr11:16235572-16235891	K562	blood:	n/a	chr11:16235739-16235750
39	CEBPB	chr11:16301103-16301437	IMR90	lung:	n/a	chr11:16301249-16301258 chr11:16301263-16301274 chr11:16301247-16301260 chr11:16301263-16301276 chr11:16301249-16301260 chr11:16301249-16301260 chr11:16301249-16301258 chr11:16301247-16301260 chr11:16301249-16301258 chr11:16301264-16301275 chr11:16301247-16301258 chr11:16301247-16301260 chr11:16301249-16301258
40	CEBPB	chr11:16243293-16243394	A549	lung:	n/a	n/a
41	CEBPB	chr11:16236581-16236894	IMR90	lung:	n/a	chr11:16236707-16236718
42	CEBPB	chr11:16301281-16301308	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr11:16236628-16236796	A549	lung:	n/a	chr11:16236707-16236718
44	CEBPB	chr11:16235689-16235763	HepG2	liver:	n/a	chr11:16235739-16235750
45	CEBPB	chr11:16236561-16236882	HepG2	liver:	n/a	chr11:16236707-16236718
46	CEBPB	chr11:16301138-16301697	A549	lung:	n/a	chr11:16301249-16301258 chr11:16301263-16301274 chr11:16301247-16301260 chr11:16301263-16301276 chr11:16301249-16301260 chr11:16301249-16301260 chr11:16301249-16301258 chr11:16301247-16301260 chr11:16301249-16301258 chr11:16301264-16301275 chr11:16301247-16301258 chr11:16301247-16301260 chr11:16301249-16301258
47	CEBPB	chr11:16301953-16302185	Hela-S3	cervix:	n/a	chr11:16302151-16302163
48	CEBPZ	chr11:16247850-16247882	HepG2	liver:	n/a	n/a
49	CTCF	chr11:16274040-16274190	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr11:16274080-16274230	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:16298618-16298668	U87	brain:	n/a
2	chr11:16298618-16298668	HMEC	breast:	n/a
3	chr11:16298618-16298668	NHDF-neo	bronchial:	n/a
4	chr11:16298618-16298668	HAEpiC	amniotic membrane:	n/a
5	chr11:16298618-16298668	HRPEpiC	eye:	n/a
6	chr11:16298618-16298668	GM12878	blood:	n/a
7	chr11:16298618-16298668	NT2-D1	testis:	n/a
8	chr11:16298618-16298668	MCF-7	breast:	n/a
9	chr11:16298618-16298668	PFSK-1	brain:	n/a
10	chr11:16298618-16298668	PANC-1	pancreas:	n/a
11	chr11:16298618-16298668	Hepatocyte	liver:	n/a
12	chr11:16298618-16298668	AG10803	skin:	n/a
13	chr11:16298618-16298668	BJ	skin:	n/a
14	chr11:16298618-16298668	PrEC	prostate:	n/a
15	chr11:16298618-16298668	NH-A	brain:	n/a
16	chr11:16298618-16298668	RPTEC	kidney:	n/a
17	chr11:16298618-16298668	NB4	blood:	n/a
18	chr11:16298618-16298668	GM06990	blood:	n/a
19	chr11:16298618-16298668	ProgFib	skin:	n/a
20	chr11:16298618-16298668	Caco-2	colon:	n/a
21	chr11:16298618-16298668	AG04450	lung:	fetal
22	chr11:16298618-16298668	HL-60	blood:	n/a
23	chr11:16298618-16298668	HEK293	kidney:	embryo
24	chr11:16298618-16298668	GM12892	blood:	n/a
25	chr11:16298618-16298668	SK-N-SH	brain:	n/a
26	chr11:16298618-16298668	SKMC	muscle:	n/a
27	chr11:16298618-16298668	HCPEpiC	choroid plexus:	n/a
28	chr11:16298618-16298668	AG09319	gingival:	n/a
29	chr11:16298618-16298668	A549	lung:	n/a
30	chr11:16298618-16298668	HNPCEpiC	eye:	n/a
31	chr11:16298618-16298668	HRCEpiC	kidney:	n/a
32	chr11:16298618-16298668	AG09309	skin:	n/a
33	chr11:16298618-16298668	NHBE	bronchial:	n/a
34	chr11:16298618-16298668	GM12891	blood:	n/a
35	chr11:16298618-16298668	GM19239	blood:	n/a
36	chr11:16298618-16298668	ECC-1	luminal epithelium:	n/a
37	chr11:16298618-16298668	HCT-116	colon:	n/a
38	chr11:16298618-16298668	LNCaP	prostate:	n/a
39	chr11:16298618-16298668	ovcar-3	ovarian:	n/a
40	chr11:16298618-16298668	HCM	heart:	n/a
41	chr11:16298618-16298668	HIPEpiC	eye:	n/a
42	chr11:16298618-16298668	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:16298618-16298668	HRE	kidney:	n/a
44	chr11:16298618-16298668	SK-N-SH_RA	brain:	n/a
45	chr11:16298618-16298668	SK-N-MC	brain:	n/a
46	chr11:16298618-16298668	H1-hESC	embryonic stem cell:	embryo
47	chr11:16298618-16298668	HEEpiC	esophagus:	n/a
48	chr11:16298618-16298668	HepG2	liver:	n/a
49	chr11:16298618-16298668	AoSMC	blood vessel:	n/a
50	chr11:16298618-16298668	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:16277289..16281774-chr11:16284462..16288431,5	K562	blood:
2	chr11:16251614..16253946-chr11:16259376..16260960,2	K562	blood:
3	chr11:16218926..16220596-chr11:16221268..16223735,2	K562	blood:
4	chr11:16223882..16226263-chr11:16229633..16231626,2	K562	blood:
5	chr11:16288582..16290827-chr11:16311133..16313839,2	K562	blood:
6	chr11:16306276..16308117-chr11:16316163..16319101,2	K562	blood:
7	chr11:16253830..16255900-chr11:16301377..16303054,2	K562	blood:
8	chr11:16273998..16276548-chr11:16285283..16288177,2	K562	blood:
9	chr11:16301382..16303241-chr11:16318945..16321849,2	K562	blood:
10	chr11:16258646..16260759-chr11:16262336..16265198,2	K562	blood:
11	chr11:16304365..16307291-chr11:16625396..16627357,2	K562	blood:
12	chr11:16262539..16264266-chr11:16264896..16266667,2	K562	blood:
13	chr11:16277289..16281774-chr11:16284462..16288431,5	K562	blood:
14	chr11:16289702..16293016-chr11:16300436..16303911,5	K562	blood:
15	chr11:16218926..16220596-chr11:16221268..16223735,2	K562	blood:
16	chr11:16252253..16255458-chr11:16256326..16259202,3	K562	blood:
17	chr11:16248287..16249803-chr11:16256816..16258558,2	K562	blood:
18	chr11:16299175..16301880-chr11:16312711..16315686,3	K562	blood:
19	chr11:16209269..16212267-chr11:16243598..16245269,2	K562	blood:
20	chr11:16219560..16222671-chr11:16224548..16227962,3	K562	blood:
21	chr11:16254286..16256657-chr11:16264384..16267054,2	K562	blood:
22	chr11:16253250..16255469-chr11:16319154..16321553,2	K562	blood:
23	chr11:16235541..16237281-chr11:16252412..16254092,2	K562	blood:
24	chr11:16262539..16264266-chr11:16264896..16266667,2	K562	blood:
25	chr11:16297975..16301797-chr11:16627660..16630721,4	K562	blood:
26	chr11:16272523..16274102-chr11:16278731..16281096,3	K562	blood:
27	chr11:16263238..16264748-chr11:16273911..16275537,2	K562	blood:
28	chr11:16245998..16247921-chr11:16262395..16264566,2	K562	blood:
29	chr11:16265955..16267897-chr11:16366139..16368672,2	K562	blood:
30	chr11:16226649..16230230-chr11:16231608..16235450,4	K562	blood:
31	chr11:16245998..16247921-chr11:16262395..16264566,2	K562	blood:
32	chr11:16302806..16305054-chr11:16360203..16362191,2	K562	blood:
33	chr11:16254762..16258115-chr11:16260794..16264082,4	K562	blood:
34	chr11:16265440..16267766-chr11:16271349..16273913,2	K562	blood:
35	chr11:16293209..16295889-chr11:16296244..16299615,4	K562	blood:
36	chr11:16273763..16275411-chr11:16283126..16284650,2	K562	blood:
37	chr11:16287380..16289427-chr11:16291127..16292666,2	K562	blood:
38	chr11:16256169..16258785-chr11:16346996..16349123,2	K562	blood:
39	chr11:16253958..16256004-chr11:16256326..16259109,2	K562	blood:
40	chr11:16251614..16253946-chr11:16259376..16260960,2	K562	blood:
41	chr11:16240077..16244324-chr11:16251034..16255034,5	K562	blood:
42	chr11:16273658..16274622-chr11:16627404..16628365,5	MCF-7	breast:
43	chr11:16296567..16299036-chr11:16300156..16302132,2	K562	blood:
44	chr11:16215320..16217059-chr11:16240927..16242475,2	K562	blood:
45	chr11:16240077..16244324-chr11:16251034..16255034,5	K562	blood:
46	chr11:16289702..16293016-chr11:16300436..16303911,5	K562	blood:
47	chr11:16213165..16216422-chr11:16216965..16220387,3	K562	blood:
48	chr11:16248287..16249803-chr11:16256816..16258558,2	K562	blood:
49	chr11:16235541..16237281-chr11:16252412..16254092,2	K562	blood:
50	chr11:16300623..16303536-chr11:16310934..16312660,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHA7-5	chr11:16221974-16222435	NONHSAT018173

Variant related genes	Relation type
SOX6	TF binding region
SOX6	CpG island
ENSG00000110693	chromatin interactions

Extended variants
information (count: 2756 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2756 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7122351	chr11:16220289-16220290	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367810933	chr11:16220315-16220316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572194793	chr11:16220324-16220325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188384992	chr11:16220340-16220341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569859995	chr11:16220378-16220379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537390181	chr11:16220452-16220453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556278561	chr11:16220462-16220463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs180753249	chr11:16220477-16220478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541902291	chr11:16220495-16220496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553867707	chr11:16220558-16220559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572280139	chr11:16220563-16220564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545598566	chr11:16220643-16220644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369491041	chr11:16220649-16220650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs71484704	chr11:16220671-16220672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187235678	chr11:16220682-16220683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs16932711	chr11:16220750-16220751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs36062416	chr11:16220771-16220772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531903580	chr11:16220787-16220788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567296008	chr11:16220840-16220841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544142867	chr11:16220841-16220842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201642253	chr11:16220853-16220854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561506585	chr11:16220868-16220869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6486277	chr11:16220882-16220883	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs149732273	chr11:16220887-16220888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559493154	chr11:16220910-16220911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562094887	chr11:16220921-16220922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192115299	chr11:16221004-16221005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200091199	chr11:16221097-16221098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533118693	chr11:16221098-16221099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551591078	chr11:16221104-16221105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569877811	chr11:16221120-16221121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6486278	chr11:16221145-16221146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs6486279	chr11:16221178-16221179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568331982	chr11:16221200-16221201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535481874	chr11:16221305-16221306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553804447	chr11:16221402-16221403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183453288	chr11:16221601-16221602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186056618	chr11:16221604-16221605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34648239	chr11:16221624-16221625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34968902	chr11:16221630-16221631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539587099	chr11:16221668-16221669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1455118	chr11:16221683-16221684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1455117	chr11:16221699-16221700	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs546471192	chr11:16221708-16221709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543744092	chr11:16221730-16221731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145634112	chr11:16221772-16221773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11023869	chr11:16221780-16221781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs190474864	chr11:16221872-16221873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541035156	chr11:16221927-16221928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559430079	chr11:16221932-16221933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16207200-16221200	Weak transcription	Fetal Intestine Large	intestine
2	chr11:16217600-16224600	Weak transcription	Fetal Heart	heart
3	chr11:16218200-16223400	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr11:16218400-16225800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:16220000-16221000	Enhancers	K562	blood
6	chr11:16224000-16224400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
7	chr11:16224400-16247200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr11:16224600-16224800	Enhancers	Fetal Heart	heart
9	chr11:16224800-16225200	Flanking Active TSS	Fetal Heart	heart
10	chr11:16225200-16227000	Enhancers	Fetal Heart	heart
11	chr11:16225400-16226800	Enhancers	HepG2	liver
12	chr11:16225800-16226000	Enhancers	Psoas Muscle	Psoas
13	chr11:16225800-16226400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr11:16226000-16238400	Weak transcription	Psoas Muscle	Psoas
15	chr11:16231600-16231800	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr11:16231800-16237000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:16231800-16240400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr11:16232800-16233200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr11:16233000-16233400	Enhancers	Fetal Heart	heart
20	chr11:16233000-16233600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:16233000-16233600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:16234600-16234800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr11:16235000-16237000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr11:16235800-16236200	Enhancers	Fetal Intestine Large	intestine
25	chr11:16237000-16239600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:16237000-16239800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr11:16238400-16238600	Enhancers	Psoas Muscle	Psoas
28	chr11:16238600-16260800	Weak transcription	Psoas Muscle	Psoas
29	chr11:16239600-16248200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:16240400-16241200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr11:16241200-16242000	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr11:16242000-16242600	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr11:16242600-16245000	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr11:16243200-16243600	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr11:16244800-16245200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr11:16244800-16245400	Enhancers	HUVEC	blood vessel
37	chr11:16245000-16245200	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr11:16245200-16245400	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr11:16245200-16245400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr11:16245400-16246200	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr11:16245400-16247400	Weak transcription	HUVEC	blood vessel
42	chr11:16245800-16246000	Enhancers	Duodenum Mucosa	Duodenum
43	chr11:16246000-16247000	Weak transcription	Duodenum Mucosa	Duodenum
44	chr11:16246200-16246400	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr11:16246400-16246600	Enhancers	Fetal Intestine Large	intestine
46	chr11:16246400-16247000	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr11:16246600-16258600	Weak transcription	Fetal Intestine Large	intestine
48	chr11:16247000-16247200	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr11:16247000-16248400	Enhancers	Duodenum Mucosa	Duodenum
50	chr11:16247000-16248400	Enhancers	Fetal Heart	heart

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