Variant report

Variant	nsv897015
Chromosome Location	chr11:16235962-16307700
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	chr11:16274129-16274292	K562	blood:	n/a	n/a
3	ARID3A	chr11:16292843-16293227	K562	blood:	n/a	n/a
4	ARID3A	chr11:16301328-16302542	K562	blood:	n/a	chr11:16301883-16301899
5	ARID3A	chr11:16274051-16274250	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:16247839-16248178	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:16299166-16299541	K562	blood:	n/a	n/a
8	ARID3A	chr11:16283929-16284325	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:16261422-16261856	K562	blood:	n/a	n/a
10	ATF1	chr11:16301903-16302256	K562	blood:	n/a	n/a
11	ATF1	chr11:16283956-16284156	K562	blood:	n/a	n/a
12	BACH1	chr11:16261791-16261801	K562	blood:	n/a	n/a
13	BACH1	chr11:16273238-16273356	K562	blood:	n/a	n/a
14	BHLHE40	chr11:16248034-16248148	K562	blood:	n/a	n/a
15	BHLHE40	chr11:16262212-16262324	K562	blood:	n/a	n/a
16	BHLHE40	chr11:16301906-16302158	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:16261173-16261323	K562	blood:	n/a	n/a
18	BHLHE40	chr11:16301649-16302234	K562	blood:	n/a	n/a
19	CBX3	chr11:16287608-16287923	K562	blood:	n/a	n/a
20	CBX3	chr11:16287556-16287971	K562	blood:	n/a	n/a
21	CBX3	chr11:16269564-16270388	K562	blood:	n/a	n/a
22	CCNT2	chr11:16301921-16302409	K562	blood:	n/a	n/a
23	CEBPB	chr11:16287647-16287968	K562	blood:	n/a	chr11:16287808-16287819
24	CEBPB	chr11:16287670-16287919	IMR90	lung:	n/a	chr11:16287808-16287819
25	CEBPB	chr11:16236683-16236798	H1-hESC	embryonic stem cell:	n/a	chr11:16236707-16236718
26	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
27	CEBPB	chr11:16236561-16236882	HepG2	liver:	n/a	chr11:16236707-16236718
28	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
29	CEBPB	chr11:16236628-16236796	A549	lung:	n/a	chr11:16236707-16236718
30	CEBPB	chr11:16236581-16236894	IMR90	lung:	n/a	chr11:16236707-16236718
31	CEBPB	chr11:16301953-16302185	Hela-S3	cervix:	n/a	chr11:16302151-16302163
32	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
33	CEBPB	chr11:16243293-16243394	A549	lung:	n/a	n/a
34	CEBPB	chr11:16301281-16301308	H1-hESC	embryonic stem cell:	n/a	n/a
35	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
36	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
37	CEBPB	chr11:16287706-16287967	HepG2	liver:	n/a	chr11:16287808-16287819
38	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
39	CEBPB	chr11:16291993-16292148	K562	blood:	n/a	n/a
40	CEBPB	chr11:16255090-16255143	IMR90	lung:	n/a	n/a
41	CEBPZ	chr11:16247850-16247882	HepG2	liver:	n/a	n/a
42	CTCF	chr11:16274240-16274390	HAc	cerebellar:	n/a	n/a
43	CTCF	chr11:16274040-16274190	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr11:16274060-16274210	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr11:16292940-16293090	Caco-2	colon:	n/a	n/a
46	CTCF	chr11:16274020-16274170	HCM	heart:	n/a	n/a
47	CTCF	chr11:16274020-16274170	AG04449	skin:	n/a	n/a
48	CTCF	chr11:16274080-16274230	HMEC	breast:	n/a	n/a
49	CTCF	chr11:16274060-16274210	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr11:16301667-16302284	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:16298618-16298668	Hepatocyte	liver:	n/a
2	chr11:16298618-16298668	NHBE	bronchial:	n/a
3	chr11:16298618-16298668	GM06990	blood:	n/a
4	chr11:16298618-16298668	AG04450	lung:	fetal
5	chr11:16298618-16298668	SK-N-SH	brain:	n/a
6	chr11:16298618-16298668	PANC-1	pancreas:	n/a
7	chr11:16298618-16298668	RPTEC	kidney:	n/a
8	chr11:16298618-16298668	LNCaP	prostate:	n/a
9	chr11:16298618-16298668	GM12878	blood:	n/a
10	chr11:16298618-16298668	Caco-2	colon:	n/a
11	chr11:16298618-16298668	HRE	kidney:	n/a
12	chr11:16298618-16298668	NHDF-neo	bronchial:	n/a
13	chr11:16298618-16298668	NB4	blood:	n/a
14	chr11:16298618-16298668	HUVEC	blood vessel:	n/a
15	chr11:16298618-16298668	HAEpiC	amniotic membrane:	n/a
16	chr11:16298618-16298668	AG04449	skin:	fetal
17	chr11:16298618-16298668	PFSK-1	brain:	n/a
18	chr11:16298618-16298668	GM12891	blood:	n/a
19	chr11:16298618-16298668	SK-N-MC	brain:	n/a
20	chr11:16298618-16298668	MCF10A-Er-Src	breast:	n/a
21	chr11:16298618-16298668	HCF	heart:	n/a
22	chr11:16298618-16298668	BE2_C	brain:	n/a
23	chr11:16298618-16298668	U87	brain:	n/a
24	chr11:16298618-16298668	A549	lung:	n/a
25	chr11:16298618-16298668	HRCEpiC	kidney:	n/a
26	chr11:16298618-16298668	ProgFib	skin:	n/a
27	chr11:16298618-16298668	MCF-7	breast:	n/a
28	chr11:16298618-16298668	HEEpiC	esophagus:	n/a
29	chr11:16298618-16298668	GM19239	blood:	n/a
30	chr11:16298618-16298668	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:16298618-16298668	HL-60	blood:	n/a
32	chr11:16298618-16298668	Hela-S3	cervix:	n/a
33	chr11:16298618-16298668	BJ	skin:	n/a
34	chr11:16298618-16298668	HCPEpiC	choroid plexus:	n/a
35	chr11:16298618-16298668	SAEC	small airway:	n/a
36	chr11:16298618-16298668	K562	blood:	n/a
37	chr11:16298618-16298668	SKMC	muscle:	n/a
38	chr11:16298618-16298668	HEK293	kidney:	embryo
39	chr11:16298618-16298668	HepG2	liver:	n/a
40	chr11:16298618-16298668	AoSMC	blood vessel:	n/a
41	chr11:16298618-16298668	HRPEpiC	eye:	n/a
42	chr11:16298618-16298668	HIPEpiC	eye:	n/a
43	chr11:16298618-16298668	CMK	blood:	n/a
44	chr11:16298618-16298668	GM12892	blood:	n/a
45	chr11:16298618-16298668	ovcar-3	ovarian:	n/a
46	chr11:16298618-16298668	H1-hESC	embryonic stem cell:	embryo
47	chr11:16298618-16298668	AG09309	skin:	n/a
48	chr11:16298618-16298668	HMEC	breast:	n/a
49	chr11:16298618-16298668	PrEC	prostate:	n/a
50	chr11:16298618-16298668	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:16292606..16296428-chr11:16299635..16303061,5	K562	blood:
2	chr11:16248287..16249803-chr11:16256816..16258558,2	K562	blood:
3	chr11:16277289..16281774-chr11:16284462..16288431,5	K562	blood:
4	chr11:16258646..16260759-chr11:16262336..16265198,2	K562	blood:
5	chr11:16273763..16275411-chr11:16283126..16284650,2	K562	blood:
6	chr11:16254286..16256657-chr11:16264384..16267054,2	K562	blood:
7	chr11:16263238..16264748-chr11:16273911..16275537,2	K562	blood:
8	chr11:16265440..16267766-chr11:16271349..16273913,2	K562	blood:
9	chr11:16262539..16264266-chr11:16264896..16266667,2	K562	blood:
10	chr11:16254762..16258115-chr11:16260794..16264082,4	K562	blood:
11	chr11:16235541..16237281-chr11:16252412..16254092,2	K562	blood:
12	chr11:16251402..16252987-chr11:16626584..16628103,2	K562	blood:
13	chr11:16262539..16264266-chr11:16264896..16266667,2	K562	blood:
14	chr11:16209269..16212267-chr11:16243598..16245269,2	K562	blood:
15	chr11:16254762..16258115-chr11:16260794..16264082,4	K562	blood:
16	chr11:16235541..16237281-chr11:16252412..16254092,2	K562	blood:
17	chr11:16289702..16293016-chr11:16300436..16303911,5	K562	blood:
18	chr11:16248287..16249803-chr11:16256816..16258558,2	K562	blood:
19	chr11:16289702..16293016-chr11:16300436..16303911,5	K562	blood:
20	chr11:16293209..16295889-chr11:16296244..16299615,4	K562	blood:
21	chr11:16304365..16307291-chr11:16625396..16627357,2	K562	blood:
22	chr11:16289454..16292201-chr11:16321892..16324622,2	K562	blood:
23	chr11:16240077..16244324-chr11:16251034..16255034,5	K562	blood:
24	chr11:16245998..16247921-chr11:16262395..16264566,2	K562	blood:
25	chr11:16272523..16274102-chr11:16278731..16281096,3	K562	blood:
26	chr11:16253830..16255900-chr11:16301377..16303054,2	K562	blood:
27	chr11:16300623..16303536-chr11:16310934..16312660,2	K562	blood:
28	chr11:16293209..16295889-chr11:16296244..16299615,4	K562	blood:
29	chr11:16288582..16290827-chr11:16311133..16313839,2	K562	blood:
30	chr11:16302806..16305054-chr11:16360203..16362191,2	K562	blood:
31	chr11:16252253..16255458-chr11:16256326..16259202,3	K562	blood:
32	chr11:16240077..16244324-chr11:16251034..16255034,5	K562	blood:
33	chr11:16252253..16255458-chr11:16256326..16259202,3	K562	blood:
34	chr11:16287380..16289427-chr11:16291127..16292666,2	K562	blood:
35	chr11:16301382..16303241-chr11:16318945..16321849,2	K562	blood:
36	chr11:16296567..16299036-chr11:16300156..16302132,2	K562	blood:
37	chr11:16253958..16256004-chr11:16256326..16259109,2	K562	blood:
38	chr11:16273998..16276548-chr11:16285283..16288177,2	K562	blood:
39	chr11:16265955..16267897-chr11:16366139..16368672,2	K562	blood:
40	chr11:16292606..16296428-chr11:16299635..16303061,5	K562	blood:
41	chr11:16277289..16281774-chr11:16284462..16288431,5	K562	blood:
42	chr11:16245998..16247921-chr11:16262395..16264566,2	K562	blood:
43	chr11:16299175..16301880-chr11:16312711..16315686,3	K562	blood:
44	chr11:16300243..16302575-chr11:16402868..16404616,2	K562	blood:
45	chr11:16306276..16308117-chr11:16316163..16319101,2	K562	blood:
46	chr11:16258646..16260759-chr11:16262336..16265198,2	K562	blood:
47	chr11:16253830..16255900-chr11:16301377..16303054,2	K562	blood:
48	chr11:16265440..16267766-chr11:16271349..16273913,2	K562	blood:
49	chr11:16287380..16289427-chr11:16291127..16292666,2	K562	blood:
50	chr11:16306276..16309122-chr11:16315814..16317663,2	K562	blood:

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

Extended variants
information (count: 2250 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2250 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10500828	chr11:16235962-16235963	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531412861	chr11:16235968-16235969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189398440	chr11:16235988-16235989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561833291	chr11:16236007-16236008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532428094	chr11:16236037-16236038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34185930	chr11:16236072-16236073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs180884759	chr11:16236110-16236111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565953436	chr11:16236136-16236137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185490347	chr11:16236151-16236152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552520117	chr11:16236166-16236167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189816375	chr11:16236199-16236200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183527859	chr11:16236245-16236246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556260578	chr11:16236256-16236257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368038119	chr11:16236292-16236293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571933596	chr11:16236310-16236311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564627374	chr11:16236314-16236315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569148815	chr11:16236321-16236322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568266407	chr11:16236348-16236349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142343142	chr11:16236367-16236368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536699818	chr11:16236382-16236383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369905226	chr11:16236391-16236392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146885230	chr11:16236429-16236430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187120037	chr11:16236493-16236494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35547484	chr11:16236503-16236504	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs557771378	chr11:16236506-16236507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576287030	chr11:16236511-16236512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11023873	chr11:16236520-16236521	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs11023874	chr11:16236541-16236542	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs143364020	chr11:16236548-16236549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529060346	chr11:16236559-16236560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541216191	chr11:16236560-16236561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577050112	chr11:16236562-16236563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61150801	chr11:16236574-16236575	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533237493	chr11:16236585-16236586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148148983	chr11:16236596-16236597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374597727	chr11:16236599-16236600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570484380	chr11:16236648-16236649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6486280	chr11:16236658-16236659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs538131767	chr11:16236705-16236706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541032899	chr11:16236708-16236709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560830136	chr11:16236755-16236756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568206930	chr11:16236772-16236773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535623099	chr11:16236773-16236774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554321535	chr11:16236844-16236845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191978877	chr11:16236855-16236856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540094637	chr11:16236903-16236904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141184566	chr11:16236908-16236909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529631701	chr11:16236923-16236924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543316488	chr11:16236946-16236947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556856427	chr11:16237020-16237021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16224400-16247200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr11:16226000-16238400	Weak transcription	Psoas Muscle	Psoas
3	chr11:16231800-16237000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:16231800-16240400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr11:16235000-16237000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:16235800-16236200	Enhancers	Fetal Intestine Large	intestine
7	chr11:16237000-16239600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:16237000-16239800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:16238400-16238600	Enhancers	Psoas Muscle	Psoas
10	chr11:16238600-16260800	Weak transcription	Psoas Muscle	Psoas
11	chr11:16239600-16248200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr11:16240400-16241200	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr11:16241200-16242000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr11:16242000-16242600	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr11:16242600-16245000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr11:16243200-16243600	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr11:16244800-16245200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr11:16244800-16245400	Enhancers	HUVEC	blood vessel
19	chr11:16245000-16245200	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr11:16245200-16245400	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr11:16245200-16245400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr11:16245400-16246200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr11:16245400-16247400	Weak transcription	HUVEC	blood vessel
24	chr11:16245800-16246000	Enhancers	Duodenum Mucosa	Duodenum
25	chr11:16246000-16247000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr11:16246200-16246400	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr11:16246400-16246600	Enhancers	Fetal Intestine Large	intestine
28	chr11:16246400-16247000	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr11:16246600-16258600	Weak transcription	Fetal Intestine Large	intestine
30	chr11:16247000-16247200	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr11:16247000-16248400	Enhancers	Duodenum Mucosa	Duodenum
32	chr11:16247000-16248400	Enhancers	Fetal Heart	heart
33	chr11:16247200-16247400	Enhancers	K562	blood
34	chr11:16247200-16247800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr11:16247200-16248200	Enhancers	Liver	Liver
36	chr11:16247200-16248400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr11:16247200-16248600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr11:16247200-16248600	Enhancers	A549	lung
39	chr11:16247400-16248400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:16247400-16248400	Enhancers	HUVEC	blood vessel
41	chr11:16247600-16248200	Enhancers	Fetal Lung	lung
42	chr11:16247800-16248200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:16247800-16248200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:16247800-16248200	Enhancers	Pancreas	Pancrea
45	chr11:16247800-16248200	Enhancers	HepG2	liver
46	chr11:16247800-16248200	Enhancers	NHEK	skin
47	chr11:16247800-16248400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr11:16247800-16248600	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr11:16248000-16248200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr11:16248000-16248200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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