Variant report

Variant	esv2760197
Chromosome Location	chr11:76143019-76153868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:78)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:78 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:76151321-76151403	K562	blood:	n/a	n/a
2	BACH1	chr11:76147120-76147367	K562	blood:	n/a	n/a
3	BATF	chr11:76147213-76147402	GM12878	blood:	n/a	chr11:76147294-76147305
4	BATF	chr11:76147103-76147492	GM12878	blood:	n/a	chr11:76147294-76147305
5	CEBPB	chr11:76151684-76151933	K562	blood:	n/a	n/a
6	CEBPB	chr11:76152983-76153355	K562	blood:	n/a	n/a
7	CEBPB	chr11:76153155-76153255	A549	lung:	n/a	n/a
8	CEBPB	chr11:76153081-76153355	IMR90	lung:	n/a	n/a
9	CEBPB	chr11:76153154-76153291	H1-hESC	embryonic stem cell:	n/a	n/a
10	E2F4	chr11:76146943-76147091	MCF10A-Er-Src	breast:	n/a	n/a
11	GATA2	chr11:76143871-76144146	SH-SY5Y	brain:	n/a	n/a
12	IRF1	chr11:76151169-76151252	K562	blood:	n/a	n/a
13	MAFF	chr11:76147120-76147470	K562	blood:	n/a	n/a
14	MAFK	chr11:76147125-76147475	IMR90	lung:	n/a	chr11:76147287-76147302
15	MAFK	chr11:76147156-76147463	K562	blood:	n/a	chr11:76147287-76147302
16	MAFK	chr11:76147170-76147429	HepG2	liver:	n/a	chr11:76147287-76147302
17	MAFK	chr11:76147163-76147445	HepG2	liver:	n/a	chr11:76147287-76147302
18	MAX	chr11:76143645-76143982	H1-hESC	embryonic stem cell:	n/a	n/a
19	NFYB	chr11:76143716-76143926	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr11:76151475-76151476	MCF-7	breast:	n/a	n/a
21	POLR2A	chr11:76147232-76147423	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr11:76150686-76151017	HCT-116	colon:	n/a	n/a
23	POLR2A	chr11:76151259-76151587	HepG2	liver:	n/a	n/a
24	POLR2A	chr11:76148228-76148496	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr11:76153614-76153658	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr11:76150873-76151843	GM12878	blood:	n/a	n/a
27	POLR2A	chr11:76153570-76153726	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr11:76146746-76146776	Gliobla	brain:	n/a	n/a
29	POLR2A	chr11:76151449-76151472	MCF-7	breast:	n/a	n/a
30	POLR2A	chr11:76148256-76148341	K562	blood:	n/a	n/a
31	POLR2A	chr11:76147683-76147747	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr11:76149274-76149391	HepG2	liver:	n/a	n/a
33	POLR2A	chr11:76150681-76152491	K562	blood:	n/a	n/a
34	POLR2A	chr11:76150361-76150401	HepG2	liver:	n/a	n/a
35	POLR2A	chr11:76152426-76152452	HepG2	liver:	n/a	n/a
36	POLR2A	chr11:76150869-76151160	MCF-7	breast:	n/a	n/a
37	POLR2A	chr11:76153026-76153321	HepG2	liver:	n/a	n/a
38	POLR2A	chr11:76150590-76150989	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr11:76151622-76151685	HepG2	liver:	n/a	n/a
40	POLR2A	chr11:76150682-76152155	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr11:76152708-76157183	K562	blood:	n/a	n/a
42	POLR2A	chr11:76152266-76152322	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr11:76149307-76149353	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr11:76151005-76151222	HepG2	liver:	n/a	n/a
45	POLR2A	chr11:76150088-76150118	Gliobla	brain:	n/a	n/a
46	POLR2A	chr11:76150982-76151004	HepG2	liver:	n/a	n/a
47	POLR2A	chr11:76149274-76149401	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr11:76153181-76153925	SK-N-MC	brain:	n/a	n/a
49	POLR2A	chr11:76150372-76150388	K562	blood:	n/a	n/a
50	POLR2A	chr11:76153652-76154388	PFSK-1	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76152669-76152719	HRPEpiC	eye:	n/a
2	chr11:76152669-76152719	U87	brain:	n/a
3	chr11:76152669-76152719	SK-N-SH_RA	brain:	n/a
4	chr11:76152669-76152719	HRE	kidney:	n/a
5	chr11:76152669-76152719	A549	lung:	n/a
6	chr11:76152669-76152719	Caco-2	colon:	n/a
7	chr11:76152669-76152719	PANC-1	pancreas:	n/a
8	chr11:76152669-76152719	AG04450	lung:	fetal
9	chr11:76152669-76152719	HepG2	liver:	n/a
10	chr11:76152669-76152719	CMK	blood:	n/a
11	chr11:76152669-76152719	SAEC	small airway:	n/a
12	chr11:76152669-76152719	LNCaP	prostate:	n/a
13	chr11:76152669-76152719	Jurkat	blood:	n/a
14	chr11:76152669-76152719	MCF10A-Er-Src	breast:	n/a
15	chr11:76152669-76152719	GM12891	blood:	n/a
16	chr11:76152669-76152719	HCPEpiC	choroid plexus:	n/a
17	chr11:76152669-76152719	NH-A	brain:	n/a
18	chr11:76152669-76152719	SK-N-MC	brain:	n/a
19	chr11:76152669-76152719	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:76152669-76152719	HIPEpiC	eye:	n/a
21	chr11:76152669-76152719	NT2-D1	testis:	n/a
22	chr11:76152669-76152719	AG09309	skin:	n/a
23	chr11:76152669-76152719	SK-N-SH	brain:	n/a
24	chr11:76152669-76152719	HEEpiC	esophagus:	n/a
25	chr11:76152669-76152719	Hepatocyte	liver:	n/a
26	chr11:76152669-76152719	H1-hESC	embryonic stem cell:	embryo
27	chr11:76152669-76152719	HMEC	breast:	n/a
28	chr11:76152669-76152719	HCF	heart:	n/a
29	chr11:76152669-76152719	ProgFib	skin:	n/a
30	chr11:76152669-76152719	AG09319	gingival:	n/a
31	chr11:76152669-76152719	GM19239	blood:	n/a
32	chr11:76152669-76152719	T-47D	breast:	n/a
33	chr11:76152669-76152719	AG04449	skin:	fetal
34	chr11:76152669-76152719	AoSMC	blood vessel:	n/a
35	chr11:76152669-76152719	HRCEpiC	kidney:	n/a
36	chr11:76152669-76152719	NB4	blood:	n/a
37	chr11:76152669-76152719	GM06990	blood:	n/a
38	chr11:76152669-76152719	K562	blood:	n/a
39	chr11:76152669-76152719	GM12878	blood:	n/a
40	chr11:76152669-76152719	NHBE	bronchial:	n/a
41	chr11:76152669-76152719	Hela-S3	cervix:	n/a
42	chr11:76152669-76152719	HUVEC	blood vessel:	n/a
43	chr11:76152669-76152719	IMR90	lung:	fetal
44	chr11:76152669-76152719	GM12892	blood:	n/a
45	chr11:76152669-76152719	ovcar-3	ovarian:	n/a
46	chr11:76152669-76152719	PFSK-1	brain:	n/a
47	chr11:76152669-76152719	BJ	skin:	n/a
48	chr11:76152669-76152719	ECC-1	luminal epithelium:	n/a
49	chr11:76152669-76152719	AG10803	skin:	n/a
50	chr11:76152669-76152719	HNPCEpiC	eye:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76142495..76147142-chr11:76151618..76156672,5	MCF-7	breast:
2	chr11:76130194..76132353-chr11:76143690..76145227,2	MCF-7	breast:
3	chr11:76124499..76126640-chr11:76152855..76155406,3	MCF-7	breast:
4	chr11:76089758..76095735-chr11:76153234..76157826,15	MCF-7	breast:
5	chr11:76142363..76145168-chr11:76153967..76155892,2	K562	blood:
6	chr11:76149871..76150715-chr13:27720328..27720828,2	HCT-116	colon:
7	chr11:76090615..76095251-chr11:76152894..76157527,10	K562	blood:
8	chr11:76142850..76144735-chr11:76148116..76151075,2	K562	blood:
9	chr11:76124586..76126636-chr11:76140269..76143328,3	MCF-7	breast:
10	chr11:76142850..76144735-chr11:76148116..76151075,2	K562	blood:
11	chr11:76135625..76138105-chr11:76141929..76143509,2	K562	blood:
12	chr11:76096828..76101087-chr11:76152871..76156603,6	MCF-7	breast:
13	chr11:76079133..76082087-chr11:76150149..76152952,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKRIR-1	chr11:76152384-76155841	NONHSAT023169
2	lnc-PRKRIR-1	chr11:76152382-76152683	ENSG00000255135.2
3	lnc-PRKRIR-1	chr11:76153117-76155724	ENSG00000255135.2
4	lnc-PRKRIR-1	chr11:76152398-76152683	ENSG00000255135.2

No data

Variant related genes	Relation type
C11orf30	TF binding region
C11orf30	CpG island
ENSG00000158636	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000272301	chromatin interactions
ENSG00000179240	chromatin interactions
ENSG00000137492	chromatin interactions

Extended variants
information (count: 381 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10793164	chr11:76143019-76143020	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553386482	chr11:76143050-76143051	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs189976156	chr11:76143074-76143075	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573007443	chr11:76143171-76143172	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs368571522	chr11:76143177-76143178	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs181892344	chr11:76143203-76143204	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568451229	chr11:76143209-76143210	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535990590	chr11:76143222-76143223	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141980786	chr11:76143230-76143231	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs544248615	chr11:76143242-76143243	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs563623433	chr11:76143248-76143249	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs529132565	chr11:76143250-76143251	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs111448208	chr11:76143262-76143263	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs113582351	chr11:76143267-76143268	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs541847047	chr11:76143410-76143411	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528242959	chr11:76143431-76143432	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs80330016	chr11:76143462-76143463	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs4945089	chr11:76143472-76143473	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs79937892	chr11:76143533-76143534	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs146322412	chr11:76143548-76143549	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs112567003	chr11:76143560-76143561	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs558910419	chr11:76143580-76143581	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs567952336	chr11:76143582-76143583	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs536503676	chr11:76143598-76143599	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs11236750	chr11:76143599-76143600	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs186576373	chr11:76143613-76143614	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs11236751	chr11:76143633-76143634	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs538774730	chr11:76143645-76143646	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558608525	chr11:76143646-76143647	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs575309620	chr11:76143649-76143650	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs10736806	chr11:76143658-76143659	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs10736807	chr11:76143667-76143668	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs573921477	chr11:76143701-76143702	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs542554886	chr11:76143725-76143726	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs75673170	chr11:76143731-76143732	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs567125942	chr11:76143737-76143738	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569644412	chr11:76143751-76143752	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs537244223	chr11:76143789-76143790	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs541716918	chr11:76143821-76143822	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs545190172	chr11:76143870-76143871	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564994147	chr11:76143883-76143884	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs78581551	chr11:76143890-76143891	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs550558655	chr11:76143904-76143905	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs567138661	chr11:76143978-76143979	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs530468158	chr11:76144018-76144019	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs73493439	chr11:76144029-76144030	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs188435919	chr11:76144034-76144035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs191306758	chr11:76144063-76144064	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555559308	chr11:76144099-76144100	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs74862152	chr11:76144112-76144113	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76143600-76143800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:76143600-76143800	Enhancers	Aorta	Aorta
3	chr11:76143800-76144000	ZNF genes & repeats	Aorta	Aorta
4	chr11:76143800-76144000	Enhancers	Left Ventricle	heart
5	chr11:76144000-76154000	Weak transcription	Left Ventricle	heart
6	chr11:76145600-76153600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:76146000-76152400	Weak transcription	Fetal Intestine Small	intestine
8	chr11:76147000-76147600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:76147200-76148600	Enhancers	K562	blood
10	chr11:76147600-76150800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:76147600-76154400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr11:76148000-76154400	Weak transcription	HSMM	muscle
13	chr11:76148200-76154600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr11:76148400-76148600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr11:76148400-76148600	Enhancers	Fetal Heart	heart
16	chr11:76148400-76148600	Enhancers	Right Ventricle	heart
17	chr11:76148400-76148600	Active TSS	Stomach Smooth Muscle	stomach
18	chr11:76148600-76151000	Weak transcription	K562	blood
19	chr11:76148600-76152800	Weak transcription	Fetal Heart	heart
20	chr11:76148600-76154000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr11:76148600-76154200	Weak transcription	Stomach Smooth Muscle	stomach
22	chr11:76148600-76154400	Weak transcription	Right Ventricle	heart
23	chr11:76149200-76150800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:76149200-76154400	Weak transcription	Spleen	Spleen
25	chr11:76149600-76152800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr11:76149600-76153600	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr11:76149600-76153800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr11:76149600-76154000	Weak transcription	Fetal Thymus	thymus
29	chr11:76150000-76154200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr11:76150000-76154400	Weak transcription	Fetal Muscle Leg	muscle
31	chr11:76150200-76152600	Weak transcription	NHEK	skin
32	chr11:76150400-76153200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr11:76150600-76152600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr11:76150800-76151000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr11:76150800-76153400	Weak transcription	HepG2	liver
36	chr11:76150800-76153800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:76150800-76153800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr11:76150800-76154400	Weak transcription	Fetal Kidney	kidney
39	chr11:76151000-76151200	ZNF genes & repeats	Brain Angular Gyrus	brain
40	chr11:76151000-76151600	Enhancers	K562	blood
41	chr11:76151000-76152600	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr11:76151000-76154000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:76151000-76154200	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr11:76151000-76154400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr11:76151200-76152000	Enhancers	Psoas Muscle	Psoas
46	chr11:76151200-76152800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr11:76151200-76154200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr11:76151200-76154200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr11:76151200-76154200	Weak transcription	Brain Angular Gyrus	brain
50	chr11:76151200-76154200	Weak transcription	HUVEC	blood vessel

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