Variant report

Variant	esv2760182
Chromosome Location	chr11:104922670-104931988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 372 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:372 , 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	rs562704	chr11:104922670-104922671	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533797847	chr11:104922701-104922702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185471505	chr11:104922712-104922713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78144702	chr11:104922715-104922716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs137869631	chr11:104922728-104922729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12276590	chr11:104922775-104922776	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs78278859	chr11:104922803-104922804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578537	chr11:104922809-104922810	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554674367	chr11:104922811-104922812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546059804	chr11:104922847-104922848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1699073	chr11:104922910-104922911	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs35995863	chr11:104922925-104922926	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs371094060	chr11:104923031-104923032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1785882	chr11:104923075-104923076	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs581153	chr11:104923086-104923087	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs188795270	chr11:104923156-104923157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192883737	chr11:104923249-104923250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531568940	chr11:104923255-104923256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548381360	chr11:104923305-104923306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561810636	chr11:104923308-104923309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527368922	chr11:104923309-104923310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547133381	chr11:104923321-104923322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79041817	chr11:104923336-104923337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74756131	chr11:104923338-104923339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377226048	chr11:104923340-104923341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570427690	chr11:104923348-104923349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539031052	chr11:104923349-104923350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370039076	chr11:104923350-104923351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569187584	chr11:104923358-104923359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568371263	chr11:104923521-104923522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538099166	chr11:104923551-104923552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554734089	chr11:104923563-104923564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185068135	chr11:104923616-104923617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534304112	chr11:104923624-104923625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78421830	chr11:104923688-104923689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115403243	chr11:104923699-104923700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532391	chr11:104923706-104923707	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs562797177	chr11:104923710-104923711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576401063	chr11:104923720-104923721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542083290	chr11:104923730-104923731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143739623	chr11:104923768-104923769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188356431	chr11:104923783-104923784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558435985	chr11:104923814-104923815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79399172	chr11:104923842-104923843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147205843	chr11:104923873-104923874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549365305	chr11:104923894-104923895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569251786	chr11:104923907-104923908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191309905	chr11:104923917-104923918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576411991	chr11:104923934-104923935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs508760	chr11:104923951-104923952	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	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
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104916800-104924400	Weak transcription	Left Ventricle	heart
2	chr11:104918200-104925200	Weak transcription	Ovary	ovary
3	chr11:104921400-104924600	Enhancers	HepG2	liver
4	chr11:104922200-104923400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:104923200-104923800	Enhancers	Dnd41	blood
6	chr11:104924400-104924600	Enhancers	Left Ventricle	heart
7	chr11:104924600-104927000	Weak transcription	HepG2	liver
8	chr11:104925600-104926400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr11:104926400-104931600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr11:104927000-104929200	Enhancers	HepG2	liver
11	chr11:104927000-104936200	Weak transcription	Small Intestine	intestine
12	chr11:104928400-104928800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr11:104929200-104930200	Weak transcription	HepG2	liver
14	chr11:104931000-104931200	Enhancers	HepG2	liver
15	chr11:104931000-104936800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr11:104931600-104936200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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