Variant report

Variant	esv3369868
Chromosome Location	chr11:85176604-85179402
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 152 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:152 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571074297	chr11:85176618-85176619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149265995	chr11:85176621-85176622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12288531	chr11:85176632-85176633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547216564	chr11:85176635-85176636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565420121	chr11:85176665-85176666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184542391	chr11:85176678-85176679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554503667	chr11:85176730-85176731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573490285	chr11:85176784-85176785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538498614	chr11:85176789-85176790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556920626	chr11:85176799-85176800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61907126	chr11:85176811-85176812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs578257450	chr11:85176812-85176813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544047323	chr11:85176827-85176828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554444713	chr11:85176854-85176855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs286517	chr11:85176864-85176865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542755052	chr11:85176889-85176890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561292634	chr11:85176919-85176920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200842751	chr11:85177011-85177012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543284900	chr11:85177039-85177040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372522135	chr11:85177050-85177051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564814804	chr11:85177059-85177060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544952722	chr11:85177094-85177095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532305768	chr11:85177105-85177106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547187803	chr11:85177113-85177114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs286518	chr11:85177135-85177136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557877965	chr11:85177201-85177202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116570632	chr11:85177231-85177232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192612728	chr11:85177251-85177252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569608355	chr11:85177267-85177268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184523344	chr11:85177268-85177269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2457419	chr11:85177273-85177274	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs571963274	chr11:85177305-85177306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111463131	chr11:85177321-85177322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200891107	chr11:85177331-85177332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539385350	chr11:85177351-85177352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554356920	chr11:85177417-85177418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189233067	chr11:85177420-85177421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182014894	chr11:85177421-85177422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554786121	chr11:85177430-85177431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576507638	chr11:85177461-85177462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372016877	chr11:85177466-85177467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564978692	chr11:85177475-85177476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576679544	chr11:85177488-85177489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540936438	chr11:85177491-85177492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548816571	chr11:85177560-85177561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141535152	chr11:85177568-85177569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186168690	chr11:85177593-85177594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189902898	chr11:85177596-85177597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563224284	chr11:85177629-85177630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180800783	chr11:85177641-85177642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	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
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85171400-85182800	Weak transcription	Ovary	ovary

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