Variant report

Variant	esv2635496
Chromosome Location	chr11:104596829-104598338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:50 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571954857	chr11:104596833-104596834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1147022	chr11:104596896-104596897	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs550889394	chr11:104596898-104596899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375149657	chr11:104596928-104596929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567799550	chr11:104596946-104596947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536454691	chr11:104596979-104596980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553400484	chr11:104597011-104597012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566648220	chr11:104597016-104597017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187861005	chr11:104597078-104597079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558562981	chr11:104597083-104597084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575178562	chr11:104597108-104597109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535273808	chr11:104597109-104597110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552939947	chr11:104597152-104597153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574538954	chr11:104597187-104597188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540075273	chr11:104597190-104597191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560267859	chr11:104597195-104597196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112089424	chr11:104597213-104597214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532279445	chr11:104597221-104597222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs193130554	chr11:104597264-104597265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140615638	chr11:104597279-104597280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562512179	chr11:104597315-104597316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563953623	chr11:104597338-104597339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558525508	chr11:104597623-104597624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377227855	chr11:104597634-104597635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537863032	chr11:104597662-104597663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115895705	chr11:104597739-104597740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185636780	chr11:104597757-104597758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535413309	chr11:104597771-104597772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552193262	chr11:104597782-104597783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144226231	chr11:104597810-104597811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1147023	chr11:104597823-104597824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545578004	chr11:104597845-104597846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187583253	chr11:104597990-104597991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545864604	chr11:104598015-104598016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191955387	chr11:104598034-104598035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184201424	chr11:104598047-104598048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541931173	chr11:104598049-104598050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201161455	chr11:104598061-104598062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571399201	chr11:104598072-104598073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141574657	chr11:104598081-104598082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561606861	chr11:104598099-104598100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150878859	chr11:104598108-104598109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368495616	chr11:104598120-104598121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs61078356	chr11:104598160-104598161	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs560361736	chr11:104598179-104598180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532571428	chr11:104598212-104598213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552214550	chr11:104598220-104598221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373850441	chr11:104598254-104598255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140044944	chr11:104598312-104598313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188828621	chr11:104598323-104598324	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	23813976	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104595600-104597000	Enhancers	HUVEC	blood vessel
2	chr11:104596600-104597400	Enhancers	Hela-S3	cervix
3	chr11:104597600-104599000	Enhancers	Dnd41	blood

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