Variant report

Variant	esv3495436
Chromosome Location	chr11:4542646-4543868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:65 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538377853	chr11:4542803-4542804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7131138	chr11:4542813-4542814	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs190374124	chr11:4542832-4542833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571929181	chr11:4542834-4542835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80296763	chr11:4542836-4542837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529118325	chr11:4542848-4542849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10500605	chr11:4542852-4542853	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs557003755	chr11:4542854-4542855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147218618	chr11:4542954-4542955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs16907464	chr11:4543008-4543009	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs11032597	chr11:4543032-4543033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs56186485	chr11:4543045-4543046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546984932	chr11:4543046-4543047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182841143	chr11:4543079-4543080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11032598	chr11:4543123-4543124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557632018	chr11:4543126-4543127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569488444	chr11:4543131-4543132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199945040	chr11:4543173-4543174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs386750014	chr11:4543175-4543176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201144797	chr11:4543176-4543177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34860151	chr11:4543178-4543179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572572542	chr11:4543186-4543187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533656611	chr11:4543188-4543189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191174433	chr11:4543203-4543204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537094782	chr11:4543204-4543205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573278547	chr11:4543232-4543233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12285369	chr11:4543236-4543237	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs145440663	chr11:4543267-4543268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2566201	chr11:4543276-4543277	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs76218844	chr11:4543288-4543289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569391476	chr11:4543311-4543312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150202662	chr11:4543329-4543330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200699659	chr11:4543330-4543331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201395291	chr11:4543333-4543334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs67148073	chr11:4543334-4543335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200834967	chr11:4543336-4543337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527519980	chr11:4543408-4543409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs422310	chr11:4543415-4543416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547097397	chr11:4543440-4543441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555057614	chr11:4543486-4543487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573717069	chr11:4543491-4543492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74605647	chr11:4543514-4543515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77543635	chr11:4543516-4543517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs379420	chr11:4543542-4543543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs439436	chr11:4543545-4543546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2657150	chr11:4543561-4543562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540704988	chr11:4543565-4543566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539762814	chr11:4543568-4543569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2709133	chr11:4543586-4543587	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs34375820	chr11:4543594-4543595	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4542800-4544200	Enhancers	Primary T cells from cord blood	blood

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