Variant report

Variant	esv3339762
Chromosome Location	chr11:24762576-24764724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:87 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2631427	chr11:24762577-24762578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188261416	chr11:24762627-24762628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs17307110	chr11:24762675-24762676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181829861	chr11:24762680-24762681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377308532	chr11:24762774-24762775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117033121	chr11:24762807-24762808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573130459	chr11:24762819-24762820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140637593	chr11:24762841-24762842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567585072	chr11:24762881-24762882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372233685	chr11:24762918-24762919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145667823	chr11:24762924-24762925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575328736	chr11:24762929-24762930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138682591	chr11:24762937-24762938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528089379	chr11:24762961-24762962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115984519	chr11:24762965-24762966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529753697	chr11:24762991-24762992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546147954	chr11:24763047-24763048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186117341	chr11:24763065-24763066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560402256	chr11:24763106-24763107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532020905	chr11:24763169-24763170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551643198	chr11:24763180-24763181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190972885	chr11:24763258-24763259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537221343	chr11:24763276-24763277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs386751694	chr11:24763291-24763292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551173508	chr11:24763406-24763407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567615624	chr11:24763409-24763410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536749496	chr11:24763419-24763420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553553217	chr11:24763454-24763455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567268846	chr11:24763457-24763458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370844798	chr11:24763477-24763478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369193685	chr11:24763482-24763483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372253475	chr11:24763483-24763484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34363741	chr11:24763487-24763488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11028132	chr11:24763492-24763493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11028133	chr11:24763495-24763496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs58792905	chr11:24763503-24763504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148866942	chr11:24763509-24763510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71476399	chr11:24763514-24763515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34122699	chr11:24763519-24763520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35187842	chr11:24763530-24763531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs558549353	chr11:24763559-24763560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11500134	chr11:24763566-24763567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575515536	chr11:24763580-24763581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544042559	chr11:24763598-24763599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571183533	chr11:24763603-24763604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376235702	chr11:24763604-24763605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561145676	chr11:24763687-24763688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547218240	chr11:24763688-24763689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539936385	chr11:24763693-24763694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571257530	chr11:24763717-24763718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24761200-24768400	Weak transcription	Dnd41	blood

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