Variant report

Variant	esv3321717
Chromosome Location	chr11:24763126-24764224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:46 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532020905	chr11:24763169-24763170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551643198	chr11:24763180-24763181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190972885	chr11:24763258-24763259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537221343	chr11:24763276-24763277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386751694	chr11:24763291-24763292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551173508	chr11:24763406-24763407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567615624	chr11:24763409-24763410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536749496	chr11:24763419-24763420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553553217	chr11:24763454-24763455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567268846	chr11:24763457-24763458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370844798	chr11:24763477-24763478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369193685	chr11:24763482-24763483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372253475	chr11:24763483-24763484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34363741	chr11:24763487-24763488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11028132	chr11:24763492-24763493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11028133	chr11:24763495-24763496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs58792905	chr11:24763503-24763504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148866942	chr11:24763509-24763510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71476399	chr11:24763514-24763515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34122699	chr11:24763519-24763520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35187842	chr11:24763530-24763531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558549353	chr11:24763559-24763560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11500134	chr11:24763566-24763567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575515536	chr11:24763580-24763581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544042559	chr11:24763598-24763599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571183533	chr11:24763603-24763604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376235702	chr11:24763604-24763605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561145676	chr11:24763687-24763688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547218240	chr11:24763688-24763689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539936385	chr11:24763693-24763694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571257530	chr11:24763717-24763718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113700487	chr11:24763809-24763810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78693923	chr11:24763848-24763849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559851359	chr11:24763870-24763871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531959309	chr11:24763871-24763872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113281049	chr11:24763880-24763881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191410953	chr11:24763946-24763947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79348222	chr11:24763954-24763955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183121459	chr11:24763957-24763958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550850927	chr11:24763969-24763970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567859734	chr11:24764001-24764002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530356035	chr11:24764027-24764028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547097420	chr11:24764037-24764038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186742603	chr11:24764039-24764040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191302412	chr11:24764091-24764092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182376660	chr11:24764156-24764157	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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