Variant report

Variant	esv3355470
Chromosome Location	chr11:36696476-36700674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 170 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:170 , 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	rs566587091	chr11:36696485-36696486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528838567	chr11:36696486-36696487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150637108	chr11:36696499-36696500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569131638	chr11:36696503-36696504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572456459	chr11:36696540-36696541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537793546	chr11:36696657-36696658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557514654	chr11:36696658-36696659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571137071	chr11:36696673-36696674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140061302	chr11:36696686-36696687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553018816	chr11:36696737-36696738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573268274	chr11:36696773-36696774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542162253	chr11:36696780-36696781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555517195	chr11:36696825-36696826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373244275	chr11:36696865-36696866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143801145	chr11:36696918-36696919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564791371	chr11:36696946-36696947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187060924	chr11:36696964-36696965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540836935	chr11:36696985-36696986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553355086	chr11:36697008-36697009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12790889	chr11:36697014-36697015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560145755	chr11:36697048-36697049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578181485	chr11:36697081-36697082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545426537	chr11:36697087-36697088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548955163	chr11:36697148-36697149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563865891	chr11:36697174-36697175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531612991	chr11:36697204-36697205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551236142	chr11:36697205-36697206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575922463	chr11:36697225-36697226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571226396	chr11:36697261-36697262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533700294	chr11:36697281-36697282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543097050	chr11:36697292-36697293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191487388	chr11:36697296-36697297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371439355	chr11:36697313-36697314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566944776	chr11:36697328-36697329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371436111	chr11:36697341-36697342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12272732	chr11:36697345-36697346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555708349	chr11:36697372-36697373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530956405	chr11:36697393-36697394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575519363	chr11:36697405-36697406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571656953	chr11:36697412-36697413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540607393	chr11:36697535-36697536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558451401	chr11:36697551-36697552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578250553	chr11:36697590-36697591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565161572	chr11:36697618-36697619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189064039	chr11:36697620-36697621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560564742	chr11:36697640-36697641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573666036	chr11:36697651-36697652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542386517	chr11:36697676-36697677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562624924	chr11:36697710-36697711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531175941	chr11:36697788-36697789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
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
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
WAGR syndrome	19222835	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	21829676	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Bipolar disorder	19114987	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36696000-36701200	Weak transcription	Dnd41	blood

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