Variant report

Variant	esv3391597
Chromosome Location	chr11:36695876-36699074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 137 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:137 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550337921	chr11:36695985-36695986	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs111384039	chr11:36695997-36695998	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs2101987	chr11:36695998-36695999	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs542539631	chr11:36696054-36696055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183851013	chr11:36696056-36696057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531101185	chr11:36696057-36696058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113768510	chr11:36696092-36696093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564081180	chr11:36696095-36696096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188346592	chr11:36696096-36696097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191892153	chr11:36696172-36696173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566502071	chr11:36696206-36696207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535126014	chr11:36696231-36696232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555601390	chr11:36696277-36696278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2088511	chr11:36696286-36696287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs182598173	chr11:36696319-36696320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557579625	chr11:36696320-36696321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576917487	chr11:36696381-36696382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545928330	chr11:36696393-36696394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552930858	chr11:36696398-36696399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573166526	chr11:36696408-36696409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541875293	chr11:36696415-36696416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562368685	chr11:36696432-36696433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148507535	chr11:36696438-36696439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544808350	chr11:36696441-36696442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533035578	chr11:36696448-36696449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546689330	chr11:36696460-36696461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566587091	chr11:36696485-36696486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528838567	chr11:36696486-36696487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150637108	chr11:36696499-36696500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569131638	chr11:36696503-36696504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572456459	chr11:36696540-36696541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537793546	chr11:36696657-36696658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557514654	chr11:36696658-36696659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571137071	chr11:36696673-36696674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140061302	chr11:36696686-36696687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553018816	chr11:36696737-36696738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573268274	chr11:36696773-36696774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542162253	chr11:36696780-36696781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555517195	chr11:36696825-36696826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373244275	chr11:36696865-36696866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143801145	chr11:36696918-36696919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564791371	chr11:36696946-36696947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187060924	chr11:36696964-36696965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540836935	chr11:36696985-36696986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553355086	chr11:36697008-36697009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12790889	chr11:36697014-36697015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560145755	chr11:36697048-36697049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs578181485	chr11:36697081-36697082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545426537	chr11:36697087-36697088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548955163	chr11:36697148-36697149	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36694400-36696000	ZNF genes & repeats	Dnd41	blood
2	chr11:36696000-36701200	Weak transcription	Dnd41	blood

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