Variant report

Variant	esv3351163
Chromosome Location	chr11:32785476-32788174
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 136 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:136 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370682899	chr11:32785479-32785480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546966458	chr11:32785488-32785489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373827992	chr11:32785493-32785494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571559268	chr11:32785569-32785570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566026827	chr11:32785588-32785589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533599023	chr11:32785590-32785591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7117035	chr11:32785591-32785592	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs567286904	chr11:32785594-32785595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543510807	chr11:32785607-32785608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532409725	chr11:32785623-32785624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192573098	chr11:32785680-32785681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150110934	chr11:32785681-32785682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138742808	chr11:32785683-32785684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538825304	chr11:32785707-32785708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185452778	chr11:32785731-32785732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572348634	chr11:32785769-32785770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189584286	chr11:32785787-32785788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180818147	chr11:32785816-32785817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185058812	chr11:32785827-32785828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200981140	chr11:32785828-32785829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142779184	chr11:32785839-32785840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563550271	chr11:32785860-32785861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532609439	chr11:32785907-32785908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552349712	chr11:32785908-32785909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559650855	chr11:32785909-32785910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4568981	chr11:32785913-32785914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138149627	chr11:32785914-32785915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143726908	chr11:32785916-32785917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373789610	chr11:32785976-32785977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189573455	chr11:32786018-32786019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549941118	chr11:32786059-32786060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144172990	chr11:32786102-32786103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181053861	chr11:32786107-32786108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558769302	chr11:32786155-32786156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148503855	chr11:32786156-32786157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567581937	chr11:32786168-32786169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534889210	chr11:32786188-32786189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554667550	chr11:32786225-32786226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574736882	chr11:32786234-32786235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543443914	chr11:32786245-32786246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142813248	chr11:32786264-32786265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185927415	chr11:32786289-32786290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188822977	chr11:32786304-32786305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372261458	chr11:32786317-32786318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181968063	chr11:32786322-32786323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187134829	chr11:32786331-32786332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375324050	chr11:32786339-32786340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528806715	chr11:32786379-32786380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548818233	chr11:32786381-32786382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150633827	chr11:32786393-32786394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
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
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
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32777800-32790200	Weak transcription	Liver	Liver

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