Variant report

Variant	esv3327149
Chromosome Location	chr11:84487054-84490352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 133 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532342108	chr11:84487115-84487116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547264457	chr11:84487160-84487161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562800272	chr11:84487166-84487167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191778379	chr11:84487175-84487176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544800357	chr11:84487200-84487201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559943313	chr11:84487204-84487205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145957567	chr11:84487223-84487224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184099564	chr11:84487260-84487261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567571140	chr11:84487274-84487275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188099522	chr11:84487286-84487287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545318580	chr11:84487298-84487299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139376389	chr11:84487380-84487381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555571335	chr11:84487547-84487548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558690936	chr11:84487550-84487551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538769549	chr11:84487573-84487574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558370069	chr11:84487581-84487582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567475280	chr11:84487594-84487595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567038487	chr11:84487603-84487604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534419098	chr11:84487608-84487609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555737593	chr11:84487616-84487617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574284492	chr11:84487617-84487618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537842991	chr11:84487618-84487619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556568397	chr11:84487652-84487653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540864623	chr11:84487779-84487780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192800186	chr11:84487814-84487815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185552495	chr11:84487816-84487817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560229002	chr11:84487869-84487870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571879698	chr11:84487875-84487876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542414140	chr11:84487882-84487883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78110190	chr11:84487883-84487884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531670479	chr11:84487935-84487936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75950700	chr11:84487968-84487969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549506310	chr11:84487980-84487981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77788350	chr11:84488028-84488029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532161713	chr11:84488035-84488036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138781817	chr11:84488102-84488103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565785540	chr11:84488105-84488106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368642471	chr11:84488141-84488142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79618763	chr11:84488145-84488146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549595070	chr11:84488183-84488184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567861528	chr11:84488186-84488187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538557996	chr11:84488206-84488207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556266553	chr11:84488224-84488225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577581232	chr11:84488231-84488232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538668751	chr11:84488289-84488290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140207742	chr11:84488293-84488294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs386374368	chr11:84488294-84488295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74724009	chr11:84488295-84488296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200274060	chr11:84488297-84488298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201121661	chr11:84488298-84488299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Cancer	20164920	CNVD
Obesity	20622171	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21147756	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	17142309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84484400-84492000	Weak transcription	Fetal Brain Male	brain

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