Variant report

Variant	esv2104024
Chromosome Location	chr11:101370357-101370888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567847250	chr11:101370357-101370358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375668565	chr11:101370371-101370372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188305754	chr11:101370380-101370381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536876725	chr11:101370381-101370382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546388601	chr11:101370382-101370383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553262481	chr11:101370383-101370384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112936118	chr11:101370395-101370396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192457647	chr11:101370400-101370401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566967166	chr11:101370407-101370408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373577890	chr11:101370408-101370409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530350212	chr11:101370459-101370460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573328647	chr11:101370481-101370482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199579795	chr11:101370482-101370483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71462687	chr11:101370486-101370487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372490699	chr11:101370493-101370494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78877244	chr11:101370511-101370512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530930285	chr11:101370524-101370525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142857713	chr11:101370539-101370540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563226983	chr11:101370552-101370553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146581231	chr11:101370567-101370568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141314382	chr11:101370595-101370596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146059429	chr11:101370607-101370608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200570280	chr11:101370616-101370617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183841776	chr11:101370621-101370622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375203260	chr11:101370639-101370640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71462689	chr11:101370647-101370648	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs144962159	chr11:101370673-101370674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs71056614	chr11:101370684-101370685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71462690	chr11:101370699-101370700	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs199873258	chr11:101370710-101370711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368144700	chr11:101370717-101370718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140598662	chr11:101370727-101370728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71056615	chr11:101370734-101370735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557705665	chr11:101370735-101370736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559546608	chr11:101370739-101370740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191497626	chr11:101370749-101370750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150485403	chr11:101370750-101370751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183689433	chr11:101370753-101370754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71056616	chr11:101370764-101370765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371401564	chr11:101370765-101370766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201241103	chr11:101370773-101370774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11224794	chr11:101370785-101370786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71462691	chr11:101370786-101370787	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs28501622	chr11:101370794-101370795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368838540	chr11:101370796-101370797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375866669	chr11:101370797-101370798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11224795	chr11:101370798-101370799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28377128	chr11:101370809-101370810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71056617	chr11:101370810-101370811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11224796	chr11:101370811-101370812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	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
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal cancer	21851588	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101350000-101384800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:101359000-101372200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:101362400-101373400	Weak transcription	Fetal Lung	lung
4	chr11:101368400-101374800	Weak transcription	Aorta	Aorta
5	chr11:101368600-101372200	Weak transcription	Ovary	ovary
6	chr11:101370000-101371600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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