Variant report

Variant	esv1277327
Chromosome Location	chr11:101566116-101574614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 177 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:177 , 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	rs28583613	chr11:101566137-101566138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530479766	chr11:101566151-101566152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533224762	chr11:101566154-101566155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547038810	chr11:101566210-101566211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199961300	chr11:101566367-101566368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368455433	chr11:101566564-101566565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112720926	chr11:101566594-101566595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377133502	chr11:101566595-101566596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368232566	chr11:101566605-101566606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61918165	chr11:101566616-101566617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376082955	chr11:101566650-101566651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs202141747	chr11:101566709-101566710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112108689	chr11:101566720-101566721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369013449	chr11:101566850-101566851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112057414	chr11:101567208-101567209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185438199	chr11:101567284-101567285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61918166	chr11:101567300-101567301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111539636	chr11:101567319-101567320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375927962	chr11:101567469-101567470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189566618	chr11:101567479-101567480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs61918167	chr11:101567548-101567549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs61918168	chr11:101567665-101567666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61918169	chr11:101567770-101567771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112669483	chr11:101567997-101567998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112370985	chr11:101568014-101568015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200940873	chr11:101568475-101568476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202049043	chr11:101568495-101568496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200344148	chr11:101568497-101568498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201589458	chr11:101568518-101568519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547258143	chr11:101568578-101568579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs202217240	chr11:101568689-101568690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200271152	chr11:101568711-101568712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201047468	chr11:101568725-101568726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199814454	chr11:101568744-101568745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200589567	chr11:101568776-101568777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566983390	chr11:101569098-101569099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539258833	chr11:101569119-101569120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61918170	chr11:101569125-101569126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369743060	chr11:101569194-101569195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9736345	chr11:101569255-101569256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9734496	chr11:101569312-101569313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201139109	chr11:101569345-101569346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368230435	chr11:101569346-101569347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201665696	chr11:101569347-101569348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9734504	chr11:101569354-101569355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199621814	chr11:101569375-101569376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376286871	chr11:101569400-101569401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61918173	chr11:101569403-101569404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9736358	chr11:101569450-101569451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552770630	chr11:101569460-101569461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Cancer	20164920	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101561600-101568400	Weak transcription	Ovary	ovary
2	chr11:101564800-101578400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links