Variant report

Variant	esv3466208
Chromosome Location	chr11:106785822-106789811
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 126 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:126 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141121993	chr11:106785830-106785831	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs555144215	chr11:106785882-106785883	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs374534678	chr11:106785890-106785891	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs111628949	chr11:106785897-106785898	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs185143025	chr11:106785900-106785901	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs188807675	chr11:106785912-106785913	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs78139100	chr11:106785913-106785914	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs35968189	chr11:106785930-106785931	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs367953032	chr11:106785974-106785975	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs372542933	chr11:106785977-106785978	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs558068818	chr11:106785991-106785992	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs557499644	chr11:106786009-106786010	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs146939995	chr11:106786035-106786036	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs546434545	chr11:106786056-106786057	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs558029697	chr11:106786081-106786082	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs566965662	chr11:106786086-106786087	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs137964681	chr11:106786113-106786114	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs376311713	chr11:106786128-106786129	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs368693765	chr11:106786239-106786240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10458950	chr11:106786273-106786274	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs113193694	chr11:106786303-106786304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7118277	chr11:106786319-106786320	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs563457543	chr11:106786369-106786370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149064877	chr11:106786374-106786375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7102373	chr11:106786428-106786429	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs528428190	chr11:106786459-106786460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10458951	chr11:106786481-106786482	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs75376773	chr11:106786686-106786687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142281325	chr11:106786700-106786701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs397939148	chr11:106786710-106786711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34656401	chr11:106786727-106786728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375007989	chr11:106786732-106786733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568082754	chr11:106786858-106786859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535496993	chr11:106786892-106786893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192373224	chr11:106786902-106786903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569970244	chr11:106786924-106786925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184786903	chr11:106786975-106786976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10890623	chr11:106787011-106787012	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573180097	chr11:106787113-106787114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540548578	chr11:106787124-106787125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577895456	chr11:106787130-106787131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61902987	chr11:106787135-106787136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573960353	chr11:106787140-106787141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180880451	chr11:106787149-106787150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183766174	chr11:106787201-106787202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562838686	chr11:106787257-106787258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189560942	chr11:106787273-106787274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546003547	chr11:106787278-106787279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4754174	chr11:106787288-106787289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs376086504	chr11:106787295-106787296	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
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
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
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106785800-106786200	ZNF genes & repeats	Fetal Lung	lung
2	chr11:106786200-106806800	Weak transcription	Fetal Lung	lung
3	chr11:106786600-106787200	Enhancers	Fetal Heart	heart

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