Variant report

Variant	esv1941814
Chromosome Location	chr9:11432954-11433609
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145547442	chr9:11432957-11432958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575969615	chr9:11432987-11432988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185183206	chr9:11433016-11433017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561263172	chr9:11433027-11433028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188951192	chr9:11433036-11433037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540358432	chr9:11433087-11433088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2890945	chr9:11433121-11433122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2890946	chr9:11433122-11433123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2890947	chr9:11433123-11433124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2890948	chr9:11433124-11433125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2890949	chr9:11433125-11433126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2382291	chr9:11433126-11433127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2890950	chr9:11433128-11433129	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs2890951	chr9:11433129-11433130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183822240	chr9:11433234-11433235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188097117	chr9:11433244-11433245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571216473	chr9:11433275-11433276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181345885	chr9:11433276-11433277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550204972	chr9:11433291-11433292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149170692	chr9:11433344-11433345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536380344	chr9:11433352-11433353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377022877	chr9:11433374-11433375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10959799	chr9:11433421-11433422	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7854701	chr9:11433428-11433429	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138084001	chr9:11433435-11433436	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs373051301	chr9:11433446-11433447	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs116333490	chr9:11433452-11433453	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs367840070	chr9:11433457-11433458	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs184028623	chr9:11433463-11433464	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs544898833	chr9:11433498-11433499	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs138857806	chr9:11433561-11433562	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs574758797	chr9:11433593-11433594	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs140553068	chr9:11433594-11433595	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs562382980	chr9:11433601-11433602	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
Barrett''s syndrome	19417022	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11432400-11434200	Enhancers	Fetal Heart	heart
2	chr9:11433400-11433800	Active TSS	Right Atrium	heart

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