Variant report

Variant	nsv976831
Chromosome Location	chr14:41503039-41514958
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180999885	chr14:41506615-41506616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185879741	chr14:41506649-41506650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113499595	chr14:41506667-41506668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72621037	chr14:41506671-41506672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373298986	chr14:41506674-41506675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570014325	chr14:41506693-41506694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs151226608	chr14:41506711-41506712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs3944805	chr14:41506767-41506768	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs555629118	chr14:41506878-41506879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147375468	chr14:41506879-41506880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140116331	chr14:41506904-41506905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189572016	chr14:41506936-41506937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563657999	chr14:41506956-41506957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368413913	chr14:41506957-41506958	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
early-passage human iPS cells	21368824	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41506600-41507000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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