Variant report

Variant	nsv564532
Chromosome Location	chr14:41632386-41673195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 60 )

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	rs559441516	chr14:41640230-41640231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192279235	chr14:41640256-41640257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185074085	chr14:41640377-41640378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4143953	chr14:41640389-41640390	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs531159172	chr14:41640459-41640460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74799280	chr14:41640468-41640469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561610107	chr14:41640506-41640507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs56732083	chr14:41640509-41640510	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs547422829	chr14:41640517-41640518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545568763	chr14:41640538-41640539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs56804622	chr14:41640568-41640569	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs74045318	chr14:41640573-41640574	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs187903377	chr14:41640610-41640611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543091861	chr14:41640626-41640627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77634801	chr14:41640707-41640708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148447981	chr14:41669608-41669609	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs529842886	chr14:41669624-41669625	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs547664670	chr14:41669645-41669646	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs77101571	chr14:41669696-41669697	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs536217153	chr14:41669728-41669729	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs74803015	chr14:41669730-41669731	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs527448952	chr14:41669748-41669749	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs552454997	chr14:41669755-41669756	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs369923900	chr14:41669767-41669768	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs147630406	chr14:41669769-41669770	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs188703517	chr14:41669791-41669792	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs116869753	chr14:41669797-41669798	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs183485592	chr14:41673026-41673027	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs528692099	chr14:41673031-41673032	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs547146192	chr14:41673110-41673111	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs115050914	chr14:41673128-41673129	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs187268069	chr14:41673141-41673142	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs550855354	chr14:41673170-41673171	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs17111545	chr14:41673195-41673196	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Bipolar disorder	19114987	CNVD

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41640200-41640600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:41640200-41640800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr14:41669600-41669800	Bivalent Enhancer	Left Ventricle	heart
4	chr14:41673000-41673200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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