Variant report

Variant	nsv85151
Chromosome Location	chr14:84858000-84860441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2816007	chr14:84858000-84858001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529401875	chr14:84858054-84858055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144605485	chr14:84858070-84858071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs151238453	chr14:84858076-84858077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558182474	chr14:84858095-84858096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540028011	chr14:84858103-84858104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576548157	chr14:84858131-84858132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558028418	chr14:84858229-84858230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76052737	chr14:84858347-84858348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567187916	chr14:84858412-84858413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534469378	chr14:84858422-84858423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs8016103	chr14:84858426-84858427	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs138648198	chr14:84858503-84858504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537587081	chr14:84858558-84858559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556224637	chr14:84858561-84858562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74069923	chr14:84858590-84858591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148873991	chr14:84858684-84858685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559886414	chr14:84858685-84858686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572037215	chr14:84858700-84858701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542496099	chr14:84858751-84858752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555835844	chr14:84858779-84858780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529287392	chr14:84858834-84858835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371160146	chr14:84858890-84858891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs8017425	chr14:84858900-84858901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs541234643	chr14:84858955-84858956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117169722	chr14:84858969-84858970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533236510	chr14:84859028-84859029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145502835	chr14:84859046-84859047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180670986	chr14:84859049-84859050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71418956	chr14:84859053-84859054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116301650	chr14:84859096-84859097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549691070	chr14:84859121-84859122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567814327	chr14:84859175-84859176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537854107	chr14:84859189-84859190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534015473	chr14:84859193-84859194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559316857	chr14:84859201-84859202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577688319	chr14:84859217-84859218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538333119	chr14:84859263-84859264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577492139	chr14:84859325-84859326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186061986	chr14:84859346-84859347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs118086263	chr14:84859367-84859368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542559407	chr14:84859394-84859395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560853380	chr14:84859405-84859406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs137924379	chr14:84859457-84859458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544611388	chr14:84859481-84859482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562713455	chr14:84859547-84859548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190937099	chr14:84859560-84859561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551890836	chr14:84859569-84859570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182303464	chr14:84859573-84859574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142492084	chr14:84859594-84859595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84856400-84864400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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