Variant report

Variant	esv3310374
Chromosome Location	chr14:35372181-35372530
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:35370120..35372275-chr14:35372286..35374430,3	K562	blood:
2	chr14:35342338..35344567-chr14:35370175..35372509,2	MCF-7	breast:
3	chr14:35370120..35372275-chr14:35372286..35374430,3	K562	blood:

Variant related genes	Relation type
ENSG00000198604	chromatin interactions
ENSG00000258738	chromatin interactions

Extended variants
information (count: 15 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527957879	chr14:35372210-35372211	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs143927565	chr14:35372235-35372236	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs192905790	chr14:35372263-35372264	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs549703478	chr14:35372275-35372276	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs530367753	chr14:35372276-35372277	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549054246	chr14:35372284-35372285	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs183630783	chr14:35372336-35372337	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs144298630	chr14:35372338-35372339	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551371470	chr14:35372364-35372365	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs573425190	chr14:35372394-35372395	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371982368	chr14:35372397-35372398	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs148708647	chr14:35372450-35372451	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs187983752	chr14:35372465-35372466	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141421440	chr14:35372467-35372468	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs112026560	chr14:35372508-35372509	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Acute lymphoblastic leukemia	20067559	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
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:0 , 50 per page) page:

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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