Variant report

Variant	nsv597023
Chromosome Location	chr5:7917737-7920322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:7918663-7918695	GM12878	blood:	n/a	n/a
2	CEBPB	chr5:7917486-7917794	Hela-S3	cervix:	n/a	chr5:7917640-7917651
3	CEBPB	chr5:7917463-7917820	IMR90	lung:	n/a	chr5:7917640-7917651
4	CEBPB	chr5:7917518-7917789	A549	lung:	n/a	chr5:7917640-7917651
5	CEBPB	chr5:7917491-7917819	K562	blood:	n/a	chr5:7917640-7917651
6	CEBPB	chr5:7917466-7917815	HepG2	liver:	n/a	chr5:7917640-7917651
7	EP300	chr5:7918006-7918047	K562	blood:	n/a	n/a
8	FOXA2	chr5:7920040-7920268	A549	lung:	n/a	n/a
9	IRF1	chr5:7918658-7918797	K562	blood:	n/a	n/a
10	MAFF	chr5:7917902-7918187	HepG2	liver:	n/a	chr5:7917995-7918013 chr5:7918033-7918051
11	MAFF	chr5:7917890-7918184	K562	blood:	n/a	chr5:7917995-7918013 chr5:7918033-7918051
12	MAFK	chr5:7917984-7918089	K562	blood:	n/a	chr5:7918035-7918050
13	MAFK	chr5:7917905-7918186	HepG2	liver:	n/a	chr5:7918035-7918050
14	MAFK	chr5:7917863-7918214	IMR90	lung:	n/a	chr5:7918035-7918050
15	MAFK	chr5:7917898-7918155	HepG2	liver:	n/a	chr5:7918035-7918050
16	RCOR1	chr5:7917834-7917961	K562	blood:	n/a	n/a
17	WRNIP1	chr5:7919207-7919210	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:7913593..7916151-chr5:7918931..7921579,2	K562	blood:
2	chr5:7908992..7910576-chr5:7919203..7920908,2	K562	blood:

Variant related genes	Relation type
ENSG00000251168	TF binding region

Extended variants
information (count: 18 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530854375	chr5:7917737-7917738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76231165	chr5:7917739-7917740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145532675	chr5:7917741-7917742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147807567	chr5:7917767-7917768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141197386	chr5:7917781-7917782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567081157	chr5:7917813-7917814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187759577	chr5:7917836-7917837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192463357	chr5:7917839-7917840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540424280	chr5:7917882-7917883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs162273	chr5:7917934-7917935	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs28829123	chr5:7917953-7917954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148099112	chr5:7917989-7917990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374983505	chr5:7920044-7920045	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs557748709	chr5:7920077-7920078	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs562895254	chr5:7920214-7920215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186061911	chr5:7920247-7920248	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545366538	chr5:7920248-7920249	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs191344144	chr5:7920255-7920256	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
early-passage human iPS cells	21368824	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:7917600-7918000	Enhancers	Rectal Mucosa Donor 31	rectum

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