Variant report

Variant	rs7469799
Chromosome Location	chr9:110453037-110453038
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10117620	0.82[ASN][1000 genomes]
rs10123702	0.83[ASN][1000 genomes]
rs10123747	0.80[ASN][1000 genomes]
rs10759253	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10759254	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10816554	0.82[AMR][1000 genomes]
rs10816556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10816557	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10816558	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10978991	0.82[AMR][1000 genomes]
rs10978992	1.00[AFR][1000 genomes]
rs10978995	0.82[AMR][1000 genomes]
rs10979002	0.82[AMR][1000 genomes]
rs11788158	0.82[AMR][1000 genomes]
rs60173602	0.82[AMR][1000 genomes]
rs7023431	0.83[EUR][1000 genomes]
rs7047394	1.00[AFR][1000 genomes]
rs869374	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831683	chr9:110275212-110461288	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv1808541	chr9:110444938-110488612	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110448600-110453200	Weak transcription	Right Atrium	heart
2	chr9:110452200-110453600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr9:110452200-110456800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr9:110452800-110455600	Weak transcription	NHDF-Ad	bronchial
5	chr9:110453000-110454000	Enhancers	Fetal Muscle Leg	muscle

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Input of quick search could be:

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

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