Variant report

Variant	rs8008951
Chromosome Location	chr14:42455061-42455062
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17112459	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56987246	1.00[ASN][1000 genomes]
rs58876760	1.00[ASN][1000 genomes]
rs6572122	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6572123	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7158008	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73312622	1.00[ASN][1000 genomes]
rs8006773	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8009428	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901740	chr14:42386859-42477256	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42454000-42455200	Weak transcription	Primary B cells from cord blood	blood

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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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