Variant report

Variant	rs17459247
Chromosome Location	chr12:9959951-9959952
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12582047	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16907191	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17807354	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56053011	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56400313	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57144794	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57451228	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57483180	0.81[EUR][1000 genomes]
rs58848817	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58882780	0.82[ASN][1000 genomes]
rs61361909	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7137693	0.85[EUR][1000 genomes]
rs74062765	0.85[EUR][1000 genomes];0.98[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	esv3377937	chr12:9938734-9962518	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	3 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	chr12:9959600-9961000	Weak transcription	Skeletal Muscle Female	skeletal muscle

Quick Search:

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

what's new

Quick links