Variant report

Variant	rs919658
Chromosome Location	chr8:129835008-129835009
allele	C/T
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:10)

rs_ID	r²[population]
rs1879162	0.96[EUR][1000 genomes]
rs2090682	0.93[EUR][1000 genomes]
rs35208579	0.93[EUR][1000 genomes]
rs3857887	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4733651	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4733660	0.86[EUR][1000 genomes]
rs6470664	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6994324	0.97[EUR][1000 genomes]
rs7001039	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7463635	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129825400-129836800	Weak transcription	Dnd41	blood

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