Variant report

Variant	rs62450279
Chromosome Location	chr6:19499416-19499417
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10950558	0.82[ASN][1000 genomes]
rs11525792	0.81[ASN][1000 genomes]
rs11982393	0.82[ASN][1000 genomes]
rs12234378	0.84[ASN][1000 genomes]
rs59438117	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62450274	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62450291	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62450300	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62450301	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:19493600-19501600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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