Variant report

Variant	rs62512266
Chromosome Location	chr8:59159796-59159797
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10098212	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10435589	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11990667	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17198545	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4237026	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4601298	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs56395012	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56885504	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9297986	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9297987	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9643503	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59147400-59161000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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