Variant report

Variant	rs12137096
Chromosome Location	chr1:159195512-159195513
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10489848	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10908703	0.82[ASN][1000 genomes]
rs11265146	0.97[EUR][1000 genomes]
rs11265154	0.91[ASN][1000 genomes]
rs11265155	0.91[ASN][1000 genomes]
rs11265159	0.84[ASN][1000 genomes]
rs12083313	0.84[ASN][1000 genomes]
rs12084987	0.92[ASN][1000 genomes]
rs12097396	0.84[ASN][1000 genomes]
rs12561917	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16841957	0.84[ASN][1000 genomes]
rs2325914	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3027051	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3027074	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3027075	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3027077	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34497749	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34757892	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35014997	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35262301	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4083420	0.92[ASN][1000 genomes]
rs4498802	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56697178	0.84[ASN][1000 genomes]
rs60861070	0.84[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159193000-159199200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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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

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