Variant report

Variant	rs2582662
Chromosome Location	chr5:16272637-16272638
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10056479	0.85[EUR][1000 genomes]
rs10075110	0.83[EUR][1000 genomes]
rs10079067	0.83[EUR][1000 genomes]
rs1561632	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2402099	0.82[JPT][hapmap]
rs2402237	0.85[EUR][1000 genomes]
rs2582679	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4701652	0.83[EUR][1000 genomes]
rs4701653	0.83[EUR][1000 genomes]
rs6866941	0.83[EUR][1000 genomes]
rs7715586	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7715720	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs986767	0.94[AMR][1000 genomes];0.97[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	chr5:16271800-16272800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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