Variant report

Variant	rs9861541
Chromosome Location	chr3:25144041-25144042
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13325558	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1609491	0.81[AFR][1000 genomes]
rs17015764	0.81[ASN][1000 genomes]
rs2012334	0.80[AFR][1000 genomes]
rs4858142	0.80[AFR][1000 genomes]
rs4858704	0.80[AFR][1000 genomes]
rs62228548	0.91[EUR][1000 genomes]
rs62228549	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62230269	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6797206	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6801041	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7626290	0.91[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25142800-25144600	Weak transcription	Aorta	Aorta

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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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