Variant report

Variant	rs71484988
Chromosome Location	chr10:117280723-117280724
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10885729	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10885730	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11197244	0.81[EUR][1000 genomes]
rs11197246	0.81[EUR][1000 genomes]
rs11197247	0.80[EUR][1000 genomes]
rs11197259	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11197261	0.88[EUR][1000 genomes]
rs11197264	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12766723	0.80[EUR][1000 genomes]
rs12767028	0.81[EUR][1000 genomes]
rs1572401	0.82[AMR][1000 genomes]
rs2182862	0.88[EUR][1000 genomes]
rs2420083	0.80[EUR][1000 genomes]
rs35594709	0.81[EUR][1000 genomes]
rs7071124	0.81[EUR][1000 genomes]
rs7093703	0.88[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117278000-117281800	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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