Variant report

Variant	rs62521230
Chromosome Location	chr8:118569334-118569335
allele	A/C
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]
rs11995038	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1480167	0.95[ASN][1000 genomes]
rs55663437	0.91[ASN][1000 genomes]
rs62521192	0.85[EUR][1000 genomes]
rs62521196	0.85[EUR][1000 genomes]
rs62521201	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62521202	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62521205	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62521211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62521237	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62521238	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118564600-118573200	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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