Variant report

Variant	rs58094875
Chromosome Location	chr13:51584469-51584470
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs17075139	0.86[ASN][1000 genomes]
rs2281993	0.86[ASN][1000 genomes]
rs2296914	0.89[ASN][1000 genomes]
rs60194361	0.89[ASN][1000 genomes]
rs7317089	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7332491	0.85[EUR][1000 genomes]
rs7333942	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7339210	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74080382	0.89[ASN][1000 genomes]
rs74080386	0.89[ASN][1000 genomes]
rs74080387	0.89[ASN][1000 genomes]
rs74080392	0.81[ASN][1000 genomes]
rs74080393	0.89[ASN][1000 genomes]
rs74080395	0.88[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51581200-51588000	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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