Variant report

Variant	rs10890604
Chromosome Location	chr11:106705322-106705323
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]
rs10160762	0.90[EUR][1000 genomes]
rs10789547	0.92[ASN][1000 genomes]
rs10890611	0.86[EUR][1000 genomes]
rs12274602	0.86[EUR][1000 genomes]
rs12285359	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1487889	0.92[ASN][1000 genomes]
rs1487891	0.89[EUR][1000 genomes]
rs1487892	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4754169	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7924555	0.84[EUR][1000 genomes]
rs7926569	0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs7937534	0.84[EUR][1000 genomes]
rs923327	0.90[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs9651675	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106705200-106705800	Enhancers	Fetal Heart	heart

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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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