Variant report

Variant	rs11580888
Chromosome Location	chr1:159104438-159104439
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11582615	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11586482	0.87[EUR][1000 genomes]
rs2518569	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs2518570	0.82[ASN][1000 genomes]
rs3026921	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3026922	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3026925	0.90[EUR][1000 genomes]
rs3026935	0.83[EUR][1000 genomes]
rs41264463	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61400225	0.87[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159104400-159110200	Weak transcription	Brain Germinal Matrix	brain

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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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