Variant report

Variant	rs497009
Chromosome Location	chr3:118145448-118145449
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1850944	0.82[ASN][1000 genomes]
rs480491	0.86[ASN][1000 genomes]
rs491796	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs495761	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs506192	0.88[ASN][1000 genomes]
rs507145	0.84[ASN][1000 genomes]
rs508870	0.86[ASN][1000 genomes]
rs518882	0.84[ASN][1000 genomes]
rs523712	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs531289	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs557455	0.89[ASN][1000 genomes]
rs566574	0.86[ASN][1000 genomes]
rs576638	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118144600-118146000	Enhancers	Fetal Brain Male	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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