Variant report

Variant	rs13234438
Chromosome Location	chr7:48721568-48721569
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12718290	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12718292	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13244837	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34598210	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35316325	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35483521	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62447353	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62447359	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62448770	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48720600-48723200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr7:48721400-48721600	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr7:48721400-48722600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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