Variant report

Variant	rs6471836
Chromosome Location	chr8:60763956-60763957
allele	C/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]
rs12676407	0.83[EUR][1000 genomes]
rs1497041	0.91[AFR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16925454	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1955227	0.83[EUR][1000 genomes]
rs4607595	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4738787	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56203327	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58546633	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61514252	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62510024	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6471845	0.85[EUR][1000 genomes]
rs6984918	0.84[EUR][1000 genomes]
rs6996720	0.85[EUR][1000 genomes]
rs7001936	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60763600-60764400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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