Variant report

Variant	rs4571524
Chromosome Location	chr6:75754877-75754878
allele	A/T
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]
rs11754104	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11758551	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11758990	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4291062	0.88[EUR][1000 genomes]
rs4413578	0.84[EUR][1000 genomes]
rs4518462	0.89[EUR][1000 genomes]
rs4560603	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4569931	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56310973	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6453809	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6928356	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6935028	0.89[AFR][1000 genomes]
rs73462024	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75753200-75758000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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