Variant report

Variant	rs60293431
Chromosome Location	chr4:54590701-54590702
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17083326	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17083355	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28459143	0.94[ASN][1000 genomes]
rs28484855	0.98[ASN][1000 genomes]
rs28589490	0.89[ASN][1000 genomes]
rs28613767	0.98[ASN][1000 genomes]
rs56753131	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6844085	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6850721	0.91[AFR][1000 genomes]
rs728587	0.98[ASN][1000 genomes]
rs7664385	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7671090	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54584000-54600000	Weak transcription	Osteobl	bone
2	chr4:54590000-54591000	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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