Variant report

Variant	rs28483085
Chromosome Location	chr8:64725892-64725893
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10097618	0.94[AFR][1000 genomes]
rs10110399	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1425597	1.00[ASN][1000 genomes]
rs1541750	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2355594	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2859965	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6993329	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72649241	1.00[ASN][1000 genomes]
rs73258928	1.00[ASN][1000 genomes]
rs73260622	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7842563	0.86[AMR][1000 genomes];1.00[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	chr8:64725600-64729200	Weak transcription	ES-UCSF4 Cell Line	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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