Variant report

Variant	rs59245253
Chromosome Location	chr5:71036359-71036360
allele	C/G
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]
rs3914615	0.92[ASN][1000 genomes]
rs4057258	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4057259	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60286869	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62360705	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62360707	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62360710	0.88[ASN][1000 genomes]
rs62360711	0.96[ASN][1000 genomes]
rs62360715	0.81[ASN][1000 genomes]
rs6869080	0.90[EUR][1000 genomes]
rs72769463	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72769469	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:71034800-71037800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr5:71036200-71036600	Flanking Active TSS	GM12878-XiMat	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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