Variant report

Variant	rs34480242
Chromosome Location	chr11:32597750-32597751
allele	C/T
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]
rs11031883	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12276207	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12787891	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12788831	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12807888	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs34495676	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67535916	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67559057	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7111865	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71479164	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71479166	0.85[AMR][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	chr11:32597400-32604200	Weak transcription	K562	blood

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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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