Variant report

Variant	rs12213692
Chromosome Location	chr6:71811764-71811765
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10455721	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10455722	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12192717	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12193219	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12195809	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12210276	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7742804	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7755915	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9446337	0.82[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71808200-71815400	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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