Variant report

Variant	rs13409109
Chromosome Location	chr2:190760881-190760882
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10169680	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10183082	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10497707	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13408737	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13418171	0.80[AFR][1000 genomes]
rs13421595	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16832146	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1982475	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28544977	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5743173	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5743193	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5743203	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6721150	1.00[AMR][1000 genomes]
rs73042372	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73042373	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7355626	0.80[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190758000-190761200	Weak transcription	HepG2	liver

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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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