Variant report

Variant	rs73226515
Chromosome Location	chr2:21063433-21063434
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs57140039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73224603	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73224605	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73224606	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73224618	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73224621	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73224631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73224632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73226507	1.00[AMR][1000 genomes]
rs73226522	1.00[AMR][1000 genomes]
rs73226523	1.00[AMR][1000 genomes]
rs73226524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73226525	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73243138	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73919620	1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21054400-21076400	Weak transcription	Aorta	Aorta

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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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