Variant report

Variant	rs312029
Chromosome Location	chr2:21461730-21461731
allele	A/C/G
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]
rs10166144	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10170323	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10177017	0.84[EUR][1000 genomes]
rs10177492	0.82[EUR][1000 genomes]
rs10183198	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10198972	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs13387827	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13398007	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs67144154	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	chr2:21451600-21461800	Weak transcription	Aorta	Aorta

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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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