Variant report

Variant	rs60323829
Chromosome Location	chr1:179485548-179485549
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12021876	0.80[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs12216994	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12216996	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1410586	0.86[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1928005	0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs55998153	0.81[AFR][1000 genomes]
rs56392198	0.81[AFR][1000 genomes]
rs59377201	0.82[AFR][1000 genomes]
rs73036755	0.84[AFR][1000 genomes]
rs73051834	0.83[AFR][1000 genomes];0.82[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179485400-179486800	Enhancers	Stomach Mucosa	stomach

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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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