Variant report

Variant	rs12956058
Chromosome Location	chr18:30358394-30358395
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11663493	0.86[ASN][1000 genomes]
rs12373178	0.86[ASN][1000 genomes]
rs12606442	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1403750	0.89[ASN][1000 genomes]
rs1523577	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2140445	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55737004	0.86[ASN][1000 genomes]
rs715401	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7229257	0.84[ASN][1000 genomes]
rs7234579	0.81[ASN][1000 genomes]
rs8097174	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30357000-30359600	Enhancers	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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