Variant report

Variant	rs2946799
Chromosome Location	chr3:118170552-118170553
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11708487	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12330594	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13319845	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13326806	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1447592	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1827180	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4688104	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4688105	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9813744	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9815320	0.91[EUR][1000 genomes]
rs9834379	0.91[EUR][1000 genomes]
rs9880484	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9882733	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118170200-118172000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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