Variant report

Variant	rs12682003
Chromosome Location	chr8:49865454-49865455
allele	G/T
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]
rs11515036	0.83[AMR][1000 genomes]
rs13277226	0.86[ASN][1000 genomes]
rs13279837	0.83[AFR][1000 genomes]
rs1441004	0.83[AMR][1000 genomes]
rs17641604	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1837690	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1992375	0.83[AMR][1000 genomes]
rs2203065	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs870397	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49860200-49866000	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr8:49865400-49865600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:49865400-49865600	Active TSS	Gastric	stomach

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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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