Variant report

Variant	rs11515036
Chromosome Location	chr8:49854783-49854784
allele	A/G
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]
rs10097264	0.83[EUR][1000 genomes]
rs10100077	0.83[EUR][1000 genomes]
rs12682003	0.83[AMR][1000 genomes]
rs13265564	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1441004	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1441005	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17641604	0.85[AMR][1000 genomes]
rs1837690	0.81[AMR][1000 genomes]
rs1992375	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2385117	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2385120	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2582778	0.81[EUR][1000 genomes]
rs870397	0.83[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49851000-49859800	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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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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