Variant report

Variant	rs748463
Chromosome Location	chr5:151338950-151338951
allele	C/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]
rs11740638	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12188534	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13186058	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1549618	0.84[CEU][hapmap];0.88[EUR][1000 genomes]
rs4958287	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4958504	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4958505	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6579914	0.95[CEU][hapmap];0.95[EUR][1000 genomes]
rs7710098	0.88[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151338600-151339000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr5:151338800-151341400	Weak transcription	hESC Derived CD56+ Ectoderm 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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