Variant report

Variant	rs379732
Chromosome Location	chr2:76243065-76243066
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1013593	0.85[ASN][1000 genomes]
rs11126493	0.90[AFR][1000 genomes]
rs1524215	0.95[CEU][hapmap];0.84[CHB][hapmap];0.88[JPT][hapmap]
rs2422409	0.84[ASN][1000 genomes]
rs317235	0.85[AFR][1000 genomes]
rs317236	0.81[AFR][1000 genomes]
rs317242	0.81[AFR][1000 genomes]
rs367949	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3843860	0.90[AFR][1000 genomes]
rs3843861	0.88[AFR][1000 genomes]
rs3849395	0.90[AFR][1000 genomes]
rs3849396	0.87[AFR][1000 genomes]
rs3910651	0.90[AFR][1000 genomes]
rs405354	0.85[ASN][1000 genomes]
rs427171	0.85[ASN][1000 genomes]
rs436000	0.91[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs438780	0.85[ASN][1000 genomes]
rs441584	0.86[AFR][1000 genomes]
rs4853190	0.87[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76237600-76243600	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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