Variant report

Variant	rs10805623
Chromosome Location	chr5:36553835-36553836
allele	A/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]
rs10061650	0.94[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs10076624	0.80[JPT][hapmap];0.86[ASN][1000 genomes]
rs1366636	0.94[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs2115521	0.90[ASN][1000 genomes]
rs2562554	0.92[ASN][1000 genomes]
rs2562559	0.82[ASN][1000 genomes]
rs2562568	0.94[CHB][hapmap];0.88[JPT][hapmap];0.86[ASN][1000 genomes]
rs2731901	0.90[ASN][1000 genomes]
rs2731906	0.92[ASN][1000 genomes]
rs2731907	0.89[ASN][1000 genomes]
rs2731909	0.88[ASN][1000 genomes]
rs2731920	0.94[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs9800255	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36553800-36554200	Enhancers	hESC Derived CD56+ Mesoderm 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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