Variant report

Variant	rs8189173
Chromosome Location	chr13:79876681-79876682
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]
rs10219169	0.86[AMR][1000 genomes]
rs11040020	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11500651	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12269855	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12289625	0.80[AMR][1000 genomes]
rs12785858	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2865620	0.82[ASN][1000 genomes]
rs2865673	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34486360	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3938020	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7293992	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7294268	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs8175695	0.80[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:79865000-79893200	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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