Variant report

Variant	rs7869674
Chromosome Location	chr9:96510642-96510643
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11793318	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2487020	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3209003	0.83[EUR][1000 genomes]
rs3750462	0.83[EUR][1000 genomes]
rs4618758	0.83[AFR][1000 genomes]
rs4743935	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs60681214	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7850735	0.83[EUR][1000 genomes]
rs7855547	0.83[EUR][1000 genomes]
rs7865953	0.81[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96509200-96518400	ZNF genes & repeats	hESC Derived CD184+ Endoderm 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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