Variant report

Variant	rs17669960
Chromosome Location	chr8:96308367-96308368
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs17265463	0.88[CEU][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34308441	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34393748	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35084958	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35234362	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35255852	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35526423	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35790752	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71532355	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7459448	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7841148	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96307000-96309200	Enhancers	Placenta	Placenta
2	chr8:96308200-96308400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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