Variant report

Variant	rs9561132
Chromosome Location	chr13:93387498-93387499
allele	G/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:12)

rs_ID	r²[population]
rs17233850	1.00[CEU][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs7317017	0.95[CEU][hapmap]
rs7322501	0.94[CEU][hapmap]
rs9301833	0.90[CEU][hapmap]
rs9516129	1.00[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap]
rs9523776	0.95[CEU][hapmap]
rs9523787	0.95[CEU][hapmap]
rs9523788	0.93[CEU][hapmap]
rs9523790	1.00[CEU][hapmap]
rs9523791	0.94[CEU][hapmap]
rs9523792	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9523793	0.90[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93385400-93387600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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