Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs17108692	1.00[EUR][1000 genomes]
rs17108887	1.00[EUR][1000 genomes]
rs17108894	1.00[EUR][1000 genomes]
rs17388036	1.00[EUR][1000 genomes]
rs34140758	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34144152	1.00[EUR][1000 genomes]
rs34260450	1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34370865	1.00[EUR][1000 genomes]
rs34826144	1.00[EUR][1000 genomes]
rs35593536	1.00[EUR][1000 genomes]
rs35608752	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs60189638	1.00[EUR][1000 genomes]
rs7085552	1.00[EUR][1000 genomes]
rs74146649	1.00[EUR][1000 genomes]
rs74146650	1.00[EUR][1000 genomes]
rs74146651	1.00[EUR][1000 genomes]
rs74146652	1.00[EUR][1000 genomes]
rs74146653	1.00[EUR][1000 genomes]
rs7897915	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs7917439	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7917883	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs9783193	1.00[YRI][hapmap]
rs9783238	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv551837	chr10:89707265-89777788	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3387188	chr10:89743021-89767378	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 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	chr10:89758400-89785800	Weak transcription	Aorta	Aorta

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