Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10128512	0.83[YRI][hapmap]
rs10828918	1.00[YRI][hapmap]
rs10828930	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs11014881	0.82[AFR][1000 genomes]
rs11014915	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014916	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014926	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11014956	1.00[AMR][1000 genomes]
rs11498425	1.00[AMR][1000 genomes]
rs11814511	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs11814982	0.91[AFR][1000 genomes]
rs11819023	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs12241145	0.91[YRI][hapmap]
rs12247532	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs12250247	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12261092	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12263784	0.80[AFR][1000 genomes]
rs12264399	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs12265482	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs12268743	1.00[AMR][1000 genomes]
rs12385769	1.00[AMR][1000 genomes]
rs7098026	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7896360	1.00[YRI][hapmap];0.82[AFR][1000 genomes]

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	esv1792417	chr10:26263695-26395038	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26334200-26342600	Weak transcription	Aorta	Aorta
2	chr10:26337600-26338400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
3	chr10:26338200-26341200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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