Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10122746	0.84[EUR][1000 genomes]
rs10512132	0.90[EUR][1000 genomes]
rs10512133	0.93[EUR][1000 genomes]
rs11139640	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11139646	0.96[EUR][1000 genomes]
rs11139650	0.93[EUR][1000 genomes]
rs11139652	0.87[EUR][1000 genomes]
rs11139653	0.93[EUR][1000 genomes]
rs11139654	0.93[EUR][1000 genomes]
rs11139661	0.90[EUR][1000 genomes]
rs11139665	1.00[EUR][1000 genomes]
rs11139680	0.93[EUR][1000 genomes]
rs11139682	0.96[EUR][1000 genomes]
rs11139683	0.96[EUR][1000 genomes]
rs17085592	0.93[EUR][1000 genomes]
rs17085704	0.96[EUR][1000 genomes]
rs2001818	0.90[EUR][1000 genomes]
rs7022118	0.95[AFR][1000 genomes]
rs73648460	0.93[EUR][1000 genomes]
rs73648462	0.96[EUR][1000 genomes]
rs73648463	0.93[EUR][1000 genomes]
rs73650737	0.99[AFR][1000 genomes]
rs73650739	0.85[AFR][1000 genomes]
rs73650741	0.84[AFR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7853040	0.93[EUR][1000 genomes]
rs7853471	0.93[EUR][1000 genomes]
rs7857463	0.84[AFR][1000 genomes]
rs7875519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9919047	0.85[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	nsv831641	chr9:85145561-85309589	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85194600-85195200	Enhancers	HepG2	liver
2	chr9:85194800-85195200	Enhancers	Liver	Liver

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