Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10521055	0.88[EUR][1000 genomes]
rs11788485	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11792021	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11792023	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11793965	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11794505	0.88[EUR][1000 genomes]
rs16920200	0.88[EUR][1000 genomes]
rs1935242	0.88[EUR][1000 genomes]
rs4416881	0.90[AFR][1000 genomes]
rs4451365	0.91[AFR][1000 genomes]
rs4474082	0.91[AFR][1000 genomes]
rs4612403	0.91[AFR][1000 genomes]
rs55658944	0.88[EUR][1000 genomes]
rs56218359	0.82[EUR][1000 genomes]
rs58013833	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs58772170	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73492631	0.88[EUR][1000 genomes]
rs73492632	0.87[EUR][1000 genomes]
rs73492646	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73509627	0.91[AFR][1000 genomes]
rs73509628	0.88[AFR][1000 genomes]
rs73509629	0.91[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	nsv1037157	chr9:104045761-104149233	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr9:104098600-104104200	Weak transcription	HepG2	liver

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