Variant report

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10096464	0.82[EUR][1000 genomes]
rs10099399	0.83[EUR][1000 genomes]
rs10100325	0.82[EUR][1000 genomes]
rs10103144	0.82[EUR][1000 genomes]
rs10111724	0.82[EUR][1000 genomes]
rs10112178	0.83[EUR][1000 genomes]
rs10113234	0.82[EUR][1000 genomes]
rs10113425	0.82[EUR][1000 genomes]
rs10504797	0.82[EUR][1000 genomes]
rs10504798	0.85[EUR][1000 genomes]
rs10958213	0.82[EUR][1000 genomes]
rs11780481	0.82[EUR][1000 genomes]
rs11787298	0.82[EUR][1000 genomes]
rs12375329	0.83[EUR][1000 genomes]
rs12375330	0.83[EUR][1000 genomes]
rs12375429	0.83[EUR][1000 genomes]
rs13263706	0.87[EUR][1000 genomes]
rs1437515	0.82[EUR][1000 genomes]
rs16912524	0.85[EUR][1000 genomes]
rs17708185	0.85[EUR][1000 genomes]
rs17708369	0.82[EUR][1000 genomes]
rs2196615	0.82[EUR][1000 genomes]
rs2196616	0.82[EUR][1000 genomes]
rs2217977	0.82[EUR][1000 genomes]
rs2217978	0.82[EUR][1000 genomes]
rs35196647	0.82[EUR][1000 genomes]
rs55695735	0.82[EUR][1000 genomes]
rs62529180	0.82[EUR][1000 genomes]
rs766560	0.88[EUR][1000 genomes]
rs766561	0.88[EUR][1000 genomes]
rs7818732	0.82[EUR][1000 genomes]
rs7841226	0.88[EUR][1000 genomes]
rs7845564	0.88[EUR][1000 genomes]
rs9298420	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9298421	0.82[EUR][1000 genomes]
rs9298422	0.82[EUR][1000 genomes]
rs959433	0.88[EUR][1000 genomes]

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	esv2753846	chr8:84637092-85239703	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv831374	chr8:85103604-85308976	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive 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	chr8:85099000-85121000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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