Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11944224	0.83[EUR][1000 genomes]
rs12500365	1.00[EUR][1000 genomes]
rs12500372	1.00[EUR][1000 genomes]
rs2725323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2725324	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2854031	0.86[EUR][1000 genomes]
rs2854036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2854037	0.86[EUR][1000 genomes]
rs28584998	0.83[EUR][1000 genomes]
rs2968718	0.86[EUR][1000 genomes]
rs3020586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3020587	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3020588	0.86[EUR][1000 genomes]
rs3020591	0.86[EUR][1000 genomes]
rs3109845	0.86[EUR][1000 genomes]
rs3111710	0.86[EUR][1000 genomes]
rs3111712	0.86[EUR][1000 genomes]
rs3113011	0.86[EUR][1000 genomes]
rs3113013	0.86[EUR][1000 genomes]
rs34106842	0.83[EUR][1000 genomes]
rs56174986	1.00[EUR][1000 genomes]
rs56285756	1.00[EUR][1000 genomes]
rs73113354	0.83[EUR][1000 genomes]
rs7697476	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs953324	0.83[EUR][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	esv2762417	chr4:26491768-26576800	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 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	chr4:26492000-26504200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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