Variant report

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

rs_ID	r²[population]
rs12651350	1.00[EUR][1000 genomes]
rs36224744	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4349588	0.83[AMR][1000 genomes]
rs4692548	1.00[EUR][1000 genomes]
rs56656455	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56834351	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57269196	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58297498	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58551878	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58990586	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59082948	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59902050	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60016776	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60212470	1.00[EUR][1000 genomes]
rs60373412	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60930192	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61179790	1.00[EUR][1000 genomes]
rs61239973	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61299741	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61557900	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61681337	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6825731	1.00[EUR][1000 genomes]
rs6838102	1.00[EUR][1000 genomes]
rs6839766	1.00[EUR][1000 genomes]
rs6845307	1.00[EUR][1000 genomes]
rs7659656	1.00[EUR][1000 genomes]
rs7683070	1.00[EUR][1000 genomes]
rs7689334	1.00[EUR][1000 genomes]
rs9291485	1.00[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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26492000-26495000	Weak transcription	Gastric	stomach
2	chr4:26492000-26504200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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