Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11840020	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11841551	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17072549	1.00[EUR][1000 genomes]
rs17072560	1.00[AMR][1000 genomes]
rs17072573	0.94[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17072578	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17072884	1.00[EUR][1000 genomes]
rs326505	1.00[EUR][1000 genomes]
rs55987417	1.00[EUR][1000 genomes]
rs56027878	1.00[EUR][1000 genomes]
rs58460051	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60156590	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6490341	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6490342	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7319939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7321572	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7325216	1.00[AMR][1000 genomes]
rs7327807	1.00[EUR][1000 genomes]
rs7337727	1.00[EUR][1000 genomes]
rs73441370	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73441387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74045514	1.00[EUR][1000 genomes]
rs7996240	1.00[EUR][1000 genomes]
rs9783547	1.00[AMR][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	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29585000-29609600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:29601000-29605800	Weak transcription	Aorta	Aorta
3	chr13:29602600-29607800	Enhancers	Fetal Heart	heart

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