Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11124434	0.80[EUR][1000 genomes]
rs11682662	0.86[EUR][1000 genomes]
rs11683495	0.82[EUR][1000 genomes]
rs11688672	0.83[EUR][1000 genomes]
rs11690364	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12470574	0.80[EUR][1000 genomes]
rs12477767	0.83[EUR][1000 genomes]
rs12618122	0.95[ASN][1000 genomes]
rs12618519	0.83[EUR][1000 genomes]
rs12619256	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12997825	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs13003754	0.80[EUR][1000 genomes]
rs13010526	0.93[EUR][1000 genomes]
rs13022408	0.83[EUR][1000 genomes]
rs1400713	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1914457	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2030195	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs2048933	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34054060	0.83[EUR][1000 genomes]
rs34144010	0.86[EUR][1000 genomes]
rs34464539	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35168234	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4387830	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4574146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6749313	0.80[EUR][1000 genomes]
rs7557098	0.83[EUR][1000 genomes]
rs7567650	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	nsv873728	chr2:21250914-21460786	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr2:21416200-21424400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:21418600-21422800	Weak transcription	Fetal Intestine Large	intestine
3	chr2:21422000-21422200	Enhancers	Brain Anterior Caudate	brain

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