Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11709960	0.83[ASN][1000 genomes]
rs11718127	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12631680	0.99[ASN][1000 genomes]
rs12631948	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12637429	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1404744	0.94[ASN][1000 genomes]
rs1525277	0.82[ASN][1000 genomes]
rs16831219	0.82[EUR][1000 genomes]
rs2177723	0.88[EUR][1000 genomes]
rs28703130	0.99[ASN][1000 genomes]
rs4854901	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4854959	0.95[ASN][1000 genomes]
rs58582741	0.89[ASN][1000 genomes]
rs59555202	0.97[ASN][1000 genomes]
rs60202080	0.99[ASN][1000 genomes]
rs62292260	0.97[ASN][1000 genomes]
rs68014168	0.88[EUR][1000 genomes]
rs6803764	0.87[ASN][1000 genomes]
rs7635210	0.94[ASN][1000 genomes]
rs7637854	0.82[ASN][1000 genomes]
rs9821124	0.82[ASN][1000 genomes]
rs9851723	0.90[ASN][1000 genomes]
rs9857420	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534210	chr3:179666123-179899347	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv878040	chr3:179823887-180128288	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr3:179865600-179886800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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