Variant report

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

rs_ID	r²[population]
rs11173363	0.81[AFR][1000 genomes]
rs11173369	0.85[AFR][1000 genomes]
rs11830027	0.92[ASN][1000 genomes]
rs11831127	0.90[AFR][1000 genomes]
rs11831587	0.95[AFR][1000 genomes]
rs11832299	0.85[AFR][1000 genomes]
rs11835954	0.85[AFR][1000 genomes]
rs12579713	0.95[AFR][1000 genomes]
rs12580881	0.81[AFR][1000 genomes]
rs12581293	0.85[AFR][1000 genomes]
rs12582010	0.85[AFR][1000 genomes]
rs55905809	0.95[AFR][1000 genomes]
rs56158317	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56178609	0.95[AFR][1000 genomes]
rs57533761	0.95[AFR][1000 genomes]
rs57848253	0.95[AFR][1000 genomes]
rs59757360	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61561862	0.90[AFR][1000 genomes]
rs7139265	1.00[AFR][1000 genomes]
rs7310477	0.95[AFR][1000 genomes]
rs73113496	0.85[AFR][1000 genomes]
rs73113502	0.83[AFR][1000 genomes]
rs73114735	0.85[AFR][1000 genomes]
rs73114791	0.95[AFR][1000 genomes]
rs73115184	0.85[AFR][1000 genomes]
rs73120658	0.95[AFR][1000 genomes]
rs7314006	1.00[AFR][1000 genomes]
rs7960722	0.85[AFR][1000 genomes]
rs867948	0.95[AFR][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	nsv899137	chr12:60568891-60797083	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1054287	chr12:60601870-60861866	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv832431	chr12:60626292-60809233	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr12:60679600-60691000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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