Variant report

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11086835	0.87[EUR][1000 genomes]
rs11086836	0.88[EUR][1000 genomes]
rs11696790	0.87[EUR][1000 genomes]
rs11697439	0.87[EUR][1000 genomes]
rs11905262	0.90[EUR][1000 genomes]
rs11907033	0.87[EUR][1000 genomes]
rs11907414	0.87[EUR][1000 genomes]
rs12480171	0.91[EUR][1000 genomes]
rs12480310	0.87[EUR][1000 genomes]
rs12481706	0.87[EUR][1000 genomes]
rs2206905	1.00[CHB][hapmap]
rs230159	1.00[CHB][hapmap]
rs2425493	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3091840	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34733708	0.87[EUR][1000 genomes]
rs55634456	0.87[EUR][1000 genomes]
rs55953368	0.90[EUR][1000 genomes]
rs56017218	0.87[EUR][1000 genomes]
rs57287359	0.84[EUR][1000 genomes]
rs57370890	0.81[EUR][1000 genomes]
rs59669560	0.91[EUR][1000 genomes]
rs6030189	1.00[CHB][hapmap]
rs60573844	0.84[EUR][1000 genomes]
rs61076895	0.81[EUR][1000 genomes]
rs73121630	0.90[EUR][1000 genomes]
rs73121632	0.87[EUR][1000 genomes]
rs73121633	0.94[EUR][1000 genomes]
rs73121641	0.87[EUR][1000 genomes]
rs73121645	0.87[EUR][1000 genomes]
rs73121659	0.90[EUR][1000 genomes]
rs73121664	0.90[EUR][1000 genomes]
rs73123338	0.81[EUR][1000 genomes]
rs73123352	0.83[EUR][1000 genomes]
rs73123354	0.86[EUR][1000 genomes]
rs73123356	0.82[EUR][1000 genomes]
rs73123358	0.82[EUR][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	esv2751913	chr20:40422982-41269321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv532516	chr20:40451059-41097155	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv833987	chr20:41007663-41184914	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	9 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	chr20:41022400-41039400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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