Variant report

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

rs_ID	r²[population]
rs11155422	1.00[ASN][1000 genomes]
rs12110970	1.00[ASN][1000 genomes]
rs13206047	0.84[EUR][1000 genomes]
rs17797768	0.82[ASN][1000 genomes]
rs17797774	0.82[ASN][1000 genomes]
rs28800626	1.00[ASN][1000 genomes]
rs55646460	1.00[EUR][1000 genomes]
rs56220011	1.00[EUR][1000 genomes]
rs56931754	1.00[EUR][1000 genomes]
rs58271163	1.00[EUR][1000 genomes]
rs6570686	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6570687	1.00[ASN][1000 genomes]
rs6905046	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6908027	1.00[ASN][1000 genomes]
rs6910793	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6915105	1.00[ASN][1000 genomes]
rs6916625	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6925385	0.95[ASN][1000 genomes]
rs73560904	1.00[EUR][1000 genomes]
rs7738882	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7741505	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7746796	1.00[ASN][1000 genomes]
rs7757254	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9484997	1.00[ASN][1000 genomes]
rs9497313	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9497314	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9497320	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017166	chr6:145677071-145808448	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv604838	chr6:145709371-145841146	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 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	chr6:145768200-145803800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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