Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10045556	0.93[ASN][1000 genomes]
rs10076155	0.95[ASN][1000 genomes]
rs12187672	0.95[ASN][1000 genomes]
rs12188902	0.95[ASN][1000 genomes]
rs12658947	0.94[ASN][1000 genomes]
rs12659412	0.94[ASN][1000 genomes]
rs151865	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs151870	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs151872	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs151873	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs151874	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs151875	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs151876	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs151878	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696032	0.95[ASN][1000 genomes]
rs56942787	0.95[ASN][1000 genomes]
rs5868101	0.96[ASN][1000 genomes]
rs68192123	0.95[ASN][1000 genomes]
rs6858896	0.95[ASN][1000 genomes]
rs72755740	0.94[ASN][1000 genomes]
rs72755746	0.96[ASN][1000 genomes]
rs72755747	0.96[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	esv3489100	chr5:57545689-57669673	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3489101	chr5:57545689-57669673	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57590800-57597800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:57591400-57596400	Weak transcription	Primary monocytes fromperipheralblood	blood

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