Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10094445	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10096604	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10097810	0.81[ASN][1000 genomes]
rs10098559	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10956495	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1979475	0.81[ASN][1000 genomes]
rs1979476	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1988911	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2894495	0.81[ASN][1000 genomes]
rs3912318	0.81[ASN][1000 genomes]
rs4103049	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4260864	0.81[ASN][1000 genomes]
rs4500051	0.81[ASN][1000 genomes]
rs4733741	0.92[ASN][1000 genomes]
rs6470782	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6983184	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73406845	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7834217	0.81[ASN][1000 genomes]
rs7834660	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9656980	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[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	nsv428524	chr8:130731660-130894467	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv522535	chr8:130804293-130844400	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 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	chr8:130801000-130809400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:130801800-130809400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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