Variant report

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

rs_ID	r²[population]
rs11155422	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17797768	0.82[ASN][1000 genomes]
rs17797774	0.82[ASN][1000 genomes]
rs28800626	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6570686	1.00[ASN][1000 genomes]
rs6570687	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6570688	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6570690	0.85[AMR][1000 genomes]
rs6905046	1.00[ASN][1000 genomes]
rs6907972	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6908027	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6910793	1.00[ASN][1000 genomes]
rs6915105	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6916625	1.00[ASN][1000 genomes]
rs6925385	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6934750	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73781819	1.00[ASN][1000 genomes]
rs7738882	1.00[ASN][1000 genomes]
rs7741505	1.00[ASN][1000 genomes]
rs7746796	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7754527	0.85[AMR][1000 genomes]
rs7757254	0.91[ASN][1000 genomes]
rs9484997	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9497313	1.00[ASN][1000 genomes]
rs9497314	1.00[ASN][1000 genomes]
rs9497318	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497320	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];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:2 , 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
2	chr6:145789800-145791200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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