Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:88910926..88912766-chr8:88929269..88932098,2	MCF-7	breast:

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

rs_ID	r²[population]
rs1072176	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs11987992	0.91[AMR][1000 genomes]
rs11989278	0.87[AMR][1000 genomes]
rs11997724	0.91[AMR][1000 genomes]
rs57632153	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58092272	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs58257363	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59183651	0.91[AMR][1000 genomes]
rs60046421	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7003732	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs73280265	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs73280277	0.91[AMR][1000 genomes]
rs73281903	0.91[AMR][1000 genomes]
rs73281904	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73281905	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73281919	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73281921	0.87[AMR][1000 genomes]
rs73281923	0.91[AMR][1000 genomes]
rs73281927	0.87[AMR][1000 genomes]
rs73281928	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73281931	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73692202	0.91[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891169	chr8:88803575-88948825	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv831385	chr8:88807262-88965472	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1029898	chr8:88837956-89606641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv6292	chr8:88920735-88965372	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:88927600-88932000	Enhancers	Rectal Smooth Muscle	rectum
2	chr8:88928800-88932400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:88929400-88932200	Enhancers	Colon Smooth Muscle	Colon

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