Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:88945613..88947133-chr8:88952245..88954960,2	K562	blood:
2	chr8:88953944..88956078-chr8:88958944..88960542,2	MCF-7	breast:

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

rs_ID	r²[population]
rs1072176	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs11987992	0.91[AMR][1000 genomes]
rs11989278	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11997724	0.91[AMR][1000 genomes]
rs57632153	0.86[AMR][1000 genomes]
rs58092272	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58257363	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs59183651	0.91[AMR][1000 genomes]
rs60046421	0.86[AMR][1000 genomes]
rs73280265	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73280277	0.91[AMR][1000 genomes]
rs73281903	0.91[AMR][1000 genomes]
rs73281904	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73281905	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73281919	0.96[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	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73281931	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs73692202	0.91[AMR][1000 genomes]
rs7845687	0.94[AFR][1000 genomes];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	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
2	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
3	nsv6292	chr8:88920735-88965372	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv428520	chr8:88933423-89089323	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:88951600-88956000	Weak transcription	NH-A	brain
2	chr8:88951800-88955000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:88952800-88954800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:88954400-88955400	Weak transcription	Osteobl	bone

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