Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:69950771..69953657-chr8:69955628..69958429,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs13252637	0.96[EUR][1000 genomes]
rs1344618	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1344619	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1365412	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1365413	0.96[ASN][1000 genomes]
rs1365414	0.96[ASN][1000 genomes]
rs1365416	0.98[ASN][1000 genomes]
rs1365417	1.00[ASN][1000 genomes]
rs1426595	0.88[EUR][1000 genomes]
rs1541762	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1559847	0.96[ASN][1000 genomes]
rs1559848	0.96[ASN][1000 genomes]
rs2042732	0.96[ASN][1000 genomes]
rs2042733	1.00[ASN][1000 genomes]
rs2042735	1.00[ASN][1000 genomes]
rs2217103	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28437123	1.00[ASN][1000 genomes]
rs2912518	0.96[ASN][1000 genomes]
rs2912519	0.96[ASN][1000 genomes]
rs2912520	0.96[ASN][1000 genomes]
rs2981041	1.00[ASN][1000 genomes]
rs2981043	0.96[ASN][1000 genomes]
rs2981044	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2981047	0.93[EUR][1000 genomes]
rs2981062	0.96[EUR][1000 genomes]
rs34771267	0.96[EUR][1000 genomes]
rs473477	0.98[ASN][1000 genomes]
rs608067	1.00[ASN][1000 genomes]
rs609760	1.00[ASN][1000 genomes]
rs612423	1.00[ASN][1000 genomes]
rs625096	0.99[ASN][1000 genomes]
rs639293	0.88[EUR][1000 genomes]
rs6472438	0.96[ASN][1000 genomes]
rs7007693	0.88[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031633	chr8:69766575-70322790	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69952000-69959400	Weak transcription	HSMM	muscle
2	chr8:69953800-69959800	Weak transcription	Aorta	Aorta
3	chr8:69955200-69956400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:69955200-69956600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr8:69955600-69958000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:69955800-69956200	Enhancers	HUES64 Cell Line	embryonic stem cell

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