Variant report

No.	Distal block	Cell Line	Cell type
1	chr8:99304773..99308410-chr8:99356303..99359323,3	MCF-7	breast:
2	chr8:99347365..99349416-chr8:99356232..99359153,2	K562	blood:
3	chr8:99356606..99360601-chr8:99368413..99371833,4	MCF-7	breast:
4	chr8:99351707..99353474-chr8:99355817..99358709,2	MCF-7	breast:
5	chr8:99348334..99350137-chr8:99356726..99359108,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000104361	Chromatin interaction

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10955166	0.87[ASN][1000 genomes]
rs13259687	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs36067643	0.86[ASN][1000 genomes]
rs4131950	0.84[ASN][1000 genomes]
rs4131951	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4145238	0.88[ASN][1000 genomes]
rs4236847	0.82[ASN][1000 genomes]
rs4284021	0.95[ASN][1000 genomes]
rs4346964	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4346967	0.96[ASN][1000 genomes]
rs4366057	0.84[ASN][1000 genomes]
rs4458848	0.95[ASN][1000 genomes]
rs4644205	0.82[ASN][1000 genomes]
rs4734396	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4734397	0.84[ASN][1000 genomes]
rs4734398	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4734399	0.88[ASN][1000 genomes]
rs4735553	0.82[ASN][1000 genomes]
rs4735554	0.82[ASN][1000 genomes]
rs56084201	0.86[ASN][1000 genomes]
rs6468629	0.83[ASN][1000 genomes]
rs6468632	0.95[ASN][1000 genomes]
rs7829174	0.82[ASN][1000 genomes]
rs7831383	0.81[ASN][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	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831406	chr8:99290745-99482076	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv891217	chr8:99346537-99391285	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 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	chr8:99354200-99368200	Weak transcription	NHDF-Ad	bronchial
2	chr8:99354600-99369000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:99356000-99361400	Weak transcription	Ovary	ovary

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