Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:125632600..125635495-chr4:125669372..125672069,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000151458	Chromatin interaction

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs72680301	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72682183	1.00[ASN][1000 genomes]
rs72682188	1.00[ASN][1000 genomes]
rs72682190	1.00[ASN][1000 genomes]
rs72682201	1.00[ASN][1000 genomes]
rs72683808	1.00[ASN][1000 genomes]
rs72683810	1.00[ASN][1000 genomes]
rs72683817	1.00[ASN][1000 genomes]
rs72683823	1.00[ASN][1000 genomes]
rs72683854	1.00[ASN][1000 genomes]
rs72683856	1.00[ASN][1000 genomes]
rs72683857	1.00[ASN][1000 genomes]
rs72683861	1.00[ASN][1000 genomes]
rs72683864	1.00[ASN][1000 genomes]
rs72683878	1.00[ASN][1000 genomes]
rs72683881	1.00[ASN][1000 genomes]
rs72683885	1.00[ASN][1000 genomes]
rs72683888	1.00[ASN][1000 genomes]
rs72683891	1.00[ASN][1000 genomes]
rs72683895	1.00[ASN][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	nsv879882	chr4:125662969-125703938	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 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	chr4:125668000-125672000	Weak transcription	Aorta	Aorta
2	chr4:125670000-125671000	Weak transcription	Fetal Lung	lung

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