Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:212813403..212814994-chr2:212815054..212816566,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12997949	0.90[ASN][1000 genomes]
rs12998591	0.81[ASN][1000 genomes]
rs13025703	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16847207	0.84[ASN][1000 genomes]
rs16847218	0.85[ASN][1000 genomes]
rs16847357	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17414925	0.88[ASN][1000 genomes]
rs2139936	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2579980	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs34306926	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3452	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34765931	0.81[ASN][1000 genomes]
rs57175680	0.85[ASN][1000 genomes]
rs67565187	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs839509	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs839511	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs839516	0.85[AFR][1000 genomes]
rs839519	0.92[AFR][1000 genomes]
rs839525	0.96[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs839526	0.96[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs839527	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs839528	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs839530	0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs839536	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs839540	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv834525	chr2:212693190-212860356	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212806800-212816400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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