Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:27393165..27395076-chr7:27476139..27478551,2	K562	blood:
2	chr7:27476223..27478695-chr7:27480805..27482916,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10242634	0.93[ASN][1000 genomes]
rs10252511	0.97[ASN][1000 genomes]
rs10252636	0.85[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10268623	0.83[ASN][1000 genomes]
rs10269160	0.96[ASN][1000 genomes]
rs10272561	0.91[ASN][1000 genomes]
rs10276795	0.97[ASN][1000 genomes]
rs1112620	0.97[ASN][1000 genomes]
rs11763775	0.83[ASN][1000 genomes]
rs12540319	0.91[ASN][1000 genomes]
rs1524522	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1989910	0.84[ASN][1000 genomes]
rs2074340	0.96[ASN][1000 genomes]
rs2074341	0.91[ASN][1000 genomes]
rs28418930	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs28625460	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3915086	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3915089	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs4141138	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs4722699	0.83[AMR][1000 genomes]
rs4722700	0.92[ASN][1000 genomes]
rs4722702	0.88[ASN][1000 genomes]
rs4722706	0.92[ASN][1000 genomes]
rs4722707	0.97[ASN][1000 genomes]
rs56843699	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62454789	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs62454790	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs6953785	0.91[ASN][1000 genomes]
rs757141	0.84[ASN][1000 genomes]
rs9691111	0.84[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	nsv830930	chr7:27395838-27587355	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr7:27475800-27481600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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