Variant report

No.	Distal block	Cell Line	Cell type
1	chr11:76768870..76771269-chr11:76778034..76779779,2	MCF-7	breast:
2	chr11:76766352..76769639-chr11:76770714..76773550,3	MCF-7	breast:
3	chr11:76762598..76764948-chr11:76767540..76770402,2	K562	blood:

Variant related genes	Relation type
ENSG00000149260	Chromatin interaction

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10899348	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11237065	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11237072	0.83[EUR][1000 genomes]
rs11600516	0.99[ASN][1000 genomes]
rs11602496	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11603853	0.90[ASN][1000 genomes]
rs11607153	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12362167	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12422079	0.94[ASN][1000 genomes]
rs12794060	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56695052	0.90[ASN][1000 genomes]
rs58520141	0.95[ASN][1000 genomes]
rs61617479	0.93[ASN][1000 genomes]
rs61902094	0.95[ASN][1000 genomes]
rs61902097	0.95[ASN][1000 genomes]
rs61902099	0.99[ASN][1000 genomes]
rs61902104	0.93[ASN][1000 genomes]
rs72931522	0.93[ASN][1000 genomes]
rs7482827	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7925199	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7949146	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];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	esv1816632	chr11:76751285-76927014	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76765000-76770800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr11:76769000-76769400	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr11:76769000-76770000	Enhancers	Liver	Liver
4	chr11:76769200-76769400	Enhancers	Colonic Mucosa	Colon

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