Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:47717481..47720198-chr12:47722159..47724714,2	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11183848	0.85[EUR][1000 genomes]
rs11183850	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11183851	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11183852	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11183853	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11183854	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11183855	0.86[EUR][1000 genomes]
rs11183856	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11183857	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11183858	0.86[EUR][1000 genomes]
rs12228428	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12230585	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34187987	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35521464	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35839210	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs36059508	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs71462954	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs71462955	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs71462956	0.85[AMR][1000 genomes]
rs71462957	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs71462958	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs71462959	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs71462961	0.85[AMR][1000 genomes];0.80[EUR][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	esv2751100	chr12:47541390-47746157	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 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	chr12:47709200-47727000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:47717800-47722600	Weak transcription	Primary T helper cells PMA-I stimulated	--

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