Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:49130555..49133453-chr12:49139757..49141371,2	K562	blood:

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10783275	0.85[EUR][1000 genomes]
rs10783278	0.86[EUR][1000 genomes]
rs10875861	0.88[EUR][1000 genomes]
rs10875869	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10875870	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10875871	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1110432	0.81[EUR][1000 genomes]
rs11168713	0.85[ASN][1000 genomes]
rs11168714	0.84[ASN][1000 genomes]
rs12172773	0.80[ASN][1000 genomes]
rs12426435	0.81[EUR][1000 genomes]
rs12810920	0.97[ASN][1000 genomes]
rs1863541	0.81[EUR][1000 genomes]
rs2277366	0.86[EUR][1000 genomes]
rs2409085	0.81[EUR][1000 genomes]
rs2898087	0.81[EUR][1000 genomes]
rs3741629	0.81[EUR][1000 genomes]
rs3741630	0.86[EUR][1000 genomes]
rs3741632	0.87[EUR][1000 genomes]
rs3803025	0.87[EUR][1000 genomes]
rs3943899	0.81[EUR][1000 genomes]
rs4760740	0.86[EUR][1000 genomes]
rs6580690	0.81[EUR][1000 genomes]
rs6580693	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7138190	0.81[EUR][1000 genomes]
rs7299276	0.86[EUR][1000 genomes]
rs7305907	0.94[EUR][1000 genomes]
rs7306604	0.88[EUR][1000 genomes]
rs7308699	0.88[EUR][1000 genomes]
rs7314665	0.81[EUR][1000 genomes]
rs7954446	0.94[EUR][1000 genomes]
rs7964546	0.89[EUR][1000 genomes]
rs7966065	0.81[EUR][1000 genomes]
rs7974625	0.93[EUR][1000 genomes]
rs7975030	0.94[EUR][1000 genomes]
rs9634241	0.81[EUR][1000 genomes]
rs9634262	0.81[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	esv3332169	chr12:49005807-49150691	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 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	chr12:49133200-49133400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin

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