Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10483294	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11623931	0.94[ASN][1000 genomes]
rs11628356	0.95[ASN][1000 genomes]
rs17185593	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17185677	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17185684	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17185691	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17185698	0.81[EUR][1000 genomes]
rs17185705	0.93[ASN][1000 genomes]
rs17257752	0.81[ASN][1000 genomes]
rs17257808	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17257836	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17257871	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17257878	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17257885	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17257892	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1952504	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1958389	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2007289	0.94[ASN][1000 genomes]
rs58640442	0.86[ASN][1000 genomes]
rs60783613	0.85[ASN][1000 genomes]
rs61502598	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7148029	0.94[ASN][1000 genomes]
rs7159074	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74039209	0.88[ASN][1000 genomes]
rs9743589	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901504	chr14:25184210-25646203	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv901509	chr14:25398571-25743484	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv901511	chr14:25505085-25588029	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25547000-25561600	Weak transcription	Pancreas	Pancrea
2	chr14:25547600-25551400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr14:25547800-25551200	Enhancers	Monocytes-CD14+_RO01746	blood

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