Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11158920	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11158921	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12433721	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12434220	0.81[ASN][1000 genomes]
rs12897929	0.86[ASN][1000 genomes]
rs17093750	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17104493	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2067856	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2159457	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2238277	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2238280	0.91[ASN][1000 genomes]
rs2877771	0.82[ASN][1000 genomes]
rs34729701	0.82[ASN][1000 genomes]
rs35051666	0.82[ASN][1000 genomes]
rs35858041	0.82[ASN][1000 genomes]
rs3784058	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4899409	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4902958	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56067914	0.86[ASN][1000 genomes]
rs56743778	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72734102	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72735921	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72735923	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs728497	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7493353	0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[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	esv3398985	chr14:71927884-72404676	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1345	chr14:72349589-72395819	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr14:72386200-72396800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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