Variant report

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10931252	0.81[ASN][1000 genomes]
rs10931254	0.83[ASN][1000 genomes]
rs10931256	0.86[EUR][1000 genomes]
rs1123176	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11678136	0.83[ASN][1000 genomes]
rs11679597	0.88[EUR][1000 genomes]
rs11683459	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11684356	0.81[ASN][1000 genomes]
rs11684434	0.83[ASN][1000 genomes]
rs11684626	0.83[ASN][1000 genomes]
rs11685506	0.88[EUR][1000 genomes]
rs11695399	0.83[ASN][1000 genomes]
rs11885414	0.81[ASN][1000 genomes]
rs11885416	0.81[ASN][1000 genomes]
rs11886619	0.81[ASN][1000 genomes]
rs11891192	0.81[ASN][1000 genomes]
rs11891461	0.81[ASN][1000 genomes]
rs11902171	0.81[ASN][1000 genomes]
rs12612335	0.83[ASN][1000 genomes]
rs12614008	0.81[ASN][1000 genomes]
rs12619357	0.81[ASN][1000 genomes]
rs12621915	0.83[ASN][1000 genomes]
rs16828175	0.81[ASN][1000 genomes]
rs16828182	0.83[ASN][1000 genomes]
rs16828214	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2887831	0.81[ASN][1000 genomes]
rs3886170	0.83[ASN][1000 genomes]
rs61764576	0.81[ASN][1000 genomes]
rs61764580	0.81[ASN][1000 genomes]
rs72905143	0.81[ASN][1000 genomes]
rs72905150	0.81[ASN][1000 genomes]
rs72905152	0.81[ASN][1000 genomes]
rs72905160	0.81[ASN][1000 genomes]
rs72905169	0.83[ASN][1000 genomes]
rs7584329	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];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	nsv428069	chr2:187575692-187766209	ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3495864	chr2:187633495-187686087	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv3495865	chr2:187633495-187686087	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	2 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	chr2:187637600-187643800	Weak transcription	Placenta	Placenta

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