Variant report

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10828832	0.84[AMR][1000 genomes]
rs11014611	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs11014627	0.90[CHB][hapmap];0.89[ASN][1000 genomes]
rs12251283	0.89[ASN][1000 genomes]
rs12259380	0.89[ASN][1000 genomes]
rs12770280	0.89[ASN][1000 genomes]
rs12773640	0.87[ASN][1000 genomes]
rs12780774	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs1335198	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs16926123	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs16926129	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs16926165	0.82[JPT][hapmap]
rs17556478	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs17557021	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs34136900	0.89[ASN][1000 genomes]
rs34165831	0.87[ASN][1000 genomes]
rs34178991	0.89[ASN][1000 genomes]
rs34372366	0.89[ASN][1000 genomes]
rs34495386	0.89[ASN][1000 genomes]
rs34703667	0.87[ASN][1000 genomes]
rs34832714	0.88[EUR][1000 genomes]
rs35387923	0.89[ASN][1000 genomes]
rs35600435	0.90[ASN][1000 genomes]
rs4145858	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs4747531	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59110794	0.96[ASN][1000 genomes]
rs61400980	0.87[ASN][1000 genomes]
rs6482495	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs71495469	0.88[ASN][1000 genomes]
rs71495470	0.96[ASN][1000 genomes]
rs72790307	0.96[ASN][1000 genomes]
rs72796333	0.87[ASN][1000 genomes]
rs9645526	0.88[EUR][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	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv550227	chr10:25843019-25865744	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv894972	chr10:25849998-25917909	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	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	chr10:25861600-25873800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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