Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11706532	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13062883	0.87[CEU][hapmap]
rs13063680	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13069920	0.87[CEU][hapmap]
rs13070168	0.93[CEU][hapmap]
rs13070615	0.93[CEU][hapmap]
rs13070956	0.87[CEU][hapmap]
rs13077031	0.93[CEU][hapmap]
rs13077745	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13078030	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13079647	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13085088	0.93[CEU][hapmap]
rs13086539	0.87[CEU][hapmap]
rs13086617	0.87[CEU][hapmap]
rs13093003	0.83[CEU][hapmap];0.82[MEX][hapmap];0.83[TSI][hapmap];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13099875	0.87[CEU][hapmap]
rs1499053	0.87[CEU][hapmap]
rs2167144	1.00[CEU][hapmap]
rs6441048	0.82[CEU][hapmap]
rs66901908	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6770125	0.87[CEU][hapmap]
rs71623492	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7641186	0.83[CEU][hapmap];0.82[MEX][hapmap];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv592085	chr3:155827634-156012679	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1014755	chr3:155889430-156411894	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs13081735	SHOX2	cis	cerebellum	SCAN
rs13081735	GFM1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155983400-155993000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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