Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12630095	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs12634284	0.85[EUR][1000 genomes]
rs12639049	0.84[EUR][1000 genomes]
rs4128734	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4234330	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4296566	0.84[EUR][1000 genomes]
rs4345047	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4679836	0.84[CEU][hapmap]
rs4679837	0.96[CEU][hapmap];0.84[EUR][1000 genomes]
rs4680465	0.85[CEU][hapmap]
rs4680468	0.84[EUR][1000 genomes]
rs6440748	0.80[EUR][1000 genomes]
rs6440763	0.89[EUR][1000 genomes]
rs6789915	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6798066	0.89[CEU][hapmap]
rs6805953	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7375135	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7427979	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7629867	0.86[EUR][1000 genomes]
rs7629912	0.84[EUR][1000 genomes]
rs7631395	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7636304	0.89[EUR][1000 genomes]
rs7637619	0.89[EUR][1000 genomes]
rs7647576	0.90[EUR][1000 genomes]
rs9680970	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9817125	0.85[CEU][hapmap];0.83[YRI][hapmap]
rs9836445	0.80[EUR][1000 genomes]
rs9849929	0.85[CEU][hapmap];0.83[YRI][hapmap]
rs9869975	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9883254	0.85[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	nsv1000355	chr3:151108859-151243835	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv995048	chr3:151114074-151560019	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv877650	chr3:151174010-151314449	Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 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	chr3:151219000-151252400	Weak transcription	Ovary	ovary

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