Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1606174	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1606176	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1849162	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1877259	0.97[EUR][1000 genomes]
rs28630725	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6440448	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs6440449	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs6802568	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6810372	0.83[EUR][1000 genomes]
rs7629838	0.80[AFR][1000 genomes]
rs7629881	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs7650609	0.83[EUR][1000 genomes]
rs7651782	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs7651979	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs966226	0.82[EUR][1000 genomes]
rs9818011	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9831186	0.95[EUR][1000 genomes]
rs9835908	0.85[EUR][1000 genomes]
rs9836760	0.84[EUR][1000 genomes]
rs9846527	0.87[EUR][1000 genomes]
rs9856645	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9870986	0.81[EUR][1000 genomes]
rs9871947	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs9872768	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs994052	0.84[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs994053	0.85[AFR][1000 genomes];0.86[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	nsv516386	chr3:146366513-146758405	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv591961	chr3:146394094-146725217	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1007875	chr3:146401461-146776618	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146403800-146410000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:146409600-146422000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:146409800-146410400	ZNF genes & repeats	Dnd41	blood

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