Variant report

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

rs_ID	r²[population]
rs10002735	0.83[AMR][1000 genomes]
rs10021306	0.83[AMR][1000 genomes]
rs10025080	0.83[AMR][1000 genomes]
rs10033262	0.93[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11934767	0.83[AMR][1000 genomes]
rs11939350	0.83[AMR][1000 genomes]
rs11943657	0.83[AMR][1000 genomes]
rs1398832	1.00[ASW][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1513571	0.85[YRI][hapmap]
rs16871966	0.83[YRI][hapmap];0.83[AMR][1000 genomes]
rs1849541	0.80[YRI][hapmap];0.83[AMR][1000 genomes]
rs1870450	0.91[AMR][1000 genomes]
rs28379252	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28452597	0.83[AMR][1000 genomes]
rs28475189	0.83[AMR][1000 genomes]
rs28547323	0.83[AMR][1000 genomes]
rs28578495	0.91[AMR][1000 genomes]
rs28676618	0.83[AMR][1000 genomes]
rs28754425	0.83[AMR][1000 genomes]
rs55842595	0.83[AMR][1000 genomes]
rs56191003	0.84[AFR][1000 genomes]
rs6827460	0.83[AMR][1000 genomes]
rs6833077	0.83[AMR][1000 genomes]
rs73105917	0.83[AMR][1000 genomes]
rs73108038	0.83[AMR][1000 genomes]
rs7664829	0.83[AMR][1000 genomes]
rs7681022	0.83[AMR][1000 genomes]
rs7695914	0.83[AMR][1000 genomes]
rs9991759	0.83[AMR][1000 genomes]
rs9999185	0.83[AMR][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	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv4269	chr4:21761429-21806056	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1005221	chr4:21786702-21822000	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21803800-21806000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:21804600-21805600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:21805000-21813200	Weak transcription	HSMMtube	muscle

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