Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10510855	0.88[EUR][1000 genomes]
rs13088848	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1839068	0.92[EUR][1000 genomes]
rs1839069	0.87[EUR][1000 genomes]
rs1947159	0.90[EUR][1000 genomes]
rs1947160	0.90[EUR][1000 genomes]
rs2100152	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2142297	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2205354	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2223084	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2250114	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2594132	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2594136	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2736748	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2736750	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2736751	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2736752	0.98[EUR][1000 genomes]
rs2736753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs34696953	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35871234	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4974235	0.88[EUR][1000 genomes]
rs67917562	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv534038	chr3:60781917-60993082	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2757872	chr3:60781943-61019003	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2759152	chr3:60781943-61220809	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60811400-60821200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:60817600-60818800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr3:60817600-60819000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:60817600-60819000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:60818000-60819000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:60818200-60818800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:60818200-60819200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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