Variant report

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

rs_ID	r²[population]
rs10019246	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10024499	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1117139	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1119120	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1393574	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1502751	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1502752	0.90[ASN][1000 genomes]
rs1502753	0.90[ASN][1000 genomes]
rs1827464	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1847200	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2202201	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2348415	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4323062	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4690954	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4691580	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4691583	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4691592	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62337306	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6845535	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6852879	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7655576	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs990180	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][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	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv881205	chr4:160516090-160628006	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160535800-160536800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:160536200-160537400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:160536400-160537000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
4	chr4:160536400-160537000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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