Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11217980	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11217987	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11217988	0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12270409	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12273984	0.83[EUR][1000 genomes]
rs12274300	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12276408	0.98[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12276440	0.80[AMR][1000 genomes]
rs12281464	0.82[AMR][1000 genomes]
rs12281614	0.84[AMR][1000 genomes]
rs12294858	0.84[AMR][1000 genomes]
rs17124211	0.97[ASN][1000 genomes]
rs28781001	0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4567478	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61901362	0.83[EUR][1000 genomes]
rs61901368	0.81[EUR][1000 genomes]
rs61901379	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61901380	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61902685	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7103021	0.94[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7103418	0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7119619	0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7946325	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9630199	0.80[AMR][1000 genomes]
rs9630200	0.80[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	nsv1054407	chr11:120535570-120630114	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1053607	chr11:120540795-120802006	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3693392	chr11:120549745-120628012	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	Chromatin interactive region	3 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	chr11:120561600-120569200	Weak transcription	Spleen	Spleen
2	chr11:120566600-120568000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr11:120567200-120570400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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