Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1106843	0.88[EUR][1000 genomes]
rs12713473	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13410732	0.83[EUR][1000 genomes]
rs219515	0.88[EUR][1000 genomes]
rs219516	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs219518	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs219519	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs219520	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs219521	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs219522	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs219525	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2338022	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2879094	0.91[AMR][1000 genomes]
rs4504022	0.93[AMR][1000 genomes]
rs6752495	0.91[AMR][1000 genomes]
rs7558805	0.93[AMR][1000 genomes]
rs7584918	0.93[AMR][1000 genomes]
rs7601920	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7603669	0.93[AMR][1000 genomes]
rs7608111	0.91[AMR][1000 genomes]
rs892459	0.83[EUR][1000 genomes]
rs9677096	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9679011	0.93[AMR][1000 genomes];0.83[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	nsv1011486	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv535602	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv455863	chr2:21547003-21615340	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv581170	chr2:21547003-21615340	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv528844	chr2:21587225-21605003	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21582000-21634600	Weak transcription	Aorta	Aorta
2	chr2:21591000-21593200	Enhancers	Brain Germinal Matrix	brain
3	chr2:21592400-21593000	Enhancers	Placenta Amnion	Placenta Amnion

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