Variant report

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

rs_ID	r²[population]
rs10834307	0.81[EUR][1000 genomes]
rs11027789	0.92[EUR][1000 genomes]
rs11827298	0.84[EUR][1000 genomes]
rs12277966	0.95[EUR][1000 genomes]
rs12279442	0.83[EUR][1000 genomes]
rs12282611	0.93[EUR][1000 genomes]
rs12293105	0.80[EUR][1000 genomes]
rs12786638	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12801480	0.81[EUR][1000 genomes]
rs1899540	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2068454	0.80[EUR][1000 genomes]
rs2083753	0.80[EUR][1000 genomes]
rs2099889	0.80[EUR][1000 genomes]
rs59246618	0.84[EUR][1000 genomes]
rs59797575	0.84[EUR][1000 genomes]
rs6484040	0.84[EUR][1000 genomes]
rs7104550	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7104694	0.81[EUR][1000 genomes]
rs7107321	0.92[EUR][1000 genomes]
rs7114960	0.85[EUR][1000 genomes]
rs7123539	0.93[EUR][1000 genomes]
rs7124856	0.83[EUR][1000 genomes]
rs7126291	0.84[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	nsv1055026	chr11:24151133-24737122	Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1037744	chr11:24174588-24737122	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv897083	chr11:24210635-24346093	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv897086	chr11:24261507-24356464	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv7711	chr11:24332449-24358933	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24340400-24342400	Weak transcription	Fetal Heart	heart

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