Variant report

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

rs_ID	r²[population]
rs11226747	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1124519	1.00[ASN][1000 genomes]
rs12271813	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12273491	1.00[ASN][1000 genomes]
rs12276410	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12277176	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12277602	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12279551	1.00[ASN][1000 genomes]
rs12292447	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12294105	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12294519	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1945982	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59105307	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61168136	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7125192	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7129250	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73633675	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73633691	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73633692	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73634420	1.00[ASN][1000 genomes]
rs7936745	1.00[ASN][1000 genomes]
rs9988915	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949337	chr11:104950007-105510193	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv556221	chr11:105243371-105392079	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105328800-105333000	Weak transcription	Placenta	Placenta
2	chr11:105329000-105332600	Weak transcription	K562	blood

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