Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10491762	0.81[EUR][1000 genomes]
rs10733272	0.81[EUR][1000 genomes]
rs10738347	0.95[EUR][1000 genomes]
rs10738348	0.88[EUR][1000 genomes]
rs10756495	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10756502	0.94[EUR][1000 genomes]
rs10756506	0.88[EUR][1000 genomes]
rs10756512	0.81[EUR][1000 genomes]
rs10810016	0.82[AMR][1000 genomes]
rs10810024	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10810028	0.92[EUR][1000 genomes]
rs10961227	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10961228	0.94[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs10961232	0.96[EUR][1000 genomes]
rs10961234	0.94[EUR][1000 genomes]
rs10961243	0.88[EUR][1000 genomes]
rs12378052	0.94[EUR][1000 genomes]
rs12555747	0.86[AMR][1000 genomes]
rs12555754	0.86[AMR][1000 genomes]
rs17216585	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17217956	0.88[EUR][1000 genomes]
rs17217996	0.88[EUR][1000 genomes]
rs55871307	0.95[EUR][1000 genomes]
rs62533246	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62534674	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62534675	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7024746	0.89[EUR][1000 genomes]
rs72711965	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs745034	0.89[EUR][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	nsv892590	chr9:13689066-13777299	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1022001	chr9:13717736-13983738	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv892591	chr9:13763734-13828594	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	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	chr9:13758200-13787200	Weak transcription	Aorta	Aorta
2	chr9:13760000-13764600	Weak transcription	Fetal Muscle Leg	muscle

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