Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1034167	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10733270	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10756496	0.81[EUR][1000 genomes]
rs10810035	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10961229	0.83[ASN][1000 genomes]
rs10961237	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1327513	0.81[EUR][1000 genomes]
rs1327514	0.86[EUR][1000 genomes]
rs1327517	0.85[AFR][1000 genomes]
rs1562044	0.88[EUR][1000 genomes]
rs1562046	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17218101	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17805200	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17805206	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2031759	0.89[EUR][1000 genomes]
rs4741332	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs966989	0.84[EUR][1000 genomes]
rs966990	0.84[EUR][1000 genomes]
rs966991	0.84[EUR][1000 genomes]
rs966992	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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
4	nsv1033764	chr9:13764918-14226168	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13758200-13787200	Weak transcription	Aorta	Aorta

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