Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1011530	0.89[ASN][1000 genomes]
rs1011531	0.81[ASN][1000 genomes]
rs1034167	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10733267	0.89[ASN][1000 genomes]
rs10733270	0.89[EUR][1000 genomes]
rs10756493	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10810020	0.81[ASN][1000 genomes]
rs10961237	0.81[EUR][1000 genomes]
rs11789440	0.91[ASN][1000 genomes]
rs1327510	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1327513	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1327514	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1562044	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1562046	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17805200	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17805206	0.85[EUR][1000 genomes]
rs2031759	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4514742	0.81[ASN][1000 genomes]
rs4741332	0.88[EUR][1000 genomes]
rs7021821	0.81[EUR][1000 genomes]
rs966989	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs966990	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs966991	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs966992	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[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	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

No data

Chromatin state (count:3 , 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
3	chr9:13762400-13763600	Enhancers	HSMMtube	muscle

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