Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10429635	0.87[ASN][1000 genomes]
rs10817520	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10981921	0.88[ASN][1000 genomes]
rs10981922	0.91[ASN][1000 genomes]
rs10981924	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10981925	0.85[ASN][1000 genomes]
rs10981941	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10981978	0.91[ASN][1000 genomes]
rs10981981	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12376085	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12380621	0.86[ASN][1000 genomes]
rs12380863	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12555454	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1409382	0.87[ASN][1000 genomes]
rs59045685	0.86[EUR][1000 genomes]
rs7030996	0.86[EUR][1000 genomes]
rs7031010	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7035099	0.93[ASN][1000 genomes]
rs913080	0.85[EUR][1000 genomes]
rs949527	0.82[EUR][1000 genomes]
rs987073	0.91[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	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	esv1275147	chr9:116586362-116586363	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116585000-116590800	Weak transcription	Aorta	Aorta
2	chr9:116586000-116586400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:116586200-116590400	Weak transcription	NH-A	brain

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