Variant report

Variant	rs10733272
Chromosome Location	chr9:13779792-13779793
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10491762	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10738347	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10738348	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10756502	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10756504	0.89[ASN][1000 genomes]
rs10756506	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10756508	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10756512	0.86[EUR][1000 genomes]
rs10810028	0.80[ASN][1000 genomes]
rs10810034	0.82[ASN][1000 genomes]
rs10961228	0.81[EUR][1000 genomes]
rs10961232	0.80[EUR][1000 genomes]
rs10961234	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10961243	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11789856	0.81[EUR][1000 genomes]
rs12115484	0.82[EUR][1000 genomes]
rs12235162	0.86[ASN][1000 genomes]
rs12376678	0.86[ASN][1000 genomes]
rs12378052	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17217956	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17217996	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2382412	0.82[EUR][1000 genomes]
rs2382413	0.82[EUR][1000 genomes]
rs2382414	0.82[EUR][1000 genomes]
rs2890972	0.82[EUR][1000 genomes]
rs2890973	0.82[EUR][1000 genomes]
rs55871307	0.84[ASN][1000 genomes]
rs62534678	0.86[ASN][1000 genomes]
rs7024746	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs745034	0.85[ASN][1000 genomes]
rs7857269	0.87[ASN][1000 genomes]
rs9632882	0.83[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	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
2	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
3	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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13758200-13787200	Weak transcription	Aorta	Aorta
2	chr9:13778200-13779800	Enhancers	Fetal Heart	heart
3	chr9:13779000-13791600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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