Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10118592	0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10810055	0.87[AFR][1000 genomes]
rs10810057	0.89[CEU][hapmap];0.82[MEX][hapmap]
rs10961296	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs10961303	0.88[YRI][hapmap]
rs12002277	0.81[AFR][1000 genomes]
rs12343481	0.82[AMR][1000 genomes]
rs12344771	0.83[AMR][1000 genomes]
rs12350449	0.80[AMR][1000 genomes]
rs1359846	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17822351	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1822541	0.86[CHB][hapmap];0.85[YRI][hapmap];0.81[AMR][1000 genomes]
rs1969938	0.83[AMR][1000 genomes]
rs1969940	0.83[AMR][1000 genomes]
rs4548276	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7023760	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7023898	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7024597	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7027511	0.82[AFR][1000 genomes]
rs7029494	0.89[YRI][hapmap]
rs7031343	0.83[AMR][1000 genomes]
rs7035288	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7851375	0.91[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs981564	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9886719	0.86[AFR][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	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	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
3	nsv1032113	chr9:13861066-13923136	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1032447	chr9:13861066-13923673	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 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	chr9:13863400-13884200	Weak transcription	Left Ventricle	heart
2	chr9:13880400-13880800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr9:13880600-13899800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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