Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11148563	0.89[EUR][1000 genomes]
rs1538918	0.88[EUR][1000 genomes]
rs4551929	0.89[EUR][1000 genomes]
rs4884384	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4886346	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs5006270	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73213567	0.84[EUR][1000 genomes]
rs73492723	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7983113	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7999738	0.84[EUR][1000 genomes]
rs8002358	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs947025	0.89[EUR][1000 genomes]
rs9528358	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9528359	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9528360	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9528361	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9528383	0.89[EUR][1000 genomes]
rs9528384	0.89[EUR][1000 genomes]
rs9539244	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9539252	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9539253	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9539259	0.89[EUR][1000 genomes]
rs9539260	0.89[EUR][1000 genomes]
rs9539269	0.89[EUR][1000 genomes]
rs9539270	0.89[EUR][1000 genomes]
rs9539274	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948661	chr13:61906251-62179649	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2761266	chr13:61928642-62690828	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv948810	chr13:62003256-62968196	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1053698	chr13:62108064-62271909	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv900249	chr13:62133250-62218811	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv900250	chr13:62147535-62321073	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:62173600-62175200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:62173800-62175200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:62174400-62175800	Enhancers	Liver	Liver
4	chr13:62174600-62175000	Flanking Active TSS	Brain Substantia Nigra	brain
5	chr13:62174600-62175400	Enhancers	Brain Cingulate Gyrus	brain
6	chr13:62174800-62175400	Enhancers	Brain Angular Gyrus	brain
7	chr13:62174800-62175800	Enhancers	Brain Inferior Temporal Lobe	brain

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