Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11233878	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11233885	0.97[EUR][1000 genomes]
rs11233886	0.98[EUR][1000 genomes]
rs11233887	0.98[EUR][1000 genomes]
rs11233888	0.98[EUR][1000 genomes]
rs11233889	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11233891	0.98[EUR][1000 genomes]
rs11233892	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12274345	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12275051	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12275529	0.98[EUR][1000 genomes]
rs12282675	1.00[EUR][1000 genomes]
rs12286025	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12286565	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12289688	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12290311	0.97[EUR][1000 genomes]
rs12294547	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12295053	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12575693	0.95[EUR][1000 genomes]
rs1483410	0.88[EUR][1000 genomes]
rs2514164	0.87[AFR][1000 genomes]
rs28673785	0.90[EUR][1000 genomes]
rs4433587	0.89[EUR][1000 genomes]
rs56209818	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7115622	0.89[EUR][1000 genomes]
rs73513704	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7932501	0.94[EUR][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	nsv898025	chr11:83658909-83796678	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv898026	chr11:83685801-83789540	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83683800-83692000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:83687600-83693000	Weak transcription	Brain Angular Gyrus	brain
3	chr11:83688400-83692000	Weak transcription	Brain Anterior Caudate	brain
4	chr11:83689800-83692200	Enhancers	Fetal Heart	heart
5	chr11:83690400-83691400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:83690400-83691600	Enhancers	Brain Hippocampus Middle	brain
7	chr11:83690600-83691400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr11:83690600-83691600	Enhancers	Brain Cingulate Gyrus	brain
9	chr11:83690600-83692200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr11:83690600-83692200	Enhancers	Brain Substantia Nigra	brain

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