Variant report

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

rs_ID	r²[population]
rs16918904	0.87[AMR][1000 genomes]
rs16918906	0.81[AMR][1000 genomes]
rs16928235	0.87[AMR][1000 genomes]
rs16928320	0.87[AMR][1000 genomes]
rs16928330	0.87[AMR][1000 genomes]
rs60322521	0.87[AMR][1000 genomes]
rs61214522	0.86[EUR][1000 genomes]
rs72662689	0.87[AMR][1000 genomes]
rs72664004	0.87[AMR][1000 genomes]
rs72664043	0.87[AMR][1000 genomes]
rs72664091	0.93[AMR][1000 genomes]
rs72664097	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs72666306	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666307	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666308	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666309	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666310	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666317	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666319	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666321	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666340	0.86[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890955	chr8:62919691-63062581	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63032400-63034000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr8:63032400-63034600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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