Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs16918927	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16929168	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16929206	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16929308	1.00[EUR][1000 genomes]
rs16929351	1.00[EUR][1000 genomes]
rs16929371	1.00[EUR][1000 genomes]
rs16929390	1.00[EUR][1000 genomes]
rs16929430	1.00[EUR][1000 genomes]
rs16929437	1.00[EUR][1000 genomes]
rs2101043	1.00[EUR][1000 genomes]
rs2101044	1.00[EUR][1000 genomes]
rs2127581	1.00[EUR][1000 genomes]
rs57900808	1.00[EUR][1000 genomes]
rs58391948	1.00[EUR][1000 genomes]
rs58717549	1.00[EUR][1000 genomes]
rs60709086	1.00[EUR][1000 genomes]
rs6993807	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73256928	1.00[EUR][1000 genomes]
rs73256936	1.00[EUR][1000 genomes]
rs73264897	1.00[EUR][1000 genomes]
rs73266909	1.00[EUR][1000 genomes]
rs73266967	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv890959	chr8:63449156-63515522	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 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	chr8:63510600-63512400	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:63511800-63512400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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