Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs61739457	0.91[EUR][1000 genomes]
rs62511467	0.91[EUR][1000 genomes]
rs72661799	1.00[ASN][1000 genomes]
rs72663806	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs72663807	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72663809	1.00[ASN][1000 genomes]
rs72663811	1.00[ASN][1000 genomes]
rs72663816	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72663819	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72663820	1.00[ASN][1000 genomes]
rs72663825	1.00[ASN][1000 genomes]
rs72663828	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72663840	1.00[EUR][1000 genomes]
rs72663855	0.91[EUR][1000 genomes]
rs72663857	0.91[EUR][1000 genomes]
rs72663861	0.91[EUR][1000 genomes]
rs72663862	0.91[EUR][1000 genomes]
rs72663868	0.91[EUR][1000 genomes]
rs72663874	0.91[EUR][1000 genomes]
rs7838636	0.88[AFR][1000 genomes];1.00[ASN][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	nsv890967	chr8:64107847-64454446	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64363600-64364400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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