Variant report

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

rs_ID	r²[population]
rs1008854	0.89[ASN][1000 genomes]
rs1030095	0.89[ASN][1000 genomes]
rs1030096	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13381024	0.93[ASN][1000 genomes]
rs1420956	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1420957	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1420958	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1420959	0.82[ASN][1000 genomes]
rs1420960	0.94[ASN][1000 genomes]
rs28550271	0.87[ASN][1000 genomes]
rs7236882	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7238941	0.81[ASN][1000 genomes]
rs8083861	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8091034	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8096529	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs8097226	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8099487	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9955609	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9958092	0.83[ASN][1000 genomes]
rs9960073	0.97[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	esv2761996	chr18:24866083-25818618	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 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	chr18:25185200-25195000	Weak transcription	H9 Cell Line	embryonic stem cell

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