Variant report

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

rs_ID	r²[population]
rs1149456	0.89[EUR][1000 genomes]
rs1149457	0.89[EUR][1000 genomes]
rs1149470	0.87[EUR][1000 genomes]
rs1149471	0.89[EUR][1000 genomes]
rs1149472	0.88[EUR][1000 genomes]
rs1149473	0.87[EUR][1000 genomes]
rs1149474	0.89[EUR][1000 genomes]
rs1149475	0.88[EUR][1000 genomes]
rs1217098	0.84[EUR][1000 genomes]
rs1217099	0.84[EUR][1000 genomes]
rs1217107	0.88[EUR][1000 genomes]
rs1217108	0.88[EUR][1000 genomes]
rs1217109	0.88[EUR][1000 genomes]
rs1217110	0.90[EUR][1000 genomes]
rs1238050	0.89[EUR][1000 genomes]
rs751769	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs790563	0.89[EUR][1000 genomes]
rs790565	0.84[EUR][1000 genomes]
rs790566	0.83[EUR][1000 genomes]
rs790571	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs966294	0.86[EUR][1000 genomes]
rs978336	0.89[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	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr8:64561000-64569200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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