Variant report

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

rs_ID	r²[population]
rs13153590	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13155466	0.94[CEU][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13159849	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13161951	0.82[EUR][1000 genomes]
rs13168948	0.82[AMR][1000 genomes]
rs13172980	0.81[EUR][1000 genomes]
rs13172989	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13173486	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13177210	0.89[AMR][1000 genomes]
rs13177823	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13178121	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13178468	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13181295	0.93[CEU][hapmap];0.89[AMR][1000 genomes]
rs13181945	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13186099	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13188220	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34035147	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34104982	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34625696	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34881925	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35908078	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62365914	0.91[AMR][1000 genomes];0.89[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	nsv948807	chr5:79549207-79805765	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv518480	chr5:79586085-79748382	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 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	chr5:79638600-79648000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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