Variant report

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10135604	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10136394	0.84[EUR][1000 genomes]
rs10146465	0.84[EUR][1000 genomes]
rs10146659	0.83[EUR][1000 genomes]
rs10146748	0.83[EUR][1000 genomes]
rs10147245	0.84[EUR][1000 genomes]
rs10149210	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11159469	0.86[EUR][1000 genomes]
rs12587285	0.97[ASN][1000 genomes]
rs12878113	0.85[ASN][1000 genomes]
rs12881248	0.85[ASN][1000 genomes]
rs12889844	0.86[EUR][1000 genomes]
rs17110851	0.87[ASN][1000 genomes]
rs17110854	0.88[ASN][1000 genomes]
rs17110955	0.84[EUR][1000 genomes]
rs34019777	1.00[ASN][1000 genomes]
rs34481438	0.83[ASN][1000 genomes]
rs34489190	0.97[ASN][1000 genomes]
rs34946091	0.98[ASN][1000 genomes]
rs35038680	0.97[ASN][1000 genomes]
rs35426127	0.98[ASN][1000 genomes]
rs35505520	0.88[ASN][1000 genomes]
rs35930082	0.97[ASN][1000 genomes]
rs55670336	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs56256007	0.85[ASN][1000 genomes]
rs61981704	0.97[ASN][1000 genomes]
rs61981706	0.91[ASN][1000 genomes]
rs67116258	0.97[ASN][1000 genomes]
rs7144224	0.80[ASN][1000 genomes]
rs7160749	0.85[EUR][1000 genomes]
rs8008043	0.85[EUR][1000 genomes]
rs8010347	0.85[EUR][1000 genomes]
rs8016151	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8017175	0.85[ASN][1000 genomes]
rs9323688	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv902116	chr14:81018237-81082400	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island 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	chr14:81052400-81070000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr14:81054400-81061400	Weak transcription	Dnd41	blood

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