Variant report

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

rs_ID	r²[population]
rs10138951	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11620910	0.91[EUR][1000 genomes]
rs11623496	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs11624616	0.94[EUR][1000 genomes]
rs17110868	0.91[EUR][1000 genomes]
rs57289554	0.90[EUR][1000 genomes]
rs57315708	0.87[EUR][1000 genomes]
rs57759210	0.92[EUR][1000 genomes]
rs61391568	1.00[EUR][1000 genomes]
rs6574591	0.94[EUR][1000 genomes]
rs7155869	0.87[AMR][1000 genomes]
rs7156847	0.94[EUR][1000 genomes]
rs7157244	0.94[EUR][1000 genomes]
rs7159335	0.94[EUR][1000 genomes]
rs73328690	0.87[EUR][1000 genomes]
rs8008286	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8008763	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8014976	0.94[EUR][1000 genomes]
rs8016841	0.91[EUR][1000 genomes]
rs8017020	0.94[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	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	chr14:81062200-81082200	Weak transcription	Dnd41	blood

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