Variant report

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

rs_ID	r²[population]
rs12432505	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12437092	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17110796	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17110799	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17110803	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17110880	0.94[AFR][1000 genomes]
rs17530332	0.84[EUR][1000 genomes]
rs2122429	0.92[AFR][1000 genomes]
rs56341421	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58877537	0.88[AMR][1000 genomes]
rs66523873	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7160951	0.94[AFR][1000 genomes]
rs72689053	0.88[AMR][1000 genomes]
rs72689058	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs72689070	0.96[AFR][1000 genomes]
rs72689071	0.94[AFR][1000 genomes]
rs72689095	0.94[AFR][1000 genomes]
rs8008191	0.84[AFR][1000 genomes]
rs8017017	0.94[AFR][1000 genomes]
rs8017133	0.89[AFR][1000 genomes]
rs8017609	0.92[AFR][1000 genomes]
rs8017722	0.94[AFR][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	chr14:81021800-81025400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:81024800-81029400	Weak transcription	Dnd41	blood

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