Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12549995	0.85[EUR][1000 genomes]
rs1451856	0.87[EUR][1000 genomes]
rs1531657	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16929287	0.87[EUR][1000 genomes]
rs16929302	0.87[EUR][1000 genomes]
rs2127577	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2620876	0.87[EUR][1000 genomes]
rs2957797	0.85[EUR][1000 genomes]
rs4483149	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4738986	0.87[EUR][1000 genomes]
rs4738991	0.83[EUR][1000 genomes]
rs55651027	0.85[EUR][1000 genomes]
rs58103443	0.85[EUR][1000 genomes]
rs58261377	0.84[EUR][1000 genomes]
rs62509503	0.87[EUR][1000 genomes]
rs62509504	0.88[EUR][1000 genomes]
rs62509505	0.87[EUR][1000 genomes]
rs6985441	0.85[EUR][1000 genomes]
rs7812978	0.87[EUR][1000 genomes]
rs7840692	0.87[EUR][1000 genomes]
rs7844749	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs827683	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs827684	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs827687	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs862386	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs936614	0.88[EUR][1000 genomes]
rs936616	0.87[EUR][1000 genomes]
rs936618	0.87[EUR][1000 genomes]
rs936619	0.86[EUR][1000 genomes]
rs936620	1.00[EUR][1000 genomes]
rs961829	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831340	chr8:63515126-63702660	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv890960	chr8:63516962-63629549	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63517000-63521400	Weak transcription	Fetal Brain Female	brain
2	chr8:63517600-63519800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:63518400-63519600	Enhancers	Fetal Lung	lung
4	chr8:63518800-63519600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:63519000-63519600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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