Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10195421	0.82[CHB][hapmap]
rs12612816	0.84[ASN][1000 genomes]
rs12615814	0.83[ASN][1000 genomes]
rs1524215	0.94[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap]
rs365027	0.89[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs371016	0.84[ASN][1000 genomes]
rs375530	0.84[ASN][1000 genomes]
rs379749	0.83[ASN][1000 genomes]
rs380810	0.84[ASN][1000 genomes]
rs384304	0.84[ASN][1000 genomes]
rs389616	0.84[ASN][1000 genomes]
rs390189	0.84[ASN][1000 genomes]
rs390652	0.84[ASN][1000 genomes]
rs390687	0.84[ASN][1000 genomes]
rs394278	0.84[ASN][1000 genomes]
rs397424	0.84[ASN][1000 genomes]
rs403631	0.84[ASN][1000 genomes]
rs410367	0.84[ASN][1000 genomes]
rs410954	0.84[ASN][1000 genomes]
rs416093	0.84[ASN][1000 genomes]
rs416264	0.84[ASN][1000 genomes]
rs421884	0.85[ASN][1000 genomes]
rs422600	0.84[ASN][1000 genomes]
rs432117	0.84[ASN][1000 genomes]
rs454793	0.84[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834265	chr2:76275611-76450728	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:76302600-76307400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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