Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10014366	0.83[ASN][1000 genomes]
rs10213414	0.95[ASN][1000 genomes]
rs11934703	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12645768	0.96[ASN][1000 genomes]
rs13435788	0.94[ASN][1000 genomes]
rs17725979	0.88[ASN][1000 genomes]
rs2051709	0.83[ASN][1000 genomes]
rs2520490	0.84[ASN][1000 genomes]
rs2520492	0.88[ASN][1000 genomes]
rs4287984	0.89[ASN][1000 genomes]
rs4355370	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4449392	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4455396	0.90[ASN][1000 genomes]
rs4485801	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4532218	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4616731	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4835555	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67046168	0.81[ASN][1000 genomes]
rs6832649	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6851434	0.90[ASN][1000 genomes]
rs764005	0.81[ASN][1000 genomes]
rs7668770	0.96[ASN][1000 genomes]
rs7673586	0.96[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	nsv4544	chr4:149979800-150026323	Weak transcription Enhancers Flanking Active TSS	TF binding region 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	chr4:149994200-149994400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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