Variant report

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

rs_ID	r²[population]
rs2205453	0.84[ASN][1000 genomes]
rs2404032	0.84[ASN][1000 genomes]
rs2823528	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2823533	0.85[ASN][1000 genomes]
rs2823534	0.84[ASN][1000 genomes]
rs2823535	0.84[ASN][1000 genomes]
rs2823536	0.84[ASN][1000 genomes]
rs2823537	0.84[ASN][1000 genomes]
rs2823538	0.84[ASN][1000 genomes]
rs2823539	0.84[ASN][1000 genomes]
rs2823540	0.84[ASN][1000 genomes]
rs2823542	0.84[ASN][1000 genomes]
rs2823543	0.84[ASN][1000 genomes]
rs2896726	0.84[ASN][1000 genomes]
rs375736	0.92[ASN][1000 genomes]
rs387709	0.92[ASN][1000 genomes]
rs390503	0.84[ASN][1000 genomes]
rs412399	0.85[ASN][1000 genomes]
rs420519	0.84[ASN][1000 genomes]
rs422504	0.81[ASN][1000 genomes]
rs435166	0.84[ASN][1000 genomes]
rs727131	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7280084	0.93[EUR][1000 genomes];1.00[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	nsv1064664	chr21:17336936-17405756	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 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	chr21:17352600-17353600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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