Variant report

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

rs_ID	r²[population]
rs10025761	0.81[ASN][1000 genomes]
rs10033566	0.81[ASN][1000 genomes]
rs1026824	0.86[EUR][1000 genomes]
rs10518510	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1155135	0.91[AFR][1000 genomes]
rs11937459	0.87[AFR][1000 genomes]
rs12499978	0.81[ASN][1000 genomes]
rs12503648	0.81[ASN][1000 genomes]
rs12507660	0.81[ASN][1000 genomes]
rs12509041	0.81[ASN][1000 genomes]
rs12649107	0.96[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs1471556	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1480898	0.81[ASN][1000 genomes]
rs1531684	0.91[AFR][1000 genomes]
rs17291532	0.81[ASN][1000 genomes]
rs1871737	0.81[ASN][1000 genomes]
rs1871738	0.81[ASN][1000 genomes]
rs2054560	0.85[AFR][1000 genomes]
rs2127817	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2127818	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2170268	0.91[AFR][1000 genomes]
rs7659822	0.81[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	nsv879914	chr4:128005362-128123638	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:128104600-128105400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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