Variant report

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

rs_ID	r²[population]
rs10005522	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10020135	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10471032	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11098913	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12331820	1.00[EUR][1000 genomes]
rs1480912	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28366863	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28378521	1.00[AFR][1000 genomes]
rs28432794	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28434627	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28452137	1.00[EUR][1000 genomes]
rs28473454	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28479022	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28485376	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28546828	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28552074	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28562660	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28587364	1.00[EUR][1000 genomes]
rs28726160	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28758907	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4289455	1.00[EUR][1000 genomes]
rs9992427	1.00[EUR][1000 genomes]
rs9998369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128018800-128023200	Weak transcription	Fetal Lung	lung
2	chr4:128019000-128024200	Weak transcription	Fetal Brain Male	brain

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