Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs16990117	1.00[EUR][1000 genomes]
rs16990578	1.00[EUR][1000 genomes]
rs16990828	1.00[EUR][1000 genomes]
rs16992521	1.00[EUR][1000 genomes]
rs16992557	1.00[EUR][1000 genomes]
rs16992628	1.00[EUR][1000 genomes]
rs366082	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs392028	1.00[EUR][1000 genomes]
rs56141957	1.00[EUR][1000 genomes]
rs58289432	1.00[EUR][1000 genomes]
rs58297914	1.00[EUR][1000 genomes]
rs59169113	1.00[EUR][1000 genomes]
rs73346759	1.00[EUR][1000 genomes]
rs73892584	1.00[EUR][1000 genomes]
rs73892585	1.00[EUR][1000 genomes]
rs73892591	1.00[EUR][1000 genomes]
rs73892592	1.00[EUR][1000 genomes]
rs73892593	1.00[EUR][1000 genomes]
rs73892594	1.00[EUR][1000 genomes]
rs73892598	1.00[EUR][1000 genomes]
rs73892601	1.00[EUR][1000 genomes]
rs73894705	1.00[EUR][1000 genomes]
rs73894706	1.00[EUR][1000 genomes]
rs73894707	1.00[EUR][1000 genomes]
rs73894709	1.00[EUR][1000 genomes]
rs73894710	1.00[EUR][1000 genomes]
rs764003	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	nsv1064664	chr21:17336936-17405756	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs367091	MEIS2	trans	lymphoblastoid	seeQTL

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17376600-17380400	Weak transcription	Osteobl	bone

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