Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1735700	0.84[ASN][1000 genomes]
rs2205454	0.92[ASN][1000 genomes]
rs2823522	0.89[ASN][1000 genomes]
rs2823524	0.94[ASN][1000 genomes]
rs366592	0.81[ASN][1000 genomes]
rs373182	0.90[ASN][1000 genomes]
rs380087	0.81[ASN][1000 genomes]
rs413785	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs416719	0.97[ASN][1000 genomes]
rs419509	0.93[ASN][1000 genomes]
rs420590	0.94[ASN][1000 genomes]
rs433085	0.84[ASN][1000 genomes]
rs435947	1.00[ASN][1000 genomes]
rs443745	0.93[ASN][1000 genomes]
rs444390	0.94[ASN][1000 genomes]
rs446216	0.84[ASN][1000 genomes]
rs68109293	0.90[ASN][1000 genomes]
rs7348985	0.90[ASN][1000 genomes]
rs9978096	0.88[ASN][1000 genomes]
rs9984156	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834050	chr21:17146090-17348951	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
2	nsv3463	chr21:17327119-17343458	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	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
rs425252	RBM11	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17341600-17344400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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