Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11737790	0.84[AMR][1000 genomes]
rs12374391	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13119094	0.82[YRI][hapmap]
rs1587736	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17363983	0.86[AMR][1000 genomes]
rs1910423	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2389919	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs34021877	0.92[AMR][1000 genomes]
rs34463615	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs35229169	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4834817	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs62319692	0.87[AMR][1000 genomes]
rs6534157	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs67101952	0.85[AMR][1000 genomes]
rs6822154	0.88[AMR][1000 genomes]
rs6822164	0.88[AMR][1000 genomes]
rs6856110	0.81[ASN][1000 genomes]
rs6856904	0.88[AMR][1000 genomes]
rs6858155	0.84[AMR][1000 genomes]
rs72682879	0.83[AMR][1000 genomes]
rs7657393	0.81[JPT][hapmap];0.82[YRI][hapmap]

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	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1818167	FLJ14186///LOC284701///LOC441124///LOC728624	Cis_chr	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120758600-120794000	Weak transcription	Aorta	Aorta

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