Variant report

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

rs_ID	r²[population]
rs10797073	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10908789	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1138323	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12144628	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12402879	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12728784	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12736781	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1572382	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1998651	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2025516	0.82[ASN][1000 genomes]
rs2025517	0.82[ASN][1000 genomes]
rs2099604	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3816146	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4106115	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6660233	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6668760	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6692382	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7515302	0.93[ASN][1000 genomes]
rs7528976	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7534679	0.81[EUR][1000 genomes]
rs9726326	0.90[EUR][1000 genomes]
rs977019	0.87[AMR][1000 genomes];0.81[EUR][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	esv1829614	chr1:160465291-160595000	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv872491	chr1:160470258-160580549	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv831703	chr1:160496124-160643024	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6656191	CD84	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160500400-160502600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr1:160501200-160501800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:160501200-160502000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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