Variant report

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

rs_ID	r²[population]
rs1014959	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10197925	0.83[ASN][1000 genomes]
rs10432495	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11890128	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11900132	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12693384	0.83[ASN][1000 genomes]
rs13393273	0.83[ASN][1000 genomes]
rs13405270	0.80[ASN][1000 genomes]
rs16826057	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2052794	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs359892	0.83[ASN][1000 genomes]
rs4366862	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55782979	0.87[ASN][1000 genomes]
rs60269985	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73041376	0.92[EUR][1000 genomes]
rs73041379	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73043234	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73043238	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7608194	0.82[ASN][1000 genomes]
rs7608284	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532412	chr2:185347334-186108701	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	esv1818452	chr2:185428946-185503154	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:185466000-185479800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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