Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10131505	0.97[ASN][1000 genomes]
rs10132537	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10139559	0.88[ASN][1000 genomes]
rs12432538	0.92[ASN][1000 genomes]
rs12435170	0.83[ASN][1000 genomes]
rs12587047	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12587356	0.83[ASN][1000 genomes]
rs12589135	0.81[ASN][1000 genomes]
rs12590725	0.83[ASN][1000 genomes]
rs12887780	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12887904	0.97[ASN][1000 genomes]
rs17119380	0.84[ASN][1000 genomes]
rs17119453	0.85[ASN][1000 genomes]
rs1999279	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2183523	0.84[ASN][1000 genomes]
rs2210185	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34326388	0.84[ASN][1000 genomes]
rs4904151	0.84[ASN][1000 genomes]
rs6574764	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs71412380	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7142351	0.83[ASN][1000 genomes]
rs7153137	0.97[ASN][1000 genomes]
rs7155319	0.83[ASN][1000 genomes]
rs7161618	0.86[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs8007316	0.84[ASN][1000 genomes]
rs8022815	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs8022878	0.84[ASN][1000 genomes]
rs952821	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[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	nsv902159	chr14:84336944-84447356	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1039271	chr14:84405561-84467550	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84440600-84444200	Enhancers	Fetal Heart	heart
2	chr14:84441400-84443200	Enhancers	Fetal Lung	lung
3	chr14:84442000-84443400	Enhancers	HUVEC	blood vessel
4	chr14:84442200-84448000	Weak transcription	Stomach Mucosa	stomach
5	chr14:84443000-84446800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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