Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10134393	1.00[EUR][1000 genomes]
rs10136631	1.00[EUR][1000 genomes]
rs10136758	1.00[EUR][1000 genomes]
rs10138344	1.00[EUR][1000 genomes]
rs10141914	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10144184	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11846239	1.00[EUR][1000 genomes]
rs11848194	1.00[EUR][1000 genomes]
rs11850212	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11850250	1.00[EUR][1000 genomes]
rs12100761	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs140614	1.00[EUR][1000 genomes]
rs17121021	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951394	1.00[EUR][1000 genomes]
rs2182631	1.00[EUR][1000 genomes]
rs28402332	1.00[EUR][1000 genomes]
rs28680491	1.00[EUR][1000 genomes]
rs28706922	1.00[EUR][1000 genomes]
rs28729624	1.00[EUR][1000 genomes]
rs28833867	1.00[EUR][1000 genomes]
rs28871975	1.00[EUR][1000 genomes]
rs58358811	1.00[EUR][1000 genomes]
rs59459881	1.00[EUR][1000 genomes]
rs6574815	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8022920	1.00[EUR][1000 genomes]
rs9323756	1.00[EUR][1000 genomes]
rs9972170	1.00[EUR][1000 genomes]
rs9972174	1.00[EUR][1000 genomes]
rs9972265	1.00[EUR][1000 genomes]

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	nsv1047924	chr14:85826280-85868228	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85825200-85829800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:85828800-85830200	Enhancers	Fetal Lung	lung
3	chr14:85829600-85830600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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