Variant report

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

rs_ID	r²[population]
rs11916622	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11923030	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1389658	0.83[AFR][1000 genomes]
rs17011233	0.85[AFR][1000 genomes]
rs17011245	0.87[AFR][1000 genomes]
rs57865745	0.94[EUR][1000 genomes]
rs66607699	0.88[EUR][1000 genomes]
rs66747516	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66986313	0.88[EUR][1000 genomes]
rs67227208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73039270	0.94[EUR][1000 genomes]
rs73039276	0.94[EUR][1000 genomes]
rs73041314	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73041322	1.00[EUR][1000 genomes]
rs73041330	1.00[EUR][1000 genomes]
rs73140289	0.95[AFR][1000 genomes]
rs73142203	0.88[AFR][1000 genomes]
rs73142210	0.88[AFR][1000 genomes]
rs73142213	0.88[AFR][1000 genomes]
rs73144148	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003085	chr3:21887971-22415107	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv432404	chr3:22000296-22433396	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1003211	chr3:22244883-22584229	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv536520	chr3:22244883-22584229	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr3:22387400-22389200	Enhancers	Fetal Lung	lung

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