Variant report

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

rs_ID	r²[population]
rs1033599	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1033600	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12434204	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12894028	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1950445	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1950446	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1950447	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1950448	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1950450	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1951072	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1955878	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1955880	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1955882	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2207566	0.92[EUR][1000 genomes]
rs28676371	0.92[EUR][1000 genomes]
rs4981599	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7152181	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8018144	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs926911	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs995973	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][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	nsv430993	chr14:25976760-26097160	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv564073	chr14:26030013-26057695	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
3	nsv427937	chr14:26038386-26405118	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:26044800-26046600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr14:26045000-26046600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr14:26045200-26046200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr14:26045200-26046600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr14:26045400-26046400	Enhancers	H9 Cell Line	embryonic stem cell
6	chr14:26045400-26046400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:26045600-26046600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr14:26046000-26046600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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