Variant report

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

rs_ID	r²[population]
rs11622704	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1188164	0.96[ASN][1000 genomes]
rs1188165	0.90[ASN][1000 genomes]
rs1188167	0.92[ASN][1000 genomes]
rs1188168	0.92[ASN][1000 genomes]
rs1188169	0.90[ASN][1000 genomes]
rs1188170	0.93[ASN][1000 genomes]
rs1188171	0.97[ASN][1000 genomes]
rs1188172	0.97[ASN][1000 genomes]
rs1188173	0.93[ASN][1000 genomes]
rs1188177	0.93[ASN][1000 genomes]
rs1188178	0.97[ASN][1000 genomes]
rs1188182	0.93[ASN][1000 genomes]
rs1188183	0.93[ASN][1000 genomes]
rs1188189	0.81[ASN][1000 genomes]
rs1188195	0.81[ASN][1000 genomes]
rs1188201	0.82[ASN][1000 genomes]
rs1188202	0.87[ASN][1000 genomes]
rs1188205	0.95[ASN][1000 genomes]
rs966880	0.91[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	nsv901977	chr14:56213392-56492996	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv34106	chr14:56346245-56550642	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56439200-56451200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:56444800-56449200	Weak transcription	Ovary	ovary

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