Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10139165	0.83[ASN][1000 genomes]
rs11627004	0.83[ASN][1000 genomes]
rs11627476	0.83[ASN][1000 genomes]
rs11628549	0.83[ASN][1000 genomes]
rs12147222	0.83[ASN][1000 genomes]
rs17835996	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1884631	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1950712	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2176255	0.83[ASN][1000 genomes]
rs2877522	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2877523	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3742905	0.83[ASN][1000 genomes]
rs3809393	0.83[ASN][1000 genomes]
rs55975366	0.83[ASN][1000 genomes]
rs56097892	0.83[ASN][1000 genomes]
rs56274826	0.83[ASN][1000 genomes]
rs56868917	0.83[ASN][1000 genomes]
rs60900044	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72718286	0.83[ASN][1000 genomes]
rs72718291	0.83[ASN][1000 genomes]
rs72718292	0.83[ASN][1000 genomes]
rs72720212	0.83[ASN][1000 genomes]
rs72720218	0.83[ASN][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	nsv832823	chr14:69388853-69567638	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr14:69473000-69503600	Weak transcription	Right Atrium	heart
2	chr14:69486000-69503600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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