Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12184886	1.00[ASN][1000 genomes]
rs12427687	0.84[ASN][1000 genomes]
rs12428034	0.84[ASN][1000 genomes]
rs12428181	0.91[ASN][1000 genomes]
rs12429060	1.00[ASN][1000 genomes]
rs17059609	0.96[ASN][1000 genomes]
rs17059622	0.96[ASN][1000 genomes]
rs2181759	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2324253	0.96[ASN][1000 genomes]
rs4640054	0.85[ASN][1000 genomes]
rs56183908	0.85[ASN][1000 genomes]
rs58005196	0.85[ASN][1000 genomes]
rs58551847	0.96[ASN][1000 genomes]
rs59329722	0.96[ASN][1000 genomes]
rs7322559	0.85[ASN][1000 genomes]
rs7330251	1.00[ASN][1000 genomes]
rs7332991	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7334522	0.81[ASN][1000 genomes]
rs73467356	0.85[ASN][1000 genomes]
rs73467371	0.85[ASN][1000 genomes]
rs74044032	0.85[ASN][1000 genomes]
rs8001763	0.85[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	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1036674	chr13:39841482-40008117	Bivalent Enhancer Genic enhancers Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	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	chr13:39868800-39881000	Weak transcription	Aorta	Aorta

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