Variant report

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

rs_ID	r²[population]
rs1168566	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17107987	0.99[EUR][1000 genomes]
rs17107995	1.00[EUR][1000 genomes]
rs1815594	0.83[EUR][1000 genomes]
rs1815595	0.83[EUR][1000 genomes]
rs2415478	1.00[EUR][1000 genomes]
rs2899873	0.83[EUR][1000 genomes]
rs4390500	0.83[EUR][1000 genomes]
rs4570744	0.89[EUR][1000 genomes]
rs60658845	0.95[EUR][1000 genomes]
rs61486868	0.82[EUR][1000 genomes]
rs6650500	0.83[EUR][1000 genomes]
rs67146678	1.00[EUR][1000 genomes]
rs67402173	0.89[EUR][1000 genomes]
rs67712964	1.00[EUR][1000 genomes]
rs7157738	1.00[EUR][1000 genomes]
rs7159353	1.00[EUR][1000 genomes]
rs72683076	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72685131	0.95[EUR][1000 genomes]
rs8017551	0.89[EUR][1000 genomes]
rs8020485	0.83[EUR][1000 genomes]
rs913734	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs913735	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533235	chr14:38558180-39117391	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv530640	chr14:38702117-38927901	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv2754119	chr14:38825349-38988849	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv1846932	chr14:38842788-38944821	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv510632	chr14:38868313-38939927	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv564409	chr14:38870456-38930054	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38878800-38889000	Weak transcription	Aorta	Aorta

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