Variant report

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

rs_ID	r²[population]
rs17090704	1.00[ASN][1000 genomes]
rs17090707	1.00[ASN][1000 genomes]
rs17090711	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17090717	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17090721	0.82[ASN][1000 genomes]
rs17090729	0.84[ASN][1000 genomes]
rs17090731	0.84[ASN][1000 genomes]
rs17090732	0.84[ASN][1000 genomes]
rs17090736	0.85[ASN][1000 genomes]
rs4269978	0.84[ASN][1000 genomes]
rs57228232	0.87[ASN][1000 genomes]
rs57549882	1.00[ASN][1000 genomes]
rs58347456	0.83[ASN][1000 genomes]
rs59005597	1.00[ASN][1000 genomes]
rs59659255	0.84[ASN][1000 genomes]
rs59853785	1.00[ASN][1000 genomes]
rs60085326	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61162180	1.00[ASN][1000 genomes]
rs61560666	1.00[ASN][1000 genomes]
rs73272813	1.00[AMR][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	nsv899043	chr12:42058138-42313665	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv899044	chr12:42058138-42321161	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1047870	chr12:42158954-42254373	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
4	nsv1041975	chr12:42159517-42254373	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases
5	nsv1037646	chr12:42160758-42254373	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
6	esv3449289	chr12:42207677-42207941	ZNF genes & repeats	n/a	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	chr12:42207600-42208800	ZNF genes & repeats	Aorta	Aorta

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