Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10954039	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11766249	1.00[ASN][1000 genomes]
rs11769918	1.00[ASN][1000 genomes]
rs12530505	1.00[ASN][1000 genomes]
rs12536432	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12539308	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13228582	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13232332	1.00[ASN][1000 genomes]
rs13236030	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404409	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17147221	1.00[ASN][1000 genomes]
rs1917364	1.00[ASN][1000 genomes]
rs2402738	1.00[ASN][1000 genomes]
rs34000854	1.00[ASN][1000 genomes]
rs34799484	1.00[ASN][1000 genomes]
rs35966180	1.00[ASN][1000 genomes]
rs36008540	1.00[ASN][1000 genomes]
rs4532546	1.00[ASN][1000 genomes]
rs4731184	1.00[ASN][1000 genomes]
rs4731185	1.00[ASN][1000 genomes]
rs66469910	1.00[ASN][1000 genomes]
rs6962872	1.00[ASN][1000 genomes]
rs71576208	1.00[ASN][1000 genomes]
rs9768851	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1795113	chr7:123885477-124188665	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv429809	chr7:123937674-124835925	Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
3	esv1808414	chr7:123957376-124188665	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv525687	chr7:124138187-124196444	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv608340	chr7:124138187-124196444	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 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	chr7:124165800-124166400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr7:124166200-124166400	Enhancers	Pancreas	Pancrea

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