Variant report

Variant	rs2715037
Chromosome Location	chr7:84095680-84095681
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1011990	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1228866	0.87[ASN][1000 genomes]
rs1228868	0.87[ASN][1000 genomes]
rs1228946	0.96[ASN][1000 genomes]
rs1228951	0.88[ASN][1000 genomes]
rs1228956	0.88[ASN][1000 genomes]
rs12673388	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1520102	0.89[ASN][1000 genomes]
rs1634605	0.89[ASN][1000 genomes]
rs16887703	0.83[ASN][1000 genomes]
rs1715518	0.89[ASN][1000 genomes]
rs17158998	0.83[ASN][1000 genomes]
rs17159006	0.87[ASN][1000 genomes]
rs1922349	0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2214749	0.89[ASN][1000 genomes]
rs2428807	0.88[ASN][1000 genomes]
rs2527527	0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2527529	0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2527530	0.99[ASN][1000 genomes]
rs2527532	0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2527533	0.92[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2527535	0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2527536	0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2527537	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2527538	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2706903	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2706912	0.89[ASN][1000 genomes]
rs2706913	0.89[ASN][1000 genomes]
rs2706916	0.83[ASN][1000 genomes]
rs2715032	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2715044	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2715045	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2715046	0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2715047	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2888322	0.87[ASN][1000 genomes]
rs520178	0.86[ASN][1000 genomes]
rs526991	0.85[ASN][1000 genomes]
rs529539	0.83[ASN][1000 genomes]
rs530698	0.87[ASN][1000 genomes]
rs531582	0.87[ASN][1000 genomes]
rs555632	0.81[ASN][1000 genomes]
rs559041	0.87[ASN][1000 genomes]
rs56038965	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56144625	0.87[ASN][1000 genomes]
rs561955	0.87[ASN][1000 genomes]
rs625480	0.87[ASN][1000 genomes]
rs73711542	0.84[ASN][1000 genomes]
rs73711549	0.86[ASN][1000 genomes]
rs7783073	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	esv2754468	chr7:83851249-84166749	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1023848	chr7:83985028-84101774	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2761342	chr7:83985028-84101798	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv534431	chr7:84001059-84138511	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv1034270	chr7:84068277-84101774	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv888634	chr7:84086502-84196258	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv888635	chr7:84086502-84344258	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	esv1796198	chr7:84086924-84097423	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84093600-84096400	Strong transcription	NHDF-Ad	bronchial
2	chr7:84094400-84101600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr7:84095600-84100000	Weak transcription	Adipose Nuclei	Adipose

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