Variant report

Variant	rs2706910
Chromosome Location	chr7:84071654-84071655
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1014498	0.87[EUR][1000 genomes]
rs1029538	0.87[EUR][1000 genomes]
rs1228861	0.84[ASN][1000 genomes]
rs1228877	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1228881	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1228897	0.87[EUR][1000 genomes]
rs1228899	0.87[EUR][1000 genomes]
rs1228900	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1228901	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1228902	0.81[EUR][1000 genomes]
rs1228903	0.81[EUR][1000 genomes]
rs1228904	0.86[EUR][1000 genomes]
rs1228905	0.86[EUR][1000 genomes]
rs1228907	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs1228908	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1228910	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs1228911	0.89[EUR][1000 genomes]
rs1228914	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1228917	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1228918	0.87[EUR][1000 genomes]
rs1228920	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1228921	0.87[EUR][1000 genomes]
rs1228924	0.87[EUR][1000 genomes]
rs1228925	0.87[EUR][1000 genomes]
rs1228926	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1228928	0.87[EUR][1000 genomes]
rs1228932	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1228941	0.87[EUR][1000 genomes]
rs1228955	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1228957	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1228962	0.83[EUR][1000 genomes]
rs1228964	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1228967	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1228968	0.87[EUR][1000 genomes]
rs1228969	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs1228971	0.84[EUR][1000 genomes]
rs1228972	0.80[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1228973	0.80[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1228974	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1228975	0.81[EUR][1000 genomes]
rs1228977	0.87[EUR][1000 genomes]
rs1228978	0.87[EUR][1000 genomes]
rs1235296	0.92[CEU][hapmap];0.92[YRI][hapmap];0.86[EUR][1000 genomes]
rs1520106	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1634611	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1734000	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2158168	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2527524	0.87[EUR][1000 genomes]
rs2715035	0.99[ASN][1000 genomes]
rs2715041	0.97[ASN][1000 genomes]
rs2905620	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs622514	0.82[EUR][1000 genomes]
rs6947440	0.89[ASN][1000 genomes]
rs71558728	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84068200-84076400	Weak transcription	Fetal Muscle Leg	muscle

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