Variant report

Variant	rs7694769
Chromosome Location	chr4:82258475-82258476
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10013788	0.94[EUR][1000 genomes]
rs10017744	0.96[ASN][1000 genomes]
rs10021462	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10028610	0.94[EUR][1000 genomes]
rs11727754	0.96[ASN][1000 genomes]
rs11731567	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11732090	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11732106	0.94[EUR][1000 genomes]
rs11733845	0.92[EUR][1000 genomes]
rs11736471	0.94[EUR][1000 genomes]
rs11939135	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11942269	0.92[EUR][1000 genomes]
rs12332030	0.94[EUR][1000 genomes]
rs13435660	0.89[ASN][1000 genomes]
rs1377059	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1443542	0.84[EUR][1000 genomes]
rs1452364	0.92[EUR][1000 genomes]
rs1452366	0.87[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1551236	0.96[EUR][1000 genomes]
rs17428097	0.94[EUR][1000 genomes]
rs17499131	0.92[EUR][1000 genomes]
rs1993160	0.93[ASN][1000 genomes]
rs2034630	0.91[EUR][1000 genomes]
rs2041461	0.91[ASN][1000 genomes]
rs2058367	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4693234	0.94[EUR][1000 genomes]
rs62303573	0.86[EUR][1000 genomes]
rs6535243	0.91[ASN][1000 genomes]
rs6814785	0.96[ASN][1000 genomes]
rs6819909	0.96[ASN][1000 genomes]
rs6821450	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6831114	0.91[EUR][1000 genomes]
rs6853731	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7654102	0.93[ASN][1000 genomes]
rs7664953	0.96[ASN][1000 genomes]
rs7669131	0.95[ASN][1000 genomes]
rs7673578	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7677239	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7680637	0.94[EUR][1000 genomes]
rs7685645	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829985	chr4:82199328-82353656	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7694769	PRKG2	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:82258400-82258800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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