Variant report

Variant	rs6831114
Chromosome Location	chr4:82205016-82205017
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10013788	0.87[EUR][1000 genomes]
rs10021462	0.88[EUR][1000 genomes]
rs10028610	0.87[EUR][1000 genomes]
rs11099465	0.93[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11732090	0.90[EUR][1000 genomes]
rs11732106	0.87[EUR][1000 genomes]
rs11733845	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11736471	0.87[EUR][1000 genomes]
rs11942269	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12332030	0.87[EUR][1000 genomes]
rs1349641	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1377059	0.91[EUR][1000 genomes]
rs1443542	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1443543	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1452364	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1452366	0.92[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1452367	0.83[AMR][1000 genomes]
rs1551236	0.89[EUR][1000 genomes]
rs1662845	0.85[ASN][1000 genomes]
rs1712387	0.84[ASN][1000 genomes]
rs17428097	0.87[EUR][1000 genomes]
rs17499131	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2034628	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2034630	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2159656	0.83[AMR][1000 genomes]
rs3114135	1.00[JPT][hapmap]
rs4693234	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4693996	0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4694006	0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs62303573	0.80[EUR][1000 genomes]
rs6535242	0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6821450	0.90[EUR][1000 genomes]
rs6839968	0.87[CHB][hapmap];0.91[JPT][hapmap];0.85[AMR][1000 genomes]
rs6853731	0.90[EUR][1000 genomes]
rs73829540	0.83[AFR][1000 genomes]
rs7680637	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7681976	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7685645	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7694769	0.91[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
rs6831114	PRKG2	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:82199600-82208200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:82204000-82210600	Weak transcription	Fetal Intestine Large	intestine
3	chr4:82204200-82205200	Weak transcription	Fetal Intestine Small	intestine

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