Variant report

Variant	rs58368336
Chromosome Location	chr21:47111351-47111352
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1029014	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12151963	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12483018	0.82[EUR][1000 genomes]
rs12483701	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1467758	0.90[EUR][1000 genomes]
rs17004799	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1964928	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1989537	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2150460	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2183601	0.92[EUR][1000 genomes]
rs2838973	0.91[EUR][1000 genomes]
rs2838974	0.91[EUR][1000 genomes]
rs2838976	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2838978	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2838981	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2838982	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2838983	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2838985	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2838988	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28625750	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28692915	0.80[EUR][1000 genomes]
rs3920695	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4347938	0.89[EUR][1000 genomes]
rs4434082	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4818795	0.93[EUR][1000 genomes]
rs4818797	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4819144	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55912508	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55923134	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55957843	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56213918	0.89[EUR][1000 genomes]
rs56288252	0.89[EUR][1000 genomes]
rs56300316	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57057834	0.85[EUR][1000 genomes]
rs57282159	0.85[EUR][1000 genomes]
rs57328058	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57501220	0.90[EUR][1000 genomes]
rs57990579	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58925015	0.94[EUR][1000 genomes]
rs60988006	0.85[EUR][1000 genomes]
rs61329313	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62213277	0.90[EUR][1000 genomes]
rs62215031	0.89[EUR][1000 genomes]
rs62215035	0.90[EUR][1000 genomes]
rs62215040	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62215047	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62215048	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs67565220	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs725358	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7279909	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7280560	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7283803	0.89[EUR][1000 genomes]
rs7410008	0.85[EUR][1000 genomes]
rs744506	0.84[EUR][1000 genomes]
rs767137	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8133966	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9306139	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9637169	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9647229	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9975404	0.85[EUR][1000 genomes]
rs9976200	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9976878	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9978158	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9978882	0.83[EUR][1000 genomes]
rs9981586	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531546	chr21:46504151-47411772	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
2	nsv1058665	chr21:46719445-47634282	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
3	nsv544486	chr21:46719445-47634282	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
4	nsv1059230	chr21:46956877-47907990	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	n/a
5	nsv544491	chr21:46956877-47907990	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	n/a
6	nsv1058472	chr21:47027823-47797326	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	n/a
7	nsv544492	chr21:47027823-47797326	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	n/a
8	nsv1063957	chr21:47090475-47168291	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
9	nsv1056995	chr21:47094147-47120504	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
10	nsv1062702	chr21:47095762-47169369	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
11	nsv544493	chr21:47095762-47169369	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs58368336	PCBP3	cis	Heart Left Ventricle	GTEx
rs58368336	PCBP3	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47102600-47138400	Weak transcription	Fetal Thymus	thymus

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