Variant report

Variant	rs9526832
Chromosome Location	chr13:52664205-52664206
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs11616964	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11620583	0.81[EUR][1000 genomes]
rs12584961	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12585654	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs1886542	0.89[ASN][1000 genomes]
rs1886547	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1924611	0.81[EUR][1000 genomes]
rs1998696	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2004866	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2274202	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2296348	0.89[ASN][1000 genomes]
rs2296349	0.89[ASN][1000 genomes]
rs2296350	0.89[ASN][1000 genomes]
rs2408544	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2408549	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2408550	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2408551	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2408609	0.88[ASN][1000 genomes]
rs2408611	0.89[ASN][1000 genomes]
rs28393037	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2897976	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2897977	0.89[ASN][1000 genomes]
rs3368	0.89[ASN][1000 genomes]
rs35895576	0.85[ASN][1000 genomes]
rs3825528	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4297592	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55772266	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61958812	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6650383	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs723102	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs723103	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7327634	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7337430	0.85[ASN][1000 genomes]
rs755363	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7994928	0.81[EUR][1000 genomes]
rs7995946	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9316563	0.81[EUR][1000 genomes]
rs9526819	0.81[EUR][1000 genomes]
rs9526821	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9526837	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9526842	0.87[ASN][1000 genomes]
rs9535817	0.81[EUR][1000 genomes]
rs9535819	0.81[EUR][1000 genomes]
rs9535822	0.80[EUR][1000 genomes]
rs9535823	0.81[EUR][1000 genomes]
rs9535826	0.81[EUR][1000 genomes]
rs9535828	0.83[EUR][1000 genomes]
rs9535829	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9535833	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9535836	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9535849	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9535851	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9535858	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9535860	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9535862	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9535866	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9535872	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9535878	0.88[ASN][1000 genomes]
rs9535879	0.89[ASN][1000 genomes]
rs9535880	0.89[ASN][1000 genomes]
rs9535882	0.82[ASN][1000 genomes]
rs9535885	0.86[ASN][1000 genomes]
rs9535887	0.87[ASN][1000 genomes]
rs9563084	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9563089	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9563091	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9563093	0.87[ASN][1000 genomes]
rs9568693	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9568695	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9568708	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9568713	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530718	chr13:52291802-52832752	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	nsv900082	chr13:52555288-52709938	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1040931	chr13:52564792-53350914	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv541773	chr13:52564792-53350914	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv1037567	chr13:52643647-52802799	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9526832	NEK3	Cis_1M	lymphoblastoid	RTeQTL
rs9526832	CKAP2	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52664000-52664800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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