Variant report

Variant	rs9535861
Chromosome Location	chr13:52663491-52663492
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 115 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs1004576	0.81[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.97[LWK][hapmap];0.95[MEX][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1055062	0.91[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs1060631	0.91[CHB][hapmap];0.85[JPT][hapmap];0.83[YRI][hapmap];0.82[ASN][1000 genomes]
rs1134727	0.83[ASN][1000 genomes]
rs12146904	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.83[YRI][hapmap];0.84[ASN][1000 genomes]
rs12431310	0.90[CHB][hapmap];0.90[JPT][hapmap];0.81[YRI][hapmap];0.84[ASN][1000 genomes]
rs12560598	0.81[ASN][1000 genomes]
rs1571189	0.91[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs1801243	0.82[CHB][hapmap]
rs1886538	0.82[CHB][hapmap];0.81[CHD][hapmap];0.82[MEX][hapmap]
rs1886539	0.82[ASN][1000 genomes]
rs1886542	0.82[CHB][hapmap]
rs1886543	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.87[LWK][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1886544	0.91[CHB][hapmap];0.85[JPT][hapmap];0.95[YRI][hapmap];0.84[ASN][1000 genomes]
rs1886545	0.82[ASN][1000 genomes]
rs1886546	0.82[ASN][1000 genomes]
rs1886547	0.82[CHB][hapmap]
rs2004866	0.82[CHB][hapmap]
rs2005182	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2181891	0.82[CHB][hapmap]
rs2274202	0.82[CHB][hapmap]
rs2277448	0.91[CHB][hapmap];0.85[JPT][hapmap];0.80[ASN][1000 genomes]
rs2296347	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.95[YRI][hapmap];0.82[ASN][1000 genomes]
rs2296348	0.82[CHB][hapmap]
rs2296349	0.82[CHB][hapmap]
rs2408544	0.82[CHB][hapmap]
rs2408546	0.85[ASN][1000 genomes]
rs2408547	0.86[ASN][1000 genomes]
rs2408548	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2408550	0.82[CHB][hapmap]
rs2408551	0.82[CHB][hapmap]
rs2408552	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2408554	0.81[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.84[JPT][hapmap];0.91[MEX][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2408609	0.82[CHB][hapmap]
rs2408611	0.82[CHB][hapmap]
rs2897964	0.95[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.86[MEX][hapmap];0.82[ASN][1000 genomes]
rs2897965	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2897977	0.82[CHB][hapmap]
rs3368	0.82[CHB][hapmap]
rs3742289	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.86[MEX][hapmap];0.82[ASN][1000 genomes]
rs3742291	0.82[ASN][1000 genomes]
rs3783242	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.90[LWK][hapmap];0.95[YRI][hapmap];0.83[ASN][1000 genomes]
rs3818422	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.90[LWK][hapmap];0.95[YRI][hapmap];0.83[ASN][1000 genomes]
rs4261421	0.85[ASN][1000 genomes]
rs4264295	0.85[ASN][1000 genomes]
rs4297592	0.82[CHB][hapmap]
rs4497567	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap]
rs4941727	0.80[ASW][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap];0.82[LWK][hapmap];0.93[MKK][hapmap];0.88[ASN][1000 genomes]
rs4943060	0.80[ASN][1000 genomes]
rs61958804	0.82[ASN][1000 genomes]
rs61958805	0.80[ASN][1000 genomes]
rs6561656	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.86[MEX][hapmap];0.80[ASN][1000 genomes]
rs6650384	0.86[ASN][1000 genomes]
rs6650385	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs66849828	0.88[ASN][1000 genomes]
rs7318287	0.85[ASN][1000 genomes]
rs7319784	0.80[ASN][1000 genomes]
rs7320252	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7320429	0.86[ASN][1000 genomes]
rs732071	0.82[CHB][hapmap];0.82[MEX][hapmap]
rs7320831	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.86[MEX][hapmap];0.80[ASN][1000 genomes]
rs7321120	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.86[MEX][hapmap];0.83[YRI][hapmap];0.80[ASN][1000 genomes]
rs7321310	0.80[ASN][1000 genomes]
rs7321435	0.82[CHB][hapmap];0.81[CHD][hapmap];0.82[MEX][hapmap]
rs7324458	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.95[YRI][hapmap];0.84[ASN][1000 genomes]
rs7327634	0.82[CHB][hapmap]
rs7332356	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7338131	0.86[ASN][1000 genomes]
rs747781	0.82[CHB][hapmap]
rs755363	0.82[CHB][hapmap]
rs7981904	0.92[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap]
rs7991237	0.82[CHB][hapmap]
rs7995946	0.82[CHB][hapmap]
rs7998770	0.81[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.91[MEX][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9526823	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.86[MEX][hapmap];0.82[ASN][1000 genomes]
rs9526825	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs9526826	0.86[ASN][1000 genomes]
rs9526834	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9526835	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9526836	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9526837	0.82[CHB][hapmap]
rs9526841	0.91[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs9526842	0.82[CHB][hapmap]
rs9526843	0.82[ASN][1000 genomes]
rs9535812	0.82[CHB][hapmap]
rs9535825	0.92[CEU][hapmap];0.82[CHB][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.82[TSI][hapmap]
rs9535832	0.82[CHB][hapmap]
rs9535836	0.82[CHB][hapmap]
rs9535845	0.86[ASN][1000 genomes]
rs9535851	0.82[CHB][hapmap]
rs9535853	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9535856	0.82[CHB][hapmap]
rs9535858	0.82[CHB][hapmap]
rs9535862	0.82[CHB][hapmap]
rs9535866	0.82[CHB][hapmap]
rs9535867	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.86[MEX][hapmap];0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9535871	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9535873	0.81[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.97[LWK][hapmap];0.95[MEX][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9535878	0.82[CHB][hapmap]
rs9535879	0.81[CHB][hapmap]
rs9535880	0.82[CHB][hapmap]
rs9535882	0.82[CHB][hapmap]
rs9535883	0.84[ASN][1000 genomes]
rs9535887	0.82[CHB][hapmap]
rs9535888	0.81[ASN][1000 genomes]
rs9563089	0.82[CHB][hapmap]
rs9568682	0.82[CHB][hapmap];0.81[CHD][hapmap];0.82[MEX][hapmap]
rs9568692	0.86[ASN][1000 genomes]
rs9568713	0.82[CHB][hapmap]

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:4)

SNP	Gene	Cis/trans	Tissue	Source
rs9535861	CKAP2	cis	parietal	SCAN
rs9535861	ALG11	cis	parietal	SCAN
rs9535861	ALG11	cis	cerebellum	SCAN
rs9535861	CKAP2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52661200-52663800	Enhancers	HepG2	liver
2	chr13:52661400-52663600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:52663400-52663800	Enhancers	Adipose Nuclei	Adipose

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