Variant report

Variant	rs4726875
Chromosome Location	chr7:147185337-147185338
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10236878	0.82[JPT][hapmap]
rs10242834	0.88[ASW][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs10245926	0.82[JPT][hapmap];0.95[YRI][hapmap]
rs10259368	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10266867	0.82[JPT][hapmap]
rs10282302	0.82[JPT][hapmap]
rs11976387	0.95[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11982152	0.82[JPT][hapmap]
rs11982446	0.86[CEU][hapmap]
rs12111800	0.82[JPT][hapmap]
rs12112731	0.82[JPT][hapmap]
rs12113038	0.82[JPT][hapmap]
rs1404699	0.87[MEX][hapmap]
rs1525218	0.84[GIH][hapmap];0.87[MEX][hapmap];0.80[TSI][hapmap]
rs1528507	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1528519	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1528521	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1534553	0.93[YRI][hapmap];0.82[AFR][1000 genomes]
rs1542566	0.82[MEX][hapmap]
rs1585816	0.87[CEU][hapmap]
rs16883526	0.88[ASW][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap]
rs16883529	0.82[JPT][hapmap];0.95[YRI][hapmap]
rs1819068	0.87[CEU][hapmap]
rs1830342	0.81[AFR][1000 genomes]
rs1919190	0.82[JPT][hapmap]
rs1919191	0.82[JPT][hapmap];0.95[YRI][hapmap]
rs2107855	0.82[AFR][1000 genomes]
rs2107856	0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs2107857	0.82[AFR][1000 genomes]
rs2141388	0.88[ASW][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs2141389	0.94[YRI][hapmap];0.82[AFR][1000 genomes]
rs2222764	0.88[ASW][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap]
rs2286125	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2373099	0.82[JPT][hapmap]
rs2373100	0.82[JPT][hapmap]
rs2888489	0.94[YRI][hapmap];0.82[AFR][1000 genomes]
rs2888490	0.82[JPT][hapmap];0.94[YRI][hapmap]
rs2888491	0.82[JPT][hapmap];0.94[YRI][hapmap]
rs4725736	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.91[JPT][hapmap];0.96[MEX][hapmap];0.89[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4725739	0.88[ASW][hapmap];0.95[YRI][hapmap]
rs4725740	0.88[ASW][hapmap];0.95[YRI][hapmap]
rs4726877	0.82[JPT][hapmap];0.94[YRI][hapmap]
rs6956932	0.82[JPT][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs6961608	0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs6973129	0.94[YRI][hapmap]
rs6978820	0.88[ASW][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap]
rs7778685	0.82[JPT][hapmap];0.95[YRI][hapmap]
rs7782445	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7795712	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7796028	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7800366	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7803992	0.87[MEX][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4726875	CUL1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147183200-147188600	Weak transcription	Muscle Satellite Cultured Cells	--

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