Variant report

Variant	rs7105027
Chromosome Location	chr11:8551916-8551917
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11041927	0.87[CHB][hapmap]
rs11041929	0.88[YRI][hapmap]
rs11041939	0.93[CHB][hapmap];0.85[JPT][hapmap]
rs11041943	0.94[CHB][hapmap]
rs11041949	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11041955	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11041960	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11041966	0.94[CHB][hapmap];0.89[CHD][hapmap];0.81[JPT][hapmap]
rs11041982	1.00[YRI][hapmap]
rs11820339	0.80[CEU][hapmap]
rs12224971	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs12226069	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12226478	0.86[AFR][1000 genomes]
rs12576961	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12806736	0.84[LWK][hapmap];0.92[MKK][hapmap];0.95[YRI][hapmap]
rs1446464	0.87[YRI][hapmap]
rs1992756	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.90[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap]
rs2028881	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap]
rs2311390	0.93[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];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4586148	0.87[CHB][hapmap]
rs4758067	0.88[MKK][hapmap];0.87[YRI][hapmap]
rs4929950	0.87[YRI][hapmap]
rs7119274	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7126934	0.82[YRI][hapmap]
rs726007	0.87[ASW][hapmap]
rs73405938	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7931604	0.86[YRI][hapmap]
rs7950041	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9284150	0.87[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751035	chr11:8431654-8685451	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv896983	chr11:8526643-8682465	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs7105027	RNF141	cis	cerebellum	SCAN
rs7105027	CSNK2A1P	cis	cerebellum	SCAN
rs7105027	RPL27A	cis	parietal	SCAN
rs7105027	OR52W1	cis	parietal	SCAN
rs7105027	OR51L1	cis	cerebellum	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8549000-8553000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:8551000-8555200	Enhancers	Fetal Heart	heart
3	chr11:8551000-8555800	Enhancers	Primary B cells from peripheral blood	blood
4	chr11:8551600-8555000	Enhancers	Primary B cells from cord blood	blood

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