Variant report

Variant	rs1466905
Chromosome Location	chr18:45274675-45274676
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1004765	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1107933	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1107934	0.92[EUR][1000 genomes]
rs1579118	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1894150	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1910235	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1945724	0.81[EUR][1000 genomes]
rs1995413	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2097175	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2134374	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2174028	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2653629	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2653630	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653632	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2653633	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2653634	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2653635	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2653636	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2653637	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2653638	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2653639	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2653641	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653642	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2653643	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2653644	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2653645	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2653647	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2653648	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2653651	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2653652	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2653653	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2653654	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2653655	0.91[EUR][1000 genomes]
rs2653656	0.92[EUR][1000 genomes]
rs2653657	0.84[EUR][1000 genomes]
rs2852942	0.81[EUR][1000 genomes]
rs2852949	0.92[EUR][1000 genomes]
rs2852950	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2852952	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2852954	0.91[EUR][1000 genomes]
rs2852958	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2852960	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2852961	0.88[EUR][1000 genomes]
rs2852966	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2852967	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2852969	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2852970	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62086466	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs877354	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9954192	0.88[EUR][1000 genomes]

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	esv3425854	chr18:45188942-45336590	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45264600-45274800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:45274200-45275200	Enhancers	Brain Germinal Matrix	brain
3	chr18:45274600-45275200	Bivalent Enhancer	Fetal Intestine Small	intestine

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