Variant report

Variant	rs60184902
Chromosome Location	chr3:50996257-50996258
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12485524	0.90[ASN][1000 genomes]
rs12486828	0.85[ASN][1000 genomes]
rs12487821	0.85[ASN][1000 genomes]
rs12488831	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12488948	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12490502	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12490519	0.85[ASN][1000 genomes]
rs12491206	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12491402	0.88[ASN][1000 genomes]
rs12492367	0.85[ASN][1000 genomes]
rs12492850	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12494214	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12494708	0.83[ASN][1000 genomes]
rs12494776	0.85[ASN][1000 genomes]
rs12496601	0.83[ASN][1000 genomes]
rs12496621	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12497067	0.84[ASN][1000 genomes]
rs17051468	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2125368	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2262847	0.88[ASN][1000 genomes]
rs2355707	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4073739	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4078296	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4688695	0.83[ASN][1000 genomes]
rs4688696	0.83[ASN][1000 genomes]
rs4688697	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4688752	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs56844171	0.88[ASN][1000 genomes]
rs58356214	0.88[ASN][1000 genomes]
rs58720544	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs60602904	0.86[ASN][1000 genomes]
rs60882641	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs60917457	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs61627377	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61676409	0.82[ASN][1000 genomes]
rs6446239	0.96[ASN][1000 genomes]
rs72937251	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72937253	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72937262	0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs72937265	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs72937299	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs72939228	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72942530	0.82[ASN][1000 genomes]
rs72942567	0.85[ASN][1000 genomes]
rs7372342	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7427526	0.92[ASN][1000 genomes]
rs7427615	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491647	chr3:50856276-51245158	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1004881	chr3:50900793-51032918	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv536568	chr3:50900793-51032918	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50994400-50998200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr3:50995800-51000000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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