Variant report

Variant	rs10460845
Chromosome Location	chr3:139127084-139127085
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1044826	0.83[ASN][1000 genomes]
rs10935320	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10935323	0.89[ASN][1000 genomes]
rs12488939	0.83[ASN][1000 genomes]
rs12494806	0.86[ASN][1000 genomes]
rs12695698	0.87[ASN][1000 genomes]
rs12695699	0.87[ASN][1000 genomes]
rs13060697	0.84[ASN][1000 genomes]
rs13083195	0.81[ASN][1000 genomes]
rs13085888	0.86[ASN][1000 genomes]
rs13089007	0.89[ASN][1000 genomes]
rs13092507	0.89[ASN][1000 genomes]
rs13092935	0.87[ASN][1000 genomes]
rs1586861	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1586863	0.95[ASN][1000 genomes]
rs1586864	0.95[ASN][1000 genomes]
rs17336869	0.82[ASN][1000 genomes]
rs1907687	0.95[ASN][1000 genomes]
rs2233811	0.82[ASN][1000 genomes]
rs2233815	0.82[ASN][1000 genomes]
rs2349059	0.86[ASN][1000 genomes]
rs34623690	0.82[ASN][1000 genomes]
rs3772877	0.84[ASN][1000 genomes]
rs3772878	0.84[ASN][1000 genomes]
rs3772879	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3821544	0.82[ASN][1000 genomes]
rs3821545	0.84[ASN][1000 genomes]
rs4544576	0.95[ASN][1000 genomes]
rs67929453	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9289578	0.82[ASN][1000 genomes]
rs964227	0.92[ASN][1000 genomes]
rs973691	0.82[ASN][1000 genomes]
rs9812192	0.89[ASN][1000 genomes]
rs9818691	0.92[ASN][1000 genomes]
rs9825064	0.83[ASN][1000 genomes]
rs9831108	0.89[ASN][1000 genomes]
rs9848241	0.95[ASN][1000 genomes]
rs9849039	0.92[ASN][1000 genomes]
rs9849578	0.89[ASN][1000 genomes]
rs9853350	0.89[ASN][1000 genomes]
rs9860201	0.89[ASN][1000 genomes]
rs9868544	0.86[ASN][1000 genomes]
rs9882014	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877543	chr3:139021139-139327261	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv1003154	chr3:139060841-139788752	ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv536729	chr3:139060841-139788752	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv949635	chr3:139091219-139367043	Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 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	chr3:139113200-139133000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:139114200-139153800	Weak transcription	Left Ventricle	heart
3	chr3:139124200-139133400	Weak transcription	Ovary	ovary

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