Variant report

Variant	rs12497166
Chromosome Location	chr3:146468430-146468431
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1003263	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1003264	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1019897	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10935642	0.91[ASN][1000 genomes]
rs10935643	0.81[ASN][1000 genomes]
rs11705960	0.88[ASN][1000 genomes]
rs1397886	0.81[ASN][1000 genomes]
rs1549838	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1606177	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1606178	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17371141	0.99[ASN][1000 genomes]
rs17701818	0.88[ASN][1000 genomes]
rs1991715	0.82[ASN][1000 genomes]
rs2174783	0.82[ASN][1000 genomes]
rs28493260	0.88[ASN][1000 genomes]
rs28624889	0.88[ASN][1000 genomes]
rs28885973	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3843364	0.88[ASN][1000 genomes]
rs4681336	0.92[ASN][1000 genomes]
rs55895997	0.96[ASN][1000 genomes]
rs56887948	0.90[ASN][1000 genomes]
rs58890956	0.88[ASN][1000 genomes]
rs62272988	0.92[ASN][1000 genomes]
rs6440455	0.99[ASN][1000 genomes]
rs6440458	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6440459	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6440460	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6762735	0.90[ASN][1000 genomes]
rs6781142	0.86[CHB][hapmap]
rs6808136	0.88[ASN][1000 genomes]
rs7619766	0.88[ASN][1000 genomes]
rs7638634	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9289731	0.90[ASN][1000 genomes]
rs9289732	0.85[ASN][1000 genomes]
rs961897	0.95[ASN][1000 genomes]
rs981484	0.88[ASN][1000 genomes]
rs9828677	0.86[ASN][1000 genomes]
rs9831862	0.87[ASN][1000 genomes]
rs9834967	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9835606	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9840734	0.99[ASN][1000 genomes]
rs9841610	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9841625	0.88[ASN][1000 genomes]
rs9841883	0.88[ASN][1000 genomes]
rs9842074	0.99[ASN][1000 genomes]
rs9845940	0.88[ASN][1000 genomes]
rs9856265	0.88[ASN][1000 genomes]
rs9857850	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9861781	0.88[ASN][1000 genomes]
rs9861946	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516386	chr3:146366513-146758405	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv591961	chr3:146394094-146725217	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1007875	chr3:146401461-146776618	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv877624	chr3:146414837-146536741	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv998040	chr3:146416916-146729962	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv536760	chr3:146416916-146729962	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1001931	chr3:146419061-146745361	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv877625	chr3:146461435-146521978	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146464000-146468800	Enhancers	Muscle Satellite Cultured Cells	--
2	chr3:146465000-146475600	Weak transcription	NHDF-Ad	bronchial
3	chr3:146466800-146468600	Enhancers	Fetal Heart	heart
4	chr3:146467800-146468600	Enhancers	HUVEC	blood vessel
5	chr3:146468200-146468600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:146468200-146468800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:146468200-146469000	Enhancers	HMEC	breast
8	chr3:146468200-146478600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:146468400-146468600	Enhancers	HSMMtube	muscle
10	chr3:146468400-146468800	Enhancers	HSMM	muscle
11	chr3:146468400-146469000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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