Variant report

Variant	rs13082015
Chromosome Location	chr3:94581590-94581591
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:14789975..14790495-chr3:94581323..94581855,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs13314320	0.84[ASN][1000 genomes]
rs13324772	0.84[ASN][1000 genomes]
rs13324801	0.84[ASN][1000 genomes]
rs1368194	0.83[ASN][1000 genomes]
rs1368195	0.93[ASN][1000 genomes]
rs1368196	0.93[ASN][1000 genomes]
rs1368197	0.99[ASN][1000 genomes]
rs1368198	0.99[ASN][1000 genomes]
rs1368199	0.99[ASN][1000 genomes]
rs1432472	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2053009	0.92[ASN][1000 genomes]
rs2116612	0.87[ASN][1000 genomes]
rs2163680	0.91[ASN][1000 genomes]
rs2163681	0.91[ASN][1000 genomes]
rs2163682	0.99[ASN][1000 genomes]
rs300066	0.83[ASN][1000 genomes]
rs4241479	0.99[ASN][1000 genomes]
rs4461422	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4462967	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4493433	0.99[ASN][1000 genomes]
rs4583664	0.99[ASN][1000 genomes]
rs4593024	0.92[ASN][1000 genomes]
rs4857495	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6777772	0.93[ASN][1000 genomes]
rs6780216	0.84[ASN][1000 genomes]
rs6801609	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7427844	0.97[ASN][1000 genomes]
rs7642399	0.99[ASN][1000 genomes]
rs7646332	0.97[ASN][1000 genomes]
rs7649609	1.00[ASN][1000 genomes]
rs7652148	0.99[ASN][1000 genomes]
rs7653317	0.97[ASN][1000 genomes]
rs7653599	0.96[ASN][1000 genomes]
rs9637418	0.97[ASN][1000 genomes]
rs9832016	0.88[ASN][1000 genomes]
rs9832891	0.91[ASN][1000 genomes]
rs9842192	0.87[ASN][1000 genomes]
rs9842195	0.87[ASN][1000 genomes]
rs9842368	0.87[ASN][1000 genomes]
rs9847887	0.99[ASN][1000 genomes]
rs9848372	0.98[ASN][1000 genomes]
rs9867704	0.98[ASN][1000 genomes]
rs9871980	0.99[ASN][1000 genomes]
rs9872890	0.99[ASN][1000 genomes]
rs9879048	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460763	chr3:94384332-94596072	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv590988	chr3:94384332-94596072	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv877168	chr3:94430430-94614333	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv460764	chr3:94479849-94654181	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv590989	chr3:94479849-94654181	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:94579200-94583400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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