Variant report

Variant	rs12487360
Chromosome Location	chr3:156718434-156718435
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:156717926..156719479-chr3:156720084..156721767,2	MCF-7	breast:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12486875	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12491538	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12491708	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12497150	0.94[ASN][1000 genomes]
rs12497945	1.00[EUR][1000 genomes]
rs16826990	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16826999	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16827068	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16827087	0.96[ASN][1000 genomes]
rs1871969	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28436625	0.92[ASN][1000 genomes]
rs344082	1.00[YRI][hapmap]
rs56691909	0.94[ASN][1000 genomes]
rs57202263	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58069857	0.94[ASN][1000 genomes]
rs58557481	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60275122	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60826377	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73873777	0.94[ASN][1000 genomes]
rs9823211	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9846561	1.00[CEU][hapmap];0.94[ASN][1000 genomes]
rs9990369	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829765	chr3:156568263-156718496	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3349885	chr3:156685409-156878910	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156715600-156743600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:156717200-156720200	Enhancers	Fetal Intestine Small	intestine
3	chr3:156717600-156719400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:156717800-156718600	Weak transcription	Fetal Intestine Large	intestine
5	chr3:156717800-156719000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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