Variant report

Variant	rs12323974
Chromosome Location	chr15:87688321-87688322
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:87677782..87683862-chr15:87687780..87692291,5	MCF-7	breast:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11855086	1.00[ASN][1000 genomes]
rs11858636	1.00[ASN][1000 genomes]
rs12323982	1.00[ASN][1000 genomes]
rs12324067	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13380024	0.93[AFR][1000 genomes]
rs1392164	0.80[ASN][1000 genomes]
rs1499734	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1499735	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1499748	0.93[ASN][1000 genomes]
rs1499749	0.93[ASN][1000 genomes]
rs1499750	0.93[ASN][1000 genomes]
rs1499751	0.93[ASN][1000 genomes]
rs28470621	1.00[ASN][1000 genomes]
rs28538857	1.00[ASN][1000 genomes]
rs28560375	1.00[ASN][1000 genomes]
rs28565542	1.00[ASN][1000 genomes]
rs28584554	1.00[ASN][1000 genomes]
rs28614468	1.00[ASN][1000 genomes]
rs28624575	1.00[ASN][1000 genomes]
rs28703689	1.00[ASN][1000 genomes]
rs74028919	1.00[ASN][1000 genomes]
rs74028920	1.00[ASN][1000 genomes]
rs74028921	1.00[ASN][1000 genomes]
rs8031800	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039254	chr15:87070357-87942988	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1039005	chr15:87228489-87813438	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv542465	chr15:87228489-87813438	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1044157	chr15:87458558-88101699	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv428646	chr15:87612249-87759363	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv3348696	chr15:87671174-87689949	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv12490	chr15:87671272-87689759	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3330120	chr15:87681348-87690946	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv3348063	chr15:87685948-87690946	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:87687600-87689000	Enhancers	NH-A	brain
2	chr15:87687800-87688600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr15:87688200-87689400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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