Variant report

Variant	rs17094520
Chromosome Location	chr10:118076312-118076313
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:118073107..118076558-chr10:118081327..118085296,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000182645	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10490910	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11816383	0.86[AMR][1000 genomes]
rs11817085	0.98[ASN][1000 genomes]
rs11817803	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12414617	0.84[CHB][hapmap];0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs12416076	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12416239	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12416567	0.86[AMR][1000 genomes]
rs1419870	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1419872	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17094490	0.84[JPT][hapmap];0.89[AMR][1000 genomes]
rs17094504	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17094547	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1894789	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2286630	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2438177	0.81[AMR][1000 genomes]
rs2532688	0.81[AMR][1000 genomes]
rs35997739	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3740573	0.85[AMR][1000 genomes]
rs41384349	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs41386650	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4636575	0.94[JPT][hapmap]
rs58693853	0.96[ASN][1000 genomes]
rs61092077	0.82[AMR][1000 genomes]
rs6585390	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs73373010	0.85[AMR][1000 genomes]
rs73373021	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73373031	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73374910	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7902111	0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]

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	esv3449389	chr10:117806874-118102404	Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832000	chr10:117944492-118116253	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118076000-118076400	Enhancers	H9 Cell Line	embryonic stem cell
2	chr10:118076000-118076400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:118076000-118076800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr10:118076200-118077200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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