Variant report

Variant	rs12891936
Chromosome Location	chr14:71682118-71682119
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr14:71682052-71682137	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:71678893..71680669-chr14:71681076..71683305,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269945	TF binding region
ENSG00000258517	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11158896	0.82[ASN][1000 genomes]
rs11626311	0.82[ASN][1000 genomes]
rs11628388	0.82[ASN][1000 genomes]
rs11628426	0.82[ASN][1000 genomes]
rs12588587	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12589785	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12590347	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12889985	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12893350	0.82[ASN][1000 genomes]
rs2057829	0.82[ASN][1000 genomes]
rs2107667	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2189799	0.82[ASN][1000 genomes]
rs34756752	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35509608	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4899389	0.82[ASN][1000 genomes]
rs4902914	0.82[ASN][1000 genomes]
rs4902915	0.83[CHB][hapmap]
rs4902919	0.82[ASN][1000 genomes]
rs4902920	0.82[ASN][1000 genomes]
rs66549050	0.82[ASN][1000 genomes]
rs7144473	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7155368	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7155577	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	nsv1041980	chr14:71196358-71767339	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv542125	chr14:71196358-71767339	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1036929	chr14:71469148-71683412	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1044090	chr14:71496198-71780026	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	nsv832827	chr14:71676178-71833519	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71679600-71682200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:71679800-71685000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr14:71680400-71682200	Enhancers	Stomach Mucosa	stomach
4	chr14:71680600-71702600	Weak transcription	Brain Angular Gyrus	brain
5	chr14:71680800-71691600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr14:71680800-71691800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr14:71681600-71682200	Enhancers	Gastric	stomach
8	chr14:71681800-71682600	Enhancers	Pancreas	Pancrea
9	chr14:71682000-71682600	Enhancers	Spleen	Spleen

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