Variant report

Variant	rs7182436
Chromosome Location	chr15:56092454-56092455
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr15:56033747..56035690-chr15:56092424..56095396,4	MCF-7	breast:
2	chr15:56090139..56092920-chr15:56116409..56118129,2	K562	blood:
3	chr15:56032752..56035214-chr15:56091096..56094057,2	MCF-7	breast:
4	chr15:56091891..56092629-chr15:56138007..56138913,2	MCF-7	breast:
5	chr15:55939872..55941462-chr15:56091567..56092720,22	MCF-7	breast:
6	chr14:77141813..77142316-chr15:56091817..56092480,2	MCF-7	breast:
7	chr15:55940303..55941439-chr15:56091892..56092613,4	MCF-7	breast:
8	chr15:55940259..55941893-chr15:56091674..56092667,4	K562	blood:
9	chr15:55940663..55943471-chr15:56092171..56094031,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000166450	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10518822	0.93[ASN][1000 genomes]
rs11071219	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11635701	0.86[ASN][1000 genomes]
rs11853766	0.90[ASN][1000 genomes]
rs12439615	0.90[ASN][1000 genomes]
rs12594225	0.95[ASN][1000 genomes]
rs1991406	0.92[CEU][hapmap];0.86[MEX][hapmap]
rs2008672	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2014213	0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.87[TSI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2414442	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28486084	0.89[ASN][1000 genomes]
rs28673063	0.85[EUR][1000 genomes]
rs28807987	0.92[ASN][1000 genomes]
rs34593948	0.83[ASN][1000 genomes]
rs4316693	0.82[ASN][1000 genomes]
rs4395015	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4415961	0.92[ASN][1000 genomes]
rs4605102	0.81[EUR][1000 genomes]
rs56179937	0.92[ASN][1000 genomes]
rs57692605	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57725406	0.91[ASN][1000 genomes]
rs59983763	0.92[ASN][1000 genomes]
rs60503643	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62046598	0.95[ASN][1000 genomes]
rs8030099	0.92[ASN][1000 genomes]
rs8030626	0.94[ASN][1000 genomes]
rs8034279	0.95[ASN][1000 genomes]
rs8034296	0.95[ASN][1000 genomes]
rs8038986	0.95[ASN][1000 genomes]
rs933996	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv457157	chr15:55722213-56255774	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv569539	chr15:55722213-56255774	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv833017	chr15:55965957-56157912	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	esv3366380	chr15:56003224-56141650	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv1052495	chr15:56013617-56102164	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56089000-56093600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr15:56090600-56092600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr15:56090800-56092600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr15:56091400-56092600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr15:56091400-56092600	Enhancers	Hela-S3	cervix
6	chr15:56091800-56094000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:56092000-56092600	Enhancers	K562	blood
8	chr15:56092000-56093800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:56092000-56094200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr15:56092000-56095000	Weak transcription	HSMMtube	muscle
11	chr15:56092200-56092600	Enhancers	A549	lung
12	chr15:56092200-56092600	Flanking Active TSS	HepG2	liver
13	chr15:56092200-56094200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr15:56092400-56092800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:56092400-56092800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr15:56092400-56095200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr15:56092400-56095400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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