Variant report

Variant	rs12262288
Chromosome Location	chr10:49464697-49464698
allele	C/T
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	FOSL2	chr10:49464667-49464848	HepG2	liver:	n/a	chr10:49464765-49464777 chr10:49464766-49464775 chr10:49464767-49464776

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49455241..49456959-chr10:49462949..49465290,2	MCF-7	breast:
2	chr10:49464368..49465891-chr10:49470466..49472102,2	MCF-7	breast:

Variant related genes	Relation type
FRMPD2	TF binding region

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11101273	0.83[AMR][1000 genomes]
rs11816450	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12098470	0.84[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12246849	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12247274	0.85[YRI][hapmap];0.92[AMR][1000 genomes]
rs12251755	0.89[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs12257349	0.83[AMR][1000 genomes]
rs1465605	1.00[JPT][hapmap]
rs1652243	1.00[ASN][1000 genomes]
rs1652245	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs166815	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs166817	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17009533	1.00[JPT][hapmap]
rs1730444	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1730446	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1881733	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1881734	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs204006	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2455321	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2463958	1.00[ASN][1000 genomes]
rs2652408	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2698764	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs280605	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs280606	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs280608	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs280610	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs280611	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs280615	1.00[ASN][1000 genomes]
rs386570	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs399419	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs413065	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs426153	1.00[ASN][1000 genomes]
rs440943	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs477693	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs477761	1.00[ASN][1000 genomes]
rs4838592	1.00[JPT][hapmap]
rs57706664	0.83[AMR][1000 genomes]
rs60503953	1.00[ASN][1000 genomes]
rs61840508	1.00[ASN][1000 genomes]
rs7073154	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7092864	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs73294264	1.00[ASN][1000 genomes]
rs73296347	1.00[ASN][1000 genomes]
rs73296348	1.00[ASN][1000 genomes]
rs73296380	1.00[ASN][1000 genomes]
rs73296381	1.00[ASN][1000 genomes]
rs73296386	1.00[ASN][1000 genomes]
rs73296387	1.00[ASN][1000 genomes]
rs7915333	1.00[JPT][hapmap];1.00[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	nsv895366	chr10:49299274-49576454	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv895367	chr10:49333754-49491047	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv895368	chr10:49381635-49551560	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv467190	chr10:49402084-49576878	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv550811	chr10:49402084-49576878	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv895370	chr10:49421173-49484698	Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49460600-49465800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr10:49460800-49466200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr10:49460800-49469200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:49462400-49465200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:49463000-49465000	Weak transcription	Fetal Heart	heart
6	chr10:49463400-49466800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr10:49464000-49464800	Enhancers	Right Atrium	heart
8	chr10:49464600-49464800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr10:49464600-49464800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:49464600-49464800	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links