Variant report

Variant	rs4532091
Chromosome Location	chr3:139922915-139922916
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:139922220..139924561-chr3:139926417..139928588,2	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11706003	0.84[CHD][hapmap]
rs11707185	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11707235	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17402510	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2350506	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4592987	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4594581	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4683811	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.94[MEX][hapmap];0.85[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62266217	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62266218	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62266219	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6439900	1.00[CEU][hapmap];0.88[CHB][hapmap];0.92[CHD][hapmap];0.86[GIH][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6439902	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6808021	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73226989	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9756644	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9810392	0.81[CHD][hapmap]
rs9815072	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9815327	0.88[CHB][hapmap];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9816340	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9845709	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9862941	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9867592	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998423	chr3:139526446-139947336	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv829739	chr3:139797496-140002685	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1008578	chr3:139907172-139942453	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1003141	chr3:139907434-139942453	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4532091	CEP70	cis	parietal	SCAN

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139921600-139923200	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr3:139921600-139923800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:139921600-139925600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:139921600-139926000	Enhancers	H1 Cell Line	embryonic stem cell
5	chr3:139921600-139926200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr3:139921800-139925400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr3:139922000-139923400	Enhancers	Fetal Brain Female	brain
8	chr3:139922000-139926000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:139922200-139923200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr3:139922400-139923200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr3:139922400-139925400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr3:139922600-139923000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:139922600-139923200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
14	chr3:139922600-139923600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:139922600-139924200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr3:139922800-139924000	Weak transcription	H9 Cell Line	embryonic stem cell

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