Variant report

Variant	rs4626670
Chromosome Location	chr9:95679875-95679876
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:95677020..95680081-chr9:95681150..95683718,3	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10115872	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10123843	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10123870	0.87[EUR][1000 genomes]
rs10156497	0.82[ASN][1000 genomes]
rs1022833	0.81[ASN][1000 genomes]
rs10739932	0.83[ASN][1000 genomes]
rs10739933	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10739934	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10761172	0.82[ASN][1000 genomes]
rs10821021	0.82[ASN][1000 genomes]
rs10821022	0.82[ASN][1000 genomes]
rs10821028	0.82[ASN][1000 genomes]
rs10821030	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10821031	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10821032	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10821035	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10821040	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992489	0.81[ASN][1000 genomes]
rs10992529	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12336022	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12338961	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12346689	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12379300	0.82[ASN][1000 genomes]
rs13288901	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13294147	0.83[ASN][1000 genomes]
rs35449185	0.83[ASN][1000 genomes]
rs36194652	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3824428	0.82[ASN][1000 genomes]
rs4133033	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4510923	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4535796	0.97[ASN][1000 genomes]
rs4538949	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4744150	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4744151	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6479434	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7024752	0.83[ASN][1000 genomes]
rs7032277	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7035868	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7039812	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7040645	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7045305	0.82[ASN][1000 genomes]
rs7047181	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7847713	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7847998	0.82[ASN][1000 genomes]
rs7869480	0.82[ASN][1000 genomes]
rs7872848	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7872987	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7873021	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7874026	0.84[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	nsv831654	chr9:95542920-95720961	ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv893574	chr9:95580376-95688099	Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv1818795	chr9:95656340-95689158	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
4	nsv982639	chr9:95671744-95685131	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95674800-95687400	Weak transcription	Right Atrium	heart
2	chr9:95675800-95683400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:95679200-95680800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr9:95679400-95680200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr9:95679400-95680600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr9:95679600-95680000	Enhancers	Adipose Nuclei	Adipose
7	chr9:95679600-95680200	Enhancers	Primary B cells from peripheral blood	blood
8	chr9:95679600-95680200	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr9:95679600-95680200	Enhancers	Spleen	Spleen
10	chr9:95679600-95680400	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr9:95679600-95680400	Enhancers	GM12878-XiMat	blood
12	chr9:95679800-95680000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr9:95679800-95680200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr9:95679800-95680200	Enhancers	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links