Variant report

Variant	rs10937021
Chromosome Location	chr3:179915120-179915121
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	chr3:179915089-179915142	MCF-7	breast:	n/a	n/a
2	MYC	chr3:179914992-179915152	MCF-7	breast:	n/a	n/a

Variant related genes	Relation type
GAPDHP36	TF binding region

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10222466	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10937020	0.85[EUR][1000 genomes]
rs11709960	0.90[EUR][1000 genomes]
rs12487650	0.90[EUR][1000 genomes]
rs12636328	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13322790	0.94[EUR][1000 genomes]
rs1357904	0.91[EUR][1000 genomes]
rs1404744	0.84[EUR][1000 genomes]
rs1464844	0.92[EUR][1000 genomes]
rs1525269	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1525272	0.91[EUR][1000 genomes]
rs1525276	0.91[EUR][1000 genomes]
rs1525277	0.88[EUR][1000 genomes]
rs1568859	0.90[EUR][1000 genomes]
rs1581549	0.92[EUR][1000 genomes]
rs1589858	0.92[EUR][1000 genomes]
rs16831288	0.90[EUR][1000 genomes]
rs1852121	0.84[EUR][1000 genomes]
rs1852122	0.83[EUR][1000 genomes]
rs1852123	0.90[EUR][1000 genomes]
rs2091273	0.90[EUR][1000 genomes]
rs2339967	0.90[EUR][1000 genomes]
rs2339968	0.88[EUR][1000 genomes]
rs28865282	0.86[EUR][1000 genomes]
rs3849420	0.92[EUR][1000 genomes]
rs3906013	0.90[EUR][1000 genomes]
rs3906014	0.90[EUR][1000 genomes]
rs4109306	0.91[EUR][1000 genomes]
rs4854902	0.89[EUR][1000 genomes]
rs4854961	0.86[EUR][1000 genomes]
rs4854962	0.86[EUR][1000 genomes]
rs4854964	0.94[EUR][1000 genomes]
rs6790229	0.91[EUR][1000 genomes]
rs6790465	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7619775	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7621628	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7622125	0.90[EUR][1000 genomes]
rs7652322	0.91[EUR][1000 genomes]
rs9290696	0.88[EUR][1000 genomes]
rs9290697	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9812621	0.93[EUR][1000 genomes]
rs9819178	0.90[EUR][1000 genomes]
rs9821124	0.90[EUR][1000 genomes]
rs9837718	0.91[EUR][1000 genomes]
rs9840477	0.93[EUR][1000 genomes]
rs9840775	0.94[EUR][1000 genomes]
rs9845934	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9857420	0.82[EUR][1000 genomes]
rs9860526	0.93[EUR][1000 genomes]
rs9862989	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9864555	0.80[EUR][1000 genomes]
rs9868908	0.91[EUR][1000 genomes]
rs9869517	0.93[EUR][1000 genomes]
rs9871936	0.88[EUR][1000 genomes]
rs9877454	0.92[EUR][1000 genomes]
rs9880357	0.91[EUR][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	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv878040	chr3:179823887-180128288	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv997388	chr3:179899279-180172349	Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv536817	chr3:179899279-180172349	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179903000-179915800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:179914200-179924800	Weak transcription	Pancreas	Pancrea
3	chr3:179915000-179915200	Enhancers	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links