Variant report

Variant	rs11168883
Chromosome Location	chr12:49537880-49537881
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:49523953..49526231-chr12:49537682..49541779,5	MCF-7	breast:
2	chr12:49523899..49526623-chr12:49534923..49539191,5	K562	blood:
3	chr12:49531218..49534507-chr12:49536694..49541334,4	K562	blood:

Variant related genes	Relation type
ENSG00000123416	Chromatin interaction
ENSG00000258017	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs1039225	0.86[EUR][1000 genomes]
rs10783307	0.84[EUR][1000 genomes]
rs10783308	0.84[EUR][1000 genomes]
rs10875922	0.84[EUR][1000 genomes]
rs10875924	0.84[EUR][1000 genomes]
rs10875925	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10875927	0.85[EUR][1000 genomes]
rs10875928	0.84[EUR][1000 genomes]
rs10875929	0.82[EUR][1000 genomes]
rs10875930	0.84[EUR][1000 genomes]
rs10875931	0.83[EUR][1000 genomes]
rs11168874	0.86[EUR][1000 genomes]
rs11168882	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11168884	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11168885	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11168888	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11168890	0.86[EUR][1000 genomes]
rs11168894	0.86[EUR][1000 genomes]
rs11168895	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11168901	0.83[EUR][1000 genomes]
rs11168902	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11168903	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11168904	0.83[EUR][1000 genomes]
rs11168910	0.84[EUR][1000 genomes]
rs11837207	0.84[EUR][1000 genomes]
rs12227296	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12227610	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12227770	0.83[EUR][1000 genomes]
rs12228775	0.82[EUR][1000 genomes]
rs12229524	0.85[EUR][1000 genomes]
rs12229529	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12306494	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12318740	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12579015	0.86[EUR][1000 genomes]
rs1476137	0.82[EUR][1000 genomes]
rs1476138	0.80[EUR][1000 genomes]
rs1874908	0.83[EUR][1000 genomes]
rs1991427	0.86[EUR][1000 genomes]
rs1991428	0.82[EUR][1000 genomes]
rs2016107	0.81[EUR][1000 genomes]
rs2114845	0.86[EUR][1000 genomes]
rs2114846	0.85[EUR][1000 genomes]
rs2162643	0.82[EUR][1000 genomes]
rs2162644	0.85[EUR][1000 genomes]
rs2241727	0.84[EUR][1000 genomes]
rs2334930	0.83[EUR][1000 genomes]
rs2334931	0.83[EUR][1000 genomes]
rs2878287	0.84[EUR][1000 genomes]
rs35884657	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs58336603	0.86[EUR][1000 genomes]
rs58711211	0.82[EUR][1000 genomes]
rs6580701	0.83[EUR][1000 genomes]
rs6580703	0.80[EUR][1000 genomes]
rs73110168	0.85[EUR][1000 genomes]
rs7311346	0.83[EUR][1000 genomes]
rs731350	0.82[EUR][1000 genomes]
rs7953169	0.83[EUR][1000 genomes]
rs7954521	0.86[EUR][1000 genomes]
rs7954530	0.83[EUR][1000 genomes]
rs7957998	0.83[EUR][1000 genomes]
rs7969963	0.83[EUR][1000 genomes]
rs7969967	0.83[EUR][1000 genomes]
rs9325145	0.83[EUR][1000 genomes]
rs9739878	0.81[EUR][1000 genomes]
rs9788139	0.82[EUR][1000 genomes]
rs9788140	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051161	chr12:49314550-49828473	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
2	nsv541489	chr12:49314550-49828473	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
3	nsv1036452	chr12:49376285-49867760	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	315 gene(s)	inside rSNPs	diseases
4	esv3417605	chr12:49521878-49578961	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
5	nsv428801	chr12:49536659-49744884	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49527000-49555200	Weak transcription	Thymus	Thymus
2	chr12:49527600-49542400	Weak transcription	A549	lung
3	chr12:49527800-49542400	Weak transcription	Fetal Brain Male	brain
4	chr12:49527800-49542800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:49527800-49543000	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr12:49528000-49544000	Weak transcription	GM12878-XiMat	blood
7	chr12:49532800-49538200	Weak transcription	K562	blood

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