Variant report

Variant	rs9952921
Chromosome Location	chr18:7989605-7989606
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12103962	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs2099932	1.00[AMR][1000 genomes]
rs28367342	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28379285	1.00[AMR][1000 genomes]
rs28511885	0.82[AFR][1000 genomes]
rs28521877	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs28523954	0.83[AMR][1000 genomes]
rs28526245	0.82[AFR][1000 genomes]
rs28569201	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28644497	0.83[AMR][1000 genomes]
rs28709298	0.82[AFR][1000 genomes]
rs28757770	0.83[AMR][1000 genomes]
rs6506541	0.83[AMR][1000 genomes]
rs7239724	0.83[AMR][1000 genomes]
rs7239846	0.83[AMR][1000 genomes]
rs7241071	0.83[AMR][1000 genomes]
rs73385648	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73385649	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73385658	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73385659	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9945054	0.83[AMR][1000 genomes]
rs9948263	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9949297	1.00[AMR][1000 genomes]
rs9950590	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9951398	0.83[AMR][1000 genomes]
rs9952873	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9955097	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9955973	1.00[AMR][1000 genomes]
rs9958058	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9963151	0.82[AFR][1000 genomes]
rs9963467	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9963748	0.83[AMR][1000 genomes]
rs9965536	0.83[AMR][1000 genomes]
rs9966712	0.83[AMR][1000 genomes]
rs9966934	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9967327	0.83[AMR][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	nsv534374	chr18:7438812-8412546	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1062911	chr18:7561991-8088274	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv543637	chr18:7561991-8088274	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1064345	chr18:7562051-8088274	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv543638	chr18:7562051-8088274	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr18:7981200-7995600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:7987000-7995600	Weak transcription	Aorta	Aorta
3	chr18:7987200-7994800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr18:7987600-7999400	Weak transcription	Ovary	ovary
5	chr18:7987600-8033400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr18:7988200-8003600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr18:7989600-7991000	Weak transcription	Fetal Kidney	kidney

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