Variant report

Variant	rs7094800
Chromosome Location	chr10:23086523-23086524
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10508654	0.92[ASN][1000 genomes]
rs11593600	0.97[ASN][1000 genomes]
rs12571255	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12571540	0.91[ASN][1000 genomes]
rs12572450	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12572705	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12573183	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16922710	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs16922713	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16922725	0.93[ASN][1000 genomes]
rs16922729	0.92[ASN][1000 genomes]
rs34490324	0.89[ASN][1000 genomes]
rs66625374	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs67161290	0.96[ASN][1000 genomes]
rs68141405	0.98[ASN][1000 genomes]
rs7078306	0.91[ASN][1000 genomes]
rs7082819	0.91[ASN][1000 genomes]
rs7090785	0.99[ASN][1000 genomes]
rs7091463	0.87[ASN][1000 genomes]
rs7094886	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7094895	0.94[ASN][1000 genomes]
rs72648289	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs72648290	0.95[ASN][1000 genomes]
rs72648291	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs72648292	0.94[ASN][1000 genomes]
rs72648293	0.93[ASN][1000 genomes]
rs73600523	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7903799	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7908933	0.87[ASN][1000 genomes]
rs7912540	0.94[ASN][1000 genomes]
rs7913783	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv550212	chr10:23030282-23086690	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv894960	chr10:23049139-23113841	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv894961	chr10:23049139-23128475	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv466833	chr10:23050683-23110797	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv894962	chr10:23050683-23113841	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv894963	chr10:23050683-23121820	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv894964	chr10:23050683-23128475	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv894965	chr10:23071128-23113841	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23081200-23092000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:23081200-23093000	Weak transcription	Brain Hippocampus Middle	brain

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