Variant report

Variant	rs9882135
Chromosome Location	chr3:136782584-136782585
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1023765	0.85[AMR][1000 genomes]
rs10935221	0.84[AMR][1000 genomes]
rs13098923	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1351892	0.85[AMR][1000 genomes]
rs1470143	0.85[AMR][1000 genomes]
rs1484787	0.85[AMR][1000 genomes]
rs1484794	0.83[AMR][1000 genomes]
rs3899122	0.83[AMR][1000 genomes]
rs4678286	0.83[AMR][1000 genomes]
rs6439683	0.84[AMR][1000 genomes]
rs6439685	0.84[AMR][1000 genomes]
rs6439686	0.84[AMR][1000 genomes]
rs6763000	0.81[EUR][1000 genomes]
rs6773448	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6781928	0.85[AMR][1000 genomes]
rs6795587	0.84[ASN][1000 genomes]
rs6806914	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6807138	0.84[AMR][1000 genomes]
rs6808049	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6808051	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7627723	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7646139	0.85[AMR][1000 genomes]
rs9289525	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs969329	0.83[AMR][1000 genomes]
rs9810065	0.85[ASN][1000 genomes]
rs9818478	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9818918	0.85[AMR][1000 genomes]
rs9819250	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9822931	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9826507	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9838513	0.85[AMR][1000 genomes]
rs9843104	0.87[AMR][1000 genomes]
rs9843219	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9856620	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9870582	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9874836	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv524856	chr3:136693459-137190765	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1012111	chr3:136695367-137343430	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136757000-136794000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr3:136765000-136784200	Weak transcription	Esophagus	oesophagus
3	chr3:136769400-136796200	Weak transcription	NHEK	skin
4	chr3:136781600-136782600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:136781800-136782800	ZNF genes & repeats	GM12878-XiMat	blood
6	chr3:136782000-136804600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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