Variant report

Variant	rs17293359
Chromosome Location	chr4:128083879-128083880
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1000707	0.90[EUR][1000 genomes]
rs10012435	0.90[EUR][1000 genomes]
rs10518518	0.90[EUR][1000 genomes]
rs11098914	0.90[EUR][1000 genomes]
rs11098915	0.90[EUR][1000 genomes]
rs11098916	0.90[EUR][1000 genomes]
rs11098917	0.90[EUR][1000 genomes]
rs13116630	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1351425	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1351426	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1383520	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1480897	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1480909	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1480910	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17213081	0.96[AFR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17228715	0.90[EUR][1000 genomes]
rs17228756	0.90[EUR][1000 genomes]
rs17228875	0.90[EUR][1000 genomes]
rs17229246	0.90[EUR][1000 genomes]
rs17229576	0.88[EUR][1000 genomes]
rs17291337	0.96[CEU][hapmap];0.80[CHB][hapmap];0.86[JPT][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17293310	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17293345	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17294432	0.90[EUR][1000 genomes]
rs17294586	0.90[EUR][1000 genomes]
rs17294663	0.90[EUR][1000 genomes]
rs17295431	0.86[EUR][1000 genomes]
rs28524825	0.90[EUR][1000 genomes]
rs34120215	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4550943	0.90[EUR][1000 genomes]
rs4550946	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55773382	0.88[EUR][1000 genomes]
rs55824976	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56216620	0.90[EUR][1000 genomes]
rs56387802	0.90[EUR][1000 genomes]
rs62333871	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62333879	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62333900	0.89[EUR][1000 genomes]
rs62333901	0.90[EUR][1000 genomes]
rs62333902	0.90[EUR][1000 genomes]
rs62333903	0.90[EUR][1000 genomes]
rs62333904	0.90[EUR][1000 genomes]
rs62333905	0.90[EUR][1000 genomes]
rs62333906	0.90[EUR][1000 genomes]
rs62333907	0.90[EUR][1000 genomes]
rs62333908	0.90[EUR][1000 genomes]
rs62335164	0.88[EUR][1000 genomes]
rs62335489	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs62335523	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62335528	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6810678	0.90[EUR][1000 genomes]
rs6836252	0.86[EUR][1000 genomes]
rs6836483	0.90[EUR][1000 genomes]
rs6853523	0.90[EUR][1000 genomes]
rs6857872	0.89[EUR][1000 genomes]
rs6857937	0.90[EUR][1000 genomes]
rs6858838	0.90[EUR][1000 genomes]
rs72680008	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72680022	0.90[EUR][1000 genomes]
rs744559	0.80[ASN][1000 genomes]
rs7655646	0.86[EUR][1000 genomes]
rs7694318	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs976814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs998857	0.90[EUR][1000 genomes]
rs998858	0.90[EUR][1000 genomes]
rs999285	0.90[EUR][1000 genomes]
rs9999648	0.82[CHB][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879914	chr4:128005362-128123638	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:128083200-128084400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:128083200-128085200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:128083400-128084800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:128083400-128085200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:128083600-128085000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:128083800-128084400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr4:128083800-128084600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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