Variant report

Variant	rs17005833
Chromosome Location	chr3:19381389-19381390
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10510488	0.81[MEX][hapmap]
rs11709636	1.00[CEU][hapmap];0.83[JPT][hapmap]
rs11713099	1.00[CHB][hapmap];0.95[CHD][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs12637672	0.90[EUR][1000 genomes]
rs12638161	1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs12714976	0.86[EUR][1000 genomes]
rs13060503	0.83[EUR][1000 genomes]
rs13072922	0.81[MEX][hapmap]
rs13078049	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13081910	0.82[MEX][hapmap];0.83[TSI][hapmap];0.82[EUR][1000 genomes]
rs13083035	0.83[GIH][hapmap];0.82[EUR][1000 genomes]
rs13094042	0.82[EUR][1000 genomes]
rs17005834	0.85[CHD][hapmap];0.85[JPT][hapmap]
rs17570934	0.81[MEX][hapmap]
rs2053507	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35122721	0.81[AMR][1000 genomes]
rs62279477	0.94[ASN][1000 genomes]
rs62279486	0.92[ASN][1000 genomes]
rs6806328	0.81[MEX][hapmap]
rs730586	0.85[CHD][hapmap];1.00[JPT][hapmap]
rs7618649	1.00[CHB][hapmap];0.95[CHD][hapmap];0.92[JPT][hapmap];0.92[ASN][1000 genomes]
rs7622593	0.91[ASN][1000 genomes]
rs7630441	0.91[ASN][1000 genomes]
rs7635327	0.81[MEX][hapmap]
rs7645179	0.83[JPT][hapmap]
rs7653013	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9682622	0.82[EUR][1000 genomes]
rs9829484	0.82[MEX][hapmap];0.83[TSI][hapmap]
rs9836707	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9845765	0.82[MEX][hapmap];0.83[TSI][hapmap]

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	nsv517847	chr3:18845347-19483695	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1010123	chr3:18990307-19989504	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1004602	chr3:19031671-19930052	Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv536511	chr3:19031671-19930052	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised 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 miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv948636	chr3:19335802-19856585	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 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	chr3:19367400-19383600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:19378400-19392400	Weak transcription	Brain Germinal Matrix	brain

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