Variant report

Variant	rs67171651
Chromosome Location	chr3:134970008-134970009
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10608	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11923218	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13071859	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13072079	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13080641	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13080855	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13085606	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13093562	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13095925	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16842883	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17712024	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17712106	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17712383	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3182239	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34179831	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34206167	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34340628	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34344981	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34893823	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35092007	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35326767	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35533080	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35653041	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35805151	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35844472	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35943770	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35944228	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36067487	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66525503	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66645582	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67224719	0.89[EUR][1000 genomes]
rs67358622	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73220299	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1000277	chr3:134546080-134970837	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134958000-134970400	Weak transcription	GM12878-XiMat	blood
2	chr3:134958600-134977200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:134961000-134977800	Weak transcription	Fetal Brain Female	brain
4	chr3:134961400-134977800	Weak transcription	Brain Anterior Caudate	brain
5	chr3:134963400-134981800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr3:134965400-134977800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr3:134966400-134970400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr3:134968400-134977800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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