Variant report

Variant	rs16831219
Chromosome Location	chr3:179906665-179906666
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10513771	0.90[ASN][1000 genomes]
rs10937020	0.86[ASN][1000 genomes]
rs11718127	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12487650	0.90[ASN][1000 genomes]
rs12492526	0.92[ASN][1000 genomes]
rs12497420	0.82[ASN][1000 genomes]
rs12631948	0.94[EUR][1000 genomes]
rs12637429	0.94[EUR][1000 genomes]
rs13322790	0.86[ASN][1000 genomes]
rs1357904	0.85[ASN][1000 genomes]
rs1404743	0.87[ASN][1000 genomes]
rs1464845	0.88[ASN][1000 genomes]
rs1525276	0.86[ASN][1000 genomes]
rs1568859	0.90[ASN][1000 genomes]
rs1568860	0.94[ASN][1000 genomes]
rs1589858	0.83[ASN][1000 genomes]
rs16831126	0.84[ASN][1000 genomes]
rs16831288	0.81[ASN][1000 genomes]
rs1830044	0.82[EUR][1000 genomes]
rs1852121	0.85[ASN][1000 genomes]
rs1852122	0.80[ASN][1000 genomes]
rs1921676	0.83[ASN][1000 genomes]
rs1950124	0.83[ASN][1000 genomes]
rs2049472	0.83[ASN][1000 genomes]
rs2091273	0.82[ASN][1000 genomes]
rs2177723	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2178582	0.85[MKK][hapmap]
rs2339967	0.90[ASN][1000 genomes]
rs2339968	0.90[ASN][1000 genomes]
rs2879654	0.94[ASN][1000 genomes]
rs28865282	0.88[ASN][1000 genomes]
rs4854901	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4854902	0.90[ASN][1000 genomes]
rs4854903	0.90[ASN][1000 genomes]
rs4854961	0.88[ASN][1000 genomes]
rs4854962	0.88[ASN][1000 genomes]
rs4854964	0.87[ASN][1000 genomes]
rs4854966	0.89[ASN][1000 genomes]
rs56234136	0.89[ASN][1000 genomes]
rs60057308	0.84[ASN][1000 genomes]
rs62290558	0.84[ASN][1000 genomes]
rs62292283	0.90[ASN][1000 genomes]
rs62292284	0.90[ASN][1000 genomes]
rs62292290	0.89[ASN][1000 genomes]
rs62292291	0.88[ASN][1000 genomes]
rs62292292	0.86[ASN][1000 genomes]
rs6790229	0.92[ASN][1000 genomes]
rs67979781	0.84[ASN][1000 genomes]
rs68014168	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7643438	0.80[ASN][1000 genomes]
rs7644566	0.95[JPT][hapmap]
rs7652322	0.85[ASN][1000 genomes]
rs9290696	0.90[ASN][1000 genomes]
rs939440	0.95[JPT][hapmap]
rs939441	0.95[JPT][hapmap]
rs939442	0.95[JPT][hapmap]
rs9837718	0.93[ASN][1000 genomes]
rs9840477	0.85[ASN][1000 genomes]
rs9840775	0.85[ASN][1000 genomes]
rs9860526	0.85[ASN][1000 genomes]
rs9863693	0.82[ASN][1000 genomes]
rs9869517	0.88[ASN][1000 genomes]
rs9871928	0.84[ASN][1000 genomes]
rs9871936	0.82[ASN][1000 genomes]
rs9880357	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv878040	chr3:179823887-180128288	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv997388	chr3:179899279-180172349	Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv536817	chr3:179899279-180172349	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179903000-179915800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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