Variant report

Variant	rs12635502
Chromosome Location	chr3:180078836-180078837
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10513774	0.99[ASN][1000 genomes]
rs10937031	0.97[ASN][1000 genomes]
rs10937032	1.00[ASN][1000 genomes]
rs10937034	0.91[ASN][1000 genomes]
rs11707003	0.96[ASN][1000 genomes]
rs12054337	0.94[ASN][1000 genomes]
rs12630277	0.99[ASN][1000 genomes]
rs12635401	0.97[ASN][1000 genomes]
rs12636512	1.00[ASN][1000 genomes]
rs13325203	0.97[ASN][1000 genomes]
rs1356909	0.97[ASN][1000 genomes]
rs1402219	0.96[ASN][1000 genomes]
rs1402220	0.95[ASN][1000 genomes]
rs1402223	0.97[ASN][1000 genomes]
rs1402224	0.96[ASN][1000 genomes]
rs1402225	0.99[ASN][1000 genomes]
rs1402226	1.00[ASN][1000 genomes]
rs1402227	0.99[ASN][1000 genomes]
rs1402229	1.00[ASN][1000 genomes]
rs1402230	1.00[ASN][1000 genomes]
rs1464359	0.99[ASN][1000 genomes]
rs1464360	0.99[ASN][1000 genomes]
rs16831509	1.00[ASN][1000 genomes]
rs2203980	0.94[ASN][1000 genomes]
rs28823929	1.00[ASN][1000 genomes]
rs34626513	0.94[ASN][1000 genomes]
rs4306858	0.98[ASN][1000 genomes]
rs4519699	0.99[ASN][1000 genomes]
rs4553975	1.00[ASN][1000 genomes]
rs4572765	0.96[ASN][1000 genomes]
rs4854908	0.97[ASN][1000 genomes]
rs4854971	0.97[ASN][1000 genomes]
rs4854972	0.97[ASN][1000 genomes]
rs4854973	0.99[ASN][1000 genomes]
rs4854974	0.99[ASN][1000 genomes]
rs61377300	0.96[ASN][1000 genomes]
rs62290971	0.97[ASN][1000 genomes]
rs62290972	0.99[ASN][1000 genomes]
rs62290973	0.99[ASN][1000 genomes]
rs62290975	1.00[ASN][1000 genomes]
rs62290976	0.91[ASN][1000 genomes]
rs62292329	0.96[ASN][1000 genomes]
rs62292330	0.97[ASN][1000 genomes]
rs6768614	1.00[ASN][1000 genomes]
rs6785130	1.00[ASN][1000 genomes]
rs6789456	1.00[ASN][1000 genomes]
rs6792185	1.00[ASN][1000 genomes]
rs6797893	1.00[ASN][1000 genomes]
rs7431270	0.92[ASN][1000 genomes]
rs7646778	0.99[ASN][1000 genomes]
rs7646787	0.99[ASN][1000 genomes]
rs950364	1.00[ASN][1000 genomes]
rs9637447	0.97[ASN][1000 genomes]
rs9637455	0.97[ASN][1000 genomes]
rs9810983	0.96[ASN][1000 genomes]
rs9816991	0.99[ASN][1000 genomes]
rs9857022	0.91[ASN][1000 genomes]
rs9871421	1.00[ASN][1000 genomes]

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	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
5	nsv878041	chr3:179983857-180097855	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:180076800-180083800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:180078600-180079000	Enhancers	Fetal Brain Male	brain

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