Variant report

Variant	rs10070825
Chromosome Location	chr5:112834255-112834256
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10035293	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10035297	0.98[ASN][1000 genomes]
rs10038504	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs10042141	0.90[ASN][1000 genomes]
rs10043783	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10043834	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10052747	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10053052	1.00[CEU][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs10053157	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs10053622	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10055327	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs10057000	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10057264	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs10057372	0.85[EUR][1000 genomes]
rs10060179	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10066163	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs10075927	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10078576	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10155616	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10440762	0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10477492	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10477493	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10477494	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10478123	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10478124	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11950116	0.90[ASN][1000 genomes]
rs11950577	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.98[ASN][1000 genomes]
rs11952758	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs11953401	0.85[EUR][1000 genomes]
rs11960559	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12332461	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12652864	0.90[CHB][hapmap]
rs12656898	0.84[ASN][1000 genomes]
rs12659593	0.84[ASN][1000 genomes]
rs13354840	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs13355687	0.85[EUR][1000 genomes]
rs13356509	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13356904	0.84[EUR][1000 genomes]
rs13358111	0.85[EUR][1000 genomes]
rs1582487	0.90[CHB][hapmap];0.88[ASN][1000 genomes]
rs17135618	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs1816063	0.88[ASN][1000 genomes]
rs2303718	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs28566618	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28714108	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28793421	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34936289	0.85[EUR][1000 genomes]
rs35724644	0.85[EUR][1000 genomes]
rs36009332	0.98[ASN][1000 genomes]
rs36015377	0.98[ASN][1000 genomes]
rs3842916	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs3843501	1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3857436	1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs41459745	1.00[JPT][hapmap]
rs4345310	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs55912732	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56081130	0.85[EUR][1000 genomes]
rs56090613	0.84[ASN][1000 genomes]
rs59211196	0.85[EUR][1000 genomes]
rs6594702	0.85[EUR][1000 genomes]
rs6866028	0.96[ASN][1000 genomes]
rs6871995	0.80[EUR][1000 genomes]
rs6879177	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6879370	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73779003	0.85[EUR][1000 genomes]
rs73779004	0.85[EUR][1000 genomes]
rs73779005	0.85[EUR][1000 genomes]
rs73779006	0.85[EUR][1000 genomes]
rs7705430	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs7705568	0.85[EUR][1000 genomes]
rs7709433	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7709550	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7709818	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7715071	0.85[EUR][1000 genomes]
rs7715884	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs7719254	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7722421	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7726631	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7731451	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7735806	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9654506	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[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	nsv599396	chr5:112408944-112853189	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr5:112827200-112840400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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