Variant report
Variant | rs73485825 |
---|---|
Chromosome Location | chr11:63171466-63171467 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:63168551..63171520-chr3:13164041..13166803,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1152240 | 1.00[AMR][1000 genomes] |
rs1152247 | 1.00[AMR][1000 genomes] |
rs11821164 | 1.00[AMR][1000 genomes] |
rs11824742 | 1.00[AMR][1000 genomes] |
rs11828961 | 1.00[AMR][1000 genomes] |
rs1193719 | 1.00[AMR][1000 genomes] |
rs1193720 | 1.00[AMR][1000 genomes] |
rs1193728 | 1.00[AMR][1000 genomes] |
rs1193853 | 1.00[AMR][1000 genomes] |
rs1193854 | 1.00[AMR][1000 genomes] |
rs1193855 | 1.00[AMR][1000 genomes] |
rs1193863 | 1.00[AMR][1000 genomes] |
rs1193864 | 1.00[AMR][1000 genomes] |
rs1193867 | 1.00[AMR][1000 genomes] |
rs1193872 | 1.00[AMR][1000 genomes] |
rs1193901 | 1.00[AMR][1000 genomes] |
rs1193903 | 1.00[AMR][1000 genomes] |
rs1193906 | 1.00[AMR][1000 genomes] |
rs1193910 | 1.00[AMR][1000 genomes] |
rs1404609 | 1.00[AMR][1000 genomes] |
rs2514265 | 1.00[AMR][1000 genomes] |
rs2642528 | 1.00[AMR][1000 genomes] |
rs3019069 | 1.00[AMR][1000 genomes] |
rs60039724 | 1.00[AMR][1000 genomes] |
rs60661472 | 1.00[AMR][1000 genomes] |
rs61335619 | 1.00[AMR][1000 genomes] |
rs7116264 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7118013 | 1.00[AMR][1000 genomes] |
rs73483733 | 1.00[AMR][1000 genomes] |
rs73483770 | 1.00[AMR][1000 genomes] |
rs73483775 | 1.00[AMR][1000 genomes] |
rs73483785 | 1.00[AMR][1000 genomes] |
rs73485827 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73485838 | 0.91[AFR][1000 genomes] |
rs73485839 | 0.91[AFR][1000 genomes] |
rs73485855 | 0.91[AFR][1000 genomes] |
rs73485864 | 0.91[AFR][1000 genomes] |
rs73485869 | 0.91[AFR][1000 genomes] |
rs73485888 | 1.00[AMR][1000 genomes] |
rs73488052 | 1.00[AMR][1000 genomes] |
rs73488054 | 1.00[AMR][1000 genomes] |
rs7929031 | 0.81[AFR][1000 genomes] |
rs7935128 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1051171 | chr11:62987064-63835715 | Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 100 gene(s) | inside rSNPs | diseases |
2 | nsv1053585 | chr11:63057767-63180308 | Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv555178 | chr11:63078742-63197930 | Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv1822068 | chr11:63146055-63239984 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
5 | nsv1053627 | chr11:63160057-63183395 | Flanking Active TSS Weak transcription Enhancers Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | esv3434037 | chr11:63170556-63217699 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:63170600-63172800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
2 | chr11:63170600-63173800 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
3 | chr11:63171400-63171800 | Enhancers | Liver | Liver |
4 | chr11:63171400-63173200 | Enhancers | HepG2 | liver |