Variant report
Variant | rs12058457 |
---|---|
Chromosome Location | chr1:71239057-71239058 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10889894 | 1.00[AMR][1000 genomes] |
rs11209674 | 1.00[AMR][1000 genomes] |
rs11209676 | 1.00[AMR][1000 genomes] |
rs11209695 | 1.00[EUR][1000 genomes] |
rs11799545 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11809656 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12058470 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12061298 | 1.00[AMR][1000 genomes] |
rs12063164 | 1.00[AMR][1000 genomes] |
rs12067572 | 1.00[AMR][1000 genomes] |
rs12067990 | 1.00[AMR][1000 genomes] |
rs12073070 | 1.00[EUR][1000 genomes] |
rs12073536 | 1.00[AMR][1000 genomes] |
rs2068651 | 1.00[AMR][1000 genomes] |
rs6699994 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7551712 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3452322 | chr1:71237020-71240689 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | esv3452319 | chr1:71237194-71240416 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | esv3452323 | chr1:71237208-71240443 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | esv3452321 | chr1:71237251-71240423 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv17158 | chr1:71237358-71240311 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | esv3452324 | chr1:71237364-71240328 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:71238800-71243400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |