Variant report
Variant | rs853546 |
---|---|
Chromosome Location | chr12:26053458-26053459 |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr12:26052571..26054359-chr12:26055750..26057714,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10771247 | 0.85[AMR][1000 genomes] |
rs1167618 | 0.83[AMR][1000 genomes] |
rs1167619 | 0.85[AMR][1000 genomes] |
rs1177524 | 0.86[AMR][1000 genomes] |
rs1183807 | 0.86[AMR][1000 genomes] |
rs1797965 | 0.86[AMR][1000 genomes] |
rs2634170 | 0.86[AMR][1000 genomes] |
rs2643928 | 0.86[AMR][1000 genomes] |
rs4246236 | 0.83[AMR][1000 genomes] |
rs706539 | 0.86[AMR][1000 genomes] |
rs7954454 | 0.85[AMR][1000 genomes] |
rs829823 | 0.86[AMR][1000 genomes] |
rs829824 | 0.82[AMR][1000 genomes] |
rs829825 | 0.86[AMR][1000 genomes] |
rs829826 | 0.86[AMR][1000 genomes] |
rs829827 | 0.86[AMR][1000 genomes] |
rs844202 | 0.86[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2758300 | chr12:25992331-26161116 | Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 38 gene(s) | inside rSNPs | diseases |
2 | esv2759886 | chr12:25992331-26161116 | Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 38 gene(s) | inside rSNPs | diseases |
3 | nsv1035319 | chr12:26020667-26097148 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers | TF binding regionChromatin interactive regionlncRNAmiRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:26050400-26076800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |