Variant report
| Variant | rs4852854 |
|---|---|
| Chromosome Location | chr2:72334996-72334997 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:72327200-72342400 | Weak transcription | Adipose Nuclei | Adipose |
| 2 | chr2:72333000-72342800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 3 | chr2:72334000-72335200 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 4 | chr2:72334000-72337400 | Enhancers | NHEK | skin |
| 5 | chr2:72334200-72335000 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 6 | chr2:72334200-72335200 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr2:72334600-72335000 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
| 8 | chr2:72334600-72335600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 9 | chr2:72334600-72336200 | Weak transcription | HMEC | breast |
