Variant report
| Variant | rs4917740 |
|---|---|
| Chromosome Location | chr10:98263137-98263138 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:98254400-98266400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr10:98261000-98266400 | Enhancers | HMEC | breast |
| 3 | chr10:98261200-98263800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 4 | chr10:98261200-98264400 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
| 5 | chr10:98261400-98263600 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 6 | chr10:98261600-98266200 | Weak transcription | Left Ventricle | heart |
| 7 | chr10:98261600-98266200 | Weak transcription | Right Ventricle | heart |
| 8 | chr10:98261600-98266600 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 9 | chr10:98261800-98263800 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 10 | chr10:98261800-98268400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
| 11 | chr10:98262600-98263400 | Enhancers | NHEK | skin |
| 12 | chr10:98262800-98266200 | Weak transcription | Esophagus | oesophagus |
