Variant report
| Variant | rs57166953 |
|---|---|
| Chromosome Location | chr14:69469801-69469802 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr14:69447000-69471400 | Weak transcription | Esophagus | oesophagus |
| 2 | chr14:69456000-69471200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 3 | chr14:69462800-69470800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 4 | chr14:69465000-69471200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 5 | chr14:69465000-69471600 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
| 6 | chr14:69467800-69470000 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 7 | chr14:69469000-69471400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 8 | chr14:69469000-69472000 | Weak transcription | Placenta | Placenta |
| 9 | chr14:69469200-69471600 | Weak transcription | A549 | lung |
| 10 | chr14:69469600-69471200 | Weak transcription | Stomach Smooth Muscle | stomach |
| 11 | chr14:69469800-69470000 | Bivalent Enhancer | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 12 | chr14:69469800-69471000 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 13 | chr14:69469800-69473000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
