Variant report
| Variant | rs28698682 |
|---|---|
| Chromosome Location | chr14:69461607-69461608 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr14:69447000-69471400 | Weak transcription | Esophagus | oesophagus |
| 2 | chr14:69455600-69465200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr14:69456000-69464400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 4 | chr14:69456000-69471200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 5 | chr14:69460600-69463200 | Enhancers | Primary T helper naive cells fromperipheralblood | blood |
| 6 | chr14:69461200-69461800 | Enhancers | Primary T killer naive cells fromperipheralblood | blood |
| 7 | chr14:69461600-69462800 | Enhancers | Primary T helper cells PMA-I stimulated | -- |
