Variant report
| Variant | rs194763 |
|---|---|
| Chromosome Location | chr14:69211175-69211176 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr14:69198400-69214000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 2 | chr14:69201200-69222600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 3 | chr14:69202800-69224600 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
| 4 | chr14:69203600-69213800 | Weak transcription | Esophagus | oesophagus |
| 5 | chr14:69204200-69219200 | Weak transcription | Adipose Nuclei | Adipose |
| 6 | chr14:69204400-69213800 | Weak transcription | Right Atrium | heart |
| 7 | chr14:69205600-69214200 | Weak transcription | Spleen | Spleen |
| 8 | chr14:69205600-69216200 | Weak transcription | Lung | lung |
| 9 | chr14:69209200-69212000 | Weak transcription | Fetal Thymus | thymus |
| 10 | chr14:69210200-69212200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
