Variant report
| Variant | rs4293494 |
|---|---|
| Chromosome Location | chr19:41951575-41951576 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr19:41946000-41953000 | Weak transcription | Right Atrium | heart |
| 2 | chr19:41946800-41952400 | Weak transcription | Spleen | Spleen |
| 3 | chr19:41948000-41957200 | Weak transcription | Esophagus | oesophagus |
| 4 | chr19:41949200-41952400 | Weak transcription | Left Ventricle | heart |
| 5 | chr19:41949400-41953400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 6 | chr19:41949800-41955000 | Weak transcription | HepG2 | liver |
| 7 | chr19:41950000-41953000 | Weak transcription | Lung | lung |
| 8 | chr19:41950200-41955200 | Weak transcription | GM12878-XiMat | blood |
| 9 | chr19:41950400-41953000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 10 | chr19:41951000-41951800 | Transcr. at gene 5' and 3' | Fetal Intestine Small | intestine |
| 11 | chr19:41951400-41951800 | Enhancers | Fetal Intestine Large | intestine |
