Variant report
| Variant | esv2215572 |
|---|---|
| Chromosome Location | chr19:21761725-21761727 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr19:21752000-21769600 | Weak transcription | Fetal Heart | heart |
| 2 | chr19:21752800-21766200 | Weak transcription | Fetal Intestine Large | intestine |
| 3 | chr19:21753000-21768000 | Weak transcription | Fetal Intestine Small | intestine |
| 4 | chr19:21753200-21762800 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 5 | chr19:21756800-21762400 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
| 6 | chr19:21757000-21764400 | Weak transcription | Pancreas | Pancrea |
| 7 | chr19:21757400-21762800 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 8 | chr19:21759400-21764600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 9 | chr19:21760200-21768000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 10 | chr19:21760400-21769000 | Weak transcription | Fetal Kidney | kidney |
| 11 | chr19:21761200-21762200 | Weak transcription | Primary T cells from cord blood | blood |
| 12 | chr19:21761400-21762200 | Strong transcription | Dnd41 | blood |
