Variant report
| Variant | rs28605860 |
|---|---|
| Chromosome Location | chr5:35334808-35334809 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:35332600-35335600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 2 | chr5:35332800-35336000 | Weak transcription | Fetal Intestine Small | intestine |
| 3 | chr5:35332800-35336800 | Weak transcription | Fetal Intestine Large | intestine |
| 4 | chr5:35332800-35337000 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 5 | chr5:35332800-35337800 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 6 | chr5:35333000-35335200 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 7 | chr5:35333000-35336800 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 8 | chr5:35333200-35335200 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 9 | chr5:35333200-35335200 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
