Variant report
| Variant | rs3778569 |
|---|---|
| Chromosome Location | chr6:132017930-132017931 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:131993600-132020600 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
| 2 | chr6:131998600-132054000 | Weak transcription | Fetal Intestine Small | intestine |
| 3 | chr6:131998800-132043000 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
| 4 | chr6:131999400-132020600 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
| 5 | chr6:132002600-132054400 | Weak transcription | K562 | blood |
| 6 | chr6:132014600-132019400 | Strong transcription | HepG2 | liver |
| 7 | chr6:132015200-132018400 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 8 | chr6:132017400-132019400 | Strong transcription | Fetal Adrenal Gland | Adrenal Gland |
| 9 | chr6:132017600-132018000 | Enhancers | Placenta | Placenta |
| 10 | chr6:132017600-132019000 | Strong transcription | Fetal Intestine Large | intestine |
