Variant report
| Variant | rs4713297 |
|---|---|
| Chromosome Location | chr6:30116774-30116775 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:30112800-30119200 | Strong transcription | Placenta | Placenta |
| 2 | chr6:30112800-30120800 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
| 3 | chr6:30113000-30119600 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
| 4 | chr6:30113800-30118600 | Weak transcription | Fetal Intestine Large | intestine |
| 5 | chr6:30115400-30117800 | Weak transcription | Primary hematopoietic stem cells | blood |
| 6 | chr6:30115600-30117200 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
| 7 | chr6:30116000-30121800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 8 | chr6:30116400-30118600 | Weak transcription | Fetal Intestine Small | intestine |
| 9 | chr6:30116400-30119400 | Enhancers | HepG2 | liver |
