Variant report
| Variant | rs807699 |
|---|---|
| Chromosome Location | chr6:24275383-24275384 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:24263000-24283000 | Weak transcription | Fetal Intestine Large | intestine |
| 2 | chr6:24270400-24283800 | Weak transcription | Pancreas | Pancrea |
| 3 | chr6:24271200-24283400 | Weak transcription | Fetal Intestine Small | intestine |
| 4 | chr6:24274200-24283800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 5 | chr6:24274600-24279600 | Weak transcription | Fetal Kidney | kidney |
| 6 | chr6:24274800-24277000 | Weak transcription | HepG2 | liver |
| 7 | chr6:24275200-24275800 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
