| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27622305-27622369 | Common:1; Rare:13 | ||||
| chr13:27919831-27920055 | Common:3; Rare:64 | ||||
| chr13:27971366-27971594 | Rare:46 | ||||
| chr13:27988667-27988798 | Common:2; Rare:30 | ||||
| chr13:28137937-28138290 | Common:4; Rare:92 | ||||
| chr13:28138359-28138601 | Common:3; Rare:70 | ||||
| chr13:28138638-28138852 | Common:1; Rare:50 | ||||
| chr13:28139040-28139151 | Common:1; Rare:27 | ||||
| chr13:28139189-28139430 | Rare:53 | ||||
| chr13:28139434-28139509 | Common:1; Rare:25 | ||||
| chr13:28495087-28495351 | Common:1; Rare:76 | ||||
| chr13:28658937-28659382 | Common:2; Rare:158; Clinvar (pathogenic):1 | ||||
| chr13:28718679-28718754 | Common:2; Rare:12 | ||||
| chr13:28718913-28719179 | Common:1; Rare:69 | ||||
| chr13:29594793-29595234 | Common:2; Rare:105 |