| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:25307653-25307951 | Common:1; Rare:74 | ||||
| chr13:26221776-26221948 | Rare:47 | ||||
| chr13:27251269-27251802 | Common:6; Rare:151 | ||||
| chr13:27251806-27251824 | Rare:6 | ||||
| chr13:27255092-27255356 | Common:2; Rare:62 | ||||
| chr13:27270686-27270836 | Rare:51 | ||||
| chr13:27424543-27424882 | Common:2; Rare:115 | ||||
| chr13:27434036-27434185 | Rare:46 | ||||
| chr13:27449944-27450258 | Common:3; Rare:93 | ||||
| chr13:27450514-27450632 | Common:2; Rare:53 | ||||
| chr13:27620584-27620923 | Common:4; Rare:107 | ||||
| chr13:28138051-28138234 | Common:2; Rare:59 | ||||
| chr13:28139240-28139571 | Common:1; Rare:84 | ||||
| chr13:28495126-28495209 | Common:1; Rare:22 | ||||
| chr13:28658850-28659276 | Common:2; Rare:151; Clinvar (pathogenic):1 |