| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:25468673-25468975 | Common:1; Rare:107 | ||||
| chr13:26221791-26221970 | Rare:50 | ||||
| chr13:26222259-26222375 | Common:2; Rare:33 | ||||
| chr13:26557472-26557763 | Common:4; Rare:119 | ||||
| chr13:27251235-27251623 | Common:8; Rare:119 | ||||
| chr13:27424509-27424732 | Common:2; Rare:74 | ||||
| chr13:27449986-27450215 | Common:3; Rare:69 | ||||
| chr13:27450529-27450685 | Common:2; Rare:58 | ||||
| chr13:27620465-27620810 | Common:2; Rare:117 | ||||
| chr13:28138141-28138206 | Rare:17 | ||||
| chr13:28658948-28659001 | Rare:13 | ||||
| chr13:28659062-28659194 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr13:28718954-28719123 | Common:1; Rare:36 | ||||
| chr13:30306813-30307197 | Common:7; Rare:102 | ||||
| chr13:30307364-30307596 | Common:2; Rare:79 |