| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21604067-21604297 | Common:5; Rare:119 | ||||
| chr13:23579236-23579407 | Common:3; Rare:54 | ||||
| chr13:23889289-23889510 | Common:1; Rare:79 | ||||
| chr13:24512739-24512843 | Common:3; Rare:31 | ||||
| chr13:24922810-24923121 | Common:2; Rare:106; Clinvar:1 | ||||
| chr13:25301492-25301776 | Common:3; Rare:106 | ||||
| chr13:26221791-26221982 | Rare:56 | ||||
| chr13:26222258-26222415 | Common:2; Rare:46 | ||||
| chr13:26557472-26557766 | Common:4; Rare:119 | ||||
| chr13:27251237-27251606 | Common:6; Rare:112 | ||||
| chr13:27270984-27271192 | Common:1; Rare:68 | ||||
| chr13:27450113-27450259 | Common:3; Rare:48 | ||||
| chr13:27620429-27620810 | Common:2; Rare:128 | ||||
| chr13:28138139-28138224 | Common:1; Rare:24 | ||||
| chr13:28659052-28659184 | Rare:56; Clinvar (pathogenic):1 |