| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110536323-110536723 | Common:2; Rare:107 | ||||
| chr13:110575290-110575441 | Rare:22 | ||||
| chr13:110575791-110575900 | Rare:20 | ||||
| chr13:110611080-110611490 | Common:2; Rare:156 | ||||
| chr13:110614294-110614694 | Common:2; Rare:118 | ||||
| chr13:110616319-110616585 | Common:4; Rare:97 | ||||
| chr13:110636208-110636608 | Common:11; Rare:168 | ||||
| chr13:110641650-110642299 | Common:2; Rare:296; Clinvar (benign):1 | ||||
| chr13:110675870-110676450 | Common:5; Rare:134 | ||||
| chr13:110723583-110723983 | Rare:95 | ||||
| chr13:110726870-110727140 | Common:5; Rare:74 | ||||
| chr13:110811738-110812138 | Common:4; Rare:91 | ||||
| chr13:110815263-110815783 | Common:6; Rare:177 | ||||
| chr13:110874727-110874902 | Common:3; Rare:41 | ||||
| chr13:110908076-110909147 | Common:6; Rare:281 |