| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:98900599-98900773 | Common:1; Rare:41 | ||||
| chr15:99251213-99251505 | Common:4; Rare:105 | ||||
| chr15:99320241-99320608 | Common:1; Rare:67 | ||||
| chr15:99565820-99566091 | Rare:114 | ||||
| chr15:100602130-100602647 | Common:3; Rare:140 | ||||
| chr15:100879378-100880004 | Common:5; Rare:204; Clinvar (benign):1 | ||||
| chr15:100918829-100918952 | Common:1; Rare:23 | ||||
| chr15:100919288-100919442 | Rare:57 | ||||
| chr15:101277359-101277619 | Common:3; Rare:139 | ||||
| chr15:101295128-101295401 | Common:1; Rare:85 | ||||
| chr15:101489694-101489961 | Common:3; Rare:91 | ||||
| chr15:101652254-101652403 | Common:3; Rare:75 | ||||
| chr16:53571-53895 | Common:7; Rare:109 | ||||
| chr16:78090-78287 | Common:3; Rare:69 | ||||
| chr16:138600-138801 | Common:10; Rare:60 |