| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:31392377-31392518 | Rare:35 | ||||
| chr15:31870639-31871011 | Common:1; Rare:128 | ||||
| chr15:32030273-32030550 | Common:8; Rare:76 | ||||
| chr15:32615071-32615196 | Common:3; Rare:35 | ||||
| chr15:32615379-32615535 | Common:3; Rare:41 | ||||
| chr15:34038453-34038811 | Common:7; Rare:106 | ||||
| chr15:34039055-34039236 | Common:3; Rare:60 | ||||
| chr15:34039615-34039630 | Rare:6 | ||||
| chr15:34101779-34102310 | Common:1; Rare:117 | ||||
| chr15:34209665-34209882 | Common:3; Rare:60 | ||||
| chr15:34209935-34210227 | Common:2; Rare:102 | ||||
| chr15:34224530-34224556 | Rare:3 | ||||
| chr15:34224822-34225136 | Rare:104 | ||||
| chr15:34318818-34318878 | Rare:13 | ||||
| chr15:34336366-34336440 | Common:1; Rare:30; Clinvar (benign):1 |