| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44712137-44712186 | Rare:8 | ||||
| chr15:44712593-44712756 | Rare:47 | ||||
| chr15:44728669-44729246 | Common:1; Rare:111 | ||||
| chr15:44729261-44729373 | Rare:20 | ||||
| chr15:44729482-44729560 | Common:1; Rare:18 | ||||
| chr15:44729609-44729661 | Rare:8 | ||||
| chr15:44735648-44735953 | Common:6; Rare:50 | ||||
| chr15:45022957-45023276 | Common:5; Rare:88 | ||||
| chr15:45023574-45023678 | Common:1; Rare:21 | ||||
| chr15:45187906-45188147 | Common:3; Rare:86 | ||||
| chr15:45200410-45200834 | Common:2; Rare:132 | ||||
| chr15:45201031-45201170 | Common:2; Rare:52 | ||||
| chr15:45378247-45378376 | Rare:37; Clinvar (benign):1 | ||||
| chr15:45378495-45378668 | Common:3; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr15:45378684-45378807 | Rare:26; Clinvar:1 |