| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44427269-44427679 | Common:1; Rare:157 | ||||
| chr15:44536665-44537222 | Common:6; Rare:308 | ||||
| chr15:44663528-44663871 | Rare:290; Clinvar:22; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr15:44711310-44711605 | Rare:152; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr15:44711640-44712091 | Rare:134 | ||||
| chr15:44728650-44729200 | Common:2; Rare:168 | ||||
| chr15:45023050-45023293 | Common:6; Rare:125 | ||||
| chr15:45187927-45188126 | Common:6; Rare:144 | ||||
| chr15:45402161-45402445 | Common:12; Rare:176; Clinvar:1 | ||||
| chr15:45587093-45587494 | Common:2; Rare:194; Clinvar:12; Clinvar (benign):3 | ||||
| chr15:48178271-48178423 | Rare:36 | ||||
| chr15:48331825-48332243 | Common:18; Rare:230 | ||||
| chr15:49046358-49046617 | Common:2; Rare:92 | ||||
| chr15:49155533-49155842 | Common:4; Rare:197 | ||||
| chr15:49169971-49170319 | Rare:147 |