| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44427530-44427682 | Rare:44 | ||||
| chr15:44427684-44428240 | Common:7; Rare:185 | ||||
| chr15:44536852-44537441 | Common:6; Rare:340 | ||||
| chr15:44537681-44537888 | Common:1; Rare:45 | ||||
| chr15:44662860-44663320 | Common:4; Rare:193 | ||||
| chr15:44663530-44663848 | Rare:289; Clinvar:24; Clinvar (benign):12 | ||||
| chr15:44711297-44711640 | Rare:195; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr15:44711830-44712167 | Common:1; Rare:97 | ||||
| chr15:44728869-44729188 | Common:2; Rare:128 | ||||
| chr15:45023035-45023267 | Common:6; Rare:109 | ||||
| chr15:45402186-45402428 | Common:12; Rare:155 | ||||
| chr15:45522747-45522971 | Common:1; Rare:81 | ||||
| chr15:45587068-45587482 | Common:3; Rare:176; Clinvar:12; Clinvar (benign):3 | ||||
| chr15:45587510-45588070 | Common:6; Rare:273; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:45634530-45634835 | Common:2; Rare:120 |