| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44427408-44427731 | Common:2; Rare:76 | ||||
| chr15:44427755-44427907 | Common:2; Rare:46 | ||||
| chr15:44536548-44536930 | Rare:83 | ||||
| chr15:44537000-44537266 | Common:2; Rare:104 | ||||
| chr15:44537305-44537453 | Rare:43 | ||||
| chr15:44537566-44537815 | Common:1; Rare:54 | ||||
| chr15:44566442-44566745 | Common:1; Rare:67 | ||||
| chr15:44663074-44663318 | Common:1; Rare:56 | ||||
| chr15:44663333-44663389 | Common:2; Rare:23; Clinvar (benign):3 | ||||
| chr15:44663481-44663929 | Rare:191; Clinvar:13; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr15:44711163-44711759 | Common:1; Rare:151; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711845-44712018 | Rare:33 | ||||
| chr15:44712097-44712216 | Common:1; Rare:17 | ||||
| chr15:44712594-44712786 | Rare:53 | ||||
| chr15:44728684-44729452 | Common:1; Rare:157 |