| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43510602-43511106 | Rare:186 | ||||
| chr15:43746275-43746575 | Common:1; Rare:128 | ||||
| chr15:43776949-43777112 | Common:1; Rare:48 | ||||
| chr15:43777114-43777412 | Rare:65 | ||||
| chr15:44288390-44288750 | Common:38; Rare:220 | ||||
| chr15:44536632-44537401 | Common:3; Rare:248 | ||||
| chr15:44663532-44663877 | Rare:158; Clinvar:13; Clinvar (benign):6 | ||||
| chr15:44711341-44711612 | Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44712020 | Rare:32 | ||||
| chr15:44728716-44729198 | Common:1; Rare:95 | ||||
| chr15:45200496-45200674 | Common:1; Rare:48 | ||||
| chr15:45378481-45378717 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):4 | ||||
| chr15:45402225-45402387 | Common:3; Rare:49 | ||||
| chr15:45587099-45587273 | Rare:30 | ||||
| chr15:45587296-45587450 | Rare:48; Clinvar:6 |