| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70854080-70854318 | Rare:78 | ||||
| chr15:70892352-70892880 | Common:1; Rare:125 | ||||
| chr15:72117956-72118434 | Common:5; Rare:165 | ||||
| chr15:72118556-72118639 | Rare:19 | ||||
| chr15:72231114-72231523 | Common:3; Rare:131 | ||||
| chr15:72375954-72376144 | Common:3; Rare:77; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474210-72474573 | Rare:122 | ||||
| chr15:72686114-72686225 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72783653-72783881 | Common:2; Rare:108 | ||||
| chr15:73369309-73369350 | Common:1; Rare:7 | ||||
| chr15:73369720-73369904 | Common:1; Rare:29 | ||||
| chr15:73633127-73633595 | Common:2; Rare:181 | ||||
| chr15:73684124-73684449 | Rare:87 | ||||
| chr15:73926205-73926482 | Rare:59 | ||||
| chr15:73994587-73994761 | Rare:34 |