| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:38454035-38454242 | Rare:78 | ||||
| chr15:38454322-38454419 | Common:1; Rare:23 | ||||
| chr15:38454441-38454670 | Rare:61 | ||||
| chr15:38564158-38564414 | Common:1; Rare:77 | ||||
| chr15:38564700-38564917 | Common:2; Rare:58 | ||||
| chr15:39580758-39581192 | Common:2; Rare:117 | ||||
| chr15:39782408-39782689 | Common:2; Rare:76 | ||||
| chr15:39782756-39783003 | Common:1; Rare:77 | ||||
| chr15:39920883-39921108 | Common:3; Rare:82 | ||||
| chr15:39933932-39934246 | Common:4; Rare:114 | ||||
| chr15:39934267-39934343 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr15:39976387-39976571 | Rare:37; Clinvar (pathogenic):1 | ||||
| chr15:39976695-39976877 | Common:2; Rare:66; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:40002396-40002583 | Common:1; Rare:20 | ||||
| chr15:40038406-40038680 | Common:4; Rare:55 |