| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:65611097-65611390 | Common:2; Rare:99 | ||||
| chr15:66293481-66293617 | Common:4; Rare:42 | ||||
| chr15:66504786-66505151 | Common:1; Rare:139 | ||||
| chr15:67254623-67254828 | Rare:74 | ||||
| chr15:67520944-67521236 | Common:5; Rare:105 | ||||
| chr15:68054040-68054329 | Rare:78 | ||||
| chr15:68820709-68821049 | Rare:101 | ||||
| chr15:69414201-69414453 | Rare:85 | ||||
| chr15:69452731-69452915 | Common:4; Rare:84 | ||||
| chr15:70854101-70854251 | Rare:48 | ||||
| chr15:70892381-70892822 | Common:1; Rare:96 | ||||
| chr15:72118060-72118417 | Common:3; Rare:118 | ||||
| chr15:72231094-72231534 | Common:3; Rare:142 | ||||
| chr15:72375958-72376105 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72686139-72686225 | Common:2; Rare:32; Clinvar:2; Clinvar (benign):2 |