| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66504772-66505349 | Common:4; Rare:220 | ||||
| chr15:67254623-67254850 | Rare:83 | ||||
| chr15:67521632-67521784 | Rare:37 | ||||
| chr15:67542597-67542768 | Common:2; Rare:58 | ||||
| chr15:68054155-68054339 | Rare:56 | ||||
| chr15:68277359-68277466 | Common:1; Rare:25 | ||||
| chr15:68817605-68817709 | Common:1; Rare:37 | ||||
| chr15:69414209-69414463 | Rare:86 | ||||
| chr15:69452774-69453020 | Common:5; Rare:109 | ||||
| chr15:70702170-70702422 | Rare:51 | ||||
| chr15:70854101-70854289 | Rare:62 | ||||
| chr15:70892381-70892690 | Common:1; Rare:69 | ||||
| chr15:72118167-72118432 | Common:2; Rare:87 | ||||
| chr15:72231107-72231523 | Common:3; Rare:134 | ||||
| chr15:72375968-72376124 | Common:1; Rare:64; Clinvar:5; Clinvar (pathogenic):2 |