| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:69452590-69452657 | Rare:16 | ||||
| chr15:69452688-69453020 | Common:5; Rare:139 | ||||
| chr15:70097884-70098092 | Common:1; Rare:48 | ||||
| chr15:70892516-70892851 | Common:1; Rare:67 | ||||
| chr15:72118167-72118425 | Common:2; Rare:81 | ||||
| chr15:72231107-72231532 | Common:3; Rare:139 | ||||
| chr15:72375944-72376129 | Common:2; Rare:77; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72685945-72686220 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73752225-73752334 | Rare:29 | ||||
| chr15:74202770-74203049 | Common:1; Rare:70; Clinvar:2 | ||||
| chr15:74461077-74461319 | Common:1; Rare:74 | ||||
| chr15:74540915-74541342 | Common:6; Rare:152 | ||||
| chr15:74615559-74615898 | Common:4; Rare:107 | ||||
| chr15:74695987-74696069 | Rare:23 | ||||
| chr15:74843106-74843339 | Common:1; Rare:66 |