| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70854101-70854245 | Rare:47 | ||||
| chr15:72117956-72118435 | Common:5; Rare:165 | ||||
| chr15:72231114-72231504 | Common:3; Rare:120 | ||||
| chr15:72231589-72231620 | Rare:5 | ||||
| chr15:72375951-72376147 | Common:3; Rare:78; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:72474195-72474635 | Rare:158 | ||||
| chr15:72475153-72475348 | Common:1; Rare:52 | ||||
| chr15:72686173-72686220 | Common:2; Rare:21; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72783483-72783734 | Common:1; Rare:101 | ||||
| chr15:72783736-72783804 | Rare:21 | ||||
| chr15:73633127-73633300 | Rare:68 | ||||
| chr15:73994562-73994801 | Common:1; Rare:50 | ||||
| chr15:74461106-74461347 | Rare:70 | ||||
| chr15:74540966-74541283 | Common:4; Rare:112 | ||||
| chr15:74615559-74615905 | Common:4; Rare:109 |