| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72118167-72118425 | Common:2; Rare:81 | ||||
| chr15:72231117-72231516 | Common:3; Rare:126 | ||||
| chr15:72375958-72376123 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72686147-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633219-73633587 | Common:2; Rare:144 | ||||
| chr15:73926265-73926471 | Rare:51 | ||||
| chr15:73994587-73994801 | Rare:46 | ||||
| chr15:74202434-74202569 | Common:1; Rare:31 | ||||
| chr15:74202747-74203046 | Common:1; Rare:75; Clinvar:2 | ||||
| chr15:74203184-74203273 | Common:1; Rare:16 | ||||
| chr15:74461101-74461329 | Rare:67 | ||||
| chr15:74695963-74696138 | Rare:56 | ||||
| chr15:74843113-74843281 | Common:1; Rare:53 | ||||
| chr15:74873307-74873464 | Common:5; Rare:49 | ||||
| chr15:75335973-75336085 | Common:1; Rare:48 |