| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72231160-72231526 | Common:3; Rare:119 | ||||
| chr15:72375958-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474195-72474540 | Rare:118 | ||||
| chr15:72686173-72686225 | Common:2; Rare:23; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72783693-72783788 | Common:1; Rare:39 | ||||
| chr15:73633166-73633576 | Common:2; Rare:157 | ||||
| chr15:73994587-73994801 | Rare:46 | ||||
| chr15:74461094-74461319 | Rare:69 | ||||
| chr15:74540966-74541271 | Common:4; Rare:108 | ||||
| chr15:74598293-74598506 | Common:1; Rare:92 | ||||
| chr15:74615605-74615898 | Common:3; Rare:95 | ||||
| chr15:74695969-74696058 | Rare:32 | ||||
| chr15:74873003-74873109 | Rare:23 | ||||
| chr15:74906798-74906881 | Rare:34 | ||||
| chr15:74937952-74938254 | Common:2; Rare:95 |