| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72118184-72118417 | Common:2; Rare:69 | ||||
| chr15:72375932-72376147 | Common:3; Rare:85; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72686147-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633238-73633545 | Common:1; Rare:120 | ||||
| chr15:73994587-73994761 | Rare:34 | ||||
| chr15:74461106-74461314 | Rare:65 | ||||
| chr15:74540954-74541271 | Common:4; Rare:110 | ||||
| chr15:74615581-74615891 | Common:4; Rare:100 | ||||
| chr15:74781914-74782146 | Common:3; Rare:76 | ||||
| chr15:74788757-74788996 | Rare:50 | ||||
| chr15:74821428-74821673 | Common:1; Rare:42 | ||||
| chr15:74843106-74843328 | Common:1; Rare:65 | ||||
| chr15:74873292-74873488 | Common:6; Rare:60 | ||||
| chr15:74937987-74938276 | Common:2; Rare:98 | ||||
| chr15:74995427-74995611 | Common:4; Rare:76 |