| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43746271-43746643 | Common:1; Rare:153 | ||||
| chr15:43776911-43777094 | Common:1; Rare:58 | ||||
| chr15:43777116-43777132 | Rare:9 | ||||
| chr15:43824492-43824805 | Common:2; Rare:95 | ||||
| chr15:44288362-44288995 | Common:39; Rare:293 | ||||
| chr15:44427584-44427765 | Common:1; Rare:48 | ||||
| chr15:44536670-44536784 | Rare:24 | ||||
| chr15:44536854-44537236 | Common:3; Rare:140 | ||||
| chr15:44557315-44557652 | Common:1; Rare:85 | ||||
| chr15:44663393-44663470 | Rare:28; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr15:44711298-44711616 | Rare:94; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728710-44729193 | Common:1; Rare:94 | ||||
| chr15:44729289-44729371 | Rare:12 | ||||
| chr15:44729405-44729550 | Common:1; Rare:32 | ||||
| chr15:45129679-45130038 | Rare:78 |