| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:24965559-24965822 | Common:1; Rare:58 | ||||
| chr15:24969546-24969801 | Rare:43 | ||||
| chr15:24969990-24970058 | Rare:10 | ||||
| chr15:24973425-24973846 | Common:2; Rare:105 | ||||
| chr15:24974317-24974613 | Common:4; Rare:65; Clinvar:4; Clinvar (benign):2 | ||||
| chr15:24978200-24978519 | Rare:89; Clinvar (benign):1 | ||||
| chr15:24978525-24978864 | Rare:88 | ||||
| chr15:24988095-24988203 | Rare:19 | ||||
| chr15:24990775-24991227 | Common:1; Rare:84 | ||||
| chr15:24992882-24993109 | Common:4; Rare:68 | ||||
| chr15:25015976-25016305 | Common:3; Rare:49 | ||||
| chr15:25018038-25018269 | Common:1; Rare:44 | ||||
| chr15:25030754-25030959 | Common:3; Rare:44 | ||||
| chr15:25033443-25033661 | Common:1; Rare:43 | ||||
| chr15:25034509-25034703 | Rare:37 |