| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:22494616-22494916 | Common:1; Rare:38 | ||||
| chr15:23303467-23303786 | Common:1; Rare:29 | ||||
| chr15:23401726-23401930 | Common:1; Rare:33 | ||||
| chr15:24859038-24859177 | Common:1; Rare:25 | ||||
| chr15:25083453-25083588 | Common:1; Rare:40 | ||||
| chr15:25346005-25346319 | Common:1; Rare:61 | ||||
| chr15:28589195-28589521 | Common:1; Rare:10 | ||||
| chr15:28789747-28789853 | Common:1; Rare:24 | ||||
| chr15:28832106-28832377 | Common:4; Rare:79 | ||||
| chr15:29730520-29730611 | Rare:23 | ||||
| chr15:31215837-31215964 | Common:2; Rare:30 | ||||
| chr15:32536450-32536858 | Common:2; Rare:46 | ||||
| chr15:34514378-34514537 | Rare:47 | ||||
| chr15:34794010-34794365 | Common:7; Rare:58 | ||||
| chr15:34794634-34795032 | Common:2; Rare:114; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 |