| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:24954898-24954957 | Rare:24 | ||||
| chr15:24954976-24955013 | Rare:20 | ||||
| chr15:25438276-25438544 | Common:1; Rare:89; Clinvar (benign):1 | ||||
| chr15:25438905-25439308 | Common:3; Rare:144 | ||||
| chr15:29269684-29269987 | Common:2; Rare:138 | ||||
| chr15:30624515-30624570 | Common:1; Rare:10 | ||||
| chr15:30625639-30625836 | Common:4; Rare:49 | ||||
| chr15:30625993-30626149 | Common:3; Rare:38 | ||||
| chr15:30903614-30903969 | Common:3; Rare:95 | ||||
| chr15:30991510-30991807 | Common:4; Rare:102 | ||||
| chr15:30991859-30992006 | Common:2; Rare:64 | ||||
| chr15:31326090-31326489 | Common:5; Rare:169 | ||||
| chr15:31326681-31326969 | Rare:117 | ||||
| chr15:31326997-31327044 | Rare:17 | ||||
| chr15:31365742-31365764 | Rare:3 |