| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43638778-43639178 | Rare:126 | ||||
| chr15:43735020-43735490 | Common:2; Rare:79 | ||||
| chr15:43788600-43788840 | Common:2; Rare:69 | ||||
| chr15:43789291-43789854 | Common:2; Rare:160 | ||||
| chr15:43830906-43831306 | Common:1; Rare:111 | ||||
| chr15:44545501-44546723 | Common:9; Rare:389 | ||||
| chr15:44633180-44633510 | Common:1; Rare:70 | ||||
| chr15:44662590-44662805 | Common:2; Rare:76 | ||||
| chr15:44669015-44669415 | Rare:171; Clinvar:2 | ||||
| chr15:44672210-44672640 | Common:2; Rare:148; Clinvar (pathogenic):2 | ||||
| chr15:44683250-44683800 | Rare:144 | ||||
| chr15:44710313-44710449 | Rare:21 | ||||
| chr15:44713555-44713955 | Common:2; Rare:103 | ||||
| chr15:44719572-44719972 | Rare:122 | ||||
| chr15:44722088-44722305 | Common:4; Rare:56 |