| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:92908034-92908205 | Common:2; Rare:40 | ||||
| chr15:92923674-92923876 | Rare:51 | ||||
| chr15:92929028-92929301 | Rare:52 | ||||
| chr15:92933062-92933297 | Common:3; Rare:29 | ||||
| chr15:92940370-92940495 | Common:1; Rare:29 | ||||
| chr15:92990378-92990480 | Rare:20 | ||||
| chr15:93002077-93002569 | Common:4; Rare:105; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr15:94487308-94487346 | Rare:7 | ||||
| chr15:94585062-94585349 | Common:2; Rare:56 | ||||
| chr15:94607616-94607749 | Common:1; Rare:21 | ||||
| chr15:94671861-94672080 | Rare:34 | ||||
| chr15:94841253-94841535 | Common:3; Rare:47 | ||||
| chr15:94855747-94855930 | Common:2; Rare:48 | ||||
| chr15:94856876-94856891 | Rare:4 | ||||
| chr15:95252453-95252738 | Common:1; Rare:52 |