| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39933991-39934334 | Common:5; Rare:124; Clinvar (benign):2 | ||||
| chr15:40038878-40039350 | Common:1; Rare:170 | ||||
| chr15:40108840-40109125 | Common:1; Rare:75 | ||||
| chr15:40160973-40161248 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:40382678-40383076 | Common:3; Rare:155 | ||||
| chr15:40439660-40439964 | Common:1; Rare:65 | ||||
| chr15:40440683-40440972 | Rare:76 | ||||
| chr15:40564976-40565273 | Common:3; Rare:58 | ||||
| chr15:40569192-40569365 | Common:3; Rare:41 | ||||
| chr15:40694715-40694786 | Rare:18 | ||||
| chr15:40695050-40695345 | Common:3; Rare:86; Clinvar:1 | ||||
| chr15:40755209-40755448 | Common:2; Rare:81 | ||||
| chr15:40777314-40777585 | Common:3; Rare:50 | ||||
| chr15:40807050-40807118 | Rare:18 | ||||
| chr15:40807371-40807797 | Common:4; Rare:137 |