| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67254973-67255107 | Common:1; Rare:46 | ||||
| chr15:67520590-67520656 | Common:1; Rare:11 | ||||
| chr15:67521776-67522026 | Rare:72 | ||||
| chr15:67522218-67522355 | Rare:26 | ||||
| chr15:67541819-67542219 | Common:6; Rare:68 | ||||
| chr15:67542499-67542887 | Common:5; Rare:121 | ||||
| chr15:67542966-67543169 | Common:2; Rare:43 | ||||
| chr15:68054009-68054427 | Rare:128 | ||||
| chr15:68054750-68054927 | Common:3; Rare:41 | ||||
| chr15:68229170-68229323 | Common:3; Rare:43 | ||||
| chr15:68229360-68230160 | Common:7; Rare:248; Clinvar:13; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr15:68256857-68256926 | Rare:15 | ||||
| chr15:68257053-68257387 | Common:4; Rare:93 | ||||
| chr15:68277147-68277501 | Common:1; Rare:78 | ||||
| chr15:68277574-68278418 | Common:9; Rare:255 |