| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:88622288-88622500 | Common:6; Rare:120 | ||||
| chr15:88623179-88623447 | Common:2; Rare:73 | ||||
| chr15:88624454-88624596 | Common:1; Rare:24 | ||||
| chr15:88639988-88640415 | Common:2; Rare:227 | ||||
| chr15:88640661-88641642 | Common:8; Rare:232 | ||||
| chr15:88649430-88649750 | Common:5; Rare:120 | ||||
| chr15:88683295-88683695 | Rare:124 | ||||
| chr15:88982540-88982990 | Common:2; Rare:81 | ||||
| chr15:89089194-89089594 | Common:2; Rare:84 | ||||
| chr15:89090830-89091148 | Common:8; Rare:95 | ||||
| chr15:89167515-89167915 | Rare:103 | ||||
| chr15:89179920-89180514 | Common:4; Rare:213 | ||||
| chr15:89311342-89311742 | Common:10; Rare:115 | ||||
| chr15:89321636-89322838 | Common:10; Rare:380; Clinvar:20; Clinvar (benign):20; Clinvar (pathogenic):12 | ||||
| chr15:89336118-89336518 | Common:1; Rare:90 |