| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89088032-89088509 | Common:5; Rare:119 | ||||
| chr15:89221600-89221820 | Rare:50; Clinvar (benign):1 | ||||
| chr15:89243876-89244063 | Common:1; Rare:55; Clinvar:3 | ||||
| chr15:89334793-89335147 | Common:4; Rare:163 | ||||
| chr15:89575159-89575534 | Common:3; Rare:109 | ||||
| chr15:89655412-89655602 | Common:1; Rare:66; Clinvar (benign):2 | ||||
| chr15:89690696-89690819 | Common:2; Rare:37 | ||||
| chr15:89750884-89751007 | Common:1; Rare:66 | ||||
| chr15:89776566-89776758 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr15:89893947-89894353 | Common:4; Rare:121 | ||||
| chr15:89912089-89912489 | Common:1; Rare:142 | ||||
| chr15:90000428-90001325 | Common:10; Rare:324 | ||||
| chr15:90001801-90002028 | Rare:39 | ||||
| chr15:90002350-90002710 | Common:1; Rare:91 | ||||
| chr15:90102444-90102626 | Common:1; Rare:69 |