| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74872938-74873171 | Common:1; Rare:63 | ||||
| chr15:74873272-74873523 | Common:6; Rare:70 | ||||
| chr15:74889953-74890121 | Rare:71; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74890296-74890476 | Rare:33 | ||||
| chr15:74906712-74906943 | Common:1; Rare:91 | ||||
| chr15:74907308-74907355 | Rare:14 | ||||
| chr15:74937497-74937607 | Rare:20 | ||||
| chr15:74937669-74937964 | Common:2; Rare:82 | ||||
| chr15:74937970-74938314 | Common:2; Rare:110 | ||||
| chr15:74956578-74956973 | Common:1; Rare:136 | ||||
| chr15:74956977-74957272 | Common:1; Rare:83 | ||||
| chr15:74957378-74957525 | Rare:34 | ||||
| chr15:74995358-74995655 | Common:7; Rare:113 | ||||
| chr15:75023394-75023738 | Common:4; Rare:81 | ||||
| chr15:75201740-75201962 | Common:2; Rare:79 |