| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74843103-74843530 | Common:2; Rare:116 | ||||
| chr15:74872928-74873178 | Common:2; Rare:69 | ||||
| chr15:74873273-74873529 | Common:6; Rare:71 | ||||
| chr15:74889889-74890190 | Rare:119; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74890588-74890646 | Common:1; Rare:22; Clinvar:2 | ||||
| chr15:74906007-74906046 | Rare:7 | ||||
| chr15:74906731-74906949 | Common:1; Rare:90 | ||||
| chr15:74907086-74907185 | Rare:31 | ||||
| chr15:74937453-74937518 | Common:1; Rare:12 | ||||
| chr15:74937970-74938315 | Common:2; Rare:110 | ||||
| chr15:74956712-74956909 | Common:1; Rare:84 | ||||
| chr15:74956980-74957240 | Common:1; Rare:78 | ||||
| chr15:74995386-74995609 | Common:5; Rare:87 | ||||
| chr15:75023374-75023779 | Common:4; Rare:95 | ||||
| chr15:75198726-75199015 | Common:1; Rare:60 |