| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74889942-74890076 | Rare:55; Clinvar (pathogenic):1 | ||||
| chr15:74937987-74938265 | Common:2; Rare:95 | ||||
| chr15:74995352-74995636 | Common:7; Rare:109 | ||||
| chr15:75455796-75456134 | Common:1; Rare:87 | ||||
| chr15:75625601-75625871 | Common:2; Rare:63 | ||||
| chr15:75640152-75640451 | Common:2; Rare:102 | ||||
| chr15:75843511-75843773 | Rare:108 | ||||
| chr15:75903740-75903966 | Rare:86 | ||||
| chr15:76292441-76292621 | Rare:74; Clinvar:1 | ||||
| chr15:76311393-76311547 | Rare:58; Clinvar:4; Clinvar (benign):5 | ||||
| chr15:77420084-77420481 | Common:2; Rare:121 | ||||
| chr15:77420665-77420957 | Rare:75 | ||||
| chr15:78149161-78149410 | Common:1; Rare:82 | ||||
| chr15:79896989-79897243 | Common:4; Rare:81 | ||||
| chr15:79923645-79923942 | Common:6; Rare:117 |