| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:77027336-77027801 | Common:2; Rare:99 | ||||
| chr15:77035636-77035869 | Common:4; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:77420024-77420834 | Common:4; Rare:217 | ||||
| chr15:77420852-77420994 | Rare:39 | ||||
| chr15:78149161-78149410 | Common:1; Rare:82 | ||||
| chr15:78270267-78270513 | Common:1; Rare:55 | ||||
| chr15:78299571-78299780 | Common:1; Rare:75 | ||||
| chr15:78438002-78438334 | Common:3; Rare:136 | ||||
| chr15:78507433-78507617 | Rare:54 | ||||
| chr15:78540387-78540497 | Common:3; Rare:36 | ||||
| chr15:78540664-78540810 | Common:2; Rare:48 | ||||
| chr15:78937508-78937608 | Rare:15 | ||||
| chr15:78998273-78998411 | Rare:20 | ||||
| chr15:79896989-79897227 | Common:4; Rare:77 | ||||
| chr15:79923086-79923209 | Common:1; Rare:56 |