| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74782478-74782565 | Common:1; Rare:24 | ||||
| chr15:74873266-74873425 | Common:2; Rare:41 | ||||
| chr15:74906646-74906980 | Common:2; Rare:128 | ||||
| chr15:75346859-75347083 | Common:1; Rare:47 | ||||
| chr15:75347553-75347865 | Common:2; Rare:79 | ||||
| chr15:75368519-75368944 | Rare:130 | ||||
| chr15:75455750-75455985 | Rare:73 | ||||
| chr15:75625612-75625839 | Common:2; Rare:54 | ||||
| chr15:75640074-75640448 | Common:2; Rare:132 | ||||
| chr15:75647846-75648201 | Common:1; Rare:76 | ||||
| chr15:75648532-75648773 | Common:1; Rare:38 | ||||
| chr15:75843908-75844262 | Common:1; Rare:115 | ||||
| chr15:75903836-75904074 | Rare:107 | ||||
| chr15:76311350-76311516 | Rare:68; Clinvar:7; Clinvar (benign):8 | ||||
| chr15:77420021-77420032 | Rare:1 |