| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39637032-39637225 | Common:3; Rare:61 | ||||
| chr17:39665174-39665433 | Common:2; Rare:75; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr17:39688010-39688125 | Rare:37 | ||||
| chr17:39738214-39738377 | Rare:39 | ||||
| chr17:39927473-39927768 | Common:2; Rare:91 | ||||
| chr17:39927950-39928035 | Rare:14 | ||||
| chr17:39980470-39980958 | Common:2; Rare:110 | ||||
| chr17:40054385-40054516 | Rare:30 | ||||
| chr17:40100553-40100793 | Common:1; Rare:46 | ||||
| chr17:40121814-40122001 | Common:2; Rare:71 | ||||
| chr17:40140145-40140682 | Common:6; Rare:243 | ||||
| chr17:40140703-40140813 | Rare:47 | ||||
| chr17:40219174-40219417 | Common:3; Rare:86 | ||||
| chr17:40219534-40219679 | Rare:15 | ||||
| chr17:40318085-40318308 | Common:1; Rare:49 |