| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17228453-17228675 | Common:1; Rare:59 | ||||
| chr10:17228990-17229026 | Common:1; Rare:7 | ||||
| chr10:17643871-17644286 | Common:2; Rare:125 | ||||
| chr10:18651571-18651693 | Common:1; Rare:47 | ||||
| chr10:19816152-19816502 | Common:5; Rare:74 | ||||
| chr10:22316221-22316456 | Common:1; Rare:107 | ||||
| chr10:24722713-24722842 | Rare:37 | ||||
| chr10:26438061-26438393 | Common:2; Rare:76 | ||||
| chr10:27154314-27154486 | Rare:47 | ||||
| chr10:27155188-27155380 | Common:4; Rare:64; Clinvar:3; Clinvar (benign):4 | ||||
| chr10:27240474-27240634 | Common:1; Rare:53 | ||||
| chr10:27240776-27240897 | Rare:27 | ||||
| chr10:27242058-27242216 | Common:1; Rare:67 | ||||
| chr10:28532731-28532890 | Common:1; Rare:55 | ||||
| chr10:28533232-28533534 | Common:1; Rare:110 |