| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17228961-17229365 | Common:3; Rare:81 | ||||
| chr10:17233536-17233931 | Common:4; Rare:129; Clinvar (benign):1 | ||||
| chr10:17643871-17644269 | Common:2; Rare:120 | ||||
| chr10:17809140-17809353 | Rare:24 | ||||
| chr10:18651581-18651693 | Common:1; Rare:41 | ||||
| chr10:18659265-18659606 | Common:2; Rare:115 | ||||
| chr10:22316217-22316456 | Common:2; Rare:107 | ||||
| chr10:27154315-27154474 | Rare:42 | ||||
| chr10:27155227-27155376 | Common:3; Rare:48; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:27242079-27242212 | Common:1; Rare:56 | ||||
| chr10:28532517-28532862 | Common:4; Rare:144 | ||||
| chr10:29634791-29635053 | Rare:62 | ||||
| chr10:31031850-31032028 | Common:1; Rare:69 | ||||
| chr10:31319052-31319270 | Common:2; Rare:60 | ||||
| chr10:31928792-31928968 | Common:3; Rare:67 |