| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41682379-41682555 | Common:1; Rare:75 | ||||
| chr22:41688700-41689020 | Common:1; Rare:122 | ||||
| chr22:41699367-41699549 | Common:4; Rare:83 | ||||
| chr22:41752336-41752532 | Common:1; Rare:39 | ||||
| chr22:41781029-41781430 | Common:2; Rare:102 | ||||
| chr22:41800192-41800403 | Rare:48 | ||||
| chr22:41800446-41800771 | Common:2; Rare:98 | ||||
| chr22:41832524-41833302 | Common:3; Rare:225 | ||||
| chr22:41833355-41833528 | Rare:62 | ||||
| chr22:41833559-41833952 | Common:2; Rare:98 | ||||
| chr22:41915031-41915165 | Common:5; Rare:32 | ||||
| chr22:41926341-41926477 | Rare:36 | ||||
| chr22:41926671-41927016 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:41927022-41927085 | Rare:18 | ||||
| chr22:41940147-41940388 | Common:2; Rare:52 |