| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41946433-41946469 | Common:1; Rare:18 | ||||
| chr22:41946646-41947044 | Common:4; Rare:116 | ||||
| chr22:41947075-41947243 | Common:1; Rare:62 | ||||
| chr22:41998560-41998853 | Common:3; Rare:113 | ||||
| chr22:41998920-41998964 | Rare:12 | ||||
| chr22:42070446-42071109 | Common:5; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:42074536-42074682 | Common:3; Rare:36 | ||||
| chr22:42079372-42080194 | Common:4; Rare:240 | ||||
| chr22:42090312-42090413 | Common:1; Rare:26 | ||||
| chr22:42090662-42091200 | Common:3; Rare:201; Clinvar (pathogenic):1 | ||||
| chr22:42519720-42519965 | Common:1; Rare:98 | ||||
| chr22:42553669-42554008 | Common:1; Rare:104 | ||||
| chr22:42614312-42614455 | Rare:42 | ||||
| chr22:42614478-42614772 | Common:2; Rare:108 | ||||
| chr22:42614789-42615734 | Common:11; Rare:579 |