| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41800362-41800710 | Common:3; Rare:95 | ||||
| chr22:41832909-41833266 | Common:3; Rare:129 | ||||
| chr22:41946721-41946999 | Common:3; Rare:81 | ||||
| chr22:41947084-41947255 | Common:1; Rare:59 | ||||
| chr22:42079632-42079774 | Common:1; Rare:43 | ||||
| chr22:42090739-42090952 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
| chr22:42614801-42615246 | Common:5; Rare:191 | ||||
| chr22:42649336-42649482 | Common:1; Rare:58 | ||||
| chr22:43015049-43015384 | Common:2; Rare:130 | ||||
| chr22:44024128-44024335 | Common:2; Rare:68 | ||||
| chr22:44181236-44181416 | Common:3; Rare:43 | ||||
| chr22:44668458-44668785 | Common:5; Rare:124 | ||||
| chr22:45163777-45163940 | Common:2; Rare:55 | ||||
| chr22:46053786-46053863 | Rare:28 | ||||
| chr22:46250263-46250463 | Common:3; Rare:71 |