| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:27718259-27718428 | Rare:26 | ||||
| chr22:27909682-27909937 | Common:3; Rare:50 | ||||
| chr22:28430703-28430879 | Rare:19 | ||||
| chr22:28687936-28688093 | Rare:42; Clinvar:14; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:28799454-28799528 | Rare:11 | ||||
| chr22:29272052-29272251 | Common:1; Rare:65 | ||||
| chr22:29287108-29287210 | Rare:22 | ||||
| chr22:29287543-29287807 | Common:1; Rare:51 | ||||
| chr22:29287852-29288057 | Rare:47 | ||||
| chr22:29298535-29298898 | Common:1; Rare:120 | ||||
| chr22:29299595-29300475 | Common:7; Rare:258 | ||||
| chr22:29975854-29976108 | Rare:46 | ||||
| chr22:30407259-30407444 | Common:1; Rare:43 | ||||
| chr22:30412909-30412926 | Rare:1 | ||||
| chr22:30581011-30581359 | Common:1; Rare:91 |