| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41468939-41469170 | Rare:76 | ||||
| chr22:41560917-41561132 | Common:9; Rare:63 | ||||
| chr22:41589794-41590127 | Common:5; Rare:125 | ||||
| chr22:41621061-41621370 | Common:6; Rare:113 | ||||
| chr22:41800536-41800683 | Common:1; Rare:45 | ||||
| chr22:41832876-41833235 | Common:3; Rare:121 | ||||
| chr22:41946736-41946947 | Common:3; Rare:51 | ||||
| chr22:41947089-41947205 | Rare:42 | ||||
| chr22:41976430-41976582 | Rare:28 | ||||
| chr22:41998612-41998799 | Common:1; Rare:66 | ||||
| chr22:42070761-42070973 | Common:2; Rare:46 | ||||
| chr22:42079451-42079843 | Common:3; Rare:116 | ||||
| chr22:42090668-42090960 | Common:2; Rare:130; Clinvar (pathogenic):1 | ||||
| chr22:42432357-42432453 | Rare:29 | ||||
| chr22:42614828-42615244 | Common:3; Rare:176 |