| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41560903-41561135 | Common:9; Rare:66 | ||||
| chr22:41620992-41621384 | Common:7; Rare:141 | ||||
| chr22:41800517-41800683 | Common:1; Rare:54 | ||||
| chr22:41832637-41832744 | Rare:20 | ||||
| chr22:41832909-41833345 | Common:3; Rare:146 | ||||
| chr22:41946736-41946947 | Common:3; Rare:51 | ||||
| chr22:41947122-41947225 | Rare:35 | ||||
| chr22:41976237-41976521 | Common:1; Rare:42 | ||||
| chr22:41998635-41998811 | Common:1; Rare:61 | ||||
| chr22:42070770-42071003 | Common:3; Rare:51 | ||||
| chr22:42079629-42079771 | Common:1; Rare:44 | ||||
| chr22:42090657-42091020 | Common:2; Rare:158; Clinvar (pathogenic):1 | ||||
| chr22:42210690-42210779 | Rare:30 | ||||
| chr22:42614858-42615246 | Common:3; Rare:161 | ||||
| chr22:42649329-42649495 | Common:1; Rare:67 |