| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31496381-31496556 | Common:1; Rare:47 | ||||
| chr22:31662213-31662384 | Common:2; Rare:63 | ||||
| chr22:31753807-31753977 | Rare:53 | ||||
| chr22:35257394-35257501 | Common:1; Rare:27 | ||||
| chr22:35399935-35400205 | Rare:88 | ||||
| chr22:36387992-36388322 | Common:1; Rare:92 | ||||
| chr22:36529086-36529531 | Common:6; Rare:138 | ||||
| chr22:37849300-37849457 | Rare:95 | ||||
| chr22:37953618-37953756 | Rare:60 | ||||
| chr22:38656391-38656706 | Common:1; Rare:70 | ||||
| chr22:38681821-38682239 | Common:3; Rare:157 | ||||
| chr22:39399656-39399797 | Common:3; Rare:58 | ||||
| chr22:40346445-40346564 | Rare:50; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:40819268-40819513 | Common:11; Rare:114 | ||||
| chr22:40856594-40856712 | Rare:49 |