| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41976290-41976980 | Common:1; Rare:192 | ||||
| chr22:41998595-41998883 | Common:5; Rare:197 | ||||
| chr22:42070696-42071102 | Common:8; Rare:206 | ||||
| chr22:42079218-42079844 | Common:8; Rare:290 | ||||
| chr22:42079891-42080290 | Rare:191 | ||||
| chr22:42090633-42091212 | Common:7; Rare:510; Clinvar (pathogenic):3 | ||||
| chr22:42343170-42343780 | Common:4; Rare:273 | ||||
| chr22:42343800-42344160 | Common:7; Rare:136 | ||||
| chr22:42518854-42519685 | Common:21; Rare:487 | ||||
| chr22:42519704-42519967 | Common:2; Rare:178 | ||||
| chr22:42553676-42554003 | Common:2; Rare:170 | ||||
| chr22:42614509-42615246 | Common:9; Rare:369 | ||||
| chr22:42615239-42615725 | Common:6; Rare:381 | ||||
| chr22:42646601-42647001 | Common:3; Rare:113 | ||||
| chr22:42649269-42649547 | Common:6; Rare:222 |