| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41544591-41544871 | Common:4; Rare:65 | ||||
| chr22:41560889-41561127 | Common:9; Rare:67 | ||||
| chr22:41620754-41620806 | Rare:24 | ||||
| chr22:41621000-41621384 | Common:7; Rare:139 | ||||
| chr22:41800517-41800702 | Common:1; Rare:58 | ||||
| chr22:41832649-41832703 | Rare:9 | ||||
| chr22:41832909-41833355 | Common:3; Rare:149 | ||||
| chr22:41998590-41998803 | Common:2; Rare:75 | ||||
| chr22:42070770-42070963 | Common:2; Rare:41 | ||||
| chr22:42079473-42079872 | Common:2; Rare:125 | ||||
| chr22:42090607-42091054 | Common:2; Rare:178; Clinvar (pathogenic):1 | ||||
| chr22:42553606-42553941 | Common:3; Rare:97 | ||||
| chr22:42614572-42614713 | Common:1; Rare:53 | ||||
| chr22:42614846-42615272 | Common:3; Rare:185 | ||||
| chr22:42649308-42649482 | Common:1; Rare:68 |