| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41620745-41620775 | Rare:11 | ||||
| chr22:41620969-41621414 | Common:7; Rare:154 | ||||
| chr22:41800517-41800691 | Common:1; Rare:57 | ||||
| chr22:41832867-41833355 | Common:3; Rare:163 | ||||
| chr22:42070761-42070977 | Common:3; Rare:47 | ||||
| chr22:42074193-42074310 | Common:2; Rare:25 | ||||
| chr22:42079505-42079872 | Common:2; Rare:117 | ||||
| chr22:42090607-42090967 | Common:2; Rare:151; Clinvar (pathogenic):1 | ||||
| chr22:42614838-42615246 | Common:3; Rare:173 | ||||
| chr22:42649297-42649482 | Common:1; Rare:69 | ||||
| chr22:42857170-42857443 | Common:3; Rare:114 | ||||
| chr22:43015063-43015384 | Common:2; Rare:128 | ||||
| chr22:43151432-43151604 | Common:2; Rare:41 | ||||
| chr22:43812272-43812441 | Common:2; Rare:57 | ||||
| chr22:43955326-43955566 | Common:3; Rare:75 |