| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42089909-42090506 | Common:6; Rare:278 | ||||
| chr22:42090647-42091154 | Common:11; Rare:955; Clinvar (pathogenic):7 | ||||
| chr22:42343390-42344121 | Common:7; Rare:312 | ||||
| chr22:42519654-42520054 | Common:6; Rare:568 | ||||
| chr22:42553619-42554027 | Common:9; Rare:542 | ||||
| chr22:42614007-42614407 | Common:1; Rare:107 | ||||
| chr22:42614500-42614790 | Common:5; Rare:241 | ||||
| chr22:42614786-42615638 | Common:31; Rare:1736 | ||||
| chr22:42646832-42647232 | Common:7; Rare:188 | ||||
| chr22:42649116-42649603 | Common:18; Rare:529 | ||||
| chr22:42856504-42857552 | Common:26; Rare:1155 | ||||
| chr22:42959680-42960120 | Common:6; Rare:253 | ||||
| chr22:42960174-42960574 | Common:4; Rare:72 | ||||
| chr22:43002309-43002709 | Rare:62 | ||||
| chr22:43015049-43015449 | Common:12; Rare:807 |