| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41468997-41469175 | Rare:67 | ||||
| chr22:41560814-41561162 | Common:9; Rare:94 | ||||
| chr22:41621000-41621385 | Common:7; Rare:139 | ||||
| chr22:41800517-41800631 | Rare:37 | ||||
| chr22:41832838-41833149 | Common:3; Rare:102 | ||||
| chr22:42070770-42071047 | Common:3; Rare:62 | ||||
| chr22:42079513-42079771 | Common:2; Rare:71 | ||||
| chr22:42090604-42090945 | Common:2; Rare:147; Clinvar (pathogenic):1 | ||||
| chr22:42614838-42615246 | Common:3; Rare:173 | ||||
| chr22:42649308-42649452 | Rare:63 | ||||
| chr22:42857178-42857428 | Common:3; Rare:103 | ||||
| chr22:43955303-43955566 | Common:3; Rare:80 | ||||
| chr22:44024127-44024406 | Common:2; Rare:87 | ||||
| chr22:45163758-45164015 | Common:2; Rare:97 | ||||
| chr22:45309727-45309990 | Common:1; Rare:101 |