| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41699409-41699541 | Common:4; Rare:55 | ||||
| chr22:41800517-41800683 | Common:1; Rare:54 | ||||
| chr22:41832904-41833354 | Common:3; Rare:148 | ||||
| chr22:41946700-41946892 | Common:3; Rare:45 | ||||
| chr22:41947114-41947205 | Rare:29 | ||||
| chr22:41998595-41998811 | Common:2; Rare:78 | ||||
| chr22:41998867-41999211 | Common:2; Rare:89 | ||||
| chr22:42070326-42070591 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:42070770-42070963 | Common:2; Rare:41 | ||||
| chr22:42074197-42074296 | Common:2; Rare:21 | ||||
| chr22:42079616-42079763 | Common:1; Rare:47 | ||||
| chr22:42090597-42091054 | Common:2; Rare:183; Clinvar (pathogenic):1 | ||||
| chr22:42091347-42091385 | Rare:7 | ||||
| chr22:42091388-42091405 | Rare:6 | ||||
| chr22:42210684-42210960 | Rare:85 |