| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30356864-30357018 | Common:1; Rare:50 | ||||
| chr22:30607044-30607321 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):3 | ||||
| chr22:31292462-31292597 | Rare:28 | ||||
| chr22:31496394-31496563 | Common:1; Rare:42 | ||||
| chr22:31630809-31631011 | Common:5; Rare:52 | ||||
| chr22:32475159-32475320 | Common:2; Rare:43 | ||||
| chr22:37019427-37019848 | Common:5; Rare:120 | ||||
| chr22:37849307-37849446 | Rare:81 | ||||
| chr22:37953535-37953731 | Common:1; Rare:74 | ||||
| chr22:38656401-38656743 | Common:1; Rare:77 | ||||
| chr22:38681790-38682019 | Common:2; Rare:98 | ||||
| chr22:40346415-40346556 | Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:41286175-41286471 | Common:2; Rare:87 | ||||
| chr22:41468919-41469167 | Rare:79 | ||||
| chr22:41560924-41561034 | Common:1; Rare:26 |