| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:29480027-29480220 | Rare:45 | ||||
| chr22:29553530-29553773 | Rare:69 | ||||
| chr22:29580743-29580865 | Rare:14 | ||||
| chr22:29580983-29581336 | Common:4; Rare:91 | ||||
| chr22:29603225-29603627 | Common:4; Rare:94; Clinvar:1 | ||||
| chr22:29719890-29720006 | Rare:30 | ||||
| chr22:29766911-29767452 | Common:5; Rare:172 | ||||
| chr22:29838190-29838454 | Common:4; Rare:90 | ||||
| chr22:30080223-30080471 | Common:2; Rare:63 | ||||
| chr22:30356740-30357111 | Common:2; Rare:118 | ||||
| chr22:30387329-30387652 | Common:5; Rare:98 | ||||
| chr22:30425512-30425608 | Rare:27 | ||||
| chr22:30425680-30425841 | Common:1; Rare:41 | ||||
| chr22:30606629-30606870 | Common:3; Rare:59 | ||||
| chr22:30606996-30607297 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):3 |