| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53973114-53973357 | Rare:75 | ||||
| chr12:53984873-53985233 | Common:2; Rare:80 | ||||
| chr12:54000010-54000134 | Rare:29 | ||||
| chr12:55716005-55716153 | Common:1; Rare:74 | ||||
| chr12:55725470-55725943 | Rare:125 | ||||
| chr12:55726870-55727282 | Common:2; Rare:139 | ||||
| chr12:55728286-55728474 | Rare:68 | ||||
| chr12:55728681-55729185 | Common:3; Rare:103 | ||||
| chr12:55729513-55729794 | Common:1; Rare:58 | ||||
| chr12:55829506-55829793 | Rare:92 | ||||
| chr12:55830739-55830930 | Rare:62 | ||||
| chr12:55966706-55966868 | Rare:44 | ||||
| chr12:56041563-56041976 | Common:4; Rare:88; Clinvar (benign):1 | ||||
| chr12:56104372-56104755 | Common:5; Rare:141 | ||||
| chr12:56152467-56152618 | Rare:44 |