| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49264781-49265083 | Common:4; Rare:105 | ||||
| chr12:49322980-49323307 | Common:3; Rare:77 | ||||
| chr12:49367183-49367555 | Common:1; Rare:103 | ||||
| chr12:49568098-49568252 | Common:2; Rare:49 | ||||
| chr12:49741248-49741587 | Rare:93 | ||||
| chr12:49828354-49828533 | Common:1; Rare:67 | ||||
| chr12:49843083-49843227 | Common:1; Rare:48 | ||||
| chr12:49950944-49951115 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr12:50103881-50104053 | Rare:44 | ||||
| chr12:50283423-50283672 | Common:3; Rare:74 | ||||
| chr12:50400737-50400992 | Common:1; Rare:83 | ||||
| chr12:50763896-50764297 | Common:2; Rare:109 | ||||
| chr12:50764383-50764476 | Common:1; Rare:23 | ||||
| chr12:50924506-50924769 | Common:3; Rare:80 | ||||
| chr12:51026313-51026542 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):2 |