| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57459955-57460181 | Common:2; Rare:58 | ||||
| chr12:57477812-57477905 | Rare:19 | ||||
| chr12:57488796-57489048 | Common:3; Rare:52; Clinvar (benign):1 | ||||
| chr12:57517095-57517353 | Rare:78 | ||||
| chr12:57520447-57520727 | Common:2; Rare:85 | ||||
| chr12:57522520-57522982 | Common:4; Rare:164 | ||||
| chr12:57524755-57525031 | Common:1; Rare:91 | ||||
| chr12:57527367-57527871 | Common:1; Rare:152 | ||||
| chr12:57547061-57547564 | Common:3; Rare:98 | ||||
| chr12:57591123-57591455 | Common:4; Rare:135 | ||||
| chr12:57609969-57610324 | Common:3; Rare:88 | ||||
| chr12:57611163-57611473 | Rare:68 | ||||
| chr12:57694114-57694323 | Common:1; Rare:68 | ||||
| chr12:57694573-57694898 | Rare:81 | ||||
| chr12:57716088-57716744 | Common:4; Rare:171 |