| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57590893-57590918 | Rare:4 | ||||
| chr12:57590997-57591315 | Common:6; Rare:139 | ||||
| chr12:57591721-57591814 | Rare:21 | ||||
| chr12:57604810-57604849 | Rare:5 | ||||
| chr12:57611271-57611453 | Rare:32 | ||||
| chr12:57693859-57694241 | Common:1; Rare:109 | ||||
| chr12:57694536-57694829 | Rare:68 | ||||
| chr12:57744523-57744699 | Rare:40 | ||||
| chr12:57744774-57745142 | Common:1; Rare:88 | ||||
| chr12:57745228-57745416 | Common:1; Rare:44 | ||||
| chr12:57751394-57751628 | Rare:42; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:57751847-57752016 | Rare:27 | ||||
| chr12:57752090-57752155 | Common:1; Rare:13 | ||||
| chr12:57752227-57752716 | Common:1; Rare:127; Clinvar:1 | ||||
| chr12:57754843-57755129 | Common:2; Rare:72 |