| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48233796-48234080 | Common:2; Rare:65 | ||||
| chr13:48413064-48413219 | Rare:20 | ||||
| chr13:48507040-48507335 | Common:3; Rare:47 | ||||
| chr13:49661166-49661478 | Rare:74 | ||||
| chr13:52599983-52600115 | Rare:26 | ||||
| chr13:52617337-52617557 | Common:1; Rare:54 | ||||
| chr13:57629940-57630125 | Common:1; Rare:49 | ||||
| chr13:59458970-59459149 | Common:1; Rare:37 | ||||
| chr13:109265120-109265419 | Common:4; Rare:68 | ||||
| chr13:109266182-109266238 | Rare:14 | ||||
| chr13:109268941-109268999 | Common:2; Rare:5 | ||||
| chr13:109269004-109269079 | Common:4; Rare:11 | ||||
| chr13:109269523-109269633 | Common:1; Rare:26 | ||||
| chr13:110308510-110308622 | Common:1; Rare:22 | ||||
| chr13:110424793-110424980 | Common:4; Rare:61; Clinvar:3; Clinvar (benign):2 |