| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40921659-40921898 | Common:5; Rare:67 | ||||
| chr13:42271371-42271534 | Common:2; Rare:50 | ||||
| chr13:44142050-44142361 | Common:5; Rare:48 | ||||
| chr13:44917996-44918106 | Common:3; Rare:62 | ||||
| chr13:48379917-48380204 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr13:48413033-48413168 | Rare:17 | ||||
| chr13:49517868-49518073 | Common:1; Rare:37 | ||||
| chr13:50125414-50125676 | Common:1; Rare:88 | ||||
| chr13:52194398-52194481 | Rare:26 | ||||
| chr13:52600327-52600479 | Common:3; Rare:53 | ||||
| chr13:52617337-52617555 | Common:1; Rare:54 | ||||
| chr13:59458937-59459168 | Common:2; Rare:41 | ||||
| chr13:71865937-71866223 | Rare:47 | ||||
| chr13:75481140-75481292 | Common:3; Rare:36; Clinvar (benign):1 | ||||
| chr13:75481369-75481578 | Common:1; Rare:92; Clinvar (benign):1 |