| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30617579-30618039 | Common:1; Rare:140 | ||||
| chr13:30735387-30735608 | Common:2; Rare:46 | ||||
| chr13:30906069-30906282 | Common:3; Rare:42 | ||||
| chr13:30906594-30906793 | Common:1; Rare:58 | ||||
| chr13:32031261-32031435 | Common:1; Rare:47 | ||||
| chr13:32315335-32315553 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:33205897-33206146 | Rare:48 | ||||
| chr13:33285703-33286000 | Common:1; Rare:62 | ||||
| chr13:33350598-33350728 | Rare:36 | ||||
| chr13:36346247-36346454 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346642-36346797 | Common:4; Rare:46 | ||||
| chr13:37059596-37059728 | Common:1; Rare:47 | ||||
| chr13:38349541-38349929 | Common:4; Rare:133; Clinvar (pathogenic):1 | ||||
| chr13:38350231-38350281 | Rare:26 | ||||
| chr13:39038094-39038406 | Common:1; Rare:79 |