| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46553004-46553396 | Common:4; Rare:125 | ||||
| chr13:46797113-46797326 | Common:3; Rare:78 | ||||
| chr13:46896871-46897188 | Common:2; Rare:55 | ||||
| chr13:48001242-48001439 | Common:2; Rare:89; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037685-48037782 | Rare:53 | ||||
| chr13:48037920-48038027 | Common:4; Rare:39 | ||||
| chr13:48233069-48233475 | Common:3; Rare:141 | ||||
| chr13:48303674-48303768 | Rare:38; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr13:48975811-48975928 | Rare:43 | ||||
| chr13:49110233-49110392 | Common:2; Rare:45 | ||||
| chr13:49247830-49247977 | Rare:46 | ||||
| chr13:49443997-49444377 | Common:1; Rare:124 | ||||
| chr13:49585516-49585636 | Common:1; Rare:39 | ||||
| chr13:49691339-49691625 | Common:5; Rare:109 | ||||
| chr13:49792484-49792712 | Common:5; Rare:101 |