| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48094979-48095379 | Common:8; Rare:413 | ||||
| chr13:48232920-48233717 | Common:15; Rare:578 | ||||
| chr13:48303154-48303554 | Common:1; Rare:76 | ||||
| chr13:48303480-48303970 | Common:1; Rare:735; Clinvar:30; Clinvar (benign):5; Clinvar (pathogenic):8 | ||||
| chr13:48492525-48492925 | Common:4; Rare:156 | ||||
| chr13:48532088-48532512 | Common:4; Rare:129 | ||||
| chr13:48532501-48532965 | Common:27; Rare:709 | ||||
| chr13:48533045-48533173 | Common:2; Rare:60 | ||||
| chr13:48975492-48975644 | Rare:60 | ||||
| chr13:48975619-48977114 | Common:21; Rare:1372 | ||||
| chr13:48977150-48977550 | Common:1; Rare:77 | ||||
| chr13:49110040-49110459 | Common:10; Rare:278 | ||||
| chr13:49219880-49220230 | Common:1; Rare:88 | ||||
| chr13:49247522-49248074 | Common:4; Rare:449 | ||||
| chr13:49248354-49248754 | Common:1; Rare:66 |