| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30616832-30617101 | Rare:49 | ||||
| chr13:30617479-30618040 | Common:1; Rare:183 | ||||
| chr13:32031255-32031425 | Common:1; Rare:48 | ||||
| chr13:32031507-32031658 | Rare:29 | ||||
| chr13:32031678-32031777 | Common:1; Rare:35 | ||||
| chr13:32254041-32254287 | Common:2; Rare:55 | ||||
| chr13:32315426-32315525 | Rare:27; Clinvar:1 | ||||
| chr13:32428099-32428233 | Rare:30 | ||||
| chr13:33285693-33285968 | Common:1; Rare:60 | ||||
| chr13:35855665-35855803 | Rare:29 | ||||
| chr13:36131380-36131668 | Common:1; Rare:72 | ||||
| chr13:36345549-36345668 | Common:1; Rare:22 | ||||
| chr13:36346078-36346177 | Rare:21 | ||||
| chr13:36346258-36346476 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:36346632-36346787 | Common:4; Rare:44 |