| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28658919-28659009 | Rare:22 | ||||
| chr13:28659072-28659194 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr13:28718742-28719136 | Common:1; Rare:103 | ||||
| chr13:29850081-29850211 | Rare:44 | ||||
| chr13:30307001-30307197 | Common:4; Rare:46 | ||||
| chr13:30307372-30307591 | Common:2; Rare:77 | ||||
| chr13:30465760-30466117 | Common:1; Rare:111 | ||||
| chr13:30616971-30617166 | Rare:36 | ||||
| chr13:30617216-30617392 | Rare:37 | ||||
| chr13:30617396-30618040 | Common:1; Rare:211 | ||||
| chr13:30618430-30618574 | Common:2; Rare:22 | ||||
| chr13:31162345-31162424 | Common:1; Rare:18 | ||||
| chr13:32031630-32031797 | Common:1; Rare:51 | ||||
| chr13:32315358-32315531 | Common:1; Rare:45; Clinvar:1 | ||||
| chr13:32586225-32586593 | Common:2; Rare:114 |