| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:26557404-26557822 | Common:4; Rare:157 | ||||
| chr13:27171656-27172156 | Common:3; Rare:448 | ||||
| chr13:27251203-27251678 | Common:24; Rare:426 | ||||
| chr13:27270627-27270980 | Common:2; Rare:188 | ||||
| chr13:27424425-27424827 | Common:14; Rare:338 | ||||
| chr13:27429133-27430057 | Common:17; Rare:243 | ||||
| chr13:27449958-27450369 | Common:9; Rare:298 | ||||
| chr13:27450366-27450781 | Common:12; Rare:387 | ||||
| chr13:27620360-27621080 | Common:16; Rare:610 | ||||
| chr13:27621065-27621956 | Common:14; Rare:357; Clinvar:5; Clinvar (benign):5 | ||||
| chr13:27622002-27622709 | Common:14; Rare:361 | ||||
| chr13:28100420-28100850 | Common:6; Rare:147 | ||||
| chr13:28137968-28138622 | Common:17; Rare:389 | ||||
| chr13:28138614-28139487 | Common:4; Rare:329 | ||||
| chr13:28658932-28659235 | Common:1; Rare:250; Clinvar (pathogenic):3 |