| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27620443-27620828 | Common:2; Rare:128 | ||||
| chr13:27621090-27621180 | Common:1; Rare:24 | ||||
| chr13:28138011-28138229 | Common:2; Rare:64 | ||||
| chr13:28138835-28138966 | Rare:34 | ||||
| chr13:28659066-28659194 | Rare:55; Clinvar (pathogenic):1 | ||||
| chr13:29850330-29850419 | Common:1; Rare:26 | ||||
| chr13:29850566-29850774 | Common:2; Rare:83 | ||||
| chr13:30306832-30307197 | Common:6; Rare:98 | ||||
| chr13:30307398-30307596 | Common:1; Rare:70 | ||||
| chr13:30465769-30465986 | Common:1; Rare:72 | ||||
| chr13:30617346-30618052 | Common:1; Rare:225 | ||||
| chr13:32031250-32031328 | Common:1; Rare:22 | ||||
| chr13:32315342-32315531 | Common:1; Rare:49; Clinvar:1 | ||||
| chr13:32428053-32428215 | Rare:40 | ||||
| chr13:33285670-33285963 | Common:1; Rare:66 |