| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27171719-27172030 | Common:1; Rare:110 | ||||
| chr13:27251225-27251632 | Common:8; Rare:128 | ||||
| chr13:27424499-27424767 | Common:4; Rare:90 | ||||
| chr13:27449944-27450230 | Common:3; Rare:81 | ||||
| chr13:27450466-27450685 | Common:2; Rare:85 | ||||
| chr13:27620429-27621061 | Common:5; Rare:216 | ||||
| chr13:28138092-28138229 | Common:1; Rare:47 | ||||
| chr13:28308401-28308643 | Common:2; Rare:39 | ||||
| chr13:28328379-28328514 | Rare:22 | ||||
| chr13:28659042-28659194 | Rare:69; Clinvar (pathogenic):1 | ||||
| chr13:28718790-28719131 | Common:1; Rare:86 | ||||
| chr13:29850043-29850227 | Common:1; Rare:58 | ||||
| chr13:29850566-29850820 | Common:2; Rare:98 | ||||
| chr13:30306840-30307207 | Common:6; Rare:101 | ||||
| chr13:30307355-30307483 | Common:2; Rare:45 |