| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:23579236-23579471 | Common:4; Rare:73 | ||||
| chr13:23889289-23889468 | Rare:63 | ||||
| chr13:24160537-24160739 | Rare:56 | ||||
| chr13:24512729-24512818 | Common:1; Rare:26 | ||||
| chr13:24922801-24923039 | Common:1; Rare:74; Clinvar:1 | ||||
| chr13:25301502-25301684 | Common:1; Rare:73 | ||||
| chr13:26221791-26221953 | Rare:46 | ||||
| chr13:27251245-27251623 | Common:6; Rare:114 | ||||
| chr13:27450119-27450256 | Common:3; Rare:44 | ||||
| chr13:27450519-27450685 | Common:2; Rare:63 | ||||
| chr13:27620458-27620784 | Common:2; Rare:112 | ||||
| chr13:28138157-28138224 | Common:1; Rare:17 | ||||
| chr13:28659062-28659184 | Rare:53; Clinvar (pathogenic):1 | ||||
| chr13:30306970-30307197 | Common:5; Rare:53 | ||||
| chr13:30464195-30464278 | Common:1; Rare:25 |