| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:25301439-25301692 | Common:1; Rare:95 | ||||
| chr13:25468493-25469014 | Common:1; Rare:151 | ||||
| chr13:26221782-26221983 | Rare:59 | ||||
| chr13:26222186-26222345 | Common:3; Rare:44 | ||||
| chr13:26557449-26557794 | Common:4; Rare:137 | ||||
| chr13:27251225-27251637 | Common:8; Rare:129 | ||||
| chr13:27270696-27270830 | Rare:44 | ||||
| chr13:27424499-27424824 | Common:4; Rare:107 | ||||
| chr13:27449968-27450230 | Common:3; Rare:77 | ||||
| chr13:27450501-27450673 | Common:2; Rare:66 | ||||
| chr13:27620443-27620810 | Common:2; Rare:125 | ||||
| chr13:28138133-28138206 | Rare:21 | ||||
| chr13:28658808-28659021 | Common:1; Rare:49 | ||||
| chr13:28659061-28659187 | Rare:54; Clinvar (pathogenic):1 | ||||
| chr13:29428406-29428806 | Common:2; Rare:102 |