| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27251225-27251740 | Common:8; Rare:156 | ||||
| chr13:27424489-27424732 | Common:4; Rare:79 | ||||
| chr13:27449968-27450256 | Common:3; Rare:88 | ||||
| chr13:27450377-27450685 | Common:4; Rare:115 | ||||
| chr13:27620480-27620812 | Common:2; Rare:109 | ||||
| chr13:28138112-28138206 | Rare:31 | ||||
| chr13:28659066-28659184 | Rare:51; Clinvar (pathogenic):1 | ||||
| chr13:28718787-28719123 | Common:1; Rare:86 | ||||
| chr13:29428376-29428840 | Common:2; Rare:121 | ||||
| chr13:30306836-30307211 | Common:6; Rare:104 | ||||
| chr13:30307379-30307604 | Common:2; Rare:77 | ||||
| chr13:30463522-30463864 | Common:2; Rare:83 | ||||
| chr13:30464246-30464372 | Rare:40 | ||||
| chr13:30465760-30466111 | Common:1; Rare:111 | ||||
| chr13:30616972-30617166 | Rare:36 |