| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21140370-21140645 | Rare:121 | ||||
| chr13:21176482-21176704 | Common:2; Rare:98 | ||||
| chr13:23889298-23889591 | Common:1; Rare:103 | ||||
| chr13:24160521-24160798 | Common:1; Rare:82 | ||||
| chr13:24512739-24512881 | Common:3; Rare:43 | ||||
| chr13:24922801-24923039 | Common:1; Rare:74; Clinvar:1 | ||||
| chr13:25301500-25301686 | Common:1; Rare:74 | ||||
| chr13:25468646-25468891 | Rare:92 | ||||
| chr13:26221787-26221920 | Rare:33 | ||||
| chr13:27251235-27251608 | Common:7; Rare:114 | ||||
| chr13:27450102-27450215 | Common:3; Rare:37 | ||||
| chr13:27620458-27620799 | Common:2; Rare:114 | ||||
| chr13:28138116-28138220 | Rare:35 | ||||
| chr13:28659076-28659187 | Rare:49; Clinvar (pathogenic):1 | ||||
| chr13:30306980-30307207 | Common:5; Rare:57 |