| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:25301486-25301692 | Common:1; Rare:79 | ||||
| chr13:26221791-26221953 | Rare:46 | ||||
| chr13:27251268-27251617 | Common:4; Rare:99 | ||||
| chr13:27450062-27450256 | Common:3; Rare:62 | ||||
| chr13:27450522-27450718 | Common:2; Rare:77 | ||||
| chr13:27620474-27620799 | Common:2; Rare:108 | ||||
| chr13:28658951-28659181 | Rare:102; Clinvar (pathogenic):1 | ||||
| chr13:30306968-30307197 | Common:5; Rare:54 | ||||
| chr13:30307401-30307612 | Common:2; Rare:71 | ||||
| chr13:32315433-32315552 | Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:33285686-33285990 | Common:1; Rare:63 | ||||
| chr13:36346314-36346447 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37000601-37000805 | Rare:70 | ||||
| chr13:39038079-39038464 | Common:1; Rare:93 | ||||
| chr13:39655629-39655755 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 |