| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75310122-75310660 | Common:5; Rare:150; Clinvar (benign):1 | ||||
| chr13:75326756-75326881 | Common:1; Rare:23 | ||||
| chr13:75348834-75349295 | Common:14; Rare:162 | ||||
| chr13:75353870-75354190 | Common:2; Rare:59 | ||||
| chr13:75365760-75366214 | Common:4; Rare:159 | ||||
| chr13:75458650-75459000 | Common:2; Rare:61 | ||||
| chr13:75480680-75480951 | Common:32; Rare:118 | ||||
| chr13:75647606-75647761 | Common:4; Rare:30 | ||||
| chr13:75739523-75739716 | Common:1; Rare:42 | ||||
| chr13:75762538-75762758 | Common:2; Rare:44 | ||||
| chr13:76723460-76723840 | Common:5; Rare:69 | ||||
| chr13:76735424-76736034 | Common:4; Rare:211 | ||||
| chr13:76884192-76884592 | Rare:94 | ||||
| chr13:76885080-76885520 | Common:2; Rare:147 | ||||
| chr13:76918109-76918633 | Common:13; Rare:184 |