| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:21459213-21459526 | Common:1; Rare:113 | ||||
| chr13:23433665-23433963 | Common:2; Rare:55 | ||||
| chr13:24160450-24160771 | Rare:85 | ||||
| chr13:24922790-24923071 | Common:2; Rare:92; Clinvar:1 | ||||
| chr13:25301492-25301783 | Common:3; Rare:109 | ||||
| chr13:26221791-26221990 | Rare:60 | ||||
| chr13:26222255-26222365 | Common:2; Rare:30 | ||||
| chr13:26557449-26557773 | Common:4; Rare:132 | ||||
| chr13:27251227-27251632 | Common:8; Rare:127 | ||||
| chr13:27270696-27270830 | Rare:44 | ||||
| chr13:27450130-27450212 | Common:2; Rare:23 | ||||
| chr13:27450380-27450685 | Common:4; Rare:114 | ||||
| chr13:27620436-27620829 | Common:2; Rare:130 | ||||
| chr13:28658964-28659180 | Rare:99; Clinvar (pathogenic):1 | ||||
| chr13:30306829-30306982 | Common:1; Rare:48 |