| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495900-120496144 | Common:4; Rare:72 | ||||
| chr12:120529149-120529250 | Common:1; Rare:30 | ||||
| chr12:122526911-122527260 | Common:3; Rare:109 | ||||
| chr12:122980415-122980723 | Rare:103 | ||||
| chr12:123233121-123233449 | Common:2; Rare:102; Clinvar:1 | ||||
| chr12:123633632-123633845 | Common:1; Rare:97; Clinvar:8; Clinvar (benign):1 | ||||
| chr13:20773939-20774018 | Rare:25 | ||||
| chr13:21176550-21176701 | Common:1; Rare:76 | ||||
| chr13:27251245-27251608 | Common:5; Rare:109 | ||||
| chr13:30465844-30466188 | Common:1; Rare:107 | ||||
| chr13:40771169-40771289 | Common:1; Rare:31 | ||||
| chr13:41061376-41061579 | Common:2; Rare:54 | ||||
| chr13:43879743-43879888 | Common:15; Rare:48 | ||||
| chr13:44989466-44989585 | Rare:42 | ||||
| chr13:45120392-45120563 | Common:1; Rare:56 |