| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33001538-33001751 | Common:3; Rare:106; Clinvar (benign):4 | ||||
| chr9:33025071-33025383 | Common:7; Rare:127 | ||||
| chr9:33076601-33076865 | Common:2; Rare:89 | ||||
| chr9:33166867-33166956 | Rare:35 | ||||
| chr9:33264574-33265093 | Common:1; Rare:151 | ||||
| chr9:33290281-33290570 | Common:2; Rare:102 | ||||
| chr9:33473857-33474143 | Common:3; Rare:87 | ||||
| chr9:33817531-33817879 | Common:2; Rare:98 | ||||
| chr9:34048857-34048986 | Common:1; Rare:52 | ||||
| chr9:34049170-34049263 | Common:1; Rare:26 | ||||
| chr9:34126375-34126461 | Rare:34 | ||||
| chr9:34126631-34126778 | Rare:47 | ||||
| chr9:34178933-34179070 | Common:1; Rare:38 | ||||
| chr9:34329186-34329606 | Rare:134 | ||||
| chr9:34458558-34458826 | Rare:61 |