| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33264971-33265094 | Rare:38 | ||||
| chr9:33290388-33290570 | Common:2; Rare:70 | ||||
| chr9:33447424-33447671 | Common:4; Rare:74 | ||||
| chr9:33817687-33817775 | Common:1; Rare:33 | ||||
| chr9:34048886-34048998 | Common:1; Rare:46 | ||||
| chr9:34049175-34049263 | Common:1; Rare:22 | ||||
| chr9:34126561-34126781 | Rare:70 | ||||
| chr9:34178952-34179078 | Common:1; Rare:34 | ||||
| chr9:34329181-34329593 | Rare:130 | ||||
| chr9:34376891-34377076 | Rare:43 | ||||
| chr9:34458539-34458833 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:34612084-34612216 | Common:8; Rare:43 | ||||
| chr9:34652015-34652217 | Rare:58 | ||||
| chr9:34665351-34665655 | Rare:96 | ||||
| chr9:35072371-35072409 | Rare:13; Clinvar:1 |