| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34048844-34048960 | Common:1; Rare:53 | ||||
| chr9:34049170-34049211 | Rare:11 | ||||
| chr9:34126631-34126816 | Common:1; Rare:53 | ||||
| chr9:34178977-34179072 | Rare:28 | ||||
| chr9:34329195-34329640 | Common:1; Rare:139 | ||||
| chr9:34458527-34458847 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:34612073-34612223 | Common:8; Rare:54 | ||||
| chr9:34652015-34652217 | Rare:58 | ||||
| chr9:34665373-34665665 | Rare:94 | ||||
| chr9:34666020-34666219 | Common:2; Rare:45 | ||||
| chr9:34989530-34989783 | Common:2; Rare:63 | ||||
| chr9:35079932-35080153 | Common:4; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35102803-35103288 | Common:1; Rare:148 | ||||
| chr9:35489810-35490139 | Common:2; Rare:105 | ||||
| chr9:35646830-35646978 | Common:1; Rare:34 |