| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34178912-34179085 | Common:2; Rare:88 | ||||
| chr9:34179120-34179470 | Rare:134 | ||||
| chr9:34329115-34329740 | Common:4; Rare:319 | ||||
| chr9:34376828-34377221 | Common:1; Rare:152 | ||||
| chr9:34458508-34458842 | Common:3; Rare:158; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:34612059-34612238 | Common:17; Rare:114 | ||||
| chr9:34637667-34637999 | Common:4; Rare:190; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:34646475-34646800 | Common:2; Rare:137; Clinvar:6; Clinvar (pathogenic):3 | ||||
| chr9:34652001-34652208 | Rare:116 | ||||
| chr9:34665331-34665655 | Rare:97 | ||||
| chr9:34665969-34666334 | Common:5; Rare:140 | ||||
| chr9:34989300-34989770 | Common:4; Rare:234 | ||||
| chr9:35071800-35072260 | Common:3; Rare:211 | ||||
| chr9:35072493-35073200 | Rare:197; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:35079613-35079854 | Rare:93; Clinvar:1 |