| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34665351-34665649 | Rare:94 | ||||
| chr9:35103100-35103196 | Common:1; Rare:30 | ||||
| chr9:35657893-35658326 | Common:5; Rare:374; Clinvar:34; Clinvar (benign):13; Clinvar (pathogenic):37 | ||||
| chr9:35689777-35690130 | Common:4; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732082-35732320 | Common:1; Rare:66 | ||||
| chr9:35732373-35732683 | Common:3; Rare:78 | ||||
| chr9:35749005-35749338 | Common:2; Rare:124 | ||||
| chr9:35814982-35815275 | Rare:74 | ||||
| chr9:36190766-36190988 | Rare:73 | ||||
| chr9:36258430-36258599 | Common:2; Rare:41; Clinvar:1 | ||||
| chr9:36572731-36572949 | Common:1; Rare:70 | ||||
| chr9:68779920-68780070 | Common:2; Rare:50 | ||||
| chr9:69120767-69121014 | Common:2; Rare:51 | ||||
| chr9:69759939-69760143 | Common:3; Rare:92 | ||||
| chr9:70258824-70259069 | Common:4; Rare:117 |