| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9362950-9363127 | Common:2; Rare:64 | ||||
| chr3:9397434-9397693 | Common:1; Rare:96 | ||||
| chr3:9749829-9750073 | Common:1; Rare:78 | ||||
| chr3:9792382-9792493 | Rare:33 | ||||
| chr3:9792732-9793119 | Common:3; Rare:133 | ||||
| chr3:9843973-9844165 | Common:2; Rare:73 | ||||
| chr3:9917017-9917195 | Common:2; Rare:32 | ||||
| chr3:9933662-9933868 | Common:1; Rare:79 | ||||
| chr3:10011065-10011251 | Common:1; Rare:56 | ||||
| chr3:10026304-10026484 | Rare:57 | ||||
| chr3:10141654-10141967 | Common:2; Rare:146; Clinvar:36; Clinvar (benign):29 | ||||
| chr3:10290246-10290307 | Rare:24 | ||||
| chr3:10312676-10312858 | Rare:45 | ||||
| chr3:11154300-11154542 | Common:4; Rare:63 | ||||
| chr3:12484342-12484560 | Common:4; Rare:69; Clinvar:3; Clinvar (benign):2 |