| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906570-99906694 | Rare:63 | ||||
| chr9:100098964-100099314 | Common:3; Rare:99; Clinvar:2 | ||||
| chr9:100352887-100353081 | Rare:65 | ||||
| chr9:101398564-101398906 | Common:1; Rare:117 | ||||
| chr9:101533700-101533907 | Rare:64 | ||||
| chr9:106863043-106863172 | Rare:38 | ||||
| chr9:108934065-108934471 | Common:7; Rare:158; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498244-109498458 | Rare:69 | ||||
| chr9:110125345-110125553 | Rare:42 | ||||
| chr9:110256431-110256725 | Common:5; Rare:106 | ||||
| chr9:112333539-112333941 | Rare:125 | ||||
| chr9:112379800-112380150 | Common:3; Rare:141 | ||||
| chr9:112718082-112718411 | Rare:71 | ||||
| chr9:113056684-113056883 | Rare:68 | ||||
| chr9:113221262-113221633 | Rare:117 |