| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120868826-120869111 | Common:2; Rare:59 | ||||
| chr9:120877157-120877482 | Common:3; Rare:107 | ||||
| chr9:121074477-121074803 | Common:1; Rare:96 | ||||
| chr9:121074849-121074977 | Rare:62 | ||||
| chr9:121075129-121075200 | Rare:20 | ||||
| chr9:121201811-121202158 | Common:2; Rare:107 | ||||
| chr9:121268041-121268215 | Common:1; Rare:61 | ||||
| chr9:121281984-121282158 | Rare:42 | ||||
| chr9:121285940-121286121 | Common:1; Rare:34 | ||||
| chr9:121286782-121287085 | Common:1; Rare:64 | ||||
| chr9:121299693-121299997 | Common:2; Rare:106; Clinvar:3 | ||||
| chr9:121326208-121326704 | Common:4; Rare:130; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:121328596-121329015 | Common:3; Rare:115; Clinvar (benign):1 | ||||
| chr9:121370203-121370512 | Common:2; Rare:92 | ||||
| chr9:121566914-121567139 | Rare:55 |