| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113275354-113275746 | Common:5; Rare:128; Clinvar (pathogenic):1 | ||||
| chr9:113410226-113410784 | Common:4; Rare:175 | ||||
| chr9:113580675-113580957 | Common:3; Rare:52 | ||||
| chr9:114387964-114388104 | Common:1; Rare:47 | ||||
| chr9:114394479-114394773 | Rare:40 | ||||
| chr9:114505443-114505622 | Common:1; Rare:52 | ||||
| chr9:114587598-114587915 | Common:2; Rare:117 | ||||
| chr9:114930457-114930686 | Common:4; Rare:56 | ||||
| chr9:115118053-115118232 | Common:2; Rare:47 | ||||
| chr9:116153565-116153876 | Common:1; Rare:70 | ||||
| chr9:116687203-116687364 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:117703950-117704497 | Common:2; Rare:109 | ||||
| chr9:120403199-120403398 | Rare:31 | ||||
| chr9:120532545-120532738 | Rare:42 | ||||
| chr9:120580132-120580216 | Rare:25; Clinvar:3 |