| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113221221-113221640 | Common:1; Rare:135 | ||||
| chr9:113275354-113275746 | Common:5; Rare:128; Clinvar (pathogenic):1 | ||||
| chr9:113376901-113377150 | Common:8; Rare:78 | ||||
| chr9:113410219-113410728 | Common:3; Rare:150 | ||||
| chr9:113463555-113463759 | Common:2; Rare:65 | ||||
| chr9:113504988-113505191 | Rare:34 | ||||
| chr9:113536566-113536819 | Common:2; Rare:61 | ||||
| chr9:113580674-113580945 | Common:3; Rare:49 | ||||
| chr9:114077528-114077732 | Common:1; Rare:36 | ||||
| chr9:114078072-114078488 | Common:1; Rare:112 | ||||
| chr9:114078499-114078557 | Common:1; Rare:14 | ||||
| chr9:114323648-114324106 | Common:6; Rare:173 | ||||
| chr9:114387977-114388170 | Common:1; Rare:56 | ||||
| chr9:114587598-114587883 | Common:2; Rare:103 | ||||
| chr9:116687203-116687364 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):1 |