| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113056661-113056883 | Common:1; Rare:75; Clinvar:1 | ||||
| chr9:113221260-113221633 | Rare:118 | ||||
| chr9:113275376-113275737 | Common:5; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:113410232-113410592 | Common:1; Rare:111 | ||||
| chr9:113410645-113410817 | Common:2; Rare:59 | ||||
| chr9:114587415-114587849 | Common:4; Rare:151 | ||||
| chr9:115118149-115118459 | Rare:71 | ||||
| chr9:116687228-116687330 | Rare:27 | ||||
| chr9:120793255-120793534 | Common:1; Rare:102 | ||||
| chr9:120842905-120843095 | Common:1; Rare:66 | ||||
| chr9:121074840-121074981 | Rare:68 | ||||
| chr9:121201837-121202158 | Common:2; Rare:91 | ||||
| chr9:121268058-121268198 | Common:1; Rare:47 | ||||
| chr9:121370213-121370453 | Common:1; Rare:65 | ||||
| chr9:122264737-122264923 | Common:2; Rare:53 |