| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:114587554-114587888 | Common:3; Rare:132 | ||||
| chr9:115118144-115118454 | Rare:71 | ||||
| chr9:116687196-116687361 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120532549-120532709 | Rare:35 | ||||
| chr9:120714465-120714709 | Common:2; Rare:76 | ||||
| chr9:120793242-120793534 | Common:1; Rare:105 | ||||
| chr9:120842881-120843239 | Common:1; Rare:121 | ||||
| chr9:120877186-120877512 | Common:1; Rare:113 | ||||
| chr9:120929050-120929202 | Common:3; Rare:38 | ||||
| chr9:121074849-121074969 | Rare:59 | ||||
| chr9:121201772-121202158 | Common:2; Rare:120 | ||||
| chr9:121268058-121268198 | Common:1; Rare:47 | ||||
| chr9:121299605-121299972 | Common:4; Rare:108; Clinvar:3 | ||||
| chr9:121328804-121329015 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr9:121370203-121370453 | Common:2; Rare:71 |