| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:119369295-119369615 | Common:2; Rare:74 | ||||
| chr9:120793242-120793534 | Common:1; Rare:105 | ||||
| chr9:120842905-120843100 | Common:1; Rare:68 | ||||
| chr9:120877153-120877502 | Common:3; Rare:121 | ||||
| chr9:120929132-120929180 | Common:1; Rare:11 | ||||
| chr9:121074828-121074981 | Rare:75 | ||||
| chr9:121201802-121202162 | Common:2; Rare:111 | ||||
| chr9:121268000-121268198 | Common:1; Rare:67 | ||||
| chr9:121328959-121329308 | Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:121370192-121370461 | Common:2; Rare:79 | ||||
| chr9:122159703-122159953 | Rare:97 | ||||
| chr9:122264735-122264922 | Common:2; Rare:53 | ||||
| chr9:122913277-122913409 | Common:2; Rare:29 | ||||
| chr9:122931482-122931680 | Common:3; Rare:36 | ||||
| chr9:124861908-124862125 | Rare:93 |