| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121075104-121075211 | Rare:29 | ||||
| chr9:121201829-121202158 | Common:2; Rare:97 | ||||
| chr9:121268049-121268207 | Common:1; Rare:53 | ||||
| chr9:121285905-121286123 | Common:1; Rare:40 | ||||
| chr9:121328921-121329315 | Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:121370183-121370512 | Common:2; Rare:101 | ||||
| chr9:122159708-122159939 | Rare:88 | ||||
| chr9:122264549-122264691 | Common:2; Rare:32 | ||||
| chr9:122264715-122264922 | Common:3; Rare:57 | ||||
| chr9:122828509-122828706 | Rare:62 | ||||
| chr9:122931482-122931680 | Common:3; Rare:36 | ||||
| chr9:124861908-124862118 | Rare:91 | ||||
| chr9:124940969-124941215 | Common:3; Rare:92 | ||||
| chr9:125189744-125190025 | Common:1; Rare:120 | ||||
| chr9:125200493-125200590 | Rare:36 |