| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121201838-121202161 | Common:2; Rare:92 | ||||
| chr9:121370217-121370511 | Common:1; Rare:83 | ||||
| chr9:122264814-122264919 | Common:1; Rare:28 | ||||
| chr9:122931482-122931632 | Common:3; Rare:25 | ||||
| chr9:124861909-124862116 | Rare:90 | ||||
| chr9:125189728-125190039 | Common:1; Rare:141 | ||||
| chr9:125240691-125241154 | Rare:123 | ||||
| chr9:127122718-127122973 | Common:3; Rare:70 | ||||
| chr9:127451369-127451523 | Common:1; Rare:55 | ||||
| chr9:128275903-128276293 | Common:4; Rare:171 | ||||
| chr9:128724070-128724443 | Common:1; Rare:126 | ||||
| chr9:128947531-128947716 | Common:1; Rare:84; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129835210-129835471 | Common:2; Rare:108 | ||||
| chr9:130043018-130043334 | Common:2; Rare:104 | ||||
| chr9:130053861-130053990 | Common:1; Rare:57 |