| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121201837-121202125 | Common:2; Rare:82 | ||||
| chr9:122264731-122264917 | Common:2; Rare:53 | ||||
| chr9:122905281-122905533 | Common:2; Rare:104 | ||||
| chr9:124861890-124862134 | Common:1; Rare:103 | ||||
| chr9:125189753-125189819 | Rare:40 | ||||
| chr9:125200451-125200590 | Rare:53 | ||||
| chr9:125241312-125241656 | Common:2; Rare:103 | ||||
| chr9:125261691-125261841 | Common:1; Rare:61 | ||||
| chr9:127451282-127451515 | Common:2; Rare:105 | ||||
| chr9:127877667-127877785 | Rare:23 | ||||
| chr9:128275936-128276288 | Common:4; Rare:163 | ||||
| chr9:128322414-128322621 | Common:1; Rare:58 | ||||
| chr9:128322729-128322856 | Common:2; Rare:46; Clinvar (benign):5 | ||||
| chr9:128371172-128371376 | Common:1; Rare:68 | ||||
| chr9:128724095-128724470 | Common:3; Rare:123 |