| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:116874611-116874985 | Common:6; Rare:158; Clinvar (benign):1 | ||||
| chr8:116938394-116938561 | Common:6; Rare:67 | ||||
| chr8:117520533-117520782 | Common:5; Rare:62 | ||||
| chr8:119416147-119416450 | Common:1; Rare:57 | ||||
| chr8:119832746-119832903 | Common:2; Rare:60 | ||||
| chr8:119855719-119855988 | Common:2; Rare:81 | ||||
| chr8:119873564-119873849 | Common:3; Rare:84 | ||||
| chr8:120445066-120445249 | Common:1; Rare:49 | ||||
| chr8:120445352-120445532 | Rare:60 | ||||
| chr8:121641428-121641606 | Rare:39 | ||||
| chr8:123072449-123072777 | Common:1; Rare:80 | ||||
| chr8:123396219-123396562 | Common:2; Rare:155 | ||||
| chr8:123416330-123416850 | Common:1; Rare:133 | ||||
| chr8:123540979-123541297 | Common:3; Rare:105 | ||||
| chr8:123768305-123768451 | Rare:50 |