| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:101205589-101205857 | Common:4; Rare:77 | ||||
| chr8:103414972-103415492 | Common:6; Rare:255 | ||||
| chr8:108248706-108248867 | Rare:60 | ||||
| chr8:108443417-108443653 | Common:4; Rare:103 | ||||
| chr8:109334060-109334402 | Common:1; Rare:86 | ||||
| chr8:116766372-116766586 | Common:1; Rare:54 | ||||
| chr8:117520584-117520782 | Common:4; Rare:46 | ||||
| chr8:119832818-119832897 | Common:1; Rare:30 | ||||
| chr8:119873564-119873835 | Common:2; Rare:76 | ||||
| chr8:120445091-120445445 | Common:1; Rare:88 | ||||
| chr8:122781589-122781769 | Common:3; Rare:25 | ||||
| chr8:123396356-123396562 | Common:2; Rare:94 | ||||
| chr8:123416425-123416765 | Rare:88 | ||||
| chr8:124474963-124475231 | Rare:98 | ||||
| chr8:124539054-124539189 | Common:1; Rare:73; Clinvar (benign):5; Clinvar (pathogenic):1 |