| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119673316-119673430 | Rare:37 | ||||
| chr8:119832815-119832903 | Common:1; Rare:36 | ||||
| chr8:119855864-119855950 | Common:1; Rare:19 | ||||
| chr8:120124971-120125254 | Common:1; Rare:69 | ||||
| chr8:120445097-120445440 | Common:1; Rare:83 | ||||
| chr8:121641007-121641356 | Common:12; Rare:52 | ||||
| chr8:122781597-122781926 | Common:3; Rare:63 | ||||
| chr8:123541059-123541369 | Common:3; Rare:102 | ||||
| chr8:124474526-124474778 | Rare:94 | ||||
| chr8:124539016-124539287 | Common:2; Rare:137; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124673324-124673681 | Common:2; Rare:68 | ||||
| chr8:124728400-124728626 | Rare:70 | ||||
| chr8:125091699-125091938 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:126557704-126557896 | Rare:45 | ||||
| chr8:126558329-126558638 | Common:1; Rare:116 |