| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119873564-119873740 | Common:1; Rare:40 | ||||
| chr8:120445075-120445465 | Common:1; Rare:105 | ||||
| chr8:121640840-121640935 | Rare:10 | ||||
| chr8:121641317-121641456 | Rare:26 | ||||
| chr8:122781632-122781932 | Common:3; Rare:58 | ||||
| chr8:123042197-123042583 | Common:3; Rare:94 | ||||
| chr8:123274221-123274711 | Common:2; Rare:133 | ||||
| chr8:123396350-123396663 | Common:2; Rare:125 | ||||
| chr8:123416330-123416850 | Common:1; Rare:133 | ||||
| chr8:124372659-124372766 | Common:2; Rare:51 | ||||
| chr8:124450713-124450841 | Common:4; Rare:44 | ||||
| chr8:124474521-124474714 | Common:1; Rare:74 | ||||
| chr8:124474944-124475271 | Rare:117 | ||||
| chr8:124538979-124539287 | Common:2; Rare:159; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124728396-124728636 | Common:2; Rare:73 |