| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:116766328-116766586 | Common:4; Rare:66 | ||||
| chr8:116874611-116874966 | Common:6; Rare:152; Clinvar (benign):1 | ||||
| chr8:119416286-119416453 | Rare:32 | ||||
| chr8:119832811-119832908 | Common:1; Rare:40 | ||||
| chr8:119855734-119855758 | Rare:7 | ||||
| chr8:119855868-119855956 | Common:1; Rare:18 | ||||
| chr8:120445075-120445473 | Common:1; Rare:107 | ||||
| chr8:122781589-122781666 | Rare:11 | ||||
| chr8:123042178-123042367 | Common:1; Rare:55 | ||||
| chr8:123274243-123274747 | Common:2; Rare:130 | ||||
| chr8:123275351-123275440 | Rare:18 | ||||
| chr8:123416514-123416821 | Rare:83 | ||||
| chr8:124474521-124474757 | Common:1; Rare:88 | ||||
| chr8:124539032-124539198 | Common:2; Rare:94; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124728396-124728767 | Common:5; Rare:113 |