| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100239095-100239330 | Common:1; Rare:51 | ||||
| chr8:100313451-100313682 | Rare:34 | ||||
| chr8:102108039-102108314 | Common:2; Rare:58 | ||||
| chr8:102656455-102656522 | Common:1; Rare:13 | ||||
| chr8:103318338-103318775 | Rare:95; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr8:103319654-103319806 | Rare:22 | ||||
| chr8:107497270-107497393 | Common:1; Rare:33 | ||||
| chr8:116736052-116736221 | Rare:31 | ||||
| chr8:118620908-118621105 | Common:2; Rare:40 | ||||
| chr8:120548939-120549228 | Common:3; Rare:30 | ||||
| chr8:122782640-122782913 | Common:2; Rare:62 | ||||
| chr8:124658466-124658632 | Common:1; Rare:26 | ||||
| chr8:125951148-125951208 | Rare:5 | ||||
| chr8:127794377-127794567 | Rare:51 | ||||
| chr8:127876770-127876859 | Common:1; Rare:21 |