| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:33473085-33473194 | Common:3; Rare:35 | ||||
| chr8:33484993-33485212 | Common:4; Rare:78 | ||||
| chr8:37736390-37736728 | Common:3; Rare:120 | ||||
| chr8:37762455-37762678 | Common:2; Rare:81 | ||||
| chr8:37849844-37849995 | Common:1; Rare:56 | ||||
| chr8:38105422-38105544 | Common:2; Rare:36 | ||||
| chr8:38105804-38105947 | Rare:39 | ||||
| chr8:38176430-38176881 | Common:5; Rare:129 | ||||
| chr8:38996452-38996781 | Common:4; Rare:110 | ||||
| chr8:41664906-41665052 | Common:1; Rare:48 | ||||
| chr8:42207557-42207665 | Common:1; Rare:37 | ||||
| chr8:42207672-42207927 | Common:2; Rare:45 | ||||
| chr8:42391704-42391920 | Common:3; Rare:77 | ||||
| chr8:42541562-42541676 | Rare:41 | ||||
| chr8:42541678-42541910 | Common:1; Rare:76; Clinvar (benign):1 |