| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37406546-37406689 | Common:3; Rare:26 | ||||
| chr8:37406747-37406841 | Common:1; Rare:21 | ||||
| chr8:37406858-37406935 | Rare:17 | ||||
| chr8:37421340-37421400 | Common:1; Rare:14 | ||||
| chr8:37436055-37436182 | Rare:29 | ||||
| chr8:37437613-37437750 | Rare:19 | ||||
| chr8:37439696-37439874 | Common:1; Rare:36 | ||||
| chr8:37489323-37489569 | Common:2; Rare:36 | ||||
| chr8:37493755-37494131 | Common:4; Rare:67 | ||||
| chr8:37744354-37744688 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:37747900-37748094 | Rare:80 | ||||
| chr8:38167783-38167955 | Rare:35 | ||||
| chr8:38935737-38935923 | Rare:25 | ||||
| chr8:38999037-38999044 | Rare:1 | ||||
| chr8:39054277-39054573 | Common:3; Rare:64 |