| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100309881-100310284 | Common:1; Rare:143 | ||||
| chr8:100706649-100706997 | Common:10; Rare:92 | ||||
| chr8:100722066-100722089 | Rare:14 | ||||
| chr8:100953323-100953413 | Common:1; Rare:17 | ||||
| chr8:101205532-101205880 | Common:4; Rare:112 | ||||
| chr8:102123829-102123894 | Rare:23 | ||||
| chr8:102238786-102239000 | Common:4; Rare:86; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr8:102239046-102239326 | Common:2; Rare:59 | ||||
| chr8:102239371-102239513 | Rare:39 | ||||
| chr8:102412692-102412948 | Common:3; Rare:62 | ||||
| chr8:102864089-102864267 | Common:3; Rare:75 | ||||
| chr8:103298730-103298944 | Common:2; Rare:52 | ||||
| chr8:103414985-103415511 | Common:6; Rare:259 | ||||
| chr8:105319285-105319584 | Rare:69 | ||||
| chr8:106270072-106270356 | Common:1; Rare:106 |