| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100309904-100310355 | Common:1; Rare:172 | ||||
| chr8:100706649-100706997 | Common:10; Rare:92 | ||||
| chr8:100709132-100709733 | Common:11; Rare:148 | ||||
| chr8:100950427-100950712 | Common:10; Rare:120 | ||||
| chr8:100951257-100951553 | Common:3; Rare:108 | ||||
| chr8:100952848-100953445 | Common:6; Rare:143 | ||||
| chr8:101205113-101205689 | Common:5; Rare:171 | ||||
| chr8:102238587-102238727 | Common:2; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:102238734-102239110 | Common:7; Rare:141; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr8:102412212-102412580 | Common:2; Rare:104 | ||||
| chr8:102412686-102412948 | Common:3; Rare:62 | ||||
| chr8:102864061-102864355 | Common:5; Rare:123 | ||||
| chr8:103020867-103021132 | Common:1; Rare:78 | ||||
| chr8:103298702-103298944 | Common:2; Rare:60 | ||||
| chr8:103414645-103414742 | Common:5; Rare:34 |