| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:89757661-89757862 | Common:1; Rare:77 | ||||
| chr8:89902394-89902571 | Common:1; Rare:69 | ||||
| chr8:90001377-90001515 | Rare:65 | ||||
| chr8:91069979-91070382 | Common:1; Rare:143 | ||||
| chr8:93740980-93741181 | Common:1; Rare:65 | ||||
| chr8:93754771-93754947 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):5 | ||||
| chr8:93916675-93916969 | Common:3; Rare:97; Clinvar (benign):1 | ||||
| chr8:94553445-94553668 | Common:3; Rare:81 | ||||
| chr8:94640728-94641078 | Common:4; Rare:93 | ||||
| chr8:94641096-94641206 | Common:3; Rare:29 | ||||
| chr8:94719746-94719945 | Common:1; Rare:54 | ||||
| chr8:95024881-95025172 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95133597-95133938 | Common:3; Rare:110 | ||||
| chr8:96261555-96261981 | Common:6; Rare:144 | ||||
| chr8:98045374-98045642 | Common:3; Rare:82 |