| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:90791707-90791775 | Common:1; Rare:26 | ||||
| chr8:91069966-91070393 | Common:1; Rare:151 | ||||
| chr8:92095212-92095338 | Rare:33 | ||||
| chr8:93700448-93700665 | Common:1; Rare:83 | ||||
| chr8:93740935-93741188 | Common:1; Rare:81 | ||||
| chr8:93916675-93917012 | Common:3; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:94436907-94437102 | Rare:41 | ||||
| chr8:94475062-94475207 | Common:3; Rare:38 | ||||
| chr8:94553426-94553777 | Common:3; Rare:128 | ||||
| chr8:94640728-94641408 | Common:7; Rare:201 | ||||
| chr8:94719765-94720011 | Common:1; Rare:78 | ||||
| chr8:94895194-94895342 | Rare:48 | ||||
| chr8:94895643-94895846 | Common:2; Rare:59 | ||||
| chr8:94949350-94949532 | Common:1; Rare:57 | ||||
| chr8:95024939-95025203 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 |