| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17922606-17922936 | Common:4; Rare:124 | ||||
| chr8:18084779-18084893 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr8:18084919-18085041 | Rare:29 | ||||
| chr8:18209949-18210147 | Common:1; Rare:56 | ||||
| chr8:19817388-19817523 | Common:4; Rare:63 | ||||
| chr8:21919452-21919772 | Common:2; Rare:124 | ||||
| chr8:22053430-22053683 | Common:2; Rare:63 | ||||
| chr8:22585119-22585399 | Common:1; Rare:88 | ||||
| chr8:22669082-22669226 | Common:2; Rare:49 | ||||
| chr8:23068990-23069107 | Rare:53 | ||||
| chr8:23457617-23457778 | Common:2; Rare:62 | ||||
| chr8:23528650-23529053 | Rare:125 | ||||
| chr8:24955935-24956201 | Rare:97; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr8:26382928-26383153 | Common:3; Rare:102 | ||||
| chr8:26383268-26383437 | Rare:51 |