| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:24914011-24914099 | Rare:27 | ||||
| chr8:24914119-24914207 | Rare:20; Clinvar:1 | ||||
| chr8:24914211-24914661 | Rare:137; Clinvar:2 | ||||
| chr8:24914663-24915025 | Rare:107; Clinvar:1 | ||||
| chr8:24955470-24956339 | Common:1; Rare:283; Clinvar:20; Clinvar (benign):15; Clinvar (pathogenic):6 | ||||
| chr8:24956341-24956643 | Rare:96; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:26045127-26045469 | Common:3; Rare:89 | ||||
| chr8:26382912-26383154 | Common:3; Rare:107 | ||||
| chr8:26383281-26383419 | Rare:37 | ||||
| chr8:26390263-26390455 | Common:1; Rare:37 | ||||
| chr8:26513815-26514271 | Common:2; Rare:98 | ||||
| chr8:27258367-27258623 | Rare:39 | ||||
| chr8:27311246-27311499 | Common:7; Rare:93 | ||||
| chr8:27490959-27491223 | Common:3; Rare:86 | ||||
| chr8:27611315-27611593 | Common:3; Rare:56 |