| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:22367190-22367286 | Common:4; Rare:44 | ||||
| chr8:22604549-22604812 | Common:1; Rare:93 | ||||
| chr8:22669082-22669221 | Common:2; Rare:44 | ||||
| chr8:23069011-23069172 | Rare:62 | ||||
| chr8:23164028-23164119 | Rare:18 | ||||
| chr8:23225070-23225253 | Common:1; Rare:42 | ||||
| chr8:23243452-23243668 | Common:3; Rare:38 | ||||
| chr8:23457601-23457867 | Common:4; Rare:91 | ||||
| chr8:23528742-23529053 | Rare:96 | ||||
| chr8:26382916-26383097 | Rare:79 | ||||
| chr8:27311236-27311500 | Common:7; Rare:100 | ||||
| chr8:27380593-27380697 | Common:1; Rare:16 | ||||
| chr8:27772584-27772739 | Common:6; Rare:49 | ||||
| chr8:27774429-27774589 | Common:2; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:27837729-27837911 | Common:1; Rare:51 |