| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151080776-151080980 | Rare:65 | ||||
| chr7:152435944-152436284 | Rare:118 | ||||
| chr7:152676091-152676295 | Common:2; Rare:89; Clinvar (benign):10 | ||||
| chr7:155644376-155644719 | Common:2; Rare:118 | ||||
| chr7:156640556-156640756 | Common:2; Rare:97 | ||||
| chr7:157336790-157337083 | Common:2; Rare:136; Clinvar:2 | ||||
| chr8:232235-232377 | Common:2; Rare:56 | ||||
| chr8:6406527-6406668 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:10839824-10840109 | Common:3; Rare:90 | ||||
| chr8:11802446-11802791 | Common:6; Rare:187 | ||||
| chr8:17246804-17246982 | Common:1; Rare:78 | ||||
| chr8:19817318-19817489 | Common:3; Rare:65 | ||||
| chr8:21919440-21919763 | Common:2; Rare:126 | ||||
| chr8:22245024-22245164 | Rare:72 | ||||
| chr8:22367053-22367301 | Common:6; Rare:82 |