| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:67952805-67953050 | Common:1; Rare:37 | ||||
| chr8:68330450-68331080 | Common:11; Rare:159 | ||||
| chr8:69466551-69466819 | Common:1; Rare:47 | ||||
| chr8:69492852-69492980 | Common:1; Rare:37 | ||||
| chr8:69833333-69833498 | Common:1; Rare:29 | ||||
| chr8:69834972-69835092 | Common:2; Rare:21 | ||||
| chr8:70402054-70402290 | Rare:78 | ||||
| chr8:70402583-70402838 | Common:2; Rare:87 | ||||
| chr8:70403387-70403594 | Common:3; Rare:58 | ||||
| chr8:70403759-70404014 | Rare:97 | ||||
| chr8:70404110-70404347 | Common:1; Rare:54 | ||||
| chr8:70608241-70608664 | Common:3; Rare:107 | ||||
| chr8:70669112-70669373 | Common:2; Rare:94 | ||||
| chr8:71322426-71322826 | Common:1; Rare:113 | ||||
| chr8:71361718-71361950 | Common:2; Rare:69; Clinvar:4; Clinvar (benign):3 |