| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:133571814-133572163 | Rare:85 | ||||
| chr8:140511191-140511495 | Common:3; Rare:115 | ||||
| chr8:142669960-142670311 | Common:9; Rare:120 | ||||
| chr8:143018375-143018544 | Common:1; Rare:50 | ||||
| chr8:143541414-143541614 | Common:2; Rare:70 | ||||
| chr8:143558256-143558420 | Common:1; Rare:65 | ||||
| chr8:143636000-143636017 | Rare:6 | ||||
| chr8:143684412-143684508 | Common:3; Rare:19 | ||||
| chr8:143829017-143829069 | Rare:20 | ||||
| chr8:143829299-143829517 | Rare:84 | ||||
| chr8:144082520-144082696 | Common:2; Rare:60 | ||||
| chr8:144096185-144096393 | Common:1; Rare:74; Clinvar (benign):3 | ||||
| chr8:144096476-144096660 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:144103719-144103867 | Rare:48 | ||||
| chr8:144104248-144104520 | Common:1; Rare:91 |