| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143829280-143829509 | Rare:88 | ||||
| chr8:143878441-143878566 | Common:3; Rare:40 | ||||
| chr8:143926769-143927119 | Common:3; Rare:141; Clinvar:22; Clinvar (benign):11 | ||||
| chr8:143939390-143939416 | Rare:14; Clinvar (benign):1 | ||||
| chr8:143939418-143939780 | Common:3; Rare:126; Clinvar (benign):1 | ||||
| chr8:143942573-143942874 | Common:2; Rare:75 | ||||
| chr8:143943918-143944078 | Rare:62 | ||||
| chr8:143986917-143987086 | Rare:31 | ||||
| chr8:143992559-143992876 | Common:2; Rare:102 | ||||
| chr8:144060678-144060820 | Rare:42 | ||||
| chr8:144078577-144078869 | Common:1; Rare:97 | ||||
| chr8:144082513-144082758 | Common:2; Rare:74 | ||||
| chr8:144083833-144084001 | Rare:53; Clinvar (pathogenic):1 | ||||
| chr8:144096031-144096227 | Rare:81; Clinvar (benign):1 | ||||
| chr8:144103682-144103881 | Common:1; Rare:71 |