| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58440128-58440460 | Common:6; Rare:89 | ||||
| chr19:58476125-58476162 | Rare:8 | ||||
| chr19:58499216-58499655 | Common:2; Rare:156; Clinvar:7; Clinvar (benign):1 | ||||
| chr19:58519761-58520031 | Rare:71 | ||||
| chr19:58554945-58555199 | Common:2; Rare:82 | ||||
| chr19:58558952-58559151 | Common:1; Rare:57 | ||||
| chr19:58573472-58573606 | Common:1; Rare:36 | ||||
| chr2:677364-677518 | Common:1; Rare:59 | ||||
| chr2:1373929-1374245 | Common:3; Rare:76 | ||||
| chr2:1744465-1744668 | Common:2; Rare:70 | ||||
| chr2:3377811-3377931 | Rare:32 | ||||
| chr2:3379604-3379791 | Common:2; Rare:75 | ||||
| chr2:3519483-3519636 | Common:2; Rare:52 | ||||
| chr2:3558269-3558635 | Common:6; Rare:131 | ||||
| chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 |