| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58183297-58183469 | Rare:57 | ||||
| chr19:58228835-58228936 | Common:1; Rare:39 | ||||
| chr19:58278660-58278998 | Common:4; Rare:104 | ||||
| chr19:58326875-58327048 | Common:1; Rare:42 | ||||
| chr19:58347605-58347792 | Common:8; Rare:89 | ||||
| chr19:58362767-58362992 | Common:1; Rare:74 | ||||
| chr19:58408449-58408686 | Common:3; Rare:74 | ||||
| chr19:58466879-58467107 | Common:1; Rare:72 | ||||
| chr19:58499182-58499545 | Common:3; Rare:118; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:58519777-58520032 | Rare:69 | ||||
| chr19:58554955-58555262 | Common:2; Rare:109 | ||||
| chr2:677364-677588 | Common:1; Rare:91 | ||||
| chr2:3377811-3378028 | Common:2; Rare:61 | ||||
| chr2:3379600-3379785 | Common:2; Rare:75 | ||||
| chr2:3519516-3519660 | Common:1; Rare:37 |