| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58098208-58098451 | Common:8; Rare:91 | ||||
| chr19:58278733-58278994 | Common:3; Rare:82 | ||||
| chr19:58326834-58327051 | Common:1; Rare:50 | ||||
| chr19:58327231-58327309 | Rare:19 | ||||
| chr19:58347620-58347773 | Common:7; Rare:75 | ||||
| chr19:58386734-58386800 | Common:1; Rare:20 | ||||
| chr19:58408460-58408686 | Common:3; Rare:69 | ||||
| chr19:58499219-58499536 | Common:2; Rare:97; Clinvar:2 | ||||
| chr19:58519786-58520011 | Rare:64 | ||||
| chr2:677346-677525 | Common:1; Rare:73 | ||||
| chr2:3377811-3377931 | Rare:32 | ||||
| chr2:3379639-3379791 | Common:2; Rare:63 | ||||
| chr2:3519452-3519685 | Common:3; Rare:67 | ||||
| chr2:3558269-3558495 | Common:5; Rare:92 | ||||
| chr2:3575107-3575345 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):5 |