| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38728346-38728508 | Common:1; Rare:46 | ||||
| chr19:38736971-38737119 | Common:2; Rare:17 | ||||
| chr19:38831721-38831982 | Common:4; Rare:103; Clinvar (benign):1 | ||||
| chr19:38842419-38842750 | Rare:70 | ||||
| chr19:38852319-38852388 | Rare:17 | ||||
| chr19:38878237-38878353 | Rare:17 | ||||
| chr19:38899513-38900020 | Rare:153 | ||||
| chr19:38930627-38930992 | Common:4; Rare:111; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr19:39335274-39335566 | Common:2; Rare:91 | ||||
| chr19:39335650-39335724 | Common:2; Rare:14 | ||||
| chr19:39335968-39336205 | Common:1; Rare:62 | ||||
| chr19:39389123-39389496 | Common:1; Rare:83 | ||||
| chr19:39390946-39391432 | Common:1; Rare:181 | ||||
| chr19:39406684-39406928 | Rare:93 | ||||
| chr19:39407080-39407106 | Rare:5 |