| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37594753-37594879 | Rare:34 | ||||
| chr19:37907045-37907315 | Rare:56 | ||||
| chr19:38374407-38374821 | Rare:157 | ||||
| chr19:38618956-38619252 | Common:3; Rare:87 | ||||
| chr19:38647372-38647748 | Common:3; Rare:132 | ||||
| chr19:38831753-38832045 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr19:38852305-38852605 | Rare:75 | ||||
| chr19:38899528-38900020 | Rare:149 | ||||
| chr19:38930742-38931002 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975690-38975884 | Common:1; Rare:51 | ||||
| chr19:39342345-39342518 | Common:2; Rare:49 | ||||
| chr19:39390860-39390965 | Rare:39 | ||||
| chr19:39390981-39391432 | Common:1; Rare:174 | ||||
| chr19:39406702-39406861 | Rare:59 | ||||
| chr19:39412825-39412854 | Rare:5 |