| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35138450-35138892 | Common:1; Rare:100 | ||||
| chr19:35139046-35139213 | Common:2; Rare:41 | ||||
| chr19:35139294-35139643 | Common:3; Rare:69 | ||||
| chr19:35139653-35139776 | Common:1; Rare:34 | ||||
| chr19:35155148-35155230 | Rare:16 | ||||
| chr19:35248536-35248881 | Common:2; Rare:98 | ||||
| chr19:35248919-35249084 | Common:1; Rare:84 | ||||
| chr19:35268970-35269153 | Common:1; Rare:22 | ||||
| chr19:35545454-35545712 | Common:4; Rare:85 | ||||
| chr19:35628765-35629100 | Common:4; Rare:97 | ||||
| chr19:35648112-35648401 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35740380-35740728 | Common:2; Rare:133 | ||||
| chr19:35745347-35745700 | Rare:108 | ||||
| chr19:35748286-35748604 | Common:3; Rare:91 | ||||
| chr19:35757906-35758225 | Common:2; Rare:98 |