| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:70205638-70205850 | Common:3; Rare:90; Clinvar (benign):2 | ||||
| chr18:74291926-74292204 | Common:2; Rare:74 | ||||
| chr18:74499294-74499481 | Common:1; Rare:38 | ||||
| chr18:74499834-74499933 | Common:2; Rare:22 | ||||
| chr18:74597810-74597914 | Common:1; Rare:28 | ||||
| chr18:79400134-79400330 | Common:2; Rare:71 | ||||
| chr19:572311-572603 | Common:1; Rare:143 | ||||
| chr19:663143-663374 | Common:2; Rare:90 | ||||
| chr19:893155-893484 | Common:3; Rare:140 | ||||
| chr19:984225-984348 | Common:1; Rare:46 | ||||
| chr19:1103776-1104110 | Common:6; Rare:144 | ||||
| chr19:1354786-1354999 | Common:2; Rare:89 | ||||
| chr19:1401491-1401659 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:1905156-1905374 | Common:4; Rare:79 | ||||
| chr19:2269257-2269601 | Common:2; Rare:145 |