| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38735467-38736397 | Common:22; Rare:426 | ||||
| chr19:38736800-38737150 | Common:11; Rare:100 | ||||
| chr19:38769824-38770043 | Common:5; Rare:54 | ||||
| chr19:38830950-38831480 | Common:12; Rare:466; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:38831699-38832079 | Common:13; Rare:347; Clinvar (benign):3 | ||||
| chr19:38837550-38838130 | Rare:432 | ||||
| chr19:38849190-38849630 | Common:4; Rare:368 | ||||
| chr19:38849717-38850238 | Common:7; Rare:349 | ||||
| chr19:38850333-38850895 | Common:4; Rare:330 | ||||
| chr19:38851529-38851631 | Rare:26 | ||||
| chr19:38851807-38852226 | Common:7; Rare:347 | ||||
| chr19:38852311-38852689 | Rare:137 | ||||
| chr19:38869776-38870451 | Common:6; Rare:348 | ||||
| chr19:38899514-38900082 | Rare:449 | ||||
| chr19:38920485-38920706 | Common:1; Rare:60 |