| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:893148-893484 | Common:3; Rare:144 | ||||
| chr19:913144-913289 | Rare:46 | ||||
| chr19:984230-984348 | Rare:42 | ||||
| chr19:1021232-1021548 | Common:14; Rare:145 | ||||
| chr19:1077559-1077749 | Common:5; Rare:55 | ||||
| chr19:1103749-1104119 | Common:7; Rare:155 | ||||
| chr19:1132191-1132316 | Rare:57 | ||||
| chr19:1241807-1241976 | Rare:54 | ||||
| chr19:1242154-1242588 | Common:1; Rare:124; Clinvar (pathogenic):1 | ||||
| chr19:1248453-1248592 | Common:1; Rare:49 | ||||
| chr19:1249582-1249938 | Common:1; Rare:143 | ||||
| chr19:1251649-1251890 | Common:1; Rare:105 | ||||
| chr19:1269047-1269398 | Common:2; Rare:135 | ||||
| chr19:1354811-1355029 | Common:1; Rare:106 | ||||
| chr19:1383437-1383491 | Rare:27 |