| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40802917-40803114 | Common:1; Rare:38 | ||||
| chr19:41218717-41218984 | Common:7; Rare:57 | ||||
| chr19:41219095-41219421 | Common:1; Rare:85 | ||||
| chr19:41262334-41262585 | Rare:45 | ||||
| chr19:41264269-41265110 | Common:6; Rare:245 | ||||
| chr19:41265207-41265285 | Rare:15 | ||||
| chr19:41310123-41310308 | Rare:77 | ||||
| chr19:41310331-41310484 | Rare:40 | ||||
| chr19:41363859-41363999 | Rare:53; Clinvar:1 | ||||
| chr19:41364080-41364211 | Common:1; Rare:41; Clinvar:2 | ||||
| chr19:41376385-41376523 | Rare:34 | ||||
| chr19:41397321-41397460 | Common:3; Rare:45 | ||||
| chr19:41397557-41397904 | Common:8; Rare:123; Clinvar (benign):7 | ||||
| chr19:41439489-41439686 | Common:1; Rare:60 | ||||
| chr19:41439873-41439940 | Common:1; Rare:38 |