| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38845671-38845912 | Common:1; Rare:71 | ||||
| chr19:39486216-39486477 | Common:2; Rare:94; Clinvar (pathogenic):1 | ||||
| chr19:40190580-40190673 | Common:1; Rare:13 | ||||
| chr19:41389618-41389815 | Rare:47 | ||||
| chr19:42396924-42397204 | Common:1; Rare:67 | ||||
| chr19:43755586-43755725 | Common:1; Rare:48 | ||||
| chr19:45717264-45717554 | Common:1; Rare:91 | ||||
| chr19:46133322-46133594 | Rare:46 | ||||
| chr19:46180650-46180925 | Rare:61 | ||||
| chr19:46180931-46181007 | Rare:16 | ||||
| chr19:46181543-46181744 | Common:2; Rare:33 | ||||
| chr19:46860778-46861126 | Common:3; Rare:113 | ||||
| chr19:47244176-47244417 | Common:1; Rare:47 | ||||
| chr19:47598655-47598812 | Rare:33 | ||||
| chr19:48259776-48259795 | Rare:2 |