| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45769203-45769319 | Rare:35 | ||||
| chr19:46413515-46413749 | Common:1; Rare:78 | ||||
| chr19:46600913-46601110 | Common:2; Rare:82 | ||||
| chr19:46601200-46601416 | Common:3; Rare:65; Clinvar (benign):1 | ||||
| chr19:46787270-46787547 | Common:1; Rare:77 | ||||
| chr19:47112166-47112332 | Rare:51 | ||||
| chr19:47256472-47256577 | Rare:39 | ||||
| chr19:47484169-47484300 | Common:2; Rare:44 | ||||
| chr19:47778406-47778801 | Common:3; Rare:136 | ||||
| chr19:48170266-48170699 | Common:2; Rare:118 | ||||
| chr19:48255847-48255924 | Common:3; Rare:12 | ||||
| chr19:48325317-48325603 | Common:2; Rare:62 | ||||
| chr19:48445863-48446025 | Rare:57 | ||||
| chr19:48619139-48619663 | Common:1; Rare:165 | ||||
| chr19:48900164-48900372 | Common:1; Rare:69 |