| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49556945-49557143 | Rare:79 | ||||
| chr19:49580528-49580679 | Rare:49 | ||||
| chr19:49665719-49666029 | Common:3; Rare:144; Clinvar (pathogenic):1 | ||||
| chr19:49690980-49691150 | Common:2; Rare:39 | ||||
| chr19:49813193-49813339 | Rare:59 | ||||
| chr19:49850963-49851032 | Rare:28 | ||||
| chr19:49867527-49867643 | Common:2; Rare:38; Clinvar:1 | ||||
| chr19:49877278-49877726 | Common:1; Rare:117 | ||||
| chr19:49877894-49878179 | Common:2; Rare:94 | ||||
| chr19:49929404-49929567 | Common:4; Rare:59 | ||||
| chr19:49929922-49930212 | Common:1; Rare:69 | ||||
| chr19:50163160-50163251 | Rare:30 | ||||
| chr19:50377603-50377859 | Common:1; Rare:99 | ||||
| chr19:50432783-50432901 | Common:1; Rare:28 | ||||
| chr19:50476200-50476547 | Common:1; Rare:164 |