| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44747933-44748194 | Rare:53 | ||||
| chr19:45039283-45039571 | Common:3; Rare:80 | ||||
| chr19:45406355-45406662 | Common:1; Rare:71 | ||||
| chr19:45450756-45450999 | Common:4; Rare:46 | ||||
| chr19:45468155-45468322 | Rare:35 | ||||
| chr19:45468697-45469010 | Common:2; Rare:61 | ||||
| chr19:45469262-45469510 | Rare:76 | ||||
| chr19:45470101-45470357 | Rare:58 | ||||
| chr19:45584246-45584567 | Common:3; Rare:89 | ||||
| chr19:45584766-45585191 | Common:5; Rare:144; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45692372-45692704 | Common:1; Rare:75 | ||||
| chr19:46608292-46608504 | Common:1; Rare:55; Clinvar (benign):4 | ||||
| chr19:46731708-46731794 | Rare:16 | ||||
| chr19:46787270-46787382 | Rare:21 | ||||
| chr19:46787409-46787543 | Rare:43 |