| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45584760-45584966 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45632636-45632781 | Rare:40 | ||||
| chr19:45692372-45692673 | Common:1; Rare:64 | ||||
| chr19:45692755-45692828 | Rare:23 | ||||
| chr19:45692906-45693050 | Common:1; Rare:21 | ||||
| chr19:45730853-45731003 | Common:1; Rare:29 | ||||
| chr19:45733103-45733486 | Rare:71 | ||||
| chr19:45769185-45769541 | Common:1; Rare:147 | ||||
| chr19:45843005-45843223 | Common:3; Rare:43 | ||||
| chr19:45863064-45863443 | Common:5; Rare:117 | ||||
| chr19:45902645-45902943 | Common:2; Rare:89 | ||||
| chr19:45995166-45995554 | Common:1; Rare:146 | ||||
| chr19:46297019-46297062 | Rare:24 | ||||
| chr19:46346941-46347213 | Common:3; Rare:94 | ||||
| chr19:46413390-46413490 | Rare:19 |