| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18589929-18589962 | Rare:3 | ||||
| chr19:18919227-18919855 | Common:4; Rare:248 | ||||
| chr19:18941235-18941433 | Common:3; Rare:53 | ||||
| chr19:19033454-19033754 | Common:2; Rare:95 | ||||
| chr19:19033805-19033933 | Common:1; Rare:35 | ||||
| chr19:19105698-19105747 | Rare:19; Clinvar (pathogenic):1 | ||||
| chr19:19192087-19192262 | Common:1; Rare:56 | ||||
| chr19:19192558-19193097 | Common:3; Rare:132; Clinvar (benign):1 | ||||
| chr19:19320471-19320865 | Common:4; Rare:146 | ||||
| chr19:19385494-19385843 | Rare:87 | ||||
| chr19:19515629-19515768 | Rare:21 | ||||
| chr19:19516106-19516260 | Rare:92; Clinvar (pathogenic):1 | ||||
| chr19:19663671-19663732 | Rare:11 | ||||
| chr19:21836154-21836369 | Common:3; Rare:84 | ||||
| chr19:29213094-29213259 | Common:3; Rare:56 |