| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38224156-38224296 | Rare:37 | ||||
| chr19:38253294-38253459 | Common:2; Rare:22 | ||||
| chr19:38256301-38256719 | Common:5; Rare:94 | ||||
| chr19:38264157-38264682 | Common:6; Rare:125 | ||||
| chr19:38264714-38264767 | Common:1; Rare:7 | ||||
| chr19:38264770-38264977 | Rare:65 | ||||
| chr19:38315722-38316066 | Rare:125 | ||||
| chr19:38335706-38335889 | Common:1; Rare:31 | ||||
| chr19:38336301-38336470 | Common:2; Rare:35 | ||||
| chr19:38337174-38337259 | Rare:31 | ||||
| chr19:38374396-38374656 | Rare:85 | ||||
| chr19:38374658-38374958 | Common:1; Rare:122 | ||||
| chr19:38387759-38387926 | Rare:41 | ||||
| chr19:38387964-38388107 | Rare:44 | ||||
| chr19:38527717-38528051 | Common:1; Rare:83; Clinvar:2; Clinvar (pathogenic):1 |