| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:52813333-52813478 | Common:2; Rare:32 | ||||
| chr19:52923414-52923537 | Common:2; Rare:47 | ||||
| chr19:53978712-53979087 | Common:10; Rare:45 | ||||
| chr19:53979297-53979600 | Rare:48 | ||||
| chr19:53980264-53980451 | Common:3; Rare:50 | ||||
| chr19:54448005-54448218 | Common:5; Rare:47 | ||||
| chr19:54461934-54462119 | Common:2; Rare:69 | ||||
| chr19:55006063-55006274 | Common:3; Rare:82 | ||||
| chr19:55189406-55189534 | Common:3; Rare:31 | ||||
| chr19:55265887-55266275 | Rare:92 | ||||
| chr19:55580128-55580292 | Common:2; Rare:28 | ||||
| chr19:57295330-57295620 | Common:1; Rare:63 | ||||
| chr19:57826722-57826797 | Rare:22 | ||||
| chr19:57867935-57868054 | Rare:22 | ||||
| chr2:276988-277250 | Common:3; Rare:67; Clinvar (benign):1 |