| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37594739-37594892 | Rare:42 | ||||
| chr19:37655403-37655550 | Common:2; Rare:57 | ||||
| chr19:37779555-37779667 | Rare:23 | ||||
| chr19:37907009-37907284 | Common:1; Rare:64 | ||||
| chr19:38224150-38224491 | Common:1; Rare:94 | ||||
| chr19:38374427-38374853 | Rare:171 | ||||
| chr19:38618793-38619322 | Common:4; Rare:148 | ||||
| chr19:38647349-38647772 | Common:3; Rare:139 | ||||
| chr19:38647783-38647854 | Rare:21 | ||||
| chr19:38831768-38832055 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr19:38849310-38849565 | Common:1; Rare:106 | ||||
| chr19:38850682-38850710 | Rare:13 | ||||
| chr19:38852311-38852434 | Rare:36 | ||||
| chr19:38899561-38900087 | Rare:156 | ||||
| chr19:38930715-38931057 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):3 |