| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17376919-17377055 | Rare:47 | ||||
| chr19:17377061-17377380 | Common:2; Rare:124 | ||||
| chr19:17404141-17404457 | Common:2; Rare:61 | ||||
| chr19:17405289-17405847 | Common:7; Rare:137 | ||||
| chr19:17511507-17511673 | Common:2; Rare:74 | ||||
| chr19:17527072-17527394 | Common:2; Rare:85 | ||||
| chr19:17556409-17556557 | Common:1; Rare:30 | ||||
| chr19:17719402-17719533 | Common:1; Rare:60 | ||||
| chr19:17751350-17751543 | Common:1; Rare:44 | ||||
| chr19:17847960-17848162 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:17932783-17933038 | Common:2; Rare:65 | ||||
| chr19:18000990-18001177 | Common:1; Rare:42 | ||||
| chr19:18007138-18007224 | Rare:18 | ||||
| chr19:18009901-18010269 | Common:1; Rare:137 | ||||
| chr19:18086859-18087029 | Common:2; Rare:52; Clinvar (benign):1 |