| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:52222916-52223162 | Common:4; Rare:38 | ||||
| chr18:52229365-52229440 | Common:1; Rare:14 | ||||
| chr18:54087807-54088022 | Common:1; Rare:44 | ||||
| chr18:54246595-54246772 | Common:2; Rare:18 | ||||
| chr18:57600471-57600664 | Common:1; Rare:29 | ||||
| chr18:57630305-57630394 | Rare:22 | ||||
| chr18:57764450-57764750 | Common:2; Rare:37 | ||||
| chr18:58281228-58281292 | Rare:16 | ||||
| chr18:58344397-58344699 | Common:1; Rare:54 | ||||
| chr18:58350924-58351036 | Rare:27 | ||||
| chr18:58681018-58681211 | Rare:39; Clinvar (benign):1 | ||||
| chr18:58980719-58980927 | Rare:45 | ||||
| chr18:59355313-59355648 | Common:1; Rare:93; Clinvar (benign):2 | ||||
| chr18:59451142-59451426 | Common:2; Rare:52 | ||||
| chr18:59540370-59540476 | Rare:20 |