| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:24138977-24139074 | Common:2; Rare:38 | ||||
| chr18:24397788-24398076 | Common:2; Rare:108 | ||||
| chr18:24426620-24426763 | Common:3; Rare:61 | ||||
| chr18:25352019-25352426 | Common:2; Rare:157 | ||||
| chr18:26657374-26657440 | Rare:21 | ||||
| chr18:26863166-26863406 | Rare:51 | ||||
| chr18:26865209-26865342 | Rare:28 | ||||
| chr18:26865677-26865869 | Common:1; Rare:56 | ||||
| chr18:28176968-28177150 | Common:3; Rare:94 | ||||
| chr18:32092338-32092727 | Common:6; Rare:175 | ||||
| chr18:33578216-33578528 | Common:4; Rare:88 | ||||
| chr18:34048523-34048660 | Rare:24 | ||||
| chr18:34222090-34222392 | Common:2; Rare:66 | ||||
| chr18:34493166-34493434 | Common:1; Rare:60 | ||||
| chr18:34818196-34818466 | Rare:55; Clinvar:3; Clinvar (benign):1 |