| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21111251-21111324 | Rare:23 | ||||
| chr18:21111625-21111938 | Common:2; Rare:103 | ||||
| chr18:21600649-21600833 | Rare:47 | ||||
| chr18:22169311-22169435 | Common:2; Rare:33 | ||||
| chr18:22169452-22169589 | Rare:38 | ||||
| chr18:22933764-22933889 | Common:1; Rare:50 | ||||
| chr18:23453172-23453329 | Rare:51 | ||||
| chr18:23503275-23503583 | Common:2; Rare:120 | ||||
| chr18:23586387-23586553 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:23619603-23619733 | Rare:36 | ||||
| chr18:23872935-23873031 | Rare:29 | ||||
| chr18:24426613-24426775 | Common:3; Rare:62 | ||||
| chr18:25351048-25351123 | Rare:27 | ||||
| chr18:26090573-26090897 | Common:4; Rare:126 | ||||
| chr18:26133814-26133909 | Common:1; Rare:25 |