| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23872688-23873068 | Rare:94; Clinvar (pathogenic):1 | ||||
| chr18:23992729-23992858 | Rare:26 | ||||
| chr18:24271760-24272074 | Rare:69 | ||||
| chr18:24397761-24398102 | Common:2; Rare:121 | ||||
| chr18:24426603-24426756 | Common:3; Rare:63 | ||||
| chr18:25351066-25351147 | Rare:28 | ||||
| chr18:26226286-26226478 | Common:2; Rare:67 | ||||
| chr18:31101460-31101590 | Common:8; Rare:43 | ||||
| chr18:31102253-31102558 | Common:1; Rare:77; Clinvar:6 | ||||
| chr18:31497944-31498303 | Common:1; Rare:113; Clinvar:7; Clinvar (benign):6 | ||||
| chr18:31685901-31685941 | Rare:11 | ||||
| chr18:31943087-31943418 | Common:7; Rare:110 | ||||
| chr18:32018599-32018873 | Common:3; Rare:82 | ||||
| chr18:32092366-32092727 | Common:5; Rare:165 | ||||
| chr18:34976942-34977067 | Common:1; Rare:22 |