| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:58864510-58864911 | Common:1; Rare:82 | ||||
| chr18:59139689-59140035 | Common:3; Rare:92 | ||||
| chr18:59697377-59697873 | Common:2; Rare:142 | ||||
| chr18:60372740-60372940 | Rare:37 | ||||
| chr18:62186928-62187348 | Common:5; Rare:115 | ||||
| chr18:63367115-63367416 | Common:1; Rare:100 | ||||
| chr18:63422331-63422716 | Common:2; Rare:112 | ||||
| chr18:63970025-63970101 | Rare:14 | ||||
| chr18:67516705-67517026 | Common:5; Rare:84 | ||||
| chr18:68714977-68715296 | Common:7; Rare:135 | ||||
| chr18:70205638-70205780 | Common:3; Rare:62; Clinvar (benign):2 | ||||
| chr18:72868028-72868347 | Common:4; Rare:114 | ||||
| chr18:74148352-74148594 | Common:1; Rare:72 | ||||
| chr18:74291897-74292255 | Common:3; Rare:103 | ||||
| chr18:74496029-74496434 | Common:4; Rare:128 |