| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54269492-54269617 | Common:1; Rare:67 | ||||
| chr18:54357878-54357973 | Common:4; Rare:25 | ||||
| chr18:54828326-54828634 | Rare:69 | ||||
| chr18:55589757-55589996 | Common:2; Rare:82 | ||||
| chr18:56651133-56651388 | Common:3; Rare:63 | ||||
| chr18:57621718-57621964 | Common:3; Rare:88 | ||||
| chr18:58221371-58221661 | Common:2; Rare:54 | ||||
| chr18:59139714-59139969 | Common:2; Rare:67 | ||||
| chr18:62186915-62187334 | Common:5; Rare:116 | ||||
| chr18:63367130-63367328 | Common:1; Rare:72 | ||||
| chr18:63422370-63422697 | Common:2; Rare:94 | ||||
| chr18:63476631-63477141 | Common:9; Rare:104 | ||||
| chr18:63587121-63587418 | Common:2; Rare:75 | ||||
| chr18:68714981-68715254 | Common:5; Rare:123 | ||||
| chr18:70205659-70205925 | Common:4; Rare:99; Clinvar (benign):2 |