| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12991163-12991388 | Common:1; Rare:79 | ||||
| chr18:13542200-13542365 | Common:1; Rare:31 | ||||
| chr18:13612344-13612639 | Common:2; Rare:67 | ||||
| chr18:13726433-13726724 | Common:4; Rare:112 | ||||
| chr18:21111729-21111971 | Common:2; Rare:82 | ||||
| chr18:21600632-21600852 | Rare:52 | ||||
| chr18:22169345-22169589 | Common:1; Rare:64 | ||||
| chr18:22797821-22798095 | Common:2; Rare:63 | ||||
| chr18:22933807-22933889 | Common:1; Rare:31 | ||||
| chr18:23453148-23453350 | Rare:72 | ||||
| chr18:23503333-23503571 | Rare:91 | ||||
| chr18:23586369-23586541 | Common:3; Rare:77; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:23586884-23587078 | Common:1; Rare:66 | ||||
| chr18:24397767-24398112 | Common:2; Rare:123 | ||||
| chr18:24426607-24426775 | Common:3; Rare:65 |