| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:66604210-66604260 | Rare:5 | ||||
| chr18:68714987-68715296 | Common:7; Rare:132 | ||||
| chr18:70205634-70205783 | Common:3; Rare:64; Clinvar (benign):2 | ||||
| chr18:74148353-74148619 | Common:1; Rare:76 | ||||
| chr18:74149003-74149087 | Common:1; Rare:27 | ||||
| chr18:74291876-74292255 | Common:3; Rare:110 | ||||
| chr18:74457147-74457430 | Common:4; Rare:93 | ||||
| chr18:74457938-74458023 | Common:1; Rare:13 | ||||
| chr18:74496039-74496424 | Common:4; Rare:123 | ||||
| chr18:74597385-74597484 | Common:1; Rare:26 | ||||
| chr18:74597554-74597931 | Common:2; Rare:104 | ||||
| chr18:75209045-75209240 | Common:1; Rare:69 | ||||
| chr18:75210723-75210910 | Common:4; Rare:50; Clinvar:7; Clinvar (benign):1 | ||||
| chr18:76822249-76822591 | Common:11; Rare:95 | ||||
| chr18:77087441-77087508 | Common:4; Rare:18 |