| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54828132-54828536 | Common:1; Rare:129 | ||||
| chr18:54959356-54959514 | Common:2; Rare:79 | ||||
| chr18:56651124-56651435 | Common:8; Rare:156 | ||||
| chr18:56651550-56651780 | Common:8; Rare:94 | ||||
| chr18:57435128-57435601 | Common:1; Rare:202 | ||||
| chr18:57586601-57586814 | Rare:60 | ||||
| chr18:57621717-57622008 | Common:6; Rare:196 | ||||
| chr18:58043740-58044747 | Common:12; Rare:468 | ||||
| chr18:58045340-58045960 | Common:12; Rare:231 | ||||
| chr18:58221383-58221620 | Common:1; Rare:43 | ||||
| chr18:58671236-58671631 | Common:7; Rare:304; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:58862654-58862977 | Common:1; Rare:61 | ||||
| chr18:59139711-59139949 | Common:2; Rare:63 | ||||
| chr18:59359198-59359527 | Common:7; Rare:275; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:59899814-59900019 | Common:6; Rare:128 |