| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:56638353-56638403 | Rare:16 | ||||
| chr18:56638527-56638980 | Common:7; Rare:153 | ||||
| chr18:56651088-56651479 | Common:6; Rare:107 | ||||
| chr18:57586570-57586904 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr18:57621677-57622048 | Common:3; Rare:132 | ||||
| chr18:58044660-58044833 | Common:2; Rare:59 | ||||
| chr18:58195318-58195435 | Common:1; Rare:25 | ||||
| chr18:58536618-58536912 | Common:3; Rare:88 | ||||
| chr18:58670955-58670985 | Rare:6 | ||||
| chr18:58671006-58671557 | Common:4; Rare:201 | ||||
| chr18:58672035-58672073 | Rare:15 | ||||
| chr18:58863704-58863827 | Rare:25 | ||||
| chr18:59139344-59139518 | Common:1; Rare:40 | ||||
| chr18:59139703-59139969 | Common:2; Rare:70 | ||||
| chr18:59140078-59140420 | Common:3; Rare:62 |