| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54269435-54269617 | Common:2; Rare:89 | ||||
| chr18:54357842-54357984 | Common:6; Rare:46 | ||||
| chr18:55664911-55665277 | Common:4; Rare:104 | ||||
| chr18:56651129-56651382 | Common:3; Rare:62 | ||||
| chr18:57586601-57586811 | Rare:59 | ||||
| chr18:57621706-57621969 | Common:3; Rare:93 | ||||
| chr18:58045584-58045996 | Rare:94 | ||||
| chr18:58046314-58046594 | Common:1; Rare:47 | ||||
| chr18:58047385-58047549 | Common:1; Rare:28 | ||||
| chr18:59359202-59359517 | Common:4; Rare:145; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:59899818-59900017 | Common:3; Rare:65 | ||||
| chr18:62186912-62187329 | Common:5; Rare:116 | ||||
| chr18:63161851-63162051 | Common:1; Rare:36 | ||||
| chr18:63367099-63367328 | Common:1; Rare:81 | ||||
| chr18:63422339-63422687 | Common:2; Rare:98 |