| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12991137-12991395 | Common:2; Rare:92 | ||||
| chr18:13218651-13218815 | Common:1; Rare:35 | ||||
| chr18:13612361-13612632 | Common:2; Rare:61 | ||||
| chr18:13726408-13726736 | Common:4; Rare:119 | ||||
| chr18:14132389-14132553 | Common:3; Rare:47 | ||||
| chr18:21111779-21111949 | Common:2; Rare:50 | ||||
| chr18:21242187-21242325 | Common:1; Rare:58 | ||||
| chr18:21600625-21600913 | Rare:77 | ||||
| chr18:21600948-21601108 | Rare:28 | ||||
| chr18:21612204-21612441 | Common:1; Rare:70 | ||||
| chr18:21704663-21704991 | Common:3; Rare:104 | ||||
| chr18:22933781-22933903 | Common:1; Rare:50 | ||||
| chr18:23453172-23453368 | Rare:68 | ||||
| chr18:23503293-23503609 | Common:4; Rare:130 | ||||
| chr18:23586408-23586547 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):1 |