| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600860-21601056 | Common:2; Rare:53 | ||||
| chr18:21612204-21612443 | Common:1; Rare:70 | ||||
| chr18:22933230-22933430 | Common:3; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933785-22933909 | Common:1; Rare:50 | ||||
| chr18:23453172-23453345 | Rare:59 | ||||
| chr18:23503300-23503547 | Common:2; Rare:91 | ||||
| chr18:23586372-23586528 | Common:3; Rare:68; Clinvar:5; Clinvar (benign):2 | ||||
| chr18:23586836-23587060 | Common:1; Rare:75 | ||||
| chr18:24426613-24426785 | Common:3; Rare:64 | ||||
| chr18:25352092-25352397 | Common:2; Rare:122 | ||||
| chr18:26090885-26090980 | Common:1; Rare:32 | ||||
| chr18:26091123-26091299 | Common:2; Rare:46 | ||||
| chr18:28176982-28177296 | Common:3; Rare:150 | ||||
| chr18:31498079-31498259 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):5 | ||||
| chr18:32092423-32092748 | Common:4; Rare:148 |