| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22933273-22933454 | Common:2; Rare:69; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933807-22933902 | Common:1; Rare:37 | ||||
| chr18:23453115-23453325 | Rare:72 | ||||
| chr18:23586416-23586524 | Common:2; Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24138862-24139069 | Common:2; Rare:61 | ||||
| chr18:24397778-24398102 | Common:2; Rare:115 | ||||
| chr18:24426499-24426779 | Common:5; Rare:110 | ||||
| chr18:26090552-26090689 | Common:1; Rare:67 | ||||
| chr18:26091175-26091225 | Common:1; Rare:12 | ||||
| chr18:31943095-31943386 | Common:7; Rare:97 | ||||
| chr18:32018350-32018788 | Common:2; Rare:117 | ||||
| chr18:32092387-32092745 | Common:5; Rare:157 | ||||
| chr18:34493086-34493364 | Common:2; Rare:66 | ||||
| chr18:35041250-35041459 | Common:1; Rare:78 | ||||
| chr18:35240917-35241094 | Common:2; Rare:66 |