| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23529827-23530115 | Common:3; Rare:63 | ||||
| chr18:23586416-23586530 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24271613-24272057 | Common:2; Rare:112 | ||||
| chr18:24426628-24426765 | Common:3; Rare:56 | ||||
| chr18:25352092-25352410 | Common:2; Rare:129 | ||||
| chr18:31101442-31101622 | Common:9; Rare:58 | ||||
| chr18:31101967-31102030 | Rare:14; Clinvar (benign):2 | ||||
| chr18:31102194-31102451 | Common:1; Rare:59; Clinvar:7 | ||||
| chr18:31498048-31498279 | Common:1; Rare:78; Clinvar:5; Clinvar (benign):6 | ||||
| chr18:31943079-31943381 | Common:7; Rare:98 | ||||
| chr18:32092068-32092071 | Rare:1 | ||||
| chr18:32092367-32092729 | Common:5; Rare:165 | ||||
| chr18:34976956-34977061 | Common:1; Rare:15 | ||||
| chr18:35240912-35241094 | Common:2; Rare:69 | ||||
| chr18:35290183-35290421 | Common:3; Rare:83 |