| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31101967-31102107 | Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
| chr18:31498050-31498326 | Common:1; Rare:98; Clinvar:8; Clinvar (benign):7 | ||||
| chr18:31943087-31943380 | Common:7; Rare:95 | ||||
| chr18:32018558-32018873 | Common:3; Rare:93 | ||||
| chr18:32091851-32091991 | Common:3; Rare:51 | ||||
| chr18:32092382-32092774 | Common:5; Rare:177 | ||||
| chr18:33578304-33578566 | Common:3; Rare:67 | ||||
| chr18:34224719-34225089 | Common:3; Rare:70 | ||||
| chr18:34493137-34493452 | Common:1; Rare:70 | ||||
| chr18:34593203-34593427 | Rare:46 | ||||
| chr18:34976934-34977067 | Common:1; Rare:24 | ||||
| chr18:35041250-35041511 | Common:1; Rare:101 | ||||
| chr18:35240917-35241140 | Common:2; Rare:83 | ||||
| chr18:35290141-35290389 | Common:2; Rare:79 | ||||
| chr18:35497603-35497709 | Common:2; Rare:40 |