| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22170672-22170843 | Rare:34 | ||||
| chr18:22933256-22933454 | Common:2; Rare:76; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933761-22933889 | Common:1; Rare:53 | ||||
| chr18:23453172-23453353 | Rare:62 | ||||
| chr18:23503300-23503609 | Common:4; Rare:127 | ||||
| chr18:23586339-23586550 | Common:4; Rare:90; Clinvar:6; Clinvar (benign):3 | ||||
| chr18:23662769-23662976 | Common:4; Rare:65 | ||||
| chr18:23884349-23884705 | Common:2; Rare:63 | ||||
| chr18:23992725-23992887 | Common:1; Rare:30 | ||||
| chr18:24271626-24271752 | Common:2; Rare:40 | ||||
| chr18:24271760-24272073 | Rare:68 | ||||
| chr18:24397788-24398013 | Common:2; Rare:96 | ||||
| chr18:24426613-24426785 | Common:3; Rare:64 | ||||
| chr18:25351052-25351129 | Rare:27 | ||||
| chr18:25352092-25352429 | Common:2; Rare:139 |