| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23586387-23586541 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24138840-24139092 | Common:2; Rare:73 | ||||
| chr18:24397784-24398073 | Common:2; Rare:107 | ||||
| chr18:24426598-24426792 | Common:3; Rare:72 | ||||
| chr18:26090576-26090982 | Common:5; Rare:154 | ||||
| chr18:26091091-26091279 | Common:2; Rare:50 | ||||
| chr18:26226288-26226481 | Common:2; Rare:70 | ||||
| chr18:26549764-26549980 | Common:4; Rare:63 | ||||
| chr18:31101910-31101999 | Common:1; Rare:23; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr18:31498069-31498266 | Common:1; Rare:68; Clinvar:5; Clinvar (benign):5 | ||||
| chr18:31684205-31684364 | Common:2; Rare:48 | ||||
| chr18:31943095-31943380 | Common:7; Rare:93 | ||||
| chr18:32018456-32018742 | Common:2; Rare:81 | ||||
| chr18:32092367-32092733 | Common:5; Rare:167 | ||||
| chr18:34976942-34977068 | Common:1; Rare:23 |