| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12947666-12948115 | Common:3; Rare:135 | ||||
| chr18:12991137-12991445 | Common:2; Rare:110 | ||||
| chr18:13726439-13726729 | Common:3; Rare:112 | ||||
| chr18:21111698-21111923 | Common:2; Rare:82 | ||||
| chr18:21600437-21600946 | Common:2; Rare:140 | ||||
| chr18:21704762-21705005 | Rare:67 | ||||
| chr18:22169526-22169589 | Rare:21 | ||||
| chr18:22933024-22933426 | Common:4; Rare:125; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933777-22933903 | Common:1; Rare:50 | ||||
| chr18:23453032-23453376 | Rare:115 | ||||
| chr18:23503287-23503576 | Common:2; Rare:106 | ||||
| chr18:23586379-23586560 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24426480-24426785 | Common:5; Rare:117 | ||||
| chr18:26090529-26090951 | Common:4; Rare:165 | ||||
| chr18:28176979-28177302 | Common:3; Rare:154 |