| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13218695-13218786 | Common:1; Rare:16 | ||||
| chr18:13726445-13726720 | Common:3; Rare:108 | ||||
| chr18:21110968-21111340 | Common:1; Rare:95 | ||||
| chr18:21111708-21111953 | Common:2; Rare:88 | ||||
| chr18:21600474-21600521 | Rare:8 | ||||
| chr18:21600644-21600917 | Common:1; Rare:73 | ||||
| chr18:21600952-21600978 | Rare:5 | ||||
| chr18:21601005-21601033 | Rare:5 | ||||
| chr18:21704626-21704982 | Common:4; Rare:115 | ||||
| chr18:22169338-22169595 | Common:2; Rare:67 | ||||
| chr18:22933054-22933426 | Common:4; Rare:119; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933785-22933889 | Common:1; Rare:41 | ||||
| chr18:23453069-23453386 | Rare:108 | ||||
| chr18:23503293-23503621 | Common:4; Rare:139 | ||||
| chr18:23586402-23586531 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):1 |