| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:11857625-11857760 | Common:1; Rare:36 | ||||
| chr18:11908277-11908404 | Rare:34 | ||||
| chr18:12307987-12308316 | Common:5; Rare:128 | ||||
| chr18:12702658-12703094 | Common:3; Rare:176 | ||||
| chr18:12884143-12884425 | Common:4; Rare:145 | ||||
| chr18:12947694-12948092 | Common:3; Rare:110 | ||||
| chr18:12991143-12991403 | Common:2; Rare:96 | ||||
| chr18:13726423-13726720 | Common:4; Rare:114 | ||||
| chr18:21612174-21612441 | Common:1; Rare:79 | ||||
| chr18:22933781-22933889 | Common:1; Rare:43 | ||||
| chr18:23453156-23453345 | Rare:67 | ||||
| chr18:23503293-23503542 | Common:2; Rare:89 | ||||
| chr18:23586408-23586541 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:23872833-23873111 | Rare:91; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr18:24138942-24139072 | Common:2; Rare:46 |