| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13542200-13542451 | Common:3; Rare:49 | ||||
| chr18:13726490-13726726 | Common:3; Rare:88 | ||||
| chr18:21111651-21111975 | Common:2; Rare:109 | ||||
| chr18:21600648-21600856 | Rare:49 | ||||
| chr18:21704700-21704932 | Common:3; Rare:80 | ||||
| chr18:22169469-22169589 | Rare:33 | ||||
| chr18:22914064-22914166 | Rare:16 | ||||
| chr18:22933240-22933446 | Common:3; Rare:78; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933741-22933913 | Common:1; Rare:72 | ||||
| chr18:23453069-23453329 | Rare:87 | ||||
| chr18:23503293-23503542 | Common:2; Rare:89 | ||||
| chr18:23586379-23586553 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:23872683-23873059 | Rare:92; Clinvar (pathogenic):1 | ||||
| chr18:24426613-24426775 | Common:3; Rare:62 | ||||
| chr18:25351058-25351142 | Rare:30 |