| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23894874-23895295 | Common:2; Rare:122; Clinvar:3 | ||||
| chr18:23895567-23896109 | Common:2; Rare:87 | ||||
| chr18:23896367-23896545 | Common:1; Rare:38 | ||||
| chr18:23897074-23897325 | Rare:36 | ||||
| chr18:23902478-23902680 | Rare:27 | ||||
| chr18:23902683-23902758 | Rare:10 | ||||
| chr18:23902900-23903208 | Rare:67; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr18:23903442-23903501 | Common:1; Rare:5 | ||||
| chr18:23903891-23904212 | Common:1; Rare:81 | ||||
| chr18:23905496-23905737 | Rare:60; Clinvar:1 | ||||
| chr18:23906602-23906952 | Rare:68 | ||||
| chr18:23907728-23908205 | Common:2; Rare:101 | ||||
| chr18:23908566-23908943 | Common:1; Rare:69 | ||||
| chr18:23908984-23909317 | Rare:78; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr18:23909436-23909728 | Rare:48 |