| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23006061-23006458 | Common:1; Rare:92; Clinvar:1 | ||||
| chr18:23012680-23012887 | Rare:31 | ||||
| chr18:23022110-23022152 | Rare:12; Clinvar:1 | ||||
| chr18:23285208-23285299 | Rare:13 | ||||
| chr18:23506682-23506996 | Rare:51 | ||||
| chr18:23536810-23537027 | Rare:52; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr18:23543205-23543328 | Rare:27 | ||||
| chr18:23585376-23585565 | Common:1; Rare:37 | ||||
| chr18:23719630-23719654 | Rare:2 | ||||
| chr18:23826042-23826318 | Common:2; Rare:48 | ||||
| chr18:23837669-23837903 | Common:1; Rare:31 | ||||
| chr18:23875449-23875628 | Common:1; Rare:35 | ||||
| chr18:23876238-23876449 | Rare:67; Clinvar (pathogenic):4 | ||||
| chr18:23876488-23876606 | Rare:19 | ||||
| chr18:23877082-23877157 | Rare:8 |