| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46104225-46104420 | Common:3; Rare:55 | ||||
| chr18:46917477-46917859 | Common:5; Rare:126 | ||||
| chr18:47176283-47176395 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr18:47930303-47930732 | Common:2; Rare:185 | ||||
| chr18:47930795-47930997 | Rare:66 | ||||
| chr18:48942479-48942624 | Common:1; Rare:44 | ||||
| chr18:49492232-49492570 | Common:2; Rare:133 | ||||
| chr18:49813485-49814138 | Common:2; Rare:207 | ||||
| chr18:50878975-50879297 | Common:4; Rare:104 | ||||
| chr18:51029986-51030245 | Rare:82 | ||||
| chr18:51030342-51030595 | Rare:67; Clinvar:2 | ||||
| chr18:54224029-54224220 | Common:2; Rare:61 | ||||
| chr18:54224504-54224559 | Rare:11 | ||||
| chr18:54269467-54269661 | Common:4; Rare:95 | ||||
| chr18:54357859-54358080 | Common:8; Rare:62 |