| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:44680696-44681030 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967243-45967465 | Rare:83 | ||||
| chr18:46098218-46098538 | Common:11; Rare:99; Clinvar (benign):6 | ||||
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46917321-46917611 | Common:1; Rare:118 | ||||
| chr18:47150419-47150554 | Common:4; Rare:51 | ||||
| chr18:49487049-49487302 | Common:3; Rare:92 | ||||
| chr18:49813825-49814317 | Common:2; Rare:195 | ||||
| chr18:50281426-50281835 | Common:3; Rare:127 | ||||
| chr18:50878948-50879264 | Common:4; Rare:105 | ||||
| chr18:51030056-51030233 | Rare:58 | ||||
| chr18:54357856-54357936 | Common:2; Rare:25 | ||||
| chr18:55589713-55589992 | Common:2; Rare:90 | ||||
| chr18:56651133-56651388 | Common:3; Rare:63 | ||||
| chr18:56651466-56651714 | Common:4; Rare:55 |