| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36187415-36187557 | Common:4; Rare:54 | ||||
| chr18:36828752-36829140 | Common:3; Rare:143 | ||||
| chr18:45967265-45967503 | Rare:84 | ||||
| chr18:46098218-46098592 | Common:11; Rare:108; Clinvar (benign):6 | ||||
| chr18:46104135-46104405 | Common:4; Rare:78; Clinvar (benign):1 | ||||
| chr18:46173819-46174104 | Common:2; Rare:68 | ||||
| chr18:49460621-49460814 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49487198-49487328 | Common:2; Rare:48 | ||||
| chr18:49561879-49562076 | Rare:51 | ||||
| chr18:49813825-49814103 | Common:1; Rare:120 | ||||
| chr18:50374909-50375137 | Common:2; Rare:71 | ||||
| chr18:50878939-50879239 | Common:4; Rare:101 | ||||
| chr18:50967923-50968054 | Rare:41 | ||||
| chr18:51030064-51030222 | Rare:51 | ||||
| chr18:54357856-54357977 | Common:6; Rare:37 |