| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:7117787-7117931 | Common:3; Rare:42 | ||||
| chr18:9102489-9102765 | Common:2; Rare:109; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136603-9137067 | Common:1; Rare:175 | ||||
| chr18:9708132-9708408 | Common:2; Rare:79 | ||||
| chr18:9914207-9914308 | Rare:52 | ||||
| chr18:11851308-11851446 | Rare:46 | ||||
| chr18:11908257-11908404 | Rare:41 | ||||
| chr18:12307978-12308319 | Common:5; Rare:134 | ||||
| chr18:12407817-12407978 | Common:5; Rare:74 | ||||
| chr18:12702658-12703104 | Common:3; Rare:179 | ||||
| chr18:12884156-12884429 | Common:4; Rare:134 | ||||
| chr18:12947673-12948061 | Common:3; Rare:100 | ||||
| chr18:12991137-12991390 | Common:1; Rare:91 | ||||
| chr18:13218684-13218790 | Common:1; Rare:20 | ||||
| chr18:13726484-13726720 | Common:3; Rare:90 |