| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22088010-22088260 | Common:5; Rare:36 | ||||
| chr18:22166618-22166754 | Common:2; Rare:17 | ||||
| chr18:22168067-22168322 | Common:4; Rare:42 | ||||
| chr18:22168329-22168680 | Rare:76 | ||||
| chr18:22174994-22175276 | Rare:55 | ||||
| chr18:22176709-22177027 | Common:1; Rare:74; Clinvar:1 | ||||
| chr18:22181203-22181585 | Rare:77; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr18:22190603-22191133 | Common:1; Rare:101 | ||||
| chr18:22197961-22198102 | Common:3; Rare:26 | ||||
| chr18:23214225-23214369 | Rare:22 | ||||
| chr18:23474810-23475102 | Rare:57 | ||||
| chr18:23508088-23508222 | Common:1; Rare:27 | ||||
| chr18:23526108-23526265 | Rare:24 | ||||
| chr18:31101230-31101355 | Common:3; Rare:27 | ||||
| chr18:32111662-32111830 | Common:2; Rare:34 |