| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46086149-46086471 | Common:4; Rare:76; Clinvar (benign):1 | ||||
| chr18:46098314-46098568 | Common:7; Rare:55 | ||||
| chr18:46104222-46104427 | Common:3; Rare:61 | ||||
| chr18:46173728-46174135 | Common:2; Rare:93 | ||||
| chr18:46917329-46917624 | Common:1; Rare:122 | ||||
| chr18:47150445-47150544 | Common:2; Rare:37 | ||||
| chr18:47930356-47930679 | Common:1; Rare:144 | ||||
| chr18:49460534-49460856 | Common:2; Rare:97; Clinvar:6; Clinvar (benign):1 | ||||
| chr18:49492261-49492570 | Common:2; Rare:124 | ||||
| chr18:49813485-49814291 | Common:3; Rare:266 | ||||
| chr18:50281422-50281558 | Rare:52 | ||||
| chr18:50878963-50879299 | Common:4; Rare:110 | ||||
| chr18:51030029-51030265 | Rare:86; Clinvar:2 | ||||
| chr18:54224029-54224205 | Rare:55 | ||||
| chr18:54270046-54270256 | Common:2; Rare:56 |