| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:44682970-44683330 | Rare:45 | ||||
| chr18:44731620-44732160 | Common:5; Rare:100 | ||||
| chr18:44916400-44916790 | Common:2; Rare:78 | ||||
| chr18:45016600-45017040 | Common:12; Rare:79 | ||||
| chr18:45359370-45359830 | Common:1; Rare:91 | ||||
| chr18:45694870-45695190 | Common:7; Rare:69 | ||||
| chr18:45782697-45783390 | Common:10; Rare:315 | ||||
| chr18:45793260-45793750 | Common:4; Rare:155 | ||||
| chr18:45802500-45803524 | Common:21; Rare:425 | ||||
| chr18:45836101-45836550 | Common:6; Rare:116 | ||||
| chr18:45839450-45839810 | Common:1; Rare:60 | ||||
| chr18:45840670-45840920 | Common:1; Rare:31 | ||||
| chr18:46068857-46069142 | Common:4; Rare:44 | ||||
| chr18:46089351-46090248 | Common:15; Rare:478; Clinvar (benign):9 | ||||
| chr18:46208855-46209007 | Common:1; Rare:21 |