| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:267396-267671 | Common:3; Rare:104 | ||||
| chr18:267690-267890 | Common:2; Rare:93 | ||||
| chr18:267938-268288 | Common:3; Rare:265 | ||||
| chr18:596684-597100 | Common:42; Rare:358 | ||||
| chr18:657364-657818 | Common:31; Rare:319 | ||||
| chr18:658051-658594 | Common:16; Rare:301 | ||||
| chr18:667714-668715 | Common:24; Rare:343 | ||||
| chr18:712515-712911 | Common:9; Rare:440 | ||||
| chr18:812172-813141 | Common:15; Rare:582 | ||||
| chr18:2570560-2571044 | Common:2; Rare:125 | ||||
| chr18:2571171-2571640 | Common:15; Rare:302 | ||||
| chr18:2655465-2656200 | Common:21; Rare:602; Clinvar:6; Clinvar (benign):1 | ||||
| chr18:3012220-3012915 | Common:14; Rare:329 | ||||
| chr18:3013051-3013636 | Common:9; Rare:316 | ||||
| chr18:3247064-3247734 | Common:14; Rare:346 |