| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:9913923-9914292 | Common:1; Rare:142 | ||||
| chr18:11851246-11851446 | Common:1; Rare:71 | ||||
| chr18:11908276-11908404 | Rare:35 | ||||
| chr18:12702658-12703104 | Common:3; Rare:179 | ||||
| chr18:12947674-12948061 | Common:3; Rare:99 | ||||
| chr18:13726441-13726718 | Common:3; Rare:109 | ||||
| chr18:22933277-22933408 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:22933768-22933889 | Common:1; Rare:47 | ||||
| chr18:23453176-23453353 | Rare:61 | ||||
| chr18:24397733-24398088 | Common:2; Rare:122 | ||||
| chr18:28176973-28177114 | Common:3; Rare:76 | ||||
| chr18:31498069-31498259 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):5 | ||||
| chr18:34976930-34977058 | Common:1; Rare:23 | ||||
| chr18:35240917-35241064 | Common:2; Rare:48 | ||||
| chr18:35290193-35290384 | Common:2; Rare:68 |